| Tag
secuence |
ORF |
Gene |
ORF PID number |
ORF COG ID |
Exponencial |
Early |
Late |
No of Ocurrence |
No of anotations |
Cromosome |
First C tag position |
Last C tag position |
Strand |
First C ORF position |
Last C ORF position |
Strand ORF |
Total number of AAs |
Description |
Cluster |
| CATGGTTATGCAAC |
YKL175W |
ZRT3 |
6322673 |
COG0428 |
9 |
21 |
0 |
2 |
1 |
11 |
119238 |
119251 |
+ |
118798 |
120808 |
+ |
503 |
Zrt3p |
9 |
| CATGTGCCAAGGAT |
YER033C |
ZRG8 |
6320871 |
- |
3 |
0 |
3 |
2 |
1 |
5 |
217939 |
217952 |
- |
217557 |
221286 |
- |
1076 |
Zinc regulated gene |
8 |
| CATGACTATCGAAG |
YGR211W |
ZPR1 |
6321650 |
COG1779 |
0 |
0 |
6 |
1 |
1 |
7 |
916628 |
916641 |
+ |
915244 |
917042 |
+ |
486 |
Involved in nucleolar function; similar to murine ZPR1
protein |
3 |
| CATGATGAAGAAAC |
YML109W |
ZDS2 |
6323527 |
- |
0 |
0 |
17 |
2 |
1 |
13 |
52089 |
52102 |
+ |
51640 |
54792 |
+ |
942 |
multicopy suppressor of a sin4 defect |
3 |
| CATGCTTAATCGAA |
YGR270W |
YTA7 |
6321709 |
COG0464 |
3 |
0 |
3 |
1 |
1 |
7 |
1031368 |
1031381 |
+ |
1027375 |
1031795 |
+ |
1379 |
Protein of unknown function, member of CDC48/PAS1/SEC18
family of ATPases, potentially phosphorylated by Cdc28p |
8 |
| CATGGCCAAGCAAT |
YBR111C |
YSA1 |
6319587 |
COG0494 |
9 |
12 |
0 |
2 |
1 |
2 |
461147 |
461160 |
- |
460635 |
461829 |
- |
231 |
Protein with weak homology to D. melanogaster serendipity
protein and X. laevis basis fibroblast growth factor |
6 |
| CATGTTGGTCCAGT |
YBR054W |
YRO2 |
6319528 |
- |
24 |
30 |
10 |
1 |
1 |
2 |
343894 |
343907 |
+ |
343061 |
344594 |
+ |
344 |
Putative plasma membrane protein of unknown function,
transcriptionally regulated by Haa1p; green fluorescent protein (GFP)-fusion
protein localizes to the cell periphery and bud |
5 |
| CATGCTGATGGTAG |
YPL283C |
YRF1-7 |
6324972 |
COG0513 |
9 |
4 |
3 |
18 |
1 |
16 |
371 |
384 |
- |
-219 |
6007 |
- |
1859 |
Helicase encoded by the Y' element of subtelomeric
regions, highly expressed in the mutants lacking the telomerase component
TLC1; potentially phosphorylated by Cdc28p |
8 |
| CATGCTGATGGTAG |
YNL339C |
YRF1-6 |
6323990 |
COG0513 |
9 |
4 |
3 |
18 |
1 |
14 |
462 |
475 |
- |
-128 |
6098 |
- |
1859 |
Helicase encoded by the Y' element of subtelomeric
regions, highly expressed in the mutants lacking the telomerase component
TLC1; potentially phosphorylated by Cdc28p |
8 |
| CATGCTGATGGTAG |
YLR467W |
YRF1-5 |
6323500 |
COG0513 |
9 |
4 |
3 |
18 |
1 |
12 |
1077786 |
1077799 |
+ |
1072505 |
1078394 |
+ |
1796 |
Helicase encoded by the Y' element of subtelomeric
regions, highly expressed in the mutants lacking the telomerase component
TLC1; potentially phosphorylated by Cdc28p |
8 |
| CATGCTGATGGTAG |
YLR466W |
YRF1-4 |
6323498 |
COG0513 |
9 |
4 |
3 |
18 |
1 |
12 |
1071123 |
1071136 |
+ |
1067084 |
1071731 |
+ |
1382 |
Helicase encoded by the Y' element of subtelomeric
regions, highly expressed in the mutants lacking the telomerase component
TLC1; potentially phosphorylated by Cdc28p |
8 |
| CATGCTGATGGTAG |
YGR296W |
YRF1-3 |
6321735 |
COG0513 |
9 |
4 |
3 |
18 |
1 |
7 |
1090490 |
1090503 |
+ |
1084869 |
1091095 |
+ |
1859 |
Helicase encoded by the Y' element of subtelomeric
regions, highly expressed in the mutants lacking the telomerase component
TLC1; potentially phosphorylated by Cdc28p |
8 |
| CATGCTGATGGTAG |
YER190W |
YRF1-2 |
6321038 |
COG0513 |
9 |
4 |
3 |
18 |
1 |
5 |
576414 |
576427 |
+ |
571475 |
577019 |
+ |
1681 |
Helicase encoded by the Y' element of subtelomeric
regions, highly expressed in the mutants lacking the telomerase component
TLC1; potentially phosphorylated by Cdc28p |
8 |
| CATGCTGATGGTAG |
YDR545W |
YRF1-1 |
6320754 |
COG0513 |
9 |
4 |
3 |
18 |
1 |
4 |
1531583 |
1531596 |
+ |
1526302 |
1532191 |
+ |
1796 |
Helicase encoded by the Y' element of subtelomeric
regions, highly expressed in the mutants lacking the telomerase component
TLC1; potentially phosphorylated by Cdc28p |
8 |
| CATGAATATATATA |
YKR014C |
YPT52 |
6322866 |
COG1100 |
6 |
4 |
0 |
4 |
1 |
11 |
464843 |
464856 |
- |
464511 |
465714 |
- |
234 |
rab5-like GTPase involved in vacuolar protein sorting and
endocytosis |
8 |
| CATGTGAATGACTC |
YER031C |
YPT31 |
6320869 |
COG1100 |
6 |
0 |
0 |
1 |
1 |
5 |
214032 |
214045 |
- |
213576 |
214746 |
- |
223 |
probably involved in intra-Golgi transport or in the
formation of transport vesicles at the most distal Golgi compartment |
8 |
| CATGTAACTCGTAT |
YDR349C |
YPS7 |
6320556 |
- |
0 |
0 |
6 |
1 |
1 |
4 |
1172424 |
1172437 |
- |
1171877 |
1174166 |
- |
596 |
Gpi-anchored aspartic protease (Yapsin 7) |
3 |
| CATGGTACAAAGAG |
YDR368W |
YPR1 |
6320576 |
COG0656 |
3 |
0 |
3 |
1 |
1 |
4 |
1214773 |
1214786 |
+ |
1213892 |
1215329 |
+ |
312 |
homologous to the aldo-keto reductase protein family |
8 |
| CATGTACAATATAT |
YDL235C |
YPD1 |
6319966 |
COG2198 |
3 |
4 |
0 |
1 |
1 |
4 |
33347 |
33360 |
- |
32916 |
33918 |
- |
167 |
Ypd1p is an intermediate protein between Sln1p and Ssk1p
in the phosphorelay reaction. |
8 |
| CATGTCCGAATATG |
YPR028W |
YOP1 |
6325285 |
COG5052 |
3 |
12 |
0 |
1 |
1 |
16 |
623520 |
623533 |
+ |
623522 |
624696 |
+ |
180 |
Ypt Interacting Protein. Regulates vesicular traffic in
stressed cells either to facilitate membrane turnover or to decrease
unnecessary secretion. |
9 |
| CATGTTCCCTCACT |
YKL067W |
YNK1 |
6322783 |
COG0105 |
3 |
0 |
31 |
1 |
1 |
11 |
314982 |
314995 |
+ |
314457 |
315417 |
+ |
153 |
catalyzes the phosphorylation of nucleoside diphosphates
into the corresponding triphosphates for nucleic acid biosynthesis. |
2 |
| CATGGATAGCGCTG |
YHR090C |
YNG2 |
6321882 |
COG5034 |
0 |
4 |
10 |
1 |
1 |
8 |
284238 |
284251 |
- |
283300 |
284626 |
- |
282 |
Yeast homolog of mammalian Ing1 |
8 |
| CATGCGGGTCATCA |
YOR064C |
YNG1 |
6324638 |
COG5034 |
9 |
0 |
6 |
1 |
1 |
15 |
445991 |
446004 |
- |
445581 |
446739 |
- |
219 |
Yeast homolog of mammalian Ing1 |
8 |
| CATGGTGAAGGATA |
YFR049W |
YMR31 |
14318574 |
- |
6 |
17 |
0 |
2 |
1 |
6 |
248873 |
248886 |
+ |
248510 |
249380 |
+ |
123 |
Mitochondrial ribosomal protein of the small subunit, has
similarity to human mitochondrial ribosomal protein MRP-S36 |
9 |
| CATGTAGATGCATC |
YKL196C |
YKT6 |
6322652 |
COG5143 |
0 |
4 |
20 |
1 |
1 |
11 |
74929 |
74942 |
- |
74438 |
75539 |
- |
200 |
Synaptobrevin (v-SNARE) homolog with similarity to
Sec22p, Snc1p, and Snc2p, essential for endoplasmic reticulum-Golgi transport |
2 |
| CATGCATCATTGAT |
YNL044W |
YIP3 |
6681850 |
COG5130 |
0 |
0 |
24 |
1 |
1 |
14 |
545818 |
545831 |
+ |
545266 |
546374 |
+ |
176 |
Interacts with YPT proteins |
2 |
| CATGCGACGGGAGT |
YCR059C |
YIH1 |
6319904 |
COG1739 |
3 |
12 |
0 |
1 |
1 |
3 |
223397 |
223410 |
- |
223224 |
224225 |
- |
258 |
piecemeal microautophagy of the nucleus (PMN) |
9 |
| CATGAGACCATTGC |
YGR234W |
YHB1 |
6321673 |
COG1017 |
3 |
12 |
0 |
1 |
1 |
7 |
961214 |
961227 |
+ |
959906 |
961604 |
+ |
399 |
may play a role in the oxidative stress response |
9 |
| CATGAACTGATAGA |
YNL160W |
YGP1 |
6324169 |
COG0252 |
30 |
30 |
6 |
1 |
1 |
14 |
337604 |
337617 |
+ |
336545 |
338108 |
+ |
354 |
may be involved in cellular adaptations prior to
stationary phase |
5 |
| CATGGCAAAGACCT |
YLR249W |
YEF3 |
6323278 |
COG0488 |
6 |
4 |
0 |
1 |
1 |
12 |
639512 |
639525 |
+ |
636782 |
640318 |
+ |
1044 |
contains two ABC cassettes, and binds and hydrolyses ATP |
8 |
| CATGTTTCTGGTGA |
YNL064C |
YDJ1 |
6324265 |
COG0484 |
3 |
0 |
17 |
1 |
1 |
14 |
506223 |
506236 |
- |
505367 |
507095 |
- |
409 |
yeast dnaJ homolog (nuclear envelope protein); heat shock
protein |
3 |
| CATGTCGGCGGCAC |
YPL087W |
YDC1 |
6325170 |
- |
0 |
0 |
10 |
1 |
1 |
16 |
384734 |
384747 |
+ |
383450 |
384902 |
+ |
317 |
Yeast dihydro-ceramidase |
3 |
| CATGACTTGATATA |
YHR135C |
YCK1 |
6321927 |
COG0515 |
0 |
8 |
0 |
1 |
1 |
8 |
373754 |
373767 |
- |
372196 |
374311 |
- |
538 |
membrane-bound casein kinase I homolog |
8 |
| CATGTGTGAGCATA |
YLL048C |
YBT1 |
6322980 |
COG1132 |
12 |
0 |
0 |
1 |
1 |
12 |
41352 |
41365 |
- |
40780 |
46264 |
- |
1661 |
Yeast bile transporter, similar to mammalian bile
transporter |
6 |
| CATGAAGCTATAAG |
YDR259C |
YAP6 |
6320465 |
- |
3 |
0 |
3 |
2 |
1 |
4 |
974911 |
974924 |
- |
974236 |
975774 |
- |
383 |
bZIP protein |
8 |
| CATGCGGCGGTTCT |
YPL252C |
YAH1 |
6325004 |
COG0633 |
6 |
0 |
0 |
1 |
1 |
16 |
73578 |
73591 |
- |
73007 |
73881 |
- |
172 |
Yeast Adrenodoxin Homologue 1; This protein is targeted
to the mitochondrial matrix as shown by using a specific polyclonal antibody |
8 |
| CATGACAATGCCCT |
YGR194C |
XKS1 |
6321633 |
COG1070 |
3 |
0 |
10 |
1 |
1 |
7 |
885964 |
885977 |
- |
885745 |
887878 |
- |
600 |
third enzyme in the xylose pathway |
8 |
| CATGCTAAACGCGC |
YOR230W |
WTM1 |
6324804 |
COG2319 |
6 |
4 |
0 |
1 |
1 |
15 |
772117 |
772130 |
+ |
770800 |
772600 |
+ |
437 |
WD repeat containing transcriptional modulator 1 |
8 |
| CATGTGGACTTGGA |
YNL283C |
WSC2 |
6324046 |
- |
0 |
0 |
6 |
1 |
1 |
14 |
105614 |
105627 |
- |
104683 |
106693 |
- |
503 |
cell wall integrity and stress response component 2 |
3 |
| CATGTCAAGGAACT |
YMR197C |
VTI1 |
6323853 |
- |
0 |
0 |
10 |
1 |
1 |
13 |
658485 |
658498 |
- |
658045 |
659197 |
- |
217 |
Involved in cis-Golgi membrane traffic |
3 |
| CATGAAGATTCCAT |
YJL222W |
VTH2 |
6322239 |
- |
3 |
0 |
3 |
3 |
1 |
10 |
12377 |
12390 |
+ |
11475 |
16623 |
+ |
1549 |
vps ten homolog |
8 |
| CATGAAGATTCCAT |
YIL173W |
VTH1 |
6322020 |
- |
3 |
0 |
3 |
3 |
1 |
9 |
12394 |
12407 |
+ |
11492 |
16640 |
+ |
1549 |
vps ten homolog |
8 |
| CATGGCACTCTAAT |
YJR126C |
VPS70 |
6322586 |
- |
3 |
8 |
0 |
1 |
1 |
10 |
656594 |
656607 |
- |
655879 |
658604 |
- |
811 |
Vps70p |
8 |
| CATGCACAGTTTCC |
YHR012W |
VPS29 |
6321800 |
COG0622 |
0 |
8 |
0 |
1 |
1 |
8 |
130579 |
130592 |
+ |
129474 |
130940 |
+ |
282 |
vacuolar protein sorting |
8 |
| CATGGAACGGCGAA |
YPL045W |
VPS16 |
6325212 |
- |
3 |
0 |
3 |
1 |
1 |
16 |
469756 |
469769 |
+ |
467255 |
469933 |
+ |
798 |
vacuolar sorting protein |
8 |
| CATGGAAGTCGCTG |
YOR270C |
VPH1 |
6324844 |
COG1269 |
3 |
4 |
0 |
1 |
1 |
15 |
828080 |
828093 |
- |
827550 |
830571 |
- |
840 |
vacuolar ATPase V0 domain subunit a (100 kDa) |
8 |
| CATGATCGTGATAA |
YLR447C |
VMA6 |
6323480 |
COG1527 |
9 |
0 |
0 |
1 |
1 |
12 |
1027530 |
1027543 |
- |
1026353 |
1027889 |
- |
345 |
vacuolar ATPase V0 domain subunit d (36 kDa) |
8 |
| CATGCTTTCGCAAC |
YOR332W |
VMA4 |
6324907 |
COG1390 |
9 |
0 |
0 |
1 |
1 |
15 |
943856 |
943869 |
+ |
943651 |
944590 |
+ |
233 |
vacuolar ATPase V1 domain subunit E (27 kDa) |
8 |
| CATGGAGTTGCTGA |
YPR036W |
VMA13 |
6325293 |
COG5231 |
6 |
4 |
0 |
1 |
1 |
16 |
645179 |
645192 |
+ |
643831 |
645766 |
+ |
478 |
vacuolar ATPase V1 domain subunit H (54 kDa) |
8 |
| CATGTCTATGTCTA |
YBR105C |
VID24 |
6319581 |
COG5073 |
3 |
8 |
0 |
1 |
1 |
2 |
450646 |
450659 |
- |
450339 |
451926 |
- |
362 |
also involved in vacuolar protein targeting |
8 |
| CATGGTGGTATTGC |
YOR106W |
VAM3 |
6324680 |
COG5325 |
3 |
4 |
0 |
1 |
1 |
15 |
519941 |
519954 |
+ |
519121 |
520471 |
+ |
283 |
Syntaxin-related protein; required for vacuolar assembly;
PEP12 homolog |
8 |
| CATGTTAATGGTAT |
YEL005C |
VAB2 |
6320832 |
- |
3 |
4 |
0 |
1 |
1 |
5 |
145880 |
145893 |
- |
145407 |
146754 |
- |
282 |
Protein with a potential role in vacuolar function, as
suggested by its ability to bind Vac8p; green fluorescent protein
(GFP)-fusion protein localizes to the cytoplasm in a punctate pattern |
8 |
| CATGCATATAAAAA |
YEL040W |
UTR2 |
6320795 |
COG2273 |
6 |
0 |
0 |
1 |
1 |
5 |
79550 |
79563 |
+ |
78053 |
79955 |
+ |
467 |
(alias: Congo Red Hypersensitivity) |
8 |
| CATGATGTTTTCTT |
YJR049C |
UTR1 |
6322509 |
COG0061 |
9 |
0 |
0 |
1 |
1 |
10 |
527779 |
527792 |
- |
526299 |
528390 |
- |
530 |
associated with ferric reductase |
8 |
| CATGGTCGTTCCTA |
YKR042W |
UTH1 |
6322895 |
- |
9 |
12 |
0 |
1 |
1 |
11 |
519857 |
519870 |
+ |
518914 |
520765 |
+ |
450 |
Youth, involved in determining yeast longevity |
9 |
| CATGGTATTGATTT |
YNR012W |
URK1 |
6324339 |
COG0572 |
0 |
0 |
6 |
2 |
1 |
14 |
648738 |
648751 |
+ |
647431 |
649435 |
+ |
501 |
converts ATP and uridine to ADP and UMP |
3 |
| CATGAGAGACATCG |
YJR103W |
URA8 |
6322563 |
COG0504 |
0 |
8 |
0 |
1 |
1 |
10 |
622122 |
622135 |
+ |
620668 |
622861 |
+ |
564 |
Last step in pyrimidine biosynthesis pathway |
8 |
| CATGGGATATAAAT |
YJL130C |
URA2 |
6322331 |
COG0458 |
9 |
0 |
0 |
3 |
1 |
10 |
168117 |
168130 |
- |
165267 |
172285 |
- |
2214 |
First and second steps of pyrimidine biosynthesis |
8 |
| CATGGACCATTTGA |
YMR271C |
URA10 |
6323927 |
COG0461 |
9 |
4 |
0 |
1 |
1 |
13 |
806836 |
806849 |
- |
806423 |
807547 |
- |
227 |
Fifth step in pyrimidine bio5 |
8 |
| CATGGTAGGTGATG |
YBR173C |
UMP1 |
6319650 |
- |
3 |
4 |
10 |
1 |
1 |
2 |
581720 |
581733 |
- |
581330 |
582129 |
- |
148 |
Involved in ubiquitin-mediated proteolysis |
8 |
| CATGGTTTTCTTGG |
YPL186C |
UIP4 |
6325071 |
- |
6 |
4 |
0 |
3 |
1 |
16 |
194546 |
194559 |
- |
194012 |
195425 |
- |
304 |
Ulp1 Interacting Protein 4 |
8 |
| CATGTCGTTATCGC |
YDL170W |
UGA3 |
6320031 |
- |
3 |
0 |
6 |
2 |
1 |
4 |
156893 |
156906 |
+ |
156319 |
158404 |
+ |
528 |
Transcriptional activator necessary for
gamma-aminobutyrate (GABA)-dependent induction of GABA genes (such as UGA1,
UGA2, UGA4) |
8 |
| CATGATTCGTCCAA |
YGR048W |
UFD1 |
6321485 |
COG5140 |
0 |
0 |
6 |
1 |
1 |
7 |
590856 |
590869 |
+ |
589828 |
591315 |
+ |
361 |
Ubiquitin fusion degradation protein |
3 |
| CATGGACAGATACG |
YOR124C |
UBP2 |
6324698 |
- |
3 |
4 |
0 |
1 |
1 |
15 |
555398 |
555411 |
- |
554571 |
558642 |
- |
1272 |
Ubiquitin-specific protease |
8 |
| CATGGCCACTGGTA |
YNL186W |
UBP10 |
6324143 |
- |
3 |
0 |
3 |
1 |
1 |
14 |
291734 |
291747 |
+ |
289498 |
292375 |
+ |
792 |
involved in telomeric silencing |
8 |
| CATGGTCGCCTTTA |
YEL012W |
UBC8 |
6579192 |
COG5078 |
6 |
4 |
6 |
1 |
1 |
5 |
132168 |
132181 |
+ |
131772 |
133050 |
+ |
218 |
Ubiquitin-conjugating enzyme that is able to ubiquitinate
histones in vitro |
8 |
| CATGGGACCTGCCG |
YBR082C |
UBC4 |
6319556 |
COG5078 |
12 |
4 |
27 |
1 |
1 |
2 |
406904 |
406917 |
- |
406086 |
407126 |
- |
148 |
One of several UBC genes encoding ubiquitin-conjugating
enzymes that attach ubiquitin to proteins. |
2 |
| CATGACGACAACTT |
YDR092W |
UBC13 |
6320297 |
COG5078 |
0 |
4 |
10 |
1 |
1 |
4 |
630218 |
630231 |
+ |
629870 |
631098 |
+ |
153 |
ubiquitin-conjugating enzyme |
8 |
| CATGTATAACGTGT |
YHR111W |
UBA4 |
6321903 |
COG0607 |
3 |
17 |
0 |
1 |
1 |
8 |
334406 |
334419 |
+ |
333074 |
334895 |
+ |
440 |
Protein that activates Urm1p before its conjugation to
proteins (urmylation); one target is the thioredoxin peroxidase Ahp1p,
suggesting a role of urmylation in the
oxidative stress response |
9 |
| CATGTATCTACAAT |
YKL210W |
UBA1 |
6322639 |
COG0476 |
9 |
0 |
0 |
1 |
1 |
11 |
42151 |
42164 |
+ |
39164 |
42737 |
+ |
1024 |
Ubiquitin activating enzyme, involved in
ubiquitin-mediated protein degradation and essential for viability |
8 |
| CATGACGAAATTCC |
YOR344C |
TYE7 |
6324920 |
- |
3 |
4 |
0 |
1 |
1 |
15 |
976825 |
976838 |
- |
976690 |
978064 |
- |
291 |
may be involved in glycolytic gene expression |
8 |
| CATGGTAACGCCTT |
YKL034W |
TUL1 |
6322817 |
- |
0 |
8 |
0 |
1 |
1 |
11 |
373642 |
373655 |
+ |
371472 |
374147 |
+ |
758 |
Transmembrane Ubiquitin Ligase |
8 |
| CATGCTATCCAACA |
YML124C |
TUB3 |
6323511 |
COG5023 |
3 |
4 |
0 |
1 |
1 |
13 |
22242 |
22255 |
- |
21701 |
23684 |
- |
445 |
Alpha-tubulin; associates with beta-tubulin (Tub2p) to
form tubulin dimer, which polymerizes to form microtubules; expressed at
lower level than Tub1p |
8 |
| CATGTAAATGGGTT |
YML100W |
TSL1 |
6323537 |
COG0380 |
3 |
8 |
0 |
1 |
1 |
13 |
73863 |
73876 |
+ |
70624 |
74419 |
+ |
1098 |
123 kD regulatory subunit of trehalose-6-phosphate
synthase/phosphatase complex; homologous to TPS3 gene product |
8 |
| CATGGAGGATAGAG |
YBR058C-A |
TSC3 |
14270689 |
- |
9 |
8 |
0 |
1 |
1 |
2 |
356194 |
356207 |
- |
355978 |
356526 |
- |
80 |
Involved in sphingolipid biosynthesis. Stimulates the
activity of serine palmitoyltransferase (LCB1, LCB2) several-fold. |
8 |
| CATGCCACCAATTA |
YDL015C |
TSC13 |
6320189 |
- |
3 |
4 |
0 |
1 |
1 |
4 |
425856 |
425869 |
- |
425500 |
426931 |
- |
310 |
ER protein involved in very long chain fatty acid
synthesis |
8 |
| CATGGTTGGCTGTT |
YBR265W |
TSC10 |
6319742 |
COG1028 |
3 |
0 |
13 |
2 |
1 |
2 |
739434 |
739447 |
+ |
738539 |
739797 |
+ |
320 |
catalyzes the second step in the synthesis of
phytosphingosine |
3 |
| CATGCAACTGGACC |
YDR453C |
TSA2 |
6320661 |
COG0450 |
0 |
12 |
0 |
1 |
1 |
4 |
1365128 |
1365141 |
- |
1364561 |
1365650 |
- |
196 |
thioredoxin peroxidase |
9 |
| CATGTAACTGGACT |
YML028W |
TSA1 |
6323613 |
COG0450 |
15 |
17 |
6 |
1 |
1 |
13 |
220645 |
220658 |
+ |
220138 |
221227 |
+ |
196 |
antioxidant enzyme that provides protection against
oxidation systems capable of generating reactive oxygen and sulfur species |
6 |
| CATGTTTACCAGTT |
YGR209C |
TRX2 |
6321648 |
COG0526 |
15 |
17 |
0 |
1 |
1 |
7 |
912869 |
912882 |
- |
912417 |
913230 |
- |
104 |
thioredoxin |
6 |
| CATGATGATGCTCT |
YHR099W |
TRA1 |
6321891 |
COG5032 |
3 |
0 |
3 |
1 |
1 |
8 |
313250 |
313263 |
+ |
302763 |
314496 |
+ |
3744 |
TRA1 is the homolog of the human protein TRRAP which we
have isolated as an essential cofactor of c-Myc. |
8 |
| CATGGGATATAAAT |
YMR261C |
TPS3 |
6323917 |
COG0380 |
9 |
0 |
0 |
3 |
1 |
13 |
791211 |
791224 |
- |
789839 |
793368 |
- |
1054 |
115 kD regulatory subunit of trehalose-6-phosphate
synthase/phosphatase complex |
8 |
| CATGCATTCAAACC |
YPR156C |
TPO3 |
6325414 |
COG0477 |
0 |
0 |
13 |
1 |
1 |
16 |
837787 |
837800 |
- |
837408 |
839771 |
- |
622 |
Polyamine transport protein |
3 |
| CATGGGCAAACGAA |
YNL079C |
TPM1 |
6324250 |
- |
3 |
12 |
0 |
1 |
1 |
14 |
478470 |
478483 |
- |
478066 |
479164 |
- |
199 |
Actin-binding protein that stabilizes actin filaments;
Tpm1, the main tropomyosin, is required for the formation and stability of
actin cables in vivo which direct polarized cell
growth and the distribution of several organelles. |
9 |
| CATGCATATATGTA |
YKL166C |
TPK3 |
6322682 |
COG0515 |
0 |
8 |
0 |
2 |
1 |
11 |
134364 |
134377 |
- |
134140 |
135710 |
- |
398 |
Involved in nutrient control of cell growth and division |
8 |
| CATGCCACAGTTAC |
YOL006C |
TOP1 |
6324568 |
COG3569 |
3 |
0 |
6 |
1 |
1 |
15 |
312930 |
312943 |
- |
312579 |
315387 |
- |
769 |
topoisomerase I |
8 |
| CATGTACATAAAGT |
YNL070W |
TOM7 |
6324259 |
- |
6 |
0 |
0 |
1 |
1 |
14 |
493638 |
493651 |
+ |
493365 |
494046 |
+ |
60 |
Involved in mitochondrial protein import |
8 |
| CATGCAACAAGGTA |
YGR082W |
TOM20 |
6321519 |
- |
9 |
0 |
0 |
1 |
1 |
7 |
644356 |
644369 |
+ |
644046 |
645096 |
+ |
183 |
Translocase of Outer Mitochondrial membrane |
8 |
| CATGTAATAATAAT |
YKL058W |
TOA2 |
6322792 |
COG5123 |
6 |
0 |
0 |
1 |
1 |
11 |
330369 |
330382 |
+ |
329811 |
330678 |
+ |
122 |
Transcription factor IIA, small chain |
8 |
| CATGGATATGTTAT |
YDR105C |
TMS1 |
6320310 |
- |
9 |
8 |
0 |
1 |
1 |
4 |
665414 |
665427 |
- |
664905 |
666764 |
- |
473 |
Putative membrane protein, conserved in mammals |
8 |
| CATGCTACTATGAT |
YOR009W |
TIR4 |
6324583 |
- |
0 |
0 |
13 |
1 |
1 |
15 |
345784 |
345797 |
+ |
344334 |
346296 |
+ |
487 |
Tir4p |
3 |
| CATGGTACTCCTCT |
YER011W |
TIR1 |
6320848 |
- |
18 |
0 |
0 |
1 |
1 |
5 |
175532 |
175545 |
+ |
175247 |
176510 |
+ |
254 |
Cold-shock induced protein of the Srp1p/Tip1p family of
serine-alanine-rich proteins. Encodes a stress-response cell wall
mannoprotein and this gene is downregulated at
acidic pH. |
6 |
| CATGGTACACCACA |
YBR067C |
TIP1 |
6319541 |
- |
64 |
25 |
131 |
1 |
1 |
2 |
372401 |
372414 |
- |
371564 |
372695 |
- |
210 |
cold- and heat-shock induced protein of the Srp1p/Tip1p
family of serine-alanine-rich proteins |
1 |
| CATGTAAATATAAA |
YEL020W-A |
TIM9 |
6320815 |
- |
3 |
4 |
0 |
3 |
1 |
5 |
117529 |
117542 |
+ |
117211 |
117973 |
+ |
87 |
Translocase in inner membrane of mitochondria involved in
mitochondrial protein import |
8 |
| CATGCACGATCGAC |
YJL054W |
TIM54 |
6322407 |
- |
9 |
0 |
0 |
1 |
1 |
10 |
335642 |
335655 |
+ |
334181 |
335813 |
+ |
478 |
Translocase Inner Membrane, 54kD |
8 |
| CATGGTTGGAGAAC |
YPL063W |
TIM50 |
6325194 |
COG5190 |
6 |
21 |
0 |
2 |
1 |
16 |
430563 |
430576 |
+ |
429934 |
431863 |
+ |
476 |
Protein of the inner mitochondrial membrane, required for
import of mitochondrial matrix proteins |
9 |
| CATGAACAACCAGC |
YGR181W |
TIM13 |
6321620 |
- |
6 |
4 |
3 |
1 |
1 |
7 |
858957 |
858970 |
+ |
858290 |
859106 |
+ |
105 |
Translocase of the inner membrane; mitochondrial
intermembrane space protein mediating import and insertion of polytopic inner
membrane proteins |
8 |
| CATGGCGTAAGATA |
YPR041W |
TIF5 |
6325298 |
COG1601 |
12 |
4 |
0 |
2 |
1 |
16 |
649958 |
649971 |
+ |
648699 |
650415 |
+ |
405 |
eIF5 mediates hydrolysis of eIF2-GTP (SUI2,SUI3,GCD11) at
start codons |
6 |
| CATGGTTCCATACA |
YLR237W |
THI7 |
6323266 |
COG1953 |
3 |
8 |
0 |
2 |
1 |
12 |
613951 |
613964 |
+ |
612369 |
614664 |
+ |
598 |
Thiamine Metabolism |
8 |
| CATGCTGCTGAGCA |
YGR144W |
THI4 |
6321583 |
COG1635 |
9 |
25 |
0 |
1 |
1 |
7 |
781343 |
781356 |
+ |
780402 |
781769 |
+ |
326 |
Protein highly expressed in early stationary phase during
growth on molasses |
9 |
| CATGGTGCCACGAA |
YPL258C |
THI21 |
6324997 |
COG0819 |
6 |
4 |
0 |
1 |
1 |
16 |
53638 |
53651 |
- |
52999 |
55153 |
- |
551 |
THI for thiamine metabolism. Transcribed in the presence
of low level of thiamine (10-8M) and turned off in the presence of high level
(10-6M) of thiamine. Under the positive control of
THI2 and THI3. |
8 |
| CATGGATGAAGGTG |
YOL055C |
THI20 |
6324517 |
COG0819 |
0 |
8 |
0 |
1 |
1 |
15 |
224542 |
224555 |
- |
223919 |
226073 |
- |
551 |
THI for thiamine metabolism. Transcribed in the presence
of low level of thiamine (10-8M) and turned off in the presence of high level
(10-6M) of thiamine. Under the positive control of
THI2 and THI3. |
8 |
| CATGGCCCGCACTA |
YMR313C |
TGL3 |
6323973 |
COG1752 |
3 |
0 |
6 |
1 |
1 |
13 |
899449 |
899462 |
- |
898879 |
901306 |
- |
642 |
Triacylglycerol lipase of the lipid particle |
8 |
| CATGGGTAACACGC |
YLR178C |
TFS1 |
6323207 |
COG1881 |
36 |
12 |
13 |
1 |
1 |
12 |
513669 |
513682 |
- |
512665 |
513823 |
- |
219 |
Carboxypeptidase Y inhibitor |
5 |
| CATGCACTTGAGTT |
YPL234C |
TFP3 |
6325022 |
COG0636 |
3 |
12 |
0 |
1 |
1 |
16 |
105139 |
105152 |
- |
104447 |
105440 |
- |
164 |
vacuolar ATPase V0 domain subunit c' (17 kDa) |
9 |
| CATGATTCCTGCTG |
YGR186W |
TFG1 |
6321625 |
- |
0 |
0 |
6 |
1 |
1 |
7 |
868930 |
868943 |
+ |
867777 |
870483 |
+ |
735 |
Largest subunit of the RNA Polymerase general
transcription factor IIF (TFIIF), interacts with Fcp1p phosphatase and with
TFIIB; potentially phosphorylated by Cdc28p |
3 |
| CATGCACGTTAGGG |
YKR062W |
TFA2 |
6322915 |
COG5174 |
6 |
4 |
6 |
1 |
1 |
11 |
560356 |
560369 |
+ |
559308 |
560793 |
+ |
328 |
TFIIE small subunit, involved in RNA polymerase II
transcription initiation |
8 |
| CATGCCAAACATAA |
YBL088C |
TEL1 |
6319383 |
COG5032 |
3 |
4 |
0 |
1 |
1 |
2 |
54098 |
54111 |
- |
50517 |
59379 |
- |
2787 |
Protein kinase, primarily involved in telomere length
regulation; contributes to cell cycle checkpoint control in response to DNA
damage; functionally redundant with Mec1p; homolog
of human ataxia telangiectasia (ATM) gene |
8 |
| CATGTGGGCTTGGG |
YKL081W |
TEF4 |
6322769 |
COG0625 |
3 |
4 |
0 |
1 |
1 |
11 |
284024 |
284037 |
+ |
282536 |
284599 |
+ |
412 |
Translation elongation factor EF-1gamma |
8 |
| CATGAGACAAACTG |
YBR118W |
TEF2 |
6319594 |
COG5256 |
61 |
55 |
193 |
2 |
1 |
2 |
478903 |
478916 |
+ |
477627 |
479293 |
+ |
458 |
translational elongation factor EF-1 alpha |
11 |
| CATGAGACAAACTG |
YPR080W |
TEF1 |
6325337 |
COG5256 |
61 |
55 |
193 |
2 |
1 |
16 |
701866 |
701879 |
+ |
700590 |
702465 |
+ |
458 |
translational elongation factor EF-1 alpha |
11 |
| CATGGGTGTTAACG |
YGR192C |
TDH3 |
6321631 |
COG0057 |
33 |
25 |
0 |
2 |
1 |
7 |
883410 |
883423 |
- |
882316 |
883813 |
- |
332 |
Glyceraldehyde-3-phosphate dehydrogenase 3 |
5 |
| CATGACCGCCACCC |
YJR009C |
TDH2 |
6322468 |
COG0057 |
6 |
0 |
3 |
1 |
1 |
10 |
454048 |
454061 |
- |
453098 |
454595 |
- |
332 |
glyceraldehyde 3-phosphate dehydrogenase |
8 |
| CATGACCGCCACTC |
YJL052W |
TDH1 |
6322409 |
COG0057 |
98 |
163 |
103 |
1 |
1 |
10 |
338719 |
338732 |
+ |
338187 |
339684 |
+ |
332 |
Glyceraldehyde-3-phosphate dehydrogenase 1 |
10 |
| CATGTACTTCTATA |
YPL180W |
TCO89 |
6325077 |
- |
0 |
8 |
0 |
1 |
1 |
16 |
207774 |
207787 |
+ |
205247 |
208145 |
+ |
799 |
Tor Complex One, 89 kDa subunit |
8 |
| CATGTTGCCTTTCT |
YIL129C |
TAO3 |
6322062 |
- |
0 |
8 |
0 |
1 |
1 |
9 |
110843 |
110856 |
- |
105608 |
113237 |
- |
2376 |
Identified in a hunt for mutants that activate OCH1
transcription |
8 |
| CATGTACACAAGTA |
YLR354C |
TAL1 |
6323386 |
COG0176 |
18 |
0 |
0 |
1 |
1 |
12 |
836267 |
836280 |
- |
835850 |
837356 |
- |
335 |
Transaldolase, enzyme in the pentose phosphate pathway |
6 |
| CATGTACAAAGAGA |
YJR046W |
TAH11 |
6322506 |
- |
0 |
0 |
6 |
1 |
1 |
10 |
523370 |
523383 |
+ |
521962 |
524275 |
+ |
604 |
Essential protein. |
3 |
| CATGATATTTGCTA |
YIL047C |
SYG1 |
6322142 |
COG5409 |
0 |
4 |
6 |
1 |
1 |
9 |
265088 |
265101 |
- |
264615 |
267822 |
- |
902 |
Protein for which truncation and overexpression can
suppress lethality of G-alpha protein deficiency |
8 |
| CATGTGCATATATG |
YBR111W-A |
SUS1 |
41629677 |
- |
9 |
4 |
10 |
2 |
1 |
2 |
462663 |
462676 |
+ |
462095 |
463034 |
+ |
96 |
Protein involved in mRNA export coupled transcription
activation; component of the SAGA histone acetylase complex |
8 |
| CATGAAGACTGTCG |
YDR297W |
SUR2 |
6320503 |
COG3000 |
6 |
4 |
0 |
1 |
1 |
4 |
1057267 |
1057280 |
+ |
1056543 |
1058091 |
+ |
349 |
Possibly hydroxylates ceramide-1 at C-4 to give
ceramide-2. Or, hydroxylates DHS at C-4 to give PHS, which is acylated to
give ceramide-2. Not yet clear whether DHS or
ceramide-1 is the preferred substrate. |
8 |
| CATGTTACAATTTA |
YPL057C |
SUR1 |
6325200 |
COG3774 |
6 |
4 |
24 |
1 |
1 |
16 |
451614 |
451627 |
- |
451405 |
453052 |
- |
382 |
Probable catalytic subunit of a mannosylinositol
phosphorylceramide (MIPC) synthase, forms a complex with probable regulatory
subunit Csg2p; function in sphingolipid biosynthesis
is overlapping with that of Csh1p |
2 |
| CATGGGTTTTAAGT |
YNL244C |
SUI1 |
6324085 |
COG0023 |
0 |
8 |
10 |
1 |
1 |
14 |
187166 |
187179 |
- |
186885 |
187495 |
- |
108 |
translation initiation factor eIF1 |
8 |
| CATGACAGCAAACG |
YIR011C |
STS1 |
6322201 |
- |
0 |
8 |
0 |
1 |
1 |
9 |
377333 |
377346 |
- |
376785 |
378243 |
- |
319 |
restores protein transport when overexpressed and rRNA
stability to a sec23 mutation |
8 |
| CATGCTGGCAAACC |
YLR150W |
STM1 |
6323179 |
- |
3 |
4 |
0 |
1 |
1 |
12 |
441407 |
441420 |
+ |
440468 |
441788 |
+ |
273 |
Multicopy suppressor of tom1 and pop2 mutations.
Genetically interacts with CDC13 to maintain telomere structure. |
8 |
| CATGCTATGGTTGA |
YOR027W |
STI1 |
6324601 |
COG0457 |
0 |
0 |
6 |
1 |
1 |
15 |
382925 |
382938 |
+ |
381052 |
383320 |
+ |
589 |
Heat shock protein also induced by canavanine and entry
into stationary phase |
3 |
| CATGACTTATGTAA |
YGR008C |
STF2 |
6321445 |
- |
6 |
17 |
0 |
1 |
1 |
7 |
507996 |
508009 |
- |
507613 |
508366 |
- |
84 |
ATPase stabilizing factor |
9 |
| CATGGCCGTTTCTT |
YJR117W |
STE24 |
6322577 |
COG0501 |
0 |
4 |
3 |
1 |
1 |
10 |
642214 |
642227 |
+ |
641922 |
643782 |
+ |
453 |
zinc metallo-protease that catalyzes the first step of
N-terminal processing of the yeast a-factor precursor |
8 |
| CATGATGGAACTAT |
YHR064C |
SSZ1 |
37362658 |
- |
3 |
4 |
0 |
1 |
1 |
8 |
225464 |
225477 |
- |
225171 |
227142 |
- |
538 |
DnaK homolog, interacts with Zuo1p (DnaJ homolog) to form
a ribosome-associated complex (RAC) that is bound to the ribosome via the
Zuo1p subunit |
8 |
| CATGTAGGAGTCTC |
YPL092W |
SSU1 |
6325165 |
COG1275 |
12 |
4 |
0 |
1 |
1 |
16 |
375202 |
375215 |
+ |
373788 |
375496 |
+ |
458 |
putative sulfite pump |
6 |
| CATGTAGTAAGTAA |
YLR250W |
SSP120 |
6323279 |
- |
0 |
4 |
3 |
1 |
1 |
12 |
641091 |
641104 |
+ |
640319 |
641465 |
+ |
234 |
Protein of unknown function; green fluorescent protein
(GFP)-fusion protein localizes to the cytoplasm in a punctate pattern |
8 |
| CATGGAAGAACTGG |
YPL232W |
SSO1 |
6325024 |
COG5074 |
3 |
0 |
3 |
1 |
1 |
16 |
107921 |
107934 |
+ |
107275 |
108646 |
+ |
290 |
SSO1 and SSO2 encode syntaxin homologs (post-Golgi
t-SNAREs); act in late stages of secretion |
8 |
| CATGGGTTCCCAAC |
YLR006C |
SSK1 |
6323034 |
COG0784 |
3 |
4 |
0 |
1 |
1 |
12 |
163087 |
163100 |
- |
161255 |
163892 |
- |
712 |
Cytoplasmic response regulator, part of a two-component
signal transducer that mediates osmosensing via a phosphorelay mechanism;
dephosphorylated form is degraded by the
ubiquitin-proteasome system; potential Cdc28p substrate |
8 |
| CATGGACCTTGATT |
YBR169C |
SSE2 |
6319646 |
COG0443 |
3 |
4 |
24 |
1 |
1 |
2 |
573873 |
573886 |
- |
573373 |
575953 |
- |
693 |
HSP70 family member, highly homologous to Sse1p |
2 |
| CATGCCAGCGCGTA |
YPL106C |
SSE1 |
6325151 |
COG0443 |
6 |
4 |
0 |
1 |
1 |
16 |
349991 |
350004 |
- |
349690 |
352270 |
- |
693 |
HSP70 family member, highly homologous to Ssa1p and Sse2p |
8 |
| CATGAATTTTGTAC |
YDR293C |
SSD1 |
6320499 |
COG0557 |
3 |
8 |
0 |
2 |
1 |
4 |
1045497 |
1045510 |
- |
1045133 |
1049384 |
- |
1250 |
Product of gene unknown |
8 |
| CATGAAGTTCTCCA |
YJR045C |
SSC1 |
6322505 |
COG0443 |
6 |
0 |
3 |
1 |
1 |
10 |
520543 |
520556 |
- |
519100 |
521516 |
- |
654 |
Nuclear-encoded mitochondrial protein; member of the heat
shock protein 70 (HSP70) family; most similar to E. coli DnaK protein; acts
as a chaperone for protein import across the inner
membrane; subunit of Endo.SceI endonuclease |
8 |
| CATGTCTTCTCGTT |
YNL209W |
SSB2 |
6324120 |
COG0443 |
6 |
12 |
0 |
2 |
1 |
14 |
253883 |
253896 |
+ |
252058 |
254398 |
+ |
613 |
stress-seventy subfamily B |
9 |
| CATGTCTTCTCGTT |
YDL229W |
SSB1 |
6319972 |
COG0443 |
6 |
12 |
0 |
2 |
1 |
4 |
45891 |
45904 |
+ |
44066 |
46406 |
+ |
613 |
Stress-Seventy Subfamily B; involved in translation,
perhaps by guiding the nascent chain through the ribosome |
9 |
| CATGTGTTGCTCAT |
YER103W |
SSA4 |
6320950 |
COG0443 |
9 |
0 |
13 |
1 |
1 |
5 |
364624 |
364637 |
+ |
364585 |
366797 |
+ |
642 |
member of 70 kDa heat shock protein family |
8 |
| CATGCCCAACTCGG |
YBL075C |
SSA3 |
6319396 |
COG0443 |
0 |
12 |
0 |
1 |
1 |
2 |
84549 |
84562 |
- |
84260 |
86446 |
- |
649 |
heat-inducible cytosolic member of the 70 kDa heat shock
protein family |
9 |
| CATGTAACATATAT |
YAL005C |
SSA1 |
6319314 |
COG0443 |
76 |
51 |
121 |
1 |
1 |
1 |
139394 |
139407 |
- |
139008 |
141435 |
- |
642 |
Stress-seventy subfamily A |
1 |
| CATGTGTAACCTTT |
YNL138W |
SRV2 |
6324191 |
- |
0 |
0 |
6 |
1 |
1 |
14 |
368434 |
368447 |
+ |
366741 |
368820 |
+ |
526 |
N-terminal domain appears to be involved in cellular
responsiveness to RAS. |
3 |
| CATGTTTGGTGGCG |
YPR088C |
SRP54 |
6325345 |
COG0541 |
6 |
8 |
0 |
1 |
1 |
16 |
711505 |
711518 |
- |
710900 |
713024 |
- |
541 |
Signal recognition particle subunit (homolog of mammalian
SRP54) |
8 |
| CATGGCTTTGGCTA |
YKR091W |
SRL3 |
6322944 |
- |
6 |
0 |
0 |
1 |
1 |
11 |
611932 |
611945 |
+ |
611447 |
612404 |
+ |
152 |
Cytoplasmic protein that, when overexpressed, suppresses
the lethality of a rad53 null mutation; potential Cdc28p substrate |
8 |
| CATGGCCGGCAGAC |
YHR041C |
SRB2 |
6321831 |
- |
3 |
4 |
0 |
1 |
1 |
8 |
189549 |
189562 |
- |
188624 |
189856 |
- |
210 |
RNA polymerase II holoenzyme/mediator subunit |
8 |
| CATGCCTAATAACA |
YLR055C |
SPT8 |
6323084 |
COG2319 |
0 |
0 |
6 |
1 |
1 |
12 |
251520 |
251533 |
- |
250980 |
253081 |
- |
602 |
Subunit of the SAGA transcriptional regulatory complex
but not present in SAGA-like complex SLIK/SALSA, required for SAGA-mediated
inhibition at some promoters |
3 |
| CATGGTGATGATGA |
YML010W |
SPT5 |
6323632 |
COG5164 |
0 |
0 |
6 |
2 |
1 |
13 |
248303 |
248316 |
+ |
247677 |
251367 |
+ |
1063 |
Protein that forms a complex with Spt4p and mediates both
activation and inhibition of transcription elongation; Spt4p-Spt5p complex
also plays a role in pre-mRNA processing |
3 |
| CATGTATATATATA |
YMR179W |
SPT21 |
6323833 |
- |
15 |
0 |
0 |
15 |
1 |
13 |
622163 |
622176 |
+ |
619857 |
622632 |
+ |
758 |
Protein required for normal transcription at several loci
including HTA2-HTB2 and HHF2-HHT2, but not required at the other histone
loci; functionally related to Spt10p |
6 |
| CATGGTACTTTCTC |
YER148W |
SPT15 |
6320996 |
COG2101 |
3 |
4 |
3 |
1 |
1 |
5 |
465831 |
465844 |
+ |
465298 |
466519 |
+ |
240 |
TATA-binding protein, general transcription factor that
interacts with other factors to form the preinitiation complex at promoters,
essential for viability |
8 |
| CATGATGGTTCAGG |
YHR139C |
SPS100 |
6321931 |
COG0252 |
12 |
21 |
41 |
1 |
1 |
8 |
378376 |
378389 |
- |
377721 |
379200 |
- |
326 |
involved in spore development |
2 |
| CATGTTCCGAAGGA |
YOR148C |
SPP2 |
6324722 |
- |
15 |
12 |
6 |
1 |
1 |
15 |
608571 |
608584 |
- |
608141 |
609197 |
- |
185 |
Required for final stages of splicesome maturation;
promotes step 1 of splicing |
8 |
| CATGTGATGAAGAT |
YDR104C |
SPO71 |
6320309 |
- |
6 |
0 |
0 |
3 |
1 |
4 |
662747 |
662760 |
- |
660668 |
664904 |
- |
1245 |
Meiosis-specific protein of unknown function, required
for spore wall formation during sporulation; dispensible for both nuclear
divisions during meiosis |
8 |
| CATGATTATGTTGT |
YER150W |
SPI1 |
6320998 |
- |
0 |
0 |
10 |
1 |
1 |
5 |
469024 |
469037 |
+ |
468365 |
469310 |
+ |
148 |
strongly expressed during stationary phase, and
trancription is dependent on MSN2/MSN4. |
3 |
| CATGTGGATACTCA |
YOL052C |
SPE2 |
6324521 |
- |
0 |
0 |
10 |
1 |
1 |
15 |
232773 |
232786 |
- |
231945 |
233634 |
- |
396 |
S-adenosylmethionine decarboxylase |
3 |
| CATGCGAGCTTTCG |
YHR163W |
SOL3 |
6321957 |
COG0363 |
3 |
4 |
0 |
1 |
1 |
8 |
424483 |
424496 |
+ |
423631 |
424972 |
+ |
280 |
weak multicopy suppressor of los1-1 |
8 |
| CATGAATATATATA |
YGL127C |
SOH1 |
6321311 |
COG5088 |
6 |
4 |
0 |
4 |
1 |
7 |
270327 |
270340 |
- |
270149 |
270779 |
- |
127 |
Soh1p has limited sequence similarity to RNA polymerases
and interacts with a DNA repair protein, Rad5p, in a two-hybrid system assay;
may provide a link between recombination in direct
repeats and transcription |
8 |
| CATGAAAAATGAGG |
YOR353C |
SOG2 |
6324929 |
COG4886 |
9 |
0 |
0 |
2 |
1 |
15 |
998313 |
998326 |
- |
997949 |
1000823 |
- |
791 |
Protein required for cell viability |
8 |
| CATGGGTAACGTAA |
YJR104C |
SOD1 |
6322564 |
COG2032 |
36 |
51 |
3 |
1 |
1 |
10 |
622662 |
622675 |
- |
621964 |
622927 |
- |
154 |
Cu, Zn superoxide dismutase |
13 |
| CATGCTTCCAATGG |
YMR096W |
SNZ1 |
6323743 |
COG0214 |
0 |
4 |
13 |
2 |
1 |
13 |
459258 |
459271 |
+ |
458407 |
459799 |
+ |
297 |
Snooze: stationary phase-induced gene family; involved in
cellular response to nutrient limitation and growth arrest |
3 |
| CATGGGAAAAAGTA |
YJL036W |
SNX4 |
6322424 |
COG5391 |
0 |
8 |
6 |
1 |
1 |
10 |
379983 |
379996 |
+ |
378741 |
380511 |
+ |
423 |
Sorting NeXin |
8 |
| CATGGTCATATGTG |
YMR322C |
SNO4 |
6323984 |
COG0693 |
9 |
17 |
3 |
3 |
1 |
13 |
918160 |
918173 |
- |
917895 |
919077 |
- |
237 |
Possible chaperone and cysteine protease with similarity
to E. coli Hsp31 and S. cerevisiae Hsp31p, Hsp32p, and Hsp33p; member of the
DJ-1/ThiJ/PfpI superfamily; may have a role in
pyridoxine metabolism |
9 |
| CATGCCAAGAATTC |
YGR197C |
SNG1 |
6321636 |
- |
3 |
8 |
0 |
2 |
1 |
7 |
892318 |
892331 |
- |
892190 |
894143 |
- |
547 |
Involved in nitrosoguanidine resistance |
8 |
| CATGTGGATGTGTA |
YHL025W |
SNF6 |
6321762 |
- |
9 |
21 |
17 |
1 |
1 |
8 |
55909 |
55922 |
+ |
54848 |
56345 |
+ |
332 |
Involved in global regulation of transcription |
8 |
| CATGTGGTACAAGG |
YAL030W |
SNC1 |
6319289 |
COG5143 |
6 |
8 |
0 |
1 |
1 |
1 |
87652 |
87665 |
+ |
87289 |
88254 |
+ |
117 |
Involved in mediating targeting and transport of
secretory proteins; forms a complex with Snc2p and Sec9p |
8 |
| CATGATGAAGCTAC |
YDL123W |
SNA4 |
6320080 |
COG0401 |
0 |
0 |
13 |
1 |
1 |
4 |
241835 |
241848 |
+ |
241418 |
242339 |
+ |
140 |
Protein of unknown function, localized to the vacuolar
outer membrane |
3 |
| CATGCGACTGCGCC |
YJL151C |
SNA3 |
6322310 |
COG0401 |
21 |
60 |
41 |
1 |
1 |
10 |
136428 |
136441 |
- |
135852 |
136691 |
- |
133 |
Integral membrane protein localized to vacuolar
intralumenal vesicles, computational analysis of large-scale protein-protein
interaction data suggests a possible role in either
cell wall synthesis or protein-vacuolar targeting |
7 |
| CATGAACGTTCGTG |
YGR229C |
SMI1 |
6321668 |
COG4282 |
6 |
0 |
0 |
1 |
1 |
7 |
949212 |
949225 |
- |
948883 |
950899 |
- |
505 |
Protein involved in (1,3)-beta-glucan synthesis, possibly
through regulation of cell wall glucan and chitin synthesis; chromatin
binding protein |
8 |
| CATGAGCAATGGAA |
YHR050W |
SMF2 |
6321841 |
COG1914 |
3 |
4 |
0 |
1 |
1 |
8 |
209181 |
209194 |
+ |
207647 |
209467 |
+ |
549 |
SMF2 was isolated as a high copy suppressor of a
temperature sensitive mutation in the PEP ( mitochondrial matrix protease)
gene and may influence PEP-dependent protein
import |
8 |
| CATGTATATATATA |
YOL122C |
SMF1 |
6324450 |
COG1914 |
15 |
0 |
0 |
15 |
1 |
15 |
89534 |
89547 |
- |
89192 |
91418 |
- |
575 |
Isolated as high copy suppressor of a cdc1 mutation &
involved in high affinity Mn2+ uptake. SMF1 was isolated as a high copy
suppressor of a ts mutation in the PEP (mito.
matrix protease) gene & may influence PEP-dependent protein import |
6 |
| CATGTGTGTTAATA |
YER029C |
SMB1 |
6320867 |
COG1958 |
6 |
8 |
0 |
1 |
1 |
5 |
212520 |
212533 |
- |
212087 |
213176 |
- |
196 |
associated with U1, U2, U4, and U5 snRNPs as part of the
Sm-core that is common to all spliceosomal snRNPs |
8 |
| CATGTTTTAGTCGC |
YDR088C |
SLU7 |
6320293 |
- |
0 |
4 |
3 |
1 |
1 |
4 |
618647 |
618660 |
- |
618301 |
619639 |
- |
382 |
Involved in 3' splice site choices and acts in concert
with Prp18 during the 2nd step of splicing. |
8 |
| CATGACGTATAGTT |
YKL108W |
SLD2 |
6322741 |
- |
0 |
8 |
0 |
1 |
1 |
11 |
235509 |
235522 |
+ |
234072 |
235786 |
+ |
453 |
Protein required for DNA replication, phosphorylated in S
phase by S-phase cyclin-dependent kinases (Cdks), phosphorylation is
essential for DNA replication and for complex
formation with Dpb11p; potential Cdc28p substrate |
8 |
| CATGAAATTGATGC |
YDL052C |
SLC1 |
6320151 |
COG0204 |
0 |
8 |
3 |
2 |
1 |
4 |
363408 |
363421 |
- |
362257 |
363583 |
- |
303 |
fatty acyltransferase homologous to E. coli plsC gene;
functionally complements plsC mutants |
8 |
| CATGTATGAATTAT |
YDR328C |
SKP1 |
6320535 |
COG5201 |
6 |
0 |
0 |
1 |
1 |
4 |
1125281 |
1125294 |
- |
1124926 |
1126009 |
- |
194 |
Involved in kinetochore function and ubiquitin-mediated
proteolysis |
8 |
| CATGGAAGATTTAC |
YHR206W |
SKN7 |
6322000 |
COG5169 |
0 |
0 |
6 |
2 |
1 |
8 |
515052 |
515065 |
+ |
512730 |
515097 |
+ |
622 |
Protein with similarity to DNA-binding region of heat
shock transcription factors |
3 |
| CATGCAGCCCTGAG |
YOL113W |
SKM1 |
6324459 |
COG0515 |
0 |
8 |
0 |
1 |
1 |
15 |
106248 |
106261 |
+ |
104325 |
106708 |
+ |
655 |
Serine/threonine protein kinase with similarity to Ste20p
and Cla4p |
8 |
| CATGGTTTCTTGCC |
YNL032W |
SIW14 |
6324296 |
COG2365 |
9 |
12 |
0 |
1 |
1 |
14 |
575417 |
575430 |
+ |
574504 |
575848 |
+ |
281 |
Synthetic interaction with Whi2 |
6 |
| CATGCCCTCCCTAA |
YDL047W |
SIT4 |
6320156 |
COG0639 |
0 |
4 |
20 |
1 |
1 |
4 |
370712 |
370725 |
+ |
369769 |
371203 |
+ |
311 |
SIT4 suppress mutations in DBF2 |
2 |
| CATGGGGCCTCTGA |
YNL007C |
SIS1 |
6324321 |
COG2214 |
0 |
0 |
24 |
1 |
1 |
14 |
618926 |
618939 |
- |
618219 |
619564 |
- |
352 |
HSP40 family chaperone |
2 |
| CATGATGAATAAGT |
YMR175W |
SIP18 |
6323829 |
- |
6 |
0 |
0 |
1 |
1 |
13 |
611022 |
611035 |
+ |
611015 |
611312 |
+ |
79 |
Salt-Induced Protein |
8 |
| CATGACCACTAGAG |
YLR058C |
SHM2 |
6323087 |
COG0112 |
6 |
17 |
0 |
1 |
1 |
12 |
258195 |
258208 |
- |
257494 |
259402 |
- |
469 |
serine hydroxymethyltransferase |
9 |
| CATGCGCTTGCTAT |
YGL228W |
SHE10 |
6321209 |
- |
3 |
0 |
3 |
1 |
1 |
7 |
69337 |
69350 |
+ |
67597 |
69669 |
+ |
577 |
Mrna (identified by a library screen) that causes growth
arrest when overexpressed |
8 |
| CATGTTATGTAGAT |
YOR007C |
SGT2 |
6324580 |
COG0457 |
3 |
8 |
3 |
1 |
1 |
15 |
338895 |
338908 |
- |
338622 |
339978 |
- |
346 |
small glutamine-rich tetratricopeptide repeat containing
protein |
8 |
| CATGCAACCCCATC |
YJR134C |
SGM1 |
6322594 |
- |
3 |
8 |
17 |
1 |
1 |
10 |
673553 |
673566 |
- |
673145 |
675767 |
- |
707 |
involved in carbohydrate metabolism |
2 |
| CATGGATTATTGGG |
YGL066W |
SGF73 |
6321372 |
- |
0 |
4 |
3 |
1 |
1 |
7 |
379869 |
379882 |
+ |
377610 |
380082 |
+ |
657 |
SaGa associated Factor 73kDa |
8 |
| CATGCAGTGGCTCT |
YBL102W |
SFT2 |
6319366 |
COG5102 |
3 |
8 |
6 |
1 |
1 |
2 |
24879 |
24892 |
+ |
24098 |
25244 |
+ |
215 |
similar to mammalian syntaxin 5 |
8 |
| CATGCATCTATAAA |
YLR403W |
SFP1 |
6323435 |
COG5189 |
6 |
0 |
0 |
1 |
1 |
12 |
925634 |
925647 |
+ |
925566 |
928116 |
+ |
683 |
Inhibits nuclear protein localization when present in
multiple copies |
8 |
| CATGCATATTTGGG |
YJL168C |
SET2 |
6322293 |
COG2940 |
0 |
0 |
10 |
1 |
1 |
10 |
102196 |
102209 |
- |
101721 |
104421 |
- |
733 |
Contains a 'SET' or 'TROMO' domain at the N-terminus of
the protein Methyltransferase activity is important for transcriptional
repression activity |
3 |
| CATGGTTGCATAAT |
YDR023W |
SES1 |
6320226 |
COG0172 |
9 |
4 |
0 |
1 |
1 |
4 |
490984 |
490997 |
+ |
489504 |
491391 |
+ |
462 |
seryl-tRNA synthetase |
8 |
| CATGCACAAGAATA |
YOR184W |
SER1 |
6324758 |
COG1932 |
6 |
12 |
3 |
1 |
1 |
15 |
680627 |
680640 |
+ |
679357 |
681043 |
+ |
395 |
phosphoserine transaminase |
9 |
| CATGGTGGAGATTT |
YAL067C |
SEO1 |
6319250 |
COG0477 |
3 |
0 |
3 |
3 |
1 |
1 |
8723 |
8736 |
- |
6737 |
9017 |
- |
593 |
Suppressor of Sulfoxyde Ethionine resistance |
8 |
| CATGGGCCAATGGT |
YDR363W-A |
SEM1 |
6320571 |
- |
0 |
0 |
34 |
1 |
1 |
4 |
1202239 |
1202252 |
+ |
1202116 |
1202884 |
+ |
89 |
Suppressor of Exocyst Mutations; Homolog of DSS1; similar
to hypothetical protein from S. pombe |
2 |
| CATGGAACAAGGTT |
YBL066C |
SEF1 |
6319406 |
- |
0 |
0 |
10 |
1 |
1 |
2 |
96674 |
96687 |
- |
96407 |
100079 |
- |
1057 |
Suppressor of Essential Function |
3 |
| CATGTCTAGTCTCT |
YDR077W |
SED1 |
6320282 |
- |
15 |
21 |
0 |
1 |
1 |
4 |
601963 |
601976 |
+ |
600788 |
602303 |
+ |
338 |
Isolated as a suppressor of an erd2 deletion mutant (ERD2
is the HDEL receptor that sorts ER proteins), SED1 encodes a cell wall
protein. |
6 |
| CATGTACAAACCTT |
YPL094C |
SEC62 |
41629689 |
- |
3 |
0 |
3 |
1 |
1 |
16 |
369755 |
369768 |
- |
369437 |
370658 |
- |
274 |
membrane component of ER protein translocation apparatus |
8 |
| CATGGTCAATTCGG |
YER008C |
SEC3 |
6320845 |
- |
6 |
0 |
121 |
1 |
1 |
5 |
167477 |
167490 |
- |
167308 |
171817 |
- |
1336 |
Profilin synthetic lethal protein, has region of
coiled-coil structure; subunit of the Exocyst complex, which contains Sec3p,
Sec5p, Sec6p, Sec8p, Sec10p, Sec15p, and Exo70p
and is required for exocytosis; potential Cdc28p substrate |
12 |
| CATGTATATGCCTA |
YIL076W |
SEC28 |
6322114 |
- |
3 |
12 |
0 |
1 |
1 |
9 |
217602 |
217615 |
+ |
216466 |
218044 |
+ |
359 |
Part of a heptameric protein complex that regulates
retrograde Golgi-to-ER protein traffic in eukaryotic cells; coatomer forms
the COP I vesicle coat whose functions are essential |
9 |
| CATGATCTAGAATC |
YGL137W |
SEC27 |
6321301 |
COG2319 |
3 |
0 |
3 |
1 |
1 |
7 |
252192 |
252205 |
+ |
249872 |
253240 |
+ |
889 |
Involved in endoplasmic-to-Golgi protein trafficking |
8 |
| CATGTTTGAACCAC |
YDR238C |
SEC26 |
6320444 |
COG5096 |
0 |
0 |
6 |
2 |
1 |
4 |
937881 |
937894 |
- |
937388 |
940808 |
- |
973 |
Involved in endoplasmic-to-Golgi protein trafficking |
3 |
| CATGCAAATAAGGG |
YNL287W |
SEC21 |
6324042 |
COG5240 |
0 |
8 |
3 |
1 |
1 |
14 |
94879 |
94892 |
+ |
91992 |
95220 |
+ |
935 |
non-clathrin coat protein involved in transport between
ER and Golgi |
8 |
| CATGGGCAATAGAT |
YBL050W |
SEC17 |
6319421 |
- |
3 |
0 |
6 |
1 |
1 |
2 |
125768 |
125781 |
+ |
125090 |
126583 |
+ |
292 |
peripheral membrane protein required for vesicular
transport between ER and Golgisimilar to alpha-SNAP part of cis-SNARE complex
required for 'priming' step in homotypic vacuole
fusion |
8 |
| CATGGGAATCTACT |
YPL085W |
SEC16 |
6325172 |
- |
0 |
8 |
24 |
2 |
1 |
16 |
388400 |
388413 |
+ |
387062 |
394032 |
+ |
2195 |
multidomain vesicle coat protein that interacts with
Sec23p |
2 |
| CATGTGAGGCTTGC |
YBR214W |
SDS24 |
6319691 |
COG0517 |
3 |
21 |
0 |
1 |
1 |
2 |
652948 |
652961 |
+ |
651372 |
653402 |
+ |
527 |
Similar to S. pombe SDS23, suppresses DIS2, localized to
the nucleus |
9 |
| CATGCACATCTATA |
YDR178W |
SDH4 |
6320383 |
- |
18 |
30 |
0 |
1 |
1 |
4 |
818524 |
818537 |
+ |
817944 |
818988 |
+ |
181 |
Yeast succinate dehydrogenase (SDH) is a tetramer of
non-equivalent subunits--Sdh1p, Sdh2p, Sdh3p, Sdh4p--that couples the
oxidation of succinate to the transfer of electrons
to ubiquinone. |
5 |
| CATGAAAAAAAAAA |
YLL041C |
SDH2 |
6322987 |
COG0479 |
3 |
0 |
3 |
13 |
1 |
12 |
52622 |
52635 |
- |
52631 |
53930 |
- |
266 |
Yeast succinate dehydrogenase (SDH) is a tetramer of
non-equivalent subunits--Sdh1p, Sdh2p, Sdh3p, Sdh4p--that couples the
oxidation of succinate to the transfer of electrons
to ubiquinone. |
8 |
| CATGCAAGAGAGGA |
YKL148C |
SDH1 |
6322701 |
COG1053 |
3 |
8 |
0 |
1 |
1 |
11 |
169368 |
169381 |
- |
168835 |
171134 |
- |
640 |
Yeast succinate dehydrogenase (SDH) is a tetramer of
non-equivalent subunits--Sdh1p, Sdh2p, Sdh3p, Sdh4p--that couples the
oxidation of succinate to the transfer of electrons
to ubiquinone. |
8 |
| CATGGAATGGAATC |
YMR272C |
SCS7 |
6323928 |
COG5274 |
33 |
34 |
0 |
1 |
1 |
13 |
809462 |
809475 |
- |
809123 |
810776 |
- |
384 |
Required for the hydroxylation of the very long chain
fatty acid (VLCFA), located in the endoplasmic reticulum |
5 |
| CATGGTACTCCTTC |
YBR037C |
SCO1 |
6319511 |
COG1999 |
3 |
0 |
3 |
1 |
1 |
2 |
310537 |
310550 |
- |
310276 |
311413 |
- |
295 |
inner mitochondrial membrane protein |
8 |
| CATGAACGACGAAG |
YGR049W |
SCM4 |
6321486 |
- |
3 |
8 |
0 |
1 |
1 |
7 |
591874 |
591887 |
+ |
591316 |
592378 |
+ |
187 |
Protein that suppresses ts allele of CDC4 when
overexpressed |
8 |
| CATGGGAGAAGGTG |
YGL011C |
SCL1 |
6321427 |
COG0638 |
3 |
8 |
10 |
1 |
1 |
7 |
474644 |
474657 |
- |
473993 |
475250 |
- |
252 |
Proteasome subunit YC7alpha/Y8 (protease yscE subunit 7) |
8 |
| CATGAATTCAACAG |
YPL218W |
SAR1 |
6325038 |
COG1100 |
0 |
0 |
13 |
1 |
1 |
16 |
139444 |
139457 |
+ |
138697 |
139907 |
+ |
190 |
Secretion-Associated, Ras-related. Component of COPII
coat of vesicles; required for ER to Golgi protein transport |
3 |
| CATGTAGTTTTCTA |
YFR040W |
SAP155 |
37362647 |
- |
3 |
4 |
0 |
1 |
1 |
6 |
237299 |
237312 |
+ |
234229 |
237736 |
+ |
1002 |
Protein that forms a complex with the Sit4p protein
phosphatase and is required for its function; member of a family of similar
proteins including Sap4p, Sap185p, and Sap190p |
8 |
| CATGTACATTATAC |
YLR180W |
SAM1 |
6323209 |
COG0192 |
6 |
4 |
0 |
1 |
1 |
12 |
516480 |
516493 |
+ |
515264 |
516911 |
+ |
382 |
S-adenosylmethionine synthetase |
8 |
| CATGTGATACTAAG |
YER043C |
SAH1 |
6320882 |
COG0499 |
9 |
17 |
0 |
1 |
1 |
5 |
235609 |
235622 |
- |
235270 |
237118 |
- |
449 |
Putative S-adenosyl-L-homocysteine hydrolase with a
probable role in S-adenosylhomocysteine catabolism and/or methionine
degradation |
9 |
| CATGCCTCTACTGG |
YDR129C |
SAC6 |
6320334 |
COG5069 |
6 |
0 |
0 |
1 |
1 |
4 |
713101 |
713114 |
- |
712835 |
715373 |
- |
642 |
fimbrin homolog (actin-filament bundling protein) |
8 |
| CATGAAGATTCCAT |
YDR388W |
RVS167 |
6320596 |
- |
3 |
0 |
3 |
3 |
1 |
4 |
1250892 |
1250905 |
+ |
1250174 |
1252121 |
+ |
482 |
The BAR adaptor proteins encoded by RVS167 and RVS161
form a complex that regulates actin, endocytosis, and viability following
starvation or osmotic stress. |
8 |
| CATGGAAGAACGTC |
YCR009C |
RVS161 |
6319854 |
- |
3 |
4 |
0 |
1 |
1 |
3 |
131433 |
131446 |
- |
130243 |
131539 |
- |
265 |
Protein required for viability after N, C, or S
starvation. The BAR adaptor proteins encoded by RVS167 and RVS161 form a
complex that regulates actin, endocytosis, and
viability following starvation or osmotic stress. |
8 |
| CATGCAGAGAGAGA |
YGR161C |
RTS3 |
6321600 |
- |
0 |
0 |
6 |
1 |
1 |
7 |
809342 |
809355 |
- |
808133 |
809423 |
- |
263 |
Hypothetical ORF |
3 |
| CATGAAATTGATGC |
YDR233C |
RTN1 |
6320439 |
- |
0 |
8 |
3 |
2 |
1 |
4 |
929831 |
929844 |
- |
928963 |
930349 |
- |
295 |
reticulon gene member of the RTNLA (reticulon-like A)
subfamily |
8 |
| CATGTTTCTAAGCG |
YGL252C |
RTG2 |
6321185 |
COG0248 |
3 |
8 |
0 |
1 |
1 |
7 |
25958 |
25971 |
- |
25219 |
27484 |
- |
588 |
Protein involved in interorganelle communication between
mitochondria, peroxisomes, and nucleus. Likely role of Rtg2p is to antagonize
Mks1p, a negative regulator of RTG target gene
activation. |
8 |
| CATGTACATACAAA |
YGR215W |
RSM27 |
6321654 |
- |
3 |
8 |
0 |
2 |
1 |
7 |
922558 |
922571 |
+ |
922178 |
923009 |
+ |
110 |
Mitochondrial ribosomal protein of the small subunit |
8 |
| CATGGGCAAGAAGA |
YCR052W |
RSC6 |
6319900 |
- |
3 |
0 |
10 |
2 |
1 |
3 |
215401 |
215414 |
+ |
214989 |
216691 |
+ |
483 |
a subunit of RSC, a fifteen-protein chromatin remodeling
complex and related to the swi/snf complex. |
8 |
| CATGTCCAAAATAG |
YOR049C |
RSB1 |
6324623 |
- |
0 |
0 |
24 |
3 |
1 |
15 |
422705 |
422718 |
- |
422169 |
423732 |
- |
354 |
Resistance to Sphingoid long-chain Base. Putative
transporter or flippase that translocates LCBs from the cytoplasmic side
toward the extracytoplasmic side of the membrane. |
2 |
| CATGCAAAGGTGCG |
YPL193W |
RSA1 |
6325063 |
- |
6 |
0 |
0 |
1 |
1 |
16 |
182581 |
182594 |
+ |
181402 |
183046 |
+ |
381 |
RiboSome Assembly |
8 |
| CATGCTATGTCGTA |
YGR095C |
RRP46 |
37362654 |
- |
6 |
8 |
3 |
1 |
1 |
7 |
675632 |
675645 |
- |
675174 |
676344 |
- |
223 |
Ribosomal RNA Processing |
8 |
| CATGTGTATGTAAT |
YCR035C |
RRP43 |
10383796 |
- |
0 |
8 |
0 |
1 |
1 |
3 |
191751 |
191764 |
- |
191330 |
193013 |
- |
394 |
Ribosomal RNA Processing |
8 |
| CATGGTTAACAAAA |
YDL111C |
RRP42 |
6320092 |
COG2123 |
3 |
8 |
0 |
1 |
1 |
4 |
263245 |
263258 |
- |
262814 |
264110 |
- |
265 |
Ribosomal RNA Processing |
8 |
| CATGGCTATGTACA |
YHR069C |
RRP4 |
6321860 |
COG1097 |
6 |
8 |
0 |
1 |
1 |
8 |
233480 |
233493 |
- |
233081 |
234659 |
- |
359 |
Ribosomal RNA Processing |
8 |
| CATGGTTTACCTTT |
YHR065C |
RRP3 |
37362659 |
- |
0 |
8 |
0 |
1 |
1 |
8 |
227508 |
227521 |
- |
227143 |
229038 |
- |
501 |
Required for maturation of the 35S primary transcript of
pre-rRNA and is required for cleavages leading to mature 18S RNA |
8 |
| CATGTATATAAGCA |
YML043C |
RRN11 |
6323598 |
- |
3 |
4 |
0 |
1 |
1 |
13 |
190146 |
190159 |
- |
189745 |
191767 |
- |
507 |
rDNA transcription factor CF component, which also
contains Rrn6p and Rrn7p, which is required for rDNA transcription by RNA
polymerase I |
8 |
| CATGTGTATGTATA |
YOR259C |
RPT4 |
6324833 |
COG1222 |
18 |
12 |
17 |
3 |
1 |
15 |
812367 |
812380 |
- |
811894 |
813706 |
- |
437 |
Proteasome Cap Subunit |
8 |
| CATGCAGGAAGCTG |
YDR394W |
RPT3 |
6320602 |
COG1222 |
3 |
8 |
0 |
1 |
1 |
4 |
1262825 |
1262838 |
+ |
1261669 |
1263311 |
+ |
428 |
probable 26S protease subunit and member of the
CDC48/PAS1/SEC18 family of ATPases |
8 |
| CATGGATTATGCAT |
YPL081W |
RPS9A |
6325176 |
COG0522 |
0 |
0 |
6 |
1 |
1 |
16 |
405286 |
405299 |
+ |
404945 |
406538 |
+ |
197 |
Protein component of the small (40S) ribosomal subunit;
nearly identical to Rps9Ap and has similarity to E. coli S4 and rat S9
ribosomal proteins |
3 |
| CATGTACAATTTTA |
YER102W |
RPS8B |
6320949 |
COG2007 |
6 |
0 |
0 |
3 |
1 |
5 |
363727 |
363740 |
+ |
363096 |
364197 |
+ |
200 |
Protein component of the small (40S) ribosomal subunit;
identical to Rps8Bp and has similarity to rat S8 ribosomal protein |
8 |
| CATGGTTTTCCCAA |
YNL096C |
RPS7B |
6324233 |
- |
6 |
0 |
0 |
2 |
1 |
14 |
443573 |
443586 |
- |
442899 |
444315 |
- |
190 |
Protein component of the small (40S) ribosomal subunit,
nearly identical to Rps7Ap; interacts with Kti11p; deletion causes
hypersensitivity to zymocin; has similarity to rat
S7 and Xenopus S8 ribosomal proteins |
8 |
| CATGACAAGATCTT |
YOR096W |
RPS7A |
6324670 |
- |
9 |
0 |
0 |
1 |
1 |
15 |
506557 |
506570 |
+ |
505794 |
507266 |
+ |
190 |
Protein component of the small (40S) ribosomal subunit,
nearly identical to Rps7Bp; interacts with Kti11p; deletion causes
hypersensitivity to zymocin; has similarity to rat
S7 and Xenopus S8 ribosomal proteins |
8 |
| CATGGACGTCATCA |
YHR203C |
RPS4B |
6321997 |
COG1471 |
3 |
4 |
0 |
1 |
1 |
8 |
504988 |
505001 |
- |
503975 |
505528 |
- |
261 |
Protein component of the small (40S) ribosomal subunit;
identical to Rps4Bp and has similarity to rat S4 ribosomal protein |
8 |
| CATGGATGTCATCA |
YJR145C |
RPS4A |
6322605 |
COG1471 |
18 |
0 |
0 |
1 |
1 |
10 |
702456 |
702469 |
- |
701443 |
702983 |
- |
261 |
Protein component of the small (40S) ribosomal subunit;
mutation affects 20S pre-rRNA processing; identical to Rps4Bp and has
similarity to rat S4 ribosomal protein |
6 |
| CATGTGTAATTAAA |
YOR182C |
RPS30B |
6324756 |
- |
3 |
4 |
10 |
1 |
1 |
15 |
678142 |
678155 |
- |
677692 |
678793 |
- |
63 |
Protein component of the small (40S) ribosomal subunit;
nearly identical to Rps30Ap and has similarity to rat S30 ribosomal protein |
8 |
| CATGCCATCTTTAC |
YLR287C-A |
RPS30A |
6323318 |
- |
6 |
4 |
6 |
1 |
1 |
12 |
712468 |
712481 |
- |
712061 |
713160 |
- |
63 |
Protein component of the small (40S) ribosomal subunit;
nearly identical to Rps30Bp and has similarity to rat S30 ribosomal protein |
8 |
| CATGCTCTACTGTC |
YHR021C |
RPS27B |
6321809 |
COG2051 |
6 |
0 |
0 |
1 |
1 |
8 |
147925 |
147938 |
- |
147364 |
148661 |
- |
82 |
Protein component of the small (40S) ribosomal subunit;
nearly identical to Rps27Ap and has similarity to rat S27 ribosomal protein |
8 |
| CATGTGTAACATCT |
YER131W |
RPS26B |
6320978 |
COG4830 |
6 |
0 |
0 |
1 |
1 |
5 |
424726 |
424739 |
+ |
423948 |
424806 |
+ |
119 |
Protein component of the small (40S) ribosomal subunit;
nearly identical to Rps26Ap and has similarity to rat S26 ribosomal protein |
8 |
| CATGAAGGACAGAG |
YLR333C |
RPS25B |
6323365 |
COG4901 |
3 |
4 |
0 |
1 |
1 |
12 |
795793 |
795806 |
- |
795074 |
795899 |
- |
108 |
Protein component of the small (40S) ribosomal subunit;
nearly identical to Rps25Ap and has similarity to rat S25 ribosomal protein |
8 |
| CATGAAAACTGGAA |
YER074W |
RPS24A |
6320918 |
COG2004 |
3 |
4 |
0 |
1 |
1 |
5 |
306672 |
306685 |
+ |
306319 |
307648 |
+ |
135 |
Protein component of the small (40S) ribosomal subunit;
identical to Rps24Bp and has similarity to rat S24 ribosomal protein |
8 |
| CATGCAACAACTAC |
YJL136C |
RPS21B |
6322325 |
- |
27 |
34 |
0 |
1 |
1 |
10 |
156345 |
156358 |
- |
156046 |
157191 |
- |
87 |
Protein component of the small (40S) ribosomal subunit;
nearly identical to Rps21Bp and has similarity to rat S21 ribosomal protein |
5 |
| CATGTTTCCCAAGT |
YMR143W |
RPS16A |
9755341 |
COG0103 |
6 |
0 |
0 |
1 |
1 |
13 |
552689 |
552702 |
+ |
551927 |
553360 |
+ |
143 |
Protein component of the small (40S) ribosomal subunit;
identical to Rps16Bp and has similarity to E. coli S9 and rat S16 ribosomal
proteins |
8 |
| CATGGTAGAGCCGG |
YOL040C |
RPS15 |
6324533 |
COG0185 |
33 |
12 |
13 |
1 |
1 |
15 |
253180 |
253193 |
- |
252648 |
253575 |
- |
142 |
Protein component of the small (40S) ribosomal subunit;
has similarity to E. coli S19 and rat S15 ribosomal proteins |
5 |
| CATGGAAATACGGC |
YJL191W |
RPS14B |
6322270 |
COG0100 |
6 |
8 |
0 |
1 |
1 |
10 |
74636 |
74649 |
+ |
73786 |
75109 |
+ |
138 |
Ribosomal protein 59 (rp59) of the small (40S) ribosomal
subunit, required for ribosome assembly; mutations confer resistance to
cryptopleurine; nearly identical to
Rps14Ap and similar to E. coli S11 and rat S14
ribosomal proteins |
8 |
| CATGTATTGTACTT |
YCR031C |
RPS14A |
10383793 |
COG0100 |
15 |
4 |
6 |
1 |
1 |
3 |
177474 |
177487 |
- |
176996 |
178215 |
- |
137 |
Ribosomal protein 59 (rp59) of the small (40S) ribosomal
subunit, required for ribosome assembly; mutations confer resistance to
cryptopleurine; nearly identical to Rps14Bp and
similar to E. coli S11 and rat S14 ribosomal proteins |
6 |
| CATGGAACACTTCT |
YOR369C |
RPS12 |
6324945 |
COG1358 |
15 |
0 |
0 |
1 |
1 |
15 |
1028200 |
1028213 |
- |
1027691 |
1028621 |
- |
143 |
Protein component of the small (40S) ribosomal subunit;
has similarity to rat ribosomal protein S12 |
6 |
| CATGGCAATACTAC |
YMR230W |
RPS10B |
6323886 |
COG5045 |
12 |
8 |
10 |
2 |
1 |
13 |
733000 |
733013 |
+ |
732413 |
733266 |
+ |
105 |
Protein component of the small (40S) ribosomal subunit;
nearly identical to Rps10Ap and has similarity to rat ribosomal protein S10 |
8 |
| CATGGCAATACTAC |
YOR293W |
RPS10A |
6324867 |
COG5045 |
12 |
8 |
10 |
2 |
1 |
15 |
867709 |
867722 |
+ |
867095 |
868336 |
+ |
105 |
Protein component of the small (40S) ribosomal subunit;
nearly identical to Rps10Bp and has similarity to rat ribosomal protein S10 |
8 |
| CATGGGTTTTGGTT |
YDR382W |
RPP2B |
6320590 |
COG2058 |
9 |
8 |
0 |
1 |
1 |
4 |
1239787 |
1239800 |
+ |
1239480 |
1240311 |
+ |
110 |
Homology to rat P2, human P2, and E.coli L12eIA |
8 |
| CATGGGTTTCGGTT |
YOL039W |
RPP2A |
6324534 |
COG2058 |
15 |
12 |
0 |
4 |
1 |
15 |
254590 |
254603 |
+ |
254295 |
255114 |
+ |
106 |
Homology to rat P2, human P2, and E.coli L12eIB |
6 |
| CATGGGTTTCGGTT |
YDL130W |
RPP1B |
6320073 |
COG2058 |
15 |
12 |
0 |
4 |
1 |
4 |
230502 |
230515 |
+ |
229906 |
231023 |
+ |
106 |
Homology to rat P1, human P1, and E. coli L12eIIB |
6 |
| CATGGGTTTCGGTT |
YDL081C |
RPP1A |
6320122 |
COG2058 |
15 |
12 |
0 |
4 |
1 |
4 |
309812 |
309825 |
- |
309303 |
310122 |
- |
106 |
Homology to rat P1, human P1, and E.coli L12eIIA |
6 |
| CATGGGTTTCGGTT |
YLR340W |
RPP0 |
6323371 |
COG0244 |
15 |
12 |
0 |
4 |
1 |
12 |
806800 |
806813 |
+ |
805887 |
807324 |
+ |
312 |
Homology to rat P0, human P0, and E. coli L10e |
6 |
| CATGAGAGCCATAA |
YDR427W |
RPN9 |
6320635 |
- |
0 |
8 |
0 |
1 |
1 |
4 |
1323175 |
1323188 |
+ |
1322193 |
1323873 |
+ |
393 |
Regulatory Particle Non-ATPase |
8 |
| CATGTTAATTTGCT |
YOR261C |
RPN8 |
6324835 |
COG1310 |
3 |
0 |
13 |
1 |
1 |
15 |
815836 |
815849 |
- |
815414 |
816929 |
- |
338 |
Regulatory Particle Non-ATPase, homolog of mammalian
proteasomal subunit S12/p40 |
3 |
| CATGGGTTAATTAA |
YDL020C |
RPN4 |
6320184 |
- |
12 |
0 |
89 |
1 |
1 |
4 |
415105 |
415118 |
- |
414611 |
416705 |
- |
531 |
Involved in ubiquitin degradation pathway. May act as
common transcription factor on proteasomal and proteasome-related genes. |
12 |
| CATGATGATGGCAT |
YLR421C |
RPN13 |
6323453 |
- |
12 |
4 |
0 |
1 |
1 |
12 |
964965 |
964978 |
- |
964587 |
965556 |
- |
156 |
Proteasome subunit |
6 |
| CATGATCACTGGTG |
YNL067W |
RPL9B |
6324262 |
COG0097 |
12 |
0 |
0 |
3 |
1 |
14 |
499909 |
499922 |
+ |
499680 |
500754 |
+ |
191 |
Protein component of the large (60S) ribosomal subunit,
nearly identical to Rpl9Ap and has similarity to E. coli L6 and rat L9
ribosomal proteins |
6 |
| CATGATCACTGGTG |
YGL147C |
RPL9A |
6321291 |
COG0097 |
12 |
0 |
0 |
3 |
1 |
7 |
228088 |
228101 |
- |
227258 |
228332 |
- |
191 |
Protein component of the large (60S) ribosomal subunit,
nearly identical to Rpl9Bp and has similarity to E. coli L6 and rat L9
ribosomal proteins |
6 |
| CATGTTGTCTCTTT |
YLL045C |
RPL8B |
6322984 |
COG1358 |
6 |
0 |
0 |
1 |
1 |
12 |
48203 |
48216 |
- |
47463 |
48628 |
- |
256 |
Ribosomal protein L4 of the large (60S) ribosomal
subunit, nearly identical to Rpl8Ap and has similarity to rat L7a ribosomal
protein; mutation results in decreased amounts of
free 60S subunits |
8 |
| CATGCCCACCATCA |
YLR448W |
RPL6B |
6323481 |
COG2163 |
0 |
0 |
6 |
2 |
1 |
12 |
1029159 |
1029172 |
+ |
1028849 |
1030262 |
+ |
176 |
Protein component of the large (60S) ribosomal subunit,
has similarity to Rpl6Bp and to rat L6 ribosomal protein; binds to 5.8S rRNA |
3 |
| CATGGAAGAATTAG |
YPL131W |
RPL5 |
6325126 |
COG0256 |
3 |
12 |
0 |
1 |
1 |
16 |
303739 |
303752 |
+ |
303120 |
304385 |
+ |
297 |
Protein component of the large (60S) ribosomal subunit
with similarity to E. coli L18 and rat L5 ribosomal proteins; binds 5S rRNA
and is required for 60S subunit assembly |
9 |
| CATGTGTCGTGGTG |
YDR012W |
RPL4B |
6320215 |
COG0088 |
9 |
0 |
0 |
2 |
1 |
4 |
472124 |
472137 |
+ |
471850 |
473153 |
+ |
362 |
Protein component of the large (60S) ribosomal subunit,
nearly identical to Rpl4Ap and has similarity to E. coli L4 and rat L4
ribosomal proteins |
8 |
| CATGTGTCGTGGTG |
YBR031W |
RPL4A |
6319505 |
COG0088 |
9 |
0 |
0 |
2 |
1 |
2 |
300402 |
300415 |
+ |
300128 |
301715 |
+ |
362 |
N-terminally acetylated protein component of the large
(60S) ribosomal subunit, nearly identical to Rpl4Bp and has similarity to E.
coli L4 and rat L4 ribosomal proteins |
8 |
| CATGTTAGTTTCTA |
YDL184C |
RPL41A |
6320017 |
- |
9 |
4 |
10 |
1 |
1 |
4 |
130319 |
130332 |
- |
129909 |
130485 |
- |
25 |
Ribosomal protein L47 of the large (60S) ribosomal
subunit, identical to Rpl41Bp and has similarity to rat L41 ribosomal
protein; comprised of only 25 amino acids; rpl41a
rpl41b double null mutant is viable |
8 |
| CATGCTCTCCCCCA |
YIL148W |
RPL40A |
6322043 |
COG1552 |
0 |
0 |
6 |
1 |
1 |
9 |
69010 |
69023 |
+ |
68708 |
70027 |
+ |
128 |
Fusion protein, identical to Rpl40Bp, that is cleaved to
yield ubiquitin and a ribosomal protein of the large (60S) ribosomal subunit
with similarity to rat L40; ubiquitin may facilitate
assembly of the ribosomal protein into ribosomes |
3 |
| CATGTCTCCAGAAG |
YDR500C |
RPL37B |
6320708 |
COG2126 |
3 |
4 |
0 |
1 |
1 |
4 |
1450234 |
1450247 |
- |
1449687 |
1450841 |
- |
88 |
Protein component of the large (60S) ribosomal subunit,
has similarity to Rpl37Ap and to rat L37 ribosomal protein |
8 |
| CATGTTCAAAAGAA |
YLR185W |
RPL37A |
6323214 |
COG2126 |
3 |
4 |
0 |
3 |
1 |
12 |
523104 |
523117 |
+ |
522665 |
523633 |
+ |
88 |
Protein component of the large (60S) ribosomal subunit,
has similarity to Rpl37Bp and to rat L37 ribosomal protein |
8 |
| CATGGCTCTCCCCC |
YPL249C-A |
RPL36B |
6325006 |
COG5051 |
6 |
8 |
0 |
1 |
1 |
16 |
75622 |
75635 |
- |
75200 |
76239 |
- |
100 |
Protein component of the large (60S) ribosomal subunit,
nearly identical to Rpl36Bp and has similarity to rat L36 ribosomal protein;
binds to 5.8 S rRNA |
8 |
| CATGACCCCAGCTC |
YMR194W |
RPL36A |
6323848 |
COG5051 |
0 |
8 |
0 |
1 |
1 |
13 |
651662 |
651675 |
+ |
651144 |
652408 |
+ |
100 |
N-terminally acetylated protein component of the large
(60S) ribosomal subunit, nearly identical to Rpl36Ap and has similarity to
rat L36 ribosomal protein; binds to 5.8 S rRNA |
8 |
| CATGTGCCACGAAC |
YER056C-A |
RPL34A |
9755331 |
COG2174 |
3 |
4 |
3 |
1 |
1 |
5 |
269143 |
269156 |
- |
268922 |
270183 |
- |
121 |
Protein component of the large (60S) ribosomal subunit,
nearly identical to Rpl34Bp and has similarity to rat L34 ribosomal protein |
8 |
| CATGCACACCAAGA |
YBL092W |
RPL32 |
6319378 |
COG1717 |
12 |
8 |
0 |
1 |
1 |
2 |
46231 |
46244 |
+ |
45975 |
46866 |
+ |
130 |
Protein component of the large (60S) ribosomal subunit,
has similairty to rat L32 ribosomal protein; overexpression disrupts
telomeric silencing |
6 |
| CATGGGTACTGATG |
YDL075W |
RPL31A |
6320128 |
COG2097 |
6 |
0 |
3 |
1 |
1 |
4 |
322774 |
322787 |
+ |
322226 |
323487 |
+ |
113 |
Protein component of the large (60S) ribosomal subunit,
nearly identical to Rpl31Bp and has similarity to rat L31 ribosomal protein;
associates with the karyopherin Sxm1p |
8 |
| CATGGATAAATACC |
YGL103W |
RPL28 |
6321335 |
COG0200 |
3 |
4 |
0 |
1 |
1 |
7 |
311609 |
311622 |
+ |
310968 |
312193 |
+ |
149 |
Ribosomal protein L29 of the large (60S) ribosomal
subunit, has similarity to E. coli L15 and rat L27a ribosomal proteins; may
have peptidyl transferase activity; can mutate to
cycloheximide resistance |
8 |
| CATGAACTGTGCTG |
YER117W |
RPL23B |
6320963 |
COG0093 |
3 |
12 |
0 |
2 |
1 |
5 |
397300 |
397313 |
+ |
396765 |
398148 |
+ |
137 |
Protein component of the large (60S) ribosomal subunit,
identical to Rpl23Ap and has similarity to E. coli L14 and rat L23 ribosomal
proteins |
9 |
| CATGAACTGTGCTG |
YBL087C |
RPL23A |
6319384 |
COG0093 |
3 |
12 |
0 |
2 |
1 |
2 |
60152 |
60165 |
- |
59380 |
60735 |
- |
137 |
Protein component of the large (60S) ribosomal subunit,
identical to Rpl23Bp and has similarity to E. coli L14 and rat L23 ribosomal
proteins |
9 |
| CATGGTGCCGTCCA |
YBR191W |
RPL21A |
6319668 |
COG2139 |
6 |
0 |
13 |
1 |
1 |
2 |
606677 |
606690 |
+ |
606227 |
607596 |
+ |
160 |
Protein component of the large (60S) ribosomal subunit,
nearly identical to Rpl21Bp and has similarity to rat L21 ribosomal protein |
3 |
| CATGGGTCCAGCTT |
YGL135W |
RPL1B |
6321303 |
COG0081 |
12 |
8 |
0 |
2 |
1 |
7 |
255269 |
255282 |
+ |
254644 |
255665 |
+ |
217 |
N-terminally acetylated protein component of the large
(60S) ribosomal subunit, nearly identical to Rpl1Bp and has similarity to E.
coli L1 and rat L10a ribosomal proteins; rpl1a
rpl1b double null mutation is lethal |
6 |
| CATGGGTCCAGCTT |
YPL220W |
RPL1A |
6325036 |
COG0081 |
12 |
8 |
0 |
2 |
1 |
16 |
136414 |
136427 |
+ |
135789 |
136748 |
+ |
217 |
N-terminally acetylated protein component of the large
(60S) ribosomal subunit, nearly identical to Rpl1Bp and has similarity to E.
coli L1 and rat L10a ribosomal proteins; rpl1a
rpl1b double null mutation is lethal |
6 |
| CATGCTCAATCCAA |
YBL027W |
RPL19B |
6319444 |
COG2147 |
6 |
0 |
0 |
1 |
1 |
2 |
168966 |
168979 |
+ |
168388 |
169840 |
+ |
189 |
Protein component of the large (60S) ribosomal subunit,
nearly identical to Rpl19Bp and has similarity to rat L19 ribosomal protein;
rpl19a and rpl19b single null mutations result in
slow growth, while the double null mutation is lethal |
8 |
| CATGATCTTTAATT |
YKL006W |
RPL14A |
6322847 |
COG2163 |
6 |
0 |
0 |
2 |
1 |
11 |
432371 |
432384 |
+ |
431549 |
432862 |
+ |
138 |
N-terminally acetylated protein component of the large
(60S) ribosomal subunit, nearly identical to Rpl14Bp and has similarity to
rat L14 ribosomal protein; rpl14a csh5 double null
mutant exhibits synthetic slow growth |
8 |
| CATGTGATTATACC |
YEL054C |
RPL12A |
6320781 |
COG0080 |
6 |
0 |
0 |
1 |
1 |
5 |
52477 |
52490 |
- |
52222 |
53218 |
- |
165 |
Protein component of the large (60S) ribosomal subunit,
nearly identical to Rpl12Bp; rpl12a rpl12b double mutant exhibits slow growth
and slow translation; has similarity to E. coli
L11 and rat L12 ribosomal proteins |
8 |
| CATGAACAGACCAG |
YGR085C |
RPL11B |
6321522 |
COG0094 |
9 |
12 |
0 |
3 |
1 |
7 |
648506 |
648519 |
- |
648145 |
648909 |
- |
174 |
Protein component of the large (60S) ribosomal subunit,
nearly identical to Rpl11Ap; involved in ribosomal assembly; depletion causes
degradation of proteins and RNA of the 60S
subunit; has similarity to E. coli L5 and rat L11 |
6 |
| CATGAACAGACCAG |
YPR102C |
RPL11A |
6325359 |
COG0094 |
9 |
12 |
0 |
3 |
1 |
16 |
731341 |
731354 |
- |
730721 |
731744 |
- |
174 |
Protein component of the large (60S) ribosomal subunit,
nearly identical to Rpl11Bp; involved in ribosomal assembly; depletion causes
degradation of proteins and RNA of the 60S
subunit; has similarity to E. coli L5 and rat L11 |
6 |
| CATGTCTTGAGAAT |
YLR075W |
RPL10 |
6323104 |
COG0197 |
6 |
12 |
0 |
1 |
1 |
12 |
283209 |
283222 |
+ |
282928 |
283872 |
+ |
221 |
Protein component of the large (60S) ribosomal subunit,
responsible for joining the 40S and 60S subunits; regulates translation
initiation; has similarity to rat L10 ribosomal
protein and to members of the QM gene family |
9 |
| CATGTGGCAAACAA |
YIL119C |
RPI1 |
6322072 |
- |
6 |
0 |
6 |
1 |
1 |
9 |
136796 |
136809 |
- |
136152 |
137874 |
- |
407 |
possesses a transcriptional activation domain and affects
the mRNA levels of several cell wall metabolism genes. |
8 |
| CATGTGTAGAAAAG |
YER169W |
RPH1 |
6321017 |
COG5048 |
0 |
8 |
0 |
2 |
1 |
5 |
525887 |
525900 |
+ |
523364 |
525968 |
+ |
796 |
Regulator of PHR1 |
8 |
| CATGAAAAAAATAA |
YHR088W |
RPF1 |
6321880 |
COG2136 |
6 |
4 |
0 |
4 |
1 |
8 |
281564 |
281577 |
+ |
281496 |
282882 |
+ |
295 |
protein that localizes to the nucleolus |
8 |
| CATGGGAAAAATGG |
YJL121C |
RPE1 |
6322341 |
COG0036 |
3 |
4 |
0 |
1 |
1 |
10 |
190148 |
190161 |
- |
189795 |
191010 |
- |
238 |
D-ribulose-5-Phosphate 3-epimerase |
8 |
| CATGAGACAAAACT |
YPR190C |
RPC82 |
6325448 |
- |
0 |
4 |
17 |
1 |
1 |
16 |
917294 |
917307 |
- |
916572 |
919035 |
- |
654 |
RNA polymerase III subunit C82 |
3 |
| CATGCTGGCAAAGT |
YNL151C |
RPC31 |
6324178 |
- |
0 |
4 |
6 |
1 |
1 |
14 |
347989 |
348002 |
- |
347267 |
348521 |
- |
251 |
RNA polymerase III subunit C31; contains HMG-like
C-terminal domain |
8 |
| CATGTAGATGTTAC |
YNL113W |
RPC19 |
6324215 |
COG1761 |
3 |
4 |
0 |
1 |
1 |
14 |
413192 |
413205 |
+ |
412771 |
413638 |
+ |
142 |
RNA polymerase subunit, common to RNA polymerases I and
III |
8 |
| CATGTTGTTCTTTT |
YBR154C |
RPB5 |
6319630 |
COG2012 |
0 |
0 |
6 |
2 |
1 |
2 |
547834 |
547847 |
- |
547819 |
548965 |
- |
215 |
RNA polymerase subunit, found in RNA polymerase complexes
I, II, and III |
3 |
| CATGTGGCTGAGGA |
YJL148W |
RPA34 |
6322313 |
- |
6 |
17 |
0 |
1 |
1 |
10 |
140894 |
140907 |
+ |
140355 |
141555 |
+ |
233 |
RNA polymerase I subunit A34.5 |
9 |
| CATGTGAACATCTA |
YJR063W |
RPA12 |
6322523 |
COG1594 |
3 |
4 |
0 |
1 |
1 |
10 |
555542 |
555555 |
+ |
555109 |
555827 |
+ |
125 |
RNA polymerase I subunit A12.2; contains two zinc binding
domains, and the N terminal domain is responsible for anchoring to the RNA
pol I complex |
8 |
| CATGCAGTATATAT |
YBL093C |
ROX3 |
6319377 |
- |
27 |
17 |
6 |
1 |
1 |
2 |
44154 |
44167 |
- |
43754 |
44915 |
- |
220 |
RNA polymerase II holoenzyme component |
5 |
| CATGATAAGACGGC |
YPR065W |
ROX1 |
6325322 |
- |
3 |
25 |
0 |
1 |
1 |
16 |
680236 |
680249 |
+ |
679688 |
681207 |
+ |
368 |
Heme-dependent repressor of hypoxic genes; contains an
HMG domain that is responsible for DNA bending activity |
9 |
| CATGATGTGGTATA |
YLR371W |
ROM2 |
6323403 |
- |
6 |
0 |
0 |
1 |
1 |
12 |
864158 |
864171 |
+ |
862713 |
867282 |
+ |
1356 |
GDP/GTP exchange protein (GEP) for Rho1p and Rho2p;
mutations are synthetically lethal with mutations in rom1, which also encodes
a GEP |
8 |
| CATGTGACGGTAAG |
YGL144C |
ROG1 |
6321294 |
- |
0 |
0 |
10 |
2 |
1 |
7 |
232131 |
232144 |
- |
231954 |
234510 |
- |
685 |
Protein with putative serine active lipase domain |
3 |
| CATGTCTAAGTCCG |
YGR180C |
RNR4 |
6321619 |
COG0208 |
3 |
4 |
0 |
1 |
1 |
7 |
855307 |
855320 |
- |
854899 |
856304 |
- |
345 |
Ribonucleotide-diphosphate reductase (RNR), small
subunit; the RNR complex catalyzes the rate-limiting step in dNTP synthesis
and is regulated by DNA replication and DNA damage
checkpoint pathways via localization of the small subunits |
8 |
| CATGGAAAACATCT |
YJL026W |
RNR2 |
6322434 |
COG0208 |
18 |
8 |
0 |
1 |
1 |
10 |
393386 |
393399 |
+ |
392320 |
393882 |
+ |
399 |
Ribonucleotide-diphosphate reductase (RNR), small
subunit; the RNR complex catalyzes the rate-limiting step in dNTP synthesis
and is regulated by DNA replication and DNA damage
checkpoint pathways via localization of the small subunits |
6 |
| CATGGTGACACGCT |
YMR235C |
RNA1 |
6323891 |
COG5238 |
3 |
0 |
3 |
1 |
1 |
13 |
741439 |
741452 |
- |
741012 |
742734 |
- |
407 |
Protein involved in RNA processing and export from
nucleus |
8 |
| CATGTAAATATAAA |
YEL050C |
RML2 |
6320785 |
COG0090 |
3 |
4 |
0 |
3 |
1 |
5 |
59537 |
59550 |
- |
59171 |
60851 |
- |
393 |
Mitochondrial ribosomal protein of the large subunit, has
similarity to E. coli L2 ribosomal protein; fat21 mutant allele causes
inability to utilize oleate and may interfere with
activity of the Adr1p transcription factor |
8 |
| CATGCTAATCACTG |
YER083C |
RMD7 |
37362643 |
- |
3 |
4 |
0 |
1 |
1 |
5 |
326216 |
326229 |
- |
325933 |
327027 |
- |
285 |
Required for Meiotic nuclear Division; functions in DNA
replication and damage response |
8 |
| CATGGAAATCCGGT |
YDR255C |
RMD5 |
6320461 |
COG5109 |
3 |
0 |
3 |
2 |
1 |
4 |
967110 |
967123 |
- |
966050 |
967814 |
- |
421 |
Required for Meiotic nuclear Division |
8 |
| CATGTAGCTAACAA |
YNL139C |
RLR1 |
6324190 |
- |
6 |
0 |
17 |
1 |
1 |
14 |
364938 |
364951 |
- |
360425 |
365717 |
- |
1597 |
Required for LacZ RNA expression from certain plasmids;
suppressor of the Transcriptional (T) defect of Hpr1 (H) by Overexpression
(O); plays a role in transcription elongation by
RNA polymerase II |
2 |
| CATGGGATAAATAA |
YLR009W |
RLP24 |
6323037 |
COG2075 |
3 |
8 |
0 |
1 |
1 |
12 |
167188 |
167201 |
+ |
166536 |
167634 |
+ |
199 |
Ribosomal Like Protein 24 |
8 |
| CATGAGGACAAGGA |
YOR119C |
RIO1 |
6324693 |
COG1718 |
15 |
4 |
6 |
1 |
1 |
15 |
548906 |
548919 |
- |
548293 |
550246 |
- |
484 |
Essential in yeast; plays a role in cell cycle
progression. |
6 |
| CATGTGTACTTAAT |
YGL045W |
RIM8 |
27808707 |
- |
0 |
4 |
3 |
1 |
1 |
7 |
415895 |
415908 |
+ |
414104 |
416231 |
+ |
542 |
Regulator of IME2 (RIM) Involved in proteolytic
processing of Rim1p |
8 |
| CATGGTTTCAAACG |
YOR275C |
RIM20 |
6324849 |
- |
6 |
0 |
0 |
1 |
1 |
15 |
840799 |
840812 |
- |
838582 |
841066 |
- |
661 |
Regulator of IME2 |
8 |
| CATGCGCCTTACCT |
YBL033C |
RIB1 |
6319438 |
COG0807 |
0 |
8 |
0 |
1 |
1 |
2 |
158852 |
158865 |
- |
158355 |
159658 |
- |
345 |
First step in the riboflavin biosynthesis pathway |
8 |
| CATGGGTCAATGGC |
YNL163C |
RIA1 |
6324166 |
COG0480 |
6 |
4 |
0 |
2 |
1 |
14 |
329022 |
329035 |
- |
326321 |
330073 |
- |
1110 |
RIbosome Assembly; Elongation Factor Like |
8 |
| CATGACTTAATAAT |
YIL053W |
RHR2 |
6322136 |
COG0637 |
6 |
17 |
0 |
1 |
1 |
9 |
255962 |
255975 |
+ |
255050 |
256364 |
+ |
271 |
DL-glycerol-3-phosphatase |
9 |
| CATGGCAAGTCGCA |
YBL082C |
RHK1 |
6319389 |
- |
6 |
4 |
0 |
1 |
1 |
2 |
70350 |
70363 |
- |
69443 |
71124 |
- |
458 |
Resistance to Hansenula Killer 1, hypothetical F-458
protein |
8 |
| CATGCAATGAATGA |
YKL038W |
RGT1 |
6322813 |
- |
3 |
4 |
0 |
2 |
1 |
11 |
368835 |
368848 |
+ |
365248 |
369007 |
+ |
1170 |
transcriptional repressor and activator |
8 |
| CATGACACTGCATA |
YOR107W |
RGS2 |
6324681 |
- |
3 |
8 |
6 |
1 |
1 |
15 |
522562 |
522575 |
+ |
521353 |
522781 |
+ |
309 |
Regulator of G-protein Signalling for gpa2; belongs to
the RGS protein family and acts on Gpa2 |
8 |
| CATGAGTTTCAATA |
YMR182C |
RGM1 |
6323836 |
COG5048 |
0 |
0 |
6 |
2 |
1 |
13 |
625069 |
625082 |
- |
624080 |
625166 |
- |
211 |
Putative transcriptional repressor with proline-rich zinc
fingers |
3 |
| CATGGTGTTGAGAA |
YBL020W |
RFT1 |
6319451 |
- |
6 |
0 |
0 |
1 |
1 |
2 |
183798 |
183811 |
+ |
182366 |
184317 |
+ |
574 |
encodes a flippase that is required for translocation of
Man5GlcNac2-PP-Dol from the cytoplasmic side to the lumenal side of the ER
membrane |
8 |
| CATGAATATTACAT |
YJR068W |
RFC2 |
6322528 |
COG0470 |
0 |
0 |
6 |
1 |
1 |
10 |
568468 |
568481 |
+ |
567557 |
569117 |
+ |
353 |
RFC is a DNA binding protein and ATPase that acts as a
processivity factor for DNA polymerases delta and epsilon and loads
proliferating cell nuclear antigen (PCNA) on DNA |
3 |
| CATGCACACCCCTC |
YPL167C |
REV3 |
6325090 |
COG0417 |
3 |
4 |
0 |
1 |
1 |
16 |
235185 |
235198 |
- |
232093 |
237106 |
- |
1504 |
DNA polymerase zeta, which is unique in its ability to
bypass thymine dimers during replication, is composed of Rev3p and Rev7p. |
8 |
| CATGGAGCCGTTGT |
YBR049C |
REB1 |
6319523 |
COG5147 |
6 |
0 |
13 |
1 |
1 |
2 |
334150 |
334163 |
- |
333847 |
336778 |
- |
810 |
DNA binding protein which binds sites found in genes
transcribed by both RNA polymerase I and RNA polymerase II. Reb1p is required
for termination of RNA polymerase I transcription. |
3 |
| CATGAAAAAAAAAA |
YOR380W |
RDR1 |
6324956 |
- |
3 |
0 |
3 |
13 |
1 |
15 |
1052790 |
1052803 |
+ |
1051286 |
1053425 |
+ |
546 |
Repressor of drug resistance |
8 |
| CATGGCGAACCGAT |
YGL246C |
RAI1 |
6321191 |
- |
6 |
0 |
0 |
1 |
1 |
7 |
37507 |
37520 |
- |
37118 |
38780 |
- |
387 |
Product of gene unknown |
8 |
| CATGGTTATATATA |
YGL163C |
RAD54 |
6321275 |
COG0553 |
9 |
0 |
0 |
1 |
1 |
7 |
193608 |
193621 |
- |
193305 |
196407 |
- |
898 |
DNA-dependent ATPase, stimulates strand exchange by
modifying the topology of double-stranded DNA; involved in the
recombinational repair of double-strand breaks in
DNA during vegetative growth and meiosis; member of the SWI/SNF family |
8 |
| CATGAATGGTTCAG |
YNL250W |
RAD50 |
6324079 |
COG0419 |
0 |
0 |
6 |
1 |
1 |
14 |
175509 |
175522 |
+ |
175409 |
179846 |
+ |
1312 |
Subunit of MRX complex, with Mre11p and Xrs2p, involved
in processing double-strand DNA breaks in vegetative cells, initiation of
meiotic DSBs, telomere maintenance, and
nonhomologous end joining |
3 |
| CATGATTTTTGAGC |
YEL037C |
RAD23 |
6320798 |
COG5272 |
0 |
8 |
0 |
1 |
1 |
5 |
81339 |
81352 |
- |
80908 |
82603 |
- |
398 |
Protein with ubiquitin-like N terminus, recognizes and
binds damaged DNA (with Rad4p) during nucleotide excision repair; regulates
Rad4p levels, subunit of Nuclear Excision Repair
Factor 2 (NEF2); homolog of human HR23A and HR23B proteins |
8 |
| CATGTTGAGTGAGC |
YMR022W |
QRI8 |
6323664 |
COG5078 |
0 |
0 |
10 |
1 |
1 |
13 |
319052 |
319065 |
+ |
318679 |
319675 |
+ |
165 |
part of the HRDDER pathway of ER-associated protein
degradation |
3 |
| CATGTATATATTAT |
YLR204W |
QRI5 |
6323233 |
- |
6 |
0 |
0 |
3 |
1 |
12 |
552682 |
552695 |
+ |
552272 |
553106 |
+ |
111 |
Product of gene unknown |
8 |
| CATGTTCAACCCAA |
YGR183C |
QCR9 |
6321622 |
- |
3 |
4 |
0 |
1 |
1 |
7 |
858947 |
858960 |
- |
858567 |
859479 |
- |
66 |
7.3 kDa subunit 9 of the ubiquinol cytochrome c
oxidoreductase complex |
8 |
| CATGCCTCTACATT |
YJL166W |
QCR8 |
6322295 |
- |
12 |
12 |
58 |
1 |
1 |
10 |
106720 |
106733 |
+ |
106427 |
107210 |
+ |
94 |
Ubiquinol cytochrome-c reductase subunit 8 (11 kDa
protein) |
1 |
| CATGCAGACCGCTT |
YDR529C |
QCR7 |
6320738 |
- |
6 |
8 |
0 |
1 |
1 |
4 |
1496358 |
1496371 |
- |
1495654 |
1496536 |
- |
127 |
ubiquinol-cytochrome c oxidoreductase subunit 7 (14 kDa) |
8 |
| CATGTAAGACCAAA |
YPR191W |
QCR2 |
6325449 |
COG0612 |
3 |
4 |
0 |
1 |
1 |
16 |
920608 |
920621 |
+ |
919375 |
920980 |
+ |
368 |
40 kDa ubiquinol cytochrome-c reductase core protein 2 |
8 |
| CATGCTTGGGCTAT |
YHR001W-A |
QCR10 |
6321788 |
- |
3 |
8 |
0 |
1 |
1 |
8 |
107992 |
108005 |
+ |
107820 |
108615 |
+ |
77 |
8.5 kDa subunit of the ubiqunol-cytochrome c
oxidoreductase complex |
8 |
| CATGCTCTGGTTCT |
YBR218C |
PYC2 |
6319695 |
COG1038 |
3 |
4 |
0 |
2 |
1 |
2 |
660949 |
660962 |
- |
658165 |
662206 |
- |
1180 |
converts pyruvate to oxaloacetate |
8 |
| CATGAACCGGTTAG |
YGL062W |
PYC1 |
6321376 |
COG1038 |
6 |
8 |
6 |
1 |
1 |
7 |
388728 |
388741 |
+ |
385197 |
389232 |
+ |
1178 |
converts pyruvate to oxaloacetate |
8 |
| CATGGCATAATCTG |
YLR196W |
PWP1 |
6323225 |
COG2319 |
3 |
4 |
10 |
1 |
1 |
12 |
545690 |
545703 |
+ |
543970 |
546098 |
+ |
576 |
periodic tryptophan proteinProtein with periodic
trytophan residues that resembles members of beta-transducin superfamily
because of presence of WD-40 repeats |
8 |
| CATGTAAATGTTAG |
YHR037W |
PUT2 |
6321826 |
COG1012 |
3 |
38 |
0 |
2 |
1 |
8 |
183747 |
183760 |
+ |
181969 |
184057 |
+ |
575 |
delta-1-pyrroline-5-carboxylate dehydrogenase |
9 |
| CATGGGGCCCACCA |
YLR142W |
PUT1 |
6323171 |
COG0506 |
55 |
98 |
10 |
1 |
1 |
12 |
426480 |
426493 |
+ |
425187 |
427116 |
+ |
476 |
proline oxidase |
4 |
| CATGCTCGGTAAGT |
YGL063W |
PUS2 |
6321375 |
COG0101 |
3 |
0 |
3 |
1 |
1 |
7 |
385053 |
385066 |
+ |
383655 |
385196 |
+ |
370 |
pseudouridine synthase 2 |
8 |
| CATGCAAACTGGTA |
YNL016W |
PUB1 |
6324312 |
COG0724 |
0 |
8 |
0 |
2 |
1 |
14 |
603491 |
603504 |
+ |
602905 |
604765 |
+ |
453 |
abundant mRNP-component protein hypothesized to bind a
pool of non-translatable mRNAs. not reported to associate with polyribosomes. |
8 |
| CATGTATGTTTGCC |
YER075C |
PTP3 |
6320919 |
- |
3 |
0 |
3 |
1 |
1 |
5 |
310776 |
310789 |
- |
307910 |
311195 |
- |
928 |
Protein tyrosine phosphatase |
8 |
| CATGGTGCTTCTTT |
YBL056W |
PTC3 |
6319415 |
COG0631 |
0 |
0 |
6 |
1 |
1 |
2 |
114974 |
114987 |
+ |
113727 |
115632 |
+ |
468 |
protein phosphatase type 2C |
3 |
| CATGACCCGGCTTC |
YER089C |
PTC2 |
6320934 |
COG0631 |
6 |
12 |
0 |
1 |
1 |
5 |
336002 |
336015 |
- |
335443 |
337336 |
- |
464 |
Protein phosphatase type 2C |
9 |
| CATGTGTAGGGTCT |
YAL043C |
PTA1 |
6319273 |
- |
6 |
0 |
0 |
1 |
1 |
1 |
58654 |
58667 |
- |
58466 |
61055 |
- |
785 |
pre-tRNA processing |
8 |
| CATGGGGTGCGGGT |
YDR032C |
PST2 |
6320235 |
COG0655 |
9 |
0 |
0 |
1 |
1 |
4 |
504195 |
504208 |
- |
503595 |
504690 |
- |
198 |
Protoplasts-SecreTed protein; the gene product was
detected among the proteins secreted by regenerating protoplasts |
8 |
| CATGTGAACAAATA |
YDR055W |
PST1 |
6320260 |
- |
15 |
25 |
17 |
2 |
1 |
4 |
564909 |
564922 |
+ |
563523 |
565356 |
+ |
444 |
Protoplasts-secreted |
5 |
| CATGGGGTGACTAT |
YJL079C |
PRY1 |
6322382 |
COG2340 |
6 |
12 |
0 |
1 |
1 |
10 |
289862 |
289875 |
- |
289292 |
290690 |
- |
299 |
Protein of unknown function, has similarity to Pry2p and
Pry3p and to the plant PR-1 class of pathogen related proteins |
9 |
| CATGGACCCTTCCT |
YBL064C |
PRX1 |
6319407 |
COG0450 |
9 |
4 |
6 |
1 |
1 |
2 |
101066 |
101079 |
- |
100080 |
101120 |
- |
261 |
also called mTPx I, a mitochondrial isoform of
thioredoxin peroxidase (EC 1.11.1.-) |
8 |
| CATGGATGGTAGTG |
YOL061W |
PRS5 |
6324511 |
COG0462 |
3 |
17 |
0 |
1 |
1 |
15 |
213721 |
213734 |
+ |
212243 |
214232 |
+ |
496 |
Phosphoribosylpyrophosphate synthetase (ribose-phosphate
pyrophosphokinase) |
9 |
| CATGCATTTTACCC |
YHL011C |
PRS3 |
6321776 |
COG0462 |
0 |
0 |
6 |
1 |
1 |
8 |
80427 |
80440 |
- |
80150 |
81611 |
- |
320 |
ribose-phosphate pyrophosphokinase 3 |
3 |
| CATGGCTTGGGCGG |
YKL181W |
PRS1 |
6322667 |
COG0462 |
6 |
0 |
0 |
1 |
1 |
11 |
108169 |
108182 |
+ |
107321 |
109103 |
+ |
427 |
ribose-phosphate pyrophosphokinase |
8 |
| CATGCCACTGAAGA |
YGL120C |
PRP43 |
6321318 |
COG1643 |
6 |
0 |
3 |
2 |
1 |
7 |
283036 |
283049 |
- |
281162 |
283941 |
- |
767 |
RNA helicase in the DEAH-box family, involved in release
of the lariat-intron from the
spliceosome |
8 |
| CATGAAAGGAAAAG |
YDR473C |
PRP3 |
6320681 |
- |
0 |
0 |
10 |
2 |
1 |
4 |
1405114 |
1405127 |
- |
1403934 |
1405842 |
- |
469 |
Splicing factor, component of the U4/U6-U5 snRNP complex |
3 |
| CATGTCGCAGGTAA |
YER013W |
PRP22 |
6320850 |
COG1185 |
0 |
8 |
0 |
1 |
1 |
5 |
182075 |
182088 |
+ |
178840 |
182598 |
+ |
1145 |
RNA-dependent ATPase/ATP-dependent RNA helicase in the
DEAH-box family, associates with the lariat intermediate before the second
catalytic step of splicing |
8 |
| CATGGAATTGGAGA |
YMR302C |
PRP12 |
6323960 |
- |
0 |
0 |
10 |
1 |
1 |
13 |
870391 |
870404 |
- |
869627 |
872624 |
- |
850 |
Integral inner mitochondrial membrane protein with
similarity to exonucleases; prp12 mutants exhibit an increased rate of mt DNA
escape |
3 |
| CATGCTGGAGGGGA |
YIL117C |
PRM5 |
6322074 |
- |
0 |
0 |
6 |
1 |
1 |
9 |
140626 |
140639 |
- |
140111 |
141566 |
- |
318 |
Pheromone-regulated protein, predicted to have 1
transmembrane segment; induced during cell integrity signalling |
3 |
| CATGGCTATGAATT |
YPL156C |
PRM4 |
6325101 |
COG0695 |
3 |
0 |
13 |
1 |
1 |
16 |
256134 |
256147 |
- |
255413 |
256766 |
- |
284 |
Pheromone-regulated protein, predicted to have 1
transmembrane segment; transcriptionally regulated by Ste12p during mating
and by Cat8p during the diauxic shift |
3 |
| CATGGAACACAAGA |
YNL279W |
PRM1 |
6324050 |
- |
6 |
8 |
3 |
4 |
1 |
14 |
112052 |
112065 |
+ |
110915 |
113268 |
+ |
661 |
Pheromone-regulated multispanning membrane protein
involved in membrane fusion during mating; predicted to have 5 transmembrane
segments and a coiled coil domain; localizes to
the shmoo tip; regulated by Ste12p |
8 |
| CATGCTTATATAAA |
YGR135W |
PRE9 |
6321574 |
COG0638 |
3 |
0 |
13 |
2 |
1 |
7 |
762194 |
762207 |
+ |
761395 |
762430 |
+ |
258 |
20S proteasome beta-type subunit; the only nonessential
20S subunit |
3 |
| CATGGGGCTCTCGT |
YMR314W |
PRE5 |
6323974 |
COG0638 |
3 |
8 |
3 |
1 |
1 |
13 |
901913 |
901926 |
+ |
901708 |
902798 |
+ |
234 |
20S proteasome alpha-type subunit |
8 |
| CATGGCCTCGTTTA |
YPL179W |
PPQ1 |
6325078 |
COG0639 |
3 |
8 |
24 |
2 |
1 |
16 |
209980 |
209993 |
+ |
208156 |
210304 |
+ |
549 |
Putative protein serine/threonine phosphatase; null
mutation enhances efficiency of translational suppressors |
2 |
| CATGGAAGTGGACG |
YDL134C |
PPH21 |
6320067 |
COG0639 |
3 |
4 |
0 |
1 |
1 |
4 |
219753 |
219766 |
- |
219289 |
220771 |
- |
369 |
Catalytic subunit of protein phosphatase 2A, functionally
redundant with Pph22p; methylated at C terminus; forms alternate complexes
with several regulatory subunits; involved in
signal transduction and regulation of mitosis |
8 |
| CATGTGTATGTATA |
YHR026W |
PPA1 |
6321815 |
COG0636 |
18 |
12 |
17 |
3 |
1 |
8 |
161566 |
161579 |
+ |
160836 |
161976 |
+ |
213 |
Subunit c'' of the vacuolar ATPase, which functions in
acidification of the vacuole; one of three proteolipid subunits of the V0
domain |
8 |
| CATGGCTTTAAGTT |
YNL055C |
POR1 |
6324273 |
- |
6 |
4 |
0 |
1 |
1 |
14 |
518332 |
518345 |
- |
517493 |
518843 |
- |
283 |
Outer mitochondrial membrane porin (voltage-dependent
anion channel, or VDAC) |
8 |
| CATGGAAAGTGATG |
YBR167C |
POP7 |
6319644 |
- |
12 |
0 |
0 |
1 |
1 |
2 |
571498 |
571511 |
- |
571158 |
571847 |
- |
140 |
Subunit of both RNase MRP, which cleaves pre-rRNA, and
nuclear RNase P, which cleaves tRNA precursors to generate mature 5' ends |
6 |
| CATGGCATATCGAA |
YGR030C |
POP6 |
6321467 |
- |
0 |
4 |
6 |
1 |
1 |
7 |
546007 |
546020 |
- |
545184 |
546159 |
- |
158 |
Subunit of both RNase MRP, which cleaves pre-rRNA, and
nuclear RNase P, which cleaves tRNA precursors to generate mature 5' ends |
8 |
| CATGGGAGATCTTG |
YCR014C |
POL4 |
10383782 |
COG1796 |
24 |
64 |
31 |
1 |
1 |
3 |
138896 |
138909 |
- |
138683 |
140930 |
- |
582 |
Probable homolog of mammalian DNA polymerase beta; may
function in double-stranded DNA break repair |
7 |
| CATGAAAAAAAAAA |
YNL262W |
POL2 |
6324067 |
COG0417 |
3 |
0 |
3 |
13 |
1 |
14 |
154918 |
154931 |
+ |
148211 |
155098 |
+ |
2222 |
DNA polymerase II |
8 |
| CATGACGTGCAGTA |
YIL122W |
POG1 |
6322069 |
- |
6 |
0 |
0 |
1 |
1 |
9 |
131657 |
131670 |
+ |
130607 |
132161 |
+ |
351 |
Promoter of Growth; weak similarity to human
transcription adaptor protein p300 |
8 |
| CATGAACAAGTACT |
YGL037C |
PNC1 |
6321401 |
COG1335 |
3 |
4 |
6 |
1 |
1 |
7 |
427506 |
427519 |
- |
426809 |
427951 |
- |
216 |
NAD(+) salvage pathway gene |
8 |
| CATGAACGAGGATG |
YDL095W |
PMT1 |
6320107 |
COG1928 |
0 |
0 |
10 |
1 |
1 |
4 |
289379 |
289392 |
+ |
287059 |
289908 |
+ |
817 |
Transfers mannose residues from dolichyl
phosphate-D-mannose to specific serine/threonine residues of proteins in the
secretory pathway; acts in complex with Pmt2p |
3 |
| CATGTATGGGCGAC |
YGL167C |
PMR1 |
6321271 |
COG0474 |
12 |
12 |
34 |
1 |
1 |
7 |
187456 |
187469 |
- |
187121 |
190472 |
- |
950 |
Pmr1p, a member of the SERCA family of CaATPases, plays
an important role in the transport of Ca++ into Golgi. |
2 |
| CATGATATAGACGC |
YDR276C |
PMP3 |
6320482 |
COG0401 |
3 |
4 |
0 |
1 |
1 |
4 |
1013196 |
1013209 |
- |
1012969 |
1013635 |
- |
55 |
plasma membrane protein involved in salt tolerance |
8 |
| CATGGGGGTGCTAG |
YGL006W |
PMC1 |
6321432 |
COG0474 |
0 |
0 |
6 |
1 |
1 |
7 |
489257 |
489270 |
+ |
485923 |
489943 |
+ |
1173 |
May be involved in depleting cytosol of Ca2+ ions |
3 |
| CATGGCTGCTATGC |
YPL036W |
PMA2 |
6325221 |
COG0474 |
21 |
25 |
13 |
2 |
1 |
16 |
485633 |
485646 |
+ |
482839 |
486181 |
+ |
947 |
plasma membrane ATPase |
5 |
| CATGGCTGCTATGC |
YGL008C |
PMA1 |
6321430 |
COG0474 |
21 |
25 |
13 |
2 |
1 |
7 |
479947 |
479960 |
- |
479414 |
482669 |
- |
918 |
Major regulator of cytoplasmic pH. Part of the P2
subgroup of cation-transporting ATPases; functions physiologically to pump
protons out of the cell. |
5 |
| CATGCAGTACTTTC |
YMR008C |
PLB1 |
6323650 |
- |
3 |
4 |
0 |
1 |
1 |
13 |
280382 |
280395 |
- |
280091 |
282584 |
- |
664 |
Responsible for the production of the deacylation
products of phosphatidylcholine and phosphatidylethanolamine but not
phosphatidylinositol |
8 |
| CATGGTGAAGGGGA |
YDR490C |
PKH1 |
6320698 |
COG0515 |
3 |
8 |
0 |
1 |
1 |
4 |
1431903 |
1431916 |
- |
1431457 |
1434256 |
- |
766 |
Pkb-activating Kinase Homologue |
8 |
| CATGAACAAGTCGG |
YGR086C |
PIL1 |
6321523 |
- |
6 |
8 |
10 |
1 |
1 |
7 |
649642 |
649655 |
- |
649101 |
650619 |
- |
339 |
Phosphorylation Inhibited by Long chain base |
8 |
| CATGCAATCCATTT |
YBR106W |
PHO88 |
6319582 |
COG5065 |
0 |
8 |
0 |
1 |
1 |
2 |
452973 |
452986 |
+ |
452615 |
453680 |
+ |
188 |
May be a membrane protein involved in inorganic phosphate
transport and regulation of Pho81p function |
8 |
| CATGGCATCTTGTT |
YJL117W |
PHO86 |
6322344 |
- |
6 |
4 |
3 |
2 |
1 |
10 |
193426 |
193439 |
+ |
192451 |
193885 |
+ |
311 |
May collaborate with Pho87p and Pho84p in phosphate
uptake |
8 |
| CATGACACGTACTG |
YDR481C |
PHO8 |
6320689 |
COG1785 |
3 |
17 |
0 |
1 |
1 |
4 |
1418427 |
1418440 |
- |
1418039 |
1420238 |
- |
566 |
repressible alkaline phosphatase |
9 |
| CATGTGTTTTTCCG |
YDL236W |
PHO13 |
6319965 |
COG0647 |
3 |
4 |
6 |
1 |
1 |
4 |
33357 |
33370 |
+ |
32296 |
33733 |
+ |
312 |
p-nitrophenyl phosphatase |
8 |
| CATGACTATCGCTA |
YER037W |
PHM8 |
6320875 |
COG1011 |
3 |
4 |
0 |
1 |
1 |
5 |
225886 |
225899 |
+ |
225888 |
227352 |
+ |
321 |
Protein of unknown function, expression is induced by low
phosphate levels and by inactivation of Pho85p |
8 |
| CATGCACCTCAAGG |
YKL043W |
PHD1 |
6322808 |
- |
0 |
4 |
6 |
1 |
1 |
11 |
357144 |
357157 |
+ |
356393 |
357992 |
+ |
366 |
protein similar to StuA of Aspergillus nidulans |
8 |
| CATGTATGATGTGA |
YGR132C |
PHB1 |
6321571 |
COG0330 |
9 |
4 |
0 |
1 |
1 |
7 |
756358 |
756371 |
- |
755093 |
756455 |
- |
287 |
antiproliferative protein involved in determination of
replicative life span |
8 |
| CATGGTCTAAACTG |
YMR105C |
PGM2 |
6323752 |
COG0033 |
3 |
4 |
0 |
2 |
1 |
13 |
476544 |
476557 |
- |
475453 |
477605 |
- |
569 |
Phosphoglucomutase |
8 |
| CATGTCTCTACTGG |
YCR012W |
PGK1 |
10383781 |
COG0126 |
224 |
339 |
186 |
1 |
1 |
3 |
138906 |
138919 |
+ |
137743 |
139492 |
+ |
416 |
3-phosphoglycerate kinase |
10 |
| CATGTTACTTTCAC |
YBR196C |
PGI1 |
6319673 |
COG0166 |
0 |
12 |
13 |
1 |
1 |
2 |
612355 |
612368 |
- |
611840 |
613857 |
- |
554 |
Phosphoglucoisomerase |
8 |
| CATGATGCTGAGGG |
YOR122C |
PFY1 |
6324696 |
- |
6 |
17 |
24 |
1 |
1 |
15 |
552421 |
552434 |
- |
551799 |
552887 |
- |
126 |
profilin (actin-binding protein) |
2 |
| CATGGTCGGACTGC |
YIL107C |
PFK26 |
6322084 |
COG0406 |
3 |
4 |
0 |
1 |
1 |
9 |
165184 |
165197 |
- |
162776 |
165758 |
- |
827 |
6-Phosphofructose-2-kinase |
8 |
| CATGGTGGATTCTT |
YDR329C |
PEX3 |
6320536 |
- |
0 |
4 |
6 |
1 |
1 |
4 |
1126884 |
1126897 |
- |
1126010 |
1127586 |
- |
441 |
48-kDa peroxisomal integral membrane protein |
8 |
| CATGGCGTGACGAA |
YDR479C |
PEX29 |
6320687 |
- |
3 |
8 |
0 |
1 |
1 |
4 |
1415354 |
1415367 |
- |
1414699 |
1416862 |
- |
554 |
Peroxisomal integral membrane protein, involved in
regulation of peroxisome size and number; genetic interactions suggest that
Pex28p and Pex29p act at steps upstream of those
mediated by Pex30p, Pex31p, and Pex32p |
8 |
| CATGCCCATCTCTC |
YGR239C |
PEX21 |
6321678 |
- |
6 |
0 |
0 |
1 |
1 |
7 |
969013 |
969026 |
- |
968692 |
970057 |
- |
288 |
Peroxin; Pex18p and Pex21p are partially functionally
redundant. |
8 |
| CATGTTGTCAAAAT |
YJL210W |
PEX2 |
6322250 |
- |
3 |
4 |
0 |
2 |
1 |
10 |
37788 |
37801 |
+ |
36919 |
38004 |
+ |
271 |
Pex2p, Pex10p, and Pex12p together make up the RING
finger complex of the peroxisomal import machinery. |
8 |
| CATGTCCATACCTG |
YOL147C |
PEX11 |
6324425 |
- |
3 |
8 |
0 |
1 |
1 |
15 |
47818 |
47831 |
- |
47573 |
48641 |
- |
236 |
May promote peroxisomal proliferation by participating in
peroxisomal elongation or fission or segregation of peroxisomes to daughter
cells |
8 |
| CATGTGGACATCTA |
YDR265W |
PEX10 |
6320471 |
- |
0 |
8 |
0 |
1 |
1 |
4 |
999753 |
999766 |
+ |
998856 |
1000368 |
+ |
337 |
Pex2p, Pex10p, and Pex12p together make up the RING
finger complex of the peroxisomal import machinery. |
8 |
| CATGTGTAATGGTG |
YOR201C |
PET56 |
6324775 |
COG0566 |
6 |
4 |
0 |
1 |
1 |
15 |
720405 |
720418 |
- |
720066 |
721708 |
- |
412 |
Ribose methyltransferase that modifies a functionally
critical, conserved nucleotide in mitochondrial 21S rRNA |
8 |
| CATGTAAATATGTA |
YNR045W |
PET494 |
6324373 |
- |
9 |
0 |
0 |
2 |
1 |
14 |
707612 |
707625 |
+ |
706138 |
707786 |
+ |
489 |
Specific translational activator for the COX3 mRNA that
acts together with Pet54p and Pet122p; located in the mitochondrial inner
membrane |
8 |
| CATGATGGTGAGCA |
YCR020C |
PET18 |
6319866 |
COG0819 |
9 |
12 |
0 |
1 |
1 |
3 |
154135 |
154148 |
- |
153510 |
154656 |
- |
215 |
Protein required for respiratory growth and stability of
the mitochondrial genome |
6 |
| CATGTATATACGTC |
YOR158W |
PET123 |
6324732 |
- |
0 |
4 |
6 |
1 |
1 |
15 |
633228 |
633241 |
+ |
632164 |
633619 |
+ |
318 |
Mitochondrial ribosomal protein of the small subunit;
PET123 exhibits genetic interactions
with PET122, which encodes a COX3 mRNA-specific translational activator |
8 |
| CATGTACATACCTG |
YDR079W |
PET100 |
6320284 |
- |
9 |
4 |
0 |
1 |
1 |
4 |
603463 |
603476 |
+ |
603059 |
603893 |
+ |
111 |
Chaperone that specifically facilitates the assembly of
cytochrome c oxidase, located in the mitochondrial inner membrane |
8 |
| CATGGTGCCGCCAT |
YPL154C |
PEP4 |
6325103 |
- |
12 |
12 |
24 |
1 |
1 |
16 |
260052 |
260065 |
- |
259336 |
260930 |
- |
405 |
vacuolar proteinase A |
8 |
| CATGGATCAGGGTA |
YBL017C |
PEP1 |
6319454 |
- |
9 |
4 |
0 |
1 |
1 |
2 |
186972 |
186985 |
- |
186440 |
191548 |
- |
1579 |
vacuolar protein sorting receptor for carboxypeptidase Y
and proteinase A; related to Sortilin |
8 |
| CATGAGGGACTGTT |
YBR035C |
PDX3 |
6319509 |
COG0259 |
3 |
4 |
0 |
1 |
1 |
2 |
306221 |
306234 |
- |
305939 |
306917 |
- |
228 |
pyridoxine (pyridoxiamine) phosphate oxidase |
8 |
| CATGAAAAAAAAAA |
YNL264C |
PDR17 |
6324065 |
- |
3 |
0 |
3 |
13 |
1 |
14 |
145388 |
145401 |
- |
145281 |
146614 |
- |
350 |
involved in pleiotropic drug resistance by controlling
lipids in various cellular compartments; putative phosphatidylinositol
transfer protein. |
8 |
| CATGAGAGAGGTGC |
YDR406W |
PDR15 |
6320614 |
COG0842 |
3 |
4 |
0 |
1 |
1 |
4 |
1283202 |
1283215 |
+ |
1279198 |
1284286 |
+ |
1529 |
similar to Pdr5p and Pdr10p |
8 |
| CATGGTGTGGTCAC |
YCL043C |
PDI1 |
6319806 |
COG0526 |
9 |
4 |
10 |
1 |
1 |
3 |
48997 |
49010 |
- |
48365 |
50221 |
- |
522 |
Catalyzes the formation and isomerization of disulfide
bonds during the folding of secretory proteins. |
8 |
| CATGAAAACCCAAT |
YOR360C |
PDE2 |
6324936 |
- |
6 |
0 |
0 |
3 |
1 |
15 |
1013660 |
1013673 |
- |
1012738 |
1014817 |
- |
526 |
low-Km (high-affinity) cAMP phosphodiesterase |
8 |
| CATGCCCATTATCT |
YGL248W |
PDE1 |
6321189 |
COG5212 |
3 |
0 |
3 |
1 |
1 |
7 |
36493 |
36506 |
+ |
35653 |
36932 |
+ |
369 |
3',5'-Cyclic-nucleotide phosphodiesterase, low affinity |
8 |
| CATGATTCAACGTT |
YLR134W |
PDC5 |
6323163 |
COG3961 |
0 |
8 |
0 |
1 |
1 |
12 |
412433 |
412446 |
+ |
410724 |
412914 |
+ |
563 |
pyruvate decarboxylase |
8 |
| CATGTTGCCAGTCT |
YLR044C |
PDC1 |
6323073 |
COG3961 |
85 |
137 |
24 |
1 |
1 |
12 |
232455 |
232468 |
- |
232015 |
234082 |
- |
563 |
pyruvate decarboxylase |
4 |
| CATGTATGGCGTAC |
YBR221C |
PDB1 |
6319698 |
COG0022 |
21 |
25 |
3 |
1 |
1 |
2 |
664962 |
664975 |
- |
664635 |
666210 |
- |
366 |
beta subunit of pyruvate dehydrogenase (E1 beta) |
6 |
| CATGCAAAGGATCT |
YHR071W |
PCL5 |
6321862 |
- |
3 |
4 |
0 |
1 |
1 |
8 |
237478 |
237491 |
+ |
237005 |
238193 |
+ |
229 |
PHO85 cyclin |
8 |
| CATGGAAAAGTAAA |
YER129W |
PAK1 |
6320976 |
COG0515 |
3 |
8 |
13 |
2 |
1 |
5 |
417705 |
417718 |
+ |
417277 |
421204 |
+ |
1142 |
Protein kinase that activates the SNF1 complex by
phosphorylating Snf1p, identified as a high copy suppressor of cdc17 (DNA
polymerase alpha) mutations, not a p21 activated
kinase |
3 |
| CATGAGATAAGTTT |
YOR269W |
PAC1 |
6324843 |
COG2319 |
0 |
0 |
6 |
1 |
1 |
15 |
827856 |
827869 |
+ |
826382 |
828365 |
+ |
494 |
Required for viability in the absence of the
kinesin-related Cin8p mitotic motor. |
3 |
| CATGGGTCCAATTA |
YHR179W |
OYE2 |
6321973 |
COG1902 |
33 |
4 |
0 |
1 |
1 |
8 |
462833 |
462846 |
+ |
462500 |
464201 |
+ |
400 |
NAPDH dehydrogenase (old yellow enzyme), isoform 2 |
6 |
| CATGGAATCCAAAA |
YHR001W |
OSH7 |
6321787 |
- |
3 |
4 |
0 |
1 |
1 |
8 |
107341 |
107354 |
+ |
106049 |
107819 |
+ |
437 |
Member of an oxysterol-binding protein family with seven
members in S. cerevisiae; family members have overlapping, redundant
functions in sterol metabolism and collectively
perform a function essential for viability |
8 |
| CATGTGCTAGTTTA |
YOR130C |
ORT1 |
6324704 |
- |
3 |
4 |
0 |
1 |
1 |
15 |
570438 |
570451 |
- |
569559 |
570807 |
- |
292 |
Ornithine transporter of the mitochondrial inner
membrane, exports ornithine from mitochondria as part of arginine
biosynthesis; human ortholog is associated with hyperammonaemia-hyperornithinaemia-homocitrullinuria (HHH) syndrome |
8 |
| CATGATCTACGCTA |
YJR073C |
OPI3 |
6322533 |
- |
9 |
4 |
0 |
1 |
1 |
10 |
572257 |
572270 |
- |
572039 |
572849 |
- |
206 |
Phospholipid methyltransferase
(methylene-fatty-acyl-phospholipid synthase), catalyzes the last two steps in
phosphatidylcholine biosynthesis |
8 |
| CATGATTACGTTTT |
YGL055W |
OLE1 |
6321383 |
COG5274 |
70 |
94 |
38 |
1 |
1 |
7 |
400255 |
400268 |
+ |
398629 |
400660 |
+ |
510 |
Fatty acid desaturase, required for monounsaturated fatty
acid synthesis and for normal distribution of mitochondria |
4 |
| CATGGGAAAACAAA |
YPL134C |
ODC1 |
6325123 |
- |
12 |
4 |
17 |
1 |
1 |
16 |
298320 |
298333 |
- |
298071 |
299502 |
- |
310 |
Mitochondrial inner membrane transporter, exports
2-oxoadipate and 2-oxoglutarate from the mitochondrial matrix to the cytosol
for use in lysine and glutamate biosynthesis and
in lysine catabolism |
8 |
| CATGAAGAGCTGGT |
YLR093C |
NYV1 |
9755337 |
COG5143 |
0 |
0 |
6 |
1 |
1 |
12 |
326856 |
326869 |
- |
326015 |
327416 |
- |
253 |
v-SNARE component of the vacuolar SNARE complex involved
in vesicle fusion; inhibits ATP-dependent Ca(2+) transport activity of Pmc1p
in the vacuolar membrane |
3 |
| CATGTAGCAAGAGG |
YJL061W |
NUP82 |
6322400 |
- |
6 |
0 |
0 |
1 |
1 |
10 |
322140 |
322153 |
+ |
319932 |
322572 |
+ |
713 |
Subunit of the nuclear pore complex (NPC), forms a
subcomplex with Nup159p and Nsp1p, interacts with Nup116p and is required for
proper localization of Nup116p in the NPC |
8 |
| CATGGCAAAATAGT |
YIL115C |
NUP159 |
6322076 |
- |
6 |
0 |
0 |
1 |
1 |
9 |
144322 |
144335 |
- |
143825 |
148706 |
- |
1460 |
Subunit of the nuclear pore complex that is found
exclusively on the cytoplasmic side, forms a subcomplex with Nup82p and
Nsp1p, required for mRNA export |
8 |
| CATGGGCGGTGGTG |
YOR098C |
NUP1 |
6324672 |
- |
9 |
0 |
0 |
1 |
1 |
15 |
507994 |
508007 |
- |
507506 |
511178 |
- |
1076 |
Nuclear pore complex (NPC) subunit, involved in protein
import/export and in export of RNAs, possible karyopherin release factor that
accelerates release of karyopherin-cargo complexes
after transport across NPC; potential Cdc28p substrate |
8 |
| CATGTAAATGTTAG |
YBR001C |
NTH2 |
6319473 |
COG1626 |
3 |
38 |
0 |
2 |
1 |
2 |
240720 |
240733 |
- |
238406 |
241247 |
- |
780 |
Neutral trehalase, degrades trehalose; required for
thermotolerance and may mediate resistance to other cellular stresses |
9 |
| CATGATGACAAAGG |
YDR001C |
NTH1 |
6320204 |
COG1626 |
12 |
0 |
3 |
1 |
1 |
4 |
450482 |
450495 |
- |
449718 |
452472 |
- |
751 |
Neutral trehalase, degrades trehalose; required for
thermotolerance and may mediate resistance to other cellular stresses; may be
phosphorylated by Cdc28p |
6 |
| CATGATCACTGGTG |
YER009W |
NTF2 |
6320846 |
- |
12 |
0 |
0 |
3 |
1 |
5 |
172358 |
172371 |
+ |
172114 |
172990 |
+ |
125 |
Nuclear envelope protein, interacts with GDP-bound Gsp1p
and with proteins of the nuclear pore to transport Gsp1p into the nucleus
where it is an essential player in nucleocytoplasmic
transport |
6 |
| CATGAGAAACAGGC |
YNL091W |
NST1 |
6324238 |
- |
0 |
0 |
6 |
1 |
1 |
14 |
454252 |
454265 |
+ |
452408 |
456564 |
+ |
1240 |
Protein of unknown function, mediates sensitivity to salt
stress; interacts physically with the splicing factor Msl1p and also displays
genetic interaction with MSL1 |
3 |
| CATGGAGGACGCCA |
YGR159C |
NSR1 |
6321599 |
COG0724 |
3 |
4 |
0 |
1 |
1 |
7 |
806695 |
806708 |
- |
806025 |
807659 |
- |
414 |
Nucleolar protein that binds nuclear localization
sequences, required for pre-rRNA processing and ribosome biogenesis |
8 |
| CATGTAAGCAAGAA |
YLR007W |
NSE1 |
6323035 |
- |
3 |
8 |
0 |
1 |
1 |
12 |
165335 |
165348 |
+ |
164391 |
165900 |
+ |
336 |
Essential nuclear protein required for DNA repair; forms
a complex with Smc5p and Rhc18p |
8 |
| CATGCATACATACA |
YDR043C |
NRG1 |
6320248 |
COG5048 |
9 |
17 |
79 |
1 |
1 |
4 |
542584 |
542597 |
- |
542171 |
543365 |
- |
231 |
Transcriptional repressor that recruits the Cyc8p-Tup1p
complex to promoters; mediates glucose repression and negatively regulates a
variety of processes including filamentous growth
and alkaline pH response |
1 |
| CATGCAGCTAAAGA |
YOR209C |
NPT1 |
6324783 |
COG1488 |
0 |
8 |
0 |
1 |
1 |
15 |
736695 |
736708 |
- |
735938 |
737726 |
- |
429 |
Nicotinate phosphoribosyltransferase, acts in the salvage
pathway of NAD+ biosynthesis; required for silencing at rDNA and telomeres
and has a role in silencing at mating-type loci;
localized to the nucleus |
8 |
| CATGAAAAGGGCAT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
7 |
166622 |
166635 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGAAACAAAAAC |
N.A. |
NORF |
N.A. |
N.A. |
0 |
8 |
0 |
1 |
1 |
16 |
339447 |
339460 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGAAATATCTAT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
8 |
0 |
1 |
1 |
15 |
854719 |
854732 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGAAATCTTTCT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
9 |
107051 |
107064 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGAAATTTGTGT |
N.A. |
NORF |
N.A. |
N.A. |
6 |
0 |
0 |
1 |
1 |
4 |
1189609 |
1189622 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGAACCGATCAA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
5 |
348714 |
348727 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGAAGCGAAAGG |
N.A. |
NORF |
N.A. |
N.A. |
6 |
0 |
0 |
1 |
1 |
2 |
680581 |
680594 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGAAGCGGTACT |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
3 |
1 |
1 |
9 |
47885 |
47898 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGAAGTGATGAA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
3 |
1 |
1 |
6 |
76130 |
76143 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGAATACCAGCG |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
3 |
176797 |
176810 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGAATCAAGTAT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
10 |
712079 |
712092 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGAATGTCCAGA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
6 |
2 |
1 |
4 |
469993 |
470006 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGAATTATGTGA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
3 |
1 |
1 |
13 |
350325 |
350338 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGAATTTCTTCG |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
10 |
1 |
1 |
4 |
541651 |
541664 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGACAAGTCGCC |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
6 |
1 |
1 |
10 |
96671 |
96684 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGACAATATTGT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
5 |
299308 |
299321 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGACAATCACGT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
8 |
0 |
1 |
1 |
15 |
349127 |
349140 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGACACCACCAG |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
10 |
3 |
1 |
1 |
140214 |
140227 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGACACGCTTGT |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
15 |
430117 |
430130 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGACAGCAACTC |
N.A. |
NORF |
N.A. |
N.A. |
6 |
0 |
0 |
1 |
1 |
11 |
173810 |
173823 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGACAGCAGAGA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
14 |
59612 |
59625 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGACATATGTTA |
N.A. |
NORF |
N.A. |
N.A. |
9 |
4 |
0 |
1 |
1 |
4 |
916057 |
916070 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGACATCGGAAT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
11 |
283162 |
283175 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGACCAATAATA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
8 |
0 |
1 |
1 |
16 |
128501 |
128514 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGACCAATCTAC |
N.A. |
NORF |
N.A. |
N.A. |
0 |
4 |
3 |
1 |
1 |
7 |
883762 |
883775 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGACCGATAACG |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
10 |
2 |
1 |
2 |
477658 |
477671 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGACGGTCTTAC |
N.A. |
NORF |
N.A. |
N.A. |
9 |
0 |
3 |
1 |
1 |
11 |
163856 |
163869 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGACTATATGTT |
N.A. |
NORF |
N.A. |
N.A. |
15 |
8 |
0 |
1 |
1 |
16 |
582219 |
582232 |
- |
-1 |
-1 |
U |
0 |
|
6 |
| CATGACTGTCGCTG |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
34 |
2 |
1 |
16 |
14910 |
14923 |
+ |
-1 |
-1 |
U |
0 |
|
2 |
| CATGACTGTTCTAT |
N.A. |
NORF |
N.A. |
N.A. |
9 |
0 |
6 |
1 |
1 |
5 |
260967 |
260980 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGACTTAGTTTA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
14 |
117065 |
117078 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGACTTCTTGGT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
8 |
0 |
2 |
1 |
8 |
212551 |
212564 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGAGACCAATCC |
N.A. |
NORF |
N.A. |
N.A. |
0 |
4 |
3 |
1 |
1 |
8 |
391707 |
391720 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGAGACTTAGTA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
10 |
2 |
1 |
6 |
54426 |
54439 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGAGAGCTTTTA |
N.A. |
NORF |
N.A. |
N.A. |
12 |
0 |
76 |
2 |
1 |
12 |
455872 |
455885 |
- |
-1 |
-1 |
U |
0 |
|
2 |
| CATGAGAGGTGATC |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
17 |
1 |
1 |
7 |
811258 |
811271 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGAGATATATGT |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
12 |
1 |
4 |
883877 |
883890 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGAGATTTGATG |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
12 |
87697 |
87710 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGAGCCTACAGA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
7 |
326794 |
326807 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGAGGATGTTCG |
N.A. |
NORF |
N.A. |
N.A. |
6 |
4 |
0 |
1 |
1 |
2 |
735636 |
735649 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGAGGATTTCGG |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
3 |
1 |
1 |
12 |
22841 |
22854 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGAGGCTACCTA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
24 |
1 |
1 |
15 |
908509 |
908522 |
- |
-1 |
-1 |
U |
0 |
|
2 |
| CATGAGTAATCATA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
15 |
524856 |
524869 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGAGTCCAATGT |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
13 |
915583 |
915596 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGAGTTGATGGA |
N.A. |
NORF |
N.A. |
N.A. |
6 |
12 |
0 |
1 |
1 |
8 |
183737 |
183750 |
- |
-1 |
-1 |
U |
0 |
|
9 |
| CATGATAAGACAGT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
4 |
10 |
1 |
1 |
10 |
228011 |
228024 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGATAATGAGGA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
24 |
1 |
1 |
13 |
14416 |
14429 |
+ |
-1 |
-1 |
U |
0 |
|
2 |
| CATGATAATTGGCT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
11 |
207158 |
207171 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGATACCTTGGT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
2 |
1 |
12 |
515624 |
515637 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGATATGGCGAC |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
13 |
1 |
1 |
7 |
4082 |
4095 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGATGAATAAGA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
10 |
1 |
1 |
10 |
265044 |
265057 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGATGCCACGGT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
4 |
6 |
1 |
1 |
8 |
378439 |
378452 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGATGCTTTTAC |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
8 |
495334 |
495347 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGATGGCGAGTA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
8 |
10 |
1 |
1 |
11 |
279845 |
279858 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGATTAGAACAA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
4 |
652113 |
652126 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGATTATTTGGT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
4 |
135428 |
135441 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGATTGCGTTCT |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
2 |
1 |
8 |
260263 |
260276 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGCAAATAAAAA |
N.A. |
NORF |
N.A. |
N.A. |
15 |
34 |
0 |
2 |
1 |
2 |
537259 |
537272 |
- |
-1 |
-1 |
U |
0 |
|
5 |
| CATGCAAATCCAAA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
4 |
3 |
1 |
1 |
10 |
307303 |
307316 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGCAACTTGTGA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
6 |
2 |
1 |
9 |
21477 |
21490 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGCAAGACAAAA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
9 |
74287 |
74300 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGCACGAGGCCT |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
13 |
388660 |
388673 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGCACTCTTGGG |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
3 |
1 |
1 |
3 |
296942 |
296955 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGCAGACACACA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
10 |
1 |
1 |
16 |
831762 |
831775 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGCAGAGGCGAC |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
16 |
730172 |
730185 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGCAGATACGGA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
4 |
3 |
1 |
1 |
3 |
126724 |
126737 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGCAGATCTCCG |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
13 |
1 |
1 |
15 |
379671 |
379684 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGCAGATCTGAG |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
10 |
1 |
1 |
10 |
139680 |
139693 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGCAGCAAAAGA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
10 |
1 |
1 |
7 |
919587 |
919600 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGCAGTTGTAGT |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
4 |
593117 |
593130 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGCATAACGGAT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
8 |
0 |
1 |
1 |
7 |
610327 |
610340 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGCATATACGAG |
N.A. |
NORF |
N.A. |
N.A. |
15 |
4 |
0 |
2 |
1 |
4 |
588062 |
588075 |
+ |
-1 |
-1 |
U |
0 |
|
6 |
| CATGCATCACCATC |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
12 |
794701 |
794714 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGCCAATGGTTC |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
13 |
1 |
1 |
16 |
830097 |
830110 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGCCATTCTCTA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
2 |
443168 |
443181 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGCCATTTGTAC |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
10 |
112172 |
112185 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGCCCACGTAAG |
N.A. |
NORF |
N.A. |
N.A. |
0 |
4 |
34 |
1 |
1 |
4 |
954490 |
954503 |
- |
-1 |
-1 |
U |
0 |
|
2 |
| CATGCCGAAAGAAA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
27 |
1 |
1 |
15 |
407051 |
407064 |
- |
-1 |
-1 |
U |
0 |
|
2 |
| CATGCCGTTTAAAA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
7 |
754483 |
754496 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGCCTGTTTGAG |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
27 |
2 |
1 |
12 |
464559 |
464572 |
- |
-1 |
-1 |
U |
0 |
|
2 |
| CATGCCTTTGATAT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
12 |
460487 |
460500 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGCGAAAACAAT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
2 |
1 |
8 |
291326 |
291339 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGCGAAGTCAAA |
N.A. |
NORF |
N.A. |
N.A. |
6 |
8 |
6 |
1 |
1 |
2 |
680607 |
680620 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGCGCAAGCAGC |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
7 |
266323 |
266336 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGCGGGAACATA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
8 |
0 |
1 |
1 |
7 |
422131 |
422144 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGCGTACAGAAA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
4 |
3 |
1 |
1 |
2 |
697908 |
697921 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGCTAGAACGCG |
N.A. |
NORF |
N.A. |
N.A. |
24 |
25 |
134 |
3 |
1 |
12 |
452036 |
452049 |
- |
-1 |
-1 |
U |
0 |
|
1 |
| CATGCTCATTATCT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
2 |
292633 |
292646 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGCTCTCATCAA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
3 |
158413 |
158426 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGCTGAGCTATT |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
10 |
1 |
1 |
4 |
974921 |
974934 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGCTGCATCCTA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
4 |
1 |
7 |
422577 |
422590 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGCTGCTTCCTA |
N.A. |
NORF |
N.A. |
N.A. |
9 |
8 |
24 |
1 |
1 |
13 |
917516 |
917529 |
+ |
-1 |
-1 |
U |
0 |
|
2 |
| CATGCTGGGTCCCA |
N.A. |
NORF |
N.A. |
N.A. |
6 |
0 |
0 |
1 |
1 |
4 |
1385247 |
1385260 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGAAATGTTTG |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
2 |
733000 |
733013 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGAAATTCGTT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
10 |
1 |
1 |
15 |
258957 |
258970 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGAACTCCACA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
11 |
94124 |
94137 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGAAGTCGGAA |
N.A. |
NORF |
N.A. |
N.A. |
6 |
4 |
27 |
2 |
1 |
12 |
463067 |
463080 |
- |
-1 |
-1 |
U |
0 |
|
2 |
| CATGGAAGTGTTTT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
17 |
1 |
1 |
7 |
765558 |
765571 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGAATAATAGA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
3 |
2 |
1 |
12 |
456922 |
456935 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGAATTGGAAT |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
15 |
834821 |
834834 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGAATTTATAG |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
17 |
1 |
1 |
13 |
259929 |
259942 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGAGACACCCA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
8 |
0 |
1 |
1 |
8 |
451658 |
451671 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGAGCGTGGTT |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
3 |
1 |
1 |
7 |
994049 |
994062 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGAGGAGATTT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
2 |
1 |
1 |
141075 |
141088 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGAGGCTGATA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
14 |
271352 |
271365 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGAGTGAACAG |
N.A. |
NORF |
N.A. |
N.A. |
3 |
8 |
6 |
2 |
1 |
10 |
454058 |
454071 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGATAGATTAC |
N.A. |
NORF |
N.A. |
N.A. |
6 |
0 |
0 |
1 |
1 |
2 |
84421 |
84434 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGATGCCACAA |
N.A. |
NORF |
N.A. |
N.A. |
12 |
0 |
3 |
1 |
1 |
14 |
89243 |
89256 |
+ |
-1 |
-1 |
U |
0 |
|
6 |
| CATGGATGTAACAA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
14 |
356255 |
356268 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGATGTACAAC |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
3 |
1 |
1 |
4 |
1385436 |
1385449 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGATTGCAAAT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
2 |
1 |
15 |
495496 |
495509 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGCAAACAATA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
16 |
641947 |
641960 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGCAAATGGAA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
14 |
441429 |
441442 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGCAACAACTT |
N.A. |
NORF |
N.A. |
N.A. |
6 |
4 |
0 |
1 |
1 |
11 |
326776 |
326789 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGCAAGACAGT |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
13 |
220635 |
220648 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGCAATTTAAC |
N.A. |
NORF |
N.A. |
N.A. |
9 |
0 |
0 |
1 |
1 |
2 |
372411 |
372424 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGCACTGAGAA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
11 |
145331 |
145344 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGCAGAAGAAC |
N.A. |
NORF |
N.A. |
N.A. |
0 |
8 |
0 |
1 |
1 |
14 |
106357 |
106370 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGCAGCTATAC |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
6 |
1 |
1 |
16 |
525110 |
525123 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGCAGTCGGAT |
N.A. |
NORF |
N.A. |
N.A. |
6 |
0 |
0 |
2 |
1 |
1 |
183472 |
183485 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGCCAATGATA |
N.A. |
NORF |
N.A. |
N.A. |
6 |
8 |
62 |
1 |
1 |
5 |
468389 |
468402 |
- |
-1 |
-1 |
U |
0 |
|
2 |
| CATGGCCACCGTCC |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
17 |
2 |
1 |
12 |
453940 |
453953 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGCCAGGACAA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
24 |
1 |
1 |
3 |
156710 |
156723 |
+ |
-1 |
-1 |
U |
0 |
|
2 |
| CATGGCCCGGTGTG |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
10 |
1 |
1 |
15 |
422852 |
422865 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGCCGTTCGAT |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
12 |
390117 |
390130 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGCCGTTCTTA |
N.A. |
NORF |
N.A. |
N.A. |
9 |
17 |
41 |
2 |
1 |
12 |
456446 |
456459 |
- |
-1 |
-1 |
U |
0 |
|
2 |
| CATGGCCTTGTGCT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
17 |
2 |
1 |
12 |
457450 |
457463 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGCGACTTGAT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
17 |
1 |
1 |
2 |
720771 |
720784 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGCGAGTTTAG |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
4 |
691256 |
691269 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGCGATCCGTA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
8 |
271290 |
271303 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGCGGCGGGTG |
N.A. |
NORF |
N.A. |
N.A. |
3 |
8 |
0 |
1 |
1 |
3 |
41669 |
41682 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGCTCCAATAG |
N.A. |
NORF |
N.A. |
N.A. |
6 |
0 |
3 |
1 |
1 |
4 |
1130964 |
1130977 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGCTGAAATGG |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
3 |
1 |
1 |
13 |
132953 |
132966 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGCTTCATCGC |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
6 |
1 |
1 |
15 |
908802 |
908815 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGGCCCACAGT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
12 |
53735 |
53748 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGGGCAATCTT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
15 |
678657 |
678670 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGGGTAGTACT |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
3 |
1 |
1 |
13 |
671729 |
671742 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGGTAATCGAA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
27 |
1 |
1 |
4 |
832425 |
832438 |
+ |
-1 |
-1 |
U |
0 |
|
2 |
| CATGGGTACATTCA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
5 |
67151 |
67164 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGGTGGGTACA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
13 |
1 |
1 |
16 |
281072 |
281085 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGGTTCCATTG |
N.A. |
NORF |
N.A. |
N.A. |
6 |
0 |
0 |
1 |
1 |
16 |
541132 |
541145 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGGTTCTAATT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
3 |
107653 |
107666 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGTAACTAGTG |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
16 |
128011 |
128024 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGTAAGTAGAC |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
13 |
110990 |
111003 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGTAATACAAG |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
10 |
1 |
1 |
4 |
470585 |
470598 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGTACGCAAGA |
N.A. |
NORF |
N.A. |
N.A. |
9 |
12 |
0 |
2 |
1 |
10 |
742181 |
742194 |
+ |
-1 |
-1 |
U |
0 |
|
9 |
| CATGGTAGAACACC |
N.A. |
NORF |
N.A. |
N.A. |
9 |
4 |
0 |
4 |
1 |
4 |
1154314 |
1154327 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGTAGTACCTG |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
3 |
40018 |
40031 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGTAGTATTCA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
2 |
1 |
11 |
255921 |
255934 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGTATAACTGT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
24 |
2 |
1 |
12 |
457581 |
457594 |
- |
-1 |
-1 |
U |
0 |
|
2 |
| CATGGTATATGTGT |
N.A. |
NORF |
N.A. |
N.A. |
6 |
0 |
3 |
2 |
1 |
8 |
198274 |
198287 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGTCCAAAATA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
20 |
1 |
1 |
2 |
382276 |
382289 |
- |
-1 |
-1 |
U |
0 |
|
2 |
| CATGGTGCCTTTTA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
12 |
849410 |
849423 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGTGCTGGCTT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
2 |
581730 |
581743 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGTGTTTTGTG |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
20 |
2 |
1 |
12 |
454730 |
454743 |
- |
-1 |
-1 |
U |
0 |
|
2 |
| CATGGTTAAGGCAA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
10 |
1 |
1 |
10 |
294743 |
294756 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGGTTCTTGCCT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
24 |
1 |
1 |
7 |
939577 |
939590 |
- |
-1 |
-1 |
U |
0 |
|
2 |
| CATGGTTGTTCGGA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
10 |
1 |
1 |
7 |
398919 |
398932 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGGTTTCAACGG |
N.A. |
NORF |
N.A. |
N.A. |
0 |
8 |
44 |
2 |
1 |
12 |
457377 |
457390 |
- |
-1 |
-1 |
U |
0 |
|
2 |
| CATGTAAAGCCAAA |
N.A. |
NORF |
N.A. |
N.A. |
9 |
0 |
0 |
1 |
1 |
2 |
197131 |
197144 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTAAATGTGCT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
3 |
184814 |
184827 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGTAACAATGCA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
4 |
3 |
1 |
1 |
17 |
59023 |
59036 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTAACATATTA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
3 |
1 |
1 |
14 |
476791 |
476804 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTAACCCTTAA |
N.A. |
NORF |
N.A. |
N.A. |
6 |
0 |
0 |
1 |
1 |
11 |
334287 |
334300 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTAAGACAGTG |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
10 |
1 |
1 |
2 |
342647 |
342660 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTAAGACATCT |
N.A. |
NORF |
N.A. |
N.A. |
3 |
8 |
0 |
1 |
1 |
12 |
155300 |
155313 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTAAGCAGCAT |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
6 |
1 |
1 |
10 |
338304 |
338317 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTAATACGCTA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
10 |
573715 |
573728 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTACCAATGTC |
N.A. |
NORF |
N.A. |
N.A. |
12 |
25 |
6 |
1 |
1 |
4 |
1162807 |
1162820 |
+ |
-1 |
-1 |
U |
0 |
|
6 |
| CATGTACCCGAGGA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
4 |
979670 |
979683 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTACGTCTCCA |
N.A. |
NORF |
N.A. |
N.A. |
6 |
0 |
0 |
1 |
1 |
16 |
239051 |
239064 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTACTTACTCA |
N.A. |
NORF |
N.A. |
N.A. |
12 |
0 |
0 |
1 |
1 |
12 |
673943 |
673956 |
+ |
-1 |
-1 |
U |
0 |
|
6 |
| CATGTAGAACAGGG |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
10 |
348832 |
348845 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTAGACATCTA |
N.A. |
NORF |
N.A. |
N.A. |
70 |
12 |
27 |
1 |
1 |
2 |
491115 |
491128 |
+ |
-1 |
-1 |
U |
0 |
|
13 |
| CATGTAGTTGCTCC |
N.A. |
NORF |
N.A. |
N.A. |
6 |
0 |
20 |
1 |
1 |
7 |
317110 |
317123 |
+ |
-1 |
-1 |
U |
0 |
|
2 |
| CATGTATAAATAAT |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
4 |
955574 |
955587 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTATAGGTGTC |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
10 |
2 |
1 |
14 |
169817 |
169830 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGTATCATATGG |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
15 |
722133 |
722146 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGTATGCATTAG |
N.A. |
NORF |
N.A. |
N.A. |
3 |
8 |
3 |
1 |
1 |
15 |
165380 |
165393 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTATGTCCATC |
N.A. |
NORF |
N.A. |
N.A. |
6 |
0 |
20 |
1 |
1 |
7 |
986428 |
986441 |
- |
-1 |
-1 |
U |
0 |
|
2 |
| CATGTATGTGTATA |
N.A. |
NORF |
N.A. |
N.A. |
6 |
0 |
0 |
1 |
1 |
12 |
255042 |
255055 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTATTGTCAGT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
10 |
1 |
1 |
15 |
423665 |
423678 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGTATTTGTATG |
N.A. |
NORF |
N.A. |
N.A. |
9 |
12 |
0 |
1 |
1 |
5 |
327592 |
327605 |
+ |
-1 |
-1 |
U |
0 |
|
9 |
| CATGTCAGCTTGGT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
10 |
3 |
1 |
1 |
228050 |
228063 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGTCATAGTCCA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
10 |
1 |
1 |
2 |
775807 |
775820 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGTCATCGTAGT |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
3 |
1 |
1 |
1 |
72878 |
72891 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTCCAATACAC |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
17 |
1 |
1 |
2 |
259060 |
259073 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGTCTGCGTGAA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
3 |
1 |
1 |
10 |
136438 |
136451 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTCTTCAAAAC |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
15 |
849707 |
849720 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGTGAGGAGGCG |
N.A. |
NORF |
N.A. |
N.A. |
0 |
4 |
3 |
1 |
1 |
15 |
849960 |
849973 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTGATGAAGAA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
8 |
494216 |
494229 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTGCCCTGTGG |
N.A. |
NORF |
N.A. |
N.A. |
3 |
8 |
0 |
1 |
1 |
12 |
27174 |
27187 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTGGATTTCAG |
N.A. |
NORF |
N.A. |
N.A. |
6 |
0 |
6 |
1 |
1 |
4 |
1224883 |
1224896 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTGGGAACCCA |
N.A. |
NORF |
N.A. |
N.A. |
6 |
0 |
0 |
1 |
1 |
11 |
534644 |
534657 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTGGGCCCTTT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
10 |
1 |
1 |
14 |
618936 |
618949 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGTGGTTTTTTA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
5 |
471572 |
471585 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGTGTAAATTAA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
8 |
0 |
1 |
1 |
9 |
44723 |
44736 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTGTACTTTAA |
N.A. |
NORF |
N.A. |
N.A. |
6 |
0 |
0 |
1 |
1 |
13 |
465397 |
465410 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTGTAGAAGAA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
6 |
1 |
1 |
5 |
468711 |
468724 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTTAACTCGCC |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
15 |
757226 |
757239 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGTTAAGTCACG |
N.A. |
NORF |
N.A. |
N.A. |
3 |
8 |
0 |
1 |
1 |
9 |
199565 |
199578 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTTAATGTTAT |
N.A. |
NORF |
N.A. |
N.A. |
6 |
0 |
0 |
1 |
1 |
5 |
546521 |
546534 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTTAATTTGTT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
10 |
1 |
1 |
2 |
381978 |
381991 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGTTACAATTAA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
6 |
1 |
1 |
16 |
592066 |
592079 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTTACTCTTGA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
6 |
1 |
1 |
16 |
590331 |
590344 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTTAGGCCGGT |
N.A. |
NORF |
N.A. |
N.A. |
6 |
0 |
0 |
1 |
1 |
15 |
894084 |
894097 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTTAGTTTTGG |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
3 |
1 |
1 |
16 |
260927 |
260940 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTTATAGATCA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
3 |
1 |
1 |
2 |
259050 |
259063 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTTATGTTAGA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
3 |
1 |
1 |
12 |
602462 |
602475 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTTATTTTGTA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
15 |
426646 |
426659 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGTTCAACTGGG |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
3 |
1 |
1 |
16 |
254494 |
254507 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTTCAATGGCT |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
9 |
125539 |
125552 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTTCCCATCCT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
10 |
1 |
1 |
1 |
180189 |
180202 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGTTCGACCCTT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
12 |
194289 |
194302 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGTTCGCGCAGT |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
13 |
915355 |
915368 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGTTCTTCAACA |
N.A. |
NORF |
N.A. |
N.A. |
3 |
8 |
0 |
1 |
1 |
7 |
649652 |
649665 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTTGATGATTT |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
17 |
1 |
1 |
16 |
582349 |
582362 |
- |
-1 |
-1 |
U |
0 |
|
2 |
| CATGTTGCACTTCT |
N.A. |
NORF |
N.A. |
N.A. |
6 |
8 |
0 |
1 |
1 |
12 |
806824 |
806837 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTTGCATTGTC |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
11 |
576724 |
576737 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGTTGGTCTCAA |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
6 |
110435 |
110448 |
+ |
-1 |
-1 |
U |
0 |
|
3 |
| CATGTTTATGCAGT |
N.A. |
NORF |
N.A. |
N.A. |
3 |
0 |
3 |
1 |
1 |
13 |
405925 |
405938 |
- |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTTTTCCATTC |
N.A. |
NORF |
N.A. |
N.A. |
0 |
0 |
6 |
1 |
1 |
2 |
442958 |
442971 |
- |
-1 |
-1 |
U |
0 |
|
3 |
| CATGTTTTGTTTAT |
N.A. |
NORF |
N.A. |
N.A. |
3 |
4 |
0 |
1 |
1 |
5 |
79974 |
79987 |
+ |
-1 |
-1 |
U |
0 |
|
8 |
| CATGTTTTATATAT |
YNL175C |
NOP13 |
6324155 |
COG0724 |
0 |
0 |
13 |
2 |
1 |
14 |
307317 |
307330 |
- |
306981 |
308612 |
- |
403 |
Protein of unknown function, localizes to the nucleolus
and nucleoplasm; contains an RNA recognition motif (RRM) and has similarity
to Nop12p, which is required for processing of
pre-18S rRNA |
3 |
| CATGCGCTTGTGGA |
YNL078W |
NIS1 |
6324251 |
- |
0 |
0 |
10 |
1 |
1 |
14 |
479865 |
479878 |
+ |
479767 |
481389 |
+ |
407 |
Nis1p |
3 |
| CATGAAAAAATCCA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
13 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGAAAAACATTG |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGAAAACTATGT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGAAAAGGGGCA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGAAAATCCAAT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGAAACAAACTG |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGAAACAAGTTG |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGAAACTGATAG |
N.A. |
NID |
N.A. |
N.A. |
6 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGAAAGAACAGA |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGAAAGAAGGCG |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGAACAACAACT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
17 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
2 |
| CATGAACAACCCAG |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGAACAAGGTCG |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGAACAATGCTA |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGAACCGCCACT |
N.A. |
NID |
N.A. |
N.A. |
3 |
8 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGAAGAAAGGCG |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGAAGAAGTAAC |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGAAGATGCTCA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGAAGATGGCTA |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGAAGGTGGTTA |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGAAGTCAATAG |
N.A. |
NID |
N.A. |
N.A. |
6 |
4 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGAATCCTTTCT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGAATGCAAACA |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGACAAAAAAAA |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGACAAACAACT |
N.A. |
NID |
N.A. |
N.A. |
9 |
4 |
51 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
2 |
| CATGACAAATGCTA |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGACAACAAACT |
N.A. |
NID |
N.A. |
N.A. |
9 |
0 |
34 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
2 |
| CATGACAACAACTT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
13 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGACAACCAACT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
27 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
2 |
| CATGACAACCACTA |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGACAATGCCCC |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGACAGCAAAAA |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGACAGCAACTA |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGACAGCCACTC |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGACATCGGGGA |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGACCAACAACT |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
10 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGACCAAGAATT |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGACCACCACAT |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGACCCCTGTCA |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
13 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGACCCGCCACT |
N.A. |
NID |
N.A. |
N.A. |
9 |
4 |
10 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGACCCTGTCCA |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGACCGCCACCT |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGACCGCCACTT |
N.A. |
NID |
N.A. |
N.A. |
6 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGACCGCCCACT |
N.A. |
NID |
N.A. |
N.A. |
6 |
8 |
20 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
2 |
| CATGACCGGAATTA |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGACGACAACTA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGACGTCAATTG |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGACTACTGAGG |
N.A. |
NID |
N.A. |
N.A. |
9 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGACTGCTCTGG |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGACTGTCCGCT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGACTGTTATCT |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGACTTGTTGGT |
N.A. |
NID |
N.A. |
N.A. |
9 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGAGAAAAACAG |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGAGAACAAACT |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
10 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGAGAACTATGT |
N.A. |
NID |
N.A. |
N.A. |
3 |
12 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
9 |
| CATGAGACAAAAAT |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGAGACAAACCT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGAGACCAAACT |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGAGAGGAGTCT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGAGATGCCTCA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGAGATGCTTCA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGAGCCTTGAAT |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
10 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGAGGAATCTAC |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGAGGACAAACT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
10 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGAGGATACTCA |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGAGGTGCTAAG |
N.A. |
NID |
N.A. |
N.A. |
9 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGAGTGCTGTTA |
N.A. |
NID |
N.A. |
N.A. |
9 |
12 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
9 |
| CATGATAGACATCT |
N.A. |
NID |
N.A. |
N.A. |
6 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGATATTCTTTA |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGATCGCCACTC |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGATCGCCCGCT |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGATCGCCGCCT |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGATCTCCAAAT |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGATCTCTACTG |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGATCTTGTCTC |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGATGAAGCTGC |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGATGATAACAT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
13 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGATGATAACCA |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGATGATCAACC |
N.A. |
NID |
N.A. |
N.A. |
6 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGATGCAAAGGG |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGATGCCCACGG |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGATGCGGCCCT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGATGGCGAGTT |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGATGGGCGAGT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGATGTTTTTTA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGATTACGTTCT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGATTCCCTGCT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGATTGCCAGTC |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGATTGCTGTTA |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGATTGTTTTAT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGATTTACGTTT |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGATTTATATAT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGATTTTCAATG |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGCAAAAAAAAA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGCAAAATAGAA |
N.A. |
NID |
N.A. |
N.A. |
3 |
12 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
9 |
| CATGCAAACATCAC |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCAAAGTGATG |
N.A. |
NID |
N.A. |
N.A. |
3 |
17 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
9 |
| CATGCAAATAGAAA |
N.A. |
NID |
N.A. |
N.A. |
67 |
103 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
4 |
| CATGCAACAACCTA |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCAAGCGGAGA |
N.A. |
NID |
N.A. |
N.A. |
6 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCAAGGGGTTG |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCAAGTAGATT |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCACAGAAGAA |
N.A. |
NID |
N.A. |
N.A. |
9 |
21 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
9 |
| CATGCACCAAGAAT |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCACCTAATGA |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCACCTATTGA |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCAGCCGCTAC |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCAGTAAATGT |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCAGTACAAAA |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCAGTGATTGC |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCATAGGTCAA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGCATCAGAGGG |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCATCTAGAGG |
N.A. |
NID |
N.A. |
N.A. |
3 |
8 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCATCTGAGGG |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCATTAGAGGG |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCATTATGGTG |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
13 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGCCAAATAGAA |
N.A. |
NID |
N.A. |
N.A. |
6 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCCAATCTTTA |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCCACTGTCAA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGCCACTTGTCA |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCCAGGTCGTT |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCCCACTGTCA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGCCCCACGTAA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
10 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGCCCGTTTGAG |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGCCGAAAAGAA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGCCGCTCTGGG |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGCGAACTGCGC |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCGAAGGCAAA |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCGACTGCCGC |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCGACTGCGGC |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCGATTATTAT |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCGGAACCTTG |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCGGGACCTTG |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCGGGGGTATC |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGCGGGGTATCG |
N.A. |
NID |
N.A. |
N.A. |
0 |
12 |
17 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
2 |
| CATGCGGTAGTCCC |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCTAACGGACG |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCTAAGAACGC |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCTACCGGACG |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCTACGGAACG |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCTACGGACAA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGCTACGGACCG |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
13 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGCTACGGGACG |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
10 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCTAGAAACGC |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGCTAGAACCGC |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCTAGAACGGC |
N.A. |
NID |
N.A. |
N.A. |
3 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCTAGGAACGC |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCTAGGACCTA |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCTATGTCCGT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGCTCTTTCCAT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGCTGATGGTGG |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCTGCCTCTGG |
N.A. |
NID |
N.A. |
N.A. |
6 |
4 |
10 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCTGGACGCAC |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCTGGCTCTGG |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
13 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGCTTCCCAATG |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCTTGCTGAGC |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGCTTTTATGCT |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGAAACTGTTG |
N.A. |
NID |
N.A. |
N.A. |
12 |
0 |
27 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
2 |
| CATGGAAAGTCGGA |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGAAGGGGGTG |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGAAGTCGGGA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGGAAGTTCGGA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
10 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGGAATGGAAAT |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGAATGGGAAT |
N.A. |
NID |
N.A. |
N.A. |
9 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGAATGGGATA |
N.A. |
NID |
N.A. |
N.A. |
9 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGACTAAATGT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGGAGACATTCA |
N.A. |
NID |
N.A. |
N.A. |
9 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGAGGCTGGGT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGATAGATTTA |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGCAAATACTA |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGCAATTACTA |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGCACTGCCAT |
N.A. |
NID |
N.A. |
N.A. |
6 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGCATCTCATA |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGCATTCAAAA |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGCCAAATGAT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
13 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGGCCAATGATT |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGCCAATTGAT |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGCCCGCCACT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGGCCCGTTCTT |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGCCCTTGAAT |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
13 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGGCCGCCAGAG |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGGCCGCTCTTA |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGCCGTGGAAA |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGCCGTTCTTT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGGCCTCGTTTT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGGCCTTGAAAT |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
27 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
2 |
| CATGGCCTTGAGTA |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGCCTTTGAAT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
13 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGGCGGGGCAAT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGCTACGAAAC |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGCTCATTACA |
N.A. |
NID |
N.A. |
N.A. |
15 |
30 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
5 |
| CATGGCTCATTTAC |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGCTCCAAATA |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGCTGCTCAAA |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGCTTCTTTAT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGAAAAACAA |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGAAAAATGC |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGAAAACGTT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGAAAATCTT |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGAAGATCTT |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGAATATAAA |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGAGAAGGTT |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGAGATCTTT |
N.A. |
NID |
N.A. |
N.A. |
3 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGCCAATGGG |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGGGCCTTGAAT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
10 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGCGATTGGG |
N.A. |
NID |
N.A. |
N.A. |
3 |
30 |
24 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
2 |
| CATGGGCGCTAAGA |
N.A. |
NID |
N.A. |
N.A. |
12 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
6 |
| CATGGGCTCGCTTT |
N.A. |
NID |
N.A. |
N.A. |
3 |
12 |
10 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
9 |
| CATGGGGACCAAAC |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGGCCCAACC |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGGCCCACCC |
N.A. |
NID |
N.A. |
N.A. |
6 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGGCCCCACC |
N.A. |
NID |
N.A. |
N.A. |
3 |
21 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
9 |
| CATGGGGCTGAGAT |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGGGCCCACC |
N.A. |
NID |
N.A. |
N.A. |
3 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGGGGTGATA |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGGGTGGTAT |
N.A. |
NID |
N.A. |
N.A. |
6 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGGTAACGTA |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGGTGAAAAC |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGGTGCTAAG |
N.A. |
NID |
N.A. |
N.A. |
9 |
21 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
9 |
| CATGGGGTGTTAAC |
N.A. |
NID |
N.A. |
N.A. |
12 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
6 |
| CATGGGGTTAATTA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGGGTAACCGTA |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGTGAAAAAC |
N.A. |
NID |
N.A. |
N.A. |
15 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
6 |
| CATGGGTGCCCTAT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGTGCCTAAG |
N.A. |
NID |
N.A. |
N.A. |
18 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
6 |
| CATGGGTGCTAAAA |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGTGCTAAAG |
N.A. |
NID |
N.A. |
N.A. |
24 |
30 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
5 |
| CATGGGTGCTAAGG |
N.A. |
NID |
N.A. |
N.A. |
12 |
12 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
6 |
| CATGGGTGCTAGGA |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGTGCTGAGA |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGTGCTTAAG |
N.A. |
NID |
N.A. |
N.A. |
9 |
21 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
9 |
| CATGGGTGGAAAAC |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGGTGGCTAAG |
N.A. |
NID |
N.A. |
N.A. |
9 |
25 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
9 |
| CATGGGTGGTAAGA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
17 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGGGTTCTTGCC |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGGGTTGCTAAG |
N.A. |
NID |
N.A. |
N.A. |
6 |
25 |
17 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
2 |
| CATGGTACACCCAC |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
17 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGGTAGAGCCCG |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGTATGGCGAC |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGTATTTTTGC |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGTCAAATTCG |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGGTCAATTCCG |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGGTCCCGCCAA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGGTGGCGAGGT |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGTGGGGTTTT |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGTGGTGCACA |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGTGTTAGCAT |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGTTCTGCATT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGTTTATGGCC |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGTTTTTGCCT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGTAAACATATA |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
13 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGTAAACTGGAC |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTAAAGTGATG |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTAAATACGTA |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
10 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTAACAAATGC |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTAACATATAA |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTAACATATAC |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTAACCATATA |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTAACTGGGAC |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTAAGTGCCTT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGTAATGTATAT |
N.A. |
NID |
N.A. |
N.A. |
9 |
17 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
9 |
| CATGTACACCAGAT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTACACTAGAT |
N.A. |
NID |
N.A. |
N.A. |
30 |
21 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
5 |
| CATGTACCAAATGT |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTACCACCTCC |
N.A. |
NID |
N.A. |
N.A. |
9 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTACCACTAGA |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTACCACTTCC |
N.A. |
NID |
N.A. |
N.A. |
3 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTACCCACTCC |
N.A. |
NID |
N.A. |
N.A. |
6 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTAGAAACAAT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTAGACAATTC |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTAGCCACTAA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGTAGGGGCAGG |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTAGGTTAGAT |
N.A. |
NID |
N.A. |
N.A. |
6 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTAGGTTTTGC |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
10 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGTAGTTTGCTC |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTATAAGTTTA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
17 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGTATATCAGGT |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTATATGTATG |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTATGGCGTAA |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTATGTTTTGC |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTCAAAACATC |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGTCAATTCGGT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGTCACTACTGG |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTCATCCCCAG |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTCATTTAACC |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTCCGAAGTCC |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGTCCGAGGTCC |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTCCGCTATGG |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
17 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGTCCTAAGCTA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
10 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGTCCTCTACTG |
N.A. |
NID |
N.A. |
N.A. |
6 |
12 |
10 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTCGCCTTCAT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTCGCTTTATT |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTCGCTTTCAT |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTCGTACTTTT |
N.A. |
NID |
N.A. |
N.A. |
21 |
17 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
6 |
| CATGTCTCCTACTG |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTCTCTAACTG |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTCTCTACTTG |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTCTCTTACTG |
N.A. |
NID |
N.A. |
N.A. |
6 |
17 |
10 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
9 |
| CATGTCTGGTCTCT |
N.A. |
NID |
N.A. |
N.A. |
9 |
12 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
9 |
| CATGTCTTCTACTG |
N.A. |
NID |
N.A. |
N.A. |
6 |
17 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
9 |
| CATGTCTTGAGATG |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTGATTATACA |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTGCAAACCTT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGTGCGGGCCCT |
N.A. |
NID |
N.A. |
N.A. |
6 |
8 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTGGCGGCCCT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTGGGGTCACC |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTGGGTCACCG |
N.A. |
NID |
N.A. |
N.A. |
18 |
12 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
6 |
| CATGTGGGTTCACC |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGTGGTGGTATA |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTGGTTGTTAT |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
10 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTGTAAAACGC |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTGTACGGGTT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGTGTACGGTTC |
N.A. |
NID |
N.A. |
N.A. |
6 |
4 |
13 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGTGTATTTTCG |
N.A. |
NID |
N.A. |
N.A. |
9 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTGTCGGGGTG |
N.A. |
NID |
N.A. |
N.A. |
9 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTGTGCTAAGA |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTGTGGGTATA |
N.A. |
NID |
N.A. |
N.A. |
12 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
6 |
| CATGTGTGGTTATA |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTGTTGGTATA |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTAACACAAA |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTAATATTTA |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
13 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGTTACTCAAAA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGTTAGTCGAAC |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTATGTATTA |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
10 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTATTGTACT |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTCAAACCCA |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTCCCCAGGT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGTTCCCTCATT |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTCCGTTCAC |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTCGCTTCAT |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
6 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGTTCTCTACTG |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTCTGAGATG |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTGAAGTCTC |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
13 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGTTGCCAGGTC |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTGCCAGTCC |
N.A. |
NID |
N.A. |
N.A. |
12 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
6 |
| CATGTTGCCCAGTC |
N.A. |
NID |
N.A. |
N.A. |
3 |
4 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTGCGGCCCT |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTGGGTAATG |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTGGGTCCAG |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTGTCCTTTG |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTGTCTTTTG |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTGTGAAAGC |
N.A. |
NID |
N.A. |
N.A. |
6 |
0 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTGTGCTTCT |
N.A. |
NID |
N.A. |
N.A. |
0 |
4 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTGTTTTTTA |
N.A. |
NID |
N.A. |
N.A. |
0 |
0 |
10 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
3 |
| CATGTTTCAAAAGA |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
10 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTTCGGGTCA |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTTCTTGGTG |
N.A. |
NID |
N.A. |
N.A. |
3 |
0 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGTTTGCCAGTC |
N.A. |
NID |
N.A. |
N.A. |
0 |
12 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
9 |
| CATGTTTGTCTTTG |
N.A. |
NID |
N.A. |
N.A. |
0 |
8 |
3 |
-1 |
-1 |
-1 |
-1 |
-1 |
U |
-1 |
-1 |
U |
-1 |
|
8 |
| CATGGTGTGGATTA |
YML118W |
NGL3 |
6323517 |
COG5239 |
0 |
0 |
6 |
1 |
1 |
13 |
33597 |
33610 |
+ |
32334 |
34242 |
+ |
505 |
DNase/RNase (putative); CCR4 C-terminal homolog; displays
homology to drosophila Angel gene; homolog to ngl1 and ngl2 |
3 |
| CATGGAGAGAAGGC |
YHR004C |
NEM1 |
6321791 |
COG5190 |
0 |
8 |
0 |
1 |
1 |
8 |
111763 |
111776 |
- |
111312 |
113088 |
- |
446 |
Nuclear Envelope Morphology |
8 |
| CATGATCTCCAATG |
YPR149W |
NCE102 |
6325407 |
- |
12 |
21 |
31 |
1 |
1 |
16 |
830342 |
830355 |
+ |
829912 |
830932 |
+ |
173 |
involved in secretion of proteins that lack classical
secretory signal sequences |
8 |
| CATGGTGATTCCCA |
YJL116C |
NCA3 |
6322345 |
- |
9 |
0 |
10 |
2 |
1 |
10 |
194174 |
194187 |
- |
193281 |
194793 |
- |
337 |
With NCA2, regulates proper expression of subunits 6
(Atp6p) and 8 (Atp8p ) of the Fo-F1 ATP synthase |
8 |
| CATGCGCATATGCT |
YDL040C |
NAT1 |
6320164 |
COG0457 |
9 |
0 |
0 |
1 |
1 |
4 |
378783 |
378796 |
- |
378443 |
381435 |
- |
854 |
Required for entry into stationary phase, heat
shock-resistance, a mating-type functions, and sporulation; forms a complex
with Ard1p |
8 |
| CATGTAAGTGTGTA |
YKR048C |
NAP1 |
6322901 |
- |
18 |
0 |
6 |
2 |
1 |
11 |
524923 |
524936 |
- |
524717 |
526282 |
- |
417 |
nucleosome assembly protein I |
6 |
| CATGCCTCTTAACA |
YKL129C |
MYO3 |
6322720 |
COG5022 |
6 |
0 |
0 |
1 |
1 |
11 |
196286 |
196299 |
- |
196030 |
200165 |
- |
1271 |
myosin I |
8 |
| CATGCAAGTATATA |
YGR007W |
MUQ1 |
6321444 |
COG0615 |
0 |
12 |
0 |
1 |
1 |
7 |
508017 |
508030 |
+ |
506971 |
508441 |
+ |
323 |
choline phosphate cytidylyltransferase (also called
phosphoethanolamine cytidylyltransferase or phosphocholine
cytidylyltransferase) |
9 |
| CATGTAAATTGGTG |
YPL070W |
MUK1 |
6325187 |
- |
9 |
0 |
0 |
2 |
1 |
16 |
422920 |
422933 |
+ |
420943 |
423280 |
+ |
612 |
Hypothetical ORF |
8 |
| CATGGAGTGGCCTT |
YMR228W |
MTF1 |
6323884 |
- |
3 |
4 |
0 |
1 |
1 |
13 |
725577 |
725590 |
+ |
724625 |
726149 |
+ |
341 |
Mitochondrial RNA polymerase specificity factor |
8 |
| CATGCGTGAGGTGA |
YPL097W |
MSY1 |
6325160 |
COG0162 |
3 |
8 |
0 |
1 |
1 |
16 |
366463 |
366476 |
+ |
364947 |
366921 |
+ |
492 |
Tyrosyl-tRNA synthetase |
8 |
| CATGCTGGATGATC |
YDR335W |
MSN5 |
6320542 |
- |
3 |
12 |
0 |
1 |
1 |
4 |
1144771 |
1144784 |
+ |
1141158 |
1145081 |
+ |
1224 |
Multicopy suppressor of snf1 mutation |
9 |
| CATGCAGCTCAACA |
YKL062W |
MSN4 |
6322788 |
COG5048 |
9 |
4 |
0 |
1 |
1 |
11 |
324390 |
324403 |
+ |
322873 |
325264 |
+ |
630 |
Transcription factor. Multicopy suppressor of snf1
mutation. Key regulator of stress-responsive gene expression. |
8 |
| CATGATATCAAAAA |
YDL154W |
MSH5 |
6320047 |
COG0249 |
6 |
17 |
0 |
2 |
1 |
4 |
179498 |
179511 |
+ |
178335 |
181539 |
+ |
901 |
dispensable for DNA repair and meiotic intrachromosomal
reciprocal recombination, required for full reciprocal recombination between
homologs, and spore viability |
9 |
| CATGCCACTAAGAC |
YLR219W |
MSC3 |
6323248 |
- |
0 |
0 |
6 |
1 |
1 |
12 |
576237 |
576250 |
+ |
574153 |
576826 |
+ |
728 |
Protein of unknown function, green fluorescent protein
(GFP)-fusion protein localizes to the cell periphery; msc3 mutants are
defective in directing meiotic recombination events
to homologous chromatids; potential Cdc28p substrate |
3 |
| CATGGCCAAGAAAC |
YML128C |
MSC1 |
6323507 |
- |
12 |
0 |
0 |
1 |
1 |
13 |
15881 |
15894 |
- |
14755 |
16677 |
- |
513 |
Protein of unknown function, green fluorescent protein
(GFP)-fusion protein localizes to the endoplasmic reticulum; msc1 mutants are
defective in directing meiotic recombination
events to homologous chromatids |
6 |
| CATGGAATAAGCTG |
YKL009W |
MRT4 |
6322843 |
COG0244 |
0 |
4 |
13 |
2 |
1 |
11 |
426585 |
426598 |
+ |
425885 |
427094 |
+ |
236 |
mRna turnover 4 |
3 |
| CATGCAGAAAATGG |
YHR005C-A |
MRS11 |
6321793 |
- |
0 |
8 |
0 |
1 |
1 |
8 |
115645 |
115658 |
- |
115115 |
115895 |
- |
93 |
May act cooperatively with Mrs5p in mitochondrial protein
import or other related essential mitochondrial processes |
8 |
| CATGCCAGAAGAAA |
YBR146W |
MRPS9 |
6319622 |
COG0103 |
6 |
0 |
0 |
1 |
1 |
2 |
536114 |
536127 |
+ |
535216 |
536530 |
+ |
278 |
Mitochondrial ribosomal protein of the small subunit |
8 |
| CATGGTCACGTTGG |
YGR165W |
MRPS35 |
6321604 |
- |
9 |
17 |
0 |
2 |
1 |
7 |
830271 |
830284 |
+ |
829119 |
830517 |
+ |
345 |
Mitochondrial ribosomal protein of the small subunit |
9 |
| CATGGGCCACTAGT |
YPL013C |
MRPS16 |
6325244 |
COG0228 |
3 |
8 |
6 |
1 |
1 |
16 |
529036 |
529049 |
- |
528481 |
529345 |
- |
121 |
Mitochondrial ribosomal protein of the small subunit |
8 |
| CATGTACATACATC |
YGR220C |
MRPL9 |
6321659 |
COG0087 |
6 |
17 |
0 |
2 |
1 |
7 |
936030 |
936043 |
- |
935576 |
936884 |
- |
269 |
Mitochondrial ribosomal protein of the large subunit |
9 |
| CATGCTGCGAAAAG |
YPR100W |
MRPL51 |
6325356 |
- |
3 |
0 |
3 |
1 |
1 |
16 |
730182 |
730195 |
+ |
729787 |
730487 |
+ |
140 |
Mitochondrial ribosomal protein of the large subunit |
8 |
| CATGGGTACAGTTG |
YNL177C |
MRPL22 |
6324152 |
COG0091 |
0 |
12 |
0 |
1 |
1 |
14 |
303733 |
303746 |
- |
303187 |
304615 |
- |
309 |
Mitochondrial ribosomal protein of the large subunit |
9 |
| CATGTATATAACTA |
YBL038W |
MRPL16 |
6319433 |
COG0197 |
0 |
0 |
10 |
1 |
1 |
2 |
146873 |
146886 |
+ |
146152 |
147173 |
+ |
232 |
Mitochondrial ribosomal protein of the large subunit |
3 |
| CATGTACATACATC |
YDL202W |
MRPL11 |
6319999 |
COG0244 |
6 |
17 |
0 |
2 |
1 |
4 |
99276 |
99289 |
+ |
98476 |
99561 |
+ |
249 |
Mitochondrial ribosomal protein of the large subunit |
9 |
| CATGTACATACAAA |
YDR116C |
MRPL1 |
6320321 |
COG0081 |
3 |
8 |
0 |
2 |
1 |
4 |
682619 |
682632 |
- |
682219 |
683575 |
- |
285 |
Mitochondrial ribosomal protein of the large subunit |
8 |
| CATGGAAATATGTA |
YKL167C |
MRP49 |
6322681 |
- |
6 |
4 |
0 |
1 |
1 |
11 |
133661 |
133674 |
- |
133498 |
134139 |
- |
137 |
Mitochondrial ribosomal protein of the large subunit, not
essential for mitochondrial translation |
8 |
| CATGGAAAAGTACC |
YDR405W |
MRP20 |
6320613 |
- |
6 |
0 |
6 |
1 |
1 |
4 |
1278199 |
1278212 |
+ |
1277634 |
1278924 |
+ |
263 |
Mitochondrial ribosomal protein of the large subunit |
8 |
| CATGTATATTATGC |
YKL003C |
MRP17 |
6322850 |
COG0360 |
6 |
4 |
0 |
2 |
1 |
11 |
436527 |
436540 |
- |
436241 |
437135 |
- |
131 |
Mitochondrial ribosomal protein of the small subunit;
MRP17 exhibits genetic interactions with PET122, encoding a COX3-specific
translational activator |
8 |
| CATGGCCTTGTATA |
YDL045W-A |
MRP10 |
6320158 |
- |
6 |
0 |
6 |
1 |
1 |
4 |
372579 |
372592 |
+ |
372245 |
373031 |
+ |
95 |
Mitochondrial ribosomal protein of the small subunit |
8 |
| CATGTCAATTATGT |
YDR033W |
MRH1 |
6320236 |
- |
0 |
0 |
10 |
1 |
1 |
4 |
509113 |
509126 |
+ |
508142 |
509603 |
+ |
320 |
Membrane protein related to Hsp30p; Localized by
immunofluorescence to membranes, mainly the plasma membr. punctuate
immunofluorescence pattern observed in buds. The
nuclear envelope, but not vacuole or mitochondrial membranes also stained |
3 |
| CATGCGACTGCTAA |
YJL066C |
MPM1 |
6322395 |
- |
24 |
12 |
6 |
1 |
1 |
10 |
313927 |
313940 |
- |
313832 |
314788 |
- |
252 |
mitochondrial membrane protein |
6 |
| CATGTTCTGCATAT |
YKL064W |
MNR2 |
6322786 |
COG0598 |
0 |
8 |
0 |
1 |
1 |
11 |
320274 |
320287 |
+ |
317409 |
320817 |
+ |
969 |
Product of gene unknown |
8 |
| CATGGATCCCGCAA |
YBR098W |
MMS4 |
27808702 |
- |
3 |
4 |
0 |
1 |
1 |
2 |
443261 |
443274 |
+ |
441472 |
444046 |
+ |
691 |
endonuclease |
8 |
| CATGAAAAACTTTG |
YIL051C |
MMF1 |
6322138 |
COG0251 |
6 |
0 |
0 |
1 |
1 |
9 |
257969 |
257982 |
- |
257343 |
258279 |
- |
145 |
Maintenance of Mitochondrial Function |
8 |
| CATGCCTATATGAT |
YNL117W |
MLS1 |
6324212 |
COG2225 |
3 |
4 |
13 |
1 |
1 |
14 |
408061 |
408074 |
+ |
406358 |
408340 |
+ |
554 |
carbon-catabolite sensitive malate synthase |
3 |
| CATGCGACTAAAGG |
YLR035C |
MLH2 |
6323063 |
COG0323 |
3 |
4 |
0 |
1 |
1 |
12 |
212172 |
212185 |
- |
211935 |
214457 |
- |
695 |
Mutl Homolog |
8 |
| CATGTGTTATGCTA |
YNL074C |
MLF3 |
6324255 |
- |
6 |
0 |
0 |
1 |
1 |
14 |
486606 |
486619 |
- |
486266 |
488123 |
- |
452 |
Protein of unknown function |
8 |
| CATGCTAACTGGCT |
YGL106W |
MLC1 |
6321332 |
COG5126 |
6 |
0 |
0 |
1 |
1 |
7 |
306883 |
306896 |
+ |
306561 |
307437 |
+ |
149 |
may stabilize Myo2p by binding to the neck region |
8 |
| CATGGGCTATGAAA |
YPL140C |
MKK2 |
6325117 |
COG0515 |
9 |
0 |
3 |
1 |
1 |
16 |
287326 |
287339 |
- |
287014 |
289033 |
- |
506 |
Member of MAP kinase pathway involving PKC1, BCK1, and
SLT2. Shows functional redundancy with MKK1 |
8 |
| CATGCATATATATT |
YJR077C |
MIR1 |
6322537 |
- |
6 |
0 |
0 |
2 |
1 |
10 |
577136 |
577149 |
- |
576670 |
578104 |
- |
311 |
Product of gene unknown |
8 |
| CATGTAAATAGTGC |
YDR296W |
MHR1 |
6320502 |
- |
3 |
4 |
0 |
1 |
1 |
4 |
1055939 |
1055952 |
+ |
1055204 |
1056383 |
+ |
226 |
Involved in mitochondrial homologous DNA recombination.
Binds to activation domains of acidic activators. Presence in RNA pol II
holoenzyme may help recruit an Ssn3-active form of
the holoenzyme to target promoters. |
8 |
| CATGCTGCTCAATT |
YJR144W |
MGM101 |
6322604 |
- |
9 |
4 |
0 |
2 |
1 |
10 |
700832 |
700845 |
+ |
700797 |
702105 |
+ |
269 |
Involved in mitochondrial genome maintenance |
8 |
| CATGCTTTTATACT |
YOR232W |
MGE1 |
6324806 |
COG0576 |
0 |
0 |
6 |
1 |
1 |
15 |
775398 |
775411 |
+ |
774573 |
775758 |
+ |
228 |
involved in protein import into mitochondria |
3 |
| CATGTACAAATTTG |
YIR033W |
MGA2 |
6322224 |
COG0666 |
3 |
0 |
6 |
1 |
1 |
9 |
419281 |
419294 |
+ |
416121 |
419961 |
+ |
1113 |
Product of gene unknown |
8 |
| CATGTCAAATCTTA |
YML062C |
MFT1 |
6323578 |
- |
6 |
0 |
0 |
1 |
1 |
13 |
147268 |
147281 |
- |
147006 |
148683 |
- |
392 |
Protein involved in mitochondrial import of fusion
proteins |
8 |
| CATGCTTTGTATAT |
YPL169C |
MEX67 |
6325088 |
- |
0 |
0 |
6 |
1 |
1 |
16 |
228939 |
228952 |
- |
228539 |
230837 |
- |
599 |
Involved in nuclear mRNA export, binds both poly(A) |
3 |
| CATGTAGGGCAGGT |
YIL046W |
MET30 |
6322143 |
COG2319 |
0 |
4 |
10 |
1 |
1 |
9 |
270032 |
270045 |
+ |
268650 |
271071 |
+ |
640 |
F-box protein containing five copies of the WD40 motif,
controls cell cycle function, sulfur metabolism, and methionine biosynthesis
as part of the ubiquitin ligase complex; interacts
with and regulates Met4p, localizes within the nucleus |
8 |
| CATGCGATGTCATT |
YOL064C |
MET22 |
6324508 |
COG1218 |
6 |
0 |
0 |
2 |
1 |
15 |
206119 |
206132 |
- |
205885 |
207175 |
- |
357 |
Bisphosphate-3'-nucleotidase, involved in salt tolerance
and methionine biogenesis; dephosphorylates 3'-phosphoadenosine-5'-phosphate
and 3'-phosphoadenosine-5'-phosphosulfate,
intermediates of the sulfate assimilation pathway |
8 |
| CATGGCCTTGACAA |
YIL128W |
MET18 |
6322063 |
- |
3 |
4 |
0 |
1 |
1 |
9 |
115214 |
115227 |
+ |
113806 |
117403 |
+ |
1032 |
Protein of unknown function, required for both nucleotide
excision repair (NER) and RNA polymerase II (RNAP II) transcription; possible
role in assembly of a multiprotein complex(es)
required for NER and RNAP II transcription |
8 |
| CATGGAGAGATGAA |
YPL023C |
MET12 |
6325234 |
COG0685 |
0 |
0 |
6 |
1 |
1 |
16 |
504496 |
504509 |
- |
503836 |
506308 |
- |
657 |
Isozyme of methylenetetrahydrofolate reductase, catalyzes
the reduction of 5,10-methylenetetrahydrofolate to 5-methyltetrahydrofolate
in the methionine biosynthesis pathway |
3 |
| CATGAAAACATTGA |
YNL142W |
MEP2 |
6324187 |
COG0004 |
3 |
0 |
6 |
2 |
1 |
14 |
358850 |
358863 |
+ |
357453 |
359451 |
+ |
499 |
belongs to a ubiquitous family of cytoplasmic membrane
proteins that transport only ammonium (NH(4)(+) + NH(3)). |
8 |
| CATGAAAAAAATAA |
YGL197W |
MDS3 |
6321241 |
- |
6 |
4 |
0 |
4 |
1 |
7 |
128675 |
128688 |
+ |
124701 |
129663 |
+ |
1487 |
Mck1 Dosage Suppressor 3; negative regulator of early
meiotic gene expression |
8 |
| CATGTAAATACTAA |
YKL053C-A |
MDM35 |
6322797 |
- |
6 |
0 |
0 |
1 |
1 |
11 |
338777 |
338790 |
- |
338399 |
339087 |
- |
86 |
Mitochondrial Distribution and Morphology |
8 |
| CATGGAGGATAGCC |
YGL219C |
MDM34 |
6321220 |
- |
0 |
12 |
0 |
1 |
1 |
7 |
82892 |
82905 |
- |
82377 |
84255 |
- |
459 |
Mitochondrial outer membrane protein, colocalizes with
mtDNA nucleids, required for mitochondria shape |
9 |
| CATGCAACCGGGCA |
YFL016C |
MDJ1 |
14318504 |
COG0484 |
3 |
0 |
6 |
1 |
1 |
6 |
104849 |
104862 |
- |
104457 |
106230 |
- |
511 |
involved in protection against heat-induced protein
aggregation but not necessary for protein import into the mitochondrion |
8 |
| CATGGCGTTCGCGG |
YDL078C |
MDH3 |
6320125 |
COG0039 |
6 |
4 |
0 |
1 |
1 |
4 |
315667 |
315680 |
- |
314858 |
316388 |
- |
343 |
malate dehydrogenase |
8 |
| CATGCTATTCGTTG |
YKL085W |
MDH1 |
6322765 |
COG0039 |
6 |
30 |
3 |
1 |
1 |
11 |
279947 |
279960 |
+ |
278768 |
280153 |
+ |
334 |
mitochondrial malate dehydrogenase |
9 |
| CATGTGTATGACTA |
YKL150W |
MCR1 |
6322699 |
COG0543 |
12 |
4 |
0 |
1 |
1 |
11 |
167536 |
167549 |
+ |
166549 |
167956 |
+ |
302 |
NADH-cytochrome b5 reductase |
6 |
| CATGAAAAAGGCGT |
YMR043W |
MCM1 |
6323686 |
COG5068 |
0 |
0 |
10 |
1 |
1 |
13 |
353997 |
354010 |
+ |
353870 |
355229 |
+ |
286 |
Involved in cell-type-specific transcription and
pheromone response |
3 |
| CATGGGCGAGATGC |
YNL307C |
MCK1 |
6324022 |
COG0515 |
3 |
4 |
0 |
1 |
1 |
14 |
56873 |
56886 |
- |
55947 |
57573 |
- |
375 |
Disp. for mitosis, required for chr. segregation, benomyl
resist., basal IME1 transcript. in mitosis, IME1 induction in meiosis &
ascus mat. independ. of IME1; maybe in mitotic
chr. segregation specific to CDEIII |
8 |
| CATGTTTGTTGGTT |
YOR306C |
MCH5 |
6324882 |
COG0477 |
15 |
21 |
0 |
2 |
1 |
15 |
890191 |
890204 |
- |
889364 |
891428 |
- |
521 |
monocarboxylate permease homologue |
6 |
| CATGCCAAGAATTC |
YOL119C |
MCH4 |
6324453 |
COG0477 |
3 |
8 |
0 |
2 |
1 |
15 |
94716 |
94729 |
- |
94402 |
96360 |
- |
501 |
monocarboxylate permease homologue |
8 |
| CATGTGTTTTTTTA |
YOR197W |
MCA1 |
6324771 |
- |
0 |
0 |
34 |
2 |
1 |
15 |
718539 |
718552 |
+ |
717023 |
718883 |
+ |
453 |
metacaspase |
2 |
| CATGATCGTTTTAT |
YOR298C-A |
MBF1 |
42742310 |
- |
3 |
8 |
41 |
1 |
1 |
15 |
877131 |
877144 |
- |
876728 |
877682 |
- |
151 |
bridges the DNA-binding region of GCN4 and TBP; similar
to multiprotein bridging factor 1 of Bombyx mori |
2 |
| CATGCACTGATGGC |
YNR017W |
MAS6 |
6324344 |
- |
6 |
0 |
0 |
1 |
1 |
14 |
663642 |
663655 |
+ |
662912 |
664079 |
+ |
222 |
23 kDa mitochondrial inner membrane protein |
8 |
| CATGCCACTTAGTA |
YHR024C |
MAS2 |
6321813 |
COG0612 |
0 |
8 |
0 |
1 |
1 |
8 |
157569 |
157582 |
- |
157237 |
159184 |
- |
482 |
53 kDa subunit of the mitochondrial processing protease |
8 |
| CATGAAATCACAGG |
YOL060C |
MAM3 |
6324512 |
COG1253 |
0 |
4 |
3 |
1 |
1 |
15 |
213931 |
213944 |
- |
213517 |
216136 |
- |
706 |
putative hemolysin-like protein with three transmembrane
domains |
8 |
| CATGTTCCCAGGTA |
YBR142W |
MAK5 |
6319618 |
COG0513 |
0 |
0 |
6 |
2 |
1 |
2 |
529651 |
529664 |
+ |
528273 |
531093 |
+ |
773 |
Necessary for maintenance of dsRNA killer plasmids. Is
predicted to encode an DEAD-box RNA helicase |
3 |
| CATGCGTGCAGCTC |
YKL021C |
MAK11 |
6322831 |
COG2319 |
3 |
4 |
0 |
1 |
1 |
11 |
396962 |
396975 |
- |
396892 |
398393 |
- |
468 |
essential for cell growth and replication of M dsRNA
virus; contains four beta-transducin repeats |
8 |
| CATGTATTACTGAC |
YER142C |
MAG1 |
6320990 |
COG0122 |
3 |
12 |
0 |
1 |
1 |
5 |
455115 |
455128 |
- |
454642 |
456031 |
- |
296 |
3-methyladenine DNA glycosylase |
9 |
| CATGACCCATCGGT |
YKL029C |
MAE1 |
6322823 |
COG0281 |
0 |
8 |
0 |
1 |
1 |
11 |
382377 |
382390 |
- |
381860 |
384368 |
- |
669 |
Mitochondrial malic enzyme |
8 |
| CATGTGGCAATATG |
YMR038C |
LYS7 |
6323681 |
COG2608 |
3 |
8 |
0 |
1 |
1 |
13 |
347403 |
347416 |
- |
347011 |
348259 |
- |
249 |
Involved in lysine biosynthesis, oxidative stress
protection; copper chaperone for SOD1 |
8 |
| CATGCATCGGTCTA |
YDR234W |
LYS4 |
6320440 |
COG1048 |
6 |
0 |
0 |
1 |
1 |
4 |
932345 |
932358 |
+ |
931121 |
933495 |
+ |
693 |
homoaconitase |
8 |
| CATGGTAGTTTGTC |
YDR034C |
LYS14 |
6320237 |
- |
0 |
0 |
6 |
1 |
1 |
4 |
509725 |
509738 |
- |
509233 |
512104 |
- |
790 |
Transcriptional activator of lysine pathway genes with
2-aminoadipate semialdehyde as co-inducer; saccharopine reductase synthesis |
3 |
| CATGTAGCACTAAA |
YNL006W |
LST8 |
6324322 |
COG2319 |
0 |
0 |
6 |
1 |
1 |
14 |
621185 |
621198 |
+ |
620066 |
621476 |
+ |
303 |
Required for amino acid permease transport from the Golgi
to the cell surface |
3 |
| CATGTATATCAGTG |
YDR378C |
LSM6 |
6320586 |
COG1958 |
3 |
0 |
6 |
1 |
1 |
4 |
1229350 |
1229363 |
- |
1228838 |
1229708 |
- |
123 |
Like Sm-F protein |
8 |
| CATGGCAGGTGCTG |
YFR024C-A |
LSB3 |
15530184 |
COG2930 |
0 |
12 |
0 |
1 |
1 |
6 |
203056 |
203069 |
- |
201449 |
203421 |
- |
451 |
LAs17 Binding protein |
9 |
| CATGGCTGCCTATG |
YFL018C |
LPD1 |
14318501 |
COG1249 |
6 |
0 |
3 |
1 |
1 |
6 |
101641 |
101654 |
- |
101123 |
103121 |
- |
499 |
an FAD flavoprotein which contains a pair of redox-active
cysteines involved in the transfer of reducing equivalents from the FAD
cofactor to the substrate |
8 |
| CATGGCGTTTGAGG |
YKL183W |
LOT5 |
6322665 |
- |
6 |
0 |
0 |
2 |
1 |
11 |
99420 |
99433 |
+ |
98726 |
100145 |
+ |
306 |
LOw Temperature responsive |
8 |
| CATGTAATGGCACT |
YKL205W |
LOS1 |
6322644 |
- |
6 |
0 |
0 |
1 |
1 |
11 |
53487 |
53500 |
+ |
50052 |
53704 |
+ |
1100 |
Nuclear pore protein involved in pre-tRNA splicing |
8 |
| CATGGACCGCAATG |
YOR196C |
LIP5 |
6324770 |
COG0320 |
6 |
4 |
0 |
1 |
1 |
15 |
715538 |
715551 |
- |
715094 |
716837 |
- |
414 |
Involved in lipoic acid metabolism |
8 |
| CATGCTGACTCCTT |
YNL104C |
LEU4 |
6324225 |
COG0119 |
0 |
12 |
0 |
1 |
1 |
14 |
425396 |
425409 |
- |
424496 |
426754 |
- |
619 |
leucine biosynthesis |
9 |
| CATGGACGTTGGCG |
YNL323W |
LEM3 |
6324006 |
COG5035 |
0 |
0 |
17 |
1 |
1 |
14 |
33547 |
33560 |
+ |
31943 |
33686 |
+ |
414 |
plays an important role in phospholipid translocation
across the plasma membrane. |
3 |
| CATGAATTTGGTGG |
YPL213W |
LEA1 |
6325043 |
COG4886 |
6 |
0 |
0 |
2 |
1 |
16 |
151205 |
151218 |
+ |
150613 |
151828 |
+ |
238 |
Looks Exceptionally like U2A |
8 |
| CATGGAAAGAACGA |
YDR499W |
LCD1 |
6320707 |
- |
3 |
0 |
3 |
2 |
1 |
4 |
1450367 |
1450380 |
+ |
1447818 |
1450560 |
+ |
747 |
required for the DNA integrity checkpoint pathways; S.
pombe Rad26 functional homolog (putative), homolog of human ATRIP |
8 |
| CATGAACAGTGTTG |
YJL062W |
LAS21 |
6322399 |
COG1524 |
3 |
0 |
3 |
1 |
1 |
10 |
318203 |
318216 |
+ |
317200 |
319931 |
+ |
830 |
Local Anesthetics Sensitive: involved in the attachment
of glycosylphosphatidylinositol (GPI) anchors to proteins. |
8 |
| CATGCACAGCATCA |
YKL103C |
LAP4 |
6322746 |
COG1362 |
6 |
0 |
0 |
1 |
1 |
11 |
245884 |
245897 |
- |
245285 |
247328 |
- |
514 |
vacuolar aminopeptidase ysc1 |
8 |
| CATGTGGCGGACAT |
YPL053C |
KTR6 |
6325204 |
COG5020 |
3 |
0 |
10 |
1 |
1 |
16 |
457166 |
457179 |
- |
456614 |
458453 |
- |
446 |
Similar to KRE2, mannosylphosphate transferase which may
recognize any oligosaccharides with at least one alpha-1,2-linked mannobiose
unit. Required for the transfer of
mannosylphosphate to cell wall mannans. |
8 |
| CATGGCGTTTGAGG |
YBR205W |
KTR3 |
6319682 |
COG5020 |
6 |
0 |
0 |
2 |
2 |
2 |
635101 |
635114 |
+ |
633579 |
635102 |
+ |
404 |
Putative alpha-1,2-mannosyltransferase |
8 |
| CATGATACGTAGGC |
YBL071W-A |
KTI11 |
21648335 |
COG5216 |
3 |
8 |
13 |
1 |
1 |
2 |
90436 |
90449 |
+ |
89976 |
90723 |
+ |
82 |
Similar to Hemiascomycetous yeast protein (FEBS Lett.
487(1): 31-36 (2000)). |
3 |
| CATGGCAAAATGGA |
YHR082C |
KSP1 |
6321874 |
COG0515 |
3 |
0 |
10 |
1 |
1 |
8 |
268661 |
268674 |
- |
267961 |
271549 |
- |
1029 |
Serine/threonine kinase similar to casein kinase II and
other serine/threonine protein kinases |
8 |
| CATGAGAAAAGTAT |
YJL174W |
KRE9 |
6322287 |
- |
6 |
0 |
6 |
1 |
1 |
10 |
95904 |
95917 |
+ |
95090 |
96419 |
+ |
276 |
cell wall beta-glucan assembly |
8 |
| CATGGTCATAAAAA |
YPR159W |
KRE6 |
6325417 |
COG2273 |
0 |
8 |
0 |
2 |
1 |
16 |
859787 |
859800 |
+ |
857577 |
860238 |
+ |
720 |
cell wall beta-glucan assembly |
8 |
| CATGTCTGAAGATG |
YNL132W |
KRE33 |
6324197 |
COG1444 |
3 |
4 |
6 |
1 |
1 |
14 |
377320 |
377333 |
+ |
375321 |
378766 |
+ |
1056 |
Killer toxin REsistant |
8 |
| CATGATGACTGAAC |
YER038C |
KRE29 |
6320876 |
- |
0 |
4 |
13 |
2 |
1 |
5 |
226838 |
226851 |
- |
226358 |
228251 |
- |
464 |
Killer toxin REsistant |
3 |
| CATGCAATTATAGA |
YKL168C |
KKQ8 |
6322680 |
COG0515 |
6 |
4 |
0 |
1 |
1 |
11 |
131254 |
131267 |
- |
130794 |
133497 |
- |
734 |
Serine/threonine protein kinase of unknown function |
8 |
| CATGCAGGTACACA |
YOR233W |
KIN4 |
6324807 |
COG0515 |
0 |
0 |
10 |
2 |
1 |
15 |
777100 |
777113 |
+ |
775846 |
778747 |
+ |
800 |
protein kinase |
3 |
| CATGCAAAGGTATC |
YJL094C |
KHA1 |
6322367 |
COG0475 |
0 |
12 |
0 |
1 |
1 |
10 |
253200 |
253213 |
- |
251238 |
254358 |
- |
873 |
putative K+/H+ antiporter |
9 |
| CATGATTATTCTTG |
YDR148C |
KGD2 |
6320352 |
COG0508 |
6 |
0 |
0 |
1 |
1 |
4 |
753622 |
753635 |
- |
753170 |
755060 |
- |
463 |
dihydrolipoyl transsuccinylase component of
alpha-ketoglutarate dehydrogenase complex in mitochondria |
8 |
| CATGATGTTAGCAT |
YIL125W |
KGD1 |
6322066 |
COG0567 |
3 |
25 |
3 |
2 |
1 |
9 |
125875 |
125888 |
+ |
122689 |
126203 |
+ |
1014 |
alpha-ketoglutarate dehydrogenase |
9 |
| CATGCATAGCTAAT |
YJL034W |
KAR2 |
6322426 |
COG0443 |
9 |
8 |
51 |
1 |
1 |
10 |
383380 |
383393 |
+ |
381243 |
383752 |
+ |
682 |
Involved in translocation of nascent polypeptides across
the ER membrane |
2 |
| CATGATAAACCTGA |
YLR347C |
KAP95 |
6323379 |
COG5215 |
3 |
0 |
3 |
1 |
1 |
12 |
824103 |
824116 |
- |
823328 |
826412 |
- |
861 |
protein involved in nuclear import; required for the
docking of import substrate to the nuclear membrane/pore; identified as an
rna1-1 synthetic lethal |
8 |
| CATGTGTAGAAAAG |
YPR061C |
JID1 |
6325318 |
COG2214 |
0 |
8 |
0 |
2 |
1 |
16 |
676814 |
676827 |
- |
675627 |
676877 |
- |
301 |
cytosolic Hsp40 chaperone with DnaJ homology necessary
for degradation of misfolded ER proteins with a tightly folding cytoplasmic
domain |
8 |
| CATGTTATTGGCTG |
YKL032C |
IXR1 |
6322820 |
- |
0 |
0 |
13 |
1 |
1 |
11 |
379745 |
379758 |
- |
379209 |
381501 |
- |
597 |
intrastrand crosslink recognition protein |
3 |
| CATGTTTAACCGCT |
YDL115C |
IWR1 |
44829553 |
- |
3 |
4 |
10 |
1 |
1 |
4 |
253907 |
253920 |
- |
253496 |
254717 |
- |
240 |
Interacts with RNA Polymerase II |
8 |
| CATGCTTGCAGAAG |
YOR226C |
ISU2 |
6324800 |
COG0822 |
0 |
0 |
6 |
1 |
1 |
15 |
761675 |
761688 |
- |
761266 |
762084 |
- |
156 |
Iron-sulfur cluster nifU-like protein |
3 |
| CATGCATATCTTCC |
YPL135W |
ISU1 |
6325122 |
COG0822 |
3 |
4 |
0 |
1 |
1 |
16 |
298195 |
298208 |
+ |
297552 |
298548 |
+ |
165 |
Iron-sulfur cluster nifU-like protein |
8 |
| CATGAATGTACATA |
YOL081W |
IRA2 |
6324491 |
- |
0 |
0 |
10 |
1 |
1 |
15 |
180355 |
180368 |
+ |
171069 |
180807 |
+ |
3079 |
Negatively regulates cAPK by antagonizing CDC25 |
3 |
| CATGAATGAATATC |
YBR011C |
IPP1 |
6319483 |
COG0221 |
18 |
4 |
3 |
1 |
1 |
2 |
256969 |
256982 |
- |
256573 |
257935 |
- |
287 |
Cytoplasmic inorganic pyrophosphatase (PPase), catalyzes
the rapid exchange of oxygens from Pi with water, highly expressed and
essential for viability, active-site residues show
identity to those from E. coli PPase |
6 |
| CATGACTGAGTTTT |
YJL153C |
INO1 |
37362665 |
- |
18 |
8 |
13 |
1 |
1 |
10 |
134485 |
134498 |
- |
133854 |
135851 |
- |
533 |
Inositol 1-phosphate synthase, involved in synthesis of
inositol phosphates and inositol-containing phospholipids; transcription is
coregulated with other phospholipid biosynthetic
genes by Ino2p and Ino4p, which bind the UASINO DNA element |
8 |
| CATGCGTTTCCGCA |
YDL181W |
INH1 |
6320020 |
- |
15 |
4 |
3 |
1 |
1 |
4 |
135438 |
135451 |
+ |
135180 |
135896 |
+ |
85 |
Protein that inhibits ATP hydrolysis by the F1F0-ATP
synthase, inhibitory function is enhanced by stabilizing proteins Stf1p and
Stf2p; has similarity to Stf1p and both Inh1p and
Stf1p exhibit the potential to form coiled-coil structures |
6 |
| CATGTGGTCATCAA |
YCR071C |
IMG2 |
10383803 |
- |
0 |
12 |
0 |
1 |
1 |
3 |
240025 |
240038 |
- |
239599 |
240538 |
- |
146 |
Mitochondrial ribosomal protein of the small subunit |
9 |
| CATGCAAAAGACTG |
YLR432W |
IMD3 |
6323464 |
COG0517 |
12 |
0 |
13 |
4 |
1 |
12 |
1003820 |
1003833 |
+ |
1002553 |
1004623 |
+ |
523 |
Inosine monophosphate dehydrogenase, catalyzes the first
step of GMP biosynthesis, member of a four-gene family in S. cerevisiae,
constitutively expressed |
8 |
| CATGCAAAAGACTG |
YHR216W |
IMD2 |
6322012 |
COG0516 |
12 |
0 |
13 |
4 |
1 |
8 |
555661 |
555674 |
+ |
554394 |
556464 |
+ |
523 |
Inosine monophosphate dehydrogenase, catalyzes the first
step of GMP biosynthesis, expression is induced by mycophenolic acid
resulting in resistance to the drug, expression is
repressed by nutrient limitation |
8 |
| CATGAGCCTATTTA |
YCL009C |
ILV6 |
6319837 |
COG0440 |
0 |
4 |
3 |
1 |
1 |
3 |
104535 |
104548 |
- |
104350 |
105547 |
- |
309 |
Regulatory subunit of acetolactate synthase, which
catalyzes the first step of branched-chain amino acid biosynthesis; enhances
activity of the Ilv2p catalytic subunit, localizes
to mitochondria |
8 |
| CATGGAAATCTGGA |
YLR355C |
ILV5 |
6323387 |
COG0059 |
9 |
8 |
0 |
2 |
1 |
12 |
838108 |
838121 |
- |
837566 |
839252 |
- |
395 |
Acetohydroxyacid reductoisomerase, mitochondrial protein
involved in branched-chain amino acid biosynthesis, also required for
maintenance of wild-type mitochondrial DNA |
8 |
| CATGCCCAAGGTGT |
YER086W |
ILV1 |
6320930 |
COG1171 |
0 |
8 |
0 |
1 |
1 |
5 |
328880 |
328893 |
+ |
328473 |
330571 |
+ |
576 |
Threonine deaminase, catalyzes the first step in
isoleucine biosynthesis; expression is under general amino acid control; ILV1
locus exhibits highly positioned nucleosomes whose
organization is independent of known ILV1 regulation |
8 |
| CATGCTAATATGTG |
YJR118C |
ILM1 |
6322578 |
- |
6 |
0 |
0 |
2 |
1 |
10 |
643294 |
643307 |
- |
642906 |
644016 |
- |
203 |
Protein of unknown function |
8 |
| CATGTAATCTCTAG |
YFL013C |
IES1 |
14318508 |
- |
0 |
8 |
0 |
1 |
1 |
6 |
107481 |
107494 |
- |
107347 |
109924 |
- |
692 |
Subunit of the INO80 chromatin remodeling complex |
8 |
| CATGCCGGTACACC |
YJL146W |
IDS2 |
6322315 |
- |
0 |
0 |
6 |
1 |
1 |
10 |
144766 |
144779 |
+ |
143210 |
145077 |
+ |
469 |
Protein involved in modulation of Ime2p activity during
meiosis, appears to act indirectly to promote Ime2p-mediated late meiotic
functions; found in growing cells and degraded
during sporulation |
3 |
| CATGGCCGTCGCGG |
YMR195W |
ICY1 |
6323851 |
- |
24 |
17 |
0 |
1 |
1 |
13 |
654313 |
654326 |
+ |
654033 |
654915 |
+ |
127 |
Protein that interacts with the cytoskeleton and is
involved in chromatin organization and nuclear transport, interacts
genetically with TCP1 and ICY2, required for viability in rich media of cells lacking mitochondrial DNA |
6 |
| CATGCAACCAGTTT |
YIR037W |
HYR1 |
6322228 |
COG0386 |
3 |
4 |
0 |
1 |
1 |
9 |
423311 |
423324 |
+ |
423125 |
424115 |
+ |
163 |
Thiol peroxidase that functions as a hydroperoxide
receptor to sense intracellular hydroperoxide levels and transduce a redox
signal to the Yap1p transcription factor |
8 |
| CATGTACTCTTCGC |
YEL034W |
HYP2 |
6320801 |
COG0231 |
9 |
8 |
3 |
1 |
1 |
5 |
86220 |
86233 |
+ |
85676 |
86648 |
+ |
157 |
Translation initiation factor eIF-5A, promotes formation
of the first peptide bond; similar to and functionally redundant with Anb1p;
undergoes an essential hypusination modification;
expressed under aerobic conditions |
8 |
| CATGATCACGCTCT |
YDR342C |
HXT7 |
6320549 |
COG0477 |
18 |
8 |
3 |
2 |
1 |
4 |
1154169 |
1154182 |
- |
1153707 |
1155918 |
- |
570 |
High-affinity glucose transporter of the major
facilitator superfamily, nearly identical to Hxt6p, expressed at high basal
levels relative to other HXTs, expression repressed by high glucose levels |
6 |
| CATGATCACGCTCT |
YDR343C |
HXT6 |
6320550 |
COG0477 |
18 |
8 |
3 |
2 |
1 |
4 |
1159561 |
1159574 |
- |
1159099 |
1161310 |
- |
570 |
High-affinity glucose transporter of the major
facilitator superfamily, nearly identical to Hxt7p, expressed at high basal
levels relative to other HXTs, repression of expression by high glucose requires SNF3 |
6 |
| CATGATATCAAACA |
YDR345C |
HXT3 |
6320552 |
COG0477 |
3 |
4 |
0 |
1 |
1 |
4 |
1162797 |
1162810 |
- |
1162448 |
1164650 |
- |
567 |
Low affinity glucose transporter of the major facilitator
superfamily, expression is induced in low or high glucose conditions |
8 |
| CATGGAAATCTGGT |
YMR011W |
HXT2 |
6323653 |
COG0477 |
3 |
8 |
0 |
1 |
1 |
13 |
289650 |
289663 |
+ |
288078 |
290202 |
+ |
541 |
High-affinity glucose transporter of the major
facilitator superfamily, expression is induced by low levels of glucose and
repressed by high levels of glucose |
8 |
| CATGGATACCTCCT |
YFR053C |
HXK1 |
14318578 |
COG5026 |
24 |
12 |
13 |
1 |
1 |
6 |
254000 |
254013 |
- |
253080 |
255036 |
- |
485 |
Hexokinase isoenzyme 1, cytosolic protein that catalyzes
phosphorylation of glucose during glucose metabolism, expression is highest
during growth on non-glucose carbon sources and is
repressed by Hxk2p |
5 |
| CATGATGTTAGCAT |
YJR036C |
HUL4 |
6322497 |
COG5021 |
3 |
25 |
3 |
2 |
1 |
10 |
502772 |
502785 |
- |
500128 |
503305 |
- |
892 |
Protein with similarity to hect domain E3
ubiquitin-protein ligases, not essential for viability |
9 |
| CATGCTGTCTCTGA |
YDR224C |
HTB1 |
6320430 |
- |
6 |
12 |
6 |
1 |
1 |
4 |
914354 |
914367 |
- |
913810 |
914704 |
- |
131 |
Histone H2B (HTB1 and HTB2 code for nearly identical
proteins) |
9 |
| CATGCAGAGTTTGA |
YOL068C |
HST1 |
6324504 |
COG0846 |
3 |
4 |
0 |
2 |
1 |
15 |
200538 |
200551 |
- |
199868 |
201878 |
- |
503 |
Homolog of SIR2 |
8 |
| CATGGAAATAACTG |
YPL240C |
HSP82 |
6325016 |
COG0326 |
6 |
0 |
34 |
2 |
1 |
16 |
96387 |
96400 |
- |
96259 |
98625 |
- |
709 |
82 kDa heat shock protein; homolog of mammalian Hsp90 |
2 |
| CATGAAGAAGGCGA |
YDR258C |
HSP78 |
6320464 |
COG0542 |
3 |
0 |
31 |
1 |
1 |
4 |
971827 |
971840 |
- |
971467 |
974235 |
- |
811 |
Similar to E. coli ClpB protein; involved in folding of
some mitochondrial proteins |
2 |
| CATGTTAGCCACTG |
YLR259C |
HSP60 |
6323288 |
COG0459 |
9 |
4 |
55 |
1 |
1 |
12 |
663455 |
663468 |
- |
662787 |
665004 |
- |
572 |
60 kDa heat shock protein |
2 |
| CATGAGATGCTCAT |
YDR171W |
HSP42 |
6320376 |
COG0071 |
6 |
8 |
34 |
1 |
1 |
4 |
807445 |
807458 |
+ |
806615 |
808241 |
+ |
375 |
Similar to HSP26; expression is regulated by stress
conditions |
2 |
| CATGGTCATATGTG |
YOR391C |
HSP33 |
6324967 |
COG0693 |
9 |
17 |
3 |
3 |
1 |
15 |
1078337 |
1078350 |
- |
1078042 |
1079254 |
- |
237 |
Possible chaperone and cysteine protease with similarity
to E. coli Hsp31 and S. cerevisiae Hsp32p, Hsp33p, and Sno4p; member of the
DJ-1/ThiJ/PfpI superfamily, which includes human
DJ-1 involved in Parkinson's disease |
9 |
| CATGGTCATATGTG |
YPL280W |
HSP32 |
6324975 |
COG0693 |
9 |
17 |
3 |
3 |
1 |
16 |
12789 |
12802 |
+ |
11887 |
13099 |
+ |
237 |
Possible chaperone and cysteine protease with similarity
to E. coli Hsp31 and S. cerevisiae Hsp31p, Hsp33p, and Sno4p; member of the
DJ-1/ThiJ/PfpI superfamily, which includes human
DJ-1 involved in Parkinson's disease |
9 |
| CATGTCTGAGATGG |
YDR533C |
HSP31 |
6320742 |
COG0693 |
36 |
30 |
17 |
1 |
1 |
4 |
1501291 |
1501304 |
- |
1500936 |
1502148 |
- |
237 |
Possible chaperone and cysteine protease with similarity
to E. coli Hsp31 and S. cerevisiae Hsp32p, Hsp33p, and Sno4p; member of the
DJ-1/ThiJ/PfpI superfamily, which includes human
DJ-1 involved in Parkinson's disease; exists as a dimer |
5 |
| CATGGTAATCGTTT |
YCR021C |
HSP30 |
6319869 |
- |
3 |
8 |
6 |
1 |
1 |
3 |
156423 |
156436 |
- |
155605 |
157102 |
- |
332 |
Protein induced by heat shock, ethanol treatment, and
entry into stationary phase; located in plasma membrane |
8 |
| CATGTCGCTTCATT |
YEL017C-A |
HSP30 |
6320819 |
- |
33 |
42 |
83 |
1 |
1 |
5 |
122419 |
122432 |
- |
122299 |
122929 |
- |
43 |
May regulate plasma membrane H(+)-ATPase; nearly
identical to PMP1 |
1 |
| CATGTCATTTAACA |
YBR072W |
HSP26 |
6319546 |
COG0071 |
6 |
4 |
38 |
1 |
1 |
2 |
381988 |
382001 |
+ |
381990 |
383133 |
+ |
214 |
heat shock protein 26 |
2 |
| CATGGTTTTTTCTT |
YFL014W |
HSP12 |
14318506 |
- |
9 |
0 |
6 |
1 |
1 |
6 |
107603 |
107616 |
+ |
107250 |
108078 |
+ |
109 |
induced by heat shock, entry into stationary phase,
depletion of glucose, and addition of lipids (fatty acids) |
8 |
| CATGTTTAATTGGT |
YLL026W |
HSP104 |
6323002 |
COG0542 |
9 |
0 |
17 |
2 |
1 |
12 |
89243 |
89256 |
+ |
88622 |
91847 |
+ |
908 |
plays a major role in the acquisition of tolerance to a
variety of stresses such as heat, ethanol, and sodium arsenite, inheritance
of [PSI+], and reactivation of mRNA splicing after
heat shock. |
8 |
| CATGTTTTATATAT |
YMR186W |
HSC82 |
6323840 |
COG0326 |
0 |
0 |
13 |
2 |
1 |
13 |
634487 |
634500 |
+ |
632354 |
634970 |
+ |
705 |
constitutively expressed heat shock protein |
3 |
| CATGTACGTGTATT |
YOL123W |
HRP1 |
6324449 |
COG0724 |
9 |
0 |
41 |
1 |
1 |
15 |
89544 |
89557 |
+ |
87843 |
89946 |
+ |
534 |
Putative polyadenylated-RNA-binding protein located in
nucleus; similar to vertebrate hnRNP A/B protein family |
2 |
| CATGGAATCGTGGG |
YOR267C |
HRK1 |
6324841 |
COG0515 |
6 |
4 |
6 |
2 |
1 |
15 |
823722 |
823735 |
- |
822086 |
824864 |
- |
759 |
Hygromycin Resistance Kinase |
8 |
| CATGGGAATCTACT |
YDR399W |
HPT1 |
6320607 |
COG2236 |
0 |
8 |
24 |
2 |
1 |
4 |
1270629 |
1270642 |
+ |
1270056 |
1271050 |
+ |
221 |
enzyme involved in de novo purine biosynthesis |
2 |
| CATGAAGAAACGGC |
YIL112W |
HOS4 |
6322079 |
COG0666 |
0 |
0 |
6 |
1 |
1 |
9 |
153961 |
153974 |
+ |
151592 |
155218 |
+ |
1083 |
Hos4p |
3 |
| CATGTTTCAAGAAA |
YPL116W |
HOS3 |
6325141 |
COG0123 |
6 |
0 |
0 |
2 |
1 |
16 |
331653 |
331666 |
+ |
329605 |
332197 |
+ |
697 |
Protein with similarity to Hda1p, Rpd3p, Hos2p, and Hos1p |
8 |
| CATGGTTGGAGAAC |
YER062C |
HOR2 |
6320905 |
COG0637 |
6 |
21 |
0 |
2 |
1 |
5 |
280507 |
280520 |
- |
279625 |
280680 |
- |
250 |
RHR2 (GPP1) encodes another DL-glycerol-3-phosphatase |
9 |
| CATGCCATTGATGA |
YER052C |
HOM3 |
6320893 |
COG0527 |
0 |
0 |
10 |
1 |
1 |
5 |
256407 |
256420 |
- |
255875 |
257957 |
- |
527 |
First step in common pathway for methionine and threonine
biosynthesis |
3 |
| CATGGGGTTGTTCT |
YNR055C |
HOL1 |
6324383 |
COG0477 |
3 |
4 |
0 |
1 |
1 |
14 |
728705 |
728718 |
- |
727925 |
730184 |
- |
586 |
Putative ion transporter similar to the major facilitator
superfamily of transporters |
8 |
| CATGTAGCTGCAAA |
YLR113W |
HOG1 |
6323142 |
COG0515 |
6 |
4 |
3 |
1 |
1 |
12 |
372853 |
372866 |
+ |
371621 |
373427 |
+ |
435 |
Osmoregulation. Hog1p is activated under stress
conditions when the cAMP cellular content is low. |
8 |
| CATGAATAAGCCAA |
YDR305C |
HNT2 |
6320511 |
COG0537 |
0 |
8 |
0 |
1 |
1 |
4 |
1073434 |
1073447 |
- |
1072550 |
1073480 |
- |
217 |
Fhit homolog, member of the histidine triad superfamily
of nucleotide binding-proteins |
8 |
| CATGTTACTAGCCA |
YDL125C |
HNT1 |
6320078 |
COG0537 |
3 |
8 |
10 |
1 |
1 |
4 |
238900 |
238913 |
- |
238665 |
239606 |
- |
158 |
Hint homolog, member of the histidine triad superfamily
of nucleotide-binding proteins |
8 |
| CATGTCCTTGTACT |
YBR034C |
HMT1 |
6319508 |
COG0500 |
6 |
17 |
0 |
1 |
1 |
2 |
304739 |
304752 |
- |
304393 |
305938 |
- |
348 |
Nuclear SAM-dependent mono- and asymmetric arginine
dimethylating methyltransferase that modifies hnRNPs, including Npl3p and
Hrp1p, thus facilitating nuclear export of these
proteins; required for viability of npl3 mutants |
9 |
| CATGGGCTTGCTTT |
YDR174W |
HMO1 |
6320379 |
- |
3 |
4 |
0 |
1 |
1 |
4 |
812925 |
812938 |
+ |
812104 |
813343 |
+ |
246 |
Chromatin associated high mobility group (HMG) family
member involved in genome maintenance; rDNA-binding component of the Pol I
transcription system; associates with a 5'-3' DNA
helicase and Fpr1p, a prolyl isomerase |
8 |
| CATGTAATAAGAAG |
YLR450W |
HMG2 |
6323483 |
COG1257 |
6 |
0 |
0 |
1 |
1 |
12 |
1035823 |
1035836 |
+ |
1032623 |
1036088 |
+ |
1045 |
One of two isozymes of HMG-CoA reductase that convert
HMG-CoA to mevalonate, a rate-limiting step in sterol biosynthesis;
overproduction induces assembly of peripheral ER
membrane arrays and short nuclear-associated membrane stacks |
8 |
| CATGGAAATGGAAG |
YER057C |
HMF1 |
6320899 |
COG0251 |
6 |
0 |
0 |
2 |
1 |
5 |
270757 |
270770 |
- |
270236 |
271124 |
- |
129 |
Member of the p14.5 protein family with similarity to
Mmf1p, functionally complements Mmf1p function when targeted to mitochondria;
heat shock inducible; high-dosage growth
inhibitor; forms a homotrimer in vitro |
8 |
| CATGCTGCTCAATT |
YCL030C |
HIS4 |
10383761 |
COG0141 |
9 |
4 |
0 |
2 |
1 |
3 |
66969 |
66982 |
- |
65569 |
68333 |
- |
799 |
Multifunctional enzyme containing phosphoribosyl-AMP
cyclohydrolase, phosphoribosyl-ATP pyrophosphatase, and histidinol
dehydrogenase activities; catalyzes the second,
third, ninth and tenth steps in histidine biosynthesis |
8 |
| CATGTGTATATATG |
YOR202W |
HIS3 |
6324776 |
COG0131 |
6 |
4 |
0 |
1 |
1 |
15 |
722648 |
722661 |
+ |
721946 |
722910 |
+ |
220 |
Imidazoleglycerol-phosphate dehydratase, catalyzes the
sixth step in histidine biosynthesis; mutations cause histidine auxotrophy
and sensitivity to Cu, Co, and Ni salts;
transcription is regulated by general amino acid control via Gcn4p |
8 |
| CATGTACAGCTGTG |
YFR025C |
HIS2 |
14318548 |
COG1387 |
12 |
0 |
0 |
1 |
1 |
6 |
203666 |
203679 |
- |
203422 |
204738 |
- |
335 |
Histidinolphosphatase, catalyzes the eighth step in
histidine biosynthesis; mutations cause histidine auxotrophy and sensitivity
to Cu, Co, and Ni salts; transcription is regulated
by general amino acid control |
6 |
| CATGTATAATAATT |
YNL031C |
HHT2 |
6324297 |
COG2036 |
6 |
0 |
0 |
1 |
1 |
14 |
575407 |
575420 |
- |
575139 |
576048 |
- |
136 |
One of two identical histone H3 proteins (see also HHT2);
core histone required for chromatin assembly, involved in
heterochromatin-mediated telomeric and HM silencing;
regulated by acetylation, methylation, and mitotic phosphorylation |
8 |
| CATGTACTATATAT |
YNL030W |
HHF2 |
6324298 |
COG2036 |
9 |
0 |
0 |
1 |
1 |
14 |
577161 |
577174 |
+ |
576725 |
577535 |
+ |
103 |
One of two identical histone H4 proteins (see also HHF1);
core histone required for chromatin assembly and chromosome function;
contributes to telomeric silencing; N-terminal
domain involved in maintaining genomic integrity |
8 |
| CATGGCAGATCTCG |
YOR176W |
HEM15 |
6324750 |
COG0276 |
3 |
8 |
3 |
1 |
1 |
15 |
663443 |
663456 |
+ |
662401 |
664081 |
+ |
393 |
Ferrochelatase, a mitochondrial inner membrane protein,
catalyzes the insertion of ferrous iron into protoporphyrin IX, the eighth
and final step in the heme biosynthetic pathway;
Yfh1p mediates the use of iron by Hem15p |
8 |
| CATGGGCTGAGATA |
YDR232W |
HEM1 |
6320438 |
COG0156 |
15 |
8 |
0 |
1 |
1 |
4 |
929105 |
929118 |
+ |
927444 |
929589 |
+ |
548 |
5-aminolevulinate synthase, catalyzes the first step in
the heme biosynthetic pathway; an N-terminal signal sequence is required for
localization to the mitochondrial matrix;
expression is regulated by Hap2p-Hap3p |
6 |
| CATGTATACACACA |
YNL281W |
HCH1 |
6324048 |
- |
12 |
4 |
17 |
1 |
1 |
14 |
109040 |
109053 |
+ |
108465 |
109425 |
+ |
153 |
Heat shock protein regulator that binds to Hsp90p and may
stimulate ATPase activity; originally identified as a high-copy number
suppressor of a HSP90 loss-of-function mutation;
GFP-fusion protein localizes to the cytoplasm and nucleus |
8 |
| CATGAAACATCCGT |
YOR358W |
HAP5 |
6324934 |
COG5208 |
6 |
0 |
0 |
1 |
2 |
15 |
1011183 |
1011196 |
+ |
1010157 |
1011184 |
+ |
242 |
Subunit of the heme-activated, glucose-repressed
Hap2/3/4/5 CCAAT-binding complex, a transcriptional activator and global
regulator of respiratory gene expression; required
for assembly and DNA binding activity of the complex |
8 |
| CATGTTGCAATAAA |
YKL109W |
HAP4 |
6322740 |
- |
6 |
0 |
0 |
1 |
1 |
11 |
233543 |
233556 |
+ |
231873 |
234036 |
+ |
554 |
Subunit of the heme-activated, glucose-repressed
Hap2p/3p/4p/5p CCAAT-binding complex, a transcriptional activator and global
regulator of respiratory gene expression; provides
the principal activation function of the complex |
8 |
| CATGAAGACAATCG |
YFL031W |
HAC1 |
14318488 |
- |
3 |
4 |
3 |
1 |
1 |
6 |
76140 |
76153 |
+ |
75177 |
76644 |
+ |
238 |
bZIP transcription factor (ATF/CREB1 homolog) that
regulates the unfolded-protein response, via UPRE binding, and membrane
biogenesis; ER stress-induced splicing pathway
utilizing Ire1p, Trl1p and Ada5p facilitates efficient Hac1p synthesis |
8 |
| CATGCTTGAGACGA |
YJL110C |
GZF3 |
6322351 |
- |
6 |
4 |
0 |
1 |
1 |
10 |
210200 |
210213 |
- |
209340 |
211494 |
- |
551 |
GATA zinc finger protein and Dal80p homolog that
negatively regulates nitrogen catabolic gene expression by competing with
Gat1p for GATA site binding; function requires a
repressive carbon source; dimerizes with Dal80p and binds to Tor1p |
8 |
| CATGGCATCAACTT |
YPL189W |
GUP2 |
6325067 |
COG1696 |
3 |
0 |
3 |
1 |
1 |
16 |
190958 |
190971 |
+ |
189153 |
191404 |
+ |
609 |
Multimembrane-spanning protein and putative glycerol
transporter that is essential for proton symport of glycerol; Gup1p homolog |
8 |
| CATGGGAACCCGAT |
YIR038C |
GTT1 |
6322229 |
COG0625 |
6 |
0 |
0 |
1 |
1 |
9 |
423301 |
423314 |
- |
423307 |
424510 |
- |
234 |
ER associated glutathione S-transferase capable of
homodimerization; expression induced during the diauxic shift and throughout
stationary phase; functional overlap with Gtt2p,
Grx1p, and Grx2p |
8 |
| CATGATAGTTCGGA |
YML121W |
GTR1 |
6323514 |
- |
3 |
4 |
13 |
1 |
1 |
13 |
27610 |
27623 |
+ |
26930 |
28361 |
+ |
310 |
Cytoplasmic GTP binding protein and negative regulator of
the Ran/Tc4 GTPase cycle, through its homolog and binding partner, Gtr2p;
involved in phosphate transport and invasive
growth; human RagA and RagB proteins are functional homologs |
3 |
| CATGCTCTACAGTA |
YER174C |
GRX4 |
6321022 |
COG0278 |
6 |
0 |
0 |
1 |
1 |
5 |
538429 |
538442 |
- |
537930 |
539163 |
- |
244 |
Hydroperoxide and superoxide-radical responsive
glutathione-dependent oxidoreductase; monothiol glutaredoxin subfamily member
along with Grx3p and Grx5p; protects cells from
oxidative damage |
8 |
| CATGCTCTCCAATC |
YDR098C |
GRX3 |
6320303 |
COG0526 |
6 |
0 |
0 |
1 |
1 |
4 |
644175 |
644188 |
- |
643832 |
645029 |
- |
285 |
Hydroperoxide and superoxide-radical responsive
glutathione-dependent oxidoreductase; monothiol glutaredoxin subfamily member
along with Grx4p and Grx5p; protects cells from
oxidative damage |
8 |
| CATGTGTTTGTATT |
YCL035C |
GRX1 |
6319814 |
COG0695 |
6 |
8 |
3 |
1 |
1 |
3 |
60752 |
60765 |
- |
60342 |
61173 |
- |
110 |
Hydroperoxide and superoxide-radical responsive
heat-stable glutathione-dependent disulfide oxidoreductase with active site
cysteine pair; protects cells from oxidative damage |
8 |
| CATGCTCTTCTGTT |
YHR104W |
GRE3 |
6321896 |
COG0656 |
6 |
8 |
0 |
1 |
1 |
8 |
324475 |
324488 |
+ |
323411 |
324767 |
+ |
327 |
Aldose reductase involved in methylglyoxal, d-xylose and
arabinose metabolism; stress induced (osmotic, ionic, oxidative, heat shock,
starvation and heavy metals); regulated by the HOG
pathway |
8 |
| CATGATGCCACTTT |
YPL223C |
GRE1 |
6325033 |
- |
18 |
8 |
0 |
1 |
1 |
16 |
128491 |
128504 |
- |
128132 |
129137 |
- |
168 |
Hydrophilin of unknown function; stress induced (osmotic,
ionic, oxidative, heat shock and heavy metals); regulated by the HOG pathway |
6 |
| CATGGAAACTTATC |
YKR067W |
GPT2 |
6322920 |
COG0204 |
3 |
4 |
0 |
1 |
1 |
11 |
569054 |
569067 |
+ |
567560 |
570290 |
+ |
743 |
Glycerol-3-phosphate acyltransferase located in both
lipid particles and the ER; involved in the stepwise acylation of
glycerol-3-phosphate and dihydroxyacetone, which are
intermediate steps in lipid biosynthesis |
8 |
| CATGATCGCCGCTC |
YKL152C |
GPM1 |
6322697 |
COG0588 |
49 |
64 |
17 |
1 |
1 |
11 |
163846 |
163859 |
- |
163148 |
164390 |
- |
247 |
converts 3-phosphoglycerate to 2-phosphoglycerate in
glycolysis |
7 |
| CATGAATTAGTGGA |
YPR160W |
GPH1 |
6325418 |
COG0058 |
9 |
4 |
0 |
1 |
1 |
16 |
863858 |
863871 |
+ |
861300 |
864507 |
+ |
902 |
Releases glucose-1-phosphate from glycogen |
8 |
| CATGGAAGACCTAC |
YOL059W |
GPD2 |
6324513 |
COG0240 |
3 |
4 |
0 |
1 |
1 |
15 |
218395 |
218408 |
+ |
217125 |
218946 |
+ |
440 |
Involved in glycerol production via conversion of
glyerol-3-phosphate and NAD+ to glycerol phosphate and NADH |
8 |
| CATGAAGATTAGAT |
YDL022W |
GPD1 |
6320181 |
COG0240 |
3 |
12 |
0 |
1 |
1 |
4 |
412985 |
412998 |
+ |
411822 |
413496 |
+ |
391 |
glycerol-3-phosphate dehydrogenase |
9 |
| CATGATACTTGAAT |
YER020W |
GPA2 |
6320858 |
- |
6 |
0 |
0 |
1 |
1 |
5 |
196676 |
196689 |
+ |
195167 |
196946 |
+ |
449 |
Nucleotide binding alpha subunit of the heterotrimeric G
protein that interacts with the receptor Grp1p, has signaling role in
response to nutrients; green fluorescent protein
(GFP)-fusion protein localizes to the cell periphery |
8 |
| CATGTTGATCCGTG |
YHR183W |
GND1 |
6321977 |
COG0362 |
9 |
8 |
0 |
1 |
1 |
8 |
471970 |
471983 |
+ |
470958 |
472741 |
+ |
489 |
6-phosphogluconate dehydrogenase, decarboxylating;
converts 6-phosphogluconate + NADP to ribulose-5-phosphate + NADPH + CO2 |
8 |
| CATGTGGTGACTGT |
YDL171C |
GLT1 |
6320030 |
COG0069 |
0 |
0 |
6 |
1 |
1 |
4 |
149365 |
149378 |
- |
148705 |
155641 |
- |
2145 |
NAD(+)-dependent glutamate synthase (GOGAT), synthesizes
glutamate from glutamine and alpha-ketoglutarate; with Gln1p, forms the
secondary pathway for glutamate biosynthesis from
ammonia; expression regulated by nitrogen source |
3 |
| CATGCAGTCTAAAT |
YOR040W |
GLO4 |
6324614 |
COG0491 |
6 |
4 |
0 |
1 |
1 |
15 |
407924 |
407937 |
+ |
407063 |
408419 |
+ |
285 |
Mitochondrial glyoxylase-II |
8 |
| CATGGGACAGAGCT |
YDR272W |
GLO2 |
6320478 |
COG0491 |
6 |
8 |
0 |
1 |
1 |
4 |
1009770 |
1009783 |
+ |
1009002 |
1010167 |
+ |
274 |
Cytoplasmic glyoxylase-II |
8 |
| CATGCCAAATATCT |
YML004C |
GLO1 |
6323639 |
COG0346 |
6 |
0 |
3 |
1 |
1 |
13 |
261560 |
261573 |
- |
261206 |
262685 |
- |
326 |
Regulated by HOG (high osmolarity glycerol)-MAP
(mitogen-activated protein) kinase pathway in osmotic stress response |
8 |
| CATGAGAAAAAATC |
YPR035W |
GLN1 |
6325292 |
COG0174 |
6 |
4 |
0 |
2 |
1 |
16 |
643475 |
643488 |
+ |
642203 |
643814 |
+ |
370 |
Glutamine synthetase (GS), synthesizes glutamine from
glutamate and ammonia; with Glt1p, forms the secondary pathway for glutamate
biosynthesis from ammonia; expression regulated by
nitrogen source and by amino acid limitation |
8 |
| CATGCCACAACTGA |
YER107C |
GLE2 |
6320954 |
COG2319 |
3 |
0 |
13 |
1 |
1 |
5 |
373474 |
373487 |
- |
372945 |
374541 |
- |
365 |
Nuclear pore protein required for poly(A)+ RNA export,
has beta-transducin (WD-40) repeats |
3 |
| CATGACACCTCCAT |
YMR311C |
GLC8 |
6323971 |
- |
9 |
0 |
0 |
1 |
1 |
13 |
896896 |
896909 |
- |
896669 |
897602 |
- |
229 |
Homolog of mammalian protein phosphatase inhibitor 2. |
8 |
| CATGTATTGGTAGA |
YEL011W |
GLC3 |
6320826 |
COG0296 |
21 |
8 |
0 |
1 |
1 |
5 |
135287 |
135300 |
+ |
133120 |
135733 |
+ |
704 |
Glycogen branching enzyme, involved in glycogen
accumulation; green fluorescent protein (GFP)-fusion protein localizes to the
cytoplasm in a punctate pattern |
6 |
| CATGGCATTTGGAC |
YDR096W |
GIS1 |
6320301 |
COG5048 |
3 |
0 |
3 |
1 |
1 |
4 |
637736 |
637749 |
+ |
637133 |
640316 |
+ |
894 |
putative zinc finger protein; repressor of PHR1
transcription |
8 |
| CATGGATAATGACA |
YDR152W |
GIR2 |
6320356 |
- |
3 |
0 |
3 |
1 |
1 |
4 |
766534 |
766547 |
+ |
765700 |
766996 |
+ |
265 |
Genetically Interacts with ribosomal genes |
8 |
| CATGTATGCATTTA |
YMR135C |
GID8 |
6323784 |
- |
6 |
12 |
0 |
1 |
1 |
13 |
538584 |
538597 |
- |
538189 |
540055 |
- |
455 |
Protein of unknown function, involved in
proteasome-dependent catabolite inactivation of fructose-1,6-bisphosphatase;
contains LisH and CTLH domains, like Vid30p |
9 |
| CATGGTGGCTGACG |
YAL062W |
GDH3 |
6319256 |
COG0334 |
0 |
0 |
13 |
1 |
1 |
1 |
32898 |
32911 |
+ |
31568 |
33440 |
+ |
457 |
NADP(+)-dependent glutamate dehydrogenase, synthesizes
glutamate from ammonia and alpha-ketoglutarate; rate of alpha-ketoglutarate
utilization differs from Gdh1p; expression
regulated by nitrogen and carbon sources |
3 |
| CATGGCTGTATTCT |
YDL215C |
GDH2 |
6319986 |
COG2902 |
0 |
0 |
10 |
1 |
1 |
4 |
71187 |
71200 |
- |
70366 |
73919 |
- |
1092 |
NAD(+)-dependent glutamate dehydrogenase, degrades
glutamate to ammonia and alpha-ketoglutarate; expression sensitive to
nitrogen catabolite repression and intracellular
ammonia levels |
3 |
| CATGTATATTAAGG |
YEL042W |
GDA1 |
6320793 |
COG5371 |
6 |
0 |
0 |
1 |
1 |
5 |
75355 |
75368 |
+ |
73771 |
75826 |
+ |
518 |
converts nucleoside diphosphates to nucleoside
monophosphates to recycle nucleosides and promote transport of additional
nucleotide sugars into golgi |
8 |
| CATGATGACTGAAC |
YAL044C |
GCV3 |
37362609 |
- |
0 |
4 |
13 |
2 |
1 |
1 |
57950 |
57963 |
- |
57454 |
58465 |
- |
170 |
H-protein subunit of the glycine cleavage system |
3 |
| CATGCCCTTCTGTA |
YMR189W |
GCV2 |
6323843 |
COG0403 |
6 |
0 |
0 |
1 |
1 |
13 |
640562 |
640575 |
+ |
637499 |
641102 |
+ |
1034 |
Glycine CleaVage system |
8 |
| CATGTTGGAAAGGA |
YEL009C |
GCN4 |
6320828 |
- |
24 |
30 |
6 |
1 |
1 |
5 |
139179 |
139192 |
- |
138419 |
139763 |
- |
281 |
transcriptional activator of amino acid biosynthetic
genes |
5 |
| CATGTCCGCTTCAT |
YFL021W |
GAT1 |
14318498 |
- |
0 |
0 |
10 |
1 |
1 |
6 |
97529 |
97542 |
+ |
95964 |
97995 |
+ |
510 |
activator of transcription of nitrogen-regulated genes;
inactivated by increases in intracellular glutamate levels |
3 |
| CATGTCCTGATTAT |
YOL030W |
GAS5 |
6324543 |
- |
3 |
8 |
0 |
1 |
1 |
15 |
269225 |
269238 |
+ |
268187 |
270140 |
+ |
484 |
Gas5p |
8 |
| CATGTATGAATGCA |
YMR307W |
GAS1 |
6323967 |
- |
6 |
21 |
3 |
1 |
1 |
13 |
888112 |
888125 |
+ |
887002 |
889180 |
+ |
559 |
Glycophospholipid-anchored surface protein |
9 |
| CATGGGGTGGTATC |
YKR039W |
GAP1 |
6322892 |
COG0833 |
15 |
8 |
0 |
1 |
1 |
11 |
516091 |
516104 |
+ |
514705 |
517012 |
+ |
602 |
general amino acid permease |
6 |
| CATGTAACCTCTGA |
YPL248C |
GAL4 |
6325008 |
- |
0 |
12 |
0 |
1 |
1 |
16 |
79563 |
79576 |
- |
79354 |
82356 |
- |
881 |
Positive regulator of GAL genes |
9 |
| CATGTCTCAGTGAT |
YOR178C |
GAC1 |
6324752 |
- |
0 |
0 |
10 |
1 |
1 |
15 |
667961 |
667974 |
- |
667361 |
670241 |
- |
793 |
Regulatory subunit for phosphoprotein phosphatase type 1
(PP-1), also known as Glc7p, which regulates glycogen synthase-2 |
3 |
| CATGGCATCTTGTT |
YLR088W |
GAA1 |
6323117 |
- |
6 |
4 |
3 |
2 |
1 |
12 |
317381 |
317394 |
+ |
316108 |
318451 |
+ |
614 |
ER protein essential for attaching GPI
(glycosylphosphatidylinositol) to protein |
8 |
| CATGTATACGTATA |
YHR059W |
FYV4 |
6321850 |
- |
3 |
4 |
0 |
2 |
1 |
8 |
220527 |
220540 |
+ |
220109 |
220725 |
+ |
130 |
Protein of unknown function, required for survival upon
exposure to K1 killer toxin |
8 |
| CATGTGTTTTTTTA |
YBR021W |
FUR4 |
6319495 |
COG1953 |
0 |
0 |
34 |
2 |
1 |
2 |
282135 |
282148 |
+ |
281405 |
283699 |
+ |
633 |
uracil permease |
2 |
| CATGGCGTTTGAGG |
YBR207W |
FTH1 |
6319684 |
COG0672 |
6 |
0 |
0 |
2 |
1 |
2 |
635101 |
635114 |
+ |
635103 |
636999 |
+ |
465 |
FTS3 Homolog 1 |
8 |
| CATGAAGACCAAGA |
YHR049W |
FSH1 |
6321839 |
- |
0 |
0 |
6 |
1 |
1 |
8 |
206962 |
206975 |
+ |
206454 |
207646 |
+ |
243 |
Serine hydrolase that localizes to both the nucleus and
cytoplasm. Sequence similary to Fsh2p and Fsh3p |
3 |
| CATGAGAAAACAGA |
YLL043W |
FPS1 |
6322985 |
COG0580 |
0 |
0 |
10 |
2 |
1 |
12 |
51941 |
51954 |
+ |
49937 |
52445 |
+ |
669 |
Plasma membrane glycerol channel, member of the major
intrinsic protein (MIP) family of channel proteins; involved in efflux of
glycerol and in uptake of the trivalent metalloids
arsenite and antimonite |
3 |
| CATGGTTTCAAGAG |
YGR267C |
FOL2 |
6321706 |
COG0302 |
6 |
0 |
0 |
1 |
1 |
7 |
1025118 |
1025131 |
- |
1024510 |
1025740 |
- |
243 |
GTP-cyclohydrolase I, catalyzes the first step in the
folic acid biosynthetic pathway |
8 |
| CATGGACGGCGCCG |
YMR020W |
FMS1 |
6323662 |
- |
0 |
0 |
10 |
1 |
1 |
13 |
316820 |
316833 |
+ |
315376 |
317401 |
+ |
508 |
Polyamine oxidase, converts spermine to spermidine, which
is required for the essential hypusination modification of translation factor
eIF-5A; also involved in pantothenic acid
biosynthesis |
3 |
| CATGTAAAAAAAAA |
YHR176W |
FMO |
41629686 |
- |
6 |
4 |
0 |
2 |
1 |
8 |
455843 |
455856 |
+ |
454227 |
456024 |
+ |
432 |
Flavin-containing monooxygenase, localized to the
cytoplasmic face of the ER membrane; catalyzes oxidation of biological thiols
to maintain the ER redox buffer ratio for correct
folding of disulfide-bonded proteins |
8 |
| CATGCCGACTACAT |
YLR342W |
FKS1 |
6323374 |
- |
3 |
4 |
0 |
1 |
1 |
12 |
810623 |
810636 |
+ |
809997 |
815809 |
+ |
1876 |
Catalytic subunit of 1,3-beta-D-glucan synthase,
functionally redundant with alternate catalytic subunit Gsc2p; binds to
regulatory subunit Rho1p; involved in cell wall synthesis and maintenance; localizes to sites of cell wall remodeling |
8 |
| CATGAAATACGACA |
YBR101C |
FES1 |
6319577 |
- |
0 |
0 |
6 |
1 |
1 |
2 |
444262 |
444275 |
- |
443279 |
444650 |
- |
290 |
Hsp70 (Ssa1p) nucleotide exchange factor, cytosolic
homolog of Sls1p, which is the nucleotide exchange factor for BiP (Kar2p) in
the endoplasmic reticulum |
3 |
| CATGTAAACTATTT |
YER056C |
FCY2 |
6320897 |
COG1457 |
18 |
4 |
0 |
1 |
1 |
5 |
266431 |
266444 |
- |
266012 |
268112 |
- |
533 |
Purine-cytosine permease, mediates purine (adenine,
guanine, and hypoxanthine) and cytosine accumulation |
6 |
| CATGAGATTTCAAA |
YPR062W |
FCY1 |
6325319 |
COG0590 |
3 |
4 |
0 |
4 |
1 |
16 |
677311 |
677324 |
+ |
677160 |
678135 |
+ |
158 |
Cytosine deaminase, involved in salvage pathways of
pyrimidine metabolism |
8 |
| CATGGGTGCTAAGA |
YKL060C |
FBA1 |
6322790 |
COG0191 |
506 |
610 |
162 |
1 |
1 |
11 |
326096 |
326109 |
- |
325554 |
327132 |
- |
359 |
Fructose 1,6-bisphosphate adolase, required for
glycolysis and gluconeogenesis |
10 |
| CATGGTACAGCTAT |
YER183C |
FAU1 |
6321031 |
COG0212 |
6 |
0 |
13 |
1 |
1 |
5 |
553294 |
553307 |
- |
552830 |
553964 |
- |
211 |
5,10-methenyltetrahydrofolate synthetase, involved in
folic acid biosynthesis |
3 |
| CATGTAGGAACTAT |
YBR041W |
FAT1 |
41629676 |
- |
0 |
8 |
0 |
1 |
1 |
2 |
319473 |
319486 |
+ |
318228 |
320736 |
+ |
669 |
Fatty acid transporter and very long-chain fatty acyl-CoA
synthetase, may form a complex with Faa1p or Faa4p that imports and activates
exogenous fatty acids |
8 |
| CATGGTCCGCCAAA |
YPL231W |
FAS2 |
6325025 |
COG0736 |
6 |
8 |
13 |
1 |
1 |
16 |
114085 |
114098 |
+ |
108652 |
114814 |
+ |
1887 |
Alpha subunit of fatty acid synthetase, which catalyzes
the synthesis of long-chain saturated fatty acids; contains beta-ketoacyl
reductase and beta-ketoacyl synthase activities |
3 |
| CATGTTGGTATGAT |
YKL182W |
FAS1 |
6322666 |
COG2030 |
9 |
8 |
6 |
1 |
1 |
11 |
105556 |
105569 |
+ |
100676 |
107320 |
+ |
2051 |
Beta subunit of fatty acid synthetase, which catalyzes
the synthesis of long-chain saturated fatty acids; contains
acetyltransacylase, dehydratase, enoyl reductase, malonyl transacylase, and palmitoyl transacylase activities |
8 |
| CATGACTGAAAACG |
YLR300W |
EXG1 |
6323331 |
COG2730 |
0 |
8 |
0 |
1 |
1 |
12 |
729795 |
729808 |
+ |
728957 |
730802 |
+ |
448 |
Major exo-1,3-beta-glucanase of the cell wall, involved
in cell wall beta-glucan assembly; exists as three differentially
glycosylated isoenzymes |
8 |
| CATGTTATATACGC |
YNL125C |
ESBP6 |
6324204 |
COG0477 |
0 |
0 |
6 |
1 |
1 |
14 |
390111 |
390124 |
- |
389647 |
392167 |
- |
673 |
Protein with similarity to monocarboxylate permeases,
appears not to be involved in transport of monocarboxylates such as lactate,
pyruvate or acetate across the plasma membrane |
3 |
| CATGCATTTGTGTA |
YML012W |
ERV25 |
6323630 |
- |
3 |
12 |
0 |
1 |
1 |
13 |
246771 |
246784 |
+ |
246116 |
247250 |
+ |
211 |
Protein that forms a heterotrimeric comnplex with Erp1,
Erp2p, and Emp24, member of the p24 family involved in endoplasmic reticulum
to Golgi transport |
9 |
| CATGCGGGGAATGT |
YPR037C |
ERV2 |
6325296 |
COG5054 |
0 |
8 |
3 |
1 |
1 |
16 |
646661 |
646674 |
- |
645944 |
647033 |
- |
196 |
Flavin-linked sulfhydryl oxidase localized to the
endoplasmic reticulum lumen, involved in disulfide bond formation within the
ER |
8 |
| CATGTATTTGATGA |
YML130C |
ERO1 |
6323505 |
COG5061 |
6 |
8 |
10 |
1 |
1 |
13 |
11745 |
11758 |
- |
10985 |
13175 |
- |
563 |
Glycoprotein required for oxidative protein folding in
the endoplasmic reticulum |
8 |
| CATGAAACCTGAAA |
YHR190W |
ERG9 |
6321984 |
COG1562 |
0 |
0 |
10 |
1 |
1 |
8 |
485600 |
485613 |
+ |
484843 |
486676 |
+ |
444 |
Farnesyl-diphosphate farnesyl transferase (squalene
synthase), joins two farnesyl pyrophosphate moieties to form squalene in the
sterol biosynthesis pathway |
3 |
| CATGTCGACGTGGC |
YML008C |
ERG6 |
6323635 |
COG0500 |
3 |
12 |
0 |
1 |
1 |
13 |
252211 |
252224 |
- |
251517 |
252990 |
- |
383 |
Delta(24)-sterol C-methyltransferase, converts zymosterol
to fecosterol in the ergosterol biosynthetic pathway by methylating position
C-24 |
9 |
| CATGATTACCTTCG |
YMR015C |
ERG5 |
6323657 |
COG2124 |
9 |
0 |
0 |
1 |
1 |
13 |
301025 |
301038 |
- |
300369 |
302484 |
- |
538 |
C-22 sterol desaturase, a cytochrome P450 enzyme that
catalyzes the formation of the C-22(23) double bond in the sterol side chain
in ergosterol biosynthesis; may be a target of
azole antifungal drugs |
8 |
| CATGGGTCCATTGG |
YER044C |
ERG28 |
6320883 |
- |
3 |
8 |
0 |
1 |
1 |
5 |
237636 |
237649 |
- |
237119 |
238015 |
- |
148 |
Endoplasmic reticulum membrane protein, may facilitate
protein-protein interactions between the Erg26p dehydrogenase and the Erg27p
3-ketoreductase and/or tether these enzymes to the
ER |
8 |
| CATGTATGTCTGTA |
YLR100W |
ERG27 |
6323129 |
COG1028 |
9 |
4 |
0 |
1 |
1 |
12 |
342898 |
342911 |
+ |
341811 |
343353 |
+ |
347 |
3-keto sterol reductase, catalyzes the last of three
steps required to remove two C-4 methyl groups from an intermediate in
ergosterol biosynthesis; mutants are sterol auxotrophs |
8 |
| CATGTAAATAAATA |
YGL001C |
ERG26 |
6321437 |
COG0451 |
15 |
4 |
0 |
2 |
1 |
7 |
495239 |
495252 |
- |
494956 |
496504 |
- |
349 |
C-3 sterol dehydrogenase, catalyzes the second of three
steps required to remove two C-4 methyl groups from an intermediate in
ergosterol biosynthesis |
6 |
| CATGCCATTCTGGG |
YGR060W |
ERG25 |
6321497 |
COG3000 |
9 |
0 |
0 |
1 |
1 |
7 |
611308 |
611321 |
+ |
610566 |
611994 |
+ |
309 |
C-4 methyl sterol oxidase, catalyzes the first of three
steps required to remove two C-4 methyl groups from an intermediate in
ergosterol biosynthesis; mutants accumulate the
sterol intermediate 4,4-dimethylzymosterol |
8 |
| CATGTATAAGAACT |
YJL167W |
ERG20 |
6322294 |
COG0142 |
15 |
8 |
0 |
1 |
1 |
10 |
106112 |
106125 |
+ |
105007 |
106426 |
+ |
352 |
Farnesyl pyrophosphate synthetase, has both dimethylallyltranstransferase and
geranyltranstransferase activities; catalyzes the formation of C15 farnesyl
pyrophosphate units for isoprenoid and sterol
biosynthesis |
6 |
| CATGCGGTAGTCCA |
YMR202W |
ERG2 |
6323858 |
- |
30 |
17 |
0 |
1 |
1 |
13 |
668228 |
668241 |
+ |
667536 |
668490 |
+ |
222 |
C-8 sterol isomerase, catalyzes the isomerization of the
delta-8 double bond to the delta-7 position at an intermediate step in
ergosterol biosynthesis |
5 |
| CATGTACACCGCAT |
YML126C |
ERG13 |
6323509 |
COG3425 |
0 |
17 |
0 |
1 |
1 |
13 |
19410 |
19423 |
- |
18562 |
20536 |
- |
491 |
3-hydroxy-3-methylglutaryl-CoA (HMG-CoA) synthase,
catalyzes the formation of HMG-CoA from acetyl-CoA and acetoacetyl-CoA;
involved in the second step in mevalonate
biosynthesis |
9 |
| CATGGAAGAACGTG |
YGR175C |
ERG1 |
6321614 |
COG0654 |
9 |
8 |
0 |
1 |
1 |
7 |
847036 |
847049 |
- |
846437 |
848426 |
- |
496 |
Squalene epoxidase, catalyzes the epoxidation of squalene
to 2,3-oxidosqualene; plays an essential role in the ergosterol-biosynthesis
pathway and is the specific target of the
antifungal drug terbinafine |
8 |
| CATGGGATTATACA |
YBL040C |
ERD2 |
6319431 |
COG5196 |
3 |
0 |
6 |
1 |
1 |
2 |
142243 |
142256 |
- |
141578 |
142833 |
- |
219 |
Integral membrane protein that binds to the HDEL motif in
proteins destined for retention in the endoplasmic reticulum; has a role in
maintenance of normal levels of ER-resident
proteins |
8 |
| CATGAATTTACTGA |
YHR123W |
EPT1 |
6321915 |
COG5050 |
3 |
4 |
0 |
2 |
1 |
8 |
356020 |
356033 |
+ |
354817 |
356562 |
+ |
391 |
sn-1,2-diacylglycerol ethanolamine- and
cholinephosphotranferase; not essential for viability |
8 |
| CATGGTGGAGCTGT |
YJR125C |
ENT3 |
6322585 |
- |
3 |
4 |
0 |
1 |
1 |
10 |
654718 |
654731 |
- |
654154 |
655878 |
- |
408 |
Protein containing an N-terminal epsin-like domain
involved in clathrin recruitment and traffic between the Golgi and endosomes;
associates with the clathrin adaptor Gga2p |
8 |
| CATGCAACAAACTA |
YBR247C |
ENP1 |
6319724 |
- |
6 |
0 |
0 |
1 |
1 |
2 |
712526 |
712539 |
- |
712462 |
714412 |
- |
483 |
Protein associated with U3 and U14 snoRNAs, required for
pre-rRNA processing and 40S ribosomal subunit synthesis; localized in the
nucleus and concentrated in the nucleolus |
8 |
| CATGTACCACTCCT |
YHR174W |
ENO2 |
6321968 |
COG0148 |
46 |
30 |
0 |
1 |
1 |
8 |
452166 |
452179 |
+ |
451325 |
452869 |
+ |
437 |
Enolase II, catalyzes the first common step of glycolysis
and gluconeogenesis; expression is induced in response to glucose |
13 |
| CATGCATTCCCTAT |
YFL048C |
EMP47 |
14318471 |
- |
12 |
0 |
0 |
1 |
1 |
6 |
38792 |
38805 |
- |
38344 |
40180 |
- |
445 |
Integral membrane component of endoplasmic
reticulum-derived COPII-coated vesicles, which function in ER to Golgi
transport |
6 |
| CATGTTATCTATAT |
YLR080W |
EMP46 |
6323109 |
- |
9 |
4 |
0 |
1 |
1 |
12 |
289316 |
289329 |
+ |
287917 |
289750 |
+ |
444 |
Integral membrane component of endoplasmic
reticulum-derived COPII-coated vesicles, which function in ER to Golgi
transport |
8 |
| CATGTAAATAAATA |
YGL200C |
EMP24 |
6321238 |
- |
15 |
4 |
0 |
2 |
1 |
7 |
122537 |
122550 |
- |
122198 |
123308 |
- |
203 |
Integral membrane component of endoplasmic
reticulum-derived COPII-coated vesicles, which function in ER to Golgi
transport |
6 |
| CATGGCGCTGAAGA |
YLR186W |
EMG1 |
6323215 |
COG1756 |
6 |
4 |
0 |
1 |
1 |
12 |
524359 |
524372 |
+ |
523634 |
524866 |
+ |
252 |
Essential for Mitotic Growth |
8 |
| CATGCACAATATTG |
YNL230C |
ELA1 |
6324099 |
- |
0 |
0 |
6 |
1 |
1 |
14 |
217231 |
217244 |
- |
217042 |
218661 |
- |
379 |
similar to mammalian elongin A, interacts with elongin C |
3 |
| CATGAGAAGAGCTA |
YDR385W |
EFT2 |
6320593 |
COG0480 |
0 |
8 |
0 |
2 |
1 |
4 |
1245340 |
1245353 |
+ |
1243218 |
1246071 |
+ |
842 |
translation elongation factor 2 (EF-2) |
8 |
| CATGAGAAGAGCTA |
YOR133W |
EFT1 |
6324707 |
COG0480 |
0 |
8 |
0 |
2 |
1 |
15 |
577220 |
577233 |
+ |
575098 |
578125 |
+ |
842 |
translation elongation factor 2 (EF-2) |
8 |
| CATGGGATGATGAA |
YAL003W |
EFB1 |
6319315 |
COG2092 |
0 |
8 |
0 |
1 |
1 |
1 |
142928 |
142941 |
+ |
142178 |
143663 |
+ |
206 |
GDP/GTP exchange factor for Tef1p/Tef2p |
8 |
| CATGATAAGGCCCC |
YER035W |
EDC2 |
6320873 |
- |
0 |
0 |
6 |
1 |
1 |
5 |
222889 |
222902 |
+ |
222638 |
223574 |
+ |
145 |
Enhancer of mRNA Decapping |
3 |
| CATGTATAAATCGA |
YBR078W |
ECM33 |
6319552 |
- |
0 |
0 |
6 |
1 |
1 |
2 |
393417 |
393430 |
+ |
393081 |
395316 |
+ |
468 |
GPI-anchored protein of unknown function, has a possible
role in apical bud growth; GPI-anchoring on the plasma membrane crucial to
function; similar to Sps2p and Pst1p |
3 |
| CATGGATTTTTATT |
YHR132C |
ECM14 |
6321924 |
COG2866 |
3 |
0 |
3 |
2 |
1 |
8 |
368590 |
368603 |
- |
368004 |
369795 |
- |
430 |
Non-essential protein of unknown function, similar to
zinc carboxypeptidase family |
8 |
| CATGGTAGTACATA |
YDR206W |
EBS1 |
6320412 |
- |
6 |
8 |
0 |
1 |
1 |
4 |
864845 |
864858 |
+ |
862047 |
865200 |
+ |
884 |
Protein of unknown function, contains a putative RNA
recognition motif, deletion results in short telomeres; similar to Est1p, may
be partially redundant with Est1p for telomere
maintenance |
8 |
| CATGACATTATGTA |
YHR068W |
DYS1 |
6321859 |
COG1899 |
6 |
0 |
0 |
1 |
1 |
8 |
233490 |
233503 |
+ |
232134 |
233796 |
+ |
387 |
Deoxyhypusine synthase, catalyzes formation of
deoxyhypusine, the first step in hypusine biosynthesis; triggers
posttranslational hypusination of translation elongation factor eIF-5A and regulates its intracellular levels;
tetrameric |
8 |
| CATGTTTTGTGTGT |
YDR424C |
DYN2 |
6320632 |
- |
0 |
0 |
20 |
1 |
1 |
4 |
1319648 |
1319661 |
- |
1319264 |
1319829 |
- |
92 |
Cytoplasmic light chain dynein, microtubule motor protein |
2 |
| CATGGGTGAAAACG |
YKR054C |
DYN1 |
6322907 |
COG5245 |
67 |
81 |
3 |
3 |
1 |
11 |
536008 |
536021 |
- |
534924 |
547567 |
- |
4092 |
Cytoplasmic heavy chain dynein, microtubule motor
protein, required for anaphase spindle elongation; involved in spindle
assembly, chromosome movement, and spindle orientation
during cell division, targeted to microtubule tips by Pac1p |
4 |
| CATGAATTTGGTGG |
YHL016C |
DUR3 |
6321771 |
COG0591 |
6 |
0 |
0 |
2 |
1 |
8 |
72871 |
72884 |
- |
71534 |
74240 |
- |
735 |
Plasma membrane urea transporter, expression is highly
sensitive to nitrogen catabolite repression and induced by allophanate, the
last intermediate of the allantoin degradative
pathway |
8 |
| CATGTGGTAACAGA |
YGL043W |
DST1 |
6321395 |
COG1594 |
3 |
4 |
0 |
1 |
1 |
7 |
418385 |
418398 |
+ |
417485 |
418913 |
+ |
309 |
General transcription elongation factor TFIIS, enables
RNA polymerase II to read through blocks to elongation by stimulating
cleavage of nascent transcripts stalled at transcription
arrest sites |
8 |
| CATGGGCCACCTAT |
YPR017C |
DSS4 |
6325274 |
- |
3 |
4 |
0 |
1 |
1 |
16 |
593390 |
593403 |
- |
593065 |
593912 |
- |
143 |
Nucleotide release factor functioning in the post-Golgi
secretory pathway, required for ER-to-Golgi transport, binds zinc, found both
on membranes and in the cytosol; guanine
nucleotide dissociation stimulator |
8 |
| CATGTATCCATCAA |
YMR276W |
DSK2 |
6323932 |
COG5272 |
0 |
8 |
3 |
2 |
1 |
13 |
820018 |
820031 |
+ |
818826 |
820254 |
+ |
373 |
Nuclear-enriched ubiquitin-like polyubiquitin-binding
protein, required for spindle pole body (SPB) duplication and for transit
through the G2/M phase of the cell cycle, involved
in proteolysis, interacts with the proteasome |
8 |
| CATGACATACGAAA |
YDR284C |
DPP1 |
6320490 |
COG0671 |
0 |
8 |
0 |
1 |
1 |
4 |
1030503 |
1030516 |
- |
1030043 |
1031411 |
- |
289 |
Diacylglycerol pyrophosphate (DGPP) phosphatase,
zinc-regulated vacuolar membrane-associated lipid phosphatase,
dephosphorylates DGPP to phosphatidate (PA) and
Pi, then PA to diacylglycerol; involved in lipid signaling and cell
metabolism |
8 |
| CATGTTGTGGATGA |
YDR294C |
DPL1 |
6320500 |
COG0076 |
3 |
12 |
0 |
1 |
1 |
4 |
1050646 |
1050659 |
- |
1049952 |
1052220 |
- |
589 |
Dihydrosphingosine phosphate lyase, regulates
intracellular levels of sphingolipid long-chain base phosphates (LCBPs),
degrades phosphorylated long chain bases, prefers
C16 dihydrosphingosine-l-phosphate as a substrate |
9 |
| CATGAGGATGATGG |
YBR278W |
DPB3 |
6319754 |
- |
0 |
8 |
0 |
1 |
1 |
2 |
760623 |
760636 |
+ |
760252 |
761214 |
+ |
201 |
Third-largest subunit of DNA polymerase II (DNA
polymerase epsilon), required to maintain fidelity of chromosomal replication
and also for inheritance of telomeric silencing;
mRNA abundance peaks at the G1/S boundary of the cell cycle |
8 |
| CATGAGCATAGCTA |
YDR141C |
DOP1 |
6320345 |
COG5221 |
0 |
8 |
0 |
1 |
1 |
4 |
734885 |
734898 |
- |
734396 |
739991 |
- |
1698 |
Protein of unknown function, essential for viability,
involved in establishing cellular polarity and morphogenesis; green
fluorescent protein (GFP)-fusion protein localizes to the cytoplasm in a punctate pattern |
8 |
| CATGCAGATGAGTG |
YLL001W |
DNM1 |
6323028 |
COG0699 |
3 |
8 |
0 |
2 |
1 |
12 |
148230 |
148243 |
+ |
147889 |
150661 |
+ |
757 |
Dynamin-related GTPase required for mitochondrial fission
and the maintenance of mitochondrial morphology, assembles on the cytoplasmic
face of mitochondrial tubules at sites at which
division will occur; also participates in endocytosis |
8 |
| CATGGGAAATCTTC |
YMR162C |
DNF3 |
6323814 |
COG0474 |
0 |
0 |
6 |
1 |
1 |
13 |
578761 |
578774 |
- |
578451 |
583920 |
- |
1656 |
Non-essential P-type ATPase that is a potential
aminophospholipid translocase, localizes to the trans-Golgi, likely involved
in protein transport |
3 |
| CATGGAACCATAGT |
YPL265W |
DIP5 |
6324990 |
COG0833 |
0 |
17 |
0 |
1 |
1 |
16 |
43255 |
43268 |
+ |
41043 |
43368 |
+ |
608 |
Dicarboxylic amino acid permease, mediates high-affinity
and high-capacity transport of L-glutamate and L-aspartate; also a
transporter for Gln, Asn, Ser, Ala, and Gly |
9 |
| CATGAGCTCTCTTA |
YPL266W |
DIM1 |
6324989 |
COG0030 |
6 |
4 |
10 |
1 |
1 |
16 |
40072 |
40085 |
+ |
39121 |
40576 |
+ |
318 |
Essential 18S rRNA dimethylase, responsible for conserved
m6(2)Am6(2)A dimethylation in 3'-terminal loop of 18 S rRNA, part of 90S and
40S pre-particles in nucleolus, involved in
pre-ribosomal RNA processing |
8 |
| CATGCGGTTAGTAT |
YDR480W |
DIG2 |
6320688 |
- |
9 |
8 |
0 |
1 |
1 |
4 |
1418437 |
1418450 |
+ |
1417387 |
1418857 |
+ |
323 |
Regulatory protein of unknown function,
pheromone-inducible, involved in the regulation of mating-specific genes and
the invasive growth pathway, required for MAP-kinase
imposed repression, inhibits pheromone-responsive transcription |
8 |
| CATGGGTGATGAGG |
YKL002W |
DID4 |
9755336 |
- |
6 |
8 |
6 |
1 |
1 |
11 |
437946 |
437959 |
+ |
437421 |
438686 |
+ |
232 |
Class E Vps protein of the ESCRT-III complex, required
for sorting of integral membrane proteins into lumenal vesicles of
multivesicular bodies, and for delivery of newly synthesized
vacuolar enzymes to the vacuole, involved in endocytosis |
8 |
| CATGAAAAAAATAA |
YKL078W |
DHR2 |
6322772 |
COG1643 |
6 |
4 |
0 |
4 |
1 |
11 |
290955 |
290968 |
+ |
288490 |
291097 |
+ |
735 |
Predominantly nucleolar DEAH-box RNA helicase, required
for 18S rRNA synthesis |
8 |
| CATGGTTCTAATAT |
YOR204W |
DED1 |
6324778 |
COG0513 |
0 |
0 |
10 |
1 |
1 |
15 |
724954 |
724967 |
+ |
722911 |
725224 |
+ |
604 |
ATP-dependent DEAD (Asp-Glu-Ala-Asp)-box RNA helicase,
required for translation initiation of all yeast mRNAs |
3 |
| CATGAAAGTATCAC |
YOL052C-A |
DDR2 |
6324520 |
- |
6 |
0 |
0 |
1 |
1 |
15 |
231740 |
231753 |
- |
231069 |
231753 |
- |
61 |
Multistress response protein, expression is activated by
a variety of xenobiotic agents and environmental or physiological stresses |
8 |
| CATGGTCGTCAAGC |
YOR163W |
DDP1 |
6324737 |
COG0494 |
6 |
4 |
0 |
1 |
1 |
15 |
643336 |
643349 |
+ |
642741 |
643806 |
+ |
188 |
Diadenosine polyphosphate hydrolase, member of the MutT
family of nucleotide hydrolases with high specificity for diadenosine hexa-
and pentaphosphates, required for efficient
hydrolysis of diphosphorylated inositol polyphosphates |
8 |
| CATGTGCTCTGTGG |
YKL046C |
DCW1 |
6322805 |
- |
0 |
12 |
17 |
1 |
1 |
11 |
350931 |
350944 |
- |
350421 |
352269 |
- |
449 |
Mannosidase, GPI-anchored membrane protein required for
cell wall biosynthesis, homologous to Dfg5p |
2 |
| CATGTGCTGAACTT |
YOR173W |
DCS2 |
6324747 |
COG5075 |
6 |
4 |
0 |
1 |
1 |
15 |
658350 |
658363 |
+ |
657132 |
658746 |
+ |
397 |
Non-essential protein containing a HIT (histidine triad)
motif; regulated by Msn2p, Msn4p, and the Ras-cAMP-cAPK signalling pathway,
transcript accumulates under glucose limitation,
similar to Dcs1p |
8 |
| CATGAATATATATA |
YKL149C |
DBR1 |
6322700 |
- |
6 |
4 |
0 |
4 |
1 |
11 |
167526 |
167539 |
- |
167118 |
168834 |
- |
405 |
RNA lariat debranching enzyme |
8 |
| CATGAAAAAAAAAA |
YDR052C |
DBF4 |
6320258 |
COG5067 |
3 |
0 |
3 |
13 |
1 |
4 |
558161 |
558174 |
- |
558057 |
560621 |
- |
704 |
Required for Cdc7 kinase activity |
8 |
| CATGTGCGGCCCTG |
YJR150C |
DAN1 |
6322610 |
- |
39 |
85 |
17 |
1 |
1 |
10 |
708707 |
708720 |
- |
708227 |
709622 |
- |
298 |
Delayed Anaerobic |
4 |
| CATGACAGTATAAA |
YKR034W |
DAL80 |
6322885 |
- |
18 |
4 |
0 |
1 |
1 |
11 |
507365 |
507378 |
+ |
506540 |
507580 |
+ |
269 |
Negative regulator of genes in multiple nitrogen
degradation pathways; expression is regulated by nitrogen levels and by
Gln3p; member of the GATA-binding family, forms
homodimers and heterodimers with Deh1p |
6 |
| CATGACGAAAGAAA |
YOR065W |
CYT1 |
6324639 |
COG2857 |
0 |
8 |
0 |
1 |
1 |
15 |
448225 |
448238 |
+ |
447440 |
448868 |
+ |
309 |
Cytochrome c1 |
8 |
| CATGGGGAAACCGG |
YAL039C |
CYC3 |
6319278 |
- |
6 |
4 |
3 |
1 |
1 |
1 |
69038 |
69051 |
- |
68220 |
69528 |
- |
269 |
Cytochrome c heme lyase (holocytochrome c synthase),
attaches heme to apo-Cyc1p in the mitochondrial intermembrane space; human
ortholog may have a role in microphthalmia with
linear skin defects (MLS) |
8 |
| CATGTAACATTATA |
YJR048W |
CYC1 |
6322508 |
COG3474 |
6 |
0 |
10 |
1 |
1 |
10 |
526788 |
526801 |
+ |
526249 |
527077 |
+ |
109 |
Cytochrome c, isoform 1; electron carrier of the
mitochondrial intermembrane space that transfers electrons from
ubiquinone-cytochrome c oxidoreductase to cytochrome c oxidase during cellular respiration |
8 |
| CATGGAAATGGAAT |
YNL245C |
CWC25 |
6324084 |
- |
18 |
8 |
0 |
1 |
1 |
14 |
185870 |
185883 |
- |
185846 |
186884 |
- |
179 |
Complexed with Cef1p |
6 |
| CATGAATAGCAGCA |
YDR482C |
CWC21 |
6320690 |
- |
0 |
0 |
13 |
2 |
1 |
4 |
1420413 |
1420426 |
- |
1420239 |
1420826 |
- |
135 |
Complexed With Cef1p |
3 |
| CATGTTAGATAGTA |
YDR163W |
CWC15 |
6320367 |
- |
6 |
4 |
0 |
1 |
1 |
4 |
781932 |
781945 |
+ |
781417 |
782443 |
+ |
175 |
Complexed with Cef1p |
8 |
| CATGTCATTGAACG |
YPL177C |
CUP9 |
6325080 |
- |
6 |
4 |
0 |
1 |
1 |
16 |
212943 |
212956 |
- |
212542 |
213961 |
- |
306 |
Homeodomain-containing transcriptional repressor of PTR2,
which encodes a major peptide transporter; imported peptides activate
ubiquitin-dependent proteolysis, resulting in
degradation of Cup9p and de-repression of PTR2 transcription |
8 |
| CATGACAACCACAT |
YGL166W |
CUP2 |
6321272 |
- |
0 |
0 |
10 |
1 |
1 |
7 |
191545 |
191558 |
+ |
191133 |
192309 |
+ |
225 |
Copper-binding transcription factor; activates
transcription of the metallothionein genes CUP1-1 and CUP1-2 in response to
elevated copper concentrations |
3 |
| CATGAGTGCCAATG |
YHR055C |
CUP1-2 |
6321846 |
- |
3 |
0 |
6 |
2 |
1 |
8 |
214669 |
214682 |
- |
214251 |
214719 |
- |
61 |
Metallothionein, binds copper and mediates resistance to
high concentrations of copper and cadmium; locus is variably amplified in
different strains, with two copies, CUP1-1 and
CUP1-2, in the genomic sequence reference strain S288C |
8 |
| CATGAGTGCCAATG |
YHR053C |
CUP1-1 |
6321844 |
- |
3 |
0 |
6 |
2 |
1 |
8 |
212671 |
212684 |
- |
212037 |
212721 |
- |
61 |
Metallothionein, binds copper and mediates resistance to
high concentrations of copper and cadmium; locus is variably amplified in
different strains, with two copies, CUP1-1 and
CUP1-2, in the genomic sequence reference strain S288C |
8 |
| CATGTGTATACGTG |
YOR042W |
CUE5 |
6324615 |
- |
6 |
12 |
0 |
1 |
1 |
15 |
409675 |
409688 |
+ |
408424 |
410158 |
+ |
411 |
Protein containing a CUE domain that binds ubiquitin,
which may facilitate intramolecular monoubiquitination; green fluorescent
protein (GFP)-fusion protein localizes to the
cytoplasm in a punctate pattern |
9 |
| CATGTGGATCTCAA |
YMR264W |
CUE1 |
6323920 |
- |
6 |
4 |
0 |
1 |
1 |
13 |
796268 |
796281 |
+ |
795804 |
796914 |
+ |
203 |
Endoplasmic reticulum membrane protein that recruits the
ubiquitin-conjugating enzyme Ubc7p to the ER where it functions in protein
degradation; contains a CUE domain that binds
ubiquitin to facilitate intramolecular monoubiquitination |
8 |
| CATGGTCAACAAAG |
YGR088W |
CTT1 |
6321525 |
COG0753 |
3 |
4 |
0 |
2 |
1 |
7 |
655273 |
655286 |
+ |
654603 |
656823 |
+ |
573 |
Cytosolic catalase T, has a role in protection from
oxidative damage by hydrogen peroxide |
8 |
| CATGTTTCAAGAAA |
YOL145C |
CTR9 |
6324427 |
COG0457 |
6 |
0 |
0 |
2 |
1 |
15 |
51696 |
51709 |
- |
49054 |
52786 |
- |
1077 |
Component of the Paf1p complex, which is a large complex
that binds to and modulates the activity of RNA polymerase II and is required
for expression of a subset of genes, including
cyclin genes; contains TPR repeats |
8 |
| CATGTGGGGTTGTG |
YKL139W |
CTK1 |
6322710 |
COG0515 |
6 |
4 |
3 |
1 |
1 |
11 |
184050 |
184063 |
+ |
182963 |
185048 |
+ |
528 |
Catalytic (alpha) subunit of C-terminal domain kinase I
(CTDK-I), which phosphorylates the C-terminal repeated domain of the RNA
polymerase II large subunit (Rpo21p) to affect
both transcription and pre-mRNA 3' end processing |
8 |
| CATGCAACAGTTGA |
YPR030W |
CSR2 |
6325287 |
- |
0 |
0 |
6 |
1 |
1 |
16 |
630801 |
630814 |
+ |
627875 |
631509 |
+ |
1121 |
Nuclear protein with a potential regulatory role in
utilization of galactose and nonfermentable carbon sources; overproduction
suppresses the lethality at high temperature of a
chs5 spa2 double null mutation; potential Cdc28p substrate |
3 |
| CATGCATTCCTATA |
YBR161W |
CSH1 |
6319637 |
COG3774 |
6 |
0 |
0 |
4 |
1 |
2 |
562835 |
562848 |
+ |
561591 |
563220 |
+ |
376 |
Probable catalytic subunit of a mannosylinositol
phosphorylceramide (MIPC) synthase, forms a complex with probable regulatory
subunit Csg2p; function in sphingolipid biosynthesis
is overlapping with that of Sur1p |
8 |
| CATGGTAATACTTT |
YBR036C |
CSG2 |
6319510 |
- |
0 |
0 |
6 |
1 |
1 |
2 |
309374 |
309387 |
- |
308544 |
310275 |
- |
410 |
Endoplasmic reticulum membrane protein, required for
mannosylation of inositolphosphorylceramide and for growth at high calcium
concentrations |
3 |
| CATGAACTAAATAT |
YOR031W |
CRS5 |
6324605 |
- |
12 |
4 |
3 |
1 |
1 |
15 |
389494 |
389507 |
+ |
389212 |
389920 |
+ |
69 |
Copper-binding metallothionein, required for wild-type
copper resistance |
6 |
| CATGTTGCCGAATC |
YHR146W |
CRP1 |
6321940 |
- |
0 |
17 |
6 |
1 |
1 |
8 |
391717 |
391730 |
+ |
390301 |
392197 |
+ |
465 |
Protein that binds to cruciform DNA structures |
9 |
| CATGGAAAAGTAAA |
YGR218W |
CRM1 |
6321657 |
COG5101 |
3 |
8 |
13 |
2 |
1 |
7 |
935966 |
935979 |
+ |
932542 |
936295 |
+ |
1084 |
Major karyopherin, involved in export of proteins, RNAs,
and ribosomal subunits from the nucleus |
3 |
| CATGATAAACCATT |
YLR216C |
CPR6 |
6323246 |
COG0652 |
0 |
12 |
0 |
1 |
1 |
12 |
572899 |
572912 |
- |
571861 |
573213 |
- |
371 |
Peptidyl-prolyl cis-trans isomerase (cyclophilin),
catalyzes the cis-trans isomerization of peptide bonds N-terminal to proline
residues; binds to Hsp82p and contributes to
chaperone activity |
9 |
| CATGGTTGGATGGA |
YML078W |
CPR3 |
6323562 |
COG0652 |
6 |
0 |
0 |
1 |
1 |
13 |
111413 |
111426 |
+ |
111002 |
111864 |
+ |
182 |
Mitochondrial peptidyl-prolyl cis-trans isomerase
(cyclophilin), catalyzes the cis-trans isomerization of peptide bonds
N-terminal to proline residues; involved in protein refolding after import into mitochondria |
8 |
| CATGTTGTCTTTGG |
YDR155C |
CPR1 |
6320359 |
COG0652 |
9 |
21 |
31 |
2 |
1 |
4 |
768611 |
768624 |
- |
768007 |
768994 |
- |
162 |
Cytoplasmic peptidyl-prolyl cis-trans isomerase
(cyclophilin), catalyzes the cis-trans isomerization of peptide bonds
N-terminal to proline residues; binds the drug cyclosporin A |
8 |
| CATGACGTTATAGT |
YJR109C |
CPA2 |
6322569 |
COG0458 |
3 |
4 |
0 |
1 |
1 |
10 |
629551 |
629564 |
- |
629001 |
632856 |
- |
1118 |
Large subunit of carbamoyl phosphate synthetase, which
catalyzes a step in the synthesis of citrulline, an arginine precursor |
8 |
| CATGATACACCTTC |
YOR303W |
CPA1 |
6324878 |
COG0505 |
0 |
0 |
6 |
1 |
1 |
15 |
883898 |
883911 |
+ |
882895 |
884509 |
+ |
411 |
Small subunit of carbamoyl phosphate synthetase, which
catalyzes a step in the synthesis of citrulline, an arginine precursor;
translationally regulated by an attenuator peptide
encoded by YOR302W within the CPA1 mRNA 5'-leader |
3 |
| CATGAAGAGGTCAG |
YLR395C |
COX8 |
6323427 |
- |
3 |
4 |
0 |
1 |
1 |
12 |
909883 |
909896 |
- |
909230 |
909965 |
- |
78 |
Subunit VIII of cytochrome c oxidase, which is the
terminal member of the mitochondrial inner membrane electron transport chain |
8 |
| CATGATGAAGAAAC |
YHR051W |
COX6 |
6321842 |
- |
0 |
0 |
17 |
2 |
1 |
8 |
209826 |
209839 |
+ |
209698 |
210643 |
+ |
148 |
Subunit VI of cytochrome c oxidase, which is the terminal
member of the mitochondrial inner membrane electron transport chain;
expression is regulated by oxygen levels |
3 |
| CATGGAAAATTGGA |
YIL111W |
COX5B |
6322080 |
- |
6 |
0 |
0 |
1 |
1 |
9 |
155929 |
155942 |
+ |
155219 |
156041 |
+ |
151 |
Subunit Vb of cytochrome c oxidase, which is the terminal
member of the mitochondrial inner membrane electron transport chain;
predominantly expressed during anaerobic growth
while its isoform Va (Cox5Ap) is expressed during aerobic growth |
8 |
| CATGGGCATCCGCC |
YNL052W |
COX5A |
6324276 |
- |
3 |
0 |
3 |
1 |
1 |
14 |
532296 |
532309 |
+ |
531723 |
532656 |
+ |
153 |
Subunit Va of cytochrome c oxidase, which is the terminal
member of the mitochondrial inner membrane electron transport chain;
predominantly expressed during aerobic growth
while its isoform Vb (Cox5Bp) is expressed during anaerobic growth |
8 |
| CATGTCATAACTGA |
YGL187C |
COX4 |
6321251 |
- |
3 |
8 |
0 |
1 |
1 |
7 |
149416 |
149429 |
- |
149209 |
150175 |
- |
155 |
Subunit IV of cytochrome c oxidase, which is the terminal
member of the mitochondrial inner membrane electron transport chain;
N-terminal 25 residues of precursor are cleaved
during mitochondrial import |
8 |
| CATGAAGGGTTATG |
YLL009C |
COX17 |
6323020 |
- |
3 |
0 |
3 |
1 |
1 |
12 |
131229 |
131242 |
- |
130705 |
131413 |
- |
69 |
Copper metallochaperone that shuttles copper from the
cytosol to the mitochondrial intermembrane space for delivery to cytochrome c
oxidase |
8 |
| CATGATATCTTTAA |
YER141W |
COX15 |
6320989 |
COG1612 |
15 |
8 |
6 |
1 |
1 |
5 |
455125 |
455138 |
+ |
453454 |
455413 |
+ |
486 |
Protein required for the hydroxylation of heme O to form
heme A, which is an essential prosthetic group for cytochrome c oxidase |
6 |
| CATGTGCCAGACTC |
YGL191W |
COX13 |
6321247 |
- |
0 |
8 |
0 |
1 |
1 |
7 |
145066 |
145079 |
+ |
144812 |
145700 |
+ |
129 |
Subunit VIa of cytochrome c oxidase, which is the
terminal member of the mitochondrial inner membrane electron transport chain;
not essential for cytochrome c oxidase activity
but may modulate activity in response to ATP |
8 |
| CATGATGGAGCCAA |
YLR038C |
COX12 |
6323067 |
- |
3 |
4 |
3 |
1 |
1 |
12 |
224734 |
224747 |
- |
224423 |
225173 |
- |
83 |
Subunit VIb of cytochrome c oxidase, which is the
terminal member of the mitochondrial inner membrane electron transport chain;
required for assembly of fully active cytochrome c
oxidase but not required for activity after assembly |
8 |
| CATGACTTCATATT |
YPL132W |
COX11 |
6325125 |
COG3175 |
0 |
8 |
0 |
1 |
1 |
16 |
302680 |
302693 |
+ |
301715 |
303116 |
+ |
300 |
Mitochondrial membrane protein required for assembly of
active cytochrome c oxidase, probably involved in insertion of Cu(B) and
magnesium |
8 |
| CATGGAAGACAAAA |
YKL219W |
COS9 |
6322630 |
- |
6 |
0 |
0 |
3 |
1 |
11 |
15419 |
15432 |
+ |
14485 |
16207 |
+ |
407 |
Protein of unknown function, member of a family of
conserved, often subtelomerically-encoded proteins |
8 |
| CATGGAACACAAGA |
YFL062W |
COS4 |
14318457 |
- |
6 |
8 |
3 |
4 |
1 |
6 |
7276 |
7289 |
+ |
6426 |
8064 |
+ |
379 |
Protein of unknown function, member of a family of
conserved, often subtelomerically-encoded proteins |
8 |
| CATGGAACACAAGA |
YML132W |
COS3 |
6323503 |
- |
6 |
8 |
3 |
4 |
1 |
13 |
8094 |
8107 |
+ |
7244 |
8882 |
+ |
379 |
Protein of unknown function, member of a family of
conserved, often subtelomerically-encoded proteins |
8 |
| CATGGAACACAAGA |
YBR302C |
COS2 |
6319779 |
- |
6 |
8 |
3 |
4 |
1 |
2 |
810570 |
810583 |
- |
809797 |
811435 |
- |
379 |
Protein of unknown function, member of a family of
conserved, often subtelomerically-encoded proteins |
8 |
| CATGGTGCTTCATC |
YBR203W |
COS111 |
6319680 |
- |
6 |
0 |
0 |
1 |
1 |
2 |
629556 |
629569 |
+ |
629125 |
632398 |
+ |
924 |
Protein required for wild-type resistance to the
antifungal drug ciclopirox olamine; not related to the COS family of
subtelomerically-encoded proteins |
8 |
| CATGTGATAGCCAT |
YML110C |
COQ5 |
6323526 |
COG2226 |
6 |
0 |
0 |
1 |
1 |
13 |
49913 |
49926 |
- |
49532 |
50954 |
- |
307 |
2-hexaprenyl-6-methoxy-1,4-benzoquinone
methyltransferase, involved in ubiquinone (Coenzyme Q) biosynthesis; located
in mitochondria |
8 |
| CATGGTCCTGCGTT |
YOL096C |
COQ3 |
37362692 |
- |
3 |
8 |
0 |
1 |
1 |
15 |
137993 |
138006 |
- |
137825 |
139044 |
- |
312 |
O-methyltransferase, catalyzes two different
O-methylation steps in ubiquinone (Coenzyme Q) biosynthesis |
8 |
| CATGTGACAAGTCC |
YDL145C |
COP1 |
6320056 |
COG2319 |
6 |
0 |
0 |
1 |
1 |
4 |
194503 |
194516 |
- |
194073 |
198177 |
- |
1201 |
Alpha subunit of COPI vesicle coatomer complex, which
surrounds transport vesicles in the early secretory pathway |
8 |
| CATGTATAGAATTA |
YLL050C |
COF1 |
6322978 |
- |
9 |
4 |
0 |
1 |
1 |
12 |
39702 |
39715 |
- |
39471 |
40413 |
- |
143 |
yeast cortical cytoskeleton component; mammalian cofilin
homolog |
8 |
| CATGGCATTCAAAC |
YOL016C |
CMK2 |
6324557 |
COG0515 |
9 |
0 |
0 |
1 |
1 |
15 |
294672 |
294685 |
- |
294278 |
296120 |
- |
447 |
Calmodulin-dependent protein kinase |
8 |
| CATGAGAAAACAGA |
YGL215W |
CLG1 |
6321223 |
- |
0 |
0 |
10 |
2 |
1 |
7 |
89436 |
89449 |
+ |
87979 |
89836 |
+ |
452 |
cyclin-like protein that interacts with Pho85p in
affinity chromatography |
3 |
| CATGAGTATCATAC |
YGR167W |
CLC1 |
6321606 |
- |
9 |
0 |
0 |
1 |
1 |
7 |
833232 |
833245 |
+ |
832459 |
833659 |
+ |
233 |
Clathrin light chain |
8 |
| CATGACATTCCTGG |
YOR039W |
CKB2 |
6324613 |
COG5041 |
0 |
8 |
0 |
1 |
1 |
15 |
406228 |
406241 |
+ |
405767 |
407042 |
+ |
258 |
protein kinase CK2, beta' subunit |
8 |
| CATGACCATTTAGT |
YCR005C |
CIT2 |
6319850 |
COG0372 |
6 |
0 |
0 |
1 |
1 |
3 |
120881 |
120894 |
- |
120444 |
122325 |
- |
460 |
non-mitochondrial citrate synthase |
8 |
| CATGCTAAGAAGGT |
YGL029W |
CGR1 |
6321409 |
- |
3 |
4 |
0 |
1 |
1 |
7 |
440362 |
440375 |
+ |
440066 |
440927 |
+ |
120 |
Coiled-coil growth-regulated. May contribute to
compartmentalization of nucleolar constituents. |
8 |
| CATGGTGGTATCAC |
YBR029C |
CDS1 |
6319503 |
COG0575 |
0 |
4 |
3 |
1 |
1 |
2 |
296586 |
296599 |
- |
295965 |
297704 |
- |
457 |
CDP-diacylglycerol synthase, CTP-phosphatidic acid
cytidylyltransferase, CDP-diglyceride synthetase |
8 |
| CATGGACAACTTCA |
YDL126C |
CDC48 |
6320077 |
COG0464 |
9 |
4 |
6 |
1 |
1 |
4 |
237277 |
237290 |
- |
235658 |
238664 |
- |
835 |
Microsomal protein of CDC48/PAS1/SEC18 family of ATPases;
full length homology to mammalian protein VCP; involved in secretion,
peroxisome formation and gene expression |
8 |
| CATGCCTGGTCGTC |
YLR229C |
CDC42 |
6323259 |
COG1100 |
6 |
8 |
0 |
1 |
1 |
12 |
604450 |
604463 |
- |
603715 |
604789 |
- |
191 |
Small rho-like GTPase, essential for establishment and
maintenance of cell polarity; mutants have defects in the organization of
actin and septins |
8 |
| CATGGATAATAGAA |
YDR364C |
CDC40 |
6320572 |
COG2319 |
0 |
0 |
20 |
2 |
1 |
4 |
1203120 |
1203133 |
- |
1202332 |
1204198 |
- |
455 |
Pre-mRNA splicing factor, important for catalytic step II
of pre-mRNA splicing and plays a role in cell cycle progression; required for
DNA synthesis during mitosis and meiosis; has WD
repeats |
2 |
| CATGGCAGAAGGAT |
YHR166C |
CDC23 |
6321960 |
COG0457 |
6 |
0 |
6 |
1 |
1 |
8 |
437072 |
437085 |
- |
436949 |
439050 |
- |
626 |
Subunit of the anaphase-promoting complex/cyclosome
(APC/C), which is a ubiquitin-protein ligase required for degradation of
anaphase inhibitors, including mitotic cyclins,
during the metaphase/anaphase transition |
8 |
| CATGGTTTTTCTTT |
YAL038W |
CDC19 |
6319279 |
COG0469 |
12 |
47 |
34 |
1 |
1 |
1 |
73358 |
73371 |
+ |
71789 |
73790 |
+ |
500 |
Pyruvate kinase, functions as a homotetramer in
glycolysis to convert phosphoenolpyruvate to pyruvate, the input for aerobic
(TCA cycle) or anaerobic (glucose fermentation)
respiration |
7 |
| CATGACAGCAAAAC |
YKL022C |
CDC16 |
6322830 |
COG0457 |
0 |
0 |
10 |
1 |
1 |
11 |
394420 |
394433 |
- |
393870 |
396891 |
- |
840 |
Subunit of the anaphase-promoting complex/cyclosome
(APC/C), which is a ubiquitin-protein ligase required for degradation of
anaphase inhibitors, including mitotic cyclins,
during the metaphase/anaphase transition; required for sporulation |
3 |
| CATGTGACTCTTTG |
YLR390W-A |
CCW14 |
6323423 |
- |
0 |
8 |
0 |
1 |
1 |
12 |
903844 |
903857 |
+ |
903724 |
904939 |
+ |
238 |
Secretory Stress Response protein |
8 |
| CATGGCCCATCTAC |
YLR110C |
CCW12 |
6323139 |
- |
3 |
17 |
0 |
1 |
1 |
12 |
369199 |
369212 |
- |
369199 |
370099 |
- |
133 |
Ccw12p |
9 |
| CATGTGTACCTGTA |
YJL008C |
CCT8 |
6322452 |
COG0459 |
3 |
0 |
3 |
1 |
1 |
10 |
419758 |
419771 |
- |
419478 |
421578 |
- |
568 |
Subunit of the cytosolic chaperonin Cct ring complex,
related to Tcp1p, required for the assembly of actin and tubulins in vivo |
8 |
| CATGTGCTGCATAC |
YJL111W |
CCT7 |
6322350 |
COG0459 |
0 |
8 |
0 |
1 |
1 |
10 |
209462 |
209475 |
+ |
207794 |
209945 |
+ |
550 |
Subunit of the cytosolic chaperonin Cct ring complex,
related to Tcp1p, required for the assembly of actin and tubulins in vivo |
8 |
| CATGAACAAGTTGG |
YDR188W |
CCT6 |
6320393 |
COG0459 |
9 |
0 |
10 |
1 |
1 |
4 |
837702 |
837715 |
+ |
836414 |
838384 |
+ |
546 |
Subunit of the cytosolic chaperonin Cct ring complex,
related to Tcp1p, required for the assembly of actin and tubulins in vivo |
8 |
| CATGATGCTGCCCA |
YKR066C |
CCP1 |
6322919 |
COG0376 |
3 |
4 |
0 |
1 |
1 |
11 |
565939 |
565952 |
- |
565535 |
566840 |
- |
361 |
Cytochrome-c peroxidase |
8 |
| CATGAAGCCCATTT |
YDL069C |
CBS1 |
37362630 |
- |
3 |
0 |
3 |
1 |
1 |
4 |
332947 |
332960 |
- |
332622 |
333810 |
- |
229 |
translational activator of cytochrome b |
8 |
| CATGGTGGTGCAGA |
YNL161W |
CBK1 |
6324168 |
COG0515 |
3 |
0 |
3 |
1 |
1 |
14 |
334573 |
334586 |
+ |
332597 |
335366 |
+ |
756 |
Cell wall biosynthesis kinase; required for efficient
apical growth, proper mating projection morphology, bipolar bud site
selection in diploid cells, and cell separation. |
8 |
| CATGATGCTGTTAT |
YPL178W |
CBC2 |
6325079 |
COG0724 |
18 |
8 |
0 |
1 |
1 |
16 |
212884 |
212897 |
+ |
212157 |
213282 |
+ |
208 |
cap binding complex |
6 |
| CATGCTTTCTTCAG |
YOR276W |
CAF20 |
6324850 |
- |
6 |
0 |
0 |
2 |
1 |
15 |
841825 |
841838 |
+ |
841330 |
842314 |
+ |
161 |
binds to eIF-4E, the mRNA cap-binding protein, and
represses cap-dependent translation initiation by interfering with the
interaction of eIF4E and eIF4G |
8 |
| CATGCCATTTCGAA |
YKL005C |
BYE1 |
6322848 |
- |
0 |
0 |
6 |
1 |
1 |
11 |
433252 |
433265 |
- |
432237 |
434520 |
- |
594 |
Negative regulator of transcription elongation, may act
by competing with Dst1p for binding to the large subunit of RNA polymerase II
(Rpo21p); contains PHD finger and TFIIS-like
domains, which are implicated in transcription regulation |
3 |
| CATGAGTATGTGTA |
YER159C |
BUR6 |
6321007 |
COG5247 |
3 |
0 |
10 |
1 |
1 |
5 |
491318 |
491331 |
- |
491026 |
491953 |
- |
142 |
Homolog of DRAP1 (NC2alpha) |
8 |
| CATGAAAAGACGTG |
YCR047C |
BUD23 |
6319895 |
COG0500 |
0 |
0 |
10 |
1 |
1 |
3 |
210771 |
210784 |
- |
210419 |
211540 |
- |
275 |
Protein involved in bud-site selection; diploid mutants
display a random budding pattern instead of the wild-type bipolar pattern |
3 |
| CATGGTTGGCTGTT |
YBR290W |
BSD2 |
6319767 |
- |
3 |
0 |
13 |
2 |
1 |
2 |
783392 |
783405 |
+ |
782549 |
784013 |
+ |
321 |
metal homeostasis protein; putative membrane protein |
3 |
| CATGCGAAAAGGTC |
YOL137W |
BSC6 |
6324435 |
COG0738 |
6 |
4 |
0 |
1 |
1 |
15 |
67441 |
67454 |
+ |
65620 |
67612 |
+ |
497 |
Bypass of Stop Codon
transcript encoded by this ORF shows a high level of stop codon bypass |
8 |
| CATGTCCTTCAGTA |
YOL077C |
BRX1 |
6324496 |
COG5154 |
6 |
8 |
0 |
1 |
1 |
15 |
186181 |
186194 |
- |
185348 |
186722 |
- |
291 |
Essential nucleolar protein required for biogenesis of
the 60S ribosomal subunit |
8 |
| CATGCATAGTGTAT |
YGL247W |
BRR6 |
6321190 |
COG5085 |
6 |
0 |
0 |
1 |
1 |
7 |
37517 |
37530 |
+ |
36933 |
38025 |
+ |
197 |
Bad Response to Refrigeration |
8 |
| CATGCTAATATGTG |
YER172C |
BRR2 |
6321020 |
COG1204 |
6 |
0 |
0 |
2 |
1 |
5 |
534455 |
534468 |
- |
529026 |
536016 |
- |
2163 |
RNA helicase-related protein required for pre-mRNA
splicing; Snurp 246 kDa protein (Snurp = Small nuclear ribonucleoprotein
particle) |
8 |
| CATGAGTCCGGAGT |
YNR051C |
BRE5 |
6324379 |
- |
0 |
0 |
6 |
1 |
1 |
14 |
717793 |
717806 |
- |
716280 |
718326 |
- |
515 |
protein of unknown function |
3 |
| CATGTATATATATA |
YPL217C |
BMS1 |
6325039 |
COG5192 |
15 |
0 |
0 |
15 |
1 |
16 |
139599 |
139612 |
- |
139120 |
143170 |
- |
1183 |
GTP-binding protein required for processing of 35S
pre-rRNA at sites A0, |
6 |
| CATGTCCGAGTCCG |
YER177W |
BMH1 |
6321025 |
COG5040 |
30 |
21 |
13 |
1 |
1 |
5 |
546312 |
546325 |
+ |
545606 |
546811 |
+ |
267 |
14-3-3 protein, major isoform; binds proteins and DNA,
involved in regulation of many processes including exocytosis and vesicle
transport, Ras/MAPK signaling during pseudohyphal
development, rapamycin-sentitive signaling, and others |
5 |
| CATGCATCTAAGAT |
YNR056C |
BIO5 |
6324384 |
COG0531 |
3 |
4 |
0 |
1 |
1 |
14 |
731611 |
731624 |
- |
731116 |
733300 |
- |
561 |
transmembrane regulator of KAPA/DAPA transport |
8 |
| CATGGCACCAAAGA |
YJL031C |
BET4 |
41629687 |
- |
0 |
4 |
6 |
1 |
1 |
10 |
386703 |
386716 |
- |
385785 |
387354 |
- |
327 |
catalyzes prenylation of Ypt1p (as a subunit of
PGGTase-II) |
8 |
| CATGTATATATATA |
YPL161C |
BEM4 |
6325096 |
- |
15 |
0 |
0 |
15 |
1 |
16 |
244259 |
244272 |
- |
244027 |
246219 |
- |
633 |
Involved in polarity establishment and bud emergence;
interacts with the Rho1p small GTP-binding protein |
6 |
| CATGTAAAAAAAAA |
YBR200W |
BEM1 |
6319677 |
- |
6 |
4 |
0 |
2 |
1 |
2 |
622800 |
622813 |
+ |
620829 |
622939 |
+ |
551 |
SH3-domain protein that binds Cdc24p, Ste5p and Ste20p,
and the Rsr1p/Bud2p/Bup5p GTPase |
8 |
| CATGCCCTAATTAA |
YDL070W |
BDF2 |
6320132 |
COG5076 |
3 |
4 |
24 |
1 |
1 |
4 |
332957 |
332970 |
+ |
331025 |
333440 |
+ |
638 |
bromodomain protein, homolog of BDF1 |
2 |
| CATGTTCCACTATT |
YHR208W |
BAT1 |
6322002 |
COG0115 |
3 |
17 |
0 |
1 |
1 |
8 |
518582 |
518595 |
+ |
517530 |
519210 |
+ |
393 |
BAT1 highly expressed during logarithmic phase and is
repressed during stationary phase, whereas BAT2 has the opposite pattern of
expression. |
9 |
| CATGTCCTTAGCGC |
YBR068C |
BAP2 |
6319542 |
COG0833 |
0 |
4 |
3 |
1 |
1 |
2 |
373746 |
373759 |
- |
373322 |
375650 |
- |
609 |
contains 12 predicted transmembrane domains |
8 |
| CATGACATTATTGG |
YOR134W |
BAG7 |
6324708 |
- |
0 |
4 |
6 |
2 |
1 |
15 |
580151 |
580164 |
+ |
578564 |
580249 |
+ |
409 |
Structural homolog of SAC7 |
8 |
| CATGTGATGAAGAT |
YER119C |
AVT6 |
6320965 |
COG0814 |
6 |
0 |
0 |
3 |
1 |
5 |
400149 |
400162 |
- |
399052 |
400838 |
- |
448 |
Vacuolar transporter, exports aspartate and glutamate
from the vacuole; member of a family of seven S. cerevisiae genes (AVT1-7)
related to vesicular GABA-glycine transporters |
8 |
| CATGCTTTATACGT |
YNL101W |
AVT4 |
6324228 |
COG0814 |
6 |
0 |
0 |
1 |
1 |
14 |
437100 |
437113 |
+ |
434999 |
437612 |
+ |
713 |
Vacuolar transporter, exports large neutral amino acids
from the vacuole; member of a family of seven S. cerevisiae genes (AVT1-7)
related to vesicular GABA-glycine transporters |
8 |
| CATGTACAGACACA |
YKL146W |
AVT3 |
6322702 |
COG0814 |
12 |
0 |
3 |
1 |
1 |
11 |
173890 |
173903 |
+ |
171788 |
174217 |
+ |
692 |
Vacuolar transporter, exports large neutral amino acids
from the vacuole; member of a family of seven S. cerevisiae genes (AVT1-7)
related to vesicular GABA-glycine transporters |
6 |
| CATGATAATGTAAA |
YOL078W |
AVO1 |
6324494 |
- |
0 |
0 |
10 |
2 |
1 |
15 |
184995 |
185008 |
+ |
181681 |
185436 |
+ |
1176 |
Component of a membrane-bound complex containing the
Tor2p kinase and other proteins, which may have a role in regulation of cell
growth |
3 |
| CATGACCTGCTCGG |
YNL259C |
ATX1 |
6324070 |
COG2608 |
6 |
0 |
0 |
1 |
1 |
14 |
157815 |
157828 |
- |
157455 |
157864 |
- |
73 |
Cytosolic copper metallochaperone that transports copper
to the secretory vesicle copper transporter Ccc2p for eventual insertion into
Fet3p, which is a multicopper oxidase required for
high-affinity iron uptake |
8 |
| CATGCGATTATATA |
YML116W |
ATR1 |
6323520 |
COG0477 |
6 |
0 |
0 |
1 |
1 |
13 |
39868 |
39881 |
+ |
38196 |
40323 |
+ |
542 |
Multidrug efflux pump of the major facilitator
superfamily, required for resistance to aminotriazole and
4-nitroquinoline-N-oxide |
8 |
| CATGTTTAATAGAG |
YDR298C |
ATP5 |
6320504 |
COG0712 |
3 |
4 |
0 |
1 |
1 |
4 |
1058793 |
1058806 |
- |
1057669 |
1058806 |
- |
212 |
Subunit 5 of the stator stalk of mitochondrial F1F0 ATP
synthase, which is a large, evolutionarily conserved enzyme complex required
for ATP synthesis; homologous to bovine subunit
OSCP (oligomycin sensitivity-conferring protein) |
8 |
| CATGTAAATTGTTA |
YPL078C |
ATP4 |
6325179 |
- |
0 |
0 |
6 |
1 |
1 |
16 |
407620 |
407633 |
- |
407506 |
408739 |
- |
244 |
Subunit b of the stator stalk of mitochondrial F1F0 ATP
synthase, which is a large, evolutionarily conserved enzyme complex required
for ATP synthesis |
3 |
| CATGGGGAAAGCTA |
YOL077W-A |
ATP19 |
6324495 |
- |
0 |
0 |
10 |
1 |
1 |
15 |
185456 |
185469 |
+ |
185437 |
186142 |
+ |
68 |
Subunit k of the mitochondrial F1F0 ATP synthase, which
is a large enzyme complex required for ATP synthesis; associated only with
the dimeric form of ATP synthase |
3 |
| CATGCAAAGAGAAG |
YDR377W |
ATP17 |
6320585 |
- |
12 |
8 |
0 |
1 |
1 |
4 |
1228959 |
1228972 |
+ |
1228599 |
1229403 |
+ |
101 |
Subunit f of the F0 sector of mitochondrial F1F0 ATP
synthase, which is a large, evolutionarily conserved enzyme complex required
for ATP synthesis |
6 |
| CATGTTGCTAAAGA |
YLR295C |
ATP14 |
6323326 |
- |
9 |
0 |
6 |
1 |
1 |
12 |
722082 |
722095 |
- |
721502 |
722375 |
- |
124 |
Subunit h of the F0 sector of mitochondrial F1F0 ATP
synthase, which is a large, evolutionarily conserved enzyme complex required
for ATP synthesis |
8 |
| CATGAAGTACTCTA |
YBL099W |
ATP1 |
6319370 |
COG0056 |
9 |
0 |
0 |
1 |
1 |
2 |
37834 |
37847 |
+ |
37050 |
39141 |
+ |
545 |
Alpha subunit of the F1 sector of mitochondrial F1F0 ATP
synthase, which is a large, evolutionarily conserved enzyme complex required
for ATP synthesis |
8 |
| CATGTATAAGTTTT |
YMR301C |
ATM1 |
6323959 |
COG5265 |
0 |
0 |
10 |
1 |
1 |
13 |
867512 |
867525 |
- |
867091 |
869626 |
- |
690 |
Mitochondrial inner membrane transporter, exports
mitochondrially synthesized precursors of iron-sulfur (Fe/S) clusters to the
cytosol; member of the ATP-binding cassette (ABC)
transporter family |
3 |
| CATGATTGTTCAGC |
YPR026W |
ATH1 |
6325283 |
COG1554 |
0 |
0 |
10 |
1 |
1 |
16 |
616407 |
616420 |
+ |
615374 |
619508 |
+ |
1211 |
Vacuolar acid trehalase, required for trehalose
utilization |
3 |
| CATGATGTAATAGA |
YDL149W |
ATG9 |
6320052 |
- |
0 |
0 |
6 |
1 |
1 |
4 |
187796 |
187809 |
+ |
184926 |
188418 |
+ |
997 |
Integral membrane protein |
3 |
| CATGGTTTTGCCAT |
YLR189C |
ATG26 |
6323218 |
COG1819 |
3 |
4 |
0 |
2 |
1 |
12 |
532519 |
532532 |
- |
530300 |
534395 |
- |
1198 |
Udp-glycosyltransferase |
8 |
| CATGAGTTTCAATA |
YPR049C |
ATG11 |
6325306 |
- |
0 |
0 |
6 |
2 |
1 |
16 |
662734 |
662747 |
- |
660633 |
664668 |
- |
1178 |
Peripheral membrane protein required for delivery of
aminopeptidase I (Lap4p) to the vacuole in the cytoplasm-to-vacuole targeting
pathway; also required for peroxisomal degradation
(pexophagy) |
3 |
| CATGTTTGTTGGTT |
YOR377W |
ATF1 |
6324953 |
- |
15 |
21 |
0 |
2 |
1 |
15 |
1047178 |
1047191 |
+ |
1046222 |
1048298 |
+ |
525 |
Alcohol acetyltransferase with a potential role in fatty
acid metabolism; forms volatile esters during fermentation, which is
important in brewing |
6 |
| CATGGGAGCAGTTA |
YGL017W |
ATE1 |
6321421 |
COG2935 |
6 |
0 |
0 |
2 |
1 |
7 |
460478 |
460491 |
+ |
459857 |
461668 |
+ |
503 |
Arginyl-tRNA-protein transferase, catalyzes
post-translational conjugation of arginine to the amino termini of acceptor
proteins which are then subject to degradation via the N-end rule pathway |
8 |
| CATGTAGCACCGCC |
YDL197C |
ASF2 |
6320004 |
- |
3 |
4 |
0 |
1 |
1 |
4 |
104788 |
104801 |
- |
104553 |
106495 |
- |
525 |
anti-silencing protein that causes depression of silent
loci when overexpressed |
8 |
| CATGTTTAAAATGG |
YMR116C |
ASC1 |
6323763 |
COG2319 |
3 |
8 |
0 |
1 |
1 |
13 |
499390 |
499403 |
- |
498956 |
500687 |
- |
319 |
WD repeat protein (G-beta like protein) that interacts
with the translational machinery |
8 |
| CATGCAAAATTAAC |
YMR033W |
ARP9 |
6323676 |
COG5277 |
3 |
0 |
6 |
1 |
1 |
13 |
339392 |
339405 |
+ |
337787 |
339775 |
+ |
467 |
involved in transcriptional regulation |
8 |
| CATGTATAGATTGT |
YOL140W |
ARG8 |
6324432 |
COG4992 |
3 |
4 |
0 |
1 |
1 |
15 |
60047 |
60060 |
+ |
58758 |
60528 |
+ |
423 |
Acetylornithine aminotransferase, catalyzes the fourth
step in the biosynthesis of the arginine precursor ornithine |
8 |
| CATGTATTGATTTT |
YER069W |
ARG5,6 |
6320913 |
COG0002 |
0 |
8 |
0 |
1 |
1 |
5 |
298117 |
298130 |
+ |
295408 |
298498 |
+ |
863 |
Bifunctional enzyme with
N-acetyl-gamma-glutamyl-phosphate reductase and acetylglutamate kinase
activities, catalyzes the second and third steps in the biosynthesis of the arginine precursor ornithine; forms a complex
with Arg2p |
8 |
| CATGAATAATGATA |
YJL088W |
ARG3 |
6322373 |
COG0078 |
9 |
0 |
0 |
1 |
1 |
10 |
269780 |
269793 |
+ |
268715 |
270230 |
+ |
338 |
Ornithine carbamoyltransferase
(carbamoylphosphate:L-ornithine carbamoyltransferase), catalyzes the sixth
step in the biosynthesis of the arginine precursor ornithine |
8 |
| CATGCGGACCTTGT |
YDL137W |
ARF2 |
6320064 |
COG1100 |
27 |
38 |
58 |
1 |
1 |
4 |
217099 |
217112 |
+ |
216529 |
217573 |
+ |
181 |
ADP-ribosylation factor 2 |
7 |
| CATGGTTTATCCAA |
YDL192W |
ARF1 |
6320009 |
COG1100 |
3 |
4 |
6 |
1 |
1 |
4 |
116775 |
116788 |
+ |
116322 |
117366 |
+ |
181 |
implicated in signal transduction and intracellular
protein transport to or within the Golgi apparatus |
8 |
| CATGGAATAAGCTG |
YCR048W |
ARE1 |
6319896 |
COG5056 |
0 |
4 |
13 |
2 |
1 |
3 |
212566 |
212579 |
+ |
211924 |
214065 |
+ |
610 |
Acyl-CoA:sterol acyltransferase, isozyme of Are2p;
endoplasmic reticulum enzyme that contributes the major sterol esterification
activity in the absence of oxygen |
3 |
| CATGTGTATGTGAA |
YKL013C |
ARC19 |
6322839 |
- |
3 |
17 |
0 |
1 |
1 |
11 |
417005 |
417018 |
- |
416652 |
417666 |
- |
171 |
Arp complex subunit |
9 |
| CATGTTTGAACCAC |
YPL259C |
APM1 |
6324996 |
- |
0 |
0 |
6 |
2 |
1 |
16 |
52515 |
52528 |
- |
50745 |
52671 |
- |
475 |
medium subunit of the clathrin-associated protein complex |
3 |
| CATGCAGTAATGTT |
YNL077W |
APJ1 |
6324252 |
COG0484 |
18 |
0 |
27 |
1 |
1 |
14 |
482988 |
483001 |
+ |
481390 |
483475 |
+ |
528 |
Putative chaperone of the HSP40 (DNAJ) family;
overexpression interferes with propagation of the [Psi+] prion |
2 |
| CATGTTGGTGGTCA |
YBR151W |
APD1 |
6319627 |
- |
6 |
8 |
0 |
1 |
1 |
2 |
545745 |
545758 |
+ |
544984 |
546331 |
+ |
316 |
Protein of unknown function, required for normal
localization of actin patches and for normal tolerance of sodium ions and
hydrogen peroxide; localizes to both cytoplasm and
nucleus |
8 |
| CATGTATATATATA |
YOR249C |
APC5 |
6324823 |
- |
15 |
0 |
0 |
15 |
1 |
15 |
798466 |
798479 |
- |
798175 |
800731 |
- |
685 |
subunit of the Anaphase Promoting Complex; all known APC
subunits co-immunoprecipitate with epitope-tagged Apc5 |
6 |
| CATGGTCTTTTACA |
YCL050C |
APA1 |
10383757 |
COG4360 |
0 |
0 |
6 |
1 |
1 |
3 |
38368 |
38381 |
- |
37337 |
38801 |
- |
321 |
Diadenosine 5',5''-P1,P4-tetraphosphate phosphorylase I
(AP4A phosphorylase), involved in catabolism of bis(5'-nucleosidyl)
tetraphosphates; has similarity to Apa2p |
3 |
| CATGGCTTGGATGG |
YEL036C |
ANP1 |
6320799 |
- |
3 |
4 |
0 |
1 |
1 |
5 |
83444 |
83457 |
- |
82604 |
84552 |
- |
500 |
Mannan 8; Protein of the endoplasmic reticulum with a
role in retention of glycosyltransferases in the Golgi, also involved in
osmotic sensitivity and resistance to aminonitrophenyl
propanediol |
8 |
| CATGATAACCAAAA |
YGL156W |
AMS1 |
6321282 |
COG0383 |
3 |
4 |
0 |
1 |
1 |
7 |
213728 |
213741 |
+ |
210419 |
214083 |
+ |
1083 |
vacuolar alpha mannosidase |
8 |
| CATGCATACACTGA |
YPL061W |
ALD6 |
6325196 |
COG1012 |
0 |
12 |
0 |
1 |
1 |
16 |
434043 |
434056 |
+ |
432583 |
434517 |
+ |
500 |
Utilizes NADP+ as the preferred coenzyme. Activated by
Mg2+. |
9 |
| CATGTCATCATTTC |
YOR374W |
ALD4 |
6324950 |
COG1012 |
3 |
12 |
0 |
1 |
1 |
15 |
1041470 |
1041483 |
+ |
1039836 |
1041894 |
+ |
519 |
Glucose repressed. Utilizes NADP+ or NAD+ as a coenzyme
equally well. (sold by SIGMA under the catalogue number A5550, according to
A. Blomberg). |
9 |
| CATGTTTGCTCGCG |
YMR169C |
ALD3 |
6323821 |
COG1012 |
0 |
8 |
0 |
2 |
1 |
13 |
599517 |
599530 |
- |
599158 |
600871 |
- |
506 |
Expression induced in response to heat shock, oxidative
and osmotic stress. NAD+ is preferred coenzyme. |
8 |
| CATGTTTGCTCGCG |
YMR170C |
ALD2 |
6323822 |
COG1012 |
0 |
8 |
0 |
2 |
1 |
13 |
601727 |
601740 |
- |
601062 |
603081 |
- |
506 |
Expression induced in response to high osmotic stress.
NAD+ is preferred coenzyme. |
8 |
| CATGGAAGATTTAC |
YOR023C |
AHC1 |
6324597 |
- |
0 |
0 |
6 |
2 |
1 |
15 |
376165 |
376178 |
- |
375857 |
377711 |
- |
566 |
Ada Histone acetyltransferase complex component |
3 |
| CATGTAGTTCTGTA |
YDR214W |
AHA1 |
6320420 |
- |
9 |
4 |
0 |
1 |
1 |
4 |
894000 |
894013 |
+ |
892868 |
894419 |
+ |
350 |
Activator of Heat Shock Protein 90 ATPase |
8 |
| CATGAGATCAGTAA |
YPL202C |
AFT2 |
6325054 |
- |
6 |
12 |
0 |
1 |
1 |
16 |
167758 |
167771 |
- |
167588 |
169337 |
- |
416 |
Activator of Iron (Fe) Transcription |
9 |
| CATGTATATATATA |
YER017C |
AFG3 |
6320854 |
COG0465 |
15 |
0 |
0 |
15 |
1 |
5 |
189386 |
189399 |
- |
189003 |
191787 |
- |
761 |
ATPase family gene |
6 |
| CATGTTGTGCAAAA |
YDR216W |
ADR1 |
6320422 |
COG5048 |
0 |
0 |
10 |
1 |
1 |
4 |
897699 |
897712 |
+ |
895027 |
899497 |
+ |
1323 |
Controls the expression of ADH2, peroxisomal protein
genes, and genes required for ethanol, glycerol, and fatty acid utilization. |
3 |
| CATGAAAGACAATG |
YCR011C |
ADP1 |
10383780 |
COG0842 |
6 |
0 |
0 |
1 |
1 |
3 |
134157 |
134170 |
- |
133222 |
136870 |
- |
1049 |
Shows homology to ATP-dependent permeases |
8 |
| CATGGGTCAATGGC |
YJR105W |
ADO1 |
6322565 |
COG0524 |
6 |
4 |
0 |
2 |
1 |
10 |
624434 |
624447 |
+ |
623494 |
624750 |
+ |
340 |
adenosine kinase |
8 |
| CATGTTTTGGGTCT |
YMR318C |
ADH6 |
6323980 |
COG1064 |
9 |
21 |
0 |
1 |
1 |
13 |
910998 |
911011 |
- |
910560 |
912141 |
- |
360 |
NADPH-dependent alcohol dehydrogenase |
9 |
| CATGGGTGAAAACG |
YMR303C |
ADH2 |
6323961 |
COG1064 |
67 |
81 |
3 |
3 |
1 |
13 |
874098 |
874111 |
- |
872791 |
874336 |
- |
348 |
Glucose-repressible alcohol dehydrogenase II catalyzes
activities for the production of certain carboxylate esters. |
4 |
| CATGGGTGAAAACG |
YOL086C |
ADH1 |
6324486 |
COG1064 |
67 |
81 |
3 |
3 |
1 |
15 |
160355 |
160368 |
- |
159048 |
160593 |
- |
348 |
Adh protein catalyzes activities for the production of
certain carboxylate esters. |
4 |
| CATGTGTAAACGCT |
YDR408C |
ADE8 |
6320616 |
COG0299 |
3 |
4 |
3 |
1 |
1 |
4 |
1288033 |
1288046 |
- |
1287927 |
1288847 |
- |
214 |
Phosphoribosyl-glycinamide transformylase, catalyzes a
step in the 'de novo' purine nucleotide biosynthetic pathway |
8 |
| CATGGGTGTTGGTA |
YGL234W |
ADE5,7 |
6321203 |
COG0151 |
3 |
0 |
10 |
1 |
1 |
7 |
58726 |
58739 |
+ |
56481 |
59120 |
+ |
802 |
Bifunctional enzyme of the 'de novo' purine nucleotide
biosynthetic pathway, contains aminoimidazole ribotide synthetase and
glycinamide ribotide synthetase activities |
8 |
| CATGGCCAAGGAAT |
YMR300C |
ADE4 |
6323958 |
COG0034 |
3 |
0 |
10 |
1 |
1 |
13 |
865916 |
865929 |
- |
865350 |
867090 |
- |
510 |
Phosphoribosylpyrophosphate amidotransferase (PRPPAT;
amidophosphoribosyltransferase), catalyzes first step of the 'de novo' purine
nucleotide biosynthetic pathway |
8 |
| CATGGCCGTGGAAG |
YGR204W |
ADE3 |
6321643 |
COG0190 |
3 |
0 |
13 |
1 |
1 |
7 |
908728 |
908741 |
+ |
905937 |
909215 |
+ |
946 |
Cytoplasmic trifunctional enzyme C1-tetrahydrofolate
synthase, involved in single carbon metabolism and required for biosynthesis
of purines, thymidylate, methionine, and histidine |
3 |
| CATGAGTTCAGAGT |
YMR120C |
ADE17 |
6323768 |
COG0138 |
3 |
8 |
0 |
1 |
1 |
13 |
507482 |
507495 |
- |
507002 |
509279 |
- |
592 |
Enzyme of 'de novo' purine biosynthesis containing both
5-aminoimidazole-4-carboxamide ribonucleotide transformylase and inosine
monophosphate cyclohydrolase activities, isozyme
of Ade16p; ade16 ade17 mutants require adenine and histidine |
8 |
| CATGACATTTTTTA |
YNL220W |
ADE12 |
6324109 |
COG0104 |
3 |
4 |
0 |
1 |
1 |
14 |
235793 |
235806 |
+ |
234412 |
236212 |
+ |
433 |
Adenylosuccinate synthase, catalyzes the first committed
step in the 'de novo' biosynthesis of adenosine |
8 |
| CATGTTCCCAGGTA |
YFL039C |
ACT1 |
14318479 |
COG5277 |
0 |
0 |
6 |
2 |
1 |
6 |
53462 |
53475 |
- |
52761 |
54695 |
- |
375 |
Structural protein involved in cell polarization,
endocytosis, and other cytoskeletal functions |
3 |
| CATGATGGTTACTA |
YLR153C |
ACS2 |
6323182 |
COG0365 |
3 |
8 |
0 |
1 |
1 |
12 |
445999 |
446012 |
- |
445026 |
447576 |
- |
683 |
one of 2 acetyl-coA synthetases in yeast |
8 |
| CATGGGATGCTGTG |
YLR304C |
ACO1 |
6323335 |
COG1048 |
18 |
8 |
0 |
1 |
1 |
12 |
735300 |
735313 |
- |
734715 |
737550 |
- |
778 |
Mitochondrial aconitase, required for the tricarboxylic
acid (TCA) cycle; mutation leads to glutamate auxotrophy |
6 |
| CATGACAATGCTAT |
YNR016C |
ACC1 |
6324343 |
COG4799 |
24 |
30 |
10 |
1 |
1 |
14 |
654744 |
654757 |
- |
654173 |
661373 |
- |
2233 |
Acetyl-CoA carboxylase, biotin containing enzyme that
catalyzes the carboxylation of acetyl-CoA to form malonyl-CoA; required for
de novo biosynthesis of long-chain fatty acids |
5 |
| CATGTAAGGAGTTT |
YGR037C |
ACB1 |
6321474 |
COG4281 |
3 |
4 |
0 |
1 |
1 |
7 |
559699 |
559712 |
- |
559234 |
559996 |
- |
87 |
Acyl-CoA-binding protein, transports newly synthesized
acyl-CoA esters from fatty acid synthetase (Fas1p-Fas2p) to
acyl-CoA-consuming processes |
8 |
| CATGGTGTGACGAT |
YNL141W |
AAH1 |
6324188 |
COG1816 |
6 |
8 |
0 |
1 |
1 |
14 |
360565 |
360578 |
+ |
359596 |
361138 |
+ |
347 |
Adenine deaminase (adenine aminohydrolase), involved in
purine salvage and nitrogen catabolism |
8 |
| CATGTTTTCCCATT |
YJR155W |
AAD10 |
6322615 |
COG0667 |
3 |
0 |
3 |
1 |
1 |
10 |
727967 |
727980 |
+ |
727320 |
728685 |
+ |
288 |
Putative aryl-alcohol dehydrogenase with similarity to P.
chrysosporium aryl-alcohol dehydrogenase; mutational analysis has not yet
revealed a physiological role |
8 |
| CATGGTTTTGCCAT |
YAL027W |
- |
6319292 |
- |
3 |
4 |
0 |
2 |
1 |
1 |
94727 |
94740 |
+ |
94690 |
95974 |
+ |
261 |
Hypothetical ORF |
8 |
| CATGATTGTGATTG |
YAL061W |
- |
6319257 |
COG1063 |
9 |
0 |
0 |
1 |
1 |
1 |
34697 |
34710 |
+ |
33449 |
35155 |
+ |
417 |
putative polyol dehydrogenase |
8 |
| CATGCAAAAGACTG |
YAR075W |
- |
6319353 |
COG0516 |
12 |
0 |
13 |
4 |
1 |
1 |
229006 |
229019 |
+ |
228837 |
229809 |
+ |
157 |
Hypothetical ORF |
8 |
| CATGATGCAGAGTA |
YBL029W |
- |
6319442 |
- |
12 |
0 |
62 |
1 |
1 |
2 |
167162 |
167175 |
+ |
166099 |
167728 |
+ |
376 |
Hypothetical ORF |
2 |
| CATGTTAATGAAAA |
YBL036C |
- |
6319435 |
COG0325 |
6 |
0 |
0 |
1 |
1 |
2 |
151072 |
151085 |
- |
149913 |
151185 |
- |
257 |
Single-domain racemase, possibly non-specific due to the
lack of the second domain, which presumably determines specificity |
8 |
| CATGTACACACACA |
YBL054W |
- |
6319417 |
- |
3 |
4 |
0 |
2 |
1 |
2 |
119196 |
119209 |
+ |
117554 |
119630 |
+ |
525 |
Hypothetical ORF |
8 |
| CATGGCTTTTTGCA |
YBL059C-A |
- |
6681845 |
- |
3 |
4 |
3 |
1 |
1 |
2 |
109927 |
109940 |
- |
109590 |
110503 |
- |
109 |
Hypothetical ORF |
8 |
| CATGGAAATGTTGA |
YBL086C |
- |
6319385 |
- |
0 |
0 |
24 |
2 |
1 |
2 |
60949 |
60962 |
- |
60736 |
62599 |
- |
466 |
Protein of unknown function; green fluorescent protein
(GFP)-fusion protein localizes to the cell periphery |
2 |
| CATGCACTTCAACT |
YBL101W-B |
- |
6319369 |
- |
12 |
8 |
3 |
20 |
1 |
2 |
34907 |
34920 |
+ |
29932 |
35245 |
+ |
1770 |
TyB Gag-Pol protein; proteolytically processed to make
the Gag, RT, PR, and IN proteins that are required for retrotransposition |
6 |
| CATGCTGATGGTAG |
YBL113C |
- |
6319355 |
- |
9 |
4 |
3 |
18 |
1 |
2 |
374 |
387 |
- |
-219 |
2658 |
- |
792 |
Hypothetical ORF |
8 |
| CATGTATGTAATAC |
YBR016W |
- |
6319490 |
- |
6 |
12 |
0 |
1 |
1 |
2 |
270737 |
270750 |
+ |
270209 |
271094 |
+ |
128 |
Plasma membrane protein of unknown function; has
similarity to hydrophilins, which are hydrophilic, glycine-rich proteins
involved in the adaptive response to hyperosmotic
conditions |
9 |
| CATGTTTACGCCCT |
YBR025C |
- |
6319499 |
COG0012 |
0 |
4 |
44 |
1 |
1 |
2 |
290458 |
290471 |
- |
290144 |
291827 |
- |
394 |
Hypothetical ORF |
2 |
| CATGTAACTAGCGT |
YBR053C |
- |
6319527 |
COG3386 |
12 |
12 |
0 |
1 |
1 |
2 |
339575 |
339588 |
- |
339313 |
340711 |
- |
358 |
Hypothetical ORF |
6 |
| CATGCGTCTCCGGA |
YBR077C |
- |
6319551 |
- |
9 |
0 |
3 |
1 |
1 |
2 |
391712 |
391725 |
- |
391263 |
392250 |
- |
162 |
Hypothetical ORF |
8 |
| CATGTTCTATTAGG |
YBR085C-A |
- |
9755326 |
- |
6 |
8 |
3 |
1 |
1 |
2 |
418742 |
418755 |
- |
418365 |
419121 |
- |
85 |
Hypothetical ORF |
8 |
| CATGGAGGTGCTGT |
YBR137W |
- |
6319613 |
COG4702 |
3 |
4 |
0 |
1 |
1 |
2 |
513380 |
513393 |
+ |
513000 |
514038 |
+ |
179 |
Hypothetical ORF |
8 |
| CATGGCTTATGTAT |
YBR159W |
- |
6319635 |
COG0300 |
0 |
8 |
0 |
1 |
1 |
2 |
559754 |
559767 |
+ |
558641 |
560033 |
+ |
347 |
microsomal beta-keto-reductase |
8 |
| CATGCTCTGGTTCT |
YBR242W |
- |
6319719 |
COG1896 |
3 |
4 |
0 |
2 |
1 |
2 |
704654 |
704667 |
+ |
704627 |
705842 |
+ |
238 |
Hypothetical ORF |
8 |
| CATGTCTACTTATA |
YBR255C-A |
- |
41629679 |
- |
3 |
0 |
6 |
1 |
1 |
2 |
726550 |
726563 |
- |
726076 |
727031 |
- |
120 |
Hypothetical ORF identified by homology. See FEBS Letters
[2000] 487:31-36. |
8 |
| CATGGATTTTTGTT |
YBR273C |
- |
6319750 |
- |
6 |
0 |
0 |
4 |
1 |
2 |
747910 |
747923 |
- |
747761 |
749328 |
- |
436 |
Hypothetical ORF |
8 |
| CATGGGGTATTGAA |
YBR280C |
- |
37362624 |
- |
6 |
0 |
0 |
1 |
1 |
2 |
762936 |
762949 |
- |
762243 |
764655 |
- |
637 |
Hypothetical ORF |
8 |
| CATGAATGAAAGTC |
YBR287W |
- |
6319764 |
COG0679 |
3 |
0 |
3 |
1 |
1 |
2 |
777843 |
777856 |
+ |
776529 |
778311 |
+ |
427 |
Ybr287wp |
8 |
| CATGCACTTCAACT |
YCL019W |
- |
10383770 |
- |
12 |
8 |
3 |
20 |
1 |
3 |
90076 |
90089 |
+ |
85101 |
90414 |
+ |
1770 |
TyB Gag-Pol protein; proteolytically processed to make
the Gag, RT, PR, and IN proteins that are required for retrotransposition |
6 |
| CATGGGTTTTGGCG |
YCL057C-A |
- |
10383755 |
- |
6 |
4 |
3 |
1 |
1 |
3 |
24174 |
24187 |
- |
23982 |
24325 |
- |
97 |
Hypothetical ORF, has similarity to proteins in S. pombe,
C. elegans, D. melanogaster. |
8 |
| CATGCAGCCTCATT |
YCR007C |
- |
6319852 |
- |
0 |
0 |
6 |
1 |
1 |
3 |
126714 |
126727 |
- |
125509 |
126727 |
- |
239 |
Putative integral membrane protein, member of DUP240 gene
family |
3 |
| CATGGATACGACAA |
YCR026C |
- |
10383789 |
COG1524 |
3 |
4 |
0 |
1 |
1 |
3 |
164697 |
164710 |
- |
163607 |
166334 |
- |
742 |
Hypothetical ORF |
8 |
| CATGGGGAGAAAGG |
YCR079W |
- |
10383808 |
COG0631 |
6 |
8 |
0 |
1 |
1 |
3 |
253047 |
253060 |
+ |
252841 |
254366 |
+ |
442 |
Hypothetical ORF |
8 |
| CATGATAAACGTTT |
YCR095C |
- |
6319938 |
COG2365 |
0 |
0 |
6 |
1 |
1 |
3 |
288119 |
288132 |
- |
287667 |
289254 |
- |
362 |
Hypothetical ORF |
3 |
| CATGCAAGTAGATA |
YDL012C |
- |
6320192 |
- |
0 |
8 |
10 |
1 |
1 |
4 |
430975 |
430988 |
- |
430606 |
431514 |
- |
107 |
Plasma membrane protein of unknown function |
8 |
| CATGGAATCGTGGG |
YDL025C |
- |
6320179 |
COG0515 |
6 |
4 |
6 |
2 |
1 |
4 |
405791 |
405804 |
- |
404955 |
407203 |
- |
620 |
Protein of unknown function, potentially phosphorylated
by Cdc28p |
8 |
| CATGTCATTACATT |
YDL046W |
- |
6320157 |
- |
3 |
8 |
0 |
1 |
1 |
4 |
372013 |
372026 |
+ |
371237 |
372244 |
+ |
173 |
Putative homolog of human NPC2/He1, which is a
cholesterol-binding protein whose deficiency causes Niemann-Pick type C2
disease involving retention of cholesterol in
lysosomes |
8 |
| CATGCGTTCATCCG |
YDL086W |
- |
6320117 |
COG0412 |
0 |
8 |
0 |
1 |
1 |
4 |
302078 |
302091 |
+ |
301413 |
302733 |
+ |
273 |
Hypothetical ORF |
8 |
| CATGACCACTTGGA |
YDL099W |
- |
6320104 |
- |
6 |
4 |
0 |
1 |
1 |
4 |
284395 |
284408 |
+ |
283419 |
284943 |
+ |
341 |
Protein of unknown function; green fluorescent protein
(GFP)-fusion protein localizes to the cytoplasm in a punctate pattern |
8 |
| CATGCAAAAGACTG |
YDL203C |
- |
6319998 |
COG0790 |
12 |
0 |
13 |
4 |
1 |
4 |
96672 |
96685 |
- |
95584 |
97954 |
- |
623 |
Hypothetical ORF |
8 |
| CATGGTAGCAGCAA |
YDL233W |
- |
6319968 |
- |
0 |
8 |
0 |
1 |
1 |
4 |
38247 |
38260 |
+ |
36798 |
38487 |
+ |
458 |
Hypothetical ORF |
8 |
| CATGGCATCGTCAT |
YDL237W |
- |
6319964 |
- |
6 |
4 |
0 |
1 |
1 |
4 |
31807 |
31820 |
+ |
30657 |
32295 |
+ |
390 |
Hypothetical ORF |
8 |
| CATGACTTGCGGTA |
YDR003W |
- |
6320206 |
- |
3 |
4 |
0 |
1 |
2 |
4 |
454777 |
454790 |
+ |
454119 |
454778 |
+ |
210 |
Hypothetical ORF |
8 |
| CATGAGCGAATGTA |
YDR031W |
- |
6320234 |
- |
3 |
4 |
0 |
1 |
1 |
4 |
503669 |
503682 |
+ |
503494 |
504346 |
+ |
117 |
Hypothetical ORF |
8 |
| CATGCACTTCAACT |
YDR034C-D |
- |
7839150 |
- |
12 |
8 |
3 |
20 |
1 |
4 |
514361 |
514374 |
- |
513539 |
519351 |
- |
1770 |
TyB Gag-Pol protein; proteolytically processed to make
the Gag, RT, PR, and IN proteins that are required for retrotransposition |
6 |
| CATGAAGCTGAGGA |
YDR056C |
- |
6320261 |
- |
6 |
0 |
0 |
1 |
1 |
4 |
565380 |
565393 |
- |
564520 |
565636 |
- |
205 |
Hypothetical ORF |
8 |
| CATGTAGTTTCTGT |
YDR070C |
- |
6320275 |
- |
21 |
12 |
3 |
1 |
1 |
4 |
588052 |
588065 |
- |
587716 |
588375 |
- |
93 |
The authentic, non-tagged protein was localized to the
mitochondria |
6 |
| CATGTGGTTACATA |
YDR089W |
- |
6320294 |
- |
0 |
0 |
6 |
1 |
1 |
4 |
624770 |
624783 |
+ |
622106 |
625214 |
+ |
869 |
Hypothetical ORF |
3 |
| CATGCACTTCAACT |
YDR098C-B |
- |
7839152 |
- |
12 |
8 |
3 |
20 |
1 |
4 |
646175 |
646188 |
- |
645353 |
651120 |
- |
1755 |
TyB Gag-Pol protein; proteolytically processed to make
the Gag, RT, PR, and IN proteins that are required for retrotransposition |
6 |
| CATGGGAGGATGGG |
YDR186C |
- |
6320392 |
- |
3 |
4 |
0 |
1 |
1 |
4 |
832874 |
832887 |
- |
832467 |
835485 |
- |
877 |
Hypothetical ORF |
8 |
| CATGTCATAGCTTA |
YDR196C |
- |
6320402 |
COG0237 |
3 |
12 |
0 |
1 |
1 |
4 |
850190 |
850203 |
- |
849768 |
850992 |
- |
241 |
predicted to catalyze the final step in synthesis of
Coenzyme A |
9 |
| CATGCACTTCAACT |
YDR210C-D |
- |
20336767 |
- |
12 |
8 |
3 |
20 |
1 |
4 |
878975 |
878988 |
- |
878153 |
883920 |
- |
1755 |
TyB Gag-Pol protein; proteolytically processed to make
the Gag, RT, PR, and IN proteins that are required for retrotransposition |
6 |
| CATGCACTTCAACT |
YDR210W-B |
- |
7839154 |
- |
12 |
8 |
3 |
20 |
1 |
4 |
877080 |
877093 |
+ |
872105 |
877418 |
+ |
1770 |
TyB Gag-Pol protein; proteolytically processed to make
the Gag, RT, PR, and IN proteins that are required for retrotransposition |
6 |
| CATGCACAATATGT |
YDR249C |
- |
6320455 |
- |
6 |
0 |
0 |
1 |
1 |
4 |
958621 |
958634 |
- |
958332 |
959794 |
- |
373 |
Hypothetical ORF |
8 |
| CATGCACTTCAACT |
YDR261W-B |
- |
7839158 |
- |
12 |
8 |
3 |
20 |
1 |
4 |
986429 |
986442 |
+ |
981454 |
986767 |
+ |
1770 |
TyB Gag-Pol protein; proteolytically processed to make
the Gag, RT, PR, and IN proteins that are required for retrotransposition |
6 |
| CATGCCGTCGAGAG |
YDR262W |
- |
6320468 |
- |
3 |
4 |
6 |
1 |
1 |
4 |
993869 |
993882 |
+ |
993126 |
994443 |
+ |
272 |
Hypothetical ORF |
8 |
| CATGTTGTTCGTTT |
YDR282C |
- |
6320488 |
COG1723 |
6 |
8 |
3 |
28 |
1 |
4 |
1023213 |
1023226 |
- |
1023004 |
1024747 |
- |
414 |
Hypothetical ORF |
8 |
| CATGGTAGAGGTCA |
YDR316W |
- |
6320522 |
COG0500 |
3 |
4 |
0 |
1 |
1 |
4 |
1094838 |
1094851 |
+ |
1093756 |
1095670 |
+ |
471 |
Ydr316wp |
8 |
| CATGACAGGCGTTA |
YDR348C |
- |
6320555 |
- |
6 |
0 |
0 |
1 |
1 |
4 |
1170581 |
1170594 |
- |
1169817 |
1171815 |
- |
499 |
Protein of unknown function; green fluorescent protein
(GFP)-fusion protein localizes to the cell periphery and bud neck; potential
Cdc28p substrate |
8 |
| CATGCACTTCAACT |
YDR365W-B |
- |
7839164 |
- |
12 |
8 |
3 |
20 |
1 |
4 |
1211915 |
1211928 |
+ |
1206985 |
1212253 |
+ |
1755 |
TyB Gag-Pol protein; proteolytically processed to make
the Gag, RT, PR, and IN proteins that are required for retrotransposition |
6 |
| CATGGTCACTGGTA |
YDR504C |
- |
6320712 |
- |
3 |
4 |
0 |
1 |
1 |
4 |
1456327 |
1456340 |
- |
1455855 |
1456682 |
- |
127 |
Protein required for survival at high temperature during
stationary phase |
8 |
| CATGACGAGAGGAG |
YDR517W |
- |
6320725 |
COG5233 |
0 |
0 |
6 |
1 |
1 |
4 |
1477697 |
1477710 |
+ |
1477227 |
1478595 |
+ |
372 |
Golgi localized protein component of the spindle assembly
checkpoint; homolog of human GRASP65, which functions in postmitotic
reassembly of Golgi stacks |
3 |
| CATGTTCGTTCACT |
YDR524C-B |
- |
33438785 |
- |
30 |
30 |
41 |
1 |
1 |
4 |
1489379 |
1489392 |
- |
1489087 |
1489786 |
- |
66 |
Ydr524c-bp |
7 |
| CATGAAAAGATCAT |
YDR524W-A |
- |
33438784 |
- |
3 |
4 |
3 |
1 |
1 |
4 |
1489389 |
1489402 |
+ |
1489391 |
1489979 |
+ |
29 |
Identified by SAGE |
8 |
| CATGTATATATATA |
YEL020C |
- |
6320816 |
COG0028 |
15 |
0 |
0 |
15 |
1 |
5 |
118594 |
118607 |
- |
118118 |
120299 |
- |
560 |
Hypothetical ORF |
6 |
| CATGGCGCCAATAG |
YEL047C |
- |
6320788 |
COG1053 |
3 |
8 |
0 |
2 |
1 |
5 |
65463 |
65476 |
- |
65168 |
66797 |
- |
470 |
Fumurate ReDuctase Soluble |
8 |
| CATGCTGATGGTAG |
YEL077C |
- |
6320756 |
COG0513 |
9 |
4 |
3 |
18 |
1 |
5 |
358 |
371 |
- |
-235 |
4097 |
- |
1277 |
Hypothetical ORF |
8 |
| CATGTGATGAAGAT |
YER049W |
- |
6320890 |
- |
6 |
0 |
0 |
3 |
1 |
5 |
253626 |
253639 |
+ |
251727 |
254160 |
+ |
644 |
Hypothetical ORF |
8 |
| CATGATCGGTACTT |
YER053C |
- |
6320894 |
- |
0 |
0 |
13 |
1 |
1 |
5 |
258803 |
258816 |
- |
258237 |
259638 |
- |
300 |
sequence similarity to mitochondrial phosphate
transporters |
3 |
| CATGGATGCCGAAA |
YER138W-A |
- |
6320986 |
- |
6 |
4 |
0 |
1 |
1 |
5 |
449825 |
449838 |
+ |
449470 |
450073 |
+ |
34 |
Similar to TyB and TyA |
8 |
| CATGCAGCAGGTTT |
YER156C |
- |
6321004 |
COG4286 |
3 |
4 |
0 |
1 |
1 |
5 |
483380 |
483393 |
- |
482844 |
484336 |
- |
338 |
Hypothetical ORF |
8 |
| CATGGATATCAATG |
YER187W |
- |
6321035 |
- |
3 |
4 |
0 |
1 |
1 |
5 |
566327 |
566340 |
+ |
566225 |
567149 |
+ |
141 |
Hypothetical ORF |
8 |
| CATGCACTTCAACT |
YFL002W-A |
- |
14318520 |
- |
12 |
8 |
3 |
20 |
1 |
6 |
143174 |
143187 |
+ |
138199 |
143512 |
+ |
1770 |
TyB Gag-Pol protein; proteolytically processed to make
the Gag, RT, PR, and IN proteins that are required for retrotransposition |
6 |
| CATGCAATGGCTGA |
YFL046W |
- |
14318473 |
- |
0 |
0 |
10 |
1 |
1 |
6 |
43365 |
43378 |
+ |
42815 |
43937 |
+ |
207 |
The authentic, non-tagged protein was localized to the
mitochondria |
3 |
| CATGTATGTCGGTG |
YFR006W |
- |
14318528 |
COG0006 |
3 |
17 |
0 |
1 |
1 |
6 |
157589 |
157602 |
+ |
156139 |
158245 |
+ |
535 |
Hypothetical ORF |
9 |
| CATGTATATAAAAT |
YFR011C |
- |
14318533 |
- |
6 |
0 |
0 |
2 |
1 |
6 |
166678 |
166691 |
- |
166240 |
167251 |
- |
170 |
Hypothetical ORF |
8 |
| CATGTTTGGAGAGA |
YFR017C |
- |
14318539 |
- |
0 |
8 |
10 |
1 |
1 |
6 |
182266 |
182279 |
- |
181763 |
182849 |
- |
195 |
Hypothetical ORF |
8 |
| CATGCATTAACAAG |
YGL010W |
- |
6321428 |
COG4539 |
3 |
4 |
17 |
1 |
1 |
7 |
476128 |
476141 |
+ |
475548 |
476571 |
+ |
174 |
Hypothetical ORF |
3 |
| CATGTAAATATGTT |
YGL068W |
- |
6321369 |
COG0222 |
6 |
0 |
3 |
1 |
1 |
7 |
375748 |
375761 |
+ |
375088 |
376101 |
+ |
194 |
Protein required for cell viability |
8 |
| CATGCTGATTACGG |
YGL101W |
- |
6321337 |
COG1896 |
3 |
4 |
0 |
1 |
1 |
7 |
312399 |
312412 |
+ |
312194 |
313234 |
+ |
215 |
Hypothetical ORF |
8 |
| CATGAAAGTGTGGC |
YGL231C |
- |
6321206 |
- |
0 |
0 |
10 |
4 |
1 |
7 |
62682 |
62695 |
- |
62548 |
63619 |
- |
190 |
Hypothetical ORF |
3 |
| CATGCCAAAGCTGC |
YGL245W |
- |
37362649 |
- |
12 |
4 |
0 |
1 |
1 |
7 |
39673 |
39686 |
+ |
39023 |
41497 |
+ |
708 |
Glutamyl-tRNA synthetase (GluRS), forms a complex with
methionyl-tRNA synthetase (Mes1p) and Arc1p; complex formation increases the
catalytic efficiency of both tRNA synthetases and
ensures their correct localization to the cytoplasm |
6 |
| CATGGAATTGTGGC |
YGR031W |
- |
6321468 |
COG0596 |
3 |
4 |
0 |
1 |
1 |
7 |
547676 |
547689 |
+ |
546443 |
547970 |
+ |
342 |
Hypothetical ORF |
8 |
| CATGCACTTCAACT |
YGR038C-B |
- |
7839173 |
- |
12 |
8 |
3 |
20 |
1 |
7 |
562524 |
562537 |
- |
561702 |
567469 |
- |
1755 |
TyB Gag-Pol protein; proteolytically processed to make
the Gag, RT, PR, and IN proteins that are required for retrotransposition |
6 |
| CATGGTTATGCAAC |
YGR043C |
- |
6321480 |
COG0176 |
9 |
21 |
0 |
2 |
1 |
7 |
580743 |
580756 |
- |
579938 |
581438 |
- |
333 |
Hypothetical ORF |
9 |
| CATGGAACAAAGAT |
YGR052W |
- |
6321489 |
COG0515 |
3 |
4 |
0 |
1 |
1 |
7 |
594552 |
594565 |
+ |
593598 |
595206 |
+ |
369 |
The authentic, non-tagged protein was localized to the
mitochondria |
8 |
| CATGTATATATATA |
YGR131W |
- |
6321570 |
- |
15 |
0 |
0 |
15 |
1 |
7 |
755407 |
755420 |
+ |
754729 |
755752 |
+ |
174 |
Hypothetical ORF |
6 |
| CATGGAAATGGAAG |
YGR153W |
- |
6321592 |
- |
6 |
0 |
0 |
2 |
1 |
7 |
796718 |
796731 |
+ |
796095 |
797247 |
+ |
217 |
Hypothetical ORF |
8 |
| CATGCACTTCAACT |
YGR161W-B |
- |
7839176 |
- |
12 |
8 |
3 |
20 |
1 |
7 |
816716 |
816729 |
+ |
811741 |
817054 |
+ |
1770 |
TyB Gag-Pol protein; proteolytically processed to make
the Gag, RT, PR, and IN proteins that are required for retrotransposition |
6 |
| CATGGAGGTCTAAG |
YGR201C |
- |
37362656 |
- |
3 |
8 |
0 |
1 |
1 |
7 |
902630 |
902643 |
- |
902274 |
903200 |
- |
225 |
Hypothetical ORF |
8 |
| CATGGGTGGCGAGG |
YGR210C |
- |
6321649 |
COG0012 |
0 |
0 |
10 |
1 |
1 |
7 |
913618 |
913631 |
- |
913231 |
914741 |
- |
411 |
Hypothetical ORF |
3 |
| CATGTAAGGGAATT |
YGR236C |
- |
6321675 |
- |
3 |
0 |
10 |
1 |
1 |
7 |
962524 |
962537 |
- |
962064 |
962820 |
- |
129 |
Protein required for survival at high temperature during
stationary phase |
8 |
| CATGTATTAGTTGG |
YGR250C |
- |
6321689 |
COG0724 |
3 |
0 |
3 |
1 |
1 |
7 |
991121 |
991134 |
- |
990681 |
993525 |
- |
781 |
Hypothetical ORF |
8 |
| CATGTAGTGCGCTG |
YGR251W |
- |
6321690 |
- |
6 |
0 |
0 |
1 |
1 |
7 |
996536 |
996549 |
+ |
995643 |
996732 |
+ |
196 |
Protein required for cell viability |
8 |
| CATGCATTCCTATA |
YHL009W-B |
- |
7839180 |
- |
6 |
0 |
0 |
4 |
1 |
8 |
90059 |
90072 |
+ |
85904 |
91313 |
+ |
1802 |
TyB Gag-Pol protein; proteolytically processed to make
the Gag, RT, PR, and IN proteins that are required for retrotransposition |
8 |
| CATGTGCGAACTCT |
YHL026C |
- |
6321761 |
- |
9 |
17 |
0 |
1 |
1 |
8 |
53178 |
53191 |
- |
52718 |
54023 |
- |
268 |
Hypothetical ORF |
9 |
| CATGCGTCAGTGTG |
YHL048C-A |
- |
33438802 |
- |
9 |
17 |
0 |
9 |
1 |
8 |
5662 |
5675 |
- |
5163 |
5796 |
- |
44 |
Identified by expression profiling and mass spectrometry |
9 |
| CATGCTGATGGTAG |
YHL050C |
- |
6321737 |
COG0513 |
9 |
4 |
3 |
18 |
1 |
8 |
539 |
552 |
- |
-54 |
3310 |
- |
697 |
Protein of unknown function, potential Cdc28p substrate |
8 |
| CATGGCCAAGCAAT |
YHR032W |
- |
6321821 |
COG0534 |
9 |
12 |
0 |
2 |
1 |
8 |
173716 |
173729 |
+ |
173336 |
175539 |
+ |
581 |
Hypothetical ORF |
6 |
| CATGAAGAAGTACA |
YHR078W |
- |
6321869 |
- |
0 |
0 |
6 |
1 |
1 |
8 |
258120 |
258133 |
+ |
256361 |
258518 |
+ |
552 |
Hypothetical ORF |
3 |
| CATGTATAGGTCAA |
YHR112C |
- |
6321904 |
COG0626 |
6 |
0 |
6 |
1 |
1 |
8 |
334396 |
334409 |
- |
334030 |
335665 |
- |
378 |
Hypothetical ORF |
8 |
| CATGACCAACGATA |
YHR116W |
- |
6321908 |
- |
0 |
0 |
6 |
1 |
1 |
8 |
341731 |
341744 |
+ |
341667 |
342350 |
+ |
151 |
Hypothetical ORF |
3 |
| CATGCTCTAAACCG |
YHR138C |
- |
6321930 |
- |
12 |
8 |
0 |
1 |
1 |
8 |
377374 |
377387 |
- |
376857 |
377700 |
- |
114 |
Homologous to PBI2 |
6 |
| CATGGCTCATTGTA |
YHR140W |
- |
6321933 |
- |
3 |
0 |
3 |
1 |
1 |
8 |
381062 |
381075 |
+ |
380573 |
381791 |
+ |
239 |
Hypothetical ORF |
8 |
| CATGTAGTTAGTTT |
YHR181W |
- |
6321975 |
- |
0 |
0 |
41 |
2 |
1 |
8 |
467930 |
467943 |
+ |
467226 |
468216 |
+ |
228 |
Sed5-Vesicle Protein of 26 kDa |
2 |
| CATGACTGTTTCAG |
YHR199C |
- |
6321993 |
- |
6 |
8 |
0 |
1 |
1 |
8 |
497719 |
497732 |
- |
497279 |
498420 |
- |
310 |
The authentic, non-tagged protein was localized to the
mitochondria |
8 |
| CATGCTGATGGTAG |
YHR219W |
- |
6322015 |
COG0513 |
9 |
4 |
3 |
18 |
1 |
8 |
561936 |
561949 |
+ |
560171 |
562544 |
+ |
624 |
Hypothetical ORF |
8 |
| CATGGGAAATAGGA |
YIL001W |
- |
6322190 |
COG0666 |
3 |
0 |
6 |
1 |
1 |
9 |
355149 |
355162 |
+ |
353937 |
355977 |
+ |
513 |
Hypothetical ORF |
8 |
| CATGAGGAGAGAGA |
YIL046W-A |
- |
33438815 |
- |
0 |
0 |
6 |
2 |
2 |
9 |
268648 |
268661 |
+ |
268308 |
268649 |
+ |
54 |
Identified by expression profiling and mass spectrometry |
3 |
| CATGAATTTTGTAC |
YIL056W |
- |
6322133 |
- |
3 |
8 |
0 |
2 |
1 |
9 |
252098 |
252111 |
+ |
249989 |
252410 |
+ |
640 |
Hypothetical ORF |
8 |
| CATGAATCCGATAT |
YIL077C |
- |
6322113 |
- |
0 |
8 |
0 |
1 |
1 |
9 |
215096 |
215109 |
- |
214489 |
215950 |
- |
320 |
Hypothetical ORF |
8 |
| CATGAATGGATTTG |
YIL087C |
- |
6322104 |
- |
3 |
4 |
0 |
1 |
1 |
9 |
199555 |
199568 |
- |
199401 |
200116 |
- |
157 |
Hypothetical ORF |
8 |
| CATGCGATTGAATA |
YIL103W |
- |
6322088 |
COG1736 |
0 |
8 |
0 |
1 |
1 |
9 |
173010 |
173023 |
+ |
171748 |
173524 |
+ |
425 |
Hypothetical ORF |
8 |
| CATGTGTTGCAATA |
YIL152W |
- |
6322039 |
- |
3 |
4 |
0 |
1 |
1 |
9 |
57612 |
57625 |
+ |
56545 |
57751 |
+ |
235 |
Hypothetical ORF |
8 |
| CATGCTGATGGTAG |
YIL177C |
- |
6322017 |
COG0513 |
9 |
4 |
3 |
18 |
1 |
9 |
574 |
587 |
- |
-16 |
6147 |
- |
1758 |
Hypothetical ORF |
8 |
| CATGACAAGTCGAT |
YIR014W |
- |
37362663 |
- |
0 |
0 |
6 |
1 |
1 |
9 |
381733 |
381746 |
+ |
381083 |
381944 |
+ |
242 |
Hypothetical ORF |
3 |
| CATGATTTGTCGAT |
YIR018C-A |
- |
33438817 |
- |
0 |
0 |
6 |
1 |
1 |
9 |
385301 |
385314 |
- |
385062 |
385698 |
- |
45 |
Identified by expression profiling and mass spectrometry |
3 |
| CATGGTATTCCTGA |
YIR035C |
- |
6322226 |
COG1028 |
3 |
8 |
0 |
1 |
1 |
9 |
421083 |
421096 |
- |
420734 |
421787 |
- |
254 |
Hypothetical ORF |
8 |
| CATGAATACAAAAG |
YJL016W |
- |
37362668 |
- |
0 |
4 |
3 |
2 |
1 |
10 |
407126 |
407139 |
+ |
405504 |
407472 |
+ |
561 |
Hypothetical ORF |
8 |
| CATGGTGTCGGACG |
YJL048C |
- |
6322413 |
- |
3 |
4 |
0 |
1 |
1 |
10 |
347547 |
347560 |
- |
346864 |
348553 |
- |
396 |
Protein of unknown function; green fluorescent protein
(GFP)-fusion protein localizes to the nuclear periphery |
8 |
| CATGGAACCATTAC |
YJL084C |
- |
6322377 |
- |
0 |
4 |
6 |
1 |
1 |
10 |
275190 |
275203 |
- |
274279 |
277918 |
- |
1046 |
Cytoplasmic protein of unknown function that interacts
with Pcl7p, phosphorylated in vitro; potential Cdc28p substrate |
8 |
| CATGCATTCCTATA |
YJL113W |
- |
6322347 |
- |
6 |
0 |
0 |
4 |
1 |
10 |
201992 |
202005 |
+ |
197834 |
203246 |
+ |
1803 |
TyB Gag-Pol protein; proteolytically processed to make
the Gag, RT, PR, and IN proteins that are required for retrotransposition |
8 |
| CATGACTTTTTCAG |
YJL133C-A |
- |
33438820 |
- |
9 |
12 |
38 |
1 |
1 |
10 |
159422 |
159435 |
- |
159042 |
159765 |
- |
74 |
Yjl133c-ap |
2 |
| CATGCCACTGTCAG |
YJL144W |
- |
6322317 |
- |
6 |
8 |
93 |
1 |
1 |
10 |
146689 |
146702 |
+ |
146277 |
147018 |
+ |
104 |
Hypothetical ORF |
12 |
| CATGAGACAAACTT |
YJL200C |
- |
6322261 |
COG1048 |
0 |
0 |
6 |
1 |
1 |
10 |
56711 |
56724 |
- |
55945 |
58813 |
- |
789 |
Hypothetical ORF |
3 |
| CATGCTGATGGTAG |
YJL225C |
- |
6322237 |
COG0513 |
9 |
4 |
3 |
18 |
1 |
10 |
557 |
570 |
- |
-33 |
6130 |
- |
1758 |
Hypothetical ORF |
8 |
| CATGTGACAAGTAT |
YJR008W |
- |
6322467 |
COG1355 |
6 |
0 |
0 |
1 |
1 |
10 |
453297 |
453310 |
+ |
452344 |
453859 |
+ |
338 |
Hypothetical ORF |
8 |
| CATGAAGAAGTTTG |
YJR061W |
- |
6322521 |
- |
0 |
0 |
13 |
1 |
1 |
10 |
552664 |
552677 |
+ |
550425 |
553731 |
+ |
935 |
Hypothetical ORF |
3 |
| CATGAGCTCATTGG |
YJR072C |
- |
6322532 |
COG1100 |
3 |
4 |
0 |
1 |
1 |
10 |
571386 |
571399 |
- |
570513 |
572038 |
- |
385 |
Protein required for cell viability |
8 |
| CATGCATATATGTA |
YJR080C |
- |
6322540 |
- |
0 |
8 |
0 |
2 |
1 |
10 |
580252 |
580265 |
- |
579847 |
581530 |
- |
394 |
The authentic, non-tagged protein was localized to the
mitochondria |
8 |
| CATGTAGCTTTTTC |
YJR096W |
- |
6322556 |
COG0656 |
6 |
21 |
3 |
1 |
1 |
10 |
612034 |
612047 |
+ |
611112 |
612329 |
+ |
282 |
Protein with similarity to aldo-keto reductases |
9 |
| CATGGGTGCTTCCG |
YKL027W |
- |
6322825 |
COG1179 |
3 |
4 |
13 |
1 |
1 |
11 |
387833 |
387846 |
+ |
387205 |
389047 |
+ |
447 |
Hypothetical ORF |
3 |
| CATGAGAAAAAATC |
YKL033W |
- |
6322819 |
- |
6 |
4 |
0 |
2 |
1 |
11 |
377981 |
377994 |
+ |
375099 |
378714 |
+ |
1038 |
The authentic, non-tagged protein was localized to the
mitochondria |
8 |
| CATGCTGTTTTGGG |
YKL033W-A |
- |
42759861 |
- |
0 |
8 |
0 |
1 |
1 |
11 |
374762 |
374775 |
+ |
374148 |
375098 |
+ |
236 |
Similar to S. pombe hypothetical proteins |
8 |
| CATGTGAGAGAGAT |
YKL047W |
- |
6322804 |
- |
0 |
0 |
6 |
1 |
1 |
11 |
350678 |
350691 |
+ |
349108 |
351157 |
+ |
516 |
Hypothetical ORF |
3 |
| CATGTTGAACTACC |
YKL056C |
- |
6322794 |
- |
3 |
8 |
0 |
2 |
1 |
11 |
334121 |
334134 |
- |
333615 |
334560 |
- |
167 |
Hypothetical ORF |
8 |
| CATGGTCTTTTCAC |
YKL061W |
- |
6322789 |
- |
0 |
8 |
0 |
1 |
1 |
11 |
326106 |
326119 |
+ |
325416 |
326256 |
+ |
113 |
Hypothetical ORF |
8 |
| CATGTAGAAACCAG |
YKL063C |
- |
6322787 |
- |
3 |
4 |
6 |
1 |
1 |
11 |
320493 |
320506 |
- |
320161 |
321163 |
- |
167 |
Hypothetical ORF |
8 |
| CATGTCTATTGTCA |
YKL065C |
- |
6322785 |
COG5374 |
0 |
8 |
0 |
1 |
1 |
11 |
316326 |
316339 |
- |
315583 |
316702 |
- |
206 |
Yeast homolog of human BAP31 protein |
8 |
| CATGCATACTCTAT |
YKL091C |
- |
6322759 |
- |
6 |
4 |
0 |
1 |
1 |
11 |
269308 |
269321 |
- |
269105 |
270295 |
- |
310 |
Sec14p homolog |
8 |
| CATGCGACCATCGT |
YKL107W |
- |
6322742 |
COG1028 |
6 |
8 |
0 |
1 |
1 |
11 |
236771 |
236784 |
+ |
235787 |
237181 |
+ |
309 |
Hypothetical ORF |
8 |
| CATGTCTGCAAATA |
YKL121W |
- |
6322728 |
COG2319 |
0 |
8 |
0 |
1 |
1 |
11 |
216400 |
216413 |
+ |
213788 |
216845 |
+ |
852 |
Hypothetical ORF |
8 |
| CATGCAGTGATGCA |
YKL151C |
- |
6322698 |
COG0063 |
30 |
34 |
6 |
1 |
1 |
11 |
164905 |
164918 |
- |
164423 |
165935 |
- |
337 |
Hypothetical ORF |
5 |
| CATGGGCAATAGCC |
YKR045C |
- |
37362675 |
- |
3 |
0 |
13 |
2 |
1 |
11 |
522971 |
522984 |
- |
522561 |
523611 |
- |
183 |
Hypothetical ORF |
3 |
| CATGAGAACTTCGT |
YKR049C |
- |
6322902 |
- |
9 |
0 |
0 |
1 |
1 |
11 |
526686 |
526699 |
- |
526283 |
526873 |
- |
133 |
The authentic, non-tagged protein was localized to the
mitochondria |
8 |
| CATGCGATGTCATT |
YKR089C |
- |
6322942 |
COG1752 |
6 |
0 |
0 |
2 |
1 |
11 |
607533 |
607546 |
- |
605060 |
608006 |
- |
910 |
Protein of unknown function found in lipid particles;
potential Cdc28p substrate |
8 |
| CATGACAACAGTAT |
YLL014W |
- |
6323015 |
- |
3 |
0 |
3 |
1 |
1 |
12 |
121767 |
121780 |
+ |
121321 |
122146 |
+ |
108 |
Hypothetical ORF |
8 |
| CATGTGTGCGTATA |
YLL049W |
- |
6322979 |
- |
6 |
0 |
0 |
1 |
1 |
12 |
41205 |
41218 |
+ |
40665 |
41703 |
+ |
179 |
Hypothetical ORF |
8 |
| CATGCTGATGGTAG |
YLL066C |
- |
6322962 |
COG0513 |
9 |
4 |
3 |
18 |
1 |
12 |
6214 |
6227 |
- |
5621 |
9836 |
- |
1205 |
Hypothetical ORF |
8 |
| CATGCTGATGGTAG |
YLL067C |
- |
6322961 |
COG0513 |
9 |
4 |
3 |
18 |
1 |
12 |
578 |
591 |
- |
86 |
4301 |
- |
1205 |
Hypothetical ORF |
8 |
| CATGCAACACCTCC |
YLR004C |
- |
6323032 |
COG0477 |
6 |
4 |
0 |
1 |
1 |
12 |
158223 |
158236 |
- |
157730 |
159504 |
- |
523 |
Hypothetical ORF |
8 |
| CATGGCGCAGTTGG |
YLR035C-A |
- |
6323064 |
- |
3 |
4 |
0 |
5 |
1 |
12 |
214937 |
214950 |
- |
214942 |
218908 |
- |
1155 |
Ty ORF |
8 |
| CATGGCGAATAGTG |
YLR049C |
- |
6323078 |
- |
3 |
4 |
0 |
1 |
1 |
12 |
243776 |
243789 |
- |
243388 |
245173 |
- |
428 |
Hypothetical ORF |
8 |
| CATGCTACACAGGT |
YLR065C |
- |
6323094 |
- |
6 |
4 |
3 |
1 |
1 |
12 |
266268 |
266281 |
- |
265875 |
266919 |
- |
181 |
Hypothetical ORF |
8 |
| CATGTATATATGGT |
YLR077W |
- |
6323106 |
COG5184 |
6 |
0 |
0 |
1 |
1 |
12 |
285689 |
285702 |
+ |
283873 |
286123 |
+ |
583 |
The authentic, non-tagged protein was localized to the
mitochondria |
8 |
| CATGGGCAAGAAGA |
YLR149C |
- |
6323178 |
- |
3 |
0 |
10 |
2 |
1 |
12 |
437658 |
437671 |
- |
437133 |
439824 |
- |
730 |
Hypothetical ORF |
8 |
| CATGTGGTGATCAC |
YLR152C |
- |
6323181 |
COG0679 |
6 |
4 |
0 |
1 |
1 |
12 |
443066 |
443079 |
- |
442739 |
444689 |
- |
576 |
Hypothetical ORF |
8 |
| CATGCCAGGTCGTA |
YLR154C-G |
- |
33438833 |
- |
6 |
17 |
44 |
2 |
1 |
12 |
462484 |
462497 |
- |
462024 |
462672 |
- |
49 |
Identified by fungal homology and RT-PCR |
2 |
| CATGCTCTTGCCAA |
YLR154W-E |
- |
33438831 |
- |
0 |
0 |
20 |
2 |
2 |
12 |
455882 |
455895 |
+ |
455434 |
455883 |
+ |
67 |
Identified by gene-trapping, microarray-based expression
analysis, and genome-wide homology searching |
2 |
| CATGCTCTTGCCAA |
YLR154W-F |
- |
33438832 |
- |
0 |
0 |
20 |
2 |
1 |
12 |
455882 |
455895 |
+ |
455884 |
456523 |
+ |
46 |
Identified by expression profiling and mass spectrometry |
2 |
| CATGGCACTGCATA |
YLR168C |
- |
6323197 |
- |
39 |
34 |
6 |
1 |
1 |
12 |
499543 |
499556 |
- |
499081 |
500272 |
- |
230 |
possibly involved in intramitochondrial sorting |
13 |
| CATGCCGAACGGTT |
YLR179C |
- |
6323208 |
COG1881 |
3 |
0 |
17 |
1 |
1 |
12 |
514016 |
514029 |
- |
513824 |
514715 |
- |
201 |
Protein of unknown function, transcription is activated
by paralogous transcription factors Yrm1p and Yrr1p along with genes involved
in multidrug resistance |
3 |
| CATGTTTCCGCGGA |
YLR221C |
- |
6323250 |
- |
3 |
4 |
6 |
1 |
1 |
12 |
578314 |
578327 |
- |
577865 |
579026 |
- |
220 |
RiboSome Assembly |
8 |
| CATGGAGTTTGGCC |
YLR224W |
- |
6323253 |
- |
0 |
0 |
10 |
2 |
1 |
12 |
587384 |
587397 |
+ |
586466 |
588074 |
+ |
369 |
Hypothetical ORF |
3 |
| CATGCAAACTGGTA |
YLR225C |
- |
6323254 |
- |
0 |
8 |
0 |
2 |
1 |
12 |
587374 |
587387 |
- |
587198 |
588920 |
- |
407 |
Hypothetical ORF |
8 |
| CATGCACTTCAACT |
YLR227W-B |
- |
7839187 |
- |
12 |
8 |
3 |
20 |
1 |
12 |
598370 |
598383 |
+ |
593440 |
598708 |
+ |
1755 |
TyB Gag-Pol protein; proteolytically processed to make
the Gag, RT, PR, and IN proteins that are required for retrotransposition |
6 |
| CATGGCAAAAACTA |
YLR254C |
- |
6323283 |
- |
0 |
8 |
0 |
1 |
1 |
12 |
644488 |
644501 |
- |
643907 |
644975 |
- |
189 |
Hypothetical ORF |
8 |
| CATGTTTAATTGGT |
YLR257W |
- |
6323286 |
- |
9 |
0 |
17 |
2 |
1 |
12 |
658852 |
658865 |
+ |
658828 |
660292 |
+ |
321 |
Hypothetical ORF |
8 |
| CATGCCATACAGGT |
YLR264C-A |
- |
33438841 |
- |
6 |
0 |
0 |
1 |
1 |
12 |
673843 |
673856 |
- |
673331 |
673946 |
- |
38 |
Identified by SAGE |
8 |
| CATGCAGATGAGTG |
YLR271W |
- |
6323301 |
- |
3 |
8 |
0 |
2 |
1 |
12 |
683019 |
683032 |
+ |
682739 |
684062 |
+ |
274 |
Hypothetical ORF |
8 |
| CATGATAGTAACGA |
YLR297W |
- |
6323328 |
- |
6 |
17 |
6 |
2 |
1 |
12 |
724505 |
724518 |
+ |
724046 |
724934 |
+ |
129 |
Hypothetical ORF |
9 |
| CATGTCAAACATCC |
YLR327C |
- |
6323359 |
- |
6 |
4 |
41 |
1 |
1 |
12 |
783007 |
783020 |
- |
782628 |
783387 |
- |
86 |
Hypothetical ORF |
2 |
| CATGTTAAGCTATC |
YLR346C |
- |
6323378 |
- |
6 |
0 |
0 |
1 |
1 |
12 |
822257 |
822270 |
- |
821788 |
822592 |
- |
101 |
Protein of unknown function; expression regulated by PDR1 |
8 |
| CATGGATATGTACC |
YLR375W |
- |
6323406 |
COG5048 |
3 |
4 |
10 |
1 |
1 |
12 |
872471 |
872484 |
+ |
871696 |
873226 |
+ |
343 |
Involved in pre-tRNA splicing and in uptake of
branched-chain amino acids |
8 |
| CATGTCAGGTCCAT |
YLR387C |
- |
6323419 |
- |
6 |
12 |
6 |
1 |
1 |
12 |
896308 |
896321 |
- |
895875 |
897672 |
- |
432 |
Hypothetical ORF |
9 |
| CATGCACTTCAACT |
YLR410W-B |
- |
7839190 |
- |
12 |
8 |
3 |
20 |
1 |
12 |
946455 |
946468 |
+ |
941480 |
946793 |
+ |
1770 |
TyB Gag-Pol protein; proteolytically processed to make
the Gag, RT, PR, and IN proteins that are required for retrotransposition |
6 |
| CATGCAACATCACC |
YLR413W |
- |
6323445 |
- |
3 |
8 |
10 |
2 |
1 |
12 |
953196 |
953209 |
+ |
951152 |
953678 |
+ |
675 |
Protein of unknown function; green fluorescent protein
(GFP)-fusion protein localizes to the cell periphery |
8 |
| CATGTATGCGTTGA |
YML005W |
- |
6323638 |
COG2520 |
9 |
4 |
3 |
1 |
1 |
13 |
261570 |
261583 |
+ |
260221 |
262108 |
+ |
462 |
Putative S-adenosylmethionine-dependent methyltransferase
of the seven beta-strand family |
8 |
| CATGTCTGCGCTCT |
YML018C |
- |
6323623 |
COG0697 |
6 |
0 |
6 |
1 |
1 |
13 |
234901 |
234914 |
- |
234272 |
235952 |
- |
393 |
Hypothetical ORF |
8 |
| CATGGTAAGATTGA |
YML131W |
- |
6323504 |
COG2130 |
9 |
4 |
0 |
1 |
1 |
13 |
11152 |
11165 |
+ |
10199 |
11795 |
+ |
365 |
Hypothetical ORF |
8 |
| CATGCTGATGGTAG |
YML133C |
- |
6323502 |
COG0513 |
9 |
4 |
3 |
18 |
1 |
13 |
555 |
568 |
- |
-38 |
4684 |
- |
1374 |
Hypothetical ORF |
8 |
| CATGTCGAAGTCGT |
YMR073C |
- |
6323718 |
COG5274 |
3 |
4 |
0 |
1 |
1 |
13 |
412742 |
412755 |
- |
411768 |
412872 |
- |
201 |
Hypothetical ORF |
8 |
| CATGAAAACATTGA |
YMR086W |
- |
6323732 |
- |
3 |
0 |
6 |
2 |
1 |
13 |
440199 |
440212 |
+ |
439207 |
442525 |
+ |
960 |
Protein of unknown function; green fluorescent protein
(GFP)-fusion protein localizes to the cell periphery |
8 |
| CATGCGAAAAGGCT |
YMR090W |
- |
6323737 |
COG0702 |
24 |
17 |
13 |
1 |
1 |
13 |
449553 |
449566 |
+ |
449244 |
450426 |
+ |
227 |
Hypothetical ORF |
5 |
| CATGGCTAGTGTTC |
YMR105W-A |
- |
33438854 |
- |
0 |
0 |
10 |
1 |
1 |
13 |
478169 |
478182 |
+ |
478063 |
478756 |
+ |
64 |
Identified by gene-trapping, microarray-based expression
analysis, and genome-wide homology searching |
3 |
| CATGTTTCCTATAA |
YMR122W-A |
- |
9755340 |
- |
6 |
0 |
0 |
1 |
1 |
13 |
511750 |
511763 |
+ |
511314 |
512067 |
+ |
84 |
Hypothetical ORF |
8 |
| CATGCCAAAAGGCA |
YMR178W |
- |
6323832 |
COG1058 |
3 |
0 |
3 |
1 |
1 |
13 |
618851 |
618864 |
+ |
618478 |
619801 |
+ |
274 |
Hypothetical ORF |
8 |
| CATGGGGCTTCTTT |
YMR181C |
- |
6323835 |
- |
0 |
0 |
10 |
1 |
1 |
13 |
623575 |
623588 |
- |
623213 |
624079 |
- |
154 |
Hypothetical ORF |
3 |
| CATGTAACATAATA |
YMR182W-A |
- |
33438856 |
- |
9 |
0 |
0 |
1 |
1 |
13 |
625834 |
625847 |
+ |
625810 |
626395 |
+ |
28 |
Identified by gene-trapping, microarray-based expression
analysis, and genome-wide homology searching |
8 |
| CATGAAGGCGAAAA |
YMR187C |
- |
6323841 |
- |
0 |
0 |
13 |
1 |
1 |
13 |
634477 |
634490 |
- |
634189 |
635983 |
- |
431 |
Hypothetical ORF |
3 |
| CATGGACGCACGTT |
YMR191W |
- |
37362682 |
- |
9 |
4 |
34 |
1 |
1 |
13 |
646832 |
646845 |
+ |
645655 |
647116 |
+ |
373 |
Protein required for survival at high temperature during
stationary phase |
2 |
| CATGCCAGAAGGAG |
YMR194C-B |
- |
33438857 |
- |
3 |
4 |
10 |
1 |
1 |
13 |
652862 |
652875 |
- |
652094 |
652886 |
- |
73 |
Identified based on homology to Ashbya gossypii |
8 |
| CATGTAGATACAAA |
YMR244C-A |
- |
6323902 |
- |
12 |
0 |
0 |
1 |
1 |
13 |
758420 |
758433 |
- |
758017 |
758830 |
- |
104 |
Hypothetical ORF |
6 |
| CATGCCAAGCGTGG |
YMR244W |
- |
6323900 |
- |
0 |
0 |
6 |
1 |
1 |
13 |
757377 |
757390 |
+ |
757249 |
758815 |
+ |
355 |
Hypothetical ORF |
3 |
| CATGGCTGTGACTT |
YMR251W |
- |
6323906 |
COG0435 |
6 |
0 |
0 |
1 |
1 |
13 |
774297 |
774310 |
+ |
772914 |
774513 |
+ |
366 |
Hypothetical ORF |
8 |
| CATGGACGAGCACA |
YMR252C |
- |
6323908 |
- |
3 |
4 |
0 |
1 |
1 |
13 |
775459 |
775472 |
- |
774815 |
775718 |
- |
134 |
Hypothetical ORF |
8 |
| CATGATAAGGATGG |
YMR278W |
- |
6323934 |
COG1109 |
3 |
4 |
0 |
1 |
1 |
13 |
824078 |
824091 |
+ |
822762 |
825129 |
+ |
622 |
Hypothetical ORF |
8 |
| CATGTTCTGTGTGA |
YMR295C |
- |
6323953 |
- |
6 |
8 |
13 |
1 |
1 |
13 |
858641 |
858654 |
- |
857797 |
858889 |
- |
197 |
Protein of unknown function; green fluorescent protein
(GFP)-fusion protein localizes to the cell periphery and bud |
3 |
| CATGCAATCGAGGC |
YNL045W |
- |
6324283 |
COG0308 |
3 |
4 |
0 |
1 |
1 |
14 |
545108 |
545121 |
+ |
542961 |
545265 |
+ |
671 |
Similar to human LTA4 hydrolase but in vivo substrates
not yet defined. |
8 |
| CATGAAAAAAAAAA |
YNL067W-B |
- |
33438868 |
- |
3 |
0 |
3 |
13 |
1 |
14 |
499551 |
499564 |
+ |
499416 |
499679 |
+ |
46 |
Ynl067w-bp |
8 |
| CATGAAAAAAATAA |
YNL080C |
- |
6324249 |
- |
6 |
4 |
0 |
4 |
1 |
14 |
476921 |
476934 |
- |
476619 |
478031 |
- |
366 |
Deletion causes slight growth defect, similar to U.
maydis myp1 protein |
8 |
| CATGAGTATAGCTA |
YNL081C |
- |
6324248 |
COG0099 |
3 |
4 |
0 |
1 |
1 |
14 |
476440 |
476453 |
- |
475688 |
476618 |
- |
143 |
Putative mitochondrial ribosomal protein of the small
subunit, has similarity to E. coli S13 ribosomal protein |
8 |
| CATGTATAGCATAA |
YNL086W |
- |
6324243 |
- |
0 |
8 |
0 |
1 |
1 |
14 |
466653 |
466666 |
+ |
466334 |
467130 |
+ |
102 |
Hypothetical ORF |
8 |
| CATGATGAAGCTGT |
YNL108C |
- |
6324221 |
COG0406 |
6 |
0 |
0 |
1 |
1 |
14 |
418936 |
418949 |
- |
418515 |
419826 |
- |
270 |
Hypothetical ORF |
8 |
| CATGCTCTCATATC |
YNL116W |
- |
6324213 |
COG1716 |
3 |
4 |
3 |
1 |
1 |
14 |
409731 |
409744 |
+ |
408341 |
410408 |
+ |
522 |
Hypothetical ORF |
8 |
| CATGGGTAGGTAAG |
YNL144C |
- |
6324185 |
- |
3 |
0 |
3 |
1 |
1 |
14 |
353023 |
353036 |
- |
352321 |
355042 |
- |
740 |
Hypothetical ORF |
8 |
| CATGGGTGGATACC |
YNL149C |
- |
6324180 |
- |
3 |
8 |
0 |
1 |
1 |
14 |
349723 |
349736 |
- |
348868 |
349756 |
- |
129 |
Protein required for cell viability |
8 |
| CATGGATTTTTATT |
YNL156C |
- |
6324173 |
- |
3 |
0 |
3 |
2 |
1 |
14 |
341121 |
341134 |
- |
340570 |
341968 |
- |
299 |
Protein of unknown function, potential homolog of
mammalian Insig 1 |
8 |
| CATGCAGAAAAGAA |
YNL157W |
- |
6324172 |
- |
6 |
0 |
0 |
1 |
1 |
14 |
340515 |
340528 |
+ |
340352 |
341357 |
+ |
168 |
Hypothetical ORF |
8 |
| CATGGTTTCCTTTC |
YNL190W |
- |
6324139 |
- |
3 |
4 |
6 |
3 |
1 |
14 |
283329 |
283342 |
+ |
282394 |
283507 |
+ |
204 |
Hypothetical ORF |
8 |
| CATGAGCACACGCT |
YNL191W |
- |
6324138 |
COG0121 |
3 |
4 |
0 |
1 |
1 |
14 |
281499 |
281512 |
+ |
280431 |
282003 |
+ |
357 |
Hypothetical ORF |
8 |
| CATGATTCTCTTTT |
YNL200C |
- |
6324129 |
COG0062 |
3 |
4 |
0 |
1 |
1 |
14 |
263625 |
263638 |
- |
263213 |
264452 |
- |
246 |
Hypothetical ORF; similarity to human TGR-CL10C,
thyroidal receptor for N-acetylglucosamine |
8 |
| CATGTCCAAAATAG |
YNL201C |
- |
6324128 |
- |
0 |
0 |
24 |
3 |
1 |
14 |
260394 |
260407 |
- |
260127 |
263202 |
- |
858 |
Platinum Sensitivity |
2 |
| CATGCGGCAGTGAA |
YNL227C |
- |
6324103 |
COG2214 |
3 |
4 |
0 |
1 |
1 |
14 |
220700 |
220713 |
- |
220201 |
222430 |
- |
590 |
Protein that may function as a cochaperone, as suggested
by the presence of a DnaJ-like domain |
8 |
| CATGGTTGTGAATA |
YNL274C |
- |
6324055 |
COG1052 |
0 |
8 |
0 |
1 |
1 |
14 |
121545 |
121558 |
- |
120617 |
122168 |
- |
350 |
Putative hydroxyisocaproate dehydrogenase |
8 |
| CATGATGCTTTACC |
YNL305C |
- |
6324024 |
COG0670 |
0 |
8 |
10 |
1 |
1 |
14 |
58962 |
58975 |
- |
58399 |
59791 |
- |
297 |
Hypothetical ORF |
8 |
| CATGTATATATATA |
YNR014W |
- |
6324341 |
- |
15 |
0 |
0 |
15 |
1 |
14 |
653199 |
653212 |
+ |
652464 |
653385 |
+ |
212 |
Hypothetical ORF |
6 |
| CATGTTATCAGAGG |
YNR036C |
- |
6324364 |
COG0048 |
3 |
8 |
13 |
1 |
1 |
14 |
694438 |
694451 |
- |
694047 |
694821 |
- |
153 |
Putative mitochondrial ribosomal protein of the small
subunit, has similarity to E. coli and human mitochondrial S12 ribosomal
proteins |
3 |
| CATGTCCAAAATAG |
YOL022C |
- |
6324551 |
- |
0 |
0 |
24 |
3 |
1 |
15 |
281485 |
281498 |
- |
279773 |
281498 |
- |
408 |
Protein required for cell viability |
2 |
| CATGGTGGGACAAA |
YOL032W |
- |
6324541 |
- |
3 |
0 |
13 |
1 |
1 |
15 |
266098 |
266111 |
+ |
265429 |
266668 |
+ |
246 |
Hypothetical ORF |
3 |
| CATGTAACATTGTG |
YOR006C |
- |
6324579 |
COG2042 |
6 |
0 |
0 |
1 |
1 |
15 |
337618 |
337631 |
- |
337344 |
338621 |
- |
313 |
Hypothetical ORF |
8 |
| CATGATTTGGCCAT |
YOR044W |
- |
6324618 |
- |
0 |
0 |
6 |
2 |
1 |
15 |
413568 |
413581 |
+ |
413006 |
413850 |
+ |
157 |
Hypothetical ORF |
3 |
| CATGCTTGTAATGG |
YOR052C |
- |
6324626 |
COG3582 |
0 |
4 |
3 |
1 |
1 |
15 |
426860 |
426873 |
- |
426274 |
427225 |
- |
150 |
Hypothetical ORF |
8 |
| CATGGCACGACATA |
YOR097C |
- |
6324671 |
- |
3 |
12 |
0 |
1 |
1 |
15 |
506982 |
506995 |
- |
506479 |
507505 |
- |
175 |
Hypothetical ORF |
9 |
| CATGGTTCCATACA |
YOR192C |
- |
6324766 |
COG1953 |
3 |
8 |
0 |
2 |
1 |
15 |
698970 |
698983 |
- |
698269 |
700567 |
- |
599 |
Hypothetical ORF |
8 |
| CATGCACTTCAACT |
YOR192C-B |
- |
7839201 |
- |
12 |
8 |
3 |
20 |
1 |
15 |
704742 |
704755 |
- |
704225 |
709732 |
- |
1770 |
TyB Gag-Pol protein; proteolytically processed to make
the Gag, RT, PR, and IN proteins that are required for retrotransposition |
6 |
| CATGTATGTTTGCA |
YOR220W |
- |
6324794 |
- |
6 |
4 |
20 |
1 |
1 |
15 |
756277 |
756290 |
+ |
755328 |
756624 |
+ |
265 |
Hypothetical ORF |
2 |
| CATGTTTCTGCTGG |
YOR228C |
- |
6324802 |
- |
0 |
0 |
6 |
2 |
1 |
15 |
767424 |
767437 |
- |
766370 |
767777 |
- |
302 |
Hypothetical ORF |
3 |
| CATGCGTGTATTTT |
YOR283W |
- |
6324857 |
COG0406 |
6 |
0 |
0 |
1 |
1 |
15 |
848219 |
848232 |
+ |
847450 |
848474 |
+ |
230 |
Hypothetical ORF |
8 |
| CATGGGGGTGATAA |
YOR285W |
- |
6324859 |
COG0607 |
6 |
12 |
13 |
1 |
1 |
15 |
850024 |
850037 |
+ |
849632 |
850276 |
+ |
139 |
Hypothetical ORF |
8 |
| CATGTAGCGCAACC |
YOR289W |
- |
6324863 |
COG2078 |
6 |
4 |
13 |
1 |
1 |
15 |
853888 |
853901 |
+ |
853354 |
854608 |
+ |
251 |
Hypothetical ORF |
3 |
| CATGGTTTTCCCAA |
YOR291W |
- |
6324865 |
COG0474 |
6 |
0 |
0 |
2 |
1 |
15 |
863204 |
863217 |
+ |
861172 |
866089 |
+ |
1472 |
Hypothetical ORF |
8 |
| CATGTGATCTTTAT |
YOR338W |
- |
6324914 |
- |
0 |
0 |
10 |
1 |
1 |
15 |
957790 |
957803 |
+ |
956893 |
958483 |
+ |
363 |
Hypothetical ORF |
3 |
| CATGCACTTCAACT |
YOR343W-B |
- |
20336770 |
- |
12 |
8 |
3 |
20 |
1 |
15 |
975548 |
975561 |
+ |
970573 |
975886 |
+ |
1770 |
TyB Gag-Pol protein; proteolytically processed to make
the Gag, RT, PR, and IN proteins that are required for retrotransposition |
6 |
| CATGCCAGCAAGAT |
YOR389W |
- |
6324965 |
- |
0 |
0 |
6 |
2 |
1 |
15 |
1076221 |
1076234 |
+ |
1074209 |
1076582 |
+ |
624 |
Hypothetical ORF |
3 |
| CATGCTGATGGTAG |
YOR396W |
- |
9755360 |
COG0513 |
9 |
4 |
3 |
18 |
1 |
15 |
1090750 |
1090763 |
+ |
1087185 |
1091358 |
+ |
1224 |
Hypothetical ORF |
8 |
| CATGGTGGTGCTTT |
YPL009C |
- |
6325248 |
COG1293 |
3 |
4 |
0 |
1 |
1 |
16 |
536948 |
536961 |
- |
535316 |
538931 |
- |
1038 |
Hypothetical ORF |
8 |
| CATGACCTATAATG |
YPL014W |
- |
6325243 |
- |
3 |
4 |
0 |
1 |
1 |
16 |
528717 |
528730 |
+ |
527542 |
529186 |
+ |
381 |
Hypothetical ORF |
8 |
| CATGAAACCGTTCA |
YPL017C |
- |
6325240 |
COG1249 |
3 |
4 |
0 |
1 |
1 |
16 |
519781 |
519794 |
- |
518231 |
520229 |
- |
499 |
Putative S-adenosylmethionine-dependent methyltransferase
of the seven beta-strand family |
8 |
| CATGGAATCTCAAT |
YPL052W |
- |
6325205 |
- |
3 |
4 |
0 |
1 |
1 |
16 |
459066 |
459079 |
+ |
459068 |
459957 |
+ |
201 |
Hypothetical ORF |
8 |
| CATGACACCTGCTG |
YPL088W |
- |
6325169 |
COG0667 |
0 |
0 |
6 |
1 |
1 |
16 |
383052 |
383065 |
+ |
381960 |
383449 |
+ |
342 |
Putative aryl alcohol dehydrogenase; transcription is
activated by paralogous transcription factors Yrm1p and Yrr1p along with
genes involved in multidrug resistance |
3 |
| CATGAGGAGAGAGA |
YPL099C |
- |
6325158 |
- |
0 |
0 |
6 |
2 |
1 |
16 |
363659 |
363672 |
- |
363016 |
364063 |
- |
182 |
The authentic, non-tagged protein was localized to the
mitochondria |
3 |
| CATGCATACATATA |
YPL107W |
- |
6325150 |
- |
9 |
4 |
0 |
1 |
1 |
16 |
350013 |
350026 |
+ |
349114 |
350359 |
+ |
248 |
Hypothetical ORF |
8 |
| CATGTGCTTAACTA |
YPL110C |
- |
6325147 |
COG5408 |
3 |
0 |
6 |
1 |
1 |
16 |
340991 |
341004 |
- |
340568 |
344738 |
- |
1223 |
Hypothetical ORF |
8 |
| CATGAAACCGTCCC |
YPL183W-A |
- |
6325073 |
COG0257 |
3 |
4 |
3 |
1 |
1 |
16 |
199140 |
199153 |
+ |
199094 |
199874 |
+ |
93 |
Putative mitochondrial ribosomal protein of the large
subunit, has similarity to E. coli L36 ribosomal protein |
8 |
| CATGTTCAACGCAA |
YPL221W |
- |
6325035 |
- |
9 |
21 |
0 |
1 |
1 |
16 |
134405 |
134418 |
+ |
133042 |
135788 |
+ |
793 |
Protein of unknown function, overproduction suppresses a
pam1 slv3 double null mutation |
9 |
| CATGTAATATGGCG |
YPL222W |
- |
6325034 |
COG0397 |
9 |
4 |
0 |
1 |
1 |
16 |
132282 |
132295 |
+ |
130161 |
132726 |
+ |
688 |
The authentic, non-tagged protein was localized to the
mitochondria. |
8 |
| CATGCATATATATT |
YPL225W |
- |
6325031 |
- |
6 |
0 |
0 |
2 |
1 |
16 |
126447 |
126460 |
+ |
126006 |
126945 |
+ |
146 |
Hypothetical ORF |
8 |
| CATGCCATTTTTCT |
YPL229W |
- |
6325027 |
- |
3 |
4 |
0 |
2 |
1 |
16 |
117956 |
117969 |
+ |
117067 |
118186 |
+ |
206 |
Hypothetical ORF |
8 |
| CATGCCAGCAAGAT |
YPL278C |
- |
6324977 |
- |
0 |
0 |
6 |
2 |
1 |
16 |
14900 |
14913 |
- |
14554 |
15355 |
- |
100 |
Hypothetical ORF |
3 |
| CATGCAGCAATTTA |
YPR004C |
- |
6325261 |
COG2025 |
6 |
0 |
0 |
1 |
1 |
16 |
564796 |
564809 |
- |
563764 |
565036 |
- |
344 |
Hypothetical ORF |
8 |
| CATGAAAGGAAAAG |
YPR013C |
- |
6325270 |
COG5048 |
0 |
0 |
10 |
2 |
1 |
16 |
584651 |
584664 |
- |
584128 |
585580 |
- |
317 |
Hypothetical ORF |
3 |
| CATGTCGACAACCC |
YPR093C |
- |
37362706 |
- |
6 |
0 |
3 |
1 |
1 |
16 |
719161 |
719174 |
- |
719055 |
720420 |
- |
288 |
Hypothetical ORF |
8 |
| CATGTGCATATATG |
YPR114W |
- |
6325371 |
- |
9 |
4 |
10 |
2 |
1 |
16 |
754264 |
754277 |
+ |
753297 |
754743 |
+ |
315 |
Hypothetical ORF |
8 |
| CATGTGCTGAATTG |
YPR127W |
- |
6325384 |
COG0667 |
9 |
0 |
0 |
1 |
1 |
16 |
790683 |
790696 |
+ |
790077 |
791613 |
+ |
345 |
Hypothetical ORF |
8 |
| CATGCACTTCAACT |
YPR137C-B |
- |
7839207 |
- |
12 |
8 |
3 |
20 |
1 |
16 |
805318 |
805331 |
- |
804496 |
810263 |
- |
1755 |
TyB Gag-Pol protein; proteolytically processed to make
the Gag, RT, PR, and IN proteins that are required for retrotransposition |
6 |
| CATGTAAATATGTA |
YPR147C |
- |
6325405 |
- |
9 |
0 |
0 |
2 |
1 |
16 |
825476 |
825489 |
- |
825140 |
826553 |
- |
304 |
Hypothetical ORF |
8 |
| CATGGAAGTACAAT |
YPR151C |
- |
6325409 |
- |
3 |
0 |
24 |
1 |
1 |
16 |
831222 |
831235 |
- |
830550 |
831669 |
- |
206 |
Ypr151cp |
2 |
| CATGTCTGCAGACA |
YPR158W |
- |
6325416 |
- |
3 |
4 |
38 |
1 |
1 |
16 |
843785 |
843798 |
+ |
843256 |
844513 |
+ |
252 |
Hypothetical ORF |
2 |
| CATGGGATCAAGAA |
YPR169W |
- |
6325427 |
COG2319 |
6 |
0 |
0 |
1 |
1 |
16 |
880132 |
880145 |
+ |
878618 |
880661 |
+ |
514 |
Jumonji Interacting Protein |
8 |
| CATGGAAGACAAAA |
YPR174C |
- |
6325432 |
- |
6 |
0 |
0 |
3 |
1 |
16 |
887870 |
887883 |
- |
887832 |
888702 |
- |
221 |
Protein of unknown function; green fluorescent protein
(GFP)-fusion protein localizes to the nuclear periphery; potential Cdc28p
substrate |
8 |
| CATGCTGATGGTAG |
YPR204W |
- |
6325462 |
COG0513 |
9 |
4 |
3 |
18 |
1 |
16 |
947589 |
947602 |
+ |
944597 |
948194 |
+ |
1032 |
subtelomerically-encoded DNA helicase |
8 |
| CATGCCAAAGGAAG |
YLR348C |
Dic-01 |
6323381 |
- |
3 |
0 |
3 |
1 |
1 |
12 |
826983 |
826996 |
- |
826477 |
827872 |
- |
298 |
Mitochondrial dicarboxylate carrier, integral membrane
protein, catalyzes a dicarboxylate-phosphate exchange across the inner
mitochondrial membrane, transports cytoplasmic
dicarboxylates into the mitochondrial matrix |
8 |
|
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