chr. |
ORF's name |
start |
stop |
length |
S1 |
S2 |
V1 |
V2 |
D |
cod. prob. |
YZ score |
MIPS |
Genol. |
T |
Wood's
annotation |
brief ID |
7 |
TY1A_GR1 |
536051 |
537370 |
440 |
-7.35 |
-53.60 |
2.98 |
5.86 |
2.22 |
0.79 |
0.61 |
1 |
|
|
|
TY1A protein |
7 |
TY1A_GR2 |
567461 |
566142 |
440 |
-9.16 |
-54.89 |
2.99 |
5.89 |
2.29 |
0.78 |
0.62 |
1 |
|
|
|
TY1A protein |
7 |
TY1A_GR3 |
823010 |
821691 |
440 |
-8.13 |
-54.78 |
3.03 |
5.95 |
2.24 |
0.79 |
0.57 |
1 |
|
|
|
TY1A protein |
7 |
TY1B_GR1 |
536051 |
541316 |
1755 |
10.17 |
-47.95 |
6.35 |
8.20 |
1.43 |
0.93 |
0.59 |
1 |
|
|
|
TY1B protein |
7 |
TY1B_GR2 |
567461 |
562196 |
1755 |
10.86 |
-48.37 |
6.59 |
8.34 |
1.40 |
0.93 |
0.60 |
1 |
|
|
|
TY1B protein |
7 |
TY1B_GR3 |
823010 |
817745 |
1755 |
11.02 |
-48.20 |
6.37 |
8.17 |
1.39 |
0.93 |
0.59 |
1 |
|
|
|
TY1B protein |
7 |
TY2A_GR1 |
574136 |
573090 |
349 |
-1.82 |
-44.49 |
3.37 |
4.28 |
1.96 |
0.84 |
0.57 |
1 |
|
|
|
putative pseudo-TY2A |
7 |
TY2A_GR2 |
811733 |
813046 |
438 |
-7.59 |
-46.38 |
2.89 |
5.61 |
2.25 |
0.78 |
0.60 |
1 |
|
|
|
TY2A protein |
7 |
TY2B_A_GR1 |
571392 |
569092 |
767 |
21.25 |
-33.22 |
6.28 |
4.88 |
1.07 |
0.97 |
0.59 |
1 |
|
|
|
putative pseudo-TY2B |
7 |
TY2B_B_GR1 |
573130 |
571967 |
388 |
-2.39 |
-50.86 |
2.44 |
2.81 |
2.17 |
0.80 |
0.53 |
1 |
|
|
|
putative pseudo-TY2B |
7 |
TY2B_GR2 |
811733 |
817043 |
1770 |
11.23 |
-41.16 |
6.83 |
8.52 |
1.40 |
0.93 |
0.59 |
1 |
|
|
|
TY2B protein |
7 |
TY3A_G |
707604 |
708473 |
290 |
13.50 |
-23.20 |
3.02 |
2.24 |
1.65 |
0.90 |
0.53 |
1 |
|
|
|
TY3A protein |
7 |
TY3B_G |
707604 |
712245 |
1547 |
14.20 |
-49.88 |
6.43 |
5.29 |
1.27 |
0.95 |
0.57 |
1 |
|
|
|
TY3B protein |
7 |
YGL001c |
496497 |
495451 |
349 |
56.50 |
-64.36 |
4.36 |
1.48 |
0.97 |
0.97 |
0.72 |
1 |
1 |
5 |
|
C-3 sterol dehydrogenase (C-4
decarboxylase) |
7 |
YGL002w |
494512 |
495159 |
216 |
86.99 |
90.00 |
2.59 |
0.27 |
3.96 |
0.37 |
0.52 |
2 |
1 |
2 |
|
strong similarity to human gp25L2 protein |
7 |
YGL003c |
494169 |
492472 |
566 |
48.01 |
-61.31 |
3.39 |
2.54 |
0.62 |
0.99 |
0.57 |
1 |
1 |
6 |
|
substrate-specific activator of
APC-dependent proteolysis |
7 |
YGL004c |
491951 |
490701 |
417 |
55.55 |
-31.83 |
5.11 |
1.67 |
0.90 |
0.98 |
0.66 |
3 |
1 |
2 |
|
weak similarity to Tup1p |
7 |
YGL005c |
490542 |
489706 |
279 |
55.24 |
-51.55 |
3.57 |
2.60 |
0.55 |
0.99 |
0.61 |
3 |
2 |
4 |
|
weak similarity to Xenopus kinesin-related
protein Eg5 |
7 |
YGL006w |
485916 |
489434 |
1173 |
61.24 |
-88.68 |
7.16 |
2.54 |
1.08 |
0.96 |
0.61 |
1 |
1 |
6 |
|
Ca2+-transporting P-type ATPase |
7 |
YGL006w-a |
485419 |
485526 |
36 |
-54.46 |
-180.00 |
1.43 |
0.67 |
5.34 |
0.09 |
0.35 |
5 |
3 |
0 |
|
hypothetical protein - identified by SAGE |
7 |
YGL007w |
483256 |
483630 |
125 |
47.12 |
-160.35 |
1.71 |
1.33 |
3.07 |
0.59 |
0.57 |
6 |
0 |
0 |
|
questionable ORF |
7 |
YGL008c |
482662 |
479909 |
918 |
83.06 |
-112.66 |
9.01 |
3.68 |
2.00 |
0.83 |
0.72 |
1 |
1 |
7 |
|
H+-transporting P-type ATPase, major
isoform, plasma membrane |
7 |
YGL009c |
478648 |
476312 |
779 |
62.27 |
-51.56 |
7.08 |
2.88 |
0.59 |
0.99 |
0.71 |
1 |
1 |
7 |
|
3-isopropylmalate dehydratase |
7 |
YGL010w |
475541 |
476062 |
174 |
-18.43 |
169.99 |
0.24 |
2.62 |
4.70 |
0.21 |
0.41 |
4 |
2 |
4 |
|
similarity to hypothetical S. pombe protein |
7 |
YGL011c |
475243 |
474488 |
252 |
58.76 |
-61.50 |
4.49 |
2.51 |
0.60 |
0.99 |
0.74 |
1 |
1 |
5 |
|
20S proteasome subunit YC7ALPHA/Y8 (alpha1) |
7 |
YGL012w |
472851 |
474269 |
473 |
123.69 |
-133.15 |
2.16 |
1.01 |
3.88 |
0.39 |
0.46 |
1 |
1 |
6 |
|
sterol C-24 reductase |
7 |
YGL013c |
472294 |
469091 |
1068 |
43.41 |
-40.43 |
4.68 |
3.26 |
0.25 |
1.00 |
0.55 |
1 |
1 |
4 |
|
transcription factor |
7 |
YGL014w |
466137 |
468800 |
888 |
17.04 |
-54.93 |
4.35 |
5.78 |
1.17 |
0.96 |
0.64 |
3 |
1 |
7 |
|
similarity to Drosophila pumilio protein
and Mpt5p protein |
7 |
YGL015c |
465431 |
465042 |
130 |
0.00 |
-29.05 |
1.40 |
1.81 |
2.57 |
0.71 |
0.48 |
5 |
2 |
1 |
|
hypothetical protein |
7 |
YGL016w |
461662 |
464904 |
1081 |
47.21 |
-93.41 |
3.90 |
2.56 |
1.06 |
0.97 |
0.55 |
1 |
1 |
5 |
|
Member of the karyopherin-beta family,
nuclear import |
7 |
YGL017w |
459850 |
461358 |
503 |
62.50 |
-2.54 |
3.67 |
2.01 |
1.39 |
0.93 |
0.60 |
1 |
1 |
5 |
|
arginyl tRNA transferase |
7 |
YGL018c |
459660 |
459109 |
184 |
3.37 |
-25.91 |
1.26 |
2.87 |
2.47 |
0.74 |
0.58 |
1 |
1 |
4 |
|
molecular chaperone |
7 |
YGL019w |
458152 |
458985 |
278 |
97.59 |
1.40 |
3.63 |
2.46 |
2.32 |
0.77 |
0.60 |
1 |
1 |
6 |
|
casein kinase II, beta subunit |
7 |
YGL020c |
457866 |
457162 |
235 |
72.90 |
-74.93 |
2.66 |
1.76 |
1.62 |
0.90 |
0.61 |
4 |
2 |
4 |
|
weak similarity to TRCDSEMBL:SPBC543_10
putative coiled-coil protein S. pombe |
7 |
YGL021w |
454781 |
457060 |
760 |
20.82 |
-53.69 |
2.76 |
3.74 |
1.33 |
0.94 |
0.50 |
1 |
2 |
2 |
|
DNA damage-responsive protein |
7 |
YGL022w |
452400 |
454553 |
718 |
90.00 |
-142.80 |
5.00 |
3.89 |
2.70 |
0.68 |
0.57 |
1 |
1 |
5 |
|
oligosaccharyl transferase subunit |
7 |
YGL023c |
452100 |
450196 |
635 |
26.95 |
-21.64 |
5.34 |
5.17 |
1.01 |
0.97 |
0.64 |
1 |
1 |
6 |
|
phosphatidylinositol 3-phosphate binding |
7 |
YGL024w |
449784 |
450116 |
111 |
107.10 |
-160.14 |
1.29 |
3.63 |
3.83 |
0.40 |
0.41 |
6 |
0 |
0 |
spurious |
questionable ORF |
7 |
YGL025c |
450055 |
448763 |
431 |
1.46 |
-55.05 |
5.69 |
4.88 |
1.77 |
0.88 |
0.66 |
1 |
2 |
1 |
|
mediator complex subunit |
7 |
YGL026c |
448531 |
446411 |
707 |
72.28 |
-75.12 |
6.67 |
2.49 |
1.17 |
0.96 |
0.73 |
1 |
1 |
6 |
|
tryptophan synthase |
7 |
YGL027c |
446139 |
443641 |
833 |
55.74 |
3.97 |
4.86 |
2.50 |
1.30 |
0.94 |
0.59 |
1 |
1 |
7 |
|
ER glucosidase I |
7 |
YGL028c |
442905 |
441280 |
542 |
64.29 |
-84.05 |
3.86 |
7.04 |
1.05 |
0.97 |
0.68 |
3 |
2 |
8 |
|
similarity to glucanase |
7 |
YGL029w |
440059 |
440418 |
120 |
32.47 |
6.34 |
4.76 |
3.31 |
1.40 |
0.93 |
0.60 |
1 |
2 |
2 |
|
Coiled-coil protein, may play a role in
ribosome biogenesis |
7 |
YGL030w |
439087 |
439631 |
105 |
81.57 |
-90.00 |
2.66 |
1.46 |
2.04 |
0.83 |
0.66 |
1 |
1 |
3 |
|
60S large subunit ribosomal protein L30.e |
7 |
YGL031c |
437930 |
437466 |
155 |
42.36 |
-30.65 |
3.70 |
2.52 |
0.63 |
0.99 |
0.67 |
1 |
1 |
3 |
|
60S large subunit ribosomal protein L24.e.A |
7 |
YGL032c |
436829 |
436569 |
87 |
75.96 |
-107.53 |
0.44 |
2.14 |
2.82 |
0.65 |
0.48 |
1 |
3 |
0 |
|
a-agglutinin binding subunit |
7 |
YGL033w |
435247 |
436344 |
185 |
29.90 |
-46.47 |
3.39 |
2.03 |
0.99 |
0.97 |
0.64 |
1 |
2 |
2 |
|
required for pairing of homologous
chromosomes |
7 |
YGL034c |
433575 |
433213 |
121 |
55.49 |
-56.31 |
1.77 |
0.33 |
2.07 |
0.82 |
0.56 |
6 |
0 |
0 |
|
questionable ORF |
7 |
YGL035c |
433058 |
431547 |
504 |
-15.14 |
-48.69 |
3.92 |
3.91 |
2.41 |
0.75 |
0.53 |
1 |
1 |
4 |
|
transcriptional repressor |
7 |
YGL036w |
428597 |
431323 |
909 |
17.26 |
-61.32 |
4.58 |
4.42 |
1.18 |
0.95 |
0.57 |
4 |
2 |
2 |
|
similarity to Ede1p |
7 |
YGL037c |
427944 |
427297 |
216 |
53.62 |
-35.54 |
3.21 |
2.34 |
0.81 |
0.98 |
0.73 |
4 |
1 |
6 |
|
similarity to PIR:B70386
pyrazinamidase/nicotinamidase - Aquifex aeolicus |
7 |
YGL038c |
426801 |
425362 |
480 |
29.25 |
-52.43 |
2.62 |
2.99 |
1.16 |
0.96 |
0.58 |
1 |
2 |
5 |
|
alpha-1,6-mannosyltransferase |
7 |
YGL039w |
423958 |
425001 |
348 |
63.43 |
-57.26 |
4.32 |
1.78 |
0.94 |
0.97 |
0.68 |
3 |
1 |
11 |
|
similarity to V. vinifera dihydroflavonol
reductase |
7 |
YGL040c |
420552 |
419527 |
342 |
72.65 |
-82.87 |
3.63 |
0.87 |
1.74 |
0.88 |
0.65 |
1 |
1 |
3 |
|
porphobilinogen synthase |
7 |
YGL041c |
419222 |
418911 |
104 |
-120.96 |
-156.25 |
0.57 |
2.68 |
7.24 |
0.00 |
0.32 |
4 |
1 |
0 |
very hypoth. |
weak similarity to YJL109c |
7 |
YGL042c |
418588 |
418286 |
101 |
-138.81 |
-148.57 |
1.06 |
2.10 |
7.34 |
0.00 |
0.38 |
6 |
2 |
2 |
spurious |
questionable ORF |
7 |
YGL043w |
417478 |
418404 |
309 |
37.57 |
-24.88 |
4.67 |
4.33 |
0.67 |
0.99 |
0.71 |
1 |
1 |
3 |
|
TFIIS (transcription elongation factor) |
7 |
YGL044c |
417031 |
416144 |
296 |
35.79 |
-14.04 |
3.08 |
1.92 |
1.29 |
0.94 |
0.60 |
1 |
1 |
3 |
|
component of pre-mRNA 3'-end processing
factor CF I |
7 |
YGL045w |
415036 |
415722 |
229 |
31.22 |
-48.65 |
2.55 |
2.20 |
1.23 |
0.95 |
0.62 |
4 |
2 |
1 |
|
similarity to TRCDSEMBL:AF173842_1
Rim8p C. albicans |
7 |
YGL046w |
414100 |
414885 |
262 |
22.17 |
-47.60 |
3.60 |
1.92 |
1.19 |
0.95 |
0.53 |
3 |
2 |
3 |
|
similarity to TRCDSEMBL:AF173842_1
Rim8p C. albicans |
7 |
YGL047w |
411549 |
412154 |
202 |
76.61 |
-168.69 |
1.52 |
0.36 |
3.64 |
0.45 |
0.52 |
4 |
1 |
3 |
|
similarity to hypothetical S. pombe protein |
7 |
YGL048c |
411283 |
410069 |
405 |
46.80 |
-72.65 |
5.59 |
0.83 |
1.30 |
0.94 |
0.69 |
1 |
1 |
5 |
|
26S proteasome regulatory subunit |
7 |
YGL049c |
409601 |
406860 |
914 |
34.86 |
-24.99 |
7.18 |
7.52 |
0.73 |
0.99 |
0.68 |
1 |
1 |
5 |
|
mRNA cap-binding protein (eIF4F), 130K
subunit |
7 |
YGL050w |
405773 |
406591 |
273 |
45.63 |
-14.04 |
3.89 |
1.25 |
1.28 |
0.94 |
0.59 |
4 |
1 |
1 |
|
similarity to hypothetical protein
SPAC25B8.15c S. pombe |
7 |
YGL051w |
403684 |
404385 |
234 |
45.00 |
-64.98 |
1.57 |
1.08 |
1.89 |
0.86 |
0.59 |
4 |
3 |
0 |
very hypoth. |
strong similarity to YAR033w protein |
7 |
YGL052w |
403434 |
403736 |
101 |
-41.99 |
-4.09 |
1.34 |
1.40 |
4.06 |
0.35 |
0.44 |
6 |
0 |
0 |
very hypoth. |
questionable ORF |
7 |
YGL053w |
402586 |
403296 |
237 |
56.82 |
-50.91 |
2.02 |
1.34 |
1.61 |
0.90 |
0.60 |
4 |
3 |
0 |
|
strong similarity to hypothetical proteins
YAR031w, YGL051w, YAR028w, YAR033w and YCR007c |
7 |
YGL054c |
401284 |
400871 |
138 |
106.70 |
-169.70 |
1.78 |
1.90 |
3.90 |
0.38 |
0.47 |
1 |
1 |
3 |
|
ER-derived Vesicles |
7 |
YGL055w |
398625 |
400154 |
510 |
65.45 |
-42.80 |
3.94 |
1.63 |
1.06 |
0.97 |
0.62 |
1 |
1 |
6 |
|
stearoyl-CoA desaturase |
7 |
YGL056c |
397618 |
396038 |
527 |
6.01 |
-75.45 |
2.50 |
4.68 |
1.97 |
0.84 |
0.57 |
2 |
1 |
7 |
|
strong similarity to pombe SDS23 |
7 |
YGL057c |
395829 |
394969 |
287 |
16.86 |
-90.00 |
2.04 |
1.24 |
2.18 |
0.80 |
0.53 |
5 |
2 |
1 |
|
hypothetical protein |
7 |
YGL058w |
393986 |
394501 |
172 |
72.35 |
-42.80 |
3.52 |
2.81 |
1.07 |
0.96 |
0.77 |
1 |
1 |
6 |
|
E2 ubiquitin-conjugating enzyme |
7 |
YGL059w |
392223 |
393557 |
445 |
33.34 |
-44.17 |
2.16 |
2.31 |
1.37 |
0.93 |
0.53 |
3 |
1 |
6 |
|
similarity to rat branched-chain
alpha-ketoacid dehydrogenase kinase |
7 |
YGL060w |
390065 |
391987 |
641 |
33.85 |
-75.77 |
3.90 |
2.89 |
0.82 |
0.98 |
0.60 |
4 |
2 |
5 |
|
strong similarity to hypothetical protein
YBR216c |
7 |
YGL061c |
389709 |
388969 |
247 |
19.71 |
-31.22 |
4.53 |
2.46 |
1.18 |
0.95 |
0.59 |
1 |
2 |
1 |
|
essential mitotic spindle protein |
7 |
YGL062w |
385194 |
388727 |
1178 |
67.30 |
-76.24 |
7.93 |
2.94 |
0.99 |
0.97 |
0.70 |
1 |
1 |
8 |
|
pyruvate carboxylase 1 |
7 |
YGL063w |
383652 |
384761 |
370 |
32.91 |
-18.43 |
1.05 |
0.33 |
2.51 |
0.73 |
0.52 |
1 |
1 |
1 |
|
pseudouridine synthase 2 |
7 |
YGL064c |
383206 |
381524 |
561 |
20.06 |
-83.56 |
5.17 |
2.63 |
1.32 |
0.94 |
0.59 |
4 |
1 |
7 |
|
similarity to YLR276c and YKR024c |
7 |
YGL065c |
381269 |
379761 |
503 |
69.89 |
-88.49 |
3.37 |
1.69 |
1.53 |
0.91 |
0.58 |
1 |
1 |
4 |
|
mannosyltransferase |
7 |
YGL066w |
377607 |
379577 |
657 |
11.22 |
-16.55 |
4.81 |
7.12 |
1.58 |
0.91 |
0.64 |
4 |
2 |
5 |
|
similarity to human ATAXIN 7 |
7 |
YGL067w |
376099 |
377250 |
384 |
70.87 |
-64.98 |
2.65 |
1.69 |
1.52 |
0.91 |
0.55 |
1 |
1 |
6 |
|
NADH pyrophosphatase I of the Nudix family
of hydrolases, has a peroxisomal targeting signal |
7 |
YGL068w |
375085 |
375666 |
194 |
52.94 |
-91.47 |
4.41 |
2.80 |
0.99 |
0.97 |
0.76 |
2 |
1 |
4 |
|
strong similarity to Cricetus mitochrondial
ribosomal L12 protein |
7 |
YGL069c |
375512 |
375051 |
154 |
85.36 |
-145.12 |
2.99 |
3.24 |
2.74 |
0.67 |
0.59 |
6 |
0 |
0 |
spurious |
questionable ORF |
7 |
YGL070c |
374825 |
374460 |
122 |
90.00 |
-6.34 |
0.91 |
0.82 |
2.97 |
0.62 |
0.45 |
1 |
1 |
2 |
|
DNA-directed RNA polymerase II, 14.2 KD
subunit |
7 |
YGL071w |
372010 |
374079 |
690 |
11.77 |
-37.63 |
3.73 |
6.30 |
1.42 |
0.93 |
0.63 |
1 |
2 |
5 |
|
iron-regulated transcriptional repressor |
7 |
YGL072c |
371360 |
371004 |
119 |
111.80 |
156.57 |
0.49 |
3.00 |
4.82 |
0.18 |
0.42 |
6 |
2 |
1 |
spurious |
questionable ORF |
7 |
YGL073w |
368751 |
371249 |
833 |
18.35 |
-26.84 |
7.59 |
6.52 |
1.23 |
0.95 |
0.67 |
1 |
1 |
2 |
|
heat shock transcription factor |
7 |
YGL074c |
368920 |
368597 |
108 |
150.26 |
-149.53 |
1.55 |
3.80 |
4.84 |
0.18 |
0.41 |
6 |
2 |
1 |
spurious |
questionable ORF |
7 |
YGL075c |
368086 |
366926 |
387 |
36.71 |
-17.88 |
3.74 |
1.66 |
1.15 |
0.96 |
0.56 |
1 |
1 |
1 |
|
Protein of the nuclear envelope/endoplasmic
reticulum required for spindle pole body assembly and normal chromosome
segregation |
7 |
YGL076c |
365994 |
364336 |
244 |
48.01 |
-47.49 |
3.45 |
2.08 |
0.69 |
0.99 |
0.67 |
1 |
1 |
4 |
|
60S large subunit ribosomal protein L7.e.A |
7 |
YGL077c |
363914 |
362226 |
563 |
106.10 |
-140.19 |
4.25 |
3.62 |
3.08 |
0.59 |
0.53 |
1 |
1 |
9 |
|
choline permease |
7 |
YGL078c |
361857 |
360289 |
523 |
49.54 |
-34.06 |
5.86 |
3.75 |
0.37 |
1.00 |
0.73 |
1 |
1 |
10 |
|
putative RNA helicase required for pre-rRNA
processing |
7 |
YGL079w |
359442 |
360095 |
218 |
50.36 |
-39.29 |
3.08 |
2.89 |
0.72 |
0.99 |
0.72 |
5 |
2 |
2 |
|
hypothetical protein |
7 |
YGL080w |
358634 |
359023 |
130 |
45.00 |
-62.35 |
1.12 |
2.08 |
1.89 |
0.86 |
0.59 |
4 |
1 |
1 |
|
strong similarity to C.elegans R07E5.13
protein |
7 |
YGL081w |
357375 |
358334 |
320 |
38.00 |
-16.19 |
4.54 |
1.80 |
1.07 |
0.96 |
0.61 |
5 |
2 |
1 |
|
hypothetical protein |
7 |
YGL082w |
355825 |
356967 |
381 |
33.48 |
-14.04 |
3.81 |
3.17 |
1.00 |
0.97 |
0.63 |
4 |
1 |
5 |
|
strong similarity to hypothetical protein
YPL191c |
7 |
YGL083w |
353056 |
355467 |
804 |
43.09 |
-81.72 |
2.99 |
3.92 |
1.04 |
0.97 |
0.54 |
3 |
1 |
4 |
|
weak similarity to bovine rhodopsin kinase
and to YGR052w |
7 |
YGL084c |
352296 |
350617 |
560 |
67.38 |
-161.10 |
2.20 |
3.26 |
2.92 |
0.63 |
0.45 |
4 |
1 |
5 |
|
similarity to Gup2p - putative glycerol
transporter |
7 |
YGL085w |
349614 |
350435 |
274 |
45.00 |
31.76 |
2.73 |
1.49 |
2.22 |
0.79 |
0.49 |
3 |
2 |
4 |
|
weak similarity to Staphylococcus aureus
nuclease (SNase) |
7 |
YGL086w |
347117 |
349363 |
749 |
24.11 |
-7.01 |
5.72 |
6.59 |
1.32 |
0.94 |
0.58 |
1 |
1 |
8 |
|
spindle assembly checkpoint protein |
7 |
YGL087c |
346902 |
346407 |
137 |
33.02 |
-33.69 |
2.04 |
1.54 |
1.63 |
0.90 |
0.57 |
1 |
1 |
3 |
|
part of the error-free postreplication
repair pathway |
7 |
YGL088w |
345834 |
346196 |
121 |
157.38 |
-177.14 |
1.18 |
1.82 |
5.49 |
0.07 |
0.38 |
6 |
2 |
1 |
|
questionable ORF |
7 |
YGL089c |
345151 |
344792 |
120 |
68.96 |
-84.29 |
2.54 |
1.83 |
1.65 |
0.90 |
0.73 |
1 |
2 |
2 |
|
mating pheromone alpha-2 factor |
7 |
YGL090w |
343317 |
344579 |
421 |
48.20 |
-0.95 |
5.56 |
2.92 |
1.11 |
0.96 |
0.64 |
1 |
1 |
1 |
|
DNA ligase IV interacting factor |
7 |
YGL091c |
343040 |
342057 |
328 |
70.64 |
-57.99 |
4.33 |
1.04 |
1.42 |
0.93 |
0.66 |
1 |
1 |
6 |
|
nucleotide-binding protein |
7 |
YGL092w |
337904 |
341854 |
1317 |
57.43 |
-52.93 |
5.89 |
4.66 |
0.40 |
1.00 |
0.59 |
1 |
1 |
6 |
|
nuclear pore protein |
7 |
YGL093w |
334884 |
337634 |
917 |
33.83 |
-34.04 |
7.35 |
4.54 |
0.62 |
0.99 |
0.66 |
1 |
1 |
4 |
|
spindle pole body protein |
7 |
YGL094c |
334463 |
331119 |
1115 |
45.24 |
-37.72 |
5.06 |
2.84 |
0.30 |
1.00 |
0.56 |
1 |
1 |
7 |
|
component of Pab1p-stimulated poly(A)
ribonuclease |
7 |
YGL095c |
330605 |
328875 |
577 |
39.88 |
-31.53 |
4.29 |
2.15 |
0.69 |
0.99 |
0.59 |
1 |
1 |
2 |
|
vacuolar protein sorting-associated protein |
7 |
YGL096w |
325329 |
326156 |
276 |
-3.81 |
-45.00 |
3.62 |
2.30 |
2.04 |
0.83 |
0.57 |
3 |
1 |
2 |
|
similarity to copper homeostasis protein
Cup9p |
7 |
YGL097w |
321780 |
323225 |
482 |
70.31 |
-19.98 |
5.27 |
2.13 |
1.22 |
0.95 |
0.68 |
1 |
1 |
6 |
|
GDP/GTP exchange factor for Gsp1p/Gsp2p |
7 |
YGL098w |
317340 |
318074 |
245 |
52.88 |
-8.43 |
2.96 |
1.74 |
1.40 |
0.93 |
0.61 |
5 |
2 |
5 |
|
hypothetical protein |
7 |
YGL099w |
314629 |
316548 |
640 |
55.62 |
-25.08 |
5.46 |
4.10 |
0.65 |
0.99 |
0.67 |
3 |
1 |
6 |
|
similarity to putative human GTP-binding
protein MMR1 |
7 |
YGL100w |
313232 |
314278 |
349 |
73.20 |
-16.86 |
2.96 |
1.85 |
1.59 |
0.91 |
0.59 |
1 |
1 |
5 |
|
nuclear pore protein |
7 |
YGL101w |
312191 |
312835 |
215 |
40.60 |
0.00 |
3.14 |
1.84 |
1.47 |
0.92 |
0.61 |
4 |
1 |
4 |
|
strong similarity to hypothetical protein
YBR242w |
7 |
YGL102c |
311931 |
311506 |
142 |
26.57 |
-171.87 |
1.50 |
1.19 |
3.46 |
0.49 |
0.49 |
6 |
1 |
1 |
spurious |
questionable ORF |
7 |
YGL103w |
310965 |
311922 |
149 |
48.37 |
8.75 |
2.96 |
1.08 |
1.85 |
0.86 |
0.64 |
1 |
1 |
2 |
|
60S large subunit ribosomal protein L27a.e |
7 |
YGL104c |
310171 |
308714 |
486 |
43.67 |
-173.81 |
2.76 |
3.79 |
2.97 |
0.61 |
0.45 |
3 |
1 |
5 |
|
similarity to glucose transport proteins |
7 |
YGL105w |
307435 |
308562 |
376 |
61.70 |
-43.98 |
4.57 |
4.08 |
0.58 |
0.99 |
0.76 |
1 |
1 |
8 |
|
protein with specific affinity for G4
quadruplex nucleic acids |
7 |
YGL106w |
306558 |
307004 |
149 |
59.59 |
-28.07 |
4.37 |
1.39 |
1.12 |
0.96 |
0.76 |
1 |
1 |
3 |
|
Myo2p light chain |
7 |
YGL107c |
306271 |
304334 |
646 |
45.00 |
-47.39 |
3.73 |
2.67 |
0.36 |
1.00 |
0.57 |
4 |
2 |
4 |
|
strong similarity to hypothetical protein
YBR238c |
7 |
YGL108c |
304069 |
303650 |
140 |
17.78 |
-14.35 |
4.70 |
3.75 |
1.39 |
0.93 |
0.69 |
4 |
2 |
1 |
|
weak similarity to hypotetical S.pombe
protein |
7 |
YGL109w |
303511 |
303831 |
107 |
-128.16 |
-57.26 |
1.72 |
1.61 |
6.96 |
0.00 |
0.43 |
6 |
0 |
0 |
spurious |
questionable ORF |
7 |
YGL110c |
303409 |
301538 |
624 |
53.97 |
-12.68 |
4.36 |
3.28 |
0.88 |
0.98 |
0.59 |
4 |
2 |
5 |
|
similarity to hypothetical protein
SPCC1906.02c S. pombe |
7 |
YGL111w |
299976 |
301364 |
463 |
56.60 |
-40.16 |
5.07 |
1.95 |
0.72 |
0.99 |
0.66 |
4 |
2 |
5 |
|
weak similarity to hypothetical protein S.
pombe |
7 |
YGL112c |
299726 |
298179 |
516 |
53.97 |
-75.53 |
3.59 |
2.82 |
0.76 |
0.99 |
0.63 |
1 |
1 |
6 |
|
TFIID and SAGA subunit |
7 |
YGL113w |
295930 |
297933 |
668 |
18.73 |
-33.69 |
4.70 |
3.63 |
1.15 |
0.96 |
0.54 |
4 |
2 |
5 |
|
weak similarity to YOR165w |
7 |
YGL114w |
293458 |
295632 |
725 |
70.48 |
-162.78 |
4.33 |
3.89 |
2.75 |
0.67 |
0.53 |
3 |
1 |
5 |
|
weak similarity to H.influenzae permease |
7 |
YGL115w |
292031 |
292996 |
322 |
50.57 |
-135.00 |
3.25 |
1.02 |
2.31 |
0.77 |
0.60 |
1 |
1 |
3 |
|
nuclear regulatory protein |
7 |
YGL116w |
289807 |
291636 |
610 |
43.53 |
-45.00 |
4.47 |
2.75 |
0.23 |
1.00 |
0.56 |
1 |
1 |
8 |
|
cell division control protein |
7 |
YGL117w |
288513 |
289307 |
265 |
28.22 |
-24.78 |
2.86 |
0.88 |
1.68 |
0.89 |
0.59 |
5 |
2 |
1 |
|
hypothetical protein |
7 |
YGL118c |
288452 |
288018 |
145 |
36.87 |
-139.40 |
1.25 |
0.77 |
2.97 |
0.61 |
0.44 |
6 |
0 |
0 |
|
questionable ORF |
7 |
YGL119w |
284443 |
285945 |
501 |
52.67 |
-63.43 |
4.49 |
1.90 |
0.72 |
0.99 |
0.58 |
1 |
1 |
8 |
|
ubiquinol--cytochrome-c reductase complex
assembly protein |
7 |
YGL120c |
283938 |
281638 |
767 |
59.12 |
-50.67 |
4.29 |
3.36 |
0.46 |
1.00 |
0.65 |
1 |
1 |
10 |
|
involved in spliceosome disassembly |
7 |
YGL121c |
281158 |
280781 |
126 |
69.44 |
-74.05 |
1.52 |
1.30 |
2.09 |
0.82 |
0.62 |
5 |
2 |
1 |
|
hypothetical protein |
7 |
YGL122c |
280524 |
278950 |
525 |
0.00 |
-26.57 |
2.75 |
4.39 |
2.08 |
0.82 |
0.61 |
1 |
2 |
7 |
|
nuclear poly(A)-binding protein |
7 |
YGL123w |
277618 |
278379 |
254 |
55.08 |
-90.00 |
4.06 |
1.13 |
1.42 |
0.93 |
0.66 |
1 |
1 |
5 |
|
40S small subunit ribosomal protein |
7 |
YGL124c |
276715 |
274784 |
644 |
42.56 |
-50.19 |
2.62 |
1.85 |
1.14 |
0.96 |
0.50 |
4 |
1 |
5 |
|
similarity to S.pombe hypothetical protein |
7 |
YGL125w |
272524 |
274320 |
599 |
49.40 |
-49.94 |
2.64 |
2.35 |
0.99 |
0.97 |
0.59 |
1 |
1 |
7 |
|
putative methylene tetrahydrofolate
reductase |
7 |
YGL126w |
271001 |
272140 |
380 |
98.13 |
-180.00 |
1.09 |
1.85 |
4.06 |
0.35 |
0.47 |
1 |
2 |
2 |
|
inositol phospholipid synthesis protein |
7 |
YGL127c |
270779 |
270399 |
127 |
-26.57 |
-53.13 |
0.60 |
1.33 |
3.65 |
0.45 |
0.51 |
1 |
1 |
3 |
|
allows hpr1 null mutant to grow at 37 deg. |
7 |
YGL128c |
270340 |
269300 |
347 |
-26.57 |
-47.35 |
2.28 |
2.77 |
3.06 |
0.59 |
0.52 |
3 |
1 |
1 |
|
weak similarity to dnaJ proteins |
7 |
YGL129c |
269192 |
267729 |
488 |
32.59 |
-68.05 |
3.28 |
3.27 |
0.89 |
0.98 |
0.57 |
4 |
1 |
5 |
|
similarity to S.pombe hypothetical protein
SPBC29A3.15C - putative mitochondrial function |
7 |
YGL130w |
266148 |
267524 |
459 |
57.32 |
-24.78 |
2.94 |
2.00 |
1.16 |
0.96 |
0.59 |
1 |
1 |
6 |
|
mRNA guanylyltransferase (mRNA capping
enzyme, alpha subunit) |
7 |
YGL131c |
265862 |
261654 |
1403 |
32.08 |
-11.03 |
6.33 |
5.44 |
1.06 |
0.97 |
0.55 |
4 |
1 |
6 |
|
weak similarity to S.pombe hypothetical
protein C3H1.12C |
7 |
YGL132w |
261583 |
261915 |
111 |
111.80 |
-103.24 |
0.51 |
1.66 |
3.59 |
0.46 |
0.42 |
6 |
0 |
0 |
spurious |
questionable ORF |
7 |
YGL133w |
257710 |
261501 |
1264 |
43.10 |
-18.62 |
7.20 |
5.64 |
0.72 |
0.99 |
0.62 |
1 |
2 |
3 |
|
subunit of Isw2 chromatin remodelling
complex |
7 |
YGL134w |
255666 |
256964 |
433 |
48.48 |
-21.80 |
3.92 |
1.81 |
0.93 |
0.98 |
0.59 |
1 |
2 |
3 |
|
cyclin like protein interacting with Pho85p |
7 |
YGL135w |
254644 |
255294 |
217 |
78.96 |
-72.47 |
2.84 |
1.35 |
1.80 |
0.87 |
0.62 |
1 |
1 |
4 |
|
60S large subunit ribosomal protein |
7 |
YGL136c |
253862 |
252903 |
320 |
22.89 |
-22.75 |
2.73 |
1.88 |
1.54 |
0.91 |
0.59 |
3 |
1 |
5 |
|
weak similarity to E.coli ftsJ protein |
7 |
YGL137w |
249872 |
252738 |
889 |
79.74 |
-42.31 |
7.53 |
3.54 |
1.27 |
0.95 |
0.69 |
1 |
1 |
7 |
|
coatomer complex beta' chain (beta'-cop) of
secretory pathway vesicles |
7 |
YGL138c |
249534 |
248500 |
345 |
12.91 |
-26.00 |
2.65 |
2.46 |
1.72 |
0.88 |
0.51 |
5 |
2 |
1 |
|
hypothetical protein |
7 |
YGL139w |
245719 |
248124 |
802 |
71.57 |
-120.74 |
4.24 |
3.04 |
1.88 |
0.86 |
0.55 |
4 |
1 |
7 |
|
strong similarity to hypothetical protein
YPL221w |
7 |
YGL140c |
245015 |
241359 |
1219 |
53.46 |
-97.83 |
5.92 |
2.31 |
1.20 |
0.95 |
0.58 |
3 |
2 |
4 |
|
weak similarity to Lactobacillus putative
histidine protein kinase SppK |
7 |
YGL141w |
238356 |
241085 |
910 |
67.77 |
-51.34 |
4.12 |
2.55 |
0.84 |
0.98 |
0.55 |
1 |
1 |
5 |
|
ubiquitin-protein ligase (E3) |
7 |
YGL142c |
238122 |
236275 |
616 |
140.71 |
-150.07 |
1.15 |
3.07 |
4.64 |
0.22 |
0.42 |
1 |
1 |
4 |
|
required for Glycosyl Phosphatdyl Inositol
synthesis |
7 |
YGL143c |
235961 |
234723 |
413 |
42.59 |
-37.35 |
4.14 |
2.35 |
0.49 |
1.00 |
0.63 |
1 |
1 |
5 |
|
peptide chain release factor, mitochondrial |
7 |
YGL144c |
234510 |
232456 |
685 |
49.50 |
-54.55 |
4.47 |
2.77 |
0.20 |
1.00 |
0.66 |
4 |
2 |
7 |
|
strong similarity to hypothetical protein
YDL109c |
7 |
YGL145w |
230246 |
232348 |
701 |
37.26 |
-47.19 |
3.37 |
3.50 |
0.63 |
0.99 |
0.57 |
1 |
1 |
5 |
|
required for ER to Golgi transport |
7 |
YGL146c |
229689 |
228757 |
311 |
37.04 |
-165.96 |
3.77 |
0.70 |
2.99 |
0.61 |
0.56 |
5 |
2 |
1 |
|
hypothetical protein |
7 |
YGL147c |
228332 |
227760 |
191 |
48.08 |
-29.74 |
4.77 |
0.58 |
1.40 |
0.93 |
0.75 |
1 |
1 |
4 |
|
ribosomal protein L9.e |
7 |
YGL148w |
226402 |
227529 |
376 |
63.43 |
-72.41 |
4.84 |
2.22 |
0.93 |
0.98 |
0.70 |
1 |
1 |
6 |
|
chorismate synthase |
7 |
YGL149w |
225575 |
225877 |
101 |
-146.31 |
-153.43 |
3.23 |
4.23 |
6.88 |
0.00 |
0.20 |
6 |
2 |
1 |
very hypoth. |
questionable ORF |
7 |
YGL150c |
225576 |
221110 |
1489 |
39.56 |
-20.42 |
9.48 |
7.80 |
0.73 |
0.99 |
0.69 |
3 |
1 |
8 |
|
similarity to Snf2p and human SNF2alpha |
7 |
YGL151w |
217527 |
220922 |
1132 |
50.06 |
-72.55 |
4.77 |
4.36 |
0.54 |
0.99 |
0.59 |
1 |
2 |
4 |
|
negative transcription regulator from
artifical reporters |
7 |
YGL152c |
217372 |
216698 |
225 |
149.86 |
-143.56 |
2.39 |
5.39 |
4.63 |
0.22 |
0.34 |
6 |
0 |
0 |
spurious |
questionable ORF |
7 |
YGL153w |
216276 |
217298 |
341 |
43.95 |
-27.38 |
6.24 |
3.42 |
0.52 |
0.99 |
0.75 |
1 |
1 |
2 |
|
peroxisomal protein involved in protein
import - peroxin |
7 |
YGL154c |
216099 |
215284 |
272 |
69.30 |
-145.30 |
2.92 |
0.96 |
2.72 |
0.68 |
0.54 |
1 |
2 |
2 |
|
L-aminoadipate-semialdehyde dehydrogenase,
small subunit |
7 |
YGL155w |
214084 |
215211 |
376 |
79.70 |
-3.01 |
2.31 |
0.98 |
2.27 |
0.78 |
0.50 |
1 |
1 |
4 |
|
geranylgeranyltransferase beta subunit |
7 |
YGL156w |
210419 |
213667 |
1083 |
68.53 |
-25.42 |
4.90 |
3.40 |
0.99 |
0.97 |
0.58 |
1 |
1 |
7 |
|
alpha-mannosidase |
7 |
YGL157w |
209009 |
210049 |
347 |
60.50 |
-65.06 |
4.69 |
2.55 |
0.68 |
0.99 |
0.70 |
3 |
1 |
11 |
|
similarity to V.vinifera dihydroflavonol
4-reductase |
7 |
YGL158w |
207036 |
208571 |
512 |
67.11 |
-23.20 |
4.32 |
2.69 |
1.00 |
0.97 |
0.59 |
1 |
1 |
3 |
|
ser/thr protein kinase |
7 |
YGL159w |
202725 |
203834 |
370 |
42.75 |
-51.34 |
3.75 |
0.67 |
1.32 |
0.94 |
0.55 |
5 |
1 |
2 |
|
hypothetical protein |
7 |
YGL160w |
200565 |
202274 |
570 |
30.58 |
-104.62 |
2.14 |
1.99 |
1.94 |
0.85 |
0.49 |
3 |
1 |
3 |
|
similarity to hypothetical protein YLR047c
and Fre2p |
7 |
YGL161c |
200146 |
199217 |
310 |
51.95 |
-78.69 |
3.32 |
0.58 |
1.59 |
0.90 |
0.60 |
4 |
1 |
4 |
|
weak similarity to
TRCDSEMBL:HS167A19_1 dJ167A19.1 human |
7 |
YGL162w |
198142 |
199038 |
299 |
8.91 |
-78.93 |
2.99 |
2.71 |
1.78 |
0.87 |
0.58 |
1 |
2 |
3 |
|
hypoxic protein involved in sterol uptake |
7 |
YGL163c |
196407 |
193714 |
898 |
37.41 |
-17.62 |
5.71 |
2.98 |
0.82 |
0.98 |
0.60 |
1 |
1 |
3 |
|
DNA-dependent ATPase of the Snf2p family |
7 |
YGL164c |
193304 |
191985 |
440 |
46.21 |
-14.59 |
6.41 |
3.60 |
0.80 |
0.98 |
0.69 |
4 |
2 |
2 |
|
similarity to S.pombe hypothetical protein
SPAC31A2.10 |
7 |
YGL165c |
191980 |
191405 |
192 |
135.00 |
-147.53 |
1.43 |
1.88 |
4.42 |
0.27 |
0.42 |
6 |
0 |
0 |
spurious |
questionable ORF |
7 |
YGL166w |
191133 |
191807 |
225 |
28.22 |
-4.24 |
3.10 |
1.80 |
1.57 |
0.91 |
0.59 |
1 |
2 |
1 |
|
copper-dependent transcription factor |
7 |
YGL167c |
190472 |
187623 |
950 |
50.75 |
-112.62 |
7.33 |
3.37 |
1.45 |
0.92 |
0.66 |
1 |
1 |
4 |
|
Ca2+-transporting P-type ATPase |
7 |
YGL168w |
187468 |
187797 |
110 |
12.53 |
-144.46 |
1.76 |
1.64 |
3.02 |
0.60 |
0.45 |
6 |
0 |
0 |
spurious |
questionable ORF |
7 |
YGL169w |
186063 |
187340 |
426 |
48.95 |
-93.01 |
3.98 |
2.77 |
1.02 |
0.97 |
0.65 |
1 |
1 |
4 |
|
translation initiation protein |
7 |
YGL170c |
185398 |
184160 |
413 |
31.43 |
-17.77 |
3.11 |
4.03 |
1.15 |
0.96 |
0.55 |
5 |
2 |
1 |
|
hypothetical protein |
7 |
YGL171w |
182394 |
184085 |
564 |
41.46 |
-32.66 |
6.74 |
1.95 |
0.73 |
0.99 |
0.64 |
1 |
1 |
7 |
|
ATP-dependent RNA helicase |
7 |
YGL172w |
180704 |
182119 |
472 |
34.70 |
-51.63 |
3.64 |
2.82 |
0.60 |
0.99 |
0.61 |
1 |
2 |
3 |
|
nuclear pore protein |
7 |
YGL173c |
180117 |
175534 |
1528 |
47.73 |
-35.28 |
6.08 |
5.36 |
0.33 |
1.00 |
0.63 |
1 |
1 |
8 |
|
multifunctional nuclease |
7 |
YGL174w |
174549 |
175346 |
266 |
26.94 |
-21.14 |
4.20 |
4.93 |
1.01 |
0.97 |
0.66 |
4 |
2 |
5 |
|
weak similarity to C.elegans hypothetical
protein R08D7.1 |
7 |
YGL175c |
174326 |
173292 |
345 |
35.42 |
-16.44 |
2.97 |
3.42 |
1.14 |
0.96 |
0.61 |
1 |
2 |
4 |
|
meiotic recombination protein |
7 |
YGL176c |
173083 |
171422 |
554 |
36.87 |
-53.33 |
2.97 |
2.49 |
0.88 |
0.98 |
0.56 |
3 |
2 |
1 |
|
weak similarity to Oryctolagus calcium
channel BIII |
7 |
YGL177w |
167563 |
167907 |
115 |
0.00 |
-90.00 |
0.47 |
0.28 |
3.33 |
0.53 |
0.44 |
6 |
0 |
0 |
very hypoth. |
questionable ORF |
7 |
YGL178w |
167356 |
170572 |
859 |
7.50 |
-65.84 |
3.92 |
5.09 |
1.58 |
0.91 |
0.59 |
1 |
1 |
5 |
|
multicopy suppressor of POP2 |
7 |
YGL179c |
165095 |
163416 |
560 |
62.74 |
-68.70 |
3.14 |
2.68 |
1.00 |
0.97 |
0.56 |
2 |
1 |
4 |
|
strong similarity to Pak1p, Elm1p and
Kin82p |
7 |
YGL180w |
160069 |
162759 |
897 |
55.83 |
-44.06 |
4.40 |
4.32 |
0.36 |
1.00 |
0.59 |
1 |
1 |
9 |
|
essential for autophagocytosis |
7 |
YGL181w |
157910 |
159097 |
396 |
51.52 |
-13.84 |
2.50 |
3.57 |
1.30 |
0.94 |
0.61 |
1 |
1 |
5 |
|
transcription factor of the
Gcs1p/Glo3p/Sps18p family |
7 |
YGL182c |
157600 |
157280 |
107 |
-56.31 |
-81.25 |
1.05 |
1.27 |
4.55 |
0.24 |
0.42 |
6 |
0 |
0 |
very hypoth. |
questionable ORF |
7 |
YGL183c |
157071 |
156550 |
174 |
21.19 |
4.90 |
3.98 |
2.66 |
1.62 |
0.90 |
0.59 |
4 |
2 |
5 |
|
weak similarity to hypothetical coiled-coil
protein S. pombe |
7 |
YGL184c |
156016 |
154622 |
465 |
43.36 |
-78.31 |
3.44 |
1.37 |
1.21 |
0.95 |
0.61 |
2 |
1 |
5 |
|
strong similarity to Emericella nidulans
and similarity to other cystathionine beta-lyase and Cys3p |
7 |
YGL185c |
154310 |
153174 |
379 |
55.81 |
4.97 |
3.29 |
1.19 |
1.72 |
0.88 |
0.55 |
3 |
1 |
3 |
|
weak similarity to dehydrogenases |
7 |
YGL186c |
152780 |
151044 |
579 |
94.05 |
-165.07 |
4.71 |
3.23 |
3.21 |
0.56 |
0.49 |
3 |
1 |
2 |
|
similarity to hypothetical protein Fcy21p
and weak similarity to FCY2 protein |
7 |
YGL187c |
150175 |
149711 |
155 |
63.43 |
-53.97 |
1.98 |
1.09 |
1.79 |
0.87 |
0.63 |
1 |
1 |
3 |
|
cytochrome-c oxidase chain IV |
7 |
YGL188c |
149520 |
149350 |
57 |
5.71 |
50.19 |
1.33 |
1.03 |
3.42 |
0.50 |
0.42 |
5 |
3 |
0 |
very hypoth. |
hypothetical protein |
7 |
YGL189c |
148592 |
148236 |
119 |
41.63 |
-30.47 |
3.31 |
1.81 |
0.98 |
0.97 |
0.67 |
1 |
1 |
6 |
|
40S small subunit ribosomal protein S26e.c7 |
7 |
YGL190c |
147393 |
145816 |
526 |
37.21 |
-7.70 |
5.91 |
3.26 |
1.03 |
0.97 |
0.60 |
1 |
1 |
7 |
|
ser/thr phosphatase 2A regulatory subunit B |
7 |
YGL191w |
144812 |
145198 |
129 |
74.05 |
-53.13 |
1.92 |
2.20 |
1.75 |
0.88 |
0.68 |
1 |
1 |
3 |
|
cytochrome-c oxidase chain VIa |
7 |
YGL192w |
142250 |
144049 |
600 |
23.68 |
-11.31 |
2.54 |
3.12 |
1.59 |
0.90 |
0.55 |
1 |
1 |
6 |
|
positive transcription factor for IME2 |
7 |
YGL193c |
142231 |
141923 |
103 |
-77.91 |
-112.62 |
1.41 |
1.28 |
5.37 |
0.08 |
0.38 |
6 |
0 |
0 |
very hypoth. |
questionable ORF |
7 |
YGL194c |
141730 |
140375 |
452 |
58.09 |
-28.50 |
2.94 |
1.87 |
1.17 |
0.96 |
0.58 |
1 |
1 |
7 |
|
putative histone deacetylase |
7 |
YGL195w |
131529 |
139544 |
2672 |
71.50 |
-104.30 |
10.18 |
6.11 |
1.57 |
0.91 |
0.65 |
1 |
1 |
5 |
|
translational activator |
7 |
YGL196w |
130553 |
131047 |
165 |
76.50 |
-94.76 |
2.00 |
0.94 |
2.30 |
0.77 |
0.55 |
4 |
2 |
4 |
|
similarity to hypothetical protein
SPAC1039.06 S. pombe |
7 |
YGL197w |
124701 |
129161 |
1487 |
36.87 |
-53.70 |
4.54 |
5.70 |
0.41 |
1.00 |
0.55 |
1 |
2 |
9 |
|
negative regulator of early meiotic
expression |
7 |
YGL198w |
123594 |
124376 |
261 |
64.80 |
-152.02 |
1.16 |
2.24 |
3.05 |
0.60 |
0.52 |
3 |
2 |
3 |
|
weak similarity to Yip1p |
7 |
YGL199c |
124045 |
123578 |
156 |
52.59 |
-112.38 |
1.71 |
1.47 |
2.22 |
0.79 |
0.52 |
6 |
2 |
2 |
spurious |
questionable ORF |
7 |
YGL200c |
123308 |
122700 |
203 |
73.14 |
-84.29 |
2.42 |
0.71 |
2.08 |
0.82 |
0.59 |
1 |
1 |
3 |
|
component of the COPII-coated vesicles, 24
kDa |
7 |
YGL201c |
120909 |
117859 |
1017 |
56.44 |
-38.57 |
7.94 |
2.97 |
0.44 |
1.00 |
0.67 |
1 |
1 |
8 |
|
involved in replication |
7 |
YGL202w |
116061 |
117560 |
500 |
72.70 |
-61.70 |
2.86 |
3.30 |
1.30 |
0.94 |
0.64 |
1 |
1 |
8 |
|
aromatic amino acid aminotransferase I |
7 |
YGL203c |
114666 |
112480 |
729 |
62.87 |
-10.90 |
6.74 |
5.09 |
1.07 |
0.96 |
0.71 |
1 |
1 |
9 |
|
carboxypeptidase (YSC-alpha) |
7 |
YGL204c |
112007 |
111705 |
101 |
30.26 |
-168.23 |
1.38 |
2.44 |
3.26 |
0.54 |
0.43 |
6 |
0 |
0 |
very hypoth. |
questionable ORF |
7 |
YGL205w |
108160 |
110403 |
748 |
67.48 |
-62.53 |
4.87 |
2.06 |
0.99 |
0.97 |
0.62 |
1 |
1 |
8 |
|
acyl-CoA oxidase |
7 |
YGL206c |
107506 |
102548 |
1653 |
69.62 |
-63.55 |
7.56 |
5.30 |
0.93 |
0.98 |
0.66 |
1 |
1 |
9 |
|
clathrin heavy chain |
7 |
YGL207w |
98971 |
102075 |
1035 |
58.44 |
-22.53 |
6.71 |
4.54 |
0.76 |
0.99 |
0.65 |
1 |
1 |
7 |
|
general chromatin factor |
7 |
YGL208w |
97340 |
98584 |
415 |
25.53 |
-40.19 |
3.64 |
3.73 |
0.92 |
0.98 |
0.66 |
1 |
1 |
4 |
|
dominant suppressor of some ts mutations in
RPO21 and PRP4 |
7 |
YGL209w |
95860 |
97005 |
382 |
-1.91 |
-56.31 |
3.07 |
3.69 |
2.01 |
0.83 |
0.59 |
1 |
1 |
4 |
|
C2H2 zinc-finger protein |
7 |
YGL210w |
93795 |
94460 |
222 |
53.47 |
-24.78 |
4.51 |
1.92 |
0.86 |
0.98 |
0.67 |
1 |
1 |
7 |
|
small GTP-binding protein essential for
Golgi function |
7 |
YGL211w |
92515 |
93093 |
193 |
55.71 |
-50.19 |
1.92 |
0.56 |
1.92 |
0.85 |
0.56 |
4 |
1 |
4 |
|
similarity to M.jannaschii hypothetical
proteins MJ1157 and MJ1478 |
7 |
YGL212w |
91435 |
92382 |
316 |
31.26 |
8.84 |
3.69 |
2.56 |
1.53 |
0.91 |
0.62 |
1 |
1 |
2 |
|
vacuolar morphogenesis protein |
7 |
YGL213c |
91250 |
90060 |
397 |
88.55 |
-64.36 |
3.97 |
1.39 |
1.87 |
0.86 |
0.57 |
1 |
2 |
3 |
|
antiviral protein of the beta-transducin
(WD-40) repeat family |
7 |
YGL214w |
90010 |
90495 |
162 |
-96.34 |
-88.67 |
0.71 |
3.38 |
5.96 |
0.00 |
0.49 |
6 |
0 |
0 |
spurious |
questionable ORF |
7 |
YGL215w |
87979 |
89334 |
452 |
-27.47 |
-57.93 |
1.33 |
4.16 |
3.33 |
0.52 |
0.57 |
1 |
2 |
3 |
|
cyclin-like protein |
7 |
YGL216w |
84883 |
87297 |
805 |
27.91 |
-55.71 |
6.02 |
2.82 |
0.76 |
0.99 |
0.60 |
1 |
1 |
6 |
|
kinesin-related protein required for
nuclear migration |
7 |
YGL217c |
85178 |
84840 |
113 |
38.66 |
-138.81 |
0.60 |
3.00 |
2.94 |
0.62 |
0.48 |
6 |
0 |
0 |
spurious |
questionable ORF |
7 |
YGL218w |
83648 |
84295 |
216 |
66.80 |
-162.98 |
1.55 |
3.49 |
3.12 |
0.58 |
0.41 |
6 |
2 |
2 |
spurious |
questionable ORF |
7 |
YGL219c |
84255 |
82879 |
459 |
2.68 |
-73.94 |
2.99 |
3.21 |
1.94 |
0.85 |
0.53 |
4 |
2 |
2 |
|
similarity to hypothetical protein
SPBC19C2.11c - S. pombe |
7 |
YGL220w |
82372 |
82731 |
120 |
38.66 |
15.26 |
2.34 |
1.04 |
2.16 |
0.80 |
0.60 |
3 |
2 |
2 |
|
weak similarity to V.alginolyticus bolA
protein |
7 |
YGL221c |
82290 |
81427 |
288 |
59.04 |
-41.42 |
4.12 |
1.34 |
1.04 |
0.97 |
0.70 |
1 |
1 |
3 |
|
Ngg1p-interacting factor 3 |
7 |
YGL222c |
81184 |
80660 |
175 |
-18.08 |
-32.74 |
3.90 |
3.77 |
2.55 |
0.72 |
0.58 |
4 |
2 |
3 |
|
weak similarity to EDC2 |
7 |
YGL223c |
80363 |
79113 |
417 |
0.00 |
-60.55 |
1.62 |
3.49 |
2.37 |
0.76 |
0.57 |
3 |
1 |
1 |
|
weak similarity to Clostridium regulatory
protein |
7 |
YGL224c |
78855 |
78016 |
280 |
51.12 |
-56.89 |
2.38 |
1.64 |
1.32 |
0.94 |
0.60 |
4 |
1 |
3 |
|
strong similarity to hypothetical protein
YER037w |
7 |
YGL225w |
76892 |
77902 |
337 |
102.41 |
-138.42 |
2.79 |
4.51 |
3.06 |
0.59 |
0.53 |
1 |
2 |
5 |
|
GDP-mannose transporter into the lumen of
the Golgi |
7 |
YGL226c-a |
73156 |
72750 |
86 |
129.81 |
-135.00 |
1.68 |
2.13 |
4.05 |
0.35 |
0.45 |
1 |
2 |
1 |
|
subunit of N-oligosaccharyltransferase,
zeta subunit |
7 |
YGL226w |
73338 |
73706 |
123 |
47.12 |
50.19 |
1.72 |
0.70 |
2.98 |
0.61 |
0.49 |
3 |
2 |
1 |
|
similarity to N.crassa cytochrome-c oxidase
chain V |
7 |
YGL227w |
69670 |
72543 |
958 |
61.90 |
-11.46 |
7.54 |
4.88 |
1.04 |
0.97 |
0.67 |
3 |
1 |
5 |
|
weak similarity to human RANBPM NP_005484.1 |
7 |
YGL228w |
67597 |
69327 |
577 |
54.03 |
-29.00 |
5.81 |
3.95 |
0.54 |
0.99 |
0.68 |
4 |
2 |
4 |
|
similarity to hypothetical protein YFR039c |
7 |
YGL229c |
66958 |
64505 |
818 |
50.64 |
-36.87 |
4.02 |
3.15 |
0.34 |
1.00 |
0.62 |
1 |
1 |
3 |
|
Sit4p-associated protein |
7 |
YGL230c |
64214 |
63774 |
147 |
21.25 |
-58.39 |
1.59 |
1.26 |
2.06 |
0.82 |
0.52 |
5 |
3 |
0 |
|
hypothetical protein |
7 |
YGL231c |
63619 |
63050 |
190 |
6.84 |
-75.47 |
1.83 |
2.02 |
2.23 |
0.79 |
0.52 |
4 |
1 |
0 |
|
similarity to hypothetical protein
SPCC1281.03c - S. pombe |
7 |
YGL232w |
62074 |
62998 |
289 |
47.89 |
-2.96 |
4.12 |
3.42 |
1.07 |
0.96 |
0.63 |
3 |
1 |
0 |
|
weak similarity to P.falciparum
dihydropteroate synthase |
7 |
YGL233w |
59121 |
61850 |
910 |
45.00 |
-72.85 |
4.64 |
2.81 |
0.55 |
0.99 |
0.56 |
1 |
1 |
4 |
|
vesicular traffic control protein |
7 |
YGL234w |
56481 |
58886 |
802 |
69.25 |
-101.31 |
7.17 |
2.88 |
1.46 |
0.92 |
0.74 |
1 |
1 |
6 |
|
phosphoribosylamine-glycine ligase and
phosphoribosylformylglycinamidine cyclo-ligase |
7 |
YGL235w |
55278 |
55811 |
178 |
73.61 |
-140.19 |
1.33 |
2.34 |
2.88 |
0.64 |
0.50 |
6 |
0 |
0 |
spurious |
questionable ORF |
7 |
YGL236c |
55795 |
53759 |
679 |
34.95 |
-79.46 |
3.89 |
1.68 |
1.13 |
0.96 |
0.60 |
2 |
1 |
4 |
|
strong similarity to gidA E.coli protein |
7 |
YGL237c |
53528 |
52734 |
265 |
13.13 |
-41.19 |
1.89 |
4.57 |
1.89 |
0.86 |
0.65 |
1 |
1 |
1 |
|
CCAAT-binding factor subunit |
7 |
YGL238w |
49552 |
52431 |
960 |
47.25 |
-108.15 |
4.66 |
4.14 |
1.34 |
0.94 |
0.59 |
1 |
1 |
6 |
|
importin-beta-like protein |
7 |
YGL239c |
49745 |
49434 |
104 |
59.04 |
-126.25 |
0.57 |
1.82 |
2.85 |
0.64 |
0.52 |
6 |
2 |
1 |
spurious |
questionable ORF |
7 |
YGL240w |
48514 |
49362 |
283 |
24.34 |
-17.65 |
2.74 |
1.37 |
1.69 |
0.89 |
0.61 |
1 |
1 |
3 |
|
component of the anaphase promoting complex |
7 |
YGL241w |
45445 |
48456 |
1004 |
64.03 |
-87.80 |
5.48 |
3.28 |
1.09 |
0.96 |
0.61 |
1 |
1 |
6 |
|
Member of the karyopherin-beta family,
nuclear import |
7 |
YGL242c |
45197 |
44655 |
181 |
62.99 |
-4.51 |
4.25 |
2.83 |
1.20 |
0.95 |
0.82 |
3 |
2 |
2 |
|
weak similarity to Drosophila ANK protein |
7 |
YGL243w |
43307 |
44506 |
400 |
35.73 |
4.09 |
3.51 |
1.40 |
1.63 |
0.90 |
0.53 |
1 |
1 |
7 |
|
tRNA-specific adenosine deaminase 1 |
7 |
YGL244w |
41498 |
43171 |
558 |
56.83 |
-3.16 |
6.42 |
6.91 |
1.13 |
0.96 |
0.72 |
1 |
1 |
7 |
|
regulates DNA binding properties of TBP |
7 |
YGL245w |
38975 |
41146 |
724 |
59.53 |
-35.05 |
7.33 |
3.04 |
0.58 |
0.99 |
0.71 |
2 |
1 |
10 |
|
strong similarity to glutamine--tRNA ligase |
7 |
YGL246c |
38780 |
37620 |
387 |
65.88 |
-15.95 |
3.73 |
1.85 |
1.27 |
0.95 |
0.59 |
3 |
1 |
7 |
|
weak similarity to C.elegans dom-3 protein |
7 |
YGL247w |
36933 |
37523 |
197 |
46.27 |
159.44 |
2.27 |
0.61 |
3.87 |
0.39 |
0.51 |
4 |
1 |
5 |
|
similarity to hypothetical protein YHR036w |
7 |
YGL248w |
35653 |
36759 |
369 |
53.81 |
-19.44 |
2.64 |
0.94 |
1.63 |
0.90 |
0.55 |
1 |
2 |
8 |
|
low affinity 3',5'-cyclic-nucleotide
phosphodiesterase |
7 |
YGL249w |
33098 |
35209 |
704 |
36.20 |
-12.38 |
4.53 |
3.16 |
0.95 |
0.97 |
0.55 |
1 |
1 |
3 |
|
required for meiotic recombination and
disjunction |
7 |
YGL250w |
31898 |
32632 |
245 |
63.84 |
-37.48 |
4.06 |
2.42 |
0.78 |
0.98 |
0.74 |
4 |
1 |
2 |
|
weak similarity to hypothetical protein S.
pombe |
7 |
YGL251c |
31061 |
27924 |
1046 |
36.42 |
-47.53 |
4.69 |
2.98 |
0.42 |
1.00 |
0.53 |
1 |
1 |
6 |
|
DNA/RNA helicase |
7 |
YGL252c |
27484 |
25721 |
588 |
57.86 |
-38.66 |
5.50 |
0.53 |
1.44 |
0.93 |
0.62 |
1 |
1 |
6 |
|
retrograde regulation protein |
7 |
YGL253w |
23935 |
25392 |
486 |
64.80 |
-62.53 |
5.11 |
2.56 |
0.79 |
0.98 |
0.70 |
1 |
1 |
6 |
|
hexokinase II |
7 |
YGL254w |
22304 |
23200 |
299 |
0.00 |
-6.23 |
1.91 |
3.20 |
2.46 |
0.74 |
0.52 |
1 |
1 |
3 |
|
sulfite resistance protein |
7 |
YGL255w |
20978 |
22105 |
376 |
85.71 |
-155.32 |
4.14 |
2.10 |
2.89 |
0.64 |
0.58 |
1 |
1 |
4 |
|
high-affinity zinc transport protein |
7 |
YGL256w |
14910 |
16304 |
465 |
54.97 |
-70.79 |
5.49 |
3.24 |
0.57 |
0.99 |
0.74 |
1 |
1 |
3 |
|
alcohol dehydrogenase IV |
7 |
YGL257c |
14157 |
12484 |
558 |
67.04 |
-13.39 |
2.71 |
0.91 |
1.83 |
0.87 |
0.54 |
1 |
2 |
5 |
|
alpha-1,3-mannosyltransferases responsible
for adding the terminal mannose residues of O-linked oligosaccharides |
7 |
YGL258w |
11110 |
11727 |
206 |
66.80 |
-107.24 |
3.18 |
2.12 |
1.71 |
0.89 |
0.69 |
4 |
2 |
2 |
|
strong similarity to hypothetical protein
YOR387c |
7 |
YGL258w-a |
9162 |
9392 |
77 |
47.73 |
-90.00 |
1.69 |
0.11 |
2.34 |
0.76 |
|
4 |
2 |
1 |
|
similarity to S. bayanus |
7 |
YGL259w |
8470 |
8964 |
165 |
58.57 |
-110.73 |
1.64 |
3.08 |
2.09 |
0.82 |
0.59 |
3 |
3 |
0 |
|
similarity to hypothetical aspartyl
proteinase YIR039C |
7 |
YGL260w |
6860 |
7087 |
76 |
135.00 |
174.81 |
0.49 |
1.27 |
5.17 |
0.12 |
0.38 |
4 |
3 |
0 |
very hypoth. |
strong similarity to subtelomeric encoded
proteins |
7 |
YGL261c |
6652 |
6293 |
120 |
68.50 |
-99.16 |
3.24 |
2.87 |
1.52 |
0.91 |
0.78 |
2 |
2 |
1 |
very hypoth. |
strong similarity to members of the
Srp1/Tip1 family |
7 |
YGL262w |
5312 |
5836 |
175 |
54.64 |
-10.30 |
2.87 |
0.85 |
1.70 |
0.89 |
0.61 |
3 |
2 |
1 |
|
similarity to hypothetical protein YER187w |
7 |
YGL263w |
2790 |
3929 |
380 |
91.85 |
-90.00 |
1.59 |
1.33 |
2.64 |
0.70 |
0.48 |
4 |
3 |
0 |
|
similarity to subtelomeric encoded proteins |
7 |
YGR001c |
497802 |
497131 |
193 |
72.07 |
-46.74 |
2.57 |
1.68 |
1.54 |
0.91 |
0.60 |
4 |
1 |
4 |
|
similarity to C.elegans hypothetical M142.5
protein |
7 |
YGR002c |
499901 |
498474 |
476 |
19.06 |
-36.63 |
2.67 |
4.46 |
1.44 |
0.93 |
0.58 |
4 |
2 |
5 |
|
similarity to hypothetical S. pombe protein |
7 |
YGR003w |
500127 |
502358 |
744 |
39.29 |
-60.07 |
4.17 |
1.40 |
0.97 |
0.97 |
0.54 |
3 |
1 |
8 |
|
similarity to D.melanogaster lin19 protein |
7 |
YGR004w |
502933 |
504318 |
462 |
43.94 |
-115.35 |
3.55 |
1.96 |
1.67 |
0.89 |
0.53 |
4 |
1 |
4 |
|
strong similarity to hypothetical protein
YLR324w |
7 |
YGR005c |
505854 |
504655 |
400 |
45.00 |
-4.76 |
5.37 |
4.82 |
1.03 |
0.97 |
0.69 |
1 |
1 |
6 |
|
TFIIF subunit (transcription initiation
factor), 54 kD |
7 |
YGR006w |
506065 |
506721 |
219 |
9.73 |
-65.38 |
2.40 |
1.78 |
1.94 |
0.85 |
0.61 |
1 |
2 |
2 |
|
U5 snRNA-associated protein |
7 |
YGR007w |
506963 |
507931 |
323 |
61.45 |
-15.12 |
4.31 |
2.13 |
1.08 |
0.96 |
0.69 |
1 |
1 |
5 |
|
choline phosphate cytidylyltransferase |
7 |
YGR008c |
508358 |
508107 |
84 |
41.19 |
1.97 |
2.32 |
3.17 |
1.63 |
0.90 |
0.66 |
1 |
2 |
2 |
|
ATPase stabilizing factor |
7 |
YGR009c |
510996 |
509044 |
651 |
38.39 |
-10.66 |
6.50 |
7.42 |
0.95 |
0.97 |
0.70 |
1 |
2 |
6 |
|
protein transport protein |
7 |
YGR010w |
511539 |
512723 |
395 |
37.97 |
-55.41 |
2.62 |
1.77 |
1.21 |
0.95 |
0.61 |
4 |
1 |
7 |
|
strong similarity to hypothetical protein
YLR328w |
7 |
YGR011w |
512491 |
512814 |
108 |
-14.04 |
-150.95 |
0.79 |
1.98 |
3.90 |
0.38 |
0.32 |
6 |
2 |
1 |
spurious |
questionable ORF |
7 |
YGR012w |
513153 |
514331 |
393 |
53.03 |
-36.87 |
5.87 |
1.26 |
1.03 |
0.97 |
0.69 |
3 |
1 |
7 |
|
similarity to E.nidulans cysteine synthase |
7 |
YGR013w |
514548 |
516407 |
620 |
53.47 |
-14.88 |
5.40 |
5.32 |
0.83 |
0.98 |
0.68 |
1 |
2 |
3 |
|
associated with U1 snRNP, no counterpart in
mammalian U1 snRNP |
7 |
YGR014w |
516937 |
520854 |
1306 |
70.68 |
-91.01 |
4.52 |
11.04 |
1.31 |
0.94 |
0.58 |
1 |
2 |
3 |
|
multicopy suppressor of a cdc24 bud
emergence defect |
7 |
YGR015c |
522070 |
521087 |
328 |
14.04 |
-73.30 |
1.37 |
1.15 |
2.38 |
0.76 |
0.53 |
4 |
1 |
2 |
|
similarity to hypothetical protein YGR031w |
7 |
YGR016w |
522255 |
522824 |
190 |
42.14 |
167.01 |
2.05 |
0.97 |
3.70 |
0.43 |
0.47 |
4 |
2 |
3 |
|
weak similarity to M.jannaschii
hypothetical protein MJ1317 |
7 |
YGR017w |
523781 |
524671 |
297 |
54.83 |
-16.34 |
3.12 |
3.51 |
1.04 |
0.97 |
0.64 |
4 |
2 |
3 |
|
weak similarity to TRCDSEMBL:AC006418_11 A.
thaliana |
7 |
YGR018c |
524688 |
524362 |
109 |
-162.65 |
-101.89 |
1.61 |
1.86 |
6.14 |
0.00 |
0.35 |
6 |
0 |
0 |
spurious |
questionable ORF |
7 |
YGR019w |
525223 |
526635 |
471 |
88.59 |
-44.45 |
3.73 |
3.42 |
1.63 |
0.90 |
0.64 |
1 |
1 |
5 |
|
4-aminobutyrate aminotransferase (GABA
transaminase) |
7 |
YGR020c |
527323 |
526970 |
118 |
45.00 |
-57.09 |
3.25 |
1.86 |
0.87 |
0.98 |
0.79 |
1 |
1 |
5 |
|
H+-ATPase V1 domain 14 kDa subunit,
vacuolar |
7 |
YGR021w |
527626 |
528495 |
290 |
43.34 |
-40.24 |
5.73 |
2.00 |
0.61 |
0.99 |
0.73 |
3 |
1 |
3 |
|
similarity to M.leprae yfcA protein |
7 |
YGR022c |
529580 |
529254 |
109 |
64.06 |
-180.00 |
3.94 |
0.67 |
3.32 |
0.53 |
0.80 |
6 |
0 |
0 |
spurious |
questionable ORF |
7 |
YGR023w |
529258 |
530910 |
551 |
143.70 |
-87.85 |
2.59 |
9.08 |
3.94 |
0.37 |
0.47 |
1 |
2 |
5 |
|
potential cell wall stres sensor |
7 |
YGR024c |
532590 |
531880 |
237 |
63.43 |
-33.02 |
2.18 |
1.55 |
1.60 |
0.90 |
0.53 |
4 |
1 |
5 |
|
weak similarity to Methanobacterium
thermoautotrophicum hypothetical protein MTH972 |
7 |
YGR025w |
532633 |
532932 |
100 |
26.57 |
-57.99 |
0.89 |
1.89 |
2.17 |
0.80 |
0.43 |
6 |
0 |
0 |
very hypoth. |
questionable ORF |
7 |
YGR026w |
532979 |
533812 |
278 |
52.59 |
-140.19 |
1.28 |
0.94 |
2.92 |
0.63 |
0.45 |
5 |
2 |
2 |
|
hypothetical protein |
7 |
YGR027c |
534452 |
534129 |
108 |
54.46 |
-52.13 |
2.48 |
2.19 |
1.14 |
0.96 |
0.71 |
1 |
1 |
6 |
|
ribosomal protein S25.e.c7 |
7 |
YGR028w |
542197 |
543282 |
362 |
59.04 |
-94.90 |
3.37 |
1.85 |
1.40 |
0.93 |
0.57 |
1 |
1 |
5 |
|
intra-mitochondrial sorting protein |
7 |
YGR029w |
543547 |
544196 |
189 |
48.81 |
-3.27 |
2.32 |
2.55 |
1.55 |
0.91 |
0.57 |
1 |
1 |
4 |
|
mitochondrial biogenesis and regulation of
cell cycle |
7 |
YGR030c |
546151 |
545678 |
158 |
17.35 |
-11.31 |
2.67 |
1.22 |
1.96 |
0.84 |
0.52 |
1 |
2 |
1 |
|
required for processing of tRNAs and rRNAs |
7 |
YGR031w |
546435 |
547460 |
342 |
29.05 |
-63.43 |
3.34 |
0.73 |
1.55 |
0.91 |
0.62 |
4 |
1 |
5 |
|
similarity to hypothetical protein YGR015c
and weak similarity H.influenzae dihydrolipoamide acetyltransferase |
7 |
YGR032w |
548258 |
553942 |
1895 |
86.39 |
-87.21 |
5.48 |
2.83 |
1.75 |
0.88 |
0.56 |
1 |
1 |
8 |
|
1,3-beta-D-glucan synthase subunit |
7 |
YGR033c |
554961 |
554245 |
239 |
31.22 |
-51.84 |
2.50 |
1.15 |
1.55 |
0.91 |
0.53 |
4 |
2 |
4 |
|
weak similarity to TRCDSEMBLNEW:AP002861_10
Oryza sativa |
7 |
YGR034w |
555923 |
556663 |
129 |
68.20 |
-48.37 |
2.37 |
1.06 |
1.72 |
0.89 |
0.62 |
1 |
1 |
6 |
|
60S large subunit ribosomal protein |
7 |
YGR035c |
557416 |
557069 |
116 |
12.99 |
-40.60 |
3.72 |
1.71 |
1.54 |
0.91 |
0.56 |
5 |
3 |
0 |
|
hypothetical protein |
7 |
YGR036c |
558862 |
558146 |
239 |
96.01 |
-146.31 |
1.24 |
1.63 |
3.47 |
0.49 |
0.44 |
1 |
1 |
6 |
|
required for full levels of dolichol-linked
oligosaccharides in the endoplasmic reticulum |
7 |
YGR037c |
559988 |
559728 |
87 |
75.96 |
-30.58 |
2.21 |
2.74 |
1.67 |
0.89 |
0.77 |
1 |
1 |
5 |
|
acyl-coenzyme-A-binding protein (diazepam
binding inhibitor) |
7 |
YGR038w |
560676 |
561341 |
222 |
41.99 |
-102.99 |
1.81 |
1.79 |
1.98 |
0.84 |
0.59 |
4 |
1 |
2 |
|
strong similarity to hypothetical protein
YLR350w |
7 |
YGR039w |
574882 |
575190 |
103 |
-126.87 |
-172.41 |
0.49 |
1.49 |
7.63 |
0.00 |
0.35 |
6 |
1 |
0 |
|
questionable ORF |
7 |
YGR040w |
575392 |
576495 |
368 |
36.67 |
-60.52 |
3.05 |
1.38 |
1.22 |
0.95 |
0.57 |
1 |
1 |
5 |
|
ser/thr protein kinase of the MAP kinase
family |
7 |
YGR041w |
577481 |
579121 |
547 |
37.13 |
-55.81 |
3.75 |
2.74 |
0.52 |
0.99 |
0.58 |
1 |
2 |
1 |
|
budding protein |
7 |
YGR042w |
579470 |
580282 |
271 |
17.77 |
-17.97 |
4.98 |
2.36 |
1.39 |
0.93 |
0.64 |
3 |
2 |
1 |
|
weak similarity to TRCDSEMBL:CH20111_1
Troponin-I; Clupea harengus |
7 |
YGR043c |
581430 |
580432 |
333 |
65.40 |
-56.58 |
5.00 |
3.28 |
0.72 |
0.99 |
0.75 |
2 |
1 |
4 |
|
strong similarity to transaldolase |
7 |
YGR044c |
583886 |
582987 |
300 |
31.76 |
-22.89 |
1.43 |
2.82 |
1.83 |
0.87 |
0.54 |
1 |
1 |
0 |
|
zinc-finger transcription factor |
7 |
YGR045c |
584290 |
583931 |
120 |
53.13 |
-151.70 |
0.91 |
1.35 |
3.16 |
0.57 |
0.43 |
6 |
0 |
0 |
|
questionable ORF |
7 |
YGR046w |
584889 |
586043 |
385 |
29.95 |
-12.88 |
3.47 |
1.83 |
1.33 |
0.94 |
0.55 |
3 |
1 |
2 |
|
similarity to proline transport helper PTH1
C. albicans |
7 |
YGR047c |
589463 |
586389 |
1025 |
65.63 |
-14.14 |
6.21 |
4.09 |
1.08 |
0.96 |
0.63 |
1 |
1 |
3 |
|
TFIIIC (transcription initiation factor)
subunit, 131 kD |
7 |
YGR048w |
589820 |
590902 |
361 |
47.73 |
-49.64 |
3.91 |
1.38 |
0.91 |
0.98 |
0.63 |
1 |
1 |
5 |
|
ubiquitin fusion degradation protein |
7 |
YGR049w |
591308 |
591868 |
187 |
75.38 |
-104.04 |
1.74 |
1.51 |
2.34 |
0.76 |
0.52 |
1 |
2 |
2 |
|
cdc4 suppressor |
7 |
YGR050c |
592436 |
592083 |
118 |
23.20 |
-90.00 |
0.70 |
0.37 |
2.81 |
0.65 |
0.50 |
6 |
1 |
0 |
very hypoth. |
questionable ORF |
7 |
YGR051c |
593223 |
592903 |
107 |
-56.31 |
-73.30 |
1.05 |
1.01 |
4.56 |
0.24 |
0.43 |
6 |
0 |
0 |
very hypoth. |
questionable ORF |
7 |
YGR052w |
593590 |
594696 |
369 |
52.25 |
-28.22 |
2.04 |
2.42 |
1.40 |
0.93 |
0.56 |
3 |
1 |
3 |
|
similarity to ser/thr protein kinases |
7 |
YGR053c |
595831 |
594983 |
283 |
44.31 |
-26.57 |
3.49 |
1.46 |
1.09 |
0.96 |
0.57 |
4 |
2 |
2 |
|
weak similarity to PIR:T49786 hypothetical
protein B9J10.230 Neurospora crassa |
7 |
YGR054w |
596687 |
598612 |
642 |
62.57 |
-58.84 |
3.51 |
3.97 |
0.76 |
0.99 |
0.59 |
4 |
1 |
4 |
|
similarity to C.elegans E04D5.1 protein |
7 |
YGR055w |
599411 |
601132 |
574 |
82.41 |
-147.26 |
5.05 |
2.78 |
2.62 |
0.70 |
0.61 |
1 |
1 |
6 |
|
high affinity methionine permease |
7 |
YGR056w |
601655 |
604438 |
928 |
21.67 |
-42.94 |
5.16 |
5.16 |
0.99 |
0.97 |
0.61 |
1 |
1 |
6 |
|
member of RSC complex, which remodels the
structure of chromatin |
7 |
YGR057c |
605504 |
604770 |
245 |
53.84 |
-70.02 |
2.06 |
0.75 |
1.84 |
0.86 |
0.50 |
1 |
2 |
5 |
|
required for amino acid permease transport
from the Golgi to the cell surface |
7 |
YGR058w |
606130 |
607134 |
335 |
22.71 |
-41.63 |
2.55 |
3.29 |
1.36 |
0.93 |
0.62 |
3 |
1 |
2 |
|
similarity to mouse calcium-binding protein |
7 |
YGR059w |
607557 |
609092 |
512 |
38.96 |
-1.68 |
5.34 |
3.01 |
1.14 |
0.96 |
0.58 |
1 |
1 |
5 |
|
sporulation-specific septin |
7 |
YGR060w |
610558 |
611484 |
309 |
133.26 |
-79.11 |
1.33 |
1.51 |
3.87 |
0.39 |
0.50 |
1 |
1 |
5 |
|
C-4 sterol methyl oxidase |
7 |
YGR061c |
615959 |
611886 |
1358 |
69.96 |
-71.27 |
7.37 |
3.30 |
1.01 |
0.97 |
0.64 |
1 |
1 |
10 |
|
5'-phosphoribosylformyl glycinamidine
synthetase |
7 |
YGR062c |
617272 |
616325 |
316 |
-18.43 |
-149.38 |
2.31 |
3.20 |
3.59 |
0.46 |
0.43 |
1 |
2 |
5 |
|
required for activity of mitochondrial
cytochrome oxidase |
7 |
YGR063c |
617818 |
617513 |
102 |
62.35 |
71.57 |
2.35 |
0.31 |
3.37 |
0.51 |
0.61 |
1 |
1 |
2 |
|
transcription elongation protein |
7 |
YGR064w |
617615 |
617980 |
122 |
-40.24 |
-101.31 |
1.54 |
0.92 |
4.06 |
0.35 |
0.43 |
6 |
0 |
0 |
spurious |
questionable ORF |
7 |
YGR065c |
619852 |
618074 |
593 |
90.00 |
-95.04 |
3.16 |
1.40 |
2.23 |
0.79 |
0.52 |
1 |
1 |
7 |
|
plasma membrane H+-biotin symporter |
7 |
YGR066c |
621793 |
620918 |
292 |
90.00 |
-21.04 |
2.11 |
2.45 |
2.18 |
0.80 |
0.58 |
4 |
1 |
0 |
|
similarity to hypothetical protein YBR105c |
7 |
YGR067c |
624780 |
622399 |
794 |
49.09 |
-93.29 |
1.41 |
3.09 |
1.91 |
0.85 |
0.50 |
3 |
1 |
3 |
|
weak similarity to transcription factors |
7 |
YGR068c |
627078 |
625321 |
586 |
13.64 |
-22.38 |
4.38 |
0.76 |
1.89 |
0.86 |
0.55 |
3 |
2 |
1 |
|
weak similarity to Rod1p |
7 |
YGR069w |
627077 |
627409 |
111 |
-143.13 |
-167.91 |
1.42 |
1.36 |
7.32 |
0.00 |
0.33 |
6 |
2 |
1 |
very hypoth. |
questionable ORF |
7 |
YGR070w |
627800 |
631264 |
1155 |
30.87 |
-58.19 |
3.15 |
3.74 |
0.91 |
0.98 |
0.53 |
1 |
1 |
3 |
|
GDP/GTP exchange protein for Rho1p |
7 |
YGR071c |
634057 |
631478 |
860 |
39.73 |
-65.77 |
3.15 |
2.99 |
0.78 |
0.98 |
0.52 |
4 |
2 |
1 |
|
similarity to hypothetical protein YLR373c |
7 |
YGR072w |
634298 |
635458 |
387 |
27.82 |
-6.40 |
6.21 |
5.47 |
1.24 |
0.95 |
0.63 |
1 |
2 |
2 |
|
nonsense-mediated mRNA decay protein |
7 |
YGR073c |
635980 |
635612 |
123 |
139.40 |
-169.00 |
0.83 |
3.31 |
4.90 |
0.17 |
0.29 |
6 |
2 |
1 |
spurious |
questionable ORF |
7 |
YGR074w |
635706 |
636143 |
146 |
-1.47 |
-45.00 |
3.23 |
0.47 |
2.41 |
0.75 |
0.52 |
1 |
1 |
2 |
|
snRNA-associated protein |
7 |
YGR075c |
636869 |
636144 |
242 |
47.20 |
12.09 |
2.37 |
1.84 |
1.89 |
0.86 |
0.55 |
1 |
2 |
2 |
|
pre-mRNA splicing factor |
7 |
YGR076c |
637571 |
637101 |
157 |
11.89 |
-29.98 |
1.55 |
2.40 |
2.13 |
0.81 |
0.55 |
1 |
2 |
2 |
|
ribosomal protein YmL25, mitochondrial |
7 |
YGR077c |
639507 |
637741 |
589 |
33.02 |
-119.31 |
0.98 |
2.69 |
2.52 |
0.72 |
0.50 |
3 |
1 |
1 |
|
similarity to Hansenula polymorpha PER1
protein and weak similarity to Pichia pastoris PER3 protein |
7 |
YGR078c |
640365 |
639769 |
199 |
39.81 |
-22.48 |
2.77 |
2.22 |
1.17 |
0.96 |
0.65 |
1 |
1 |
2 |
|
GIM4 - Gim complex component |
7 |
YGR079w |
640714 |
641823 |
370 |
48.65 |
-41.73 |
3.46 |
2.58 |
0.54 |
0.99 |
0.61 |
5 |
2 |
1 |
|
hypothetical protein |
7 |
YGR080w |
642004 |
642999 |
332 |
40.10 |
-59.04 |
2.73 |
2.56 |
0.97 |
0.97 |
0.61 |
1 |
1 |
5 |
|
twinfilin, an actin monomer sequestering
protein |
7 |
YGR081c |
643774 |
643145 |
210 |
18.43 |
-6.01 |
5.02 |
2.64 |
1.50 |
0.92 |
0.65 |
3 |
2 |
2 |
|
weak similarity to mammalian myosin heavy
chain |
7 |
YGR082w |
644038 |
644586 |
183 |
58.82 |
-66.19 |
3.28 |
2.75 |
0.82 |
0.98 |
0.74 |
1 |
1 |
4 |
|
mitochondrial outer membrane import
receptor subunit, 20 kD |
7 |
YGR083c |
646809 |
644857 |
651 |
40.21 |
-69.27 |
5.65 |
4.65 |
0.53 |
0.99 |
0.65 |
1 |
1 |
2 |
|
translation initiation factor eIF2B, 71 kDa
(delta) subunit |
7 |
YGR084c |
648136 |
647120 |
339 |
18.76 |
-58.30 |
3.04 |
2.17 |
1.39 |
0.93 |
0.56 |
1 |
1 |
2 |
|
ribosomal protein of the small subunit,
mitochondrial |
7 |
YGR085c |
648901 |
648380 |
174 |
54.21 |
-9.46 |
4.02 |
0.92 |
1.50 |
0.92 |
0.66 |
1 |
1 |
4 |
|
ribosomal protein |
7 |
YGR086c |
650611 |
649595 |
339 |
77.64 |
-27.28 |
4.06 |
3.91 |
1.29 |
0.94 |
0.71 |
4 |
2 |
9 |
|
strong similarity to hypothetical protein
YPL004c |
7 |
YGR087c |
652975 |
651287 |
563 |
66.46 |
-85.66 |
4.64 |
3.34 |
1.11 |
0.96 |
0.69 |
1 |
1 |
11 |
|
pyruvate decarboxylase 3 |
7 |
YGR088w |
654595 |
656313 |
573 |
53.79 |
-26.57 |
2.90 |
3.83 |
0.97 |
0.97 |
0.62 |
1 |
1 |
7 |
|
catalase T, cytosolic |
7 |
YGR089w |
656954 |
659761 |
936 |
36.10 |
-58.55 |
3.88 |
3.95 |
0.51 |
0.99 |
0.55 |
3 |
1 |
5 |
|
weak similarity to rat tropomyosin |
7 |
YGR090w |
662352 |
666062 |
1237 |
55.10 |
-66.76 |
4.47 |
4.61 |
0.50 |
1.00 |
0.57 |
4 |
1 |
9 |
|
similarity to PIR:T40678 hypothetical
protein SPBC776.08c S. pombe |
7 |
YGR091w |
666335 |
667816 |
494 |
26.26 |
-45.00 |
3.76 |
2.67 |
0.88 |
0.98 |
0.58 |
1 |
1 |
5 |
|
pre-mRNA splicing protein |
7 |
YGR092w |
668183 |
669898 |
572 |
50.27 |
-26.03 |
3.86 |
2.00 |
0.81 |
0.98 |
0.55 |
1 |
1 |
8 |
|
ser/thr protein kinase related to Dbf20p |
7 |
YGR093w |
670382 |
671902 |
507 |
33.33 |
-31.11 |
3.88 |
3.01 |
0.71 |
0.99 |
0.60 |
4 |
1 |
6 |
|
similarity to hypothetical S.pombe protein |
7 |
YGR094w |
672180 |
675491 |
1104 |
62.25 |
-36.63 |
7.18 |
4.39 |
0.65 |
0.99 |
0.69 |
1 |
1 |
6 |
|
valyl-tRNA synthetase |
7 |
YGR095c |
676435 |
675668 |
256 |
41.99 |
-90.00 |
3.36 |
0.63 |
1.69 |
0.89 |
0.61 |
1 |
1 |
4 |
|
involved in rRNA processing |
7 |
YGR096w |
676615 |
677556 |
314 |
41.82 |
-143.97 |
2.88 |
1.54 |
2.45 |
0.74 |
0.53 |
3 |
1 |
4 |
|
similarity to bovine Graves disease carrier
protein |
7 |
YGR097w |
678689 |
682126 |
1146 |
19.87 |
-48.92 |
5.21 |
7.33 |
1.05 |
0.97 |
0.63 |
1 |
2 |
5 |
|
involved in Skn7p-dependent transcription |
7 |
YGR098c |
687452 |
682563 |
1630 |
17.91 |
-89.42 |
5.15 |
2.45 |
1.48 |
0.92 |
0.51 |
1 |
1 |
6 |
|
required for sister chromatid separation |
7 |
YGR099w |
687893 |
689956 |
688 |
39.56 |
-113.20 |
3.41 |
0.58 |
2.05 |
0.83 |
0.55 |
1 |
1 |
3 |
|
involved in controlling telomere length and
position effect |
7 |
YGR100w |
690239 |
693088 |
950 |
60.30 |
-52.85 |
5.57 |
2.69 |
0.55 |
0.99 |
0.61 |
1 |
1 |
6 |
|
Mac1p interacting protein |
7 |
YGR101w |
693357 |
694394 |
346 |
118.61 |
-164.98 |
1.35 |
2.28 |
4.19 |
0.32 |
0.41 |
3 |
1 |
3 |
|
weak similarity to B.subtilis YqgP |
7 |
YGR102c |
695129 |
694581 |
183 |
38.93 |
0.00 |
2.47 |
1.85 |
1.68 |
0.89 |
0.57 |
5 |
2 |
4 |
|
hypothetical protein |
7 |
YGR103w |
695411 |
697225 |
605 |
49.83 |
-18.58 |
6.49 |
5.10 |
0.72 |
0.99 |
0.71 |
3 |
1 |
8 |
|
similarity to zebrafish essential for
embryonic development gene pescadillo |
7 |
YGR104c |
698362 |
697442 |
307 |
30.80 |
-64.36 |
3.46 |
1.58 |
1.15 |
0.96 |
0.58 |
1 |
2 |
2 |
|
DNA-directed RNA polymerase II holoenzyme
and Kornberg's mediator (SRB) subcomplex subunit |
7 |
YGR105w |
698593 |
698823 |
77 |
49.90 |
-141.84 |
2.83 |
2.03 |
2.33 |
0.77 |
0.85 |
1 |
2 |
1 |
|
ATPase assembly integral membrane protein |
7 |
YGR106c |
699780 |
698986 |
265 |
99.02 |
-88.32 |
3.92 |
2.09 |
2.26 |
0.78 |
0.61 |
5 |
2 |
0 |
|
hypothetical protein |
7 |
YGR107w |
702661 |
703107 |
149 |
-104.04 |
-120.47 |
0.34 |
1.62 |
6.50 |
0.00 |
0.41 |
6 |
0 |
0 |
|
questionable ORF |
7 |
YGR108w |
703630 |
705042 |
471 |
43.63 |
-18.78 |
4.07 |
2.43 |
0.79 |
0.98 |
0.58 |
1 |
1 |
4 |
|
cyclin, G2/M-specific |
7 |
YGR109c |
706495 |
705356 |
380 |
26.15 |
-45.00 |
3.14 |
2.03 |
1.16 |
0.96 |
0.55 |
1 |
1 |
4 |
|
cyclin, B-type |
7 |
YGR110w |
713703 |
715037 |
445 |
54.69 |
-29.25 |
1.39 |
1.36 |
1.94 |
0.85 |
0.50 |
4 |
1 |
5 |
|
weak similarity to YLR099c and YDR125c |
7 |
YGR111w |
715822 |
717021 |
400 |
59.38 |
4.40 |
2.85 |
2.61 |
1.56 |
0.91 |
0.56 |
3 |
1 |
5 |
|
weak similarity to mosquito
carboxylesterase |
7 |
YGR112w |
717352 |
718518 |
389 |
21.25 |
-43.88 |
2.94 |
1.83 |
1.41 |
0.93 |
0.53 |
1 |
1 |
4 |
|
SURF homologue protein |
7 |
YGR113w |
718887 |
719915 |
343 |
31.85 |
-27.05 |
4.20 |
2.85 |
0.79 |
0.98 |
0.58 |
1 |
2 |
2 |
|
essential mitotic spindle pole protein |
7 |
YGR114c |
720648 |
720262 |
129 |
-174.29 |
-178.70 |
0.88 |
3.87 |
6.41 |
0.00 |
0.31 |
6 |
2 |
1 |
spurious |
questionable ORF |
7 |
YGR115c |
721145 |
720369 |
259 |
177.90 |
-110.75 |
5.10 |
6.31 |
5.24 |
0.11 |
0.32 |
6 |
0 |
0 |
spurious |
questionable ORF |
7 |
YGR116w |
720403 |
724755 |
1451 |
51.88 |
-13.69 |
9.14 |
7.32 |
0.84 |
0.98 |
0.69 |
1 |
1 |
9 |
|
transcription elongation protein |
7 |
YGR117c |
726473 |
725046 |
476 |
44.23 |
-69.78 |
4.80 |
1.86 |
0.79 |
0.98 |
0.60 |
5 |
1 |
4 |
|
hypothetical protein |
7 |
YGR118w |
726968 |
727722 |
145 |
62.78 |
26.57 |
3.27 |
0.93 |
2.24 |
0.79 |
0.61 |
1 |
1 |
6 |
|
40S small subunit ribosomal protein S23.e |
7 |
YGR119c |
729666 |
728044 |
541 |
20.50 |
-23.11 |
4.91 |
3.51 |
1.19 |
0.95 |
0.59 |
1 |
1 |
7 |
|
nuclear pore protein |
7 |
YGR120c |
730855 |
730031 |
275 |
34.29 |
-34.59 |
1.61 |
2.12 |
1.70 |
0.89 |
0.57 |
1 |
1 |
1 |
|
required for ER to golgi vesicle docking |
7 |
YGR121c |
732922 |
731447 |
492 |
82.33 |
-156.37 |
4.73 |
1.57 |
2.91 |
0.63 |
0.57 |
1 |
1 |
5 |
|
ammonia permease of high capacity and
moderate affinity |
7 |
YGR122c-a |
735753 |
735628 |
42 |
146.31 |
-114.44 |
1.11 |
1.86 |
4.52 |
0.24 |
0.42 |
6 |
|
|
spurious |
questionable ORF - identified by SAGE |
7 |
YGR122w |
733930 |
735135 |
402 |
36.03 |
-62.74 |
2.71 |
1.85 |
1.20 |
0.95 |
0.53 |
5 |
2 |
1 |
|
hypothetical protein |
7 |
YGR123c |
738198 |
736660 |
513 |
60.41 |
-25.08 |
4.11 |
2.29 |
0.86 |
0.98 |
0.64 |
1 |
1 |
3 |
|
protein ser/thr phosphatase |
7 |
YGR124w |
739939 |
741654 |
572 |
72.58 |
-49.48 |
4.47 |
3.02 |
0.98 |
0.97 |
0.69 |
1 |
1 |
6 |
|
asparagine synthetase |
7 |
YGR125w |
742320 |
745427 |
1036 |
61.65 |
-135.97 |
4.91 |
2.59 |
2.07 |
0.82 |
0.52 |
4 |
1 |
9 |
|
similarity to S.pombe hypothetical protein
SPAC24H6.11c |
7 |
YGR126w |
745830 |
746519 |
230 |
45.00 |
-39.92 |
2.98 |
4.21 |
0.76 |
0.99 |
0.73 |
4 |
2 |
2 |
|
weak similarity to hypothetical protein
YPR156c |
7 |
YGR127w |
746793 |
747728 |
312 |
60.95 |
-42.40 |
2.91 |
1.76 |
1.16 |
0.96 |
0.58 |
3 |
2 |
5 |
|
weak similarity to mouse T10 protein |
7 |
YGR128c |
750086 |
747948 |
713 |
42.35 |
-63.07 |
4.00 |
2.65 |
0.44 |
1.00 |
0.56 |
5 |
2 |
4 |
|
hypothetical protein |
7 |
YGR129w |
750395 |
751039 |
215 |
39.70 |
0.00 |
4.70 |
4.43 |
1.17 |
0.96 |
0.66 |
1 |
2 |
2 |
|
synthetic lethal with CDC40 |
7 |
YGR130c |
753839 |
751392 |
816 |
37.87 |
-29.17 |
7.18 |
10.34 |
0.59 |
0.99 |
0.76 |
3 |
1 |
4 |
|
weak similarity to myosin heavy chain
proteins |
7 |
YGR131w |
754721 |
755242 |
174 |
62.35 |
-162.65 |
1.80 |
2.54 |
3.02 |
0.60 |
0.48 |
2 |
2 |
3 |
|
strong similarity to Nce2p |
7 |
YGR132c |
756447 |
755587 |
287 |
58.61 |
-82.87 |
4.08 |
1.43 |
1.24 |
0.95 |
0.68 |
1 |
1 |
1 |
|
prohibitin, antiproliferative protein |
7 |
YGR133w |
756891 |
757439 |
183 |
19.03 |
-26.57 |
2.27 |
0.50 |
2.15 |
0.81 |
0.56 |
1 |
1 |
1 |
|
E2 ubiquitin-conjugating enzyme - peroxin |
7 |
YGR134w |
757765 |
761130 |
1122 |
55.56 |
-57.15 |
5.07 |
2.81 |
0.39 |
1.00 |
0.59 |
5 |
2 |
5 |
|
hypothetical protein |
7 |
YGR135w |
761387 |
762160 |
258 |
52.52 |
-41.05 |
4.71 |
2.56 |
0.38 |
1.00 |
0.74 |
1 |
1 |
4 |
|
20S proteasome subunit Y13 (alpha3) |
7 |
YGR136w |
762423 |
763145 |
241 |
76.76 |
-52.37 |
1.12 |
3.90 |
2.12 |
0.81 |
0.63 |
3 |
1 |
6 |
|
weak similarity to chicken growth factor
receptor-binding protein GRB2 homolog |
7 |
YGR137w |
762883 |
763254 |
124 |
-34.38 |
150.26 |
2.07 |
1.45 |
5.06 |
0.14 |
0.41 |
6 |
0 |
0 |
spurious |
questionable ORF |
7 |
YGR138c |
765601 |
763760 |
614 |
90.00 |
-129.09 |
4.44 |
3.33 |
2.46 |
0.74 |
0.60 |
3 |
1 |
9 |
|
similarity to multidrug resistance proteins |
7 |
YGR139w |
765721 |
766056 |
112 |
22.38 |
18.43 |
1.74 |
0.90 |
2.59 |
0.71 |
0.36 |
6 |
0 |
0 |
very hypoth. |
questionable ORF |
7 |
YGR140w |
767424 |
770291 |
956 |
36.31 |
-33.50 |
3.33 |
5.51 |
0.76 |
0.99 |
0.57 |
1 |
2 |
6 |
|
kinetochore protein complex CBF3, 110 KD
subunit |
7 |
YGR141w |
770564 |
771964 |
467 |
69.44 |
45.88 |
2.77 |
2.13 |
2.54 |
0.72 |
0.49 |
4 |
1 |
6 |
|
strong similarity to hypothetical protein
YPR157w |
7 |
YGR142w |
772449 |
773678 |
410 |
56.98 |
-13.61 |
4.71 |
4.83 |
0.91 |
0.98 |
0.66 |
1 |
2 |
3 |
|
Gene/protein whose expression is elevated
in a btn1 minus/Btn1p lacking yeast strain |
7 |
YGR143w |
775188 |
777500 |
771 |
71.08 |
-36.42 |
4.00 |
4.61 |
0.98 |
0.97 |
0.61 |
1 |
2 |
9 |
|
glucan synthase subunit |
7 |
YGR144w |
780394 |
781371 |
326 |
78.96 |
-97.13 |
4.63 |
1.79 |
1.77 |
0.88 |
0.73 |
1 |
1 |
3 |
|
involved in thiamine biosynthesis and DNA
repair |
7 |
YGR145w |
781762 |
783882 |
707 |
52.52 |
-1.32 |
7.11 |
4.89 |
1.12 |
0.96 |
0.65 |
4 |
1 |
6 |
|
similarity to C.elegans hypothetical
protein |
7 |
YGR146c |
784853 |
784221 |
211 |
-56.31 |
-47.29 |
0.74 |
3.65 |
4.47 |
0.26 |
0.54 |
5 |
2 |
1 |
|
hypothetical protein |
7 |
YGR147c |
786915 |
786052 |
288 |
23.63 |
45.00 |
4.12 |
0.67 |
2.68 |
0.69 |
0.56 |
1 |
2 |
2 |
|
N-acetyltransferase for N-terminal
methionine |
7 |
YGR148c |
787774 |
787310 |
155 |
47.56 |
-29.25 |
3.81 |
2.30 |
0.66 |
0.99 |
0.68 |
1 |
1 |
3 |
|
60S large subunit ribosomal protein L24.e.B |
7 |
YGR149w |
789026 |
790321 |
432 |
120.96 |
-84.81 |
0.84 |
1.06 |
3.70 |
0.43 |
0.45 |
4 |
1 |
3 |
|
similarity to PIR:T40675 hypothetical
protein SPBC776.05 S. pombe |
7 |
YGR150c |
793048 |
790457 |
864 |
36.65 |
-41.48 |
5.30 |
3.13 |
0.44 |
1.00 |
0.56 |
4 |
2 |
7 |
|
similarity to PIR:T39838 hypothetical
protein SPBC19G7.07c S. pombe |
7 |
YGR151c |
794985 |
794653 |
111 |
-32.83 |
14.04 |
3.50 |
0.39 |
3.72 |
0.43 |
0.38 |
6 |
0 |
0 |
spurious |
questionable ORF |
7 |
YGR152c |
795487 |
794672 |
272 |
46.22 |
-28.61 |
4.03 |
1.52 |
0.96 |
0.97 |
0.61 |
1 |
1 |
6 |
|
GTP-binding protein |
7 |
YGR153w |
796087 |
796737 |
217 |
57.26 |
29.74 |
3.39 |
2.74 |
1.93 |
0.85 |
0.53 |
5 |
3 |
0 |
|
hypothetical protein |
7 |
YGR154c |
797863 |
796796 |
356 |
59.35 |
-18.43 |
3.33 |
1.01 |
1.48 |
0.92 |
0.58 |
4 |
1 |
5 |
|
strong similarity to hypothetical proteins
YKR076w and YMR251w |
7 |
YGR155w |
798538 |
800058 |
507 |
59.74 |
-56.98 |
5.55 |
3.18 |
0.52 |
0.99 |
0.74 |
1 |
1 |
6 |
|
cystathionine beta-synthase |
7 |
YGR156w |
800541 |
801815 |
425 |
-5.97 |
-73.84 |
4.19 |
3.48 |
2.12 |
0.81 |
0.58 |
4 |
2 |
4 |
|
weak similarity to PIR:A40220 cleavage
stimulation factor 64K chain - human |
7 |
YGR157w |
802435 |
805041 |
869 |
66.46 |
-112.62 |
3.74 |
1.32 |
1.89 |
0.86 |
0.52 |
1 |
1 |
4 |
|
phosphatidylethanolamine
N-methyltransferase |
7 |
YGR158c |
806016 |
805267 |
250 |
49.76 |
-40.91 |
3.23 |
1.26 |
1.14 |
0.96 |
0.62 |
1 |
2 |
3 |
|
involved in mRNA transport |
7 |
YGR159c |
807651 |
806410 |
414 |
93.21 |
-27.90 |
6.15 |
5.67 |
1.85 |
0.86 |
0.72 |
1 |
1 |
3 |
|
nuclear localization sequence binding
protein |
7 |
YGR160w |
807068 |
807676 |
203 |
140.05 |
-73.84 |
7.32 |
5.04 |
3.63 |
0.45 |
0.65 |
4 |
2 |
1 |
spurious |
weak similarity to C. elegans Y113G7B.12
protein of unknown function |
7 |
YGR161c |
809415 |
808627 |
263 |
12.09 |
-69.04 |
2.65 |
3.10 |
1.69 |
0.89 |
0.58 |
5 |
2 |
2 |
|
hypothetical protein |
7 |
YGR161w-a |
810222 |
810497 |
92 |
28.30 |
11.31 |
1.54 |
0.53 |
2.59 |
0.71 |
|
4 |
2 |
1 |
very hypoth. |
similarity to S. bayanus |
7 |
YGR162w |
824054 |
826909 |
952 |
42.70 |
-27.20 |
7.98 |
7.80 |
0.54 |
0.99 |
0.71 |
1 |
1 |
6 |
|
mRNA cap-binding protein (eIF4F), 150K
subunit |
7 |
YGR163w |
827547 |
828569 |
341 |
58.89 |
-87.61 |
3.67 |
1.30 |
1.40 |
0.93 |
0.66 |
3 |
1 |
4 |
|
similarity to human ragA protein and Gtr1p |
7 |
YGR164w |
828620 |
828952 |
111 |
-9.46 |
-26.57 |
2.89 |
0.21 |
2.82 |
0.65 |
0.48 |
6 |
2 |
2 |
spurious |
questionable ORF |
7 |
YGR165w |
829111 |
830145 |
345 |
33.39 |
-21.80 |
2.84 |
2.03 |
1.27 |
0.95 |
0.56 |
4 |
2 |
5 |
|
similarity to PIR:T39444 hypothetical
protein SPBC14C8.16c S. pombe |
7 |
YGR166w |
830510 |
832189 |
560 |
17.45 |
-54.66 |
3.10 |
2.85 |
1.33 |
0.94 |
0.55 |
1 |
2 |
3 |
|
beta-glucan synthesis-associated protein |
7 |
YGR167w |
832451 |
833149 |
233 |
67.09 |
-13.65 |
5.05 |
4.72 |
1.13 |
0.96 |
0.85 |
1 |
2 |
4 |
|
clathrin light chain |
7 |
YGR168c |
834477 |
833350 |
376 |
11.77 |
-164.74 |
2.53 |
1.76 |
3.20 |
0.56 |
0.42 |
5 |
1 |
2 |
|
hypothetical protein |
7 |
YGR169c |
835898 |
834687 |
404 |
35.54 |
-34.22 |
3.42 |
1.50 |
1.11 |
0.96 |
0.59 |
3 |
1 |
7 |
|
similarity to Rib2p |
7 |
YGR170w |
837137 |
840550 |
1138 |
39.01 |
-40.65 |
6.03 |
3.87 |
0.37 |
1.00 |
0.58 |
1 |
1 |
5 |
|
phosphatidylserine decarboxylase 2 |
7 |
YGR171c |
842546 |
840822 |
575 |
39.35 |
-24.54 |
2.70 |
2.11 |
1.20 |
0.95 |
0.54 |
1 |
1 |
4 |
|
methionyl-tRNA synthetase |
7 |
YGR172c |
843586 |
842843 |
248 |
93.81 |
-150.42 |
0.95 |
2.70 |
3.49 |
0.49 |
0.49 |
1 |
1 |
5 |
|
golgi membrane protein |
7 |
YGR173w |
843849 |
844952 |
368 |
59.04 |
-20.77 |
5.17 |
1.62 |
1.11 |
0.96 |
0.69 |
2 |
1 |
5 |
|
strong similarity to human GTP-binding
protein |
7 |
YGR174c |
846400 |
845891 |
170 |
25.56 |
9.46 |
1.96 |
1.87 |
2.15 |
0.81 |
0.54 |
1 |
2 |
3 |
|
ubiquinol--cytochrome-c reductase assembly
factor |
7 |
YGR175c |
848418 |
846931 |
496 |
64.48 |
-157.62 |
5.52 |
0.83 |
2.83 |
0.65 |
0.68 |
1 |
1 |
4 |
|
squalene monooxygenase |
7 |
YGR176w |
848715 |
849059 |
115 |
-97.59 |
75.96 |
1.41 |
0.38 |
6.64 |
0.00 |
0.30 |
6 |
0 |
0 |
spurious |
questionable ORF |
7 |
YGR177c |
850431 |
848827 |
535 |
59.49 |
-20.41 |
2.81 |
1.98 |
1.29 |
0.94 |
0.59 |
1 |
2 |
5 |
|
alcohol O-acetyltransferase |
7 |
YGR178c |
853210 |
851045 |
722 |
45.92 |
-32.40 |
6.58 |
4.58 |
0.40 |
1.00 |
0.68 |
1 |
1 |
7 |
|
Pab1p interacting protein |
7 |
YGR179c |
854890 |
853673 |
406 |
25.67 |
-11.58 |
4.24 |
4.20 |
1.20 |
0.95 |
0.62 |
5 |
1 |
2 |
|
hypothetical protein |
7 |
YGR180c |
856296 |
855262 |
345 |
65.61 |
-45.74 |
4.43 |
2.93 |
0.72 |
0.99 |
0.70 |
1 |
1 |
1 |
|
ribonucleotide reductase small subunit |
7 |
YGR181w |
858282 |
858596 |
105 |
49.90 |
-60.26 |
2.42 |
2.36 |
1.13 |
0.96 |
0.68 |
1 |
1 |
4 |
|
Translocase of the inner membrane |
7 |
YGR182c |
858899 |
858549 |
117 |
38.66 |
139.40 |
0.59 |
0.85 |
4.61 |
0.23 |
0.36 |
6 |
0 |
0 |
very hypoth. |
questionable ORF |
7 |
YGR183c |
859471 |
859061 |
66 |
87.27 |
-66.80 |
2.59 |
0.94 |
2.18 |
0.80 |
0.72 |
1 |
1 |
2 |
|
ubiquinol--cytochrome-c reductase subunit 9 |
7 |
YGR184c |
865748 |
859899 |
1950 |
54.74 |
-40.88 |
6.43 |
4.01 |
0.35 |
1.00 |
0.58 |
1 |
1 |
7 |
|
ubiquitin-protein ligase |
7 |
YGR185c |
867515 |
866334 |
394 |
57.09 |
-57.20 |
4.08 |
2.70 |
0.47 |
1.00 |
0.68 |
1 |
1 |
4 |
|
tyrosyl-tRNA synthetase |
7 |
YGR186w |
867769 |
869973 |
735 |
44.50 |
-19.46 |
8.95 |
5.87 |
0.70 |
0.99 |
0.74 |
1 |
2 |
6 |
|
TFIIF subunit (transcription initiation
factor), 105 kD |
7 |
YGR187c |
871411 |
870230 |
394 |
63.90 |
-27.65 |
5.50 |
1.19 |
1.29 |
0.94 |
0.67 |
3 |
1 |
7 |
|
weak similarity to human Hmg1p and Hmg2p |
7 |
YGR188c |
875104 |
872042 |
1021 |
29.02 |
-24.21 |
5.55 |
4.43 |
0.91 |
0.98 |
0.57 |
1 |
1 |
2 |
|
ser/thr protein kinase |
7 |
YGR189c |
878187 |
876667 |
507 |
94.28 |
-81.25 |
4.77 |
6.43 |
1.96 |
0.84 |
0.64 |
1 |
1 |
7 |
|
family of putative glycosidases might exert
a common role in cell wall organization |
7 |
YGR190c |
880656 |
880294 |
121 |
112.93 |
-126.03 |
2.57 |
1.24 |
3.37 |
0.51 |
0.52 |
6 |
0 |
0 |
spurious |
questionable ORF |
7 |
YGR191w |
880415 |
882223 |
603 |
80.70 |
-141.84 |
4.79 |
3.63 |
2.48 |
0.73 |
0.57 |
1 |
1 |
7 |
|
histidine permease |
7 |
YGR192c |
883805 |
882810 |
332 |
76.09 |
-81.25 |
6.16 |
2.89 |
1.33 |
0.94 |
0.81 |
1 |
1 |
8 |
|
glyceraldehyde-3-phosphate dehydrogenase 3 |
7 |
YGR193c |
885736 |
884507 |
410 |
51.34 |
-60.82 |
4.43 |
4.36 |
0.31 |
1.00 |
0.71 |
1 |
1 |
6 |
|
pyruvate dehydrogenase complex protein X |
7 |
YGR194c |
887870 |
886071 |
600 |
47.68 |
-38.80 |
3.70 |
2.67 |
0.44 |
1.00 |
0.62 |
1 |
1 |
9 |
|
xylulokinase |
7 |
YGR195w |
888877 |
889614 |
246 |
38.05 |
-104.04 |
3.72 |
0.53 |
1.90 |
0.85 |
0.61 |
1 |
1 |
2 |
|
3'->5' exoribonuclease required for 3'
end formation of 5.8S rRNA |
7 |
YGR196c |
892181 |
889731 |
817 |
50.93 |
-15.03 |
8.38 |
8.77 |
0.80 |
0.98 |
0.74 |
3 |
2 |
2 |
|
weak similarity to Tetrahymena acidic
repetitive protein arp1 |
7 |
YGR197c |
894135 |
892495 |
547 |
72.69 |
-104.57 |
3.45 |
2.21 |
1.72 |
0.88 |
0.57 |
1 |
1 |
7 |
|
involved in nitroguanidine resistance |
7 |
YGR198w |
894688 |
897138 |
817 |
50.58 |
-43.08 |
3.31 |
3.69 |
0.57 |
0.99 |
0.59 |
4 |
1 |
2 |
|
weak similarity to PIR:T38996 hypothetical
protein SPAC637.04 S. pombe |
7 |
YGR199w |
897497 |
899773 |
759 |
95.55 |
-100.54 |
2.63 |
1.59 |
2.51 |
0.73 |
0.50 |
1 |
1 |
7 |
|
putative mannosyltransferase |
7 |
YGR200c |
902265 |
899902 |
788 |
68.66 |
-36.87 |
5.78 |
1.42 |
1.24 |
0.95 |
0.58 |
3 |
1 |
7 |
|
weak similarity to rape guanine nucleotide
regulatory protein |
7 |
YGR201c |
903339 |
902518 |
274 |
77.28 |
-82.57 |
1.92 |
1.40 |
2.11 |
0.81 |
0.59 |
2 |
1 |
3 |
|
strong similarity to translation elongation
factor eEF1 alpha chain Cam1p |
7 |
YGR202c |
904743 |
903472 |
424 |
22.89 |
-19.13 |
4.74 |
5.04 |
1.17 |
0.96 |
0.66 |
1 |
1 |
4 |
|
cholinephosphate cytidylyltransferase |
7 |
YGR203w |
905232 |
905675 |
148 |
161.57 |
29.05 |
0.78 |
0.85 |
5.30 |
0.10 |
0.48 |
3 |
2 |
3 |
|
weak similarity to X.laevis
protein-tyrosin-phosphatase cdc homolog 2 and to hypothetical protein YPR200c |
7 |
YGR204w |
905929 |
908766 |
946 |
56.31 |
-84.72 |
7.97 |
3.89 |
0.88 |
0.98 |
0.75 |
1 |
1 |
7 |
|
C1-tetrahydrofolate synthase (trifunctional
enzyme),cytoplasmic |
7 |
YGR205w |
909208 |
910077 |
290 |
56.69 |
0.00 |
2.46 |
1.41 |
1.80 |
0.87 |
0.56 |
4 |
2 |
4 |
|
similarity to S.pombe hypothetical protein
D89234 |
7 |
YGR206w |
910427 |
910729 |
101 |
-20.56 |
-17.53 |
0.85 |
1.98 |
3.38 |
0.51 |
0.50 |
3 |
2 |
3 |
|
similarity to Xenopus transcription factor
Oct-1.17 |
7 |
YGR207c |
911623 |
910841 |
261 |
43.58 |
-69.44 |
5.30 |
1.59 |
0.91 |
0.98 |
0.73 |
1 |
1 |
6 |
|
electron-transferring flavoprotein, beta
chain |
7 |
YGR208w |
911878 |
912804 |
309 |
51.13 |
-31.33 |
4.90 |
1.53 |
0.92 |
0.98 |
0.73 |
1 |
1 |
4 |
|
phosphoserine phosphatase |
7 |
YGR209c |
913222 |
912911 |
104 |
86.82 |
-87.27 |
3.54 |
2.06 |
1.88 |
0.86 |
0.81 |
1 |
1 |
4 |
|
thioredoxin II |
7 |
YGR210c |
914733 |
913501 |
411 |
51.34 |
-63.43 |
5.37 |
0.55 |
1.39 |
0.93 |
0.67 |
4 |
1 |
8 |
|
similarity to M.jannaschii GTP-binding
protein and to M.capricolum hypothetical protein SGC3 |
7 |
YGR211w |
915236 |
916693 |
486 |
56.31 |
-30.43 |
4.58 |
3.31 |
0.56 |
0.99 |
0.68 |
3 |
1 |
4 |
|
similarity to M.musculus zinc finger
protein ZPR1 |
7 |
YGR212w |
917035 |
918438 |
468 |
10.30 |
-41.05 |
2.07 |
1.90 |
1.99 |
0.84 |
0.51 |
4 |
2 |
4 |
|
weak similarity to S.pombe hypothetical
protein SPAC18B11.03c |
7 |
YGR213c |
919460 |
918510 |
317 |
73.91 |
-163.56 |
3.04 |
3.57 |
2.89 |
0.63 |
0.53 |
1 |
1 |
3 |
|
involved in 7-aminocholesterol resistance |
7 |
YGR214w |
920570 |
921780 |
252 |
74.60 |
-75.65 |
4.51 |
2.80 |
1.22 |
0.95 |
0.78 |
1 |
1 |
6 |
|
40S ribosomal protein p40 homolog A |
7 |
YGR215w |
922170 |
922499 |
110 |
36.03 |
-26.57 |
2.59 |
1.71 |
1.36 |
0.93 |
0.65 |
4 |
2 |
4 |
|
strong similarity to hypothetical S. pombe
protein |
7 |
YGR216c |
924457 |
922631 |
609 |
43.73 |
-128.53 |
1.29 |
2.80 |
2.48 |
0.73 |
0.48 |
1 |
1 |
3 |
|
required for N-acetylglucosaminyl
phosphatidylinositol synthesis |
7 |
YGR217w |
924689 |
930805 |
2039 |
52.19 |
-127.18 |
5.13 |
2.42 |
1.82 |
0.87 |
0.50 |
1 |
1 |
5 |
|
calcium channel protein |
7 |
YGR218w |
932534 |
935785 |
1084 |
58.71 |
-84.51 |
5.44 |
3.17 |
0.92 |
0.98 |
0.61 |
1 |
1 |
6 |
|
nuclear export factor, exportin |
7 |
YGR219w |
936028 |
936366 |
113 |
16.70 |
-143.13 |
0.98 |
1.41 |
3.20 |
0.56 |
0.46 |
6 |
1 |
1 |
spurious |
questionable ORF |
7 |
YGR220c |
936876 |
936070 |
269 |
41.71 |
-23.96 |
3.76 |
0.60 |
1.48 |
0.92 |
0.61 |
1 |
1 |
4 |
|
ribosomal protein of the large subunit,
mitochondrial |
7 |
YGR221c |
938985 |
937120 |
622 |
17.35 |
-55.70 |
2.69 |
5.19 |
1.46 |
0.92 |
0.59 |
4 |
2 |
2 |
|
similarity to hypothetical protein YHR149c |
7 |
YGR222w |
939916 |
940794 |
293 |
43.45 |
-28.39 |
1.53 |
2.46 |
1.66 |
0.89 |
0.52 |
1 |
2 |
4 |
|
splicing protein and translational
activator, mitochondrial |
7 |
YGR223c |
942208 |
940865 |
448 |
25.87 |
-28.50 |
3.47 |
1.88 |
1.22 |
0.95 |
0.55 |
4 |
1 |
9 |
|
weak similarity to hypothetical protein
YFR021w |
7 |
YGR224w |
942799 |
944637 |
613 |
64.74 |
-154.95 |
3.97 |
4.10 |
2.51 |
0.73 |
0.54 |
2 |
1 |
4 |
|
strong similarity to drug resistance
protein SGE1, YKR105c and YCL069W |
7 |
YGR225w |
945138 |
946916 |
562 |
52.43 |
-46.79 |
2.77 |
1.91 |
1.06 |
0.97 |
0.50 |
1 |
1 |
7 |
|
required for sporulation |
7 |
YGR226c |
946993 |
946397 |
199 |
42.71 |
-130.60 |
1.25 |
1.96 |
2.60 |
0.71 |
0.50 |
5 |
2 |
7 |
spurious |
hypothetical protein |
7 |
YGR227w |
947412 |
948986 |
525 |
5.86 |
-158.84 |
1.71 |
4.35 |
3.30 |
0.53 |
0.40 |
1 |
1 |
5 |
|
ITR1 expression promoting protein |
7 |
YGR228w |
949357 |
949698 |
114 |
167.20 |
-135.00 |
4.23 |
5.56 |
5.03 |
0.14 |
0.21 |
6 |
0 |
0 |
spurious |
questionable ORF |
7 |
YGR229c |
950891 |
949377 |
505 |
53.58 |
-23.14 |
5.70 |
5.32 |
0.65 |
0.99 |
0.74 |
1 |
1 |
2 |
|
beta-1,3-glucan synthesis protein |
7 |
YGR230w |
951886 |
952296 |
137 |
-11.77 |
-31.33 |
2.09 |
2.30 |
2.65 |
0.69 |
0.52 |
1 |
2 |
3 |
|
Bypasses Need for Spo12p |
7 |
YGR231c |
953473 |
952529 |
315 |
57.36 |
-97.59 |
4.28 |
0.85 |
1.66 |
0.89 |
0.64 |
1 |
1 |
4 |
|
Prohibitin |
7 |
YGR232w |
953953 |
954636 |
228 |
91.64 |
-41.19 |
2.32 |
1.41 |
2.23 |
0.79 |
0.63 |
1 |
1 |
5 |
|
possible homolog of human 26S proteasome
regulatory subunit p28 |
7 |
YGR233c |
958203 |
954670 |
1178 |
30.96 |
-48.69 |
5.44 |
3.84 |
0.62 |
0.99 |
0.60 |
1 |
1 |
9 |
|
cyclin-dependent kinase inhibitor |
7 |
YGR234w |
959898 |
961094 |
399 |
56.50 |
-65.77 |
4.08 |
3.29 |
0.53 |
0.99 |
0.73 |
1 |
1 |
6 |
|
flavohemoglobin |
7 |
YGR235c |
962055 |
961357 |
233 |
42.83 |
-46.74 |
3.66 |
1.53 |
0.89 |
0.98 |
0.64 |
5 |
2 |
2 |
|
hypothetical protein |
7 |
YGR236c |
962812 |
962426 |
129 |
63.43 |
-129.81 |
2.95 |
0.69 |
2.44 |
0.74 |
0.63 |
5 |
2 |
1 |
|
hypothetical protein |
7 |
YGR237c |
965651 |
963297 |
785 |
31.80 |
-41.22 |
6.30 |
4.98 |
0.62 |
0.99 |
0.61 |
4 |
2 |
3 |
|
weak similarity to YOR019w |
7 |
YGR238c |
968683 |
966038 |
882 |
21.37 |
-27.28 |
4.99 |
4.85 |
1.12 |
0.96 |
0.61 |
1 |
1 |
4 |
|
involved in cell fusion and morphogenesis |
7 |
YGR239c |
970049 |
969186 |
288 |
8.13 |
-29.88 |
1.67 |
3.19 |
2.15 |
0.80 |
0.56 |
1 |
3 |
0 |
|
peroxin, essential for peroxisomal
targeting by the PTS2 pathway |
7 |
YGR240c |
973730 |
970770 |
987 |
72.59 |
-67.07 |
8.41 |
2.70 |
1.08 |
0.96 |
0.70 |
1 |
1 |
7 |
|
6-phosphofructokinase, alpha subunit |
7 |
YGR241c |
976577 |
974874 |
568 |
-9.34 |
-47.10 |
3.36 |
4.87 |
2.24 |
0.79 |
0.60 |
1 |
1 |
7 |
|
Yeast Adaptor Protein, member of AP180
protein family |
7 |
YGR242w |
976411 |
976716 |
102 |
78.69 |
-176.63 |
1.01 |
1.69 |
3.73 |
0.42 |
0.51 |
6 |
0 |
0 |
spurious |
questionable ORF |
7 |
YGR243w |
977332 |
977769 |
146 |
48.37 |
-111.80 |
1.99 |
1.78 |
2.04 |
0.83 |
0.57 |
4 |
1 |
5 |
|
strong similarity to hypothetical protein
YHR162w |
7 |
YGR244c |
979315 |
978035 |
427 |
57.35 |
-42.18 |
5.92 |
2.09 |
0.66 |
0.99 |
0.71 |
1 |
1 |
6 |
|
succinate-CoA ligase beta subunit |
7 |
YGR245c |
982064 |
979764 |
767 |
54.36 |
-13.63 |
7.06 |
3.68 |
0.87 |
0.98 |
0.68 |
1 |
1 |
6 |
|
required for normal organization of the
actin cytoskeleton; required for passage through Start |
7 |
YGR246c |
984268 |
982481 |
596 |
60.66 |
-29.29 |
6.44 |
3.85 |
0.70 |
0.99 |
0.70 |
1 |
1 |
4 |
|
TFIIIB subunit, 70 kD |
7 |
YGR247w |
984962 |
985678 |
239 |
83.48 |
-82.41 |
2.28 |
0.98 |
2.24 |
0.79 |
0.59 |
5 |
2 |
4 |
|
hypothetical protein |
7 |
YGR248w |
985968 |
986732 |
255 |
61.63 |
-68.20 |
3.56 |
0.34 |
1.67 |
0.89 |
0.62 |
2 |
1 |
3 |
|
strong similarity to Sol3p |
7 |
YGR249w |
988045 |
989412 |
456 |
-27.90 |
-64.54 |
3.60 |
4.36 |
2.94 |
0.62 |
0.55 |
3 |
1 |
3 |
|
similarity to heat shock transcription
factors |
7 |
YGR250c |
993517 |
991175 |
781 |
38.31 |
-18.32 |
4.56 |
5.69 |
0.79 |
0.98 |
0.62 |
3 |
1 |
2 |
|
weak similarity to human cleavage
stimulation factor 64K chain |
7 |
YGR251w |
995635 |
996222 |
196 |
30.65 |
-2.29 |
4.48 |
3.57 |
1.26 |
0.95 |
0.67 |
5 |
2 |
2 |
|
hypothetical protein |
7 |
YGR252w |
996865 |
998181 |
439 |
43.18 |
-15.33 |
5.30 |
3.07 |
0.80 |
0.98 |
0.66 |
1 |
1 |
7 |
|
histone acetyltransferase |
7 |
YGR253c |
999136 |
998357 |
260 |
79.02 |
-47.73 |
4.23 |
1.84 |
1.39 |
0.93 |
0.71 |
1 |
1 |
5 |
|
20S proteasome subunit(alpha5) |
7 |
YGR254w |
1000923 |
1002233 |
437 |
83.70 |
-70.23 |
6.98 |
3.25 |
1.49 |
0.92 |
0.79 |
1 |
1 |
7 |
|
enolase I (2-phosphoglycerate dehydratase) |
7 |
YGR255c |
1003958 |
1002522 |
479 |
61.65 |
-93.30 |
3.95 |
2.38 |
1.21 |
0.95 |
0.61 |
1 |
1 |
5 |
|
monooxygenase |
7 |
YGR256w |
1004621 |
1006096 |
492 |
73.39 |
-80.54 |
5.36 |
1.65 |
1.45 |
0.92 |
0.66 |
1 |
1 |
10 |
|
phosphogluconate dehydrogenase |
7 |
YGR257c |
1007302 |
1006205 |
366 |
38.29 |
-149.93 |
3.80 |
1.15 |
2.55 |
0.72 |
0.51 |
4 |
1 |
7 |
|
similarity to C.elegans C16C10.1 |
7 |
YGR258c |
1010763 |
1007671 |
1031 |
47.03 |
-18.97 |
8.09 |
5.27 |
0.70 |
0.99 |
0.67 |
1 |
1 |
9 |
|
structure-specific nuclease of the
nucleotide excision repairosome |
7 |
YGR259c |
1012918 |
1012481 |
146 |
111.80 |
-141.01 |
1.78 |
2.24 |
3.58 |
0.46 |
0.38 |
6 |
2 |
1 |
spurious |
questionable ORF |
7 |
YGR260w |
1012482 |
1014083 |
534 |
68.32 |
-149.93 |
3.87 |
1.90 |
2.53 |
0.72 |
0.57 |
3 |
1 |
9 |
|
similarity to allantoate transport protein |
7 |
YGR261c |
1016747 |
1014321 |
809 |
64.06 |
-65.70 |
4.34 |
3.59 |
0.75 |
0.99 |
0.59 |
1 |
1 |
8 |
|
AP-3 complex subunit, beta3-adaptin, 91 KD |
7 |
YGR262c |
1017756 |
1016974 |
261 |
46.40 |
-3.58 |
1.80 |
0.99 |
2.07 |
0.82 |
0.57 |
3 |
1 |
6 |
|
weak similarity to protein kinases and
M.jannaschii O-sialoglycoprotein endopeptidase homolog |
7 |
YGR263c |
1019238 |
1017967 |
424 |
42.21 |
-59.04 |
2.82 |
0.85 |
1.46 |
0.92 |
0.58 |
3 |
1 |
3 |
|
weak similarity to E.coli lipase like
enzyme |
7 |
YGR264c |
1021850 |
1019598 |
751 |
74.19 |
-34.40 |
4.29 |
4.07 |
1.10 |
0.96 |
0.63 |
1 |
1 |
3 |
|
methionyl-tRNA synthetase |
7 |
YGR265w |
1021645 |
1022052 |
136 |
104.04 |
-158.63 |
0.71 |
2.12 |
3.93 |
0.38 |
0.35 |
6 |
1 |
1 |
spurious |
questionable ORF |
7 |
YGR266w |
1022653 |
1024755 |
701 |
51.26 |
-17.16 |
4.16 |
2.69 |
0.78 |
0.98 |
0.58 |
5 |
2 |
4 |
|
hypothetical protein |
7 |
YGR267c |
1025732 |
1025004 |
243 |
38.66 |
-63.43 |
3.70 |
0.43 |
1.51 |
0.92 |
0.62 |
1 |
1 |
3 |
|
GTP cyclohydrolase I |
7 |
YGR268c |
1026650 |
1026057 |
198 |
-75.96 |
-29.93 |
1.17 |
2.71 |
5.09 |
0.13 |
0.44 |
4 |
2 |
2 |
|
weak similarity to S.pombe hypothetical
protein SPAC17A5 |
7 |
YGR269w |
1026633 |
1026956 |
108 |
37.87 |
105.26 |
2.19 |
1.10 |
3.90 |
0.39 |
0.54 |
6 |
0 |
0 |
very hypoth. |
questionable ORF |
7 |
YGR270w |
1027367 |
1031503 |
1379 |
44.62 |
-26.57 |
8.63 |
6.20 |
0.53 |
0.99 |
0.67 |
1 |
1 |
5 |
|
26S proteasome subunit |
7 |
YGR271c-a |
1037988 |
1037800 |
63 |
87.40 |
-21.80 |
2.77 |
2.04 |
1.95 |
0.84 |
|
4 |
2 |
1 |
very hypoth. |
similarity to S. bayanus |
7 |
YGR271w |
1031788 |
1037688 |
1967 |
48.88 |
-73.05 |
7.30 |
3.02 |
0.54 |
0.99 |
0.60 |
2 |
1 |
5 |
|
strong similarity to S.pombe RNA helicase |
7 |
YGR272c |
1038497 |
1038042 |
152 |
22.52 |
-22.17 |
3.60 |
2.36 |
1.25 |
0.95 |
0.53 |
4 |
2 |
5 |
|
similarity to hypothetical S.pombe protein
SPAC12G12.02 |
7 |
YGR273c |
1039235 |
1038714 |
174 |
31.76 |
-37.23 |
1.87 |
2.38 |
1.55 |
0.91 |
0.56 |
4 |
2 |
4 |
|
similarity to hypothetical protein YMR295c |
7 |
YGR274c |
1043092 |
1039895 |
1066 |
35.21 |
-19.22 |
7.38 |
5.68 |
0.83 |
0.98 |
0.65 |
1 |
1 |
8 |
|
TFIID subunit (TBP-associated factor), 145
kD |
7 |
YGR275w |
1043186 |
1043743 |
186 |
30.58 |
-7.77 |
3.75 |
3.26 |
1.18 |
0.95 |
0.66 |
1 |
3 |
0 |
|
Regulator of Ty1 Transposition |
7 |
YGR276c |
1045477 |
1043819 |
553 |
40.10 |
-37.07 |
5.28 |
2.40 |
0.52 |
0.99 |
0.64 |
1 |
1 |
5 |
|
ribonuclease H |
7 |
YGR277c |
1046558 |
1045644 |
305 |
39.94 |
116.57 |
3.21 |
0.13 |
4.17 |
0.32 |
0.55 |
4 |
1 |
2 |
|
similarity to hypothetical S.pombe protein |
7 |
YGR278w |
1046728 |
1048458 |
577 |
24.29 |
-31.83 |
3.75 |
1.42 |
1.33 |
0.94 |
0.53 |
3 |
1 |
1 |
|
similarity to C.elegans LET-858 |
7 |
YGR279c |
1049955 |
1048798 |
386 |
88.48 |
-71.92 |
5.75 |
5.25 |
1.68 |
0.89 |
0.81 |
3 |
2 |
3 |
|
similarity to glucanase |
7 |
YGR280c |
1051722 |
1050910 |
271 |
33.86 |
0.00 |
5.56 |
5.04 |
1.24 |
0.95 |
0.65 |
3 |
1 |
7 |
|
weak similarity to Cbf5p |
7 |
YGR281w |
1052821 |
1057251 |
1477 |
55.45 |
-112.02 |
8.21 |
2.50 |
1.50 |
0.92 |
0.61 |
1 |
1 |
10 |
|
ATP-binding cassette transporter protein |
7 |
YGR282c |
1058721 |
1057783 |
313 |
94.55 |
-68.01 |
4.99 |
3.17 |
1.88 |
0.86 |
0.73 |
1 |
1 |
4 |
|
endo-beta-1,3-glucanase of the cell wall |
7 |
YGR283c |
1060037 |
1059015 |
341 |
31.61 |
-51.84 |
2.48 |
2.89 |
1.18 |
0.96 |
0.58 |
4 |
2 |
5 |
|
similarity to hypothetical protein YMR310c |
7 |
YGR284c |
1061587 |
1060658 |
310 |
85.03 |
-157.62 |
2.62 |
2.09 |
3.06 |
0.59 |
0.47 |
3 |
1 |
3 |
|
similarity to mouse Surf-4 protein |
7 |
YGR285c |
1063150 |
1061852 |
433 |
68.05 |
-36.45 |
6.68 |
5.26 |
0.86 |
0.98 |
0.83 |
1 |
1 |
6 |
|
zuotin, a putative Z-DNA binding protein |
7 |
YGR286c |
1064937 |
1063813 |
375 |
42.75 |
-47.42 |
4.64 |
2.59 |
0.29 |
1.00 |
0.64 |
1 |
1 |
8 |
|
biotin synthetase |
7 |
YGR287c |
1068988 |
1067222 |
589 |
71.05 |
-17.46 |
4.31 |
3.84 |
1.18 |
0.95 |
0.62 |
2 |
1 |
6 |
|
strong similarity to maltase |
7 |
YGR288w |
1070290 |
1071708 |
473 |
38.66 |
-41.99 |
2.06 |
1.86 |
1.45 |
0.92 |
0.54 |
1 |
2 |
2 |
|
maltose pathway regulatory protein |
7 |
YGR289c |
1075810 |
1073963 |
616 |
70.17 |
-137.49 |
5.23 |
1.31 |
2.39 |
0.75 |
0.57 |
1 |
1 |
6 |
|
general alpha-glucoside permease |
7 |
YGR290w |
1075479 |
1075919 |
147 |
150.75 |
-124.44 |
2.36 |
3.50 |
4.48 |
0.25 |
0.36 |
5 |
0 |
0 |
spurious |
hypothetical protein |
7 |
YGR291c |
1076501 |
1076283 |
73 |
-20.56 |
-153.43 |
1.00 |
0.79 |
4.17 |
0.32 |
0.41 |
5 |
3 |
0 |
very hypoth. |
hypothetical protein |
7 |
YGR292w |
1076596 |
1078347 |
584 |
66.80 |
-12.20 |
4.10 |
3.13 |
1.15 |
0.96 |
0.61 |
1 |
1 |
6 |
|
alpha-glucosidase of the MAL1 locus |
7 |
YGR293c |
1080343 |
1079885 |
153 |
-20.56 |
-124.51 |
0.69 |
1.57 |
3.81 |
0.41 |
0.48 |
4 |
3 |
0 |
very hypoth. |
strong similarity to hypothetical protein
YBR300c |
7 |
YGR294w |
1080303 |
1080662 |
120 |
67.25 |
-97.13 |
3.07 |
2.94 |
1.50 |
0.92 |
0.77 |
4 |
2 |
1 |
|
strong similarity to members of the
Srp1p/Tip1p family |
7 |
YGR295c |
1082726 |
1081584 |
381 |
83.42 |
-138.01 |
1.34 |
0.69 |
3.23 |
0.55 |
0.48 |
4 |
2 |
2 |
|
strong similarity to subtelomeric encoded
proteins |
7 |
YGR296w |
1084861 |
1090585 |
1859 |
46.24 |
-29.74 |
8.32 |
2.43 |
0.56 |
0.99 |
0.62 |
4 |
|
|
|
strong similarity to YPL283c; YNL339c and
other Y' encoded proteins |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|