Chr |
ORF |
Gene |
Observations |
Best log(e) |
EC |
Description |
A |
YAR050W |
FLO1 |
35 |
-45.4 |
3 |
Lectin-like protein involved in flocculation, cell wall protein that binds to mannose chains on the surface of other cells, confers floc-forming ability that is chymotrypsin sensitive and heat resistant; similar to Flo5p [Source:SGD;Acc:S000000084] |
B |
YBL014C |
RRN6 |
66 |
-61.5 |
3 |
Component of the core factor (CF) rDNA transcription factor complex; CF is required for transcription of 35S rRNA genes by RNA polymerase I and is composed of Rrn6p, Rrn7p, and Rrn11p [Source:SGD;Acc:S000000110] |
B |
YBR040W |
FIG1 |
38 |
-16.6 |
3 |
Integral membrane protein required for efficient mating; may participate in or regulate the low affinity Ca2+ influx system, which affects intracellular signaling and cell-cell fusion during mating [Source:SGD;Acc:S000000244] |
B |
YBR148W |
YSW1 |
39 |
-22.6 |
3 |
Protein required for normal prospore membrane formation; interacts with Gip1p, which is the meiosis-specific regulatory subunit of the Glc7p protein phosphatase; expressed specifically in spores and localizes to the prospore membrane [Source:SGD;Acc:S000000352] |
B |
YBR270C |
BIT2 |
38 |
-82.1 |
3 |
Subunit of TORC2, a membrane-associated complex that regulates actin cytoskeletal dynamics during polarized growth and cell wall integrity; interacts with Slm1p and Slm2p, homologous PH domain-containing TORC2 substrates; similar to Bit61p [Source:SGD;Acc:S000000474] |
C |
YCL036W |
GFD2 |
52 |
-34.8 |
3 |
Protein of unknown function, identified as a high-copy suppressor of a dbp5 mutation [Source:SGD;Acc:S000000541] |
C |
YCL058W-A |
ADF1 |
74 |
-22.4 |
3 |
Transcriptional repressor encoded by the antisense strand of the FYV5 gene; negatively regulates transcription of FYV5 by binding to the promoter on the sense strand [Source:SGD;Acc:S000028518] |
C |
YCR018C |
SRD1 |
33 |
-22.6 |
3 |
Protein involved in the processing of pre-rRNA to mature rRNA; contains a C2/C2 zinc finger motif; srd1 mutation suppresses defects caused by the rrp1-1 mutation [Source:SGD;Acc:S000000611] |
C |
YCR028C |
FEN2 |
22 |
-14.6 |
3 |
Plasma membrane H+-pantothenate symporter; confers sensitivity to the antifungal agent fenpropimorph [Source:SGD;Acc:S000000623] |
D |
YDL020C |
RPN4 |
26 |
-25.7 |
3 |
Transcription factor that stimulates expression of proteasome genes; Rpn4p levels are in turn regulated by the 26S proteasome in a negative feedback control mechanism; RPN4 is transcriptionally regulated by various stress responses [Source:SGD;Acc:S000002178] |
D |
YDR125C |
ECM18 |
22 |
-83.3 |
3 |
Protein of unknown function, similar to Rlp24p [Source:SGD;Acc:S000002532] |
D |
YDR133C |
YDR133C |
16 |
-11.3 |
3 |
Dubious open reading frame unlikely to encode a protein, based on available experimental and comparative sequence data; partially overlaps YDR134C [Source:SGD;Acc:S000002540] |
D |
YDR191W |
HST4 |
27 |
-13.8 |
3 |
Member of the Sir2 family of NAD(+)-dependent protein deacetylases; involved along with Hst3p in silencing at telomeres, cell cycle progression, radiation resistance, genomic stability and short-chain fatty acid metabolism [Source:SGD;Acc:S000002599] |
D |
YDR242W |
AMD2 |
24 |
-50 |
3 |
Putative amidase [Source:SGD;Acc:S000002650] |
D |
YDR253C |
MET32 |
22 |
-19.3 |
3 |
Zinc-finger DNA-binding protein, involved in transcriptional regulation of the methionine biosynthetic genes, similar to Met31p [Source:SGD;Acc:S000002661] |
D |
YDR259C |
YAP6 |
53 |
-34.5 |
3 |
Basic leucine zipper (bZIP) transcription factor; physically interacts with the Tup1-Cyc8 complex and recruits Tup1p to its targets; overexpression increases sodium and lithium tolerance; computational analysis suggests a role in regulation of expre of genes involved in carbohydrate metabolism [Source:SGD;Acc:S000002667] |
D |
YDR273W |
DON1 |
35 |
-33.3 |
3 |
Meiosis-specific component of the spindle pole body, part of the leading edge protein (LEP) coat, forms a ring-like structure at the leading edge of the prospore membrane during meiosis II [Source:SGD;Acc:S000002681] |
D |
YDR306C |
YDR306C |
22 |
-80.6 |
3 |
F-box protein of unknown function; interacts with Sgt1p via a Leucine-Rich Repeat (LRR) domain [Source:SGD;Acc:S000002714] |
D |
YDR315C |
IPK1 |
21 |
-47.1 |
3 |
Inositol 1,3,4,5,6-pentakisphosphate 2-kinase, nuclear protein required for synthesis of 1,2,3,4,5,6-hexakisphosphate (phytate), which is integral to cell function; has 2 motifs conserved in other fungi; ipk1 gle1 double mutant is inviable [Source:SGD;Acc:S000002723] |
D |
YDR524C-B |
YDR524C-B |
11 |
-8 |
3 |
Putative protein of unknown function [Source:SGD;Acc:S000028739] |
E |
YEL073C |
YEL073C |
15 |
-15.2 |
3 |
Putative protein of unknown function; located adjacent to ARS503 and the telomere on the left arm of chromosome V; regulated by inositol/choline [Source:SGD;Acc:S000000799] |
E |
YER028C |
MIG3 |
26 |
-57.9 |
3 |
Probable transcriptional repressor involved in response to toxic agents such as hydroxyurea that inhibit ribonucleotide reductase; phosphorylation by Snf1p or the Mec1p pathway inactivates Mig3p, allowing induction of damage response genes [Source:SGD;Acc:S000000830] |
E |
YER066W |
RRT13 |
7 |
-16.2 |
3 |
Putative protein of unknown function; non-essential gene identified in a screen for mutants with decreased levels of rDNA transcription [Source:SGD;Acc:S000000868] |
E |
YER104W |
RTT105 |
47 |
-35.6 |
3 |
Protein with a role in regulation of Ty1 transposition [Source:SGD;Acc:S000000906] |
E |
YER185W |
PUG1 |
16 |
-5.9 |
3 |
Plasma membrane protein with roles in the uptake of protoprophyrin IX and the efflux of heme; expression is induced under both low-heme and low-oxygen conditions; member of the fungal lipid-translocating exporter (LTE) family of proteins [Source:SGD;Acc:S000000987] |
F |
YFL011W |
HXT10 |
126 |
-33 |
3 |
Putative hexose transporter, expressed at low levels and expression is repressed by glucose [Source:SGD;Acc:S000001883] |
F |
YFL017W-A |
SMX2 |
97 |
-23 |
3 |
Core Sm protein Sm G; part of heteroheptameric complex (with Smb1p, Smd1p, Smd2p, Smd3p, Sme1p, and Smx3p) that is part of the spliceosomal U1, U2, U4, and U5 snRNPs; homolog of human Sm G [Source:SGD;Acc:S000002965] |
F |
YFL050C |
ALR2 |
164 |
-37.4 |
3 |
Probable Mg(2+) transporter; overexpression confers increased tolerance to Al(3+) and Ga(3+) ions; plays a role in regulating Ty1 transposition [Source:SGD;Acc:S000001844] |
G |
YGL010W |
MPO1 |
57 |
-24.2 |
3 |
Putative protein of unknown function; YGL010W is not an essential gene [Source:SGD;Acc:S000002978] |
G |
YGL116W |
CDC20 |
80 |
-16.8 |
3 |
Cell-cycle regulated activator of anaphase-promoting complex/cyclosome (APC/C), which is required for metaphase/anaphase transition; directs ubiquitination of mitotic cyclins, Pds1p, and other anaphase inhibitors; potential Cdc28p substrate [Source:SGD;Acc:S000003084] |
G |
YGL131C |
SNT2 |
72 |
-47.1 |
3 |
DNA binding protein with similarity to the S. pombe Snt2 protein; computational analysis suggests a role in regulation of expression of genes encoding amine transporters [Source:SGD;Acc:S000003099] |
G |
YGL146C |
RRT6 |
14 |
-43.5 |
3 |
Putative protein of unknown function; non-essential gene identified in a screen for mutants with increased levels of rDNA transcription; contains two putative transmembrane spans, but no significant homology to other known proteins [Source:SGD;Acc:S000003114] |
G |
YGL154C |
LYS5 |
11 |
-16.8 |
3 |
Phosphopantetheinyl transferase involved in lysine biosynthesis; converts inactive apo-form of Lys2p (alpha-aminoadipate reductase) into catalytically active holo-form by posttranslational addition of phosphopantetheine [Source:SGD;Acc:S000003122] |
G |
YGL176C |
YGL176C |
30 |
-19.1 |
3 |
Putative protein of unknown function; deletion mutant is viable and has no detectable phenotype [Source:SGD;Acc:S000003144] |
G |
YGL209W |
MIG2 |
42 |
-46.3 |
3 |
Protein containing zinc fingers, involved in repression, along with Mig1p, of SUC2 (invertase) expression by high levels of glucose; binds to Mig1p-binding sites in SUC2 promoter [Source:SGD;Acc:S000003177] |
G |
YGR026W |
YGR026W |
234 |
-98.8 |
3 |
Putative protein of unknown function; green fluorescent protein (GFP)-fusion protein localizes to the cell periphery [Source:SGD;Acc:S000003258] |
G |
YGR101W |
PCP1 |
32 |
-23 |
3 |
Mitochondrial serine protease required for the processing of various mitochondrial proteins and maintenance of mitochondrial DNA and morphology; belongs to the rhomboid-GlpG superfamily of intramembrane peptidases [Source:SGD;Acc:S000003333] |
G |
YGR105W |
VMA21 |
20 |
-16.2 |
3 |
Integral membrane protein that is required for vacuolar H+-ATPase (V-ATPase) function, although not an actual component of the V-ATPase complex; functions in the assembly of the V-ATPase; localized to the yeast endoplasmic reticulum (ER) [Source:SGD;Acc:S000003337] |
G |
YGR121C |
MEP1 |
71 |
-32 |
3 |
Ammonium permease; belongs to a ubiquitous family of cytoplasmic membrane proteins that transport only ammonium (NH4+); expression is under the nitrogen catabolite repression regulation [Source:SGD;Acc:S000003353] |
G |
YGR168C |
YGR168C |
166 |
-58.1 |
3 |
Putative protein of unknown function; YGR168C is not an essential gene [Source:SGD;Acc:S000003400] |
G |
YGR212W |
SLI1 |
26 |
-90.5 |
3 |
N-acetyltransferase, confers resistance to the sphingolipid biosynthesis inhibitor myriocin (ISP-1) by converting it into N-acetyl-myriocin, co-operates with Ypk1p in mediating resistance to myriocin [Source:SGD;Acc:S000003444] |
H |
YHR143W |
DSE2 |
15 |
-11.7 |
3 |
Daughter cell-specific secreted protein with similarity to glucanases, degrades cell wall from the daughter side causing daughter to separate from mother; expression is repressed by cAMP [Source:SGD;Acc:S000001186] |
H |
YHR211W |
FLO5 |
35 |
-39.2 |
3 |
Lectin-like cell wall protein (flocculin) involved in flocculation, binds to mannose chains on the surface of other cells, confers floc-forming ability that is chymotrypsin resistant but heat labile; similar to Flo1p [Source:SGD;Acc:S000001254] |
I |
YIL006W |
YIA6 |
11 |
-113.6 |
3 |
Mitochondrial NAD+ transporter, involved in the transport of NAD+ into the mitochondria (see also YEA6); member of the mitochondrial carrier subfamily; disputed role as a pyruvate transporter; has putative mouse and human orthologs [Source:SGD;Acc:S000001268] |
I |
YIL049W |
DFG10 |
15 |
-32.2 |
3 |
Probable polyprenol reductase that catalyzes conversion of polyprenol to dolichol, the precursor for N-glycosylation; involved in filamentous growth; mutations in human ortholog SRD5A3 confer CDG (Congenital Disorders of Glycosylation) [Source:SGD;Acc:S000001311] |
I |
YIL099W |
SGA1 |
27 |
-88.6 |
3 |
Intracellular sporulation-specific glucoamylase involved in glycogen degradation; induced during starvation of a/a diploids late in sporulation, but dispensable for sporulation [Source:SGD;Acc:S000001361] |
I |
YIR027C |
DAL1 |
51 |
-31.3 |
3 |
Allantoinase, converts allantoin to allantoate in the first step of allantoin degradation; expression sensitive to nitrogen catabolite repression [Source:SGD;Acc:S000001466] |
J |
YJL059W |
YHC3 |
13 |
-13.8 |
3 |
Vacuolar membrane protein involved in the ATP-dependent transport of arginine into the vacuole and possibly in balancing ion homeostasis; homolog of human CLN3 involved in Batten disease (juvenile onset neuronal ceroid lipofuscinosis) [Source:SGD;Acc:S000003595] |
J |
YJL079C |
PRY1 |
99 |
-43.1 |
3 |
Protein of unknown function [Source:SGD;Acc:S000003615] |
J |
YJL113W |
YJL113W |
41 |
-27.7 |
3 |
Retrotransposon TYA Gag and TYB Pol genes; transcribed/translated as one unit; polyprotein is processed to make a nucleocapsid-like protein (Gag), reverse transcriptase (RT), protease (PR), and integrase (IN); similar to retroviral genes [Source:SGD;Acc:S000003649] |
J |
YJL199C |
MBB1 |
19 |
-20.1 |
3 |
Dubious open reading frame, unlikely to encode a protein; not conserved in closely related Saccharomyces species; protein detected in large-scale protein-protein interaction studies [Source:SGD;Acc:S000003735] |
J |
YJL214W |
HXT8 |
129 |
-22.1 |
3 |
Protein of unknown function with similarity to hexose transporter family members, expression is induced by low levels of glucose and repressed by high levels of glucose [Source:SGD;Acc:S000003750] |
J |
YJR116W |
TDA4 |
19 |
-29.5 |
3 |
Putative protein of unknown function; null mutant is sensitive to expression of the top1-T722A allele [Source:SGD;Acc:S000003877] |
J |
YJR153W |
PGU1 |
13 |
-93.1 |
3 |
Endo-polygalacturonase, pectolytic enzyme that hydrolyzes the alpha-1,4-glycosidic bonds in the rhamnogalacturonan chains in pectins [Source:SGD;Acc:S000003914] |
K |
YKR011C |
YKR011C |
37 |
-108 |
3 |
Putative protein of unknown function; green fluorescent protein (GFP)-fusion protein localizes to the nucleus [Source:SGD;Acc:S000001719] |
K |
YKR051W |
YKR051W |
43 |
-28.6 |
3 |
Putative protein of unknown function [Source:SGD;Acc:S000001759] |
K |
YKR102W |
FLO10 |
19 |
-31.3 |
3 |
Lectin-like protein with similarity to Flo1p, thought to be involved in flocculation [Source:SGD;Acc:S000001810] |
L |
YLL052C |
AQY2 |
8 |
-25 |
3 |
Water channel that mediates the transport of water across cell membranes, only expressed in proliferating cells, controlled by osmotic signals, may be involved in freeze tolerance; disrupted by a stop codon in many S. cerevisiae strains [Source:SGD;Acc:S000003975] |
L |
YLL053C |
YLL053C |
51 |
-15.7 |
3 |
Putative protein; in the Sigma 1278B strain background YLL053C is contiguous with AQY2 which encodes an aquaporin [Source:SGD;Acc:S000003976] |
L |
YLR165C |
PUS5 |
15 |
-102.7 |
3 |
Pseudouridine synthase, catalyzes only the formation of pseudouridine (Psi)-2819 in mitochondrial 21S rRNA; not essential for viability [Source:SGD;Acc:S000004155] |
L |
YLR168C |
UPS2 |
38 |
-19.1 |
3 |
Mitochondrial intermembrane space protein involved in regulation of mitochondrial cardiolipin and phosphatidylethanolamine levels; null has defects in mitochondrial morphology; similar to Ups1p, Ups3p and to human PRELI [Source:SGD;Acc:S000004158] |
L |
YLR254C |
NDL1 |
14 |
-16.4 |
3 |
Homolog of nuclear distribution factor NudE, NUDEL; interacts with Pac1p and regulates dynein targeting to microtubule plus ends [Source:SGD;Acc:S000004244] |
L |
YLR307C-A |
YLR307C-A |
17 |
-71.4 |
3 |
Putative protein of unknown function [Source:SGD;Acc:S000028525] |
L |
YLR408C |
BLS1 |
22 |
-24 |
3 |
Putative protein of unknown function; likely member of BLOC complex involved in endosomal cargo sorting; green fluorescent protein (GFP)-fusion protein localizes to the endosome; YLR408C is not an essential gene [Source:SGD;Acc:S000004400] |
M |
YML068W |
ITT1 |
35 |
-54.7 |
3 |
Protein that modulates the efficiency of translation termination, interacts with translation release factors eRF1 (Sup45p) and eRF3 (Sup35p) in vitro, contains a zinc finger domain characteristic of the TRIAD class of proteins [Source:SGD;Acc:S000004533] |
M |
YML116W |
ATR1 |
52 |
-33.2 |
3 |
Multidrug efflux pump of the major facilitator superfamily, required for resistance to aminotriazole and 4-nitroquinoline-N-oxide [Source:SGD;Acc:S000004584] |
M |
YMR034C |
YMR034C |
17 |
-8.6 |
3 |
Putative transporter, member of the SLC10 carrier family; identified in a transposon mutagenesis screen as a gene involved in azole resistance; YMR034C is not an essential gene [Source:SGD;Acc:S000004637] |
M |
YMR137C |
PSO2 |
46 |
-81.8 |
3 |
Nuclease required for a post-incision step in the repair of DNA single and double-strand breaks that result from interstrand crosslinks produced by a variety of mono- and bi-functional psoralen derivatives; induced by UV-irradiation [Source:SGD;Acc:S000004745] |
M |
YMR195W |
ICY1 |
8 |
-5.4 |
3 |
Protein of unknown function, required for viability in rich media of cells lacking mitochondrial DNA; mutants have an invasive growth defect with elongated morphology; induced by amino acid starvation [Source:SGD;Acc:S000004808] |
M |
YMR274C |
RCE1 |
8 |
-18.7 |
3 |
Type II CAAX prenyl protease involved in the proteolysis and maturation of Ras and the a-factor mating pheromone [Source:SGD;Acc:S000004887] |
N |
YNL083W |
SAL1 |
59 |
-32.4 |
3 |
ADP/ATP transporter; member of the Ca2+-binding subfamily of mitochondrial carriers, with two EF-hand motifs; transport activity of either Sal1p or Pet9p is critical for viability; polymorphic in different S. cerevisiae strains [Source:SGD;Acc:S000005027] |
N |
YNL146W |
YNL146W |
7 |
-6.2 |
3 |
Putative protein of unknown function; green fluorescent protein (GFP)-fusion protein localizes to the endoplasmic reticulum; YNL146W is not an essential gene [Source:SGD;Acc:S000005090] |
N |
YNL187W |
SWT21 |
14 |
-78.9 |
3 |
Protein involved in mRNA splicing; contains a consensus nuclear export signal (NES) sequence similar to the consensus sequence recognized by Crm1p; interacts genetically with Prp40p and Tgs1p; contains WD40 repeats [Source:SGD;Acc:S000005131] |
N |
YNR071C |
YNR071C |
26 |
-54.4 |
3 |
Putative protein of unknown function [Source:SGD;Acc:S000005354] |
O |
YOL026C |
MIM1 |
23 |
-17.8 |
3 |
Mitochondrial protein required for outer membrane protein import; cooperates with Tom70p to import the subset of proteins with multiple alpha-helical transmembrane segments, including Ugo1p, Tom20p, and others; present as an oligomer in the outer me that may create a local environment that facilitates membrane insertion of substrate proteins; also has a role in assembly of Tom20p into the TOM complex [Source:SGD;Acc:S000005386] |
O |
YOL159C |
YOL159C |
23 |
-20.1 |
3 |
Soluble protein of unknown function; deletion mutants are viable and have elevated levels of Ty1 retrotransposition and Ty1 cDNA [Source:SGD;Acc:S000005519] |
O |
YOR005C |
DNL4 |
40 |
-39.6 |
3 |
DNA ligase required for nonhomologous end-joining (NHEJ), forms stable heterodimer with required cofactor Lif1p, interacts with Nej1p; involved in meiosis, not essential for vegetative growth [Source:SGD;Acc:S000005531] |
O |
YOR025W |
HST3 |
62 |
-25.2 |
3 |
Member of the Sir2 family of NAD(+)-dependent protein deacetylases; involved along with Hst4p in telomeric silencing, cell cycle progression, radiation resistance, genomic stability and short-chain fatty acid metabolism [Source:SGD;Acc:S000005551] |
O |
YOR047C |
STD1 |
19 |
-11.1 |
3 |
Protein involved in control of glucose-regulated gene expression; interacts with kinase Snf1p, glucose sensors Snf3p and Rgt2p, TATA-binding Spt15p; regulator of transcription factor Rgt1p; interactions with Pma1p appear to propagate [GAR+] [Source:SGD;Acc:S000005573] |
O |
YOR060C |
SLD7 |
28 |
-27.6 |
3 |
Protein with a role in chromosomal DNA replication; interacts with Sld3p and reduces its affinity for Cdc45p; deletion mutant has aberrant mitochondria [Source:SGD;Acc:S000005586] |
O |
YOR137C |
SIA1 |
28 |
-60.5 |
3 |
Protein of unassigned function involved in activation of the Pma1p plasma membrane H+-ATPase by glucose [Source:SGD;Acc:S000005663] |
O |
YOR156C |
NFI1 |
60 |
-54.3 |
3 |
SUMO E3 ligase, catalyzes the covalent attachment of SUMO (Smt3p) to proteins; primary E3 ligase for Sir4p; sumoylates Yku70p/Yku80p and Sir4p in vivo to promote chromatin anchoring; promotes telomere anchoring to the nuclear envelope; involved in m ance of proper telomere length [Source:SGD;Acc:S000005682] |
O |
YOR228C |
MCP1 |
62 |
-64 |
3 |
Protein of unknown function, localized to the mitochondrial outer membrane [Source:SGD;Acc:S000005754] |
O |
YOR380W |
RDR1 |
37 |
-22.6 |
3 |
Transcriptional repressor involved in the control of multidrug resistance; negatively regulates expression of the PDR5 gene; member of the Gal4p family of zinc cluster proteins [Source:SGD;Acc:S000005907] |
O |
YOR381W |
FRE3 |
12 |
-27.5 |
3 |
Ferric reductase, reduces siderophore-bound iron prior to uptake by transporters; expression induced by low iron levels [Source:SGD;Acc:S000005908] |
O |
YOR384W |
FRE5 |
27 |
-160.8 |
3 |
Putative ferric reductase with similarity to Fre2p; expression induced by low iron levels; the authentic, non-tagged protein is detected in highly purified mitochondria in high-throughput studies [Source:SGD;Acc:S000005911] |
O |
YOR390W |
FEX1 |
53 |
-74.5 |
3 |
Putative protein of unknown function [Source:SGD;Acc:S000005917] |
P |
YPL024W |
RMI1 |
26 |
-17.7 |
3 |
Subunit of the RecQ (Sgs1p) - Topo III (Top3p) complex; stimulates superhelical relaxing and ssDNA binding activities of Top3p; involved in response to DNA damage; null mutants display increased rates of recombination and delayed S phase [Source:SGD;Acc:S000005945] |
P |
YPL052W |
OAZ1 |
38 |
-45.8 |
3 |
Regulator of ornithine decarboxylase (Spe1p), antizyme that binds to Spe1p to stimulate ubiquitin-independent degradation by the proteasome; binding of polyamines to nascent Oaz1p during translation stimulates +1 ribosomal frameshifting, allowing tr ion of full-length Oaz1p [Source:SGD;Acc:S000005973] |
P |
YPL159C |
PET20 |
110 |
-26.6 |
3 |
Mitochondrial protein, required for respiratory growth under some conditions and for stability of the mitochondrial genome [Source:SGD;Acc:S000006080] |
P |
YPL164C |
MLH3 |
70 |
-124 |
3 |
Protein involved in DNA mismatch repair and crossing-over during meiotic recombination; forms a complex with Mlh1p; mammalian homolog is implicated mammalian microsatellite instability [Source:SGD;Acc:S000006085] |
P |
YPL272C |
PBI1 |
27 |
-14.6 |
3 |
Putative protein of unknown function; gene expression induced in response to ketoconazole; YPL272C is not an essential gene [Source:SGD;Acc:S000006193] |
P |
YPL279C |
FEX2 |
52 |
-74.5 |
3 |
Putative protein of unknown function [Source:SGD;Acc:S000006200] |
P |
YPR009W |
SUT2 |
39 |
-10.4 |
3 |
Putative transcription factor; multicopy suppressor of mutations that cause low activity of the cAMP/protein kinase A pathway; highly similar to Sut1p [Source:SGD;Acc:S000006213] |
P |
YPR061C |
JID1 |
32 |
-50.1 |
3 |
Probable Hsp40p co-chaperone, has a DnaJ-like domain and appears to be involved in ER-associated degradation of misfolded proteins containing a tightly folded cytoplasmic domain; inhibits replication of Brome mosaic virus in S. cerevisiae [Source:SGD;Acc:S000006265] |
P |
YPR138C |
MEP3 |
54 |
-17.3 |
3 |
Ammonium permease of high capacity and low affinity; belongs to a ubiquitous family of cytoplasmic membrane proteins that transport only ammonium (NH4+); expression is under the nitrogen catabolite repression regulation ammonia permease [Source:SGD;Acc:S000006342] |
P |
YPR169W-A |
YPR169W-A |
16 |
-7.4 |
3 |
Dubious open reading frame unlikely to encode a protein, based on available experimental and comparative sequence data; partially overlaps two other dubious ORFs: YPR170C and YPR170W-B [Source:SGD;Acc:S000028591] |
Q |
Q0055 |
AI2 |
44 |
-115.2 |
3 |
Reverse transcriptase required for splicing of the COX1 pre-mRNA, encoded by a mobile group II intron within the mitochondrial COX1 gene [Source:SGD;Acc:S000007262] |
Q |
Q0070 |
AI5_ALPHA |
22 |
-61.1 |
3 |
Endonuclease I-SceIV, involved in intron mobility; encoded by a mobile group I intron within the mitochondrial COX1 gene [Source:SGD;Acc:S000007265] |
Q |
Q0105 |
COB |
89 |
-54.1 |
3 |
Cytochrome b, mitochondrially encoded subunit of the ubiquinol-cytochrome c reductase complex which includes Cobp, Rip1p, Cyt1p, Cor1p, Qcr2p, Qcr6p, Qcr7p, Qcr8p, Qcr9p, and Qcr10p [Source:SGD;Acc:S000007270] |
Q |
Q0110 |
BI2 |
89 |
-68.6 |
3 |
Mitochondrial mRNA maturase with a role in splicing, encoded by both exon and intron sequences of partially processed COB mRNA [Source:SGD;Acc:S000007271] |
Q |
Q0115 |
BI3 |
82 |
-36.6 |
3 |
Mitochondrial mRNA maturase, forms a complex with Mrs1p to mediate splicing of the bI3 intron of the COB gene; encoded by both exon and intron sequences of partially processed COB mRNA [Source:SGD;Acc:S000007272] |
Q |
Q0120 |
BI4 |
92 |
-83.2 |
3 |
Mitochondrial mRNA maturase, forms a complex with Nam2p to mediate splicing of the bI4 intron of the COB gene; encoded by both exon and intron sequences of partially processed COB mRNA [Source:SGD;Acc:S000007273] |
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