| ORF |
Std. Name |
|
ACV104_A1B |
|
YKL054c
|
DEF1 |
|
0.465
|
| Rad26-interacting protein |
|
YPL061w
|
ALD6 |
|
0.465
|
| aldehyde dehydrogenase |
|
YNL228w
|
|
|
0.465
|
| Hypothetical ORF |
|
YLR169w
|
|
|
0.465
|
| Hypothetical ORF |
|
YPL004c
|
LSP1 |
|
0.465
|
| Long chain base-responsive inhibitor of protein kinases Phk1p and Phk2p, acts along with Pil1p to down-regulate heat stress resistance via regulation of the Pkc1p and Ypk1p pathways; phosphorylated by Phk1p and Phk2p |
|
YDR382w
|
RPP2B |
|
0.465
|
| ribosomal protein P2B (YP2beta) (L45) |
|
YEL057c
|
|
|
0.465
|
| Hypothetical ORF |
|
YDR233c
|
RTN1 |
|
0.465
|
| reticulon gene member of the RTNLA (reticulon-like A) subfamily |
|
YDR255c
|
RMD5 |
|
0.465
|
| Cytosolic protein required for sporulation; also required for the ubiquitination of the gluconeogenetic enzyme fructose-1,6-bisphosphatase, which is degraded rapidly after the switch from gluconeogenesis to glycolysis |
|
YLR357w
|
RSC2 |
|
0.465
|
| RSC complex member |
|
YNL119w
|
NCS2 |
|
0.466
|
| plays a role in invasive growth |
|
YDL088c
|
ASM4 |
|
0.466
|
| Nuclear pore complex subunit, part of a subcomplex also containing Nup53p, Nup170p, and Pse1p |
|
YGL162w
|
SUT1 |
|
0.466
|
| Involved in sterol uptake |
|
YDR032c
|
PST2 |
|
0.466
|
| Protoplasts-SecreTed protein; the gene product was detected among the proteins secreted by regenerating protoplasts |
|
YIL071c
|
PCI8 |
|
0.466
|
| translational regulator (putative)|COP9 signalosome (CSN) subunit |
|
YMR319c
|
FET4 |
|
0.466
|
| low affinity Fe2+ transport protein |
|
YHL023c
|
RMD11 |
|
0.466
|
| Protein required for sporulation |
|
YKL096w
|
CWP1 |
|
0.466
|
| Cell wall mannoprotein, linked to a beta-1,3- and beta-1,6-glucan heteropolymer through a phosphodiester bond: involved in cell wall organization |
|
YBR031w
|
RPL4A |
|
0.466
|
| ribosomal protein L4A (L2A) (rp2) (YL2) |
|
YPR139c
|
VPS66 |
|
0.466
|
|
|
YEL066w
|
HPA3 |
|
0.466
|
| Histone acetyltransferase of the Gcn5-related N-acetyltransferase (GNAT) superfamily that is most similar to Hpa2p; acetylates histones weakly in vitro and autoacetylates |
|
YBR023c
|
CHS3 |
|
0.466
|
| Chitin synthase III, catalyzes the transfer of N-acetylglucosamine (GlcNAc) to chitin: required for synthesis of the majority of cell wall chitin, the chitin ring during bud emergence, and spore wall chitosan |
|
YOR228c
|
|
|
0.466
|
| Hypothetical ORF |
|
YDR134c
|
|
|
0.466
|
| Hypothetical ORF |
|
YGR269w
|
|
|
0.466
|
| Hypothetical ORF |
|
YLR437c
|
|
|
0.467
|
| Hypothetical ORF |
|
YOR312c
|
RPL20B |
|
0.467
|
| Protein component of the large (60S) ribosomal subunit, nearly identical to Rpl20Ap and has similarity to rat L18a ribosomal protein |
|
YGL221c
|
NIF3 |
|
0.467
|
| similar to Listeria monocytogenes major sigma factor (rpoD gene product) |
|
YMR016c
|
SOK2 |
|
0.467
|
| transcription factor (putative) |
|
YDR290w
|
|
|
0.467
|
| Dubious open reading frame, unlikely to encode a protein; not conserved in closely related Saccharomyces species; 42% of ORF overlaps the verified gene RTT103; deletion causes hydroxyuracil sensitivity |
|
YKL124w
|
SSH4 |
|
0.467
|
| Suppressor of SHR3; confers leflunomide resistance when overexpressed |
|
YER142c
|
MAG1 |
|
0.467
|
| 3-methyladenine DNA glycosylase |
|
YMR224c
|
MRE11 |
|
0.467
|
| Subunit of a complex with Rad50p and Xrs2p (RMX complex) that functions in repair of DNA double-strand breaks and in telomere stability, exhibits nuclease activity that appears to be required for RMX function: widely conserved |
|
YIR020c
|
|
|
0.467
|
| Hypothetical ORF |
|
YGR069w
|
|
|
0.467
|
| Hypothetical ORF |
|
YHR051w
|
COX6 |
|
0.468
|
| cytochrome c oxidase subunit |
|
YKR096w
|
|
|
0.468
|
| Hypothetical ORF |
|
YOR315w
|
|
|
0.468
|
| Protein of unknown function, found in the cytoplasm and the nucleus; potential Cdc28p substrate |
|
YDR101c
|
ARX1 |
|
0.468
|
|
|
YJR130c
|
STR2 |
|
0.468
|
| cystathionine gamma-synthase |
|
YDR123c
|
INO2 |
|
0.468
|
| Component of the heteromeric Ino2p/Ino4p basic helix-loop-helix transcription activator that binds inositol/choline-responsive elements (ICREs), required for derepression of phospholipid biosynthetic genes in response to inositol depletion |
|
YMR032w
|
HOF1 |
|
0.468
|
| Bud neck-localized, SH3 domain-containing protein required for cytokinesis: regulates actomyosin ring dynamics and septin localization: interacts with the formins, Bni1p and Bnr1p, and with Cyk3p, Vrp1p, and Bni5p |
|
YIR019c
|
MUC1 |
|
0.468
|
| GPI-anchored cell surface glycoprotein required for diploid pseudohyphal formation and haploid invasive growth, transcriptionally regulated by the MAPK pathway (via Ste12p and Tec1p) and the cAMP pathway (via Flo8p) |
|
YEL042w
|
GDA1 |
|
0.468
|
| Guanosine diphosphatase located in the Golgi, involved in the transport of GDP-mannose into the Golgi lumen by converting GDP to GMP after mannose is transferred its substrate |
|
YKL123w
|
|
|
0.468
|
| Hypothetical ORF |
|
YER173w
|
RAD24 |
|
0.468
|
| Checkpoint protein, involved in the activation of the DNA damage and meiotic pachytene checkpoints: subunit of a clamp loader that loads Rad17p-Mec3p-Ddc1p onto DNA: homolog of human and S. pombe Rad17 protein |
|
YGL224c
|
SDT1 |
|
0.468
|
| suppressor of deletion of TFIIS |
|
YJR010w
|
MET3 |
|
0.468
|
| ATP sulfurylase |
|
YLR028c
|
ADE16 |
|
0.468
|
| 5-aminoimidazole-4-carboxamide ribonucleotide (AICAR) transformylase/IMP cyclohydrolase |
|
YNL022c
|
|
|
0.468
|
| Non-essential protein with similarity to S. pombe hypothetical protein E349594 |
