| ORF |
Std. Name |
|
A8-1_A1B |
|
YDR131c
|
|
|
3.28E+3
|
| Hypothetical ORF |
|
YML041c
|
VPS71 |
|
3.29E+3
|
| Protein of unknown function, component of the Swr1p complex that incorporates Htz1p into chromatin: required for vacuolar protein sorting |
|
YIL135c
|
VHS2 |
|
3.29E+3
|
| Gene whose overexpression suppresses the synthetic lethality of the hal3 sit4 double mutation |
|
YDL149w
|
ATG9 |
|
3.29E+3
|
| Transmembrane protein involved in formation of Cvt and autophagic vesicles: cycles between the pre-autophagosomal structure and other cytosolic punctate structures, not found in autophagosomes |
|
YBR176w
|
ECM31 |
|
3.29E+3
|
| Ketopantoate hydroxymethyltransferase, required for pantothenic acid biosynthesis, converts 2-oxoisovalerate into 2-dehydropantoate |
|
YNL171c
|
|
|
3.30E+3
|
| Hypothetical ORF |
|
YGR149w
|
|
|
3.30E+3
|
| Hypothetical ORF |
|
YJR031c
|
GEA1 |
|
3.30E+3
|
| GDP/GTP exchange factor |
|
YJL147c
|
|
|
3.31E+3
|
| Hypothetical ORF |
|
YGR042w
|
|
|
3.31E+3
|
| Hypothetical ORF |
|
YDL184c
|
RPL41A |
|
3.31E+3
|
| Ribosomal protein L47 of the large (60S) ribosomal subunit, identical to Rpl41Bp and has similarity to rat L41 ribosomal protein: comprised of only 25 amino acids: rpl41a rpl41b double null mutant is viable |
|
YNL001w
|
DOM34 |
|
3.31E+3
|
| Probable RNA-binding protein, functions in protein translation to promote G1 progression and differentiation, required for meiotic cell division |
|
YER007c-A
|
|
|
3.31E+3
|
| Hypothetical ORF |
|
YDL090c
|
RAM1 |
|
3.31E+3
|
| farnesyltransferase beta subunit |
|
YNL198c
|
|
|
3.32E+3
|
| Hypothetical ORF |
|
YLR373c
|
VID22 |
|
3.32E+3
|
| Vacuole import and degradation |
|
YMR291w
|
|
|
3.32E+3
|
| Hypothetical ORF |
|
YDR101c
|
ARX1 |
|
3.32E+3
|
|
|
YCR034w
|
FEN1 |
|
3.32E+3
|
| Fatty acid elongase, involved in sphingolipid biosynthesis; acts on fatty acids of up to 24 carbons in length; mutations have regulatory effects on 1,3-beta-glucan synthase, vacuolar ATPase, and the secretory pathway |
|
YLR143w
|
|
|
3.32E+3
|
| Hypothetical ORF |
|
YER049w
|
|
|
3.33E+3
|
| Hypothetical ORF |
|
YDR479c
|
PEX29 |
|
3.33E+3
|
| peroxin |
|
YGR043c
|
|
|
3.33E+3
|
| Hypothetical ORF |
|
YBR170c
|
NPL4 |
|
3.33E+3
|
| Endoplasmic reticulum and nuclear membrane protein, forms a complex with Cdc48p and Ufd1p that recognizes ubiquitinated proteins in the endoplasmic reticulum and delivers them to the proteasome for degradation |
|
YGR173w
|
|
|
3.33E+3
|
| Protein with similarity to mammalian developmentally regulated GTP-binding protein |
|
YOR271c
|
|
|
3.33E+3
|
| Hypothetical ORF |
|
YER169w
|
RPH1 |
|
3.34E+3
|
| binds to PHR1 URS|transcriptional repressor |
|
YCL026c-A
|
FRM2 |
|
3.34E+3
|
| Protein of unknown function, involved in the integration of lipid signaling pathways with cellular homeostasis |
|
YNL212w
|
VID27 |
|
3.34E+3
|
| Vacuole import and degradation |
|
YLL026w
|
HSP104 |
|
3.34E+3
|
| heat shock protein 104 |
|
YDR115w
|
|
|
3.34E+3
|
| Putative mitochondrial ribosomal protein of the large subunit, has similarity to E. coli L34 ribosomal protein; required for respiratory growth, as are most mitochondrial ribosomal proteins |
|
YPR171w
|
BSP1 |
|
3.34E+3
|
| Binding protein of Synaptojanin Polyphosphoinositide phosphatase domain; may function to link synaptojanins Inp52p and Inp53p to the cortical actin cytoskeleton |
|
YIL136w
|
OM45 |
|
3.34E+3
|
| 45 kDa mitochondrial outer membrane protein |
|
YCR025c
|
|
|
3.34E+3
|
| Hypothetical ORF |
|
YCR081w
|
SRB8 |
|
3.35E+3
|
| activation mediator subcomplex of RNA polymerase I holoenzyme |
|
YJR080c
|
|
|
3.35E+3
|
| The authentic, non-tagged protein was localized to the mitochondria |
|
YIL045w
|
PIG2 |
|
3.35E+3
|
| 30% identity to YER054C/GIP2 |
|
YJL108c
|
PRM10 |
|
3.35E+3
|
| Pheromone-regulated protein, predicted to have 5 transmembrane segments |
|
YGR143w
|
SKN1 |
|
3.35E+3
|
| highly homologous to Kre6p|type II membrane protein (putative) |
|
YPL018w
|
CTF19 |
|
3.35E+3
|
| kinetochore protein |
|
YGR151c
|
|
|
3.35E+3
|
| Hypothetical ORF |
|
YDR153c
|
ENT5 |
|
3.36E+3
|
| Protein containing an N-terminal epsin-like domain involved in clathrin recruitment and traffic between the Golgi and endosomes; associates with the clathrin adaptor Gga2p, clathrin adaptor complex AP-1, and clathrin |
|
YGL228w
|
SHE10 |
|
3.36E+3
|
| Putative glycosylphosphatidylinositol (GPI)-anchored protein of unknown function; overexpression causes growth arrest |
|
YLR374c
|
|
|
3.36E+3
|
| Hypothetical ORF |
|
YHR176w
|
FMO1 |
|
3.36E+3
|
| Flavin-containing monooxygenase, localized to the cytoplasmic face of the ER membrane: catalyzes oxidation of biological thiols to maintain the ER redox buffer ratio for correct folding of disulfide-bonded proteins |
|
YDR083w
|
RRP8 |
|
3.36E+3
|
| nucleolar protein required for efficient processing of pre-rRNA at site A2; methyltransferase homolog |
|
YNL242w
|
ATG2 |
|
3.37E+3
|
| Peripheral membrane protein required for the formation of cytosolic sequestering vesicles involved in vacuolar import through both the Cvt pathway and autophagy: interacts with Atg9p and is necessary for its trafficking |
|
YLR182w
|
SWI6 |
|
3.37E+3
|
| Transcription cofactor, forms complexes with DNA-binding proteins Swi4p and Mbp1p to regulate transcription at the G1/S transition: involved in meiotic gene expression: localization regulated by phosphorylation: potential Cdc28p substrate |
|
YGR163w
|
GTR2 |
|
3.37E+3
|
| similar to Gtr1|small GTPase (putative) |
|
YCL014w
|
BUD3 |
|
3.38E+3
|
| Protein involved in bud-site selection and required for axial budding pattern: localizes with septins to bud neck in mitosis and may constitute an axial landmark for next round of budding |
