Protein required for the negative regulation by ammonia of Gap1p, which is a general amino acid permease
Zygosity: Homozygous strain
fixedexpanded
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Top fitness defect scores for YFL010W-A deletion by condition
Download Fitness data (tab-delimited text) (excel) |
Correlation | pval | ORF | Gene | Zygosity | Description |
---|---|---|---|---|---|
0.123 | 9.28E-13 | YMR297W | PRC1 | hom | Vacuolar carboxypeptidase Y (proteinase C; CPY), broad-specificity C-terminal exopeptidase involved in non-specific protein degradation in the vacuole; member of the serine carboxypeptidase family |
0.100 | 5.78E-9 | YIL084C | SDS3 | hom | Component of the Rpd3p/Sin3p deacetylase complex required for its structural integrity and catalytic activity, involved in transcriptional silencing and required for sporulation; cells defective in SDS3 display pleiotropic phenotypes |
0.089 | 2.26E-7 | YOL028C | YAP7 | hom | Putative basic leucine zipper (bZIP) transcription factor; YAP7 has a paralog, YAP5, that arose from the whole genome duplication |
0.081 | 2.53E-6 | YLR128W | DCN1 | hom | Scaffold-type E3 ligase required for cullin neddylation and ubiquitin ligase activation; contains a ubiquitin-binding domain (UBA) for ubiquitin and Nedd8 (Rub1p) interaction and a PONY domain involved in cullin binding and neddylation |
0.079 | 5.28E-6 | YPR085C | ASA1 | het | Subunit of the ASTRA complex, involved in chromatin remodeling; telomere length regulator involved in the stability or biogenesis of PIKKs such as TORC1 |
0.077 | 7.68E-6 | YKL127W | PGM1 | hom | Phosphoglucomutase, minor isoform; catalyzes the conversion from glucose-1-phosphate to glucose-6-phosphate, which is a key step in hexose metabolism |
0.077 | 7.76E-6 | YGR284C | ERV29 | hom | Protein localized to COPII-coated vesicles; involved in vesicle formation and incorporation of specific secretory cargo; protein abundance increases in response to DNA replication stress |
0.076 | 1.14E-5 | YDR132C | YDR132C | hom | Protein of unknown function; protein increases in abundance and relative distribution to the nucleus increases upon DNA replication stress; YDR132C has a paralog, YLR108C, that arose from the whole genome duplication |
0.076 | 1.15E-5 | YKR049C | FMP46 | hom | Putative redox protein containing a thioredoxin fold; the authentic, non-tagged protein is detected in highly purified mitochondria in high-throughput studies |
0.075 | 1.21E-5 | YJL058C | BIT61 | hom | Subunit of TORC2 membrane-associated complex; involved in regulation of cell cycle-dependent actin cytoskeletal dynamics during polarized growth and cell wall integrity; BIT61 has a paralog, BIT2, that arose from the whole genome duplication |
0.071 | 3.87E-5 | YLR209C | PNP1 | hom | Purine nucleoside phosphorylase, specifically metabolizes inosine and guanosine nucleosides; involved in the nicotinamide riboside salvage pathway |
0.071 | 3.89E-5 | YBL096C_d | YBL096C_d | hom | Non-essential protein of unknown function |
0.071 | 4.36E-5 | YIR020C_p | YIR020C_p | hom | Protein of unknown function; mRNA identified as translated by ribosome profiling data |
0.070 | 5.22E-5 | YLR147C | SMD3 | het | Core Sm protein Sm D3; part of heteroheptameric complex (with Smb1p, Smd1p, Smd2p, Sme1p, Smx3p, and Smx2p) that is part of the spliceosomal U1, U2, U4, and U5 snRNPs; homolog of human Sm D3 |
0.069 | 6.70E-5 | YDL133C-A | RPL41B | hom | Ribosomal 60S subunit protein L41B; comprises only 25 amino acids; rpl41a rpl41b double null mutant is viable; homologous to mammalian ribosomal protein L41, no bacterial homolog; RPL41B has a paralog, RPL41A, that arose from the whole genome duplication |