CEG_gene ID | Gene name(s) | Function | Condition | UniProt | Organism |
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CEGE0161_DEG20010405 | VHT1 | High-affinity plasma membrane H+-biotin (vitamin H) symporter; mutation results in fatty acid auxotrophy; 12 transmembrane domain containing major facilitator subfamily member; mRNA levels negatively regulated by iron deprivation and biotin | Rich medium | - | Saccharomyces cerevisiae |
CEGE0161_DEG20051462 | Slc17a5 | Sialin (Solute carrier family 17 member 5) (Sodium/sialic acid cotransporter) | Rich medium | Q8BN82 | Mus musculus |
CEGE0161_DEG20051680 | Slc17a7 | solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 [Source:RefSeq_peptide;Acc:NP_892038] | Rich medium | NP_892038 | Mus musculus |
CEGE0161_DEG20090184 | - | nicotinic acid plasma membrane transporter (predicted) | Rich medium | - | Schizosaccharomyces pombe 972h- |
CEGE0161_DEG20100385 | SLC17A6 | solute carrier family 17 (vesicular glutamate transporter), member 6 | Rich medium | Q9P2U8 | Homo sapiens |
CEGE0161_DEG20100553 | SLC17A7 | solute carrier family 17 (vesicular glutamate transporter), member 7 | Rich medium | Q9P2U7 | Homo sapiens |
CEGE0161_DEG20100910 | SLC17A5 | solute carrier family 17 (acidic sugar transporter), member 5 | Rich medium | Q9NRA2 | Homo sapiens |
CEGE0161_DEG20241211 | PIH1D1 | PIH1 domain containing 1 | Rich medium | Q9NWS0 | Homo sapiens |