Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS30007273HIVENSG00000141526.18protein_codingSLC16A3NoNo9123O15427
TVIS30002865HIVENSG00000141526.18protein_codingSLC16A3NoNo9123O15427
TVIS30007274HIVENSG00000141526.18protein_codingSLC16A3NoNo9123O15427
TVIS30088393HIVENSG00000141526.18protein_codingSLC16A3NoNo9123O15427
TVIS30078596HIVENSG00000141526.18protein_codingSLC16A3NoNo9123O15427
TVIS30020385HIVENSG00000141526.18protein_codingSLC16A3NoNo9123O15427
TVIS30046012HIVENSG00000141526.18protein_codingSLC16A3NoNo9123O15427
TVIS30046013HIVENSG00000141526.18protein_codingSLC16A3NoNo9123O15427
TVIS30046014HIVENSG00000141526.18protein_codingSLC16A3NoNo9123O15427
TVIS30046015HIVENSG00000141526.18protein_codingSLC16A3NoNo9123O15427
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Drug Information
GeneSLC16A3
DrugBank IDDB00119
Drug NamePyruvic acid
Target IDBE0000449
UniProt IDO15427
Regulation Type
PubMed IDs16213084
CitationsShimada A, Nakagawa Y, Morishige H, Yamamoto A, Fujita T: Functional characteristics of H+ -dependent nicotinate transport in primary cultures of astrocytes from rat cerebral cortex. Neurosci Lett. 2006 Jan 16;392(3):207-12. Epub 2005 Oct 5.
GroupsApproved; Investigational; Nutraceutical
Direct ClassificationAlpha-keto acids and derivatives
SMILESCC(=O)C(O)=O
PathwaysCitrullinemia Type I; 4-Hydroxybutyric Aciduria/Succinic Semialdehyde Dehydrogenase Deficiency; Glycogenosis, Type IB; Argininemia; Pyruvate Kinase Deficiency; Pyruvate Carboxylase Deficiency; Amino Sugar Metabolism; The Oncogenic Action of Fumarate; 3-Phosphoglycerate Dehydrogenase Deficiency; Glycolysis; Non-Ketotic Hyperglycinemia; 2-Hydroxyglutric Aciduria (D and L Form); Glucose-Alanine Cycle; G(M2)-Gangliosidosis: Variant B, Tay-Sachs Disease; Alanine Metabolism; Hyperglycinemia, Non-Ketotic; Cystinosis, Ocular Nonnephropathic; Dimethylglycine Dehydrogenase Deficiency; Glycogenosis, Type VII. Tarui Disease; Dihydropyrimidine Dehydrogenase Deficiency (DHPD); Lactic Acidemia; Homocarnosinosis; Primary Hyperoxaluria Type I; Ornithine Transcarbamylase Deficiency (OTC Deficiency); The Oncogenic Action of L-2-Hydroxyglutarate in Hydroxygluaricaciduria; Sarcosinemia; Urea Cycle; Phosphoenolpyruvate Carboxykinase Deficiency 1 (PEPCK1); Cysteine Metabolism
PharmGKBPA164778686
ChEMBLCHEMBL1162144