Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10010133HBVENSG00000076555.16protein_codingACACBNoNo32O00763
TVIS10018709HBVENSG00000076555.16protein_codingACACBNoNo32O00763
TVIS10052330HBVENSG00000076555.16protein_codingACACBNoNo32O00763
TVIS10047722HBVENSG00000076555.16protein_codingACACBNoNo32O00763
TVIS10045816HBVENSG00000076555.16protein_codingACACBNoNo32O00763
TVIS10045817HBVENSG00000076555.16protein_codingACACBNoNo32O00763
TVIS30033990HIVENSG00000076555.16protein_codingACACBNoNo32O00763
TVIS20000544HPVENSG00000076555.16protein_codingACACBNoNo32O00763
TVIS20050489HPVENSG00000076555.16protein_codingACACBNoNo32O00763
TVIS44026712HTLV-1ENSG00000076555.16protein_codingACACBNoNo32O00763
TCGA Plot Options
Drug Information
GeneACACB
DrugBank IDDB00121
Drug NameBiotin
Target IDBE0000702
UniProt IDO00763
Regulation Typecofactor
PubMed IDs17477831; 16772434
CitationsLiu Y, Zalameda L, Kim KW, Wang M, McCarter JD: Discovery of acetyl-coenzyme A carboxylase 2 inhibitors: comparison of a fluorescence intensity-based phosphate assay and a fluorescence polarization-based ADP Assay for high-throughput screening. Assay Drug Dev Technol. 2007 Apr;5(2):225-35.@@Hassan YI, Zempleni J: Epigenetic regulation of chromatin structure and gene function by biotin. J Nutr. 2006 Jul;136(7):1763-5.
GroupsApproved; Investigational; Nutraceutical
Direct ClassificationBiotin and derivatives
SMILES[H][C@]12CS[C@@H](CCCCC(O)=O)[C@@]1([H])NC(=O)N2
PathwaysMitochondrial Complex II Deficiency; 3-Methylglutaconic Aciduria Type III; 2-Ketoglutarate Dehydrogenase Complex Deficiency; 4-Hydroxybutyric Aciduria/Succinic Semialdehyde Dehydrogenase Deficiency; Isovaleric Aciduria; Pyruvate Carboxylase Deficiency; Warburg Effect; Isobutyryl-CoA Dehydrogenase Deficiency; Biotin Metabolism; Fructose-1,6-diphosphatase Deficiency; Methylmalonic Aciduria Due to Cobalamin-Related Disorders; Propionic Acidemia; Transfer of Acetyl Groups into Mitochondria; Malonic Aciduria; 2-Hydroxyglutric Aciduria (D and L Form); 3-Methylcrotonyl-CoA Carboxylase Deficiency Type I; Congenital Lactic Acidosis; 3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency; Fumarase Deficiency; Succinic Semialdehyde Dehydrogenase Deficiency; Alanine Metabolism; Methylmalonic Aciduria; 3-Methylglutaconic Aciduria Type IV; Lactic Acidemia; Glycogen Storage Disease Type 1A (GSD1A) or Von Gierke Disease; Primary Hyperoxaluria Type I; Triosephosphate Isomerase; The Oncogenic Action of 2-Hydroxyglutarate; Valine, Leucine, and Isoleucine Degradation; Maple Syrup Urine Disease
PharmGKBPA448625
ChEMBLCHEMBL857