VIS ID | Virus | Ensembl ID | Gene Type | Target Gene | Oncogene | Tumor Suppressor Gene | NCBI ID | Uniprot ID |
---|---|---|---|---|---|---|---|---|
TVIS10010133 | HBV | ENSG00000076555.16 | protein_coding | ACACB | No | No | 32 | O00763 |
TVIS10018709 | HBV | ENSG00000076555.16 | protein_coding | ACACB | No | No | 32 | O00763 |
TVIS10052330 | HBV | ENSG00000076555.16 | protein_coding | ACACB | No | No | 32 | O00763 |
TVIS10047722 | HBV | ENSG00000076555.16 | protein_coding | ACACB | No | No | 32 | O00763 |
TVIS10045816 | HBV | ENSG00000076555.16 | protein_coding | ACACB | No | No | 32 | O00763 |
TVIS10045817 | HBV | ENSG00000076555.16 | protein_coding | ACACB | No | No | 32 | O00763 |
TVIS30033990 | HIV | ENSG00000076555.16 | protein_coding | ACACB | No | No | 32 | O00763 |
TVIS20000544 | HPV | ENSG00000076555.16 | protein_coding | ACACB | No | No | 32 | O00763 |
TVIS20050489 | HPV | ENSG00000076555.16 | protein_coding | ACACB | No | No | 32 | O00763 |
TVIS44026712 | HTLV-1 | ENSG00000076555.16 | protein_coding | ACACB | No | No | 32 | O00763 |
Target Gene Table
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TCGA Plot Options
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Drug Information
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Gene | ACACB |
---|---|
DrugBank ID | DB00121 |
Drug Name | Biotin |
Target ID | BE0000702 |
UniProt ID | O00763 |
Regulation Type | cofactor |
PubMed IDs | 17477831; 16772434 |
Citations | Liu 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. |
Groups | Approved; Investigational; Nutraceutical |
Direct Classification | Biotin and derivatives |
SMILES | [H][C@]12CS[C@@H](CCCCC(O)=O)[C@@]1([H])NC(=O)N2 |
Pathways | Mitochondrial 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 |
PharmGKB | PA448625 |
ChEMBL | CHEMBL857 |