| VIS ID | Virus | Ensembl ID | Gene Type | Target Gene | Oncogene | Tumor Suppressor Gene | NCBI ID | Uniprot ID |
|---|---|---|---|---|---|---|---|---|
| TVIS20036440 | HPV | ENSG00000078070.14 | protein_coding | MCCC1 | No | No | 56922 | A0A0S2Z693 Q96RQ3 |
| TVIS20057084 | HPV | ENSG00000078070.14 | protein_coding | MCCC1 | No | No | 56922 | A0A0S2Z693 Q96RQ3 |
| TVIS20031632 | HPV | ENSG00000078070.14 | protein_coding | MCCC1 | No | No | 56922 | A0A0S2Z693 Q96RQ3 |
| TVIS20025033 | HPV | ENSG00000078070.14 | protein_coding | MCCC1 | No | No | 56922 | A0A0S2Z693 Q96RQ3 |
| TVIS44025026 | HTLV-1 | ENSG00000078070.14 | protein_coding | MCCC1 | No | No | 56922 | A0A0S2Z693 Q96RQ3 |
| TVIS44038278 | HTLV-1 | ENSG00000078070.14 | protein_coding | MCCC1 | No | No | 56922 | A0A0S2Z693 Q96RQ3 |
Target Gene Table
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TCGA Plot Options
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Drug Information
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| Gene | MCCC1 |
|---|---|
| DrugBank ID | DB00121 |
| Drug Name | Biotin |
| Target ID | BE0000445 |
| UniProt ID | Q96RQ3 |
| Regulation Type | cofactor |
| PubMed IDs | 16773504; 16772434 |
| Citations | Friebel D, von der Hagen M, Baumgartner ER, Fowler B, Hahn G, Feyh P, Heubner G, Baumgartner MR, Hoffmann GF: The first case of 3-methylcrotonyl-CoA carboxylase (MCC) deficiency responsive to biotin. Neuropediatrics. 2006 Apr;37(2):72-8.@@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 |
