Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS20008492HPVENSG00000170231.16protein_codingFABP6NoNo2172P51161
TVIS20029789HPVENSG00000170231.16protein_codingFABP6NoNo2172P51161
TVIS20030383HPVENSG00000170231.16protein_codingFABP6NoNo2172P51161
TVIS20060172HPVENSG00000170231.16protein_codingFABP6NoNo2172P51161
TVIS44025477HTLV-1ENSG00000170231.16protein_codingFABP6NoNo2172P51161
TCGA Plot Options
Drug Information
GeneFABP6
DrugBank IDDB04348
Drug NameTaurocholic acid
Target IDBE0001967
UniProt IDP51161
Regulation Typeligand
PubMed IDs30559664; 12486725
CitationsEthanic M, Stanimirov B, Pavlovic N, Golocorbin-Kon S, Al-Salami H, Stankov K, Mikov M: Pharmacological Applications of Bile Acids and Their Derivatives in the Treatment of Metabolic Syndrome. Front Pharmacol. 2018 Dec 3;9:1382. doi: 10.3389/fphar.2018.01382. eCollection 2018.@@Kurz M, Brachvogel V, Matter H, Stengelin S, Thuring H, Kramer W: Insights into the bile acid transportation system: the human ileal lipid-binding protein-cholyltaurine complex and its comparison with homologous structures. Proteins. 2003 Feb 1;50(2):312-28.
GroupsApproved; Experimental
Direct ClassificationTrihydroxy bile acids, alcohols and derivatives
SMILES[H][C@@]1(CC[C@@]2([H])[C@]3([H])[C@H](O)C[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])C[C@H](O)[C@]12C)[C@H](C)CCC(=O)NCCS(O)(=O)=O
PathwaysCongenital Bile Acid Synthesis Defect Type II; Familial Hypercholanemia (FHCA); Bile Acid Biosynthesis; Zellweger Syndrome; Congenital Bile Acid Synthesis Defect Type III; 27-Hydroxylase Deficiency; Cerebrotendinous Xanthomatosis (CTX)
PharmGKB
ChEMBLCHEMBL224867