Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10007115HBVENSG00000117594.10protein_codingHSD11B1NoNo3290P28845
X5D2L1
TVIS30005481HIVENSG00000117594.10protein_codingHSD11B1NoNo3290P28845
X5D2L1
TVIS30076589HIVENSG00000117594.10protein_codingHSD11B1NoNo3290P28845
X5D2L1
TVIS30026470HIVENSG00000117594.10protein_codingHSD11B1NoNo3290P28845
X5D2L1
TVIS20025360HPVENSG00000117594.10protein_codingHSD11B1NoNo3290P28845
X5D2L1
TCGA Plot Options
Drug Information
GeneHSD11B1
DrugBank IDDB04652
Drug NameCorticosterone
Target IDBE0000329
UniProt IDP28845
Regulation Typesubstrate
PubMed IDs10592235; 11755176
CitationsBerman HM, Westbrook J, Feng Z, Gilliland G, Bhat TN, Weissig H, Shindyalov IN, Bourne PE: The Protein Data Bank. Nucleic Acids Res. 2000 Jan 1;28(1):235-42.@@Pacha J, Lisa V, Miksik I: Effect of cellular differentiation on 11beta-hydroxysteroid dehydrogenase activity in the intestine. Steroids. 2002 Feb;67(2):119-26. doi: 10.1016/s0039-128x(01)00143-x.
GroupsExperimental
Direct Classification21-hydroxysteroids
SMILES[H][C@@]1(CC[C@@]2([H])[C@]3([H])CCC4=CC(=O)CC[C@]4(C)[C@@]3([H])[C@@]([H])(O)C[C@]12C)C(=O)CO
PathwaysAdrenal Hyperplasia Type 3 or Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency; Apparent Mineralocorticoid Excess Syndrome; Congenital Lipoid Adrenal Hyperplasia (CLAH) or Lipoid CAH; 3-beta-Hydroxysteroid Dehydrogenase Deficiency; Corticosterone Methyl Oxidase I Deficiency (CMO I); 11-beta-Hydroxylase Deficiency (CYP11B1); Steroidogenesis; Adrenal Hyperplasia Type 5 or Congenital Adrenal Hyperplasia Due to 17 alpha-Hydroxylase Deficiency; 17-alpha-Hydroxylase Deficiency (CYP17); Corticosterone Methyl Oxidase II Deficiency (CMO II); 21-Hydroxylase Deficiency (CYP21)
PharmGKB
ChEMBLCHEMBL110739