Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10008531HBVENSG00000164749.13protein_codingHNF4GNoNo3174Q14541
TVIS30079151HIVENSG00000164749.13protein_codingHNF4GNoNo3174Q14541
TVIS30080578HIVENSG00000164749.13protein_codingHNF4GNoNo3174Q14541
TVIS30069167HIVENSG00000164749.13protein_codingHNF4GNoNo3174Q14541
TVIS30069168HIVENSG00000164749.13protein_codingHNF4GNoNo3174Q14541
TVIS20002850HPVENSG00000164749.13protein_codingHNF4GNoNo3174Q14541
TVIS20063290HPVENSG00000164749.13protein_codingHNF4GNoNo3174Q14541
TVIS44022906HTLV-1ENSG00000164749.13protein_codingHNF4GNoNo3174Q14541
TVIS44010517HTLV-1ENSG00000164749.13protein_codingHNF4GNoNo3174Q14541
TVIS44039801HTLV-1ENSG00000164749.13protein_codingHNF4GNoNo3174Q14541
TCGA Plot Options
Drug Information
GeneHNF4G
DrugBank IDDB03796
Drug NamePalmitic Acid
Target IDBE0003179
UniProt IDQ14541
Regulation Type
PubMed IDs
Citations
GroupsApproved
Direct ClassificationLong-chain fatty acids
SMILESCCCCCCCCCCCCCCCC(O)=O
PathwaysCerivastatin Action Pathway; Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD); Ethylmalonic Encephalopathy; Familial Hypercholanemia (FHCA); Desmosterolosis; Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD Deficiency); Congenital Bile Acid Synthesis Defect Type III; Glycerolipid Metabolism; Ibandronate Action Pathway; Cerebrotendinous Xanthomatosis (CTX); Chondrodysplasia Punctata II, X-Linked Dominant (CDPX2); Smith-Lemli-Opitz Syndrome (SLOS); Carnitine Palmitoyl Transferase Deficiency II; Hyper-IgD Syndrome; Zellweger Syndrome; Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase Deficiency (LCHAD); Steroid Biosynthesis; Hypercholesterolemia; Risedronate Action Pathway; Mevalonic Aciduria; Glutaric Aciduria Type I; Alendronate Action Pathway; CHILD Syndrome; D-Glyceric Acidura; Lovastatin Action Pathway; Wolman Disease; Bile Acid Biosynthesis; Long Chain Acyl-CoA Dehydrogenase Deficiency (LCAD); Glycerol Kinase Deficiency; Atorvastatin Action Pathway
PharmGKB
ChEMBLCHEMBL82293