Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS30026886HIVENSG00000135766.9protein_codingEGLN1NoNo54583Q9GZT9
R4SCQ0
TVIS30026887HIVENSG00000135766.9protein_codingEGLN1NoNo54583Q9GZT9
R4SCQ0
TVIS30026888HIVENSG00000135766.9protein_codingEGLN1NoNo54583Q9GZT9
R4SCQ0
TVIS20037422HPVENSG00000135766.9protein_codingEGLN1NoNo54583Q9GZT9
R4SCQ0
TVIS20047823HPVENSG00000135766.9protein_codingEGLN1NoNo54583Q9GZT9
R4SCQ0
TVIS20067207HPVENSG00000135766.9protein_codingEGLN1NoNo54583Q9GZT9
R4SCQ0
TVIS20048431HPVENSG00000135766.9protein_codingEGLN1NoNo54583Q9GZT9
R4SCQ0
TCGA Plot Options
Drug Information
GeneEGLN1
DrugBank IDDB01592
Drug NameIron
Target IDBE0002217
UniProt IDQ9GZT9
Regulation Type
PubMed IDs16649251
CitationsDavidson TL, Chen H, Di Toro DM, D'Angelo G, Costa M: Soluble nickel inhibits HIF-prolyl-hydroxylases creating persistent hypoxic signaling in A549 cells. Mol Carcinog. 2006 Jul;45(7):479-89.
GroupsApproved
Direct ClassificationHomogeneous transition metal compounds
SMILES[Fe]
PathwaysCerivastatin Action Pathway; Oxidation of Branched-Chain Fatty Acids; Simvastatin Action Pathway; Chondrodysplasia Punctata II, X-Linked Dominant (CDPX2); Galactosemia III; Smith-Lemli-Opitz Syndrome (SLOS); Tyrosine Metabolism; Zellweger Syndrome; Hereditary Coproporphyria (HCP); Hypercholesterolemia; Glucose-6-phosphate Dehydrogenase Deficiency; Mevalonic Aciduria; Porphyrin Metabolism; Tryptophan Metabolism; Taurine and Hypotaurine Metabolism; Pentose Phosphate Pathway; Inositol Metabolism; Catecholamine Biosynthesis; Phenylketonuria; Vitamin A Deficiency; Congenital Erythropoietic Porphyria (CEP) or Gunther Disease; Cystinosis, Ocular Nonnephropathic; Pyrimidine Metabolism; Congenital Disorder of Glycosylation CDG-IId; Lovastatin Action Pathway; Nucleotide Sugars Metabolism; Aromatic L-Aminoacid Decarboxylase Deficiency; Cysteine Metabolism; Galactose Metabolism; The Oncogenic Action of Fumarate
PharmGKBPA450087
ChEMBL