Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10059019HBVENSG00000047457.14protein_codingCPNoNo1356A5PL27
P00450
TVIS10059018HBVENSG00000047457.14protein_codingCPNoNo1356A5PL27
P00450
TVIS30077391HIVENSG00000047457.14protein_codingCPNoNo1356A5PL27
P00450
TVIS30079596HIVENSG00000047457.14protein_codingCPNoNo1356A5PL27
P00450
TVIS30058614HIVENSG00000047457.14protein_codingCPNoNo1356A5PL27
P00450
TVIS20065716HPVENSG00000047457.14protein_codingCPNoNo1356A5PL27
P00450
TVIS44014857HTLV-1ENSG00000047457.14protein_codingCPNoNo1356A5PL27
P00450
TCGA Plot Options
Drug Information
GeneCP
DrugBank IDDB01592
Drug NameIron
Target IDBE0001140
UniProt IDP00450
Regulation Type
PubMed IDs21049900
CitationsHa-Duong NT, Eid C, Hemadi M, El Hage Chahine JM: In vitro interaction between ceruloplasmin and human serum transferrin. Biochemistry. 2010 Dec 7;49(48):10261-3. doi: 10.1021/bi1014503. Epub 2010 Nov 9.
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