Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10019086HBVENSG00000152952.14protein_codingPLOD2NoNo5352O00469
TVIS10011909HBVENSG00000152952.14protein_codingPLOD2NoNo5352O00469
TVIS10011910HBVENSG00000152952.14protein_codingPLOD2NoNo5352O00469
TVIS30076318HIVENSG00000152952.14protein_codingPLOD2NoNo5352O00469
TVIS30076817HIVENSG00000152952.14protein_codingPLOD2NoNo5352O00469
TVIS30082885HIVENSG00000152952.14protein_codingPLOD2NoNo5352O00469
TVIS30058592HIVENSG00000152952.14protein_codingPLOD2NoNo5352O00469
TVIS20032163HPVENSG00000152952.14protein_codingPLOD2NoNo5352O00469
TVIS44029684HTLV-1ENSG00000152952.14protein_codingPLOD2NoNo5352O00469
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Drug Information
GenePLOD2
DrugBank IDDB00126
Drug NameAscorbic acid
Target IDBE0002192
UniProt IDO00469
Regulation Typecofactor
PubMed IDs9344473
CitationsYeowell HN, Walker LC, Murad S, Pinnell SR: A common duplication in the lysyl hydroxylase gene of patients with Ehlers Danlos syndrome type VI results in preferential stimulation of lysyl hydroxylase activity and mRNA by hydralazine. Arch Biochem Biophys. 1997 Nov 1;347(1):126-31. doi: 10.1006/abbi.1997.0319.
GroupsApproved; Nutraceutical
Direct ClassificationButenolides
SMILES[H][C@@]1(OC(=O)C(O)=C1O)[C@@H](O)CO
PathwaysTyrosine Metabolism; Refsum Disease; The Oncogenic Action of Succinate; Disulfiram Action Pathway; Aromatic L-Aminoacid Decarboxylase Deficiency; Oxidation of Branched-Chain Fatty Acids; Catecholamine Biosynthesis; Monoamine Oxidase-A Deficiency (MAO-A); Tyrosinemia, Transient, of the Newborn; Carnitine Synthesis; Phytanic Acid Peroxisomal Oxidation; Hawkinsinuria; Dopamine beta-Hydroxylase Deficiency; Tyrosinemia Type I; Alkaptonuria; Tyrosine Hydroxylase Deficiency; The Oncogenic Action of Fumarate
PharmGKBPA451898
ChEMBLCHEMBL196