Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10038044HBVENSG00000083444.17protein_codingPLOD1NoNo5351Q02809
TVIS30079552HIVENSG00000083444.17protein_codingPLOD1NoNo5351Q02809
TVIS20047162HPVENSG00000083444.17protein_codingPLOD1NoNo5351Q02809
TVIS20032801HPVENSG00000083444.17protein_codingPLOD1NoNo5351Q02809
TVIS44011769HTLV-1ENSG00000083444.17protein_codingPLOD1NoNo5351Q02809
TVIS44021664HTLV-1ENSG00000083444.17protein_codingPLOD1NoNo5351Q02809
TVIS44037656HTLV-1ENSG00000083444.17protein_codingPLOD1NoNo5351Q02809
TVIS44037055HTLV-1ENSG00000083444.17protein_codingPLOD1NoNo5351Q02809
TVIS44037655HTLV-1ENSG00000083444.17protein_codingPLOD1NoNo5351Q02809
TVIS44037654HTLV-1ENSG00000083444.17protein_codingPLOD1NoNo5351Q02809
TCGA Plot Options
Drug Information
GenePLOD1
DrugBank IDDB00126
Drug NameAscorbic acid
Target IDBE0000087
UniProt IDQ02809
Regulation Typecofactor
PubMed IDs17100196; 11752352; 9344473
CitationsSalavoura K, Valari M, Kolialexi A, Mavrou A, Kitsiou S: A case of Ehlers Danlos syndrome type VI. Genet Couns. 2006;17(3):291-4.@@Chen X, Ji ZL, Chen YZ: TTD: Therapeutic Target Database. Nucleic Acids Res. 2002 Jan 1;30(1):412-5.@@Yeowell 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