Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS30006048HIVENSG00000139180.11protein_codingNDUFA9NoNo4704Q16795
TVIS30031847HIVENSG00000139180.11protein_codingNDUFA9NoNo4704Q16795
TVIS30031848HIVENSG00000139180.11protein_codingNDUFA9NoNo4704Q16795
TVIS30031849HIVENSG00000139180.11protein_codingNDUFA9NoNo4704Q16795
TVIS30031850HIVENSG00000139180.11protein_codingNDUFA9NoNo4704Q16795
TVIS30031851HIVENSG00000139180.11protein_codingNDUFA9NoNo4704Q16795
TVIS44017494HTLV-1ENSG00000139180.11protein_codingNDUFA9NoNo4704Q16795
TCGA Plot Options
Drug Information
GeneNDUFA9
DrugBank IDDB03147
Drug NameFlavin adenine dinucleotide
Target IDBE0000305
UniProt IDQ16795
Regulation Typecofactor
PubMed IDs25526675
CitationsBhatia C, Oerum S, Bray J, Kavanagh KL, Shafqat N, Yue W, Oppermann U: Towards a systematic analysis of human short-chain dehydrogenases/reductases (SDR): Ligand identification and structure-activity relationships. Chem Biol Interact. 2015 Jun 5;234:114-25. doi: 10.1016/j.cbi.2014.12.013. Epub 2014 Dec 16.
GroupsApproved
Direct ClassificationFlavin nucleotides
SMILESCC1=CC2=C(C=C1C)N(C[C@H](O)[C@H](O)[C@H](O)CO[P@](O)(=O)O[P@@](O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC3=C1N=CN=C3N)C1=NC(=O)NC(=O)C1=N2
PathwaysCerivastatin Action Pathway; Ethylmalonic Encephalopathy; 3-Methylglutaconic Aciduria Type III; Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD Deficiency); Caffeine Metabolism; Isovaleric Aciduria; Lysine Degradation; Riboflavin Metabolism; 5-Oxoprolinuria; Methylmalonic Aciduria Due to Cobalamin-Related Disorders; Glycerol Phosphate Shuttle; Propionic Acidemia; Hypercholesterolemia; Xanthine Dehydrogenase Deficiency (Xanthinuria); S-Adenosylhomocysteine (SAH) Hydrolase Deficiency; Tryptophan Metabolism; Glutaric Aciduria Type I; 3-Methylcrotonyl-CoA Carboxylase Deficiency Type I; Phenylketonuria; Glycine N-Methyltransferase Deficiency; Dimethylglycine Dehydrogenase Deficiency; Lovastatin Action Pathway; 3-Methylglutaconic Aciduria Type IV; Dihydropyrimidine Dehydrogenase Deficiency (DHPD); Glutathione Metabolism; Folate Metabolism; Valine, Leucine, and Isoleucine Degradation; Maple Syrup Urine Disease; Glycerol Kinase Deficiency; Adenylosuccinate Lyase Deficiency
PharmGKB
ChEMBLCHEMBL1232653