Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS42000059EBVENSG00000151376.19protein_codingME3NoNo10873Q16798
Q6TCH8
TVIS10006111HBVENSG00000151376.19protein_codingME3NoNo10873Q16798
Q6TCH8
TVIS10006112HBVENSG00000151376.19protein_codingME3NoNo10873Q16798
Q6TCH8
TVIS10004088HBVENSG00000151376.19protein_codingME3NoNo10873Q16798
Q6TCH8
TVIS10026676HBVENSG00000151376.19protein_codingME3NoNo10873Q16798
Q6TCH8
TVIS10042944HBVENSG00000151376.19protein_codingME3NoNo10873Q16798
Q6TCH8
TVIS10044213HBVENSG00000151376.19protein_codingME3NoNo10873Q16798
Q6TCH8
TVIS10050841HBVENSG00000151376.19protein_codingME3NoNo10873Q16798
Q6TCH8
TVIS10052164HBVENSG00000151376.19protein_codingME3NoNo10873Q16798
Q6TCH8
TVIS10050385HBVENSG00000151376.19protein_codingME3NoNo10873Q16798
Q6TCH8
TCGA Plot Options
Drug Information
GeneME3
DrugBank IDDB00157
Drug NameNADH
Target IDBE0000328
UniProt IDQ16798
Regulation Type
PubMed IDs16740313; 17080607; 17603759
CitationsLuo C, Wang X, Long J, Liu J: An NADH-tetrazolium-coupled sensitive assay for malate dehydrogenase in mitochondria and crude tissue homogenates. J Biochem Biophys Methods. 2006 Aug 31;68(2):101-11. Epub 2006 Apr 26.@@Wei H, Dhanaraj AL, Arora R, Rowland LJ, Fu Y, Sun L: Identification of cold acclimation-responsive Rhododendron genes for lipid metabolism, membrane transport and lignin biosynthesis: importance of moderately abundant ESTs in genomic studies. Plant Cell Environ. 2006 Apr;29(4):558-70.@@Rzem R, Vincent MF, Van Schaftingen E, Veiga-da-Cunha M: L-2-hydroxyglutaric aciduria, a defect of metabolite repair. J Inherit Metab Dis. 2007 Oct;30(5):681-9. Epub 2007 Jun 21.
GroupsApproved; Nutraceutical
Direct Classification(5'->5')-dinucleotides
SMILESNC(=O)C1=CN(C=CC1)[C@@H]1O[C@H](CO[P@](O)(=O)O[P@](O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C(N)N=CN=C23)[C@@H](O)[C@H]1O
PathwaysEthylmalonic Encephalopathy; 3-Methylglutaconic Aciduria Type III; Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD Deficiency); Caffeine Metabolism; Fructose and Mannose Degradation; Isovaleric Aciduria; Lysine Degradation; Methylmalonic Aciduria Due to Cobalamin-Related Disorders; Glycerol Phosphate Shuttle; Zellweger Syndrome; Propionic Acidemia; Glycolysis; Xanthine Dehydrogenase Deficiency (Xanthinuria); S-Adenosylhomocysteine (SAH) Hydrolase Deficiency; Tryptophan Metabolism; Glutaric Aciduria Type I; 3-Methylcrotonyl-CoA Carboxylase Deficiency Type I; Glycine N-Methyltransferase Deficiency; Dimethylglycine Dehydrogenase Deficiency; Androgen and Estrogen Metabolism; Nucleotide Sugars Metabolism; 3-Methylglutaconic Aciduria Type IV; Dihydropyrimidine Dehydrogenase Deficiency (DHPD); Malate-Aspartate Shuttle; Folate Metabolism; Valine, Leucine, and Isoleucine Degradation; Maple Syrup Urine Disease; Glycerol Kinase Deficiency; Adenylosuccinate Lyase Deficiency; Cysteine Metabolism
PharmGKBPA164755085
ChEMBLCHEMBL1234616