Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10008245HBVENSG00000196616.15protein_codingADH1BNoNo125D6RHZ6
P00325
TVIS10029746HBVENSG00000196616.15protein_codingADH1BNoNo125D6RHZ6
P00325
TVIS10029747HBVENSG00000196616.15protein_codingADH1BNoNo125D6RHZ6
P00325
TVIS10029748HBVENSG00000196616.15protein_codingADH1BNoNo125D6RHZ6
P00325
TVIS10029749HBVENSG00000196616.15protein_codingADH1BNoNo125D6RHZ6
P00325
TVIS10025493HBVENSG00000196616.15protein_codingADH1BNoNo125D6RHZ6
P00325
TVIS10025504HBVENSG00000196616.15protein_codingADH1BNoNo125D6RHZ6
P00325
TVIS10024963HBVENSG00000196616.15protein_codingADH1BNoNo125D6RHZ6
P00325
TVIS10029750HBVENSG00000196616.15protein_codingADH1BNoNo125D6RHZ6
P00325
TVIS10019430HBVENSG00000196616.15protein_codingADH1BNoNo125D6RHZ6
P00325
TCGA Plot Options
Drug Information
GeneADH1B
DrugBank IDDB00157
Drug NameNADH
Target IDBE0000400
UniProt IDP00325
Regulation Type
PubMed IDs16897483
CitationsManriquez D, El-Sharkawy I, Flores FB, El-Yahyaoui F, Regad F, Bouzayen M, Latche A, Pech JC: Two highly divergent alcohol dehydrogenases of melon exhibit fruit ripening-specific expression and distinct biochemical characteristics. Plant Mol Biol. 2006 Jul;61(4-5):675-85.
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