Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10018630HBVENSG00000178445.10protein_codingGLDCNoNo2731P23378
TVIS10042366HBVENSG00000178445.10protein_codingGLDCNoNo2731P23378
TVIS20039651HPVENSG00000178445.10protein_codingGLDCNoNo2731P23378
TVIS20046483HPVENSG00000178445.10protein_codingGLDCNoNo2731P23378
TVIS20067124HPVENSG00000178445.10protein_codingGLDCNoNo2731P23378
TVIS20045991HPVENSG00000178445.10protein_codingGLDCNoNo2731P23378
TVIS44028234HTLV-1ENSG00000178445.10protein_codingGLDCNoNo2731P23378
TVIS44013282HTLV-1ENSG00000178445.10protein_codingGLDCNoNo2731P23378
TVIS44046150HTLV-1ENSG00000178445.10protein_codingGLDCNoNo2731P23378
TCGA Plot Options
Drug Information
GeneGLDC
DrugBank IDDB00114
Drug NamePyridoxal phosphate
Target IDBE0000618
UniProt IDP23378
Regulation Typecofactor
PubMed IDs15791207; 16228305
CitationsNakai T, Nakagawa N, Maoka N, Masui R, Kuramitsu S, Kamiya N: Structure of P-protein of the glycine cleavage system: implications for nonketotic hyperglycinemia. EMBO J. 2005 Apr 20;24(8):1523-36. Epub 2005 Mar 24.@@Igamberdiev AU, Ivlev AA, Bykova NV, Threlkeld CN, Lea PJ, Gardestrom P: Decarboxylation of glycine contributes to carbon isotope fractionation in photosynthetic organisms. Photosynth Res. 2001;67(3):177-84.
GroupsApproved; Investigational; Nutraceutical
Direct ClassificationPyridoxals and derivatives
SMILESCC1=NC=C(COP(O)(O)=O)C(C=O)=C1O
PathwaysHistidinemia; 3-Methylglutaconic Aciduria Type I; Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency); beta-Ketothiolase Deficiency; Tyrosine Metabolism; Disulfiram Action Pathway; Hyperprolinemia Type II; Glutamate Metabolism; Argininosuccinic Aciduria; Tyrosinemia Type I; Hyperinsulinism-Hyperammonemia Syndrome; Porphyrin Metabolism; 2-Methyl-3-hydroxybutryl-CoA Dehydrogenase Deficiency; Glutaric Aciduria Type I; Propanoate Metabolism; Taurine and Hypotaurine Metabolism; Catecholamine Biosynthesis; Glycine and Serine Metabolism; Carnitine Synthesis; Tyrosinemia Type 3 (TYRO3); Selenoamino Acid Metabolism; Carbamoyl Phosphate Synthetase Deficiency; Hyperprolinemia Type I; Saccharopinuria/Hyperlysinemia II; Histidine Metabolism; Cystathionine beta-Synthase Deficiency; Arginine and Proline Metabolism; Starch and Sucrose Metabolism; Globoid Cell Leukodystrophy; Ammonia Recycling
PharmGKBPA164749650
ChEMBLCHEMBL82202