Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10006894HBVENSG00000171766.17protein_codingGATMNoNo2628P50440
TVIS10006879HBVENSG00000171766.17protein_codingGATMNoNo2628P50440
TVIS10006888HBVENSG00000171766.17protein_codingGATMNoNo2628P50440
TVIS10016544HBVENSG00000171766.17protein_codingGATMNoNo2628P50440
TVIS10027378HBVENSG00000171766.17protein_codingGATMNoNo2628P50440
TVIS10059178HBVENSG00000171766.17protein_codingGATMNoNo2628P50440
TVIS20033309HPVENSG00000171766.17protein_codingGATMNoNo2628P50440
TVIS20034947HPVENSG00000171766.17protein_codingGATMNoNo2628P50440
TVIS44030758HTLV-1ENSG00000171766.17protein_codingGATMNoNo2628P50440
TVIS44027190HTLV-1ENSG00000171766.17protein_codingGATMNoNo2628P50440
TCGA Plot Options
Drug Information
GeneGATM
DrugBank IDDB00129
Drug NameOrnithine
Target IDBE0000347
UniProt IDP50440
Regulation Type
PubMed IDs17139284; 17016423; 7173402; 11691635; 5335895
CitationsOverington JP, Al-Lazikani B, Hopkins AL: How many drug targets are there? Nat Rev Drug Discov. 2006 Dec;5(12):993-6.@@Imming P, Sinning C, Meyer A: Drugs, their targets and the nature and number of drug targets. Nat Rev Drug Discov. 2006 Oct;5(10):821-34.@@Thomasset N, Quash GA, Dore JF: The differential contribution of arginase and transamidinase to ornithine biosynthesis in two achromic human melanoma cell lines. FEBS Lett. 1982 Nov 1;148(1):63-6.@@Natesan S, Reddy SR: Compensatory changes in enzymes of arginine metabolism during renal hypertrophy in mice. Comp Biochem Physiol B Biochem Mol Biol. 2001 Dec;130(4):585-95.@@Mitruka BM, Costilow RN: Arginine and ornithine catabolism by Clostridium botulinum. J Bacteriol. 1967 Jan;93(1):295-301.
GroupsApproved; Nutraceutical
Direct ClassificationL-alpha-amino acids
SMILESNCCC[C@H](N)C(O)=O
PathwaysCitrullinemia Type I; Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency); Argininemia; Hyperornithinemia with Gyrate Atrophy (HOGA); Spermidine and Spermine Biosynthesis; Hyperprolinemia Type II; Argininosuccinic Aciduria; L-Arginine:Glycine Amidinotransferase Deficiency; Hyperornithinemia-Hyperammonemia-Homocitrullinuria [HHH-syndrome]; Arginine: Glycine Amidinotransferase Deficiency (AGAT Deficiency); Prolidase Deficiency (PD); Creatine Deficiency, Guanidinoacetate Methyltransferase Deficiency; Carbamoyl Phosphate Synthetase Deficiency; Ornithine Aminotransferase Deficiency (OAT Deficiency); Hyperprolinemia Type I; Arginine and Proline Metabolism; Ornithine Transcarbamylase Deficiency (OTC Deficiency); Prolinemia Type II; Urea Cycle
PharmGKBPA164783814
ChEMBLCHEMBL446143