Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10017495HBVENSG00000036473.9protein_codingOTCNoNo5009P00480
TVIS10017756HBVENSG00000036473.9protein_codingOTCNoNo5009P00480
TVIS10044584HBVENSG00000036473.9protein_codingOTCNoNo5009P00480
TVIS44043340HTLV-1ENSG00000036473.9protein_codingOTCNoNo5009P00480
TCGA Plot Options
Drug Information
GeneOTC
DrugBank IDDB00155
Drug NameCitrulline
Target IDBE0000306
UniProt IDP00480
Regulation Type
PubMed IDs10648527; 16585758
CitationsQuintero MJ, Muro-Pastor AM, Herrero A, Flores E: Arginine catabolism in the cyanobacterium Synechocystis sp. Strain PCC 6803 involves the urea cycle and arginase pathway. J Bacteriol. 2000 Feb;182(4):1008-15.@@Morizono H, Cabrera-Luque J, Shi D, Gallegos R, Yamaguchi S, Yu X, Allewell NM, Malamy MH, Tuchman M: Acetylornithine transcarbamylase: a novel enzyme in arginine biosynthesis. J Bacteriol. 2006 Apr;188(8):2974-82.
GroupsInvestigational; Nutraceutical
Direct ClassificationL-alpha-amino acids
SMILESN[C@@H](CCCNC(N)=O)C(O)=O
PathwaysCitrullinemia Type I; Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency); Argininemia; Hyperornithinemia with Gyrate Atrophy (HOGA); Canavan Disease; Hypoacetylaspartia; 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; Aspartate Metabolism; Nitric Oxide Signaling Pathway; Arginine and Proline Metabolism; Ornithine Transcarbamylase Deficiency (OTC Deficiency); Prolinemia Type II; Urea Cycle
PharmGKBPA164747225
ChEMBLCHEMBL444814