Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10020992HBVENSG00000003989.18protein_codingSLC7A2NoNo6542P52569
TVIS30068539HIVENSG00000003989.18protein_codingSLC7A2NoNo6542P52569
TVIS20011203HPVENSG00000003989.18protein_codingSLC7A2NoNo6542P52569
TVIS20046448HPVENSG00000003989.18protein_codingSLC7A2NoNo6542P52569
TVIS20023625HPVENSG00000003989.18protein_codingSLC7A2NoNo6542P52569
TVIS20066652HPVENSG00000003989.18protein_codingSLC7A2NoNo6542P52569
TVIS44035611HTLV-1ENSG00000003989.18protein_codingSLC7A2NoNo6542P52569
TCGA Plot Options
Drug Information
GeneSLC7A2
DrugBank IDDB00129
Drug NameOrnithine
Target IDBE0000562
UniProt IDP52569
Regulation Type
PubMed IDs16703566; 17065601; 12679322
CitationsYeramian A, Martin L, Arpa L, Bertran J, Soler C, McLeod C, Modolell M, Palacin M, Lloberas J, Celada A: Macrophages require distinct arginine catabolism and transport systems for proliferation and for activation. Eur J Immunol. 2006 Jun;36(6):1516-26.@@Cerec V, Piquet-Pellorce C, Aly HA, Touzalin AM, Jegou B, Bauche F: Multiple pathways for cationic amino acid transport in rat seminiferous tubule cells. Biol Reprod. 2007 Feb;76(2):241-9. Epub 2006 Oct 25.@@Endo M, Oyadomari S, Terasaki Y, Takeya M, Suga M, Mori M, Gotoh T: Induction of arginase I and II in bleomycin-induced fibrosis of mouse lung. Am J Physiol Lung Cell Mol Physiol. 2003 Aug;285(2):L313-21. Epub 2003 Apr 4.
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