Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10009465HBVENSG00000130707.18protein_codingASS1NoNo445P00966
Q5T6L4
TVIS10036839HBVENSG00000130707.18protein_codingASS1NoNo445P00966
Q5T6L4
TVIS10062550HBVENSG00000130707.18protein_codingASS1NoNo445P00966
Q5T6L4
TVIS30088707HIVENSG00000130707.18protein_codingASS1NoNo445P00966
Q5T6L4
TVIS30072166HIVENSG00000130707.18protein_codingASS1NoNo445P00966
Q5T6L4
TVIS20065430HPVENSG00000130707.18protein_codingASS1NoNo445P00966
Q5T6L4
TVIS20034622HPVENSG00000130707.18protein_codingASS1NoNo445P00966
Q5T6L4
TVIS44022964HTLV-1ENSG00000130707.18protein_codingASS1NoNo445P00966
Q5T6L4
TVIS44040355HTLV-1ENSG00000130707.18protein_codingASS1NoNo445P00966
Q5T6L4
TCGA Plot Options
Drug Information
GeneASS1
DrugBank IDDB00125
Drug NameArginine
Target IDBE0000671
UniProt IDP00966
Regulation Type
PubMed IDs16787144; 16809898; 17210712; 17354225
CitationsFeun L, Savaraj N: Pegylated arginine deiminase: a novel anticancer enzyme agent. Expert Opin Investig Drugs. 2006 Jul;15(7):815-22.@@Moradi H, Kwok V, Vaziri ND: Effect of chronic renal failure on arginase and argininosuccinate synthetase expression. Am J Nephrol. 2006;26(3):310-8. Epub 2006 Jun 29.@@Cheng PN, Lam TL, Lam WM, Tsui SM, Cheng AW, Lo WH, Leung YC: Pegylated recombinant human arginase (rhArg-peg5,000mw) inhibits the in vitro and in vivo proliferation of human hepatocellular carcinoma through arginine depletion. Cancer Res. 2007 Jan 1;67(1):309-17.@@Szlosarek PW, Grimshaw MJ, Wilbanks GD, Hagemann T, Wilson JL, Burke F, Stamp G, Balkwill FR: Aberrant regulation of argininosuccinate synthetase by TNF-alpha in human epithelial ovarian cancer. Int J Cancer. 2007 Jul 1;121(1):6-11.
GroupsInvestigational; Nutraceutical
Direct ClassificationL-alpha-amino acids
SMILESN[C@@H](CCCNC(N)=N)C(O)=O
PathwaysCitrullinemia Type I; Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency); Argininemia; Hyperornithinemia with Gyrate Atrophy (HOGA); Canavan Disease; Hypoacetylaspartia; Hyperprolinemia Type II; 3-Phosphoglycerate Dehydrogenase Deficiency; Non-Ketotic Hyperglycinemia; Argininosuccinic Aciduria; L-Arginine:Glycine Amidinotransferase Deficiency; Hyperornithinemia-Hyperammonemia-Homocitrullinuria [HHH-syndrome]; Arginine: Glycine Amidinotransferase Deficiency (AGAT Deficiency); Prolidase Deficiency (PD); Glycine and Serine Metabolism; Hyperglycinemia, Non-Ketotic; Dimethylglycine Dehydrogenase Deficiency; Creatine Deficiency, Guanidinoacetate Methyltransferase Deficiency; Carbamoyl Phosphate Synthetase Deficiency; Ornithine Aminotransferase Deficiency (OAT Deficiency); Hyperprolinemia Type I; Dihydropyrimidine Dehydrogenase Deficiency (DHPD); Aspartate Metabolism; Nitric Oxide Signaling Pathway; Arginine and Proline Metabolism; Ornithine Transcarbamylase Deficiency (OTC Deficiency); Prolinemia Type II; Urea Cycle; Sarcosinemia
PharmGKBPA448478
ChEMBLCHEMBL1485