Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10013808HBVENSG00000099810.21protein_codingMTAPNoYes4507Q13126
TVIS20008796HPVENSG00000099810.21protein_codingMTAPNoYes4507Q13126
TVIS20063595HPVENSG00000099810.21protein_codingMTAPNoYes4507Q13126
TVIS44028924HTLV-1ENSG00000099810.21protein_codingMTAPNoYes4507Q13126
TVIS44030714HTLV-1ENSG00000099810.21protein_codingMTAPNoYes4507Q13126
TVIS44036192HTLV-1ENSG00000099810.21protein_codingMTAPNoYes4507Q13126
TCGA Plot Options
Drug Information
GeneMTAP
DrugBank IDDB00173
Drug NameAdenine
Target IDBE0001128
UniProt IDQ13126
Regulation Type
PubMed IDs16631464; 17041099; 17090056
CitationsChow WA, Bedell V, Gaytan P, Borden E, Goldblum J, Hicks D, Slovak ML: Methylthioadenosine phosphorylase gene deletions are frequently detected by fluorescence in situ hybridization in conventional chondrosarcomas. Cancer Genet Cytogenet. 2006 Apr 15;166(2):95-100.@@Chattopadhyay S, Zhao R, Tsai E, Schramm VL, Goldman ID: The effect of a novel transition state inhibitor of methylthioadenosine phosphorylase on pemetrexed activity. Mol Cancer Ther. 2006 Oct;5(10):2549-55.@@Singh V, Schramm VL: Transition-state structure of human 5'-methylthioadenosine phosphorylase. J Am Chem Soc. 2006 Nov 15;128(45):14691-6.
GroupsApproved; Nutraceutical
Direct Classification6-aminopurines
SMILESNC1=C2NC=NC2=NC=N1
PathwaysGout or Kelley-Seegmiller Syndrome; Purine Metabolism; Lesch-Nyhan Syndrome (LNS); Myoadenylate Deaminase Deficiency; Molybdenum Cofactor Deficiency; Adenine Phosphoribosyltransferase Deficiency (APRT); Mercaptopurine Action Pathway; Xanthinuria Type I; Azathioprine Action Pathway; AICA-Ribosiduria; Thioguanine Action Pathway; Mitochondrial DNA Depletion Syndrome; Adenosine Deaminase Deficiency; Xanthine Dehydrogenase Deficiency (Xanthinuria); Purine Nucleoside Phosphorylase Deficiency; Adenylosuccinate Lyase Deficiency; Xanthinuria Type II
PharmGKBPA448048
ChEMBLCHEMBL226345