Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS30086869HIVENSG00000124493.14protein_codingGRM4NoNo2914A1L4F9
B7ZLU9
Q14833
TVIS30086319HIVENSG00000124493.14protein_codingGRM4NoNo2914A1L4F9
B7ZLU9
Q14833
TVIS30080842HIVENSG00000124493.14protein_codingGRM4NoNo2914A1L4F9
B7ZLU9
Q14833
TVIS30082191HIVENSG00000124493.14protein_codingGRM4NoNo2914A1L4F9
B7ZLU9
Q14833
TVIS30064521HIVENSG00000124493.14protein_codingGRM4NoNo2914A1L4F9
B7ZLU9
Q14833
TVIS20011567HPVENSG00000124493.14protein_codingGRM4NoNo2914A1L4F9
B7ZLU9
Q14833
TVIS20026247HPVENSG00000124493.14protein_codingGRM4NoNo2914A1L4F9
B7ZLU9
Q14833
TVIS20019207HPVENSG00000124493.14protein_codingGRM4NoNo2914A1L4F9
B7ZLU9
Q14833
TVIS44011413HTLV-1ENSG00000124493.14protein_codingGRM4NoNo2914A1L4F9
B7ZLU9
Q14833
TVIS44048994HTLV-1ENSG00000124493.14protein_codingGRM4NoNo2914A1L4F9
B7ZLU9
Q14833
TCGA Plot Options
Drug Information
GeneGRM4
DrugBank IDDB00142
Drug NameGlutamic acid
Target IDBE0000833
UniProt IDQ14833
Regulation Type
PubMed IDs17360958
CitationsSuzuki G, Kimura T, Satow A, Kaneko N, Fukuda J, Hikichi H, Sakai N, Maehara S, Kawagoe-Takaki H, Hata M, Azuma T, Ito S, Kawamoto H, Ohta H: Pharmacological characterization of a new, orally active and potent allosteric metabotropic glutamate receptor 1 antagonist, 4-[1-(2-fluoropyridin-3-yl)-5-methyl-1H-1,2,3-triazol-4-yl]-N-isopropyl-N-methyl- 3,6-dihydropyridine-1(2H)-carboxamide (FTIDC). J Pharmacol Exp Ther. 2007 Jun;321(3):1144-53. Epub 2007 Mar 14.
GroupsApproved; Nutraceutical
Direct ClassificationGlutamic acid and derivatives
SMILESN[C@@H](CCC(O)=O)C(O)=O
PathwaysHistidinemia; Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency); 3-Methylglutaconic Aciduria Type I; beta-Ketothiolase Deficiency; Purine Nucleoside Phosphorylase Deficiency; Tyrosine Metabolism; Ketoprofen Action Pathway; Glutamate Metabolism; Argininosuccinic Aciduria; Salla Disease/Infantile Sialic Acid Storage Disease; Tyrosinemia Type I; Hyperinsulinism-Hyperammonemia Syndrome; 2-Methyl-3-hydroxybutryl-CoA Dehydrogenase Deficiency; Glutaric Aciduria Type I; Propanoate Metabolism; Celecoxib Action Pathway; Glycine and Serine Metabolism; Suprofen Action Pathway; Indomethacin Action Pathway; Carbamoyl Phosphate Synthetase Deficiency; Sialuria or French Type Sialuria; Ibuprofen Action Pathway; Saccharopinuria/Hyperlysinemia II; Histidine Metabolism; Arginine and Proline Metabolism; Purine Metabolism; Diflunisal Action Pathway; Etodolac Action Pathway; Ammonia Recycling
PharmGKBPA449776
ChEMBLCHEMBL575060