| VIS ID | Virus | Ensembl ID | Gene Type | Target Gene | Oncogene | Tumor Suppressor Gene | NCBI ID | Uniprot ID |
|---|---|---|---|---|---|---|---|---|
| TVIS10006800 | HBV | ENSG00000145888.11 | protein_coding | GLRA1 | No | No | 2741 | P23415 Q14C71 |
| TVIS30084720 | HIV | ENSG00000145888.11 | protein_coding | GLRA1 | No | No | 2741 | P23415 Q14C71 |
| TVIS30063823 | HIV | ENSG00000145888.11 | protein_coding | GLRA1 | No | No | 2741 | P23415 Q14C71 |
| TVIS30063824 | HIV | ENSG00000145888.11 | protein_coding | GLRA1 | No | No | 2741 | P23415 Q14C71 |
| TVIS30063825 | HIV | ENSG00000145888.11 | protein_coding | GLRA1 | No | No | 2741 | P23415 Q14C71 |
| TVIS20060150 | HPV | ENSG00000145888.11 | protein_coding | GLRA1 | No | No | 2741 | P23415 Q14C71 |
| TVIS20059200 | HPV | ENSG00000145888.11 | protein_coding | GLRA1 | No | No | 2741 | P23415 Q14C71 |
| TVIS20018080 | HPV | ENSG00000145888.11 | protein_coding | GLRA1 | No | No | 2741 | P23415 Q14C71 |
Target Gene Table
▼
TCGA Plot Options
▼
Drug Information
▼
| Gene | GLRA1 |
|---|---|
| DrugBank ID | DB00145 |
| Drug Name | Glycine |
| Target ID | BE0000433 |
| UniProt ID | P23415 |
| Regulation Type | ligand |
| PubMed IDs | 17154252; 16884688 |
| Citations | Heinze L, Harvey RJ, Haverkamp S, Wassle H: Diversity of glycine receptors in the mouse retina: localization of the alpha4 subunit. J Comp Neurol. 2007 Feb 1;500(4):693-707.@@Eulenburg V, Becker K, Gomeza J, Schmitt B, Becker CM, Betz H: Mutations within the human GLYT2 (SLC6A5) gene associated with hyperekplexia. Biochem Biophys Res Commun. 2006 Sep 22;348(2):400-5. Epub 2006 Jul 26. |
| Groups | Approved; Nutraceutical; Vet_approved |
| Direct Classification | Alpha amino acids |
| SMILES | NCC(O)=O |
| Pathways | gamma-Glutamyltranspeptidase Deficiency; Lesch-Nyhan Syndrome (LNS); Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency); Molybdenum Cofactor Deficiency; AICA-Ribosiduria; Purine Nucleoside Phosphorylase Deficiency; gamma-Glutamyltransferase Deficiency; Hyperprolinemia Type II; Glutamate Metabolism; Adenine Phosphoribosyltransferase Deficiency (APRT); Mercaptopurine Action Pathway; 2-Hydroxyglutric Aciduria (D and L Form); L-Arginine:Glycine Amidinotransferase Deficiency; Hyperinsulinism-Hyperammonemia Syndrome; Congenital Bile Acid Synthesis Defect Type II; Porphyrin Metabolism; Prolidase Deficiency (PD); Glycine and Serine Metabolism; Carnitine Synthesis; Adenosine Deaminase Deficiency; Methionine Metabolism; Bile Acid Biosynthesis; Hyperprolinemia Type I; Cystathionine beta-Synthase Deficiency; Arginine and Proline Metabolism; 27-Hydroxylase Deficiency; Sarcosine Oncometabolite Pathway; Purine Metabolism; Gout or Kelley-Seegmiller Syndrome; Ammonia Recycling |
| PharmGKB | PA449789 |
| ChEMBL | CHEMBL773 |
