| VIS ID | Virus | Ensembl ID | Gene Type | Target Gene | Oncogene | Tumor Suppressor Gene | NCBI ID | Uniprot ID |
|---|---|---|---|---|---|---|---|---|
| TVIS42000057 | EBV | ENSG00000156689.7 | protein_coding | GLYATL2 | No | No | 219970 | Q8WU03 |
| TVIS30077117 | HIV | ENSG00000156689.7 | protein_coding | GLYATL2 | No | No | 219970 | Q8WU03 |
| TVIS20010630 | HPV | ENSG00000156689.7 | protein_coding | GLYATL2 | No | No | 219970 | Q8WU03 |
| TVIS20049508 | HPV | ENSG00000156689.7 | protein_coding | GLYATL2 | No | No | 219970 | Q8WU03 |
| TVIS44046675 | HTLV-1 | ENSG00000156689.7 | protein_coding | GLYATL2 | No | No | 219970 | Q8WU03 |
Target Gene Table
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TCGA Plot Options
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Drug Information
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| Gene | GLYATL2 |
|---|---|
| DrugBank ID | DB00145 |
| Drug Name | Glycine |
| Target ID | BE0002306 |
| UniProt ID | Q8WU03 |
| Regulation Type | substrate |
| PubMed IDs | 20305126 |
| Citations | Waluk DP, Schultz N, Hunt MC: Identification of glycine N-acyltransferase-like 2 (GLYATL2) as a transferase that produces N-acyl glycines in humans. FASEB J. 2010 Aug;24(8):2795-803. doi: 10.1096/fj.09-148551. Epub 2010 Mar 19. |
| 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 |
