| GENE NAME | FGFR2 |
| CHROMOSOME | 10 |
| ENSEMBL ID | None |
| ENTREZ ID | ENSG00000066468 |
| UNIPROT ACCESSION NUMBER | P21802 |
| GO MOLECULAR FUNCTION | ['protein tyrosine kinase activity', 'ATP binding', 'fibroblast growth factor binding', 'protein binding', 'heparin binding', 'protein homodimerization activity', 'protein serine/threonine/tyrosine kinase activity', 'fibroblast growth factor-activated receptor activity', 'transmembrane receptor protein tyrosine kinase activity'] |
| ESSENTIAL IN MOUSE | Essential |
| PATHWAYS | hsa01521; hsa04010; hsa04014; hsa04015; hsa04020; hsa04144; hsa04151; hsa04550; hsa04810; hsa05200; hsa05215; hsa05226; hsa05230; R-HSA-1226099; R-HSA-1643685; R-HSA-1839126; R-HSA-2023837; R-HSA-2033519; R-HSA-5655253; R-HSA-5663202; R-HSA-8851708; R-HSA-8853333 |
| 2 combinations linked to FGFR2 | OLI1520; OLI1514 |
| 2 variants linked to FGFR2 | FGFR2:c.1132A>G, p.Ile378Val; FGFR2:c.34G>A, p.Val12Met |
| 1 disease linked to FGFR2 | 46,XY disorder of sex development |