| GENE NAME | FGF17 |
| CHROMOSOME | 8 |
| ENSEMBL ID | None |
| ENTREZ ID | ENSG00000158815 |
| UNIPROT ACCESSION NUMBER | O60258 |
| GO MOLECULAR FUNCTION | ['growth factor activity', 'protein binding', 'fibroblast growth factor receptor binding', 'type 1 fibroblast growth factor receptor binding', 'type 2 fibroblast growth factor receptor binding'] |
| ESSENTIAL IN MOUSE | Non-essential |
| PATHWAYS | hsa04010; hsa04014; hsa04015; hsa04020; hsa04151; hsa04810; hsa05200; hsa05218; hsa05224; hsa05226 |
| 3 combinations linked to FGF17 | OLI367; OLI1650; OLI1347 |
| 3 variants linked to FGF17 | FGF17:c.323T>C, p.Ile108Thr; FGF17:c.580C>G, p.Gln194Glu; FGF17:c.208G>A, p.Gly70Arg |
| 1 disease linked to FGF17 | Kallmann syndrome |