| GENE NAME | FGF13 |
| CHROMOSOME | X |
| ENSEMBL ID | ENSG00000129682 |
| ENTREZ ID | 2258 |
| UNIPROT ACCESSION NUMBER | Q92913 |
| GO MOLECULAR FUNCTION | microtubule binding; protein kinase activator activity; protein binding; growth factor activity |
| ESSENTIAL IN MOUSE | None |
| PATHWAYS | R-HSA-5576892; R-HSA-5576891; R-HSA-397014 |
| 1 combination linked to FGF13 | OLI426 |
| 1 variant linked to FGF13 | FGF13:c.529T>C, p.Ser177Pro |
| 1 disease linked to FGF13 | Kallmann syndrome |