| Gene Symbol | FGF14 |
| Entrez Gene ID | 2259 |
| Full Name | fibroblast growth factor 14 |
| Synonyms | FGF-14,FHF-4,FHF4,SCA27 |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. A mutation in this gene is associated with autosomal dominant cerebral ataxia. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]. |
| Disorder MIM: | |
| Disorder Html: | Spinocerebellar ataxia 27, 609307 (3) |








































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