FGF14

FGF14
Identifiers
Aliases FGF14, FGF-14, FHF-4, FHF4, SCA27, fibroblast growth factor 14
External IDs MGI: 109189 HomoloGene: 3037 GeneCards: FGF14
Genetically Related Diseases
gestational hypertension[1]
Orthologs
Species Human Mouse
Entrez

2259

14169

Ensembl

ENSG00000102466

ENSMUSG00000025551

UniProt

Q92915

P70379

RefSeq (mRNA)

NM_010201
NM_207667

RefSeq (protein)

NP_004106.1
NP_787125.1

NP_034331.2

Location (UCSC) Chr 13: 101.71 – 102.4 Mb Chr 14: 123.98 – 124.68 Mb
PubMed search [2] [3]
Wikidata
View/Edit HumanView/Edit Mouse

Fibroblast growth factor 14 is a protein that in humans is encoded by the FGF14 gene.[4][5][6]

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.[6]

References

Further reading


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