FGF17

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Fibroblast growth factor 17 is a protein that in humans is encoded by the FGF17 gene.[5][6][7]

AliasesFGF17, FGF-13, HH20, FGF-17, fibroblast growth factor 17
End22,048,809 bp[1]
Quick facts Identifiers, Aliases ...
FGF17
Identifiers
AliasesFGF17, FGF-13, HH20, FGF-17, fibroblast growth factor 17
External IDsOMIM: 603725; MGI: 1202401; HomoloGene: 2872; GeneCards: FGF17; OMA:FGF17 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001304478
NM_003867

NM_008004
NM_001360108

RefSeq (protein)

NP_001291407
NP_003858

NP_032030
NP_001347037

Location (UCSC)Chr 8: 22.04 – 22.05 MbChr 14: 70.64 – 70.64 Mb
PubMed search[3][4]
Wikidata
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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. This gene was shown to be prominently expressed in the cerebellum and cortex. The mouse homolog of this gene was localized to specific sites in the midline structures of the forebrain, the midbrain-hindbrain junction, developing skeleton and developing arteries, which suggests a role in central nervous system, bone and vascular development. This gene was referred to as FGF-13 in reference 2, however, its amino acid sequence and chromosomal localization are identical to FGF17.[7]

References

Further reading

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