FGF3

Protein-coding gene in humans From Wikipedia, the free encyclopedia

INT-2 proto-oncogene protein also known as FGF-3 is a protein that in humans is encoded by the FGF3 gene.[5]

AliasesFGF3, HBGF-3, INT2, fibroblast growth factor 3
End69,819,416 bp[1]
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FGF3
Identifiers
AliasesFGF3, HBGF-3, INT2, fibroblast growth factor 3
External IDsOMIM: 164950; MGI: 95517; HomoloGene: 3841; GeneCards: FGF3; OMA:FGF3 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005247

NM_008007

RefSeq (protein)

NP_005238

n/a

Location (UCSC)Chr 11: 69.81 – 69.82 MbChr 7: 144.39 – 144.4 Mb
PubMed search[3][4]
Wikidata
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Function

FGF-3 is a member of the fibroblast growth factor family. FGF3 binds to Fibroblast Growth Factor Receptor 3 (FGFR3) to serve as a negative regulator of bone growth during ossification. Effectively, FGF-3 inhibits proliferation of chondrocytes within growth plate.

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.[5]

Clinical significance

The FGF3 gene was identified by its similarity with mouse fgf3/int-2, a proto-oncogene activated in virally induced mammary tumors in the mouse. Frequent amplification of this gene has been found in human tumors, which may be important for neoplastic transformation and tumor progression. Studies of the similar genes in mouse and chicken suggested the role in inner ear formation.[5] Also, haploinsufficiency in the FGF3 gene is thought to cause otodental syndrome.

Interactions

FGF3 (gene) has been shown to interact with EBNA1BP2.[6]

References

Further reading

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