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Gene : FGF12 Homo sapiens

Name  ? fibroblast growth factor 12 Cytological Location  3q28-q29
Brief Description  fibroblast growth factor 12
Description  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 growth factor lacks the N-terminal signal sequence present in most of the FGF family members, but it contains clusters of basic residues that have been demonstrated to act as a nuclear localization signal. When transfected into mammalian cells, this protein accumulated in the nucleus, but was not secreted. The specific function of this gene has not yet been determined. [provided by RefSeq, Dec 2019]
  • synonyms:
  • OTTHUMG00000156132,
  • FGF12B,
  • FHF1,
  • NM_021032,
  • fibroblast growth factor homologous factor 1,
  • FGF12B,
  • uc003fsx.4,
  • fibroblast growth factor 12B,
  • fibroblast growth factor FGF-12b,
  • FHF1,
  • HGNC:3668,
  • EIEE47,
  • FGF12,
  • U66197,
  • myocyte-activating factor
  • identifiers:
  • 2257,
  • ENSG00000114279,
  • FGF12

Genome feature

Region: gene ? Length: 588152  
Location: 3:192139390-192727541 reverse strand Cyto location: 3q28-q29

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1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

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3753 SN Ps

5 Cross References

19 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results