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Gene : FGF17 Homo sapiens

Name  ? fibroblast growth factor 17 Cytological Location  8p21.3
Brief Description  fibroblast growth factor 17
Description  This gene encodes a member of the fibroblast growth factor (FGF) family. Member of the FGF family 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 protein is expressed during embryogenesis and in the adult cerebellum and cortex and may be essential for vascular growth and normal brain development. Mutations in this gene are the cause of hypogonadotropic hypogonadism 20 with or without anosmia. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]
  • synonyms:
  • NM_003867,
  • HGNC:3673,
  • HH20,
  • AB009249,
  • OTTHUMG00000097051,
  • FGF-17,
  • uc003xag.4,
  • FGF-13,
  • FGF17,
  • FGF-13
  • identifiers:
  • 8822,
  • ENSG00000158815,
  • FGF17

Genome feature

Region: gene ? Length: 9102  
Location: 8:22039708-22048809 Cyto location: 8p21.3

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2 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



903 SN Ps

5 Cross References

19 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results