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Gene : FGF14 Homo sapiens

Name  ? fibroblast growth factor 14 Cytological Location  13q33.1
Brief Description  fibroblast growth factor 14
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. A mutation in this gene is associated with autosomal dominant cerebral ataxia. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]
  • synonyms:
  • SCA27,
  • OTTHUMG00000017303,
  • FGF-14,
  • FHF4,
  • FHF4,
  • NM_001321931,
  • HGNC:3671,
  • FHF-4,
  • uc001vpe.3,
  • SCA27,
  • FGF14
  • identifiers:
  • 2259,
  • ENSG00000102466,
  • FGF14

Genome feature

Region: gene ? Length: 691640  
Location: 13:101710804-102402443 reverse strand Cyto location: 13q33.1


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Function

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Gene -> HPO annotation (Human Phenotype Ontology)

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Genomics

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Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

1 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Expression

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

Gene Ontology

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Other

3753 SN Ps

5 Cross References

19 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results