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Gene : FGF19 Homo sapiens

Name  ? fibroblast growth factor 19 Cytological Location  11q13.3
Brief Description  fibroblast growth factor 19
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 is a high affinity, heparin dependent ligand for FGFR4. Expression of this gene was detected only in fetal but not adult brain tissue. Synergistic interaction of the chick homolog and Wnt-8c has been shown to be required for initiation of inner ear development. [provided by RefSeq, Jul 2008]
  • synonyms:
  • OTTHUMG00000167886,
  • FGF19,
  • HGNC:3675,
  • uc001opf.4,
  • NM_005117,
  • AB018122
  • identifiers:
  • 9965,
  • ENSG00000162344,
  • FGF19

Genome feature

Region: gene ? Length: 5785  
Location: 11:69698238-69704022 reverse strand Cyto location: 11q13.3


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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

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Disease

0 Diseases

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

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Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

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Expression

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Other

47 SN Ps

5 Cross References

15 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results