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Gene : FNBP4 Homo sapiens

Name  ? formin binding protein 4 Cytological Location  11p11.2
Brief Description  formin binding protein 4
Description  This gene encodes a protein containing two tryptophan-rich WW domains that binds the proline-rich formin homology 1 domains of formin family proteins, suggesting a role in the regulation of cytoskeletal dynamics during cell division and migration. It also binds intersectin family proteins suggesting a role in the maintenance of membrane curvature at sites of nascent vesicle formation. Naturally occurring mutations in this gene are associated with Waardenburg anophthalmia syndrome. [provided by RefSeq, Apr 2017]
  • synonyms:
  • OTTHUMG00000166533,
  • BC037404,
  • FBP30,
  • FNBP4,
  • uc009ylv.4,
  • KIAA1014,
  • HGNC:19752,
  • NM_001318339
  • identifiers:
  • 23360,
  • ENSG00000109920,
  • FNBP4

Genome feature

Region: gene ? Length: 50967  
Location: 11:47716494-47767460 reverse strand Cyto location: 11p11.2


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Proteins

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SNPs

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Disease

0 Diseases

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

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Mouse Gene --> Allele [Phenotype]

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Expression

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0 Pathways

3753 SN Ps

5 Cross References

17 Data Sets

3 Homologues

0 Located Features

97 Rna Seq Results