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Gene : DIAPH3 Homo sapiens

Name  ? diaphanous related formin 3 Cytological Location  13q21.2
Brief Description  diaphanous related formin 3
Description  This gene encodes a member of the diaphanous subfamily of the formin family. Members of this family are involved in actin remodeling and regulate cell movement and adhesion. Mutations in this gene are associated with autosomal dominant auditory neuropathy 1. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]
  • synonyms:
  • diap3,
  • AL137718,
  • AN,
  • uc001vht.6,
  • DRF3,
  • diaphanous homolog 3 (Drosophila),
  • DIAPH3,
  • mDia2,
  • OTTHUMG00000017004,
  • AN,
  • FLJ34705,
  • HGNC:15480,
  • NSDAN,
  • DRF3,
  • NM_001042517,
  • AUNA1,
  • auditory neuropathy, autosomal dominant 1,
  • diaphanous (Drosophila, homolog) 3,
  • NSDAN,
  • AUNA1,
  • DIA2
  • identifiers:
  • 81624,
  • ENSG00000139734,
  • DIAPH3

Genome feature

Region: gene ? Length: 498403  
Location: 13:59665583-60163985 reverse strand Cyto location: 13q21.2


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Disease

1 Diseases

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3753 SN Ps

5 Cross References

19 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results