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Gene : DIAPH2 Homo sapiens

Name  ? diaphanous related formin 2 Cytological Location  Xq21.33
Brief Description  diaphanous related formin 2
description  The product of this gene belongs to the diaphanous subfamily of the formin homology family of proteins. This gene may play a role in the development and normal function of the ovaries. Defects in this gene have been linked to premature ovarian failure 2. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
  • synonyms:
  • DIA,
  • POF2,
  • POF2,
  • NM_007309,
  • diaphanous homolog 2 (Drosophila),
  • DIA2,
  • NM_006729,
  • uc004efu.5,
  • POF,
  • DRF2,
  • DIA2,
  • POF,
  • DIAPH2,
  • OTTHUMG00000022689,
  • diaphanous (Drosophila, homolog) 2,
  • Y15909,
  • DIA,
  • POF2A,
  • HGNC:2877
  • identifiers:
  • 1730,
  • ENSG00000147202,
  • DIAPH2

Genome feature

Region: gene ? Length: 915936  
Location: X:96684663-97600598 Cyto location: Xq21.33


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Genomics

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Proteins

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SNPs

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Disease

1 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Mouse Gene --> Allele [Phenotype]

Homology

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Expression

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Other

449 SN Ps

5 Cross References

19 Data Sets

7 Homologues

0 Located Features

90 Rna Seq Results