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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:
  • NM_006729,
  • POF2,
  • DIA,
  • diaphanous (Drosophila, homolog) 2,
  • POF,
  • HGNC:2877,
  • Y15909,
  • POF2A,
  • DIA2,
  • POF2,
  • DIA,
  • DRF2,
  • POF,
  • uc004efu.5,
  • DIAPH2,
  • OTTHUMG00000022689,
  • diaphanous homolog 2 (Drosophila),
  • DIA2,
  • NM_007309
  • identifiers:
  • 1730,
  • ENSG00000147202,
  • DIAPH2

Genome feature

Region: gene ? Length: 920335  
Location: X:96684663-97604997 Cyto location: Xq21.33

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Curated Proteins Displayer


Gene Ontology Displayer

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


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]


Homologue Displayer


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Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



3753 SN Ps

5 Cross References

19 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results