DIAPH3, diaphanous related formin 3

DIAPH3, diaphanous related formin 3

• 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]

• Gene Synonyms (protein diaphanous homolog 3, diaphanous homolog 3, AN, AUNA1, DIA2, DRF3, NSDAN, diap3, mDia2,)
• NCBI Gene ID: 81624
• Species: Homo sapiens (Human)
• UNIPROT ID#>>B4DPV3
  UNIPROT ID#>>Q9NSV4
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

diaphanous related formin 3 interacts with:

• catechol-O-methyltransferase domain containing 1
  coiled-coil domain containing 183
  ectonucleotide pyrophosphatase/phosphodiesterase 6
  egl-9 family hypoxia inducible factor 3
  spindle and centriole associated protein 1
  transmembrane phosphoinositide 3-phosphatase and tensin homolog 2
  vasorin

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.