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.
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Protein Aliases: diaphanous homolog 3; diaphanous-related formin 3; Diaphanous-related formin-3; DKFZp434C0931; DKFZp686A13178; DRF3; FLJ34705; MDia2; Protein diaphanous homolog 3
Gene Aliases: AN; AUNA1; DIA2; DIAP3; DIAPH3; DRF3; mDia2; NSDAN
UniProt ID: (Human) Q9NSV4
Entrez Gene ID: (Human) 81624