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Antibody detects endogenous levels of total DIAPH3.
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: diaphanous homolog 3; diaphanous-related formin; diaphanous-related formin 3; Diaphanous-related formin-3; DKFZp434C0931; DKFZp686A13178; DRF3; FLJ34705; MDia2; p134mDIA2; Protein diaphanous homolog 3
Gene Aliases: 4930417P13Rik; AN; AUNA1; DIA2; DIAP3; DIAPH3; DRF3; mDia2; mKIAA4117; NSDAN; p134MDia2
UniProt ID: (Human) Q9NSV4, (Mouse) Q9Z207, (Rat) F1LVW7
Entrez Gene ID: (Human) 81624, (Mouse) 56419, (Rat) 290396
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