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DIAPH3

Official Full Name
diaphanous related formin 3
Organism
Homo sapiens
GeneID
81624
Background
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]
Synonyms
AN; DIA2; DRF3; AUNA1; NSDAN; diap3; mDia2;

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