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Related to ACTG1: ACTA1
ACTG1A gene on chromosome 17q25 that encodes a gamma actin which coexists with beta actin as a cytoskeletal component and mediator of internal cell motility. Actin gamma 1 is a cytoplasmic actin found in non-muscle cells.
ACTG1 mutations are associated with DFNA20/26, a type of autosomal dominant, non-syndromic sensorineural progressive hearing loss.