Recombinant DFNA5/GSDME Monoclonal Antibody

Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene.

DFNA; DFNA5; ICERE-1; GSDME; ICERE1;2310037D07Rik;4932441K13Rik; autosomal dominant 5; autosomal dominant 5 protein; Deafness; DFNA5 gene; Dfna5h; EG14210; Fin15; ICERE 1; Inversely correlated with estrogen receptor expression 1; Nonsyndromic hearing impairment protein; Non-syndromic hearing impairment protein 5; DFNA5