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dfna5

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Official Full Name
deafness, autosomal dominant 5
Background
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. T
Synonyms
DFNA5; deafness, autosomal dominant 5 (human); non-syndromic hearing impairment protein 5 homolog; EG14210; Fin15; 2310037D07Rik; 4932441K13Rik; Deafness, autosomal dominant 5; Deafness, autosomal dominant 5 protein; DFNA5_HUMAN; Dfna5h; ICERE 1; ICERE-1; Inversely correlated with estrogen receptor expression 1; Non-syndromic hearing impairment protein 5; Nonsyndromic hearing impairment protein; deafness, autosomal dominant 5 homolog