GRHL2

gene product
BOM, DFNA28, FLJ13782, TFCP2L3
The protein encoded by this gene is a transcription factor that can act as a homodimer or as a heterodimer with either GRHL1 or GRHL3. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal dominant type 28 (DFNA28). [provided by RefSeq, Mar 2009]
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