GRHL2( Human )
grainyhead like transcription factor 2
Alias
BOM|DFNA28|ECTDS|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].