基因注释：GRHL2
官方信息
官方名称：grainyhead like transcription factor 2
功能摘要：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].
作为靶基因的剪接因子
关联疾病
该基因暂无关联疾病记录