Gene Symbol | GRHL2 |
Entrez Gene ID | 79977 |
Full Name | grainyhead like transcription factor 2 |
Synonyms | BOM,DFNA28,ECTDS,TFCP2L3 |
General protein information |
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Gene Type | protein-coding |
Organism | Homo sapiens(human) |
Genome | |
Summary | 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]. |
Disorder MIM: | |
Disorder Html: | Deafness, autosomal dominant 28, 608641 (3); Ectodermal dysplasia/short stature syndrome, 616029 (3) |