| Gene Symbol | GRHL2 |
| Entrez Gene ID | 79977 |
| Full Name | grainyhead like transcription factor 2 |
| Synonyms | BOM,DFNA28,ECTDS,TFCP2L3 |
| General protein information |
|
| 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) |









































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