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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| GRHL2-20-RE | 20 (40 μL) | 200 μL |  |
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| GRHL2-20-OR | 20 (40 μL) | 200 μL |  |
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| GRHL2-20-GO | 20 (40 μL) | 200 μL |  |
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| GRHL2-20-GR | 20 (40 μL) | 200 μL |  |
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| GRHL2-20-AQ | 20 (40 μL) | 200 μL |  |
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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]
Gene Symbol : GRHL2
Gene Name : Grainyhead like transcription factor 2
Chromosome : CHR 8: 101,492,439-101,678,104
Locus : 8q22.3
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