This gene encodes a member of the diaphanous subfamily of the formin family. Members of this family are involved in actin remodeling and regulate cell movement and adhesion. Mutations in this gene are associated with autosomal dominant auditory neuropathy 1. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| DIAPH3-20-RE | 20 (40 μL) | 200 μL |  |
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| DIAPH3-20-OR | 20 (40 μL) | 200 μL |  |
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| DIAPH3-20-GO | 20 (40 μL) | 200 μL |  |
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| DIAPH3-20-GR | 20 (40 μL) | 200 μL |  |
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| DIAPH3-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the diaphanous subfamily of the formin family. Members of this family are involved in actin remodeling and regulate cell movement and adhesion. Mutations in this gene are associated with autosomal dominant auditory neuropathy 1. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]
Gene Symbol : DIAPH3
Gene Name : Diaphanous related formin 3
Chromosome : CHR 13: 601,639,84-596,655,82
Locus : 13q21.2
Alt. Genes : HIPK3
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