This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| WHRN-20-RE | 20 (40 μL) | 200 μL |  |
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| WHRN-20-OR | 20 (40 μL) | 200 μL |  |
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| WHRN-20-GO | 20 (40 μL) | 200 μL |  |
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| WHRN-20-GR | 20 (40 μL) | 200 μL |  |
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| WHRN-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]
Gene Symbol : WHRN
Gene Name : Whirlin
Chromosome : CHR 9: 114,505,508-114,402,077
Locus : 9q32
Alt. Genes : OPTN
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