This gene encodes a member of the CWF19 protein family. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia-17 and mild cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| CWF19L1-20-RE | 20 (40 μL) | 200 μL |  |
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| CWF19L1-20-OR | 20 (40 μL) | 200 μL |  |
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| CWF19L1-20-GO | 20 (40 μL) | 200 μL |  |
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| CWF19L1-20-GR | 20 (40 μL) | 200 μL |  |
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| CWF19L1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the CWF19 protein family. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia-17 and mild cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]
Gene Symbol : CWF19L1
Gene Name : CWF19 like 1, cell cycle control (S. pombe)
Chromosome : CHR 10: 100,267,680-100,232,295
Locus : 10q24.31
Alt. Genes : KIF20A
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