This gene is thought to play a role in a complex developmental pathway and the regulation of genes involved in cerebellar development. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia. [provided by RefSeq, Jan 2011]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ZNF592-20-RE | 20 (40 μL) | 200 μL |  |
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| ZNF592-20-OR | 20 (40 μL) | 200 μL |  |
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| ZNF592-20-GO | 20 (40 μL) | 200 μL |  |
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| ZNF592-20-GR | 20 (40 μL) | 200 μL |  |
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| ZNF592-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene is thought to play a role in a complex developmental pathway and the regulation of genes involved in cerebellar development. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia. [provided by RefSeq, Jan 2011]
Gene Symbol : ZNF592
Gene Name : Zinc finger protein 592
Chromosome : CHR 15: 847,485,55-848,064,31
Locus : 15q25.3
Alt. Genes : ZNF263
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