This gene encodes a multi-domain transmembrane protein which is predominantly expressed in the brain and is thought to play a role in endolysosomal trafficking. Mutations in this gene are associated with an autosomal recessive form of a syndrome exhibiting cerebellar ataxia, cognitive disability, and disequilibrium (CAMRQ2). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| WDR81-20-RE | 20 (40 μL) | 200 μL |  |
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| WDR81-20-OR | 20 (40 μL) | 200 μL |  |
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| WDR81-20-GO | 20 (40 μL) | 200 μL |  |
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| WDR81-20-GR | 20 (40 μL) | 200 μL |  |
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| WDR81-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a multi-domain transmembrane protein which is predominantly expressed in the brain and is thought to play a role in endolysosomal trafficking. Mutations in this gene are associated with an autosomal recessive form of a syndrome exhibiting cerebellar ataxia, cognitive disability, and disequilibrium (CAMRQ2). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]
Gene Symbol : WDR81
Gene Name : WD repeat domain 81
Chromosome : CHR 17: 171,652,2-173,859,8
Locus : 17p13.3
Alt. Genes : KIF20A
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