This gene encodes a member of the kinesin family of proteins. Members of this family are part of a multisubunit complex that functions as a microtubule motor in intracellular organelle transport. Mutations in this gene cause autosomal dominant spastic paraplegia 10. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| KIF5A-20-RE | 20 (40 μL) | 200 μL |  |
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| KIF5A-20-OR | 20 (40 μL) | 200 μL |  |
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| KIF5A-20-GO | 20 (40 μL) | 200 μL |  |
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| KIF5A-20-GR | 20 (40 μL) | 200 μL |  |
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| KIF5A-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the kinesin family of proteins. Members of this family are part of a multisubunit complex that functions as a microtubule motor in intracellular organelle transport. Mutations in this gene cause autosomal dominant spastic paraplegia 10. [provided by RefSeq, Jul 2008]
Gene Symbol : KIF5A
Gene Name : Kinesin family member 5A
Chromosome : CHR 12: 575,500,63-575,847,70
Locus : 12q13.3
Alt. Genes : CLEC3A
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