Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein that interacts with the huntingtin-associated protein 1, which is a huntingtin binding protein that may function in vesicle trafficking. [provided by RefSeq, Apr 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| KALRN-20-RE | 20 (40 μL) | 200 μL |  |
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| KALRN-20-OR | 20 (40 μL) | 200 μL |  |
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| KALRN-20-GO | 20 (40 μL) | 200 μL |  |
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| KALRN-20-GR | 20 (40 μL) | 200 μL |  |
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| KALRN-20-AQ | 20 (40 μL) | 200 μL |  |
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Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein that interacts with the huntingtin-associated protein 1, which is a huntingtin binding protein that may function in vesicle trafficking. [provided by RefSeq, Apr 2016]
Gene Symbol : KALRN
Gene Name : Kalirin RhoGEF kinase
Chromosome : CHR 3: 124,033,340-124,726,324
Locus : 3q21.1-q21.2
Alt. Genes : CHST4
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