This gene encodes a protein that may be involved in cilia motility. Mutations in this gene cause of autosomal recessive primary ciliary dyskinesia-5, a disorder characterized by the accumulation of cerebrospinal fluid within the ventricles of the brain. A duplicate copy of this gene has been found in humans on chromosome 1. [provided by RefSeq, Jan 2013]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| HYDIN-20-RE | 20 (40 μL) | 200 μL |  |
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| HYDIN-20-OR | 20 (40 μL) | 200 μL |  |
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| HYDIN-20-GO | 20 (40 μL) | 200 μL |  |
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| HYDIN-20-GR | 20 (40 μL) | 200 μL |  |
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| HYDIN-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a protein that may be involved in cilia motility. Mutations in this gene cause of autosomal recessive primary ciliary dyskinesia-5, a disorder characterized by the accumulation of cerebrospinal fluid within the ventricles of the brain. A duplicate copy of this gene has been found in humans on chromosome 1. [provided by RefSeq, Jan 2013]
Gene Symbol : HYDIN
Gene Name : HYDIN, axonemal central pair apparatus protein
Chromosome : CHR 16: 712,307,21-708,020,83
Locus : 16q22.2
Alt. Genes : TRAP1
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