This gene encodes a tetratricopeptide repeat domain-containing protein that localizes to ciliary axonmenes and plays a role in the docking of the outer dynein arm to cilia. Mutations in this gene cause severely reduced ciliary motility and the disorder CILD35 (ciliary dyskinesia,primary, 35). Primary ciliary dyskinesia is often associated with recurrent respiratory infections, immotile spermatozoa, and situs inversus; an inversion in left-right body symmetry. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Apr 2017]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TTC25-20-RE | 20 (40 μL) | 200 μL |  |
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| TTC25-20-OR | 20 (40 μL) | 200 μL |  |
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| TTC25-20-GO | 20 (40 μL) | 200 μL |  |
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| TTC25-20-GR | 20 (40 μL) | 200 μL |  |
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| TTC25-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a tetratricopeptide repeat domain-containing protein that localizes to ciliary axonmenes and plays a role in the docking of the outer dynein arm to cilia. Mutations in this gene cause severely reduced ciliary motility and the disorder CILD35 (ciliary dyskinesia,primary, 35). Primary ciliary dyskinesia is often associated with recurrent respiratory infections, immotile spermatozoa, and situs inversus; an inversion in left-right body symmetry. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Apr 2017]
Gene Symbol : TTC25
Gene Name : Tetratricopeptide repeat domain 25
Chromosome : CHR 17: 419,306,04-419,665,16
Locus : 17q21.2
Alt. Genes : ENAM
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