This gene encodes a protein that plays a critical role in dynein arm assembly and motile cilia function. Mutations in this gene result in primary ciliary dyskinesia. Naturally occuring readthrough transcription occurs from this locus to the downstream t-complex 10 like (TCP10L) gene. [provided by RefSeq, Apr 2017]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| C21ORF59-20-RE | 20 (40 μL) | 200 μL |  |
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| C21ORF59-20-OR | 20 (40 μL) | 200 μL |  |
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| C21ORF59-20-GO | 20 (40 μL) | 200 μL |  |
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| C21ORF59-20-GR | 20 (40 μL) | 200 μL |  |
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| C21ORF59-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a protein that plays a critical role in dynein arm assembly and motile cilia function. Mutations in this gene result in primary ciliary dyskinesia. Naturally occuring readthrough transcription occurs from this locus to the downstream t-complex 10 like (TCP10L) gene. [provided by RefSeq, Apr 2017]
Gene Symbol : C21ORF59
Gene Name : Chromosome 21 open reading frame 59
Chromosome : CHR 21: 326,126,07-326,016,73
Locus : 21q22.11
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