This gene is predominantly expressed in the retina, and mutations in this gene are the cause of autosomal recessive retinal degeneration in both humans and dogs. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| PRCD-20-RE | 20 (40 μL) | 200 μL |  |
Request Pricing |
| PRCD-20-OR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| PRCD-20-GO | 20 (40 μL) | 200 μL |  |
Request Pricing |
| PRCD-20-GR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| PRCD-20-AQ | 20 (40 μL) | 200 μL |  |
Request Pricing |
This gene is predominantly expressed in the retina, and mutations in this gene are the cause of autosomal recessive retinal degeneration in both humans and dogs. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2010]
Gene Symbol : PRCD
Gene Name : Photoreceptor disc component
Chromosome : CHR 17: 765,275,85-765,553,38
Locus : 17q25.1
Alt. Genes : TENM1
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.