PRCD 蛋白
(Progressive Rod-Cone Degeneration (PRCD))
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].
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3 results
PRCD
宿主: 人
宿主: HEK-293 Cells
Recombinant
> 80 % as determined by SDS-PAGE and Coomassie blue staining
AbP, STD
1 image
Aliases for PRCD 蛋白
photoreceptor disc component (PRCD) 蛋白RP36 蛋白
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