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|External IDs||GeneCards: |
Progressive rod-cone degeneration is a protein in humans that is encoded by the PRCD gene. 
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].
- ↑ "Entrez Gene: Progressive rod-cone degeneration". Retrieved 2012-11-28.
|This article on a gene on human chromosome 17 is a stub. You can help Wikipedia by expanding it.|