PRCD
Progressive rod-cone degeneration is a protein in humans that is encoded by the PRCD gene. [3]
PRCD | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | PRCD, RP36, progressive rod-cone degeneration, photoreceptor disc component | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 610598 HomoloGene: 135617 GeneCards: PRCD | ||||||||||||||||||||||||||||||||||||||||||||||||||
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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].
References
- GRCh38: Ensembl release 89: ENSG00000214140 - Ensembl, May 2017
- "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- "Entrez Gene: Progressive rod-cone degeneration". Retrieved 2012-11-28.
Further reading
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