PRCD

Progressive rod-cone degeneration is a protein in humans that is encoded by the PRCD gene. [3]

PRCD
Identifiers
Aliases	PRCD, RP36, progressive rod-cone degeneration, photoreceptor disc component
External IDs	OMIM: 610598 HomoloGene: 135617 GeneCards: PRCD
Gene location (Human) Chr. Chromosome 17 (human)[1] Band 17q25.1 Start 76,527,586 bp[1] End 76,553,578 bp[1]
Gene ontology Molecular function • opsin binding Cellular component • photoreceptor outer segment • cytoplasm • extracellular region • endoplasmic reticulum • Golgi apparatus • photoreceptor outer segment membrane • membrane • cell projection Biological process • response to stimulus • visual perception Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	768206	n/a
Ensembl	ENSG00000214140	n/a
UniProt	Q00LT1	n/a
RefSeq (mRNA)	NM_001077620	n/a
RefSeq (protein)	NP_001071088	n/a
Location (UCSC)	Chr 17: 76.53 – 76.55 Mb	n/a
PubMed search	[2]	n/a
Wikidata
View/Edit Human

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].