PRCD
Sign in to saveAlso known as RP36, progressive rod-cone degeneration, photoreceptor disc component
Progressive rod-cone degeneration is a protein in humans that is encoded by the PRCD gene.
Gene data
PRCD- Name
- photoreceptor disc component
- Type
- protein-coding
- Aliases
- RP36
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].
via MyGene.info
Gene · Ensembl
photoreceptor disc component
- Symbol
- PRCD
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 17:76,527,586-76,553,578
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
Show 5 more facts
- HomoloGene ID
- 135617
- exact match
- identifiers.org/ncbigene/768206
- genomic end
- 74549660
- genomic start
- 74523668
- cytogenetic location
- 17q25.1
Sources (4)
via Wikidata · CC0
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Article
2 sectionsContents
- References
- Further reading
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].