PRCD
Sign in to saveAlso known as RP36, progressive rod-cone degeneration, photoreceptor disc component
جين من أنواع جينات الإنسان العاقل
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
View on Ensembl →
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 8 more facts
- HomoloGene ID
- 135617
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/768206
- genomic end
- 74549660
- genomic start
- 74523668
- chromosome
- human chromosome 17
- cytogenetic location
- 17q25.1
- expressed in
- corpus callosum
Sources (4)
via Wikidata · CC0
Article · العربية
PRCD (Photoreceptor disc component) هوَ بروتين يُشَفر بواسطة جين PRCD في الإنسان.
Abstract from DBpedia / Wikipedia · CC BY-SA