PRCD

From Wikipedia, the free encyclopedia
PRCD
Identifiers
AliasesPRCD, RP36, progressive rod-cone degeneration, photoreceptor disc component
External IDsOMIM: 610598; MGI: 3649529; HomoloGene: 135617; GeneCards: PRCD; OMA:PRCD - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001077620

NM_001163318

RefSeq (protein)

NP_001071088

NP_001156790

Location (UCSC)Chr 17: 76.53 – 76.55 MbChr 11: 116.54 – 116.56 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Progressive rod-cone degeneration is a protein in humans that is encoded by the PRCD gene. [5]

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[edit]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000214140Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000075410Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: Progressive rod-cone degeneration". Retrieved 2012-11-28.

Further reading[edit]