PRCD

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

PRCD
Identifiers
AliasesPRCD, RP36, progressive rod-cone degeneration, photoreceptor disc component
External IDsOMIM: 610598 HomoloGene: 135617 GeneCards: PRCD
Gene location (Human)
Chr.Chromosome 17 (human)[1]
Band17q25.1Start76,527,586 bp[1]
End76,553,578 bp[1]
Orthologs
SpeciesHumanMouse
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 Mbn/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].

References

  1. GRCh38: Ensembl release 89: ENSG00000214140 - Ensembl, May 2017
  2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. "Entrez Gene: Progressive rod-cone degeneration". Retrieved 2012-11-28.

Further reading


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