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Protein-coding gene in the species Homo sapiens

PRCD

PRCD
All data from the card 17
Aliases
PRCD, RP36, progressive rod-cone degeneration, photoreceptor disc component
External IDs
OMIM: 610598; MGI: 3649529; GeneCards: PRCD
Chr.
Chromosome 17 (human)
Band
17q25.1
End
76,553,578 bp
Chr.
Chromosome 11 (mouse)
Band
11 E2|11
End
116,559,215 bp
BioGPS
n/a
Databases
NCBI: entry; OMA: entry
Species
Human
Entrez
768206
Ensembl
ENSG00000214140
UniProt
Q00LT1
RefSeq (mRNA)
NM_001077620
RefSeq (protein)
NP_001071088
Location (UCSC)
Chr 17: 76.53 – 76.55 Mb

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].

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