Version 5.4
Homo sapiens Gene: PRCD
Summary
InnateDB Gene IDBG-234944.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol PRCD
Gene Name progressive rod-cone degeneration
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000214140
Encoded Proteins
IDBP-760239
IDBP-762058
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary 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]
Gene Information
Type Protein coding
Genomic Location Chromosome 17:76527586-76553578
Strand Forward strand
Band q25.1
Transcripts
ENST00000397633
ENST00000397630
ENST00000465808
ENST00000593023
ENST00000587289
ENST00000592014 ENSP00000467661
ENST00000591317
ENST00000590555
ENST00000586148 ENSP00000465932
ENST00000587063
ENST00000592340
ENST00000592432
ENST00000587813
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
GO:0007601 visual perception
GO:0050896 response to stimulus
Cellular Component
GO:0005737 cytoplasm
GO:0016021 integral component of membrane
Orthologs
No orthologs found for this gene
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.634380 Hs.743588
RefSeq NM_001077620
HUGO
OMIM
CCDS CCDS42382
HPRD
IMGT
EMBL
GenPept
RNA Seq Atlas

If you use InnateDB for your research, please cite the following publication:

Breuer et al., InnateDB: systems biology of innate immunity and beyond - recent updates and continuing curation. Nucl. Acids Res. (2013) 41 (D1) 

InnateDB is being developed jointly by the Brinkman Laboratory (Simon Fraser University, British Columbia, Canada), the Hancock Laboratory (University of British Columbia, Vancouver, British Columbia) and the Lynn EMBL Australia Group (South Australian Health & Medical Research Institute and Flinders University, Adelaide, Australia).

Funding is currently provided by Allergen and EMBL Australia. Previous funding has been provided by Genome Canada, the Foundation for the National Institutes of Health through the Grand Challenges in Global Health initiative and by Teagasc. InnateDB curated interactions are licensed under the Design Science License. All other data is licensed under the terms of the originating database. Contact: innatedb-mail@sfu.ca