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PRCD


Official Full Name
photoreceptor disc component
Organism
Homo sapiens
Gene ID
768206
Background
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]
Synonyms
RP36

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SHH382108 shRNA set against Human PRCD (NM_001077620.2) Inquiry
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CDCB182130 Rabbit PRCD ORF clone (XM_008250902.1) Inquiry
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