Gene Symbol | PRCD |
Entrez Gene ID | 768206 |
Full Name | photoreceptor disc component |
Synonyms | RP36 |
General protein information |
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Gene Type | protein-coding |
Organism | Homo sapiens(human) |
Genome | |
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]. |
Disorder MIM: | |
Disorder Html: | Retinitis pigmentosa 36, 610599 (3) |