| Entrez gene ID | | 768206 |
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| Official gene symbol | | PRCD |
|
| Full name | | progressive rod-cone degeneration |
|
| Aliases | | ,RP36, |
|
| 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] |
|
| Location | | Chromosome: 17 Locus: 17q25.1 |
|
| Gene position | | 74523668 - 74541458 Map Viewer |
|
| Gene orientation | | plus |
|
| Gene size | | 17791 bp |
|
| Gene sequence |
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| OMIM ID | | 610598 |
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