Entrez gene ID | | 6100 |
Official gene symbol | | RP9 |
Full name | | retinitis pigmentosa 9 (autosomal dominant) |
Aliases | | ,PAP-1, |
Gene summary | | The protein encoded by this gene can be bound and phosphorylated by the protooncogene PIM1 product, a serine/threonine protein kinase . This protein localizes in nuclear speckles containing the splicing factors, and has a role in pre-mRNA splicing. CBF1-interacting protein (CIR), a corepressor of CBF1, can also bind to this protein and effects alternative splicing. Mutations in this gene result in autosomal dominant retinitis pigmentosa-9. This gene has a pseudogene (GeneID: 441212), which is located in tandem array approximately 166 kb distal to this gene. [provided by RefSeq] |
Location | | Chromosome: 7 Locus: 7p14.3 |
Gene position | | 33149002 - 33134409 Map Viewer |
Gene orientation | | minus |
Gene size | | 14594 bp |
Gene sequence |
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OMIM ID | | 607331 |
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