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Gene information for RP9 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID6100
Official gene symbolRP9
Full nameretinitis pigmentosa 9 (autosomal dominant)
Aliases,PAP-1,
Gene summaryThe 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]
LocationChromosome: 7   Locus: 7p14.3
Gene position33149002 - 33134409  Map Viewer
Gene orientationminus
Gene size14594 bp
Gene sequence
OMIM ID607331