{"symbol":"RP9","synonyms":["PAP-1"],"name":"retinitis pigmentosa 9 (autosomal dominant)","description":"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, Sep 2009]","ncbiEntrezGeneId":6100,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/6100","proteins":[{"symbol":"RP9_HUMAN","href":"/api/1.0/protein/RP9_HUMAN"}],"hgncRootFamilies":[]}