人 RP9 (NM_203288) cDNA克隆

Accession: NM_203288
基因名称: RP9
基因别名: PAP-1
基因描述: Homo sapiens retinitis pigmentosa 9 (autosomal dominant) (RP9), mRNA.
种属: Human
CDS区长度: 666 (查看编码区序列)
翻译后氨基酸长度: 221 (查看氨基酸序列)
产品编号 产品名称 载体 规格 价格
G157241 人 RP9 (NM_203288) cDNA克隆 pDONR223 2ug质粒 点击询价

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]