- accession:NM_203288
- 基因别名:RP9
- 基因描述:Homo sapiens retinitis pigmentosa 9 (autosomal dominant) (RP9), mRNA.
- 载体:现货载体
- CDS区长度:666
- 翻译后氨基酸长度:221
- 基因简介: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]
- 载体信息:自有图片地址
- 规格:10ul 质粒
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