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- accession：NM_006915
- 基因别名：RP2
- 基因描述：Homo sapiens retinitis pigmentosa 2 (X-linked recessive) (RP2), mRNA.
- 载体：现货载体
- CDS区长度：1053
- 翻译后氨基酸长度：350
- 基因简介：The RP2 locus has been implicated as one cause of X-linked retinitis pigmentosa. The predicted gene product shows homology with human cofactor C, a protein involved in the ultimate step of beta-tubulin folding. Progressive retinal degeneration may therefore be due to the accumulation of incorrectly-folded photoreceptor or neuron-specific tubulin isoforms followed by progressive cell death [provided by RefSeq, Jul 2008]
- 规格：10ul 质粒
CDS区参考序列： 点击查看序列翻译后氨基酸参数序列： 点击查看序列
