- 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]
- 载体信息:自有图片地址
- 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