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- accession：NM_001281455
- 基因别名：PMP22
- 基因描述：Homo sapiens peripheral myelin protein 22 (PMP22), transcript variant 4, mRNA.
- 载体：现货载体
- CDS区长度：483
- 翻译后氨基酸长度：160
- TranscriptVariant：This variant (4) differs in the 5' UTR, compared to variant 1. Variants 1, 2, 3 ,4, and 5 encode the same protein.
- 基因简介：This gene encodes an integral membrane protein that is a major component of myelin in the peripheral nervous system. Studies suggest two alternately used promoters drive tissue-specific expression. Various mutations of this gene are causes of Charcot-Marie-Tooth disease Type IA, Dejerine-Sottas syndrome, and hereditary neuropathy with liability to pressure palsies. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]
- 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
