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- accession：NM_014874
- 基因别名：MFN2
- 基因描述：Homo sapiens mitofusin 2 (MFN2), transcript variant 1, mRNA.
- 载体：现货载体
- CDS区长度：2274
- 翻译后氨基酸长度：757
- TranscriptVariant：This variant (1) represents the longer transcript. Both variants 1 and 2 encode the same protein.
- 基因简介：This gene encodes a mitochondrial membrane protein that participates in mitochondrial fusion and contributes to the maintenance and operation of the mitochondrial network. This protein is involved in the regulation of vascular smooth muscle cell proliferation, and it may play a role in the pathophysiology of obesity. Mutations in this gene cause Charcot-Marie-Tooth disease type 2A2, and hereditary motor and sensory neuropathy VI, which are both disorders of the peripheral nervous system. Defects in this gene have also been associated with early-onset stroke. Two transcript variants encoding the same protein have been identified. [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
