- accession:NM_000271
- 基因别名:NPC1
- 基因描述:Homo sapiens Niemann-Pick disease, type C1 (NPC1), mRNA.
- 载体:现货载体
- CDS区长度:3837
- 翻译后氨基酸长度:1278
- 基因简介:This gene encodes a large protein that resides in the limiting membrane of endosomes and lysosomes and mediates intracellular cholesterol trafficking via binding of cholesterol to its N-terminal domain. It is predicted to have a cytoplasmic C-terminus, 13 transmembrane domains, and 3 large loops in the lumen of the endosome - the last loop being at the N-terminus. This protein transports low-density lipoproteins to late endosomal/lysosomal compartments where they are hydrolized and released as free cholesterol. Defects in this gene cause Niemann-Pick type C disease, a rare autosomal recessive neurodegenerative disorder characterized by over accumulation of cholesterol and glycosphingolipids in late endosomal/lysosomal compartments.[provided by RefSeq, Aug 2009]
- 规格:10ul 质粒
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