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NPC1 NPC intracellular cholesterol transporter 1

Gene ID: 4864, updated on 11-Apr-2024
Gene type: protein coding
Also known as: NPC; POGZ; SLC65A1

Summary

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]

Associated conditions

See all available tests in GTR for this gene

DescriptionTests
Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations.
GeneReviews: Not available
Niemann-Pick disease, type C1See labs

Genomic context

Location:
18q11.2
Sequence:
Chromosome: 18; NC_000018.10 (23506184..23586506, complement)
Total number of exons:
28

Links

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