NPC Intracellular Cholesterol Transporter 1

Alternative Names

  • NPC1
  • NPC1 Gene
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OMIM Number

607623

NCBI Gene ID

4864

Uniprot ID

O15118

Length

80,323 bases

No. of Exons

28

No. of isoforms

2

Protein Name

NPC intracellular cholesterol transporter 1

Molecular Mass

142167 Da

Amino Acid Count

1278

Genomic Location

chr18:23,506,183-23,586,505

Gene Map Locus
18q11.2

Description

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. [From RefSeq]

Epidemiology in the Arab World

View Map
Variant NameCountryGenomic LocationClinvar Clinical SignificanceCTGA Clinical Significance Condition(s)HGVS ExpressionsdbSNPClinvar
NM_000271.5:c.2974G>TPalestineNC_000018.10:g.23538609C>APathogenic, Uncertain SignificancePathogenicNiemann-Pick Disease, Type C1NG_012795.1:g.53009G>T; NM_000271.5:c.2974G>T; NP_000262.2:p.Gly992Trp803582542960
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