NPC1 Chromosome 18

NPC intracellular cholesterol transporter 1
654 variants 654 Health Risk

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What This Gene Does
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]
Gene Info
Gene Group
Solute carrier family 65
Locus Type
gene with protein product
Location
18q11.2
Ensembl
ENSG00000141458
Associated Conditions (23)
Niemann-Pick disease
type C1
type C
Sphingomyelin/cholesterol lipidosis
NPC1-related disorder
Inborn genetic diseases
Dystonic disorder
Melanoma
Malignant tumor of esophagus
Papillary renal cell carcinoma type 1
Familial cancer of breast
Uterine corpus endometrial carcinoma
Russell-Silver syndrome
Nasopharyngeal carcinoma
juvenile form
Ovarian serous cystadenocarcinoma
Abnormality of metabolism/homeostasis
adult form
6 conditions
type C2
+3 more conditions
Key Variants
All Variants (654)
RSID Category Clinical Significance Conditions
RS886042268 Health Risk Pathogenic/Likely pathogenic Niemann-Pick disease, type C1, Niemann-Pick disease
RS886042270 Health Risk Pathogenic/Likely pathogenic Niemann-Pick disease, type C1, Niemann-Pick disease
RS886043131 Health Risk Pathogenic/Likely pathogenic
RS917070773 Health Risk Pathogenic/Likely pathogenic Niemann-Pick disease, type C1, Niemann-Pick disease
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