Varaico: Literature-Extracted Genetic Variants

Gene:NPC1
Variant:p.H1016R
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NPC1

NM_000271.5:p.H1016R

Associated Papers

Familial Alzheimer's disease associated with heterozygous NPC1 mutation.

Lopergolo D et al.

Journal of Medical Genetics, 2024

Signatures of natural selection and ethnic-specific prevalence of NPC1 pathogenic mutations contributing to obesity and Niemann-Pick disease type C1.

Chiorean A et al.

Scientific Reports, 2020

33139814 (PubMed )
Supplement: 41598_2020_75919_MOESM2_ESM.xlsx › LOF_and_nonsynonymous_mutations

Cholesterol binding to the sterol-sensing region of Niemann Pick C1 protein confines dynamics of its N-terminal domain.

Dubey V et al.

Plos Computational Biology, 2020

Establishing the precise evolutionary history of a gene improves prediction of disease-causing missense mutations.

Adebali O et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2016

26890452 (PubMed )
Supplement: gim2015208x1.zip › S1_Table.xls › Sheet1

Structural Insights into the Niemann-Pick C1 (NPC1)-Mediated Cholesterol Transfer and Ebola Infection.

Gong X et al.

Cell, 2016

27238017 (PubMed )
Supplement: mmc1.pdf

Identification of novel bile acids as biomarkers for the early diagnosis of Niemann-Pick C disease.

Mazzacuva F et al.

Febs Letters, 2016

27139891 (PubMed )
Supplement: FEB2-590-1651-s001.pdf

High incidence of unrecognized visceral/neurological late-onset Niemann-Pick disease, type C1, predicted by analysis of massively parallel sequencing data sets.

Wassif CA et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2016

Characterization of Disease-Associated Mutations in Human Transmembrane Proteins.

Molnár J et al.

Plos One, 2016

26986070 (PubMed )
Supplement: pone.0151760.s001.xlsx › disease

The NPC1 protein: structure implies function.

Scott C et al.

Biochimica Et Biophysica Acta, 2004

Identification of 58 novel mutations in Niemann-Pick disease type C: correlation with biochemical phenotype and importance of PTC1-like domains in NPC1.

Park WD et al.

Human Mutation, 2003

Elucidating the mutational impact in causing Niemann-Pick disease type C: an in silico approach.

Kannan P et al.

Journal of Biomolecular Structure & Dynamics, 0

36264126 (PubMed )
Supplement: supplement_1.docx
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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."