Varaico: Literature-Extracted Genetic Variants

Gene:ENPP1
Variant:p.Y513C
Back to variants list

ENPP1

NM_006208.3:p.Y513C

Associated Papers

Quantitative correlation of ENPP1 pathogenic variants with disease phenotype.

Ansh AJ et al.

Bone, 2024

ENPP1 deficiency: A clinical update on the relevance of individual variants using a locus-specific patient database.

Mercurio SA et al.

Human Mutation, 2022

Mutation update: Variants of the ENPP1 gene in pathologic calcification, hypophosphatemic rickets, and cutaneous hypopigmentation with punctate keratoderma.

Ralph D et al.

Human Mutation, 2022

Response of the ENPP1-Deficient Skeletal Phenotype to Oral Phosphate Supplementation and/or Enzyme Replacement Therapy: Comparative Studies in Humans and Mice.

Ferreira CR et al.

Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research, 2021

Prospective phenotyping of long-term survivors of generalized arterial calcification of infancy (GACI).

Ferreira CR et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021

Hypercementosis Associated with ENPP1 Mutations and GACI.

Thumbigere-Math V et al.

Journal of Dental Research, 2018

Effects of Different Variants in the ENPP1 Gene on the Functional Properties of Ectonucleotide Pyrophosphatase/Phosphodiesterase Family Member 1.

Stella J et al.

Human Mutation, 2016

Cole Disease Results from Mutations in ENPP1.

Eytan O et al.

American Journal of Human Genetics, 2013

Structure of NPP1, an ectonucleotide pyrophosphatase/phosphodiesterase involved in tissue calcification.

Jansen S et al.

Structure (london, England : 1993), 2012

Crystal structure of Enpp1, an extracellular glycoprotein involved in bone mineralization and insulin signaling.

Kato K et al.

Proceedings of the National Academy of Sciences of the United States of America, 2012

Cutaneous features of pseudoxanthoma elasticum in a patient with generalized arterial calcification of infancy due to a homozygous missense mutation in the ENPP1 gene.

Li Q et al.

The British Journal of Dermatology, 2012

Hypophosphatemia, hyperphosphaturia, and bisphosphonate treatment are associated with survival beyond infancy in generalized arterial calcification of infancy.

Rutsch F et al.

Circulation. Cardiovascular Genetics, 2008

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

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."