Varaico: Literature-Extracted Genetic Variants

Gene:GC
Variant:p.D432E
Back to variants list

GC

NM_000583.4:p.D432E

Associated Papers

Group-specific component and 25-hydroxylase gene polymorphisms in nasopharyngeal carcinoma: Associations with susceptibility and radiotherapy response.

Liu L et al.

World Journal of Clinical Oncology, 2025

Genetic insights into vitamin D deficiency: a case-control study of GC and CYP24A1 gene polymorphism.

Usama et al.

Steroids, 2025

Search for Disease-Specific Genetic Markers Originated from the Vitamin D Binding Protein Gene Polymorphisms in the Multiple Sclerosis Cohort in the Latvian Population.

Kalnina J et al.

International Journal of Molecular Sciences, 2025

Uncovering dark mass in population proteomics: Pan-analysis of single amino acid polymorphism relevant to cognition and aging.

Gao X et al.

Cell Genomics, 2025

Genetic and serum biomarkers of NSAID hypersensitivity reactions.

Amo G et al.

Frontiers in Pharmacology, 2025

Correlation between rs7041 and rs4588 polymorphisms in vitamin D binding protein gene and COVID-19-related severity and mortality.

Hamed ER et al.

Bmc Medical Genomics, 2024

Impact of gene polymorphisms involved in the vitamin D metabolic pathway on the susceptibility to and severity of autism spectrum disorder.

Saechua C et al.

Scientific Reports, 2024

Differential glycosylation in mutant vitamin D-binding protein decimates the binding stability of vitamin D.

Usama et al.

Journal of Biomolecular Structure & Dynamics, 2024

Trio-based exome sequencing and high-resolution HLA typing in families of patients with autoimmune adrenal insufficiency and autoimmune polyglandular syndrome.

Buianova A et al.

Plos One, 2024

39423205 (PubMed )
Supplement: pone.0312335.s007.xlsx › Family_B

Indicators of HSV1 Infection, ECM-Receptor Interaction, and Chromatin Modulation in a Nuclear Family with Schizophrenia.

Huang YC et al.

Journal of Personalized Medicine, 2023

37763159 (PubMed )
Supplement: jpm-13-01392-s001.zip › Supplementary_Table_S3.xlsx › Variants

Association of functional, inherited vitamin D-binding protein variants with melanoma-specific death.

Gibbs DC et al.

Jnci Cancer Spectrum, 2023

The Role of Polymorphism in the Endothelial Homeostasis and Vitamin D Metabolism Genes in the Severity of Coronary Artery Disease.

Ponasenko A et al.

Biomedicines, 2023

Single nucleotide polymorphisms in vitamin D binding protein and 25-hydroxylase genes affect vitamin D levels in adolescents of Arab ethnicity in Kuwait.

Rahman A et al.

Frontiers in Endocrinology, 2023

Genetic influence on urinary vitamin D binding protein excretion and serum levels: a focus on rs4588 C>A polymorphism in the GC gene.

Doğan D et al.

Frontiers in Endocrinology, 2023

GC1f Vitamin D Binding Protein Isoform as a Marker of Severity in Autism Spectrum Disorders.

Bolognesi E et al.

Nutrients, 2022

The association of vitamin D binding protein levels and genotypes with type 1 diabetes in the black South African population.

Cave EM et al.

Bmc Endocrine Disorders, 2022

Distribution of vitamin D-binding protein/group-specific component gene subtypes in Kuwaiti population.

Al-Shammri SN et al.

Molecular Genetics & Genomic Medicine, 2022

The Association Between VDR and GC Polymorphisms and Lung Cancer Risk: A Systematic Review and Meta-Analysis.

Duan GQ et al.

Genetic Testing and Molecular Biomarkers, 2020

Genetic variation in GC and CYP2R1 affects 25-hydroxyvitamin D concentration and skeletal parameters: A genome-wide association study in 24-month-old Finnish children.

Kämpe A et al.

Plos Genetics, 2019

Association Between Vitamin D Metabolism Gene Polymorphisms and Risk of Tunisian Adults' Asthma.

Lahmar O et al.

Lung, 2018

Evaluation of 1,25-dihydroxyvitamin D3 pathway in patients with chronic urticaria.

Nasiri-Kalmarzi R et al.

Qjm : Monthly Journal of the Association of Physicians, 2018

Common Genetic Polymorphisms Influence Blood Biomarker Measurements in COPD.

Sun W et al.

Plos Genetics, 2016

Characterization of additional vitamin D binding protein variants.

Fu L et al.

The Journal of Steroid Biochemistry and Molecular Biology, 2016

GC Gene Polymorphisms and Vitamin D-Binding Protein Levels Are Related to the Risk of Generalized Aggressive Periodontitis.

Song W et al.

International Journal of Endocrinology, 2016

The rs1803274 polymorphism of the BCHE gene is associated with an increased risk of coronary in-stent restenosis.

Pleva L et al.

Bmc Cardiovascular Disorders, 2015

Association of vitamin D binding protein polymorphisms with bronchopulmonary dysplasia: a case-control study of gc globulin and bronchopulmonary dysplasia.

Serce Pehlevan O et al.

Journal of Perinatology : Official Journal of the California Perinatal Association, 2015

Genetic and environmental influences on plasma vitamin D binding protein concentrations.

Wilson RT et al.

Translational Research : the Journal of Laboratory and Clinical Medicine, 2015

Effect of vitamin D-binding protein genotype on the development of asthma in children.

Navas-Nazario A et al.

Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology, 2014

Variations in the vitamin D-binding protein (DBP) gene are related to lower 25-hydroxyvitamin D levels in healthy girls: a cross-sectional study.

Santos BR et al.

Hormone Research in Paediatrics, 2013

Vitamin D in a northern Canadian first nation population: dietary intake, serum concentrations and functional gene polymorphisms.

Larcombe L et al.

Plos One, 2012

Association of vitamin D binding protein (VDBP) polymorphisms and serum 25(OH)D concentrations in a sample of young Canadian adults of different ancestry.

Gozdzik A et al.

The Journal of Steroid Biochemistry and Molecular Biology, 2011

Genome-wide association study of circulating vitamin D levels.

Ahn J et al.

Human Molecular Genetics, 2010

Association of molecular variants, haplotypes, and linkage disequilibrium within the human vitamin D-binding protein (DBP) gene with postmenopausal bone mineral density.

Ezura Y et al.

Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research, 2003

Use of whole exome sequencing for identification of genetic variants related to Growth Hormone Deficiency and Short Stature: A Family-Based Study.

Alharazy S et al.

Pakistan Journal of Medical Sciences, 0

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."