Varaico: Literature-Extracted Genetic Variants

Gene:GC
Variant:p.T436K
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GC

NM_000583.4:p.T436K

Associated Papers

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

39889701 (PubMed )
Supplement: mmc5.pdf

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

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_C

Vitamin D receptor rs3782905 and vitamin D binding protein rs7041 polymorphisms are associated with hepatocellular carcinoma susceptibility in cirrhotic HCV patients.

El-Masry AS et al.

Bmc Medical Genomics, 2023

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

Gibbs DC et al.

Jnci Cancer Spectrum, 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

Genetic Link Determining the Maternal-Fetal Circulation of Vitamin D.

Sampathkumar A et al.

Frontiers in Genetics, 2021

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

The effect of vitamin D pathway genes and deferasirox pharmacogenetics on liver iron in thalassaemia major patients.

Allegra S et al.

The Pharmacogenomics Journal, 2019

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

Lahmar O et al.

Lung, 2018

Role of CYP24A1, VDR and GC gene polymorphisms on deferasirox pharmacokinetics and clinical outcomes.

Allegra S et al.

The Pharmacogenomics Journal, 2018

Vitamin D binding protein rs7041 genotype alters vitamin D metabolism in pregnant women.

Ganz AB et al.

Faseb Journal : Official Publication of the Federation of American Societies for Experimental Biology, 2018

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

Maternal VDR variants rather than 25-hydroxyvitamin D concentration during early pregnancy are associated with type 1 diabetes in the offspring.

Miettinen ME et al.

Diabetologia, 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

Vitamin D binding protein is a key determinant of 25-hydroxyvitamin D levels in infants and toddlers.

Carpenter TO et al.

Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research, 2013

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

Vitamin D-related genetic variants, interactions with vitamin D exposure, and breast cancer risk among Caucasian women in Ontario.

Anderson LN et al.

Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology, 2011

Attempted replication of reported chronic obstructive pulmonary disease candidate gene associations.

Hersh CP et al.

American Journal of Respiratory Cell and Molecular Biology, 2005

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

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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."