Varaico: Literature-Extracted Genetic Variants

Gene:UCP2
Variant:p.A55V
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UCP2

NM_003355.3:p.A55V

Associated Papers

Uncoupling Proteins Variants Are Linked to Hypercholesterolemia and Abdominal Obesity in Metabolically Unhealthy Women.

Sierra-Ruelas E et al.

Lifestyle Genomics, 2025

The Outcome of Metabolic and Bariatric Surgery in Morbidly Obese Patients with Different Genetic Variants Associated with Obesity: A Systematic Review.

Zafirovska M et al.

Nutrients, 2024

Meta-analysis of genomic variants in power and endurance sports to decode the impact of genomics on athletic performance and success.

Psatha A et al.

Human Genomics, 2024

Genetic association analysis-based networks and classification of human UCP1 polymorphisms.

Li D

Genes & Diseases, 2024

In the context of the triple burden of malnutrition: A systematic review of gene-diet interactions and nutritional status.

Tan PY et al.

Critical Reviews in Food Science and Nutrition, 2024

Genetic variants in DBC1, SIRT1, UCP2 and ADRB2 as potential biomarkers for severe obesity and metabolic complications.

da Fonseca ACP et al.

Frontiers in Genetics, 2024

Association between UCP2 gene 3'UTR I/D and A55V polymorphisms and neural tube defects susceptibility: systematic review, meta-analysis, and trial sequential analysis.

Tian H et al.

Frontiers in Neurology, 2024

Functionally Significant Variants in Genes Associated with Abdominal Obesity: A Review.

Bairqdar A et al.

Journal of Personalized Medicine, 2023

The influence of six polymorphisms of uncoupling protein 3 (UCP3) gene and childhood obesity: a case-control study.

Fortes JS et al.

Bmc Pediatrics, 2023

Mitochondrial uncoupling protein 2 (UCP2) gene polymorphism - 866 G/A in the promoter region is associated with type 2 diabetes mellitus among Kashmiri population of Northern India.

Din I et al.

Molecular Biology Reports, 2023

Relationships between Uncoupling Protein Genes UCP1, UCP2 and UCP3 and Irisin Levels in Residents of the Coldest Region of Siberia.

Nikanorova AA et al.

Genes, 2022

36140780 (PubMed )
Supplement: genes-13-01612-s001.zip › genes-1894825-supplementary.pdf

Interaction Between ACTN3 (R577X), ACE (I/D), and BDKRB2 (-9/+9) Polymorphisms and Endurance Phenotypes in Brazilian Long-Distance Swimmers.

Neto SLDA et al.

Journal of Strength and Conditioning Research, 2022

Role of Uncoupling Protein 2 Gene Polymorphisms on the Risk of Ischemic Stroke in a Sardinian Population.

Stanzione R et al.

Life (basel, Switzerland), 2022

Speed and power-related gene polymorphisms associated with playing position in elite soccer players.

Petr M et al.

Biology of Sport, 2022

Prevalence of uncoupling protein one genetic polymorphisms and their relationship with cardiovascular and metabolic health.

Dinas PC et al.

Plos One, 2022

35482655 (PubMed )
Supplement: pone.0266386.s002.docx

Variability in oxidative stress-related genes (SOD2, CAT, GPX1, GSTP1, NOS3, NFE2L2, and UCP2) and susceptibility to migraine clinical phenotypes and features.

Papasavva M et al.

Frontiers in Neurology, 2022

Genetic polymorphisms associated with obesity in the Arab world: a systematic review.

Younes S et al.

International Journal of Obesity (2005), 2021

Association of the Uncoupling Protein 2-866 G/A Polymorphism with Family History and Duration of Tobacco Use Disorder in a Turkish Population.

Mervan Aytac H et al.

Psychiatry and Clinical Psychopharmacology, 2021

-866G/A and Ins/Del polymorphisms in UCP2 gene are associated with reduced short-term weight loss in patients who underwent Roux-en-Y gastric bypass.

de Oliveira MS et al.

Surgery for Obesity and Related Diseases : Official Journal of the American Society for Bariatric Surgery, 2021

Association of 45-bp ins/del polymorphism of uncoupling protein 2 (UCP2) and susceptibility to nonalcoholic fatty liver and type 2 diabetes mellitus in North-west of Iran.

Rezapour S et al.

Bmc Research Notes, 2021

The Role of Nonshivering Thermogenesis Genes on Leptin Levels Regulation in Residents of the Coldest Region of Siberia.

Nikanorova AA et al.

International Journal of Molecular Sciences, 2021

33925025 (PubMed )
Supplement: ijms-22-04657-s001.zip › ijms-1185588-supplementary.pdf

Association of UCP1 and UCP2 variants with diabetic retinopathy susceptibility in type-2 diabetes mellitus patients: a meta-analysis.

Liu X et al.

Bmc Ophthalmology, 2021

Proteogenomics Reveals Perturbed Signaling Networks in Malignant Melanoma Cells Resistant to BRAF Inhibition.

Schmitt M et al.

Molecular & Cellular Proteomics : Mcp, 2021

34673281 (PubMed )
Supplement: mmc3.xlsx › S1

Ethnicity Differences in the Association of UCP1-3826A/G, UCP2-866G/A and Ala55Val, and UCP3-55C/T Polymorphisms with Type 2 Diabetes Mellitus Susceptibility: An Updated Meta-Analysis.

Huang R et al.

Biomed Research International, 2021

Whole exome sequencing reveals novel candidate gene variants for MODY.

Yalçın Çapan Ö et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry, 2020

32645390 (PubMed )
Supplement: 1-s2.0-S0009898120303211-mmc1.xlsx › Sayfa1

Unleash the Association of Mitochondrial Uncoupling Protein (UCP2) Promoter Variant (G-866A; rs659366) with Obesity: Stepping from a Case-Control Study to a Meta-analysis.

Abd El Daim HA et al.

Biochemical Genetics, 2020

Increased Risk of High Body Fat and Altered Lipid Metabolism Associated to Suboptimal Consumption of Vitamin A Is Modulated by Genetic Variants rs5888 (SCARB1), rs1800629 (UCP1) and rs659366 (UCP2).

Galmés S et al.

Nutrients, 2020

32858880 (PubMed )
Supplement: nutrients-12-02588-s001.pdf

Association of uncoupling protein (Ucp) gene polymorphisms with cardiometabolic diseases.

Pravednikova AE et al.

Molecular Medicine (cambridge, Mass.), 2020

Analysis of association between common variants of uncoupling proteins genes and diabetic retinopathy in a Chinese population.

Jin P et al.

Bmc Medical Genetics, 2020

-866G/A and Ins/Del polymorphisms in the UCP2 gene and diabetic kidney disease: case-control study and meta-analysis.

Dieter C et al.

Genetics and Molecular Biology, 2020

UCP2 gene polymorphisms in obesity and diabetes, and the role of UCP2 in cancer.

Li J et al.

Febs Letters, 2019

Association of uncoupling protein gene polymorphisms with essential hypertension in a northeastern Han Chinese population.

Sun H et al.

Journal of Human Hypertension, 2019

Polymorphisms in the Uncoupling Protein 2 Gene Are Associated with Diabetic Retinopathy in Han Chinese Patients with Type 2 Diabetes.

Zhou TC et al.

Genetic Testing and Molecular Biomarkers, 2018

Uncoupling Protein 2 (UCP2) as Genetic Risk Factor for Obesity in Indonesia is Different in Gender Stratification.

Surniyantoro HNE et al.

The Kobe Journal of Medical Sciences, 2018

Glimepiride treatment in a patient with type A insulin resistance syndrome due to a novel heterozygous missense mutation in the insulin receptor gene.

Huang Z et al.

Journal of Diabetes Investigation, 2018

Polygenic Study of Endurance-Associated Genetic Markers NOS3 (Glu298Asp), BDKRB2 (-9/+9), UCP2 (Ala55Val), AMPD1 (Gln45Ter) and ACE (I/D) in Polish Male Half Marathoners.

Gronek P et al.

Journal of Human Kinetics, 2018

Association between Uncoupling Protein 2 Gene Ala55val Polymorphism and Sudden Sensorineural Hearing Loss.

Koide Y et al.

The Journal of International Advanced Otology, 2018

CREB1 functional polymorphisms modulating promoter transcriptional activity are associated with type 2 diabetes mellitus risk in Chinese population.

Xu Y et al.

Gene, 2018

Uncoupling Protein 2 and Peroxisome Proliferator-Activated Receptor γ Gene Polymorphisms in Association with Diabetes Susceptibility in Chinese Han Population with Variant Glucose Tolerance.

Zhou M et al.

International Journal of Endocrinology, 2018

Molecular genetics of human obesity: A comprehensive review.

Singh RK et al.

Comptes Rendus Biologies, 2017

The Ala55Val and -866G>A polymorphisms of the UCP2 gene could be biomarkers for weight loss in patients who had Roux-en-Y gastric bypass.

Nicoletti CF et al.

Nutrition (burbank, Los Angeles County, Calif.), 2017

Uncoupling protein 2 haplotype does not affect human brain structure and function in a sample of community-dwelling older adults.

Heise V et al.

Plos One, 2017

Role of MMP-1 (-519A/G, -1607 1G/2G), MMP-3 (Lys45Glu), MMP-7 (-181A/G), and MMP-12 (-82A/G) Variants and Plasma MMP Levels on Obesity-Related Phenotypes and Microvascular Reactivity in a Tunisian Population.

Boumiza S et al.

Disease Markers, 2017

The Role of Mitochondrial DNA (mtDNA) in the Development of Diabetic Retinopathy (DR): A Systematic Review.

Sarhangi N et al.

Medical Hypothesis, Discovery & Innovation Ophthalmology Journal, 2017

Association and expression analyses of the Ucp2 and Ucp3 gene polymorphisms with body measurement and meat quality traits in Qinchuan cattle.

Wang Y et al.

Journal of Genetics, 2016

Association of oxidative stress gene polymorphisms with presbycusis.

Manche SK et al.

Gene, 2016

Role of UCP2 polymorphisms on dietary intake of obese patients who underwent bariatric surgery.

Nicoletti CF et al.

Clinical Obesity, 2016

Lack of replication of associations between multiple genetic polymorphisms and endurance athlete status in Japanese population.

Yvert T et al.

Physiological Reports, 2016

Interactions between UCP2 SNPs and telomere length exist in the absence of diabetes or pre-diabetes.

Zhou Y et al.

Scientific Reports, 2016

Common UCP2 variants contribute to serum urate concentrations and the risk of hyperuricemia.

Yang L et al.

Scientific Reports, 2016

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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."