Varaico: Literature-Extracted Genetic Variants

Gene:CCR2
Variant:p.V64I
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CCR2

NM_001123396.4:p.V64I

Associated Papers

Effect of chemokine and chemokine-receptor gene polymorphisms on the development of diabetic retinopathy in the Turkish Cohort.

Alp E et al.

Experimental Eye Research, 2026

Frequency of CCR5-Δ32, CCR2-64I, and SDF1-3'A Mutations in People with HIV Diagnoses and HIV Negative Participant in Khuzestan Province, Iran.

Bavi M et al.

Aids Research and Human Retroviruses, 2026

Beyond CYP2C19: inflammation and angiogenesis gene variants drive clopidogrel resistance in CAD patients.

Hajer F et al.

Inflammation Research : Official Journal of the European Histamine Research Society ... [et Al.], 2025

Familial mast cell-mediated angioedema: Description of 4 families.

Sabaté-Brescó M et al.

The Journal of Allergy and Clinical Immunology. in Practice, 2025

Breaking new ground in CAD genetics: MCP-1 and CCR2 polymorphisms unveil pathways to personalized risk assessment.

Hajer F et al.

Human Immunology, 2025

Genetic polymorphism of CCR5 (59029A/G) and CCR2 (-64I A/G) promoters in HIV infected patients.

Khalid A et al.

Pakistan Journal of Medical Sciences, 2025

Association between chemokine genes polymorphisms and susceptibility to Parkinson's disease: a meta-analysis and systematic review.

Lee YH et al.

Acta Neurologica Belgica, 2025

The role of the 3'-UTR of the chemokine receptor CCR2 and hnRNPA0 in regulating mRNA stability and subcellular distribution in human CD4+ T cells.

Yukselten Y et al.

Frontiers in Immunology, 2025

G protein-coupled receptor (GPCR) pharmacogenomics.

Thompson MD et al.

Critical Reviews in Clinical Laboratory Sciences, 2024

Stratified analyses refine association between TLR7 rare variants and severe COVID-19.

Boos J et al.

Hgg Advances, 2024

38944683 (PubMed )
Supplement: mmc4.xlsx › single_variants_p_lt_0.05

Involvement of CXCL10 rs4256246, CXCR4 rs2228014, CCR2 rs1799864 and CXCL16 rs2277680 in the Predisposition to Schizophrenia.

Saoud H et al.

Journal of Molecular Neuroscience : Mn, 2024

Meta-analyses of the relationship between five CXCL8 gene polymorphisms and overall cancer risk, and a case-control study of oral cancer.

Peng J et al.

Bmc Oral Health, 2024

Novel NARS2 variants in a patient with early-onset status epilepticus: case study and literature review.

Yang N et al.

Bmc Pediatrics, 2024

38310242 (PubMed )
Supplement: 12887_2024_4553_MOESM1_ESM.xlsx › trio.hg38.filter

Human inherited CCR2 deficiency underlies progressive polycystic lung disease.

Neehus AL et al.

Cell, 2024

Association of Viral and Host Genetic Architecture with the Status of Neurocognitive Disorder in HIV-Infected Individuals.

Jadhav S et al.

Aids Research and Human Retroviruses, 2023

Associations between Single Nucleotide Polymorphisms from the Genes of Chemokines and the CXCR2 Chemokine Receptor and an Increased Risk of Endometrial Cancer.

Wujcicka WI et al.

Cancers, 2023

Genetic Variation and Sickle Cell Disease Severity: A Systematic Review and Meta-Analysis.

Kirkham JK et al.

Jama Network Open, 2023

37851445 (PubMed )
Supplement: jamanetwopen-e2337484-s001.pdf

New genetic and epigenetic insights into the chemokine system: the latest discoveries aiding progression toward precision medicine.

Xu H et al.

Cellular & Molecular Immunology, 2023

Decoding the genetic relationship between Alzheimer's disease and type 2 diabetes: potential risk variants and future direction for North Africa.

Boukhalfa W et al.

Frontiers in Aging Neuroscience, 2023

37342358 (PubMed )
Supplement: Table_2.XLSX › Table_2_SNPnexus_annotation

Genetic susceptibility of bladder cancer in the Lebanese population.

Kourie HR et al.

Bmc Medical Genomics, 2022

36253817 (PubMed )
Supplement: 12920_2022_1372_MOESM1_ESM.xlsx › sheet_1

Effect of Chemokine Gene Variants on Covid-19 Disease Severity.

Dogan S et al.

Immunological Investigations, 2022

The impact of MCP1-2518A/G and CCR2-V64I genetic polymorphisms in Egyptian sickle cell disease patients.

Ibrahim NS et al.

Experimental and Molecular Pathology, 2022

The Role of Genetic Factors in the Development of Acute Respiratory Viral Infection COVID-19: Predicting Severe Course and Outcomes.

Minashkin MM et al.

Biomedicines, 2022

The Relationship Between Chemokine and Chemokine Receptor Genes Polymorphisms and Chronic Obstructive Pulmonary Disease Susceptibility in Tatar Population from Russia: A Case Control Study.

Korytina GF et al.

Biochemical Genetics, 2022

Cytokines in Abdominal Aortic Aneurysm: Master Regulators With Clinical Application.

Puchenkova OA et al.

Biomarker Insights, 2022

A Common Variant at the 3'untranslated Region of the CCL7 Gene (rs17735770) Is Associated With Decreased Susceptibility to Coronary Heart Disease.

Medina-Gil JM et al.

Frontiers in Cardiovascular Medicine, 2022

35711383 (PubMed )
Supplement: Table_1.pdf

Gene polymorphisms and risk of head and neck squamous cell carcinoma: a systematic review.

Rajabi-Moghaddam M et al.

Reports of Practical Oncology and Radiotherapy : Journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology, 2022

An association of the MCP-1 and CCR2 gene polymorphisms with oral lichen planus.

Ozturk O et al.

Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology, 2021

Why does SARS-CoV-2 hit in different ways? Host genetic factors can influence the acquisition or the course of COVID-19.

Monticelli M et al.

European Journal of Medical Genetics, 2021

33872774 (PubMed )
Supplement: mmc2.xlsx › Foglio1

Evaluation of the Genetic Association and Methylation of Immune Response Pathway Genes with the Risk of Chronic Periodontitis in the Uighur Population.

Abasijiang A et al.

Genetic Testing and Molecular Biomarkers, 2021

A bioinformatic approach to investigating cytokine genes and their receptor variants in relation to COVID-19 progression.

Karakas Celik S et al.

International Journal of Immunogenetics, 2021

CCR5Δ32 in Brazil: Impacts of a European Genetic Variant on a Highly Admixed Population.

Kulmann-Leal B et al.

Frontiers in Immunology, 2021

Association of MCP-1 promotor polymorphism with disease severity of Crimean-Congo hemorrhagic fever.

Bagci B et al.

Journal of Medical Virology, 2020

A case-control association of RANTES (-28C >G) and CCR5-Delta32 polymorphisms with Parkinson's disease in Indians.

Subramanian N et al.

Neuroscience Letters, 2020

Association between Monocyte Chemoattractant Protein-1 -2518 (A/G) Single Nucleotide Polymorphism and Chronic Periodontitis in End-stage Renal Disease Patients - A Case-control Study.

Ksiazek K et al.

Immunological Investigations, 2020

Genetic determinants of fracture non-union: A systematic review from the literature.

Yan T et al.

Gene, 2020

Identification of Novel Pathogenic PKD2 Variants in Iranian Patients with Autosomal Dominant Polycystic Kidney Disease.

Bagheri M et al.

Reports of Biochemistry & Molecular Biology, 2020

Association of polymorphisms in the MCP-1 and CCR2 genes with the risk of Parkinson's disease.

Wang Y et al.

Journal of Neural Transmission (vienna, Austria : 1996), 2019

Genetic discoveries and advances in late-onset Alzheimer's disease.

Rezazadeh M et al.

Journal of Cellular Physiology, 2019

Analysis of 75 Candidate SNPs Associated With Acute Rejection in Kidney Transplant Recipients: Validation of rs2910164 in MicroRNA MIR146A.

Oetting WS et al.

Transplantation, 2019

Implication of HMOX1 and CCR5 genotypes on clinical phenotype of Egyptian patients with sickle cell anemia.

Bakr S et al.

Annals of Hematology, 2019

Cis-regulatory genetic variants in the CCR5 gene and natural HIV-1 control in black South Africans.

Koor GW et al.

Clinical Immunology (orlando, Fla.), 2019

New mechanisms of CCR5-Δ32 carriers' advantage - Impact on progenitor cells and renal function.

Skrzypkowska M et al.

The International Journal of Biochemistry & Cell Biology, 2019

Association of genetic polymorphisms of chemokines and their receptors with clearance or persistence of hepatitis C virus infection.

El-Bendary M et al.

British Journal of Biomedical Science, 2019

Novel association of five HLA alleles with HIV-1 progression in Spanish long-term non progressor patients.

Ramírez de Arellano E et al.

Plos One, 2019

The role of GPCRs in bone diseases and dysfunctions.

Luo J et al.

Bone Research, 2019

TRIM5α 136Q, CCR5 Promoter 59029G And CCR264I Alleles Impact The Progression Of HIV In Children And Adolescents.

Dambaya B et al.

The Application of Clinical Genetics, 2019

CCR2 Genetic Polymorphism And Its Potential Effect On HIV Acquisition In A Population Of Children Living In The Northern Region Of Cameroon.

Ngoufack MN et al.

The Application of Clinical Genetics, 2019

Human Genetic Variation and HIV/AIDS in Papua New Guinea: Time to Connect the Dots.

Mehlotra RK

Current Hiv/aids Reports, 2018

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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."