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Gene profile

CCR2

HGNC:1603 · SaudiVarKB evidence summary derived from retained literature mentions.

7Gene mentions
7Publications
2Linked variants
4Associated phenotypes

Associated phenotypes

Co-mentioned in CCR2 publications
PhenotypeIdentifierArticlesMentions
autism spectrum disorderHP:000072911
asthma11
celiac disease11
hepatitis C11

Linked variants

Variants normalized to CCR2
VariantHGVS / rsIDArticlesMentions
G190A11
T51C11

Population context

Reported in the same publications
Country / regionGroupCohortArticles
Not specified31
Not specified141
Not specified21
Not specified1,4601

Supporting publications

7 records
  1. 2024Mesenchymal stem cells treated with Interleukin-1 beta for mediation of an inflammatory response in human tissues.Cellular and molecular biology (Noisy-le-Grand, France)PubMed ↗
  2. 2023DNA Hypomethylation Is Associated with Increased Inflammation in Peripheral Blood Neutrophils of Children with Autism Spectrum Disorder: Understanding the Role of Ubiquitous Pollutant Di(2-ethylhexyl) Phthalate.MetabolitesPubMed ↗
  3. 2022Loss of FOCAD, operating via the SKI messenger RNA surveillance pathway, causes a pediatric syndrome with liver cirrhosis.Nature geneticsPubMed ↗
  4. 2019Association of genetic polymorphisms of chemokines and their receptors with clearance or persistence of hepatitis C virus infection.British journal of biomedical sciencePubMed ↗
  5. 2017Comprehensive Computational Analysis of GWAS Loci Identifies CCR2 as a Candidate Gene for Celiac Disease Pathogenesis.Journal of cellular biochemistryPubMed ↗
  6. 2011Allograft renal rejection and chemokine polymorphism.Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi ArabiaPubMed ↗
  7. 2010Linkage and haplotype analysis for chemokine receptors clustered on chromosome 3p21.3 and transmitted in family pedigrees with asthma and atopy.Annals of Saudi medicinePubMed ↗