CCR3, C-C motif chemokine receptor 3, 1232

N. diseases: 149; N. variants: 16
Disease: Behcet Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.120 GeneticVariation disease GWASDB Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587 2013
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.120 GeneticVariation disease GWASCAT Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587 2013
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.120 GeneticVariation disease BEFREE First stage analysis showed that ten SNPs, located in 3'UTR, 5'UTR in CCR1 or 5'UTR in CCR3, were significantly associated with Behçet's disease (P(c) = 0.018 to 1.3 × 10(-3)). 22829007 2012
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.120 Biomarker disease BEFREE Reactivity of eosinophils to the monoclonal antibody against CCR3 and the chemotaxis to eotaxin were slightly reduced in this patient as compared with healthy controls or a patient with Behçet disease homozygous for the common allele, while CCR3 mRNA level was not different. 11196669 1999