PTGDR2, prostaglandin D2 receptor 2, 11251

N. diseases: 60; N. variants: 1
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.030 Biomarker disease LHGDN The results showed that virtually all CRTH2+CD4+ lymphocytes had a pure T helper 2 phenotype and formed not all but a large proportion of circulating T helper 2 cells for both normal and atopic dermatitis subjects. 12230502 2002
CUI: C0014457
Disease: Eosinophilia
Eosinophilia
0.020 Biomarker disease BEFREE Chemoattractant receptor-homologous molecule expressed on Th2 cells activation in vivo increases blood leukocyte counts and its blockade abrogates 13,14-dihydro-15-keto-prostaglandin D2-induced eosinophilia in rats. 12975488 2003
CUI: C1306759
Disease: Eosinophilic disorder
Eosinophilic disorder
0.020 Biomarker group BEFREE Chemoattractant receptor-homologous molecule expressed on Th2 cells activation in vivo increases blood leukocyte counts and its blockade abrogates 13,14-dihydro-15-keto-prostaglandin D2-induced eosinophilia in rats. 12975488 2003
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 Biomarker group BEFREE Pharmacologically, rat CRTH2 stably transfected in mouse preB lymphoma L1.2 cells behaved very similar compared with the mouse and human orthologs, showing a binding affinity for PGD2 of 11 nM, a functional calcium mobilization when exposed to agonist, and similar sensitivity to agonists and antagonists. 12975488 2003
CUI: C1332206
Disease: Adult Lymphoma
Adult Lymphoma
0.010 Biomarker disease BEFREE Pharmacologically, rat CRTH2 stably transfected in mouse preB lymphoma L1.2 cells behaved very similar compared with the mouse and human orthologs, showing a binding affinity for PGD2 of 11 nM, a functional calcium mobilization when exposed to agonist, and similar sensitivity to agonists and antagonists. 12975488 2003
CUI: C1332979
Disease: Childhood Lymphoma
Childhood Lymphoma
0.010 Biomarker disease BEFREE Pharmacologically, rat CRTH2 stably transfected in mouse preB lymphoma L1.2 cells behaved very similar compared with the mouse and human orthologs, showing a binding affinity for PGD2 of 11 nM, a functional calcium mobilization when exposed to agonist, and similar sensitivity to agonists and antagonists. 12975488 2003
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
0.010 AlteredExpression disease BEFREE Therefore, we studied expression of DP1 and DP2 receptors by reverse transcription-polymerase chain reaction analysis of receptor mRNA levels in five human colorectal cancer cell lines (HT-29, HCA-7, HCT116, SW480 and SW48) and VACO-235 human colorectal adenoma cells. 15172124 2004
CUI: C0004096
Disease: Asthma
Asthma
0.400 GeneticVariation disease LHGDN Family-based analysis of asthma and two common SNPs [G1544C and G1651A (rs545659)] in the 3'-untranslated region of CRTH2 showed significant evidence of linkage in the presence of disequilibrium for the 1651G allele (P = 0.003) of SNP rs545659. 15345705 2004
CUI: C0004096
Disease: Asthma
Asthma
0.400 GeneticVariation disease BEFREE Family-based analysis of asthma and two common SNPs [G1544C and G1651A (rs545659)] in the 3'-untranslated region of CRTH2 showed significant evidence of linkage in the presence of disequilibrium for the 1651G allele (P = 0.003) of SNP rs545659. 15345705 2004
CUI: C0004096
Disease: Asthma
Asthma
0.400 GeneticVariation disease BEFREE Moreover, in the Chinese children the frequency of the chemoattractant receptor-homologous molecule expressed on T helper 2 cells (CRTH2) 1651G allele in near-fatal asthmatics was significantly higher than in mild-to-moderate asthmatics and normal controls. 15986064 2005
CUI: C0085129
Disease: Bronchial Hyperreactivity
Bronchial Hyperreactivity
0.010 GeneticVariation disease BEFREE The CRTH2 1651G allele of single nucleotide polymorphism re545659 was also associated with a higher degree of bronchial hyperresponsiveness. 15986064 2005
CUI: C0004096
Disease: Asthma
Asthma
0.400 GeneticVariation disease BEFREE Our data failed to support previous associations of functional polymorphisms at the 3'-UTR of the CRTH2 gene implicated in asthma. 17016057 2007
CUI: C0021368
Disease: Inflammation
Inflammation
0.010 Biomarker phenotype LHGDN The PGD(2)/CRTH2 system mediates the chemotaxis of eosinophils, basophils, and Th2 cells, which are involved in the induction of allergic inflammation. 17541272 2007
CUI: C0004096
Disease: Asthma
Asthma
0.400 Biomarker disease BEFREE CRTH2 antagonism significantly ameliorates airway hyperreactivity and downregulates inflammation-induced genes in a mouse model of airway inflammation. 18757520 2008
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.030 Biomarker disease BEFREE Prostaglandin D(2), the ligand for the G protein-coupled receptors DP1 and CRTH2, has been implicated in the pathogenesis of the allergic response in diseases such as asthma, rhinitis, and atopic dermatitis. 18757520 2008
CUI: C0013595
Disease: Eczema
Eczema
0.020 Biomarker disease BEFREE Prostaglandin D(2), the ligand for the G protein-coupled receptors DP1 and CRTH2, has been implicated in the pathogenesis of the allergic response in diseases such as asthma, rhinitis, and atopic dermatitis. 18757520 2008
CUI: C0032285
Disease: Pneumonia
Pneumonia
0.020 Biomarker disease BEFREE We investigated the role of PGD(2) and CRTH2 in allergic pulmonary inflammation by using a highly potent and specific antagonist of CRTH2. 18757520 2008
CUI: C3714636
Disease: Pneumonitis
Pneumonitis
0.020 Biomarker disease BEFREE We investigated the role of PGD(2) and CRTH2 in allergic pulmonary inflammation by using a highly potent and specific antagonist of CRTH2. 18757520 2008
CUI: C0004096
Disease: Asthma
Asthma
0.400 Biomarker disease BEFREE Genetic variations in chemoattractant receptor expressed on Th2 cells (CRTH2) is associated with asthma susceptibility in Chinese children. 18777142 2009
CUI: C0027430
Disease: Nasal Polyps
Nasal Polyps
0.020 AlteredExpression disease BEFREE Significantly greater levels of DP mRNA and conversely decreased levels of CRTH2 mRNA were observed in NP compared with UPM. 18802357 2009
CUI: C0149516
Disease: Chronic sinusitis
Chronic sinusitis
0.020 Biomarker disease BEFREE Expression and characterization of PGD2 receptors in chronic rhinosinusitis: modulation of DP and CRTH2 by PGD2. 18802357 2009
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis
0.010 Biomarker disease BEFREE We sought to determine the expression and characterization of DP and CRTH2 in CRS. 18802357 2009
CUI: C0004096
Disease: Asthma
Asthma
0.400 Biomarker disease BEFREE Furthermore, genetic association studies have shown a positive linkage of the genetic polymorphisms in DP and CRTH2, with asthma phenotypes from specific ethnic backgrounds, further highlighting the importance of PGD(2) and its receptors in the pathophysiology of asthma. 18946232 2008
CUI: C0263338
Disease: Chronic urticaria
Chronic urticaria
0.010 GeneticVariation disease BEFREE The CRTH2 -466T>C gene polymorphism may not affect on the phenotype of CU, but contributes to the required dose of antihistamines in patients with CU. 19290788 2009
CUI: C0004096
Disease: Asthma
Asthma
0.400 GeneticVariation disease BEFREE Genetic variation within CRTh2 modifies the development of allergic sensitization and asthma in a population of German children. 19392992 2009