CYSLTR2, cysteinyl leukotriene receptor 2, 57105

N. diseases: 60; N. variants: 4
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0220633
Disease: Uveal melanoma
Uveal melanoma
0.530 GeneticVariation disease BEFREE These data indicate that mutations in the PLCB4 and CYSLTR2 genes are rare in Chinese UM patients. 31614358 2019
CUI: C0220633
Disease: Uveal melanoma
Uveal melanoma
0.530 GeneticVariation disease BEFREE Uveal melanoma (UM), a rare cancer of the eye, is characterized by initiating mutations in the genes G-protein subunit alpha Q (<i>GNAQ</i>), G-protein subunit alpha 11 (<i>GNA11</i>), cysteinyl leukotriene receptor 2 (<i>CYSLTR2</i>), and phospholipase C beta 4 (<i>PLCB4</i>) and by metastasis-promoting mutations in the genes splicing factor 3B1 (<i>SF3B1</i>), serine and arginine rich splicing factor 2 (SRSF2), and BRCA1-associated protein 1 (<i>BAP1</i>). 31671564 2019
CUI: C0220633
Disease: Uveal melanoma
Uveal melanoma
0.530 Biomarker disease CTD_human Our findings implicate CYSLTR2 as a uveal melanoma oncogene and highlight the critical role of Gαq signaling in uveal melanoma pathogenesis. 27089179 2016
CUI: C0220633
Disease: Uveal melanoma
Uveal melanoma
0.530 SomaticCausalMutation disease ORPHANET Our findings implicate CYSLTR2 as a uveal melanoma oncogene and highlight the critical role of Gαq signaling in uveal melanoma pathogenesis. 27089179 2016
CUI: C0220633
Disease: Uveal melanoma
Uveal melanoma
0.530 Biomarker disease BEFREE Our findings implicate CYSLTR2 as a uveal melanoma oncogene and highlight the critical role of Gαq signaling in uveal melanoma pathogenesis. 27089179 2016
CUI: C0346373
Disease: Malignant melanoma of iris
Malignant melanoma of iris
0.400 SomaticCausalMutation disease ORPHANET Recurrent activating mutations of G-protein-coupled receptor CYSLTR2 in uveal melanoma. 27089179 2016
CUI: C0346388
Disease: Malignant melanoma of choroid
Malignant melanoma of choroid
0.400 SomaticCausalMutation disease ORPHANET Recurrent activating mutations of G-protein-coupled receptor CYSLTR2 in uveal melanoma. 27089179 2016
CUI: C0346373
Disease: Malignant melanoma of iris
Malignant melanoma of iris
0.400 Biomarker disease HPO
CUI: C0346388
Disease: Malignant melanoma of choroid
Malignant melanoma of choroid
0.400 Biomarker disease HPO
CUI: C1319853
Disease: Asthma, Aspirin-Induced
Asthma, Aspirin-Induced
0.310 Biomarker disease CTD_human Genetic and ethnic risk factors associated with drug hypersensitivity. 20485159 2010
CUI: C1319853
Disease: Asthma, Aspirin-Induced
Asthma, Aspirin-Induced
0.310 Biomarker disease CTD_human Increased expression of CYSLTR1 with CYLSTR1 and CYSLTR2 polymorphisms are new findings in AIA, while the ALOX5 promoter polymorphism has been noted in AIU. 16502481 2006
CUI: C1319853
Disease: Asthma, Aspirin-Induced
Asthma, Aspirin-Induced
0.310 GeneticVariation disease BEFREE Increased expression of CYSLTR1 with CYLSTR1 and CYSLTR2 polymorphisms are new findings in AIA, while the ALOX5 promoter polymorphism has been noted in AIU. 16502481 2006
CUI: C0013182
Disease: Drug Allergy
Drug Allergy
0.300 Biomarker group CTD_human Association analysis of cysteinyl-leukotriene receptor 2 (CYSLTR2) polymorphisms with aspirin intolerance in asthmatics. 15970796 2005
CUI: C0034069
Disease: Pulmonary Fibrosis
Pulmonary Fibrosis
0.300 Biomarker disease CTD_human Targeted gene disruption reveals the role of the cysteinyl leukotriene 2 receptor in increased vascular permeability and in bleomycin-induced pulmonary fibrosis in mice. 15328359 2004
CUI: C4721507
Disease: Alveolitis, Fibrosing
Alveolitis, Fibrosing
0.300 Biomarker disease CTD_human Targeted gene disruption reveals the role of the cysteinyl leukotriene 2 receptor in increased vascular permeability and in bleomycin-induced pulmonary fibrosis in mice. 15328359 2004
CUI: C0035126
Disease: Reperfusion Injury
Reperfusion Injury
0.200 Biomarker disease RGD Cysteinyl leukotriene receptor 2 is spatiotemporally involved in neuron injury, astrocytosis and microgliosis after focal cerebral ischemia in rats. 21664436 2011
CUI: C0004096
Disease: Asthma
Asthma
0.100 GeneticVariation disease BEFREE To evaluate the association between genetic polymorphisms in CYSLTR2 with asthma phenotypes, atopy markers and helminth infection. 31126515 2019
CUI: C0004096
Disease: Asthma
Asthma
0.100 AlteredExpression disease BEFREE On the other hand, although degrees of CysLT2 receptors expression were variable among the 5 non-asthma subjects, the expression in the asthma lung was detected on bronchial smooth muscle, epithelium and alveolar leukocytes in 2 in 2 asthma subjects. 26433531 2015
CUI: C0004096
Disease: Asthma
Asthma
0.100 Biomarker disease BEFREE Peripheral and central airway fibroblasts, from asthmatics and healthy controls, were investigated for the amount of cysteinyl-leukotriene receptors (CysLT(1) and CysLT(2)), leukotriene B(4) receptors (BLT(1) and BLT(2)), IL-13 receptor-α(1) (IL-13Rα(1)) and the IL-4 receptor (IL-4R). 21596548 2011
CUI: C0004096
Disease: Asthma
Asthma
0.100 AlteredExpression disease BEFREE PMA/ionomycin induced higher mRNA expression of CysLTR2 in B cell lines from ht2+/+ asthmatics than those from ht1+/+ asthmatics. 19840403 2009
CUI: C0004096
Disease: Asthma
Asthma
0.100 Biomarker disease BEFREE Those specific variants include 2 variants in the 5-lipoxygenase gene (ALOX5) that are both associated with response to 5-lipoxygenase inhibition and to leukotriene receptor antagonists, variants in genes encoding the 2 established cysteinyl leukotriene receptor antagonists (CYSLTR1 and CYSLTR2) that are both associated with asthma susceptibility in at least 2 independent populations, and a leukotriene C(4) synthase promoter polymorphism (LTC4s) that has been associated with asthma affection status and asthma-exacerbated respiratory disease. 19665766 2009
CUI: C0004096
Disease: Asthma
Asthma
0.100 GeneticVariation disease LHGDN CYSLTR2 and ALOX5 polymorphisms may predispose a minority of individuals to excessive cysteinyl-leukotriene concentrations, yielding a distinct asthma phenotype most likely to respond to leukotriene modifier pharmacotherapy. 17460547 2007
CUI: C0004096
Disease: Asthma
Asthma
0.100 GeneticVariation disease BEFREE GPCR genes implicated in asthma endophenotypes include variants of the cysteinyl leukotriene receptors (CYSLTR1 and CYSLTR2), and prostaglandin D2 receptors (PTGDR and CRTH2), thromboxane A2 receptor (TBXA2R), beta2-adrenergic receptor (ADRB2), chemokine receptor 5 (CCR5), and the G protein-coupled receptor associated with asthma (GPRA). 17154652 2006
CUI: C0004096
Disease: Asthma
Asthma
0.100 GeneticVariation disease BEFREE In an effort to discover additional polymorphism(s), the variant(s) of which have been implicated in asthma and aspirin intolerance, we scrutinized genetic polymorphisms of the CYSLTR2 gene, and evaluated this locus as a potential candidate for asthma. 15970796 2005
CUI: C0004096
Disease: Asthma
Asthma
0.100 Biomarker disease BEFREE Our results suggest that CYSLTR2 is one of the genes that contributes to susceptibility to asthma in the Japanese population. 15454733 2004