TSLP, thymic stromal lymphopoietin, 85480

N. diseases: 220; N. variants: 9
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.600 GeneticVariation disease BEFREE TSLP variation was determined using targeted massively parallel sequencing in a longitudinal cohort of children with AD. 31491540 2019
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.600 GeneticVariation disease BEFREE We identified that the susceptibility loci at 5q31 (RAD50/IL13, rs2158177, P = 1.08×10-3, OR = 1.15) and 5q22.1 (TSLP, rs1837253, P = 2.66×10-3, OR = 0.91) were significantly associated with AD. 28364410 2017
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.600 GeneticVariation disease BEFREE Also, TSLP polymorphisms are associated with susceptibility to asthma, atopic dermatitis, and eczema herpeticum. 22948028 2013
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.600 GeneticVariation disease BEFREE To evaluate the joint effect of allergic sensitization and TSLP polymorphisms on AD and to test whether TSLP polymorphisms increase the risk of asthma in children with AD. 26712523 2016
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.600 GeneticVariation disease BEFREE The TSLP variation is associated with less persistent AD. 24401911 2014
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.600 GeneticVariation disease BEFREE TSLP genetic variants and its dysregulated expression have been linked to atopic diseases such as atopic dermatitis, asthma, allergic rhinitis and eosinophilic esophagitis. 25340427 2014
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.600 GeneticVariation disease BEFREE Methylation status of the TSLP 5'-CpG island (CGI) was found to be significantly associated with prenatal smoke exposure (OR = 3.17, 95% CI = 1.63-6.19) and with AD (OR = 2.32, 95% CI = 1.06-5.11). 23600544 2013
CUI: C0004096
Disease: Asthma
Asthma
0.500 GeneticVariation disease BEFREE Thymic stromal lymphopoietin gene promoter polymorphisms are associated with susceptibility to bronchial asthma. 20656951 2011
CUI: C0004096
Disease: Asthma
Asthma
0.500 GeneticVariation disease GWASCAT Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct. 30929738 2019
CUI: C0004096
Disease: Asthma
Asthma
0.500 GeneticVariation disease BEFREE To analyze the polymorphism of the two SNPs Rs2289276 and Rs2289278 in TSLP gene and to evaluate the association between the two SNPs and asthma susceptibility in Chinese Han population by using case-control study. 22913730 2012
CUI: C0004096
Disease: Asthma
Asthma
0.500 GeneticVariation disease BEFREE Several unanswered questions concerning basic pathophysiological aspects of TSLP variants, the long-term safety and efficacy of tezepelumab with different phenotypes/endotypes of asthma should be addressed. 31549891 2019
CUI: C0004096
Disease: Asthma
Asthma
0.500 GeneticVariation disease BEFREE Accordingly, this study aimed to determine the associations of IL1RL1 rs3771180 and TSLP rs1837253 with asthma in Zhuang people. 31066119 2019
CUI: C0004096
Disease: Asthma
Asthma
0.500 GeneticVariation disease BEFREE Haplotype-specific score test indicated that an elevated risk for asthma was associated with a specific haplotype of TSLP involving SNP rs1898671 (OR = 1.58, 95% CI: 1.10-2.27, p = 0.01). 21966427 2011
CUI: C0004096
Disease: Asthma
Asthma
0.500 GeneticVariation disease BEFREE Identifying the polymorphisms in the thymic stromal lymphopoietin receptor (TSLPR) and their association with asthma. 20663412 2010
CUI: C0004096
Disease: Asthma
Asthma
0.500 GeneticVariation disease BEFREE TSLP variants are associated with asthma in a sex-specific fashion. 20560908 2010
CUI: C0004096
Disease: Asthma
Asthma
0.500 GeneticVariation disease BEFREE Variants in the gene encoding the TSLP protein may have differential effects on asthma phenotypes depending on gender, atopy, and the presence of allergic rhinitis. 24525665 2014
CUI: C0004096
Disease: Asthma
Asthma
0.500 GeneticVariation disease BEFREE We selected 6 single nucleotide polymorphisms in thymic stromal lymphopoietin and genotyped 5565 individuals from 4 independent asthma studies and tested for association with asthma, atopy, atopic asthma, and airway hyperresponsiveness by using a general allelic likelihood ratio test. 19539984 2009
CUI: C0004096
Disease: Asthma
Asthma
0.500 GeneticVariation disease BEFREE Sputum cells (ISCs) from 5 moderate asthmatics and 5 healthy controls (HC) were stimulated either with TNF-α or TNF-α plus recombinant IL-37 (rIL-37) comparing the suppression on TSLP production. 27528425 2016
CUI: C0004096
Disease: Asthma
Asthma
0.500 GeneticVariation disease BEFREE In addition, as our group recently found that TSLP variants are associated with asthma and reduced lung function, we assessed whether TSLP single nucleotide polymorphisms (SNPs) were associated with baseline lung function in non-COPD, nonasthmatic healthy subjects (n = 1368). 21468164 2011
CUI: C0004096
Disease: Asthma
Asthma
0.500 GeneticVariation disease BEFREE Four were at previously reported loci on 17q21, near IL1RL1, TSLP and IL33, but we report for the first time, to our knowledge, that these loci are associated with asthma risk in three ethnic groups. 21804549 2011
CUI: C0004096
Disease: Asthma
Asthma
0.500 GeneticVariation disease BEFREE In contrast, the presence or absence of TSLP minor alleles did not affect asthma risk in subjects without the SPINK5 risk alleles. 24831437 2014
CUI: C0004096
Disease: Asthma
Asthma
0.500 GeneticVariation disease BEFREE Several monoclonal antibodies (mAbs) targeting pathogenetic molecules (e.g., IgE, IL-5, IL- 5Rα, IL-4, IL-13, TSLP) are currently available or under development for the treatment of different forms of severe type 2 asthma. 29318959 2019
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.500 GeneticVariation disease BEFREE We tested for gene-environment interaction between EoE-predisposing polymorphisms (within TSLP, LOC283710/KLF13, CAPN14, CCL26, and TGFB) and implicated early-life factors (antibiotic use in infancy, cesarean delivery, breast-feeding, neonatal intensive care unit [NICU] admission, and absence of pets in the home). 29029802 2018
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.500 GeneticVariation disease BEFREE TSLP genetic variants and its dysregulated expression have been linked to atopic diseases such as atopic dermatitis, asthma, allergic rhinitis and eosinophilic esophagitis. 25340427 2014
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.500 GeneticVariation disease GWASCAT Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease. 25017104 2014