×
Entrez Id:
2205
Gene Symbol:
FCER1A
FCER1A
0.310
Biomarker
disease
LHGDN
Basophil phenotypes in chronic idiopathic urticaria in relation to disease activity and autoantibodies.
18356810
2008
×
Entrez Id:
213
Gene Symbol:
ALB
ALB
0.310
AlteredExpression
disease
BEFREE
We assessed the urticaria activity score (UAS), total antioxidant status (TAS), glutathione S-transferase (GST), superoxide dismutase (SOD), glutathione peroxidase (GPx), catalase (CAT), albumin , alpha1, alpha2, beta1 beta2, gamma globulins, c-reactive protein (CRP) and hematologic numeration.
28351163
2017
HLA-DPB1
0.310
Biomarker
disease
CTD_human
Genetic markers for differentiating aspirin-hypersensitivity.
16502481
2006
×
Entrez Id:
2205
Gene Symbol:
FCER1A
FCER1A
0.310
Biomarker
disease
CTD_human
Genetic and ethnic risk factors associated with drug hypersensitivity.
20485159
2010
×
Entrez Id:
213
Gene Symbol:
ALB
ALB
0.310
Biomarker
disease
CTD_human
Urticaria and angioedema during insemination with fluid containing bovine serum albumin.
8458210
1993
×
Entrez Id:
7040
Gene Symbol:
TGFB1
TGFB1
0.300
Biomarker
disease
CTD_human
Association between a TGFbeta1 promoter polymorphism and the phenotype of aspirin-intolerant chronic urticaria in a Korean population.
19138248
2008
×
Entrez Id:
7412
Gene Symbol:
VCAM1
VCAM1
0.300
Biomarker
disease
CTD_human
Evaluation of inflammatory parameters in physical urticarias and effects of an anti-inflammatory/antiallergic treatment.
12121561
2002
×
Entrez Id:
6401
Gene Symbol:
SELE
SELE
0.300
Biomarker
disease
CTD_human
Evaluation of inflammatory parameters in physical urticarias and effects of an anti-inflammatory/antiallergic treatment.
12121561
2002
×
Entrez Id:
3176
Gene Symbol:
HNMT
HNMT
0.300
Biomarker
disease
CTD_human
Genetic and ethnic risk factors associated with drug hypersensitivity.
20485159
2010
×
Entrez Id:
3383
Gene Symbol:
ICAM1
ICAM1
0.300
Biomarker
disease
CTD_human
Evaluation of inflammatory parameters in physical urticarias and effects of an anti-inflammatory/antiallergic treatment.
12121561
2002
×
Entrez Id:
2944
Gene Symbol:
GSTM1
GSTM1
0.300
Biomarker
disease
CTD_human
Familial aggregation of aspirin-induced urticaria and leukotriene C synthase allelic variant.
16433794
2006
×
Entrez Id:
4353
Gene Symbol:
MPO
MPO
0.300
Biomarker
disease
CTD_human
Neutrophil activation in patients with ASA-induced urticaria.
18204966
2008
×
Entrez Id:
114548
Gene Symbol:
NLRP3
NLRP3
0.160
GeneticVariation
disease
BEFREE
Urticarial rash , one of the clinical manifestations characteristic of cryopyrin-associated periodic syndrome (CAPS), is caused by a mutation in the gene encoding for NLRP3 (nucleotide-binding oligomerization domain, leucine-rich repeats containing family, pyrin domain containing 3).
20179416
2010
×
Entrez Id:
114548
Gene Symbol:
NLRP3
NLRP3
0.160
GeneticVariation
disease
LHGDN
Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis.
12355493
2002
×
Entrez Id:
114548
Gene Symbol:
NLRP3
NLRP3
0.160
Biomarker
disease
BEFREE
Dominant mutations in the CIAS1 gene cause a spectrum of autoinflammatory diseases such as familial cold autoinflammatory syndrome, FCAS , which is characterized by episodes of urticaria , arthralgia, fever and conjunctivitis after generalized exposure to cold.
15245511
2004
×
Entrez Id:
114548
Gene Symbol:
NLRP3
NLRP3
0.160
Biomarker
disease
HPO
×
Entrez Id:
114548
Gene Symbol:
NLRP3
NLRP3
0.160
GeneticVariation
disease
LHGDN
New mutations of CIAS1 that are responsible for Muckle-Wells syndrome and familial cold urticaria: a novel mutation underlies both syndromes.
11992256
2002
×
Entrez Id:
114548
Gene Symbol:
NLRP3
NLRP3
0.160
Biomarker
disease
BEFREE
Our findings implicate MCs as IL-1beta producers in the skin and mediators of histamine-independent urticaria through the NLRP3 inflammasome.
19364881
2009
×
Entrez Id:
114548
Gene Symbol:
NLRP3
NLRP3
0.160
GeneticVariation
disease
BEFREE
The cryopyrin -associated periodic fever syndrome (CAPS) is an autosomal dominant autoinflammatory disorder caused by mutations in the NLRP3 gene and is typified by recurrent episodes of systemic inflammation resulting in fever, urticarial rash and arthralgia.
26931528
2016
×
Entrez Id:
50943
Gene Symbol:
FOXP3
FOXP3
0.110
AlteredExpression
disease
BEFREE
No significant difference was detected in the expression levels of FOXP3 or TGF-beta between CU patients (n=14) and control subjects (n=7).
18440785
2008
×
Entrez Id:
50943
Gene Symbol:
FOXP3
FOXP3
0.110
Biomarker
disease
HPO
×
Entrez Id:
3815
Gene Symbol:
KIT
KIT
0.100
Biomarker
disease
HPO
×
Entrez Id:
58484
Gene Symbol:
NLRC4
NLRC4
0.100
Biomarker
disease
HPO
×
Entrez Id:
5580
Gene Symbol:
PRKCD
PRKCD
0.100
Biomarker
disease
HPO
×
Entrez Id:
25890
Gene Symbol:
ABI3BP
ABI3BP
0.100
GeneticVariation
disease
GWASCAT
Genome-wide association study in NSAID-induced acute urticaria/angioedema in Spanish and Han Chinese populations.
24236485
2013