Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
0.430 GeneticVariation disease BEFREE Among the HLA class II alleles, DRB1*04 was observed significantly more often in the study population (p < 0.001), mainly in the autoimmunological subtype of urticaria. 20559009 2010
Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
0.430 GeneticVariation disease LHGDN HLA class I and class II genotyping in patients with chronic urticaria. 18520158 2008
Entrez Id: 240
Gene Symbol: ALOX5
ALOX5
0.320 GeneticVariation disease BEFREE However, there were no differences in allele, genotype, or haplotype frequencies of ALOX5 between the AIU group and the normal control group. 16361798 2005
Entrez Id: 240
Gene Symbol: ALOX5
ALOX5
0.320 GeneticVariation disease LHGDN However, there were no differences in allele, genotype, or haplotype frequencies of ALOX5 between the AIU group and the normal control group. 16361798 2005
Entrez Id: 240
Gene Symbol: ALOX5
ALOX5
0.320 GeneticVariation disease BEFREE Copy number variation in ALOX5 and PTGER1 is associated with NSAIDs-induced urticaria and/or angioedema. 26959713 2016
Entrez Id: 3606
Gene Symbol: IL18
IL18
0.320 GeneticVariation disease BEFREE A functional promoter polymorphism of the human IL18 gene is associated with aspirin-induced urticaria. 21692767 2011
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 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 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: 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
Entrez Id: 112752
Gene Symbol: IFT43
IFT43
0.100 GeneticVariation disease GWASCAT Genome-wide association study in NSAID-induced acute urticaria/angioedema in Spanish and Han Chinese populations. 24236485 2013
Entrez Id: 1636
Gene Symbol: ACE
ACE
0.030 GeneticVariation disease BEFREE Thus, we aimed to investigate whether there is an association between ACE I/D polymorphism and chronic ordinary urticaria. 18181977 2008
Entrez Id: 1636
Gene Symbol: ACE
ACE
0.030 GeneticVariation disease BEFREE It can present with urticaria or anaphylaxis and is usually associated with angiotensin-converting enzyme inhibitors (ACEis), complement deficiencies, or the side effects of tissue plasminogen activator (tPA). 29850387 2018
Entrez Id: 3700
Gene Symbol: ITIH4
ITIH4
0.020 GeneticVariation disease BEFREE HIV-1 genomes infecting different regions of the brain of one study subject with HIV encephalitis (HIVE) had a mosaic structure, being assembled from different combinations of evolutionarily distinct lineages in p17(gag), pol, individual hypervariable regions of gp120 (V1/V2, V3, V4, and V5), and gp41/nef. 10482626 1999
Entrez Id: 154
Gene Symbol: ADRB2
ADRB2
0.020 GeneticVariation disease LHGDN Association of beta 2-adrenergic receptor polymorphism with the phenotype of aspirin-intolerant acute urticaria. 18159608 2007
Entrez Id: 90865
Gene Symbol: IL33
IL33
0.010 GeneticVariation disease BEFREE The aim of this study was to compare the clinical features, total eosinophil count, serum levels of interleukin (IL)-18, IL-18 binding protein (BP), IL-1 receptor-like (RL) 1, and IL-33 and compare with tryptase to examine if any differences could be found between patients who experienced anaphylaxis and urticaria. 31837215 2019
Entrez Id: 3106
Gene Symbol: HLA-B
HLA-B
0.010 GeneticVariation disease LHGDN HLA class I and class II genotyping in patients with chronic urticaria. 18520158 2008
Entrez Id: 1493
Gene Symbol: CTLA4
CTLA4
0.010 GeneticVariation disease BEFREE Our data suggest that there is no contribution of CTLA-4 A49G polymorphism to chronic spontaneous autoreactive urticaria susceptibility. 23597501 2015
Entrez Id: 5335
Gene Symbol: PLCG1
PLCG1
0.010 GeneticVariation disease BEFREE PLCG1 rs2228246 (angioedema vs. controls; Pc=0.044), and TNFRS11A rs1805034 (urticaria+angioedema vs. controls; Pc=0.041). 26398624 2015
Entrez Id: 5265
Gene Symbol: SERPINA1
SERPINA1
0.010 GeneticVariation disease BEFREE Deficiencies in alpha 1-antitrypsin may predispose to the development of certain types of urticaria and angio-oedema. 3873251 1985
Entrez Id: 940
Gene Symbol: CD28
CD28
0.010 GeneticVariation disease BEFREE Inducible T-cell costimulator (ICOS) and CD28 polymorphisms possibly play a role in the pathogenesis of chronic autoreactive urticaria. 28940644 2017
Entrez Id: 629
Gene Symbol: CFB
CFB
0.010 GeneticVariation disease BEFREE A new slow-moving variant of the complement factor B, named BF S075, was found in a Japanese patient with cerebral thrombosis and urticaria. 2312129 1990
Entrez Id: 181
Gene Symbol: AGRP
AGRP
0.010 GeneticVariation disease BEFREE We analyzed three microarray datasets obtained from the NCBI in order to assess the expression levels of OAS gene family network in brain biopsies of macaques with SIVE vs uninfected animals, as well as post-mortem brain of individuals with HAND (on or off ART) vs uninfected controls and three brain regions of HIV-infected individuals with both neurocognitive impairment (HAD) and encephalitis (HIVE). 28236279 2018
Entrez Id: 4056
Gene Symbol: LTC4S
LTC4S
0.010 GeneticVariation disease BEFREE The A-444C polymorphism in the leukotriene C4 synthase gene is associated with aspirin-induced urticaria. 19862937 2009