Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5243
Gene Symbol: ABCB1
ABCB1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.030 GeneticVariation BEFREE Our study showed that MDR1 genes and their polymorphisms may affect a patient's BD susceptibility and colchicine response. 22705826

2012

Entrez Id: 5243
Gene Symbol: ABCB1
ABCB1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.030 GeneticVariation BEFREE We investigated the distribution of MDR1 C3435T polymorphism in 69 patients from the Iranian Azeri Turks group with BD and 92 ethnically sex-matched healthy controls, via the polymerase chain reaction-restriction fragment length polymorphism technique. 24898446

2014

Entrez Id: 5243
Gene Symbol: ABCB1
ABCB1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.030 GeneticVariation BEFREE We concluded that ABCB1 C3435T polymorphism is not associated with a colchicine response in patients with Behçet's disease. 21218380

2011

Entrez Id: 1636
Gene Symbol: ACE
ACE
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.060 GeneticVariation BEFREE As a result of this study, ACE gene I/D polymorphism DD genotype could be a genetic marker in BD in Turkish study population. 23065219

2013

Entrez Id: 1636
Gene Symbol: ACE
ACE
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.060 GeneticVariation BEFREE A cohort of 90 patients with BD were evaluated for their ACE genotype (male/female: 49/41, mean age: 36.9+/-10.6 years, min/max: 16-66 years). 15045629

2004

Entrez Id: 1636
Gene Symbol: ACE
ACE
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.060 GeneticVariation BEFREE The distrubition of "DD", "ID" and "II" genotypes of the ACE gene were 32 (43.8%), 29 (39.8%) and 12 (16.4%) for BD patients and 32 (35.5%), 35 (38.9%) and 23 (25.6%) for healthy controls. 19255721

2009

Entrez Id: 1636
Gene Symbol: ACE
ACE
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.060 GeneticVariation BEFREE An association between Behçet's disease and ACE polymorphism may provide a useful basis for future molecular studies and therapeutic approaches in this complex disease. 15961928

2006

Entrez Id: 1636
Gene Symbol: ACE
ACE
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.060 GeneticVariation BEFREE Association of angiotensin-converting enzyme (ACE) gene insertion/deletion (I/D) polymorphism with BD has been reported in Turkish population. 23455487

2013

Entrez Id: 1636
Gene Symbol: ACE
ACE
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.060 GeneticVariation BEFREE This meta-analysis shows that the ACE I/D polymorphism is associated with vasculitis susceptibility, especially in BD and HSP. 22277255

2012

Entrez Id: 47
Gene Symbol: ACLY
ACLY
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 AlteredExpression BEFREE Therefore, SLC25A1 and ACLY upregulation suggests that metabolic reprogramming in BS involves the citrate pathway dysregulation. 30050389

2018

Entrez Id: 60
Gene Symbol: ACTB
ACTB
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 Biomarker BEFREE These results suggest that the increase of 42-merP and truncated actin in patients with Behçet's disease changes functions of neutrophils 11456109

2001

Entrez Id: 100
Gene Symbol: ADA
ADA
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 AlteredExpression BEFREE These associations include ERAP1, CCR1-CCR3, STAT4, KLRC4, GIMAP4, and TNFAIP3 in Behçet's disease; BLK and CD40 in Kawasaki disease; SERPINA1 and SEMA6A in antineutrophil cytoplasmic antibody associated vasculitides; IL12B and FCGR2A/ FCGR2A in Takayasu arteritis; and CECR1 in a newly defined vascular inflammatory syndrome associated with adenosine deaminase (ADA2) deficiency. 25405820

2015

Entrez Id: 51816
Gene Symbol: ADA2
ADA2
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.110 AlteredExpression BEFREE These associations include ERAP1, CCR1-CCR3, STAT4, KLRC4, GIMAP4, and TNFAIP3 in Behçet's disease; BLK and CD40 in Kawasaki disease; SERPINA1 and SEMA6A in antineutrophil cytoplasmic antibody associated vasculitides; IL12B and FCGR2A/ FCGR2A in Takayasu arteritis; and CECR1 in a newly defined vascular inflammatory syndrome associated with adenosine deaminase (ADA2) deficiency. 25405820

2015

Entrez Id: 9370
Gene Symbol: ADIPOQ
ADIPOQ
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.020 Biomarker BEFREE Levels of resistin (SMD = 0.51, 95% CI 0.92-0.918, P = 0.02) and adiponectin (SMD = 0.31, 95% CI 0.06-0.56, P = 0.02) were significantly higher in the BD group after adjustment for age, sex and body mass index (BMI), but not without such adjustment (resistin: (SMD = 0.38, 95% CI -0.18 to 0.93, P = 0.19; adiponectin: SMD = -0.59, 95% CI -2.23 to 1.06, P = 0.48). 29356069

2018

Entrez Id: 84890
Gene Symbol: ADO
ADO
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 Biomarker BEFREE Our findings confirmed the association of four loci (<i>LACC1</i>, <i>CEBPB-PTPN1</i>, <i>ADO-EGR2</i> and <i>RIPK2</i>) in Chinese Han patients with BD. 29907633

2018

Entrez Id: 196
Gene Symbol: AHR
AHR
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.320 AlteredExpression BEFREE In this study, we investigated the mRNA expression of AHR in the monocyte-derived and M1 macrophages in active BD patients in comparison to healthy controls. 29149781

2017

Entrez Id: 196
Gene Symbol: AHR
AHR
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.320 Biomarker BEFREE Further studies are needed to investigate whether modulation of AhR might be used in the treatment of BD. 25045206

2014

Entrez Id: 57379
Gene Symbol: AICDA
AICDA
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 GeneticVariation BEFREE Therefore, a high percentage of patients with BD have rare variants in AID genes. 30808881

2019

Entrez Id: 199
Gene Symbol: AIF1
AIF1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 GeneticVariation BEFREE In order to identify other genes of susceptibility to BD within the HLA region we investigated the distribution of human Allograft Inflammatory Factor-1 (AIF-1) gene variants among BD patients and healthy controls from Sardinia. 30252881

2018

Entrez Id: 9447
Gene Symbol: AIM2
AIM2
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 GeneticVariation BEFREE Patients and controls were genotyped and 2 tSNP (rs6940 in IFI16 and rs855873 in AIM2) were associated with BD. 25641891

2015

Entrez Id: 207
Gene Symbol: AKT1
AKT1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 AlteredExpression BEFREE AKT1 and DICER1 expression levels were higher in BD patients compared with that in SCZ patients and healthy controls, suggesting that expression of these genes is associated more specifically to manic features. 27701407

2016

Entrez Id: 213
Gene Symbol: ALB
ALB
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 AlteredExpression BEFREE Serum calprotectin and ischemia modified albumin levels as markers of disease activity in Behçet's disease. 30618530

2018

Entrez Id: 268
Gene Symbol: AMH
AMH
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 AlteredExpression BEFREE To compare ovarian reserve with anti-müllerian hormone (AMH) levels, antral follicle counts (AFCs) and ovarian volume in patients with Behçet's disease (BD) and healthy subjects. 26179772

2017

Entrez Id: 10541
Gene Symbol: ANP32B
ANP32B
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 AlteredExpression BEFREE GM-CSF, IL-11, and IL-12p40 were significantly higher in nongranulomatous uveitis (BD and HLA-B27) than in granulomatous uveitis (sarcoidosis and VKH), whereas APRIL and TWEAK were significantly higher in granulomatous uveitis. 31161935

2019

Entrez Id: 301
Gene Symbol: ANXA1
ANXA1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.020 Biomarker BEFREE Finally, in-house ELISA was developed to determine the induced anti-Annexin A1 autoantibodies in BD patients. 28963375

2018