Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3576
Gene Symbol: CXCL8
CXCL8 		0.400 Biomarker disease LHGDN Serum interleukin-8 as a serologic marker of activity in Behçet's disease. 16101867 2005
Entrez Id: 7099
Gene Symbol: TLR4
TLR4 		0.400 AlteredExpression disease LHGDN Association of reduced heme oxygenase-1 with excessive Toll-like receptor 4 expression in peripheral blood mononuclear cells in Behçet's disease. 18234118 2008
Entrez Id: 3383
Gene Symbol: ICAM1
ICAM1 		0.380 GeneticVariation disease LHGDN The ICAM1469*E is associated with susceptibility to ocular lesions and vasculitis in Korean patients with Behçet's disease. 12918698 2003
Entrez Id: 7132
Gene Symbol: TNFRSF1A
TNFRSF1A 		0.150 Biomarker disease LHGDN Soluble tumour necrosis factor receptors sTNFR1 and sTNFR2 are produced at sites of inflammation and are markers of arthritis activity in Behçet's disease. 18415772 2008
Entrez Id: 4846
Gene Symbol: NOS3
NOS3 		0.100 GeneticVariation disease LHGDN Endothelial nitric oxide synthase gene Glu298Asp polymorphism is associated with Behçet's disease. 17067432 2007
Entrez Id: 2153
Gene Symbol: F5
F5 		0.100 GeneticVariation disease LHGDN Association of factor V Leiden and prothrombin gene mutation with Behçet's disease. 11820731 2001
Entrez Id: 3553
Gene Symbol: IL1B
IL1B 		0.100 GeneticVariation disease LHGDN Specific interleukin-1 gene polymorphisms in Turkish patients with Behçet's disease. 15679582 2005
Entrez Id: 2153
Gene Symbol: F5
F5 		0.100 GeneticVariation disease LHGDN The present study was designed to analyse the role of the factor V Leiden and the prothrombin G20210A mutations and plasminogen activator inhibitor-1 4G/5G polymorphism on the thrombotic risk of patients with Behcet's disease. 12632020 2003
Entrez Id: 2153
Gene Symbol: F5
F5 		0.100 Biomarker disease LHGDN Factor V Leiden and prothrombin gene G20210A mutations in ocular Behçet disease. 12780409 2003
Entrez Id: 4846
Gene Symbol: NOS3
NOS3 		0.100 GeneticVariation disease LHGDN Endothelial nitric oxide synthase gene polymorphism is associated with Behçet's disease in Tunisian population. 18718857 2008
Entrez Id: 2147
Gene Symbol: F2
F2 		0.100 GeneticVariation disease LHGDN Association of factor V Leiden and prothrombin gene mutation with Behçet's disease. 11820731 2001
Entrez Id: 3458
Gene Symbol: IFNG
IFNG 		0.100 AlteredExpression disease LHGDN The aim of the current study was to define the expression on CD3+ T cells of six chemokine receptors associated with inflammatory sites and the expression of intracellular cytokines, such as interferon-gamma (IFN-gamma) and interleukin-4 (IL-4), in Behcet's disease (BD). 15501397 2004
Entrez Id: 7124
Gene Symbol: TNF
TNF 		0.100 Biomarker disease LHGDN The aim of the study is to compare stimulated production of TNF-alpha by PBM of BD patients with that of healthy volunteers (HV) and to examine correlations between the ability of PBM to produce TNF-alpha and organ/system involvement in patients with BD. 16897113 2007
Entrez Id: 3553
Gene Symbol: IL1B
IL1B 		0.100 GeneticVariation disease LHGDN Relationship between periodontal findings and specific polymorphisms of interleukin-1alpha and -1beta in Turkish patients with Behçet's disease. 17960403 2008
Entrez Id: 7124
Gene Symbol: TNF
TNF 		0.100 GeneticVariation disease LHGDN Six polymorphisms in the promoter region of TNFA were genotyped in 254 BD patients and 344 control subjects, via the PCR-RFLP technique. 16891799 2006
Entrez Id: 3552
Gene Symbol: IL1A
IL1A 		0.100 GeneticVariation disease LHGDN Relationship between periodontal findings and specific polymorphisms of interleukin-1alpha and -1beta in Turkish patients with Behçet's disease. 17960403 2008
Entrez Id: 3605
Gene Symbol: IL17A
IL17A 		0.100 AlteredExpression disease LHGDN The increased IL-17 (3.10% +/- 0.53%) in BD patients with active uveitis was primarily produced by CD45RO(+) memory T cells. 18579762 2008
Entrez Id: 4846
Gene Symbol: NOS3
NOS3 		0.100 GeneticVariation disease LHGDN Endothelial nitric oxide synthase gene polymorphisms in Behçet's disease. 11908569 2002
Entrez Id: 2147
Gene Symbol: F2
F2 		0.100 GeneticVariation disease LHGDN The frequencies of carriage rates of prothrombin gene G20210A and factor V Leiden polymorphisms in BD patients with and without DVT were similar. 15077257 2004
Entrez Id: 3458
Gene Symbol: IFNG
IFNG 		0.100 AlteredExpression disease LHGDN Upregulated IL-23 and IL-17 in Behçet patients with active uveitis. 18579762 2008
Entrez Id: 51561
Gene Symbol: IL23A
IL23A 		0.080 AlteredExpression disease LHGDN Results showed that the expression of IL-23p19 mRNA, IL-23, IL-17, and IFN-gamma was markedly elevated in BD patients with active uveitis. 18579762 2008
Entrez Id: 1234
Gene Symbol: CCR5
CCR5 		0.080 GeneticVariation disease LHGDN Association of chemokine receptor 5 (CCR5) delta32 mutation with Behçet's disease is dependent on gender in Iranian patients. 17067435 2007
Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA 		0.070 GeneticVariation disease LHGDN Vascular endothelial growth factor gene polymorphisms in Behçet's disease. 15338501 2004
Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1 		0.070 Biomarker disease LHGDN Class I and class II MHC polymorphisms in Mexican patients with Behçet's disease. 15158619 2004
Entrez Id: 3565
Gene Symbol: IL4
IL4 		0.060 Biomarker disease LHGDN The aim of the current study was to define the expression on CD3+ T cells of six chemokine receptors associated with inflammatory sites and the expression of intracellular cytokines, such as interferon-gamma (IFN-gamma) and interleukin-4 (IL-4), in Behcet's disease (BD). 15501397 2004