Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4210
Gene Symbol: MEFV
MEFV 		0.500 CausalMutation disease CLINVAR
Entrez Id: 64127
Gene Symbol: NOD2
NOD2 		0.180 CausalMutation disease CLINVAR
Entrez Id: 7132
Gene Symbol: TNFRSF1A
TNFRSF1A 		0.150 CausalMutation disease CLINVAR
Entrez Id: 9051
Gene Symbol: PSTPIP1
PSTPIP1 		0.120 CausalMutation disease CLINVAR
Entrez Id: 51816
Gene Symbol: ADA2
ADA2 		0.110 CausalMutation disease CLINVAR
Entrez Id: 3106
Gene Symbol: HLA-B
HLA-B 		0.700 SusceptibilityMutation disease ORPHANET Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease. 20622878 2010
Entrez Id: 3586
Gene Symbol: IL10
IL10 		0.700 SusceptibilityMutation disease ORPHANET Interleukin-10 gene polymorphisms are associated with Behcet's disease but not with Vogt-Koyanagi-Harada syndrome in the Chinese Han population. 26015771 2015
Entrez Id: 51752
Gene Symbol: ERAP1
ERAP1 		0.700 SusceptibilityMutation disease ORPHANET Brief report: association of CCR1, KLRC4, IL12A-AS1, STAT4, and ERAP1 With Behçet's disease in Iranians. 26097239 2015
Entrez Id: 3586
Gene Symbol: IL10
IL10 		0.700 SusceptibilityMutation disease ORPHANET Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease. 20622878 2010
Entrez Id: 6775
Gene Symbol: STAT4
STAT4 		0.670 SusceptibilityMutation disease ORPHANET Brief report: association of CCR1, KLRC4, IL12A-AS1, STAT4, and ERAP1 With Behçet's disease in Iranians. 26097239 2015
Entrez Id: 6775
Gene Symbol: STAT4
STAT4 		0.670 SusceptibilityMutation disease ORPHANET Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997 2012
Entrez Id: 8302
Gene Symbol: KLRC4
KLRC4 		0.630 SusceptibilityMutation disease ORPHANET Brief report: association of CCR1, KLRC4, IL12A-AS1, STAT4, and ERAP1 With Behçet's disease in Iranians. 26097239 2015
Entrez Id: 1230
Gene Symbol: CCR1
CCR1 		0.540 SusceptibilityMutation disease ORPHANET Brief report: association of CCR1, KLRC4, IL12A-AS1, STAT4, and ERAP1 With Behçet's disease in Iranians. 26097239 2015
Entrez Id: 4210
Gene Symbol: MEFV
MEFV 		0.500 SusceptibilityMutation disease ORPHANET Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease. 23633568 2013
Entrez Id: 101928376
Gene Symbol: IL12A-AS1
IL12A-AS1 		0.410 SusceptibilityMutation disease ORPHANET Brief report: association of CCR1, KLRC4, IL12A-AS1, STAT4, and ERAP1 With Behçet's disease in Iranians. 26097239 2015
Entrez Id: 7099
Gene Symbol: TLR4
TLR4 		0.400 SusceptibilityMutation disease ORPHANET Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease. 23633568 2013
Entrez Id: 149233
Gene Symbol: IL23R
IL23R 		0.400 SusceptibilityMutation disease ORPHANET Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease. 23633568 2013
Entrez Id: 337867
Gene Symbol: UBAC2
UBAC2 		0.340 SusceptibilityMutation disease ORPHANET The mRNA expression of UBAC2 transcript variant 1 was significantly decreased in PBMCs and skin of BD patients as compared with controls (P = 0.025; P = 0.047, respectively). 22455605 2012
Entrez Id: 337867
Gene Symbol: UBAC2
UBAC2 		0.340 SusceptibilityMutation disease ORPHANET A putative functional variant within the UBAC2 gene is associated with increased risk of Behçet's disease. 21918955 2011
Entrez Id: 3592
Gene Symbol: IL12A
IL12A 		0.330 SusceptibilityMutation disease ORPHANET Genome-wide association study in an admixed case series reveals IL12A as a new candidate in Behçet disease. 25799145 2015
Entrez Id: 355
Gene Symbol: FAS
FAS 		0.330 SusceptibilityMutation disease ORPHANET FAS Gene Copy Numbers are Associated with Susceptibility to Behçet Disease and VKH Syndrome in Han Chinese. 26136352 2015
Entrez Id: 720
Gene Symbol: C4A
C4A 		0.300 SusceptibilityMutation disease ORPHANET Copy number variations of complement component C4 are associated with Behçet's disease but not with ankylosing spondylitis associated with acute anterior uveitis. 23918728 2013
Entrez Id: 3586
Gene Symbol: IL10
IL10 		0.700 AlteredExpression disease BEFREE Furthermore, a positive correlation was observed between IL-10 serum levels and ocular manifestations in BD patients, in contrast to those of IL-17, showing no correlation with the different clinical manifestations. 31122907 2019
Entrez Id: 3586
Gene Symbol: IL10
IL10 		0.700 AlteredExpression disease BEFREE We revealed that hypermethylation of promoter region was the principal defect for the IL-10 mRNA low expression in patients with Behçet's disease. 29719061 2018
Entrez Id: 3586
Gene Symbol: IL10
IL10 		0.700 AlteredExpression disease BEFREE Revealing the key molecular mechanism by which IL-10 expression is regulated is crucial to understanding the pathogenesis of BD. 29096751 2017