Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
0.090 GeneticVariation disease BEFREE The index case and the two daughters with Behçet-like disease, were previously found to have a TNFAIP3 frameshift mutation. 31376265 2020
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
0.090 Biomarker disease BEFREE It has recently been recognized that TNFAIP3 deficiency leads to early onset of autoinflammatory and autoimmune syndrome resembling Behçet's disease. 30810840 2019
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
0.090 Biomarker disease BEFREE Genetic screening of TNFAIP3 should be considered for familial BD-like patients with early-onset recurrent fevers. 31164164 2019
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
0.090 GeneticVariation disease BEFREE Further functional studies are required to research whether the variant of TNFAIP3 plays a part in the development of GPP or simply causes the Behçet's disease phenotype. 31353537 2019
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
0.090 GeneticVariation disease BEFREE Mutations in tumor necrosis factor α-induced protein 3 results in a disease that can present as Behçet disease called haploinsufficiency of A20. 28582318 2017
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
0.090 Biomarker disease BEFREE Lack of association of TNFAIP3 and JAK1 with Behçet's disease in the European population. 26005883 2016
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
0.090 Biomarker disease 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: 7128
Gene Symbol: TNFAIP3
TNFAIP3
0.090 GeneticVariation disease BEFREE The aim of the study was to investigate the association of TNFα-induced protein 3 interacting with protein 1 (TNIP1) gene polymorphisms with Vogt-Koyanagi-Harada (VKH) syndrome and Behcet's disease (BD) in a Han Chinese population. 24788730 2014
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
0.090 GeneticVariation disease BEFREE TNFAIP3 gene polymorphisms confer risk for Behcet's disease in a Chinese Han population. 23161053 2013