Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 54806
Gene Symbol: AHI1
AHI1 		0.400 GeneticVariation disease GWASCAT Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. 27723758 2016
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A 		0.400 GeneticVariation disease GWASCAT Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. 27723758 2016
Entrez Id: 54806
Gene Symbol: AHI1
AHI1 		0.400 Biomarker disease CTD_human Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. 27723758 2016
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1 		0.400 GeneticVariation disease GWASCAT Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. 27723758 2016
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1 		0.400 Biomarker disease CTD_human Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. 27723758 2016
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A 		0.400 Biomarker disease CTD_human Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. 27723758 2016
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1 		0.400 Biomarker disease CTD_human Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. 20694011 2010
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A 		0.400 Biomarker disease CTD_human Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. 20694011 2010
Entrez Id: 5820
Gene Symbol: PVT1
PVT1 		0.300 Biomarker disease CTD_human Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. 27723758 2016
Entrez Id: 942
Gene Symbol: CD86
CD86 		0.100 GeneticVariation disease GWASCAT Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. 27723758 2016
Entrez Id: 3117
Gene Symbol: HLA-DQA1
HLA-DQA1 		0.100 GeneticVariation disease GWASCAT Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. 27723758 2016
Entrez Id: 1959
Gene Symbol: EGR2
EGR2 		0.100 GeneticVariation disease GWASCAT Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. 27723758 2016
Entrez Id: 115352
Gene Symbol: FCRL3
FCRL3 		0.100 GeneticVariation disease GWASCAT Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. 27723758 2016
Entrez Id: 22806
Gene Symbol: IKZF3
IKZF3 		0.100 GeneticVariation disease GWASCAT Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. 27723758 2016
Entrez Id: 105374266
Gene Symbol: LINC01991
LINC01991 		0.100 GeneticVariation disease GWASCAT Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. 27723758 2016
Entrez Id: 2625
Gene Symbol: GATA3
GATA3 		0.100 GeneticVariation disease GWASCAT Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. 27723758 2016
Entrez Id: 5771
Gene Symbol: PTPN2
PTPN2 		0.100 GeneticVariation disease GWASCAT Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. 27723758 2016
Entrez Id: 166378
Gene Symbol: SPATA5
SPATA5 		0.100 GeneticVariation disease CLINVAR
Entrez Id: 5728
Gene Symbol: PTEN
PTEN 		0.100 CausalMutation disease CLINVAR
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B 		0.070 GeneticVariation disease BEFREE Therefore, our work seems to discard a role of TNFRSF13B mutations in IgAD, concordantly with the most recent published studies. 19392801 2009
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B 		0.070 GeneticVariation disease BEFREE Mutations in TACI were also found in relatives of patients with CVID who suffered from IgA deficiency (IgAD) as well as in a patient with isolated IgAD. 17917015 2007
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B 		0.070 GeneticVariation disease LHGDN Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency. 17392797 2007
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B 		0.070 GeneticVariation disease LHGDN Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency. 17392798 2007
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B 		0.070 GeneticVariation disease BEFREE Recently, patients with CVID and IGAD have been found to have mutations of the gene TNFRSF13B encoding the TACI (transmembrane activator and calcium-modulator and cyclophilin-ligand interactor), a member of the tumor necrosis factor-receptor superfamily. 16899196 2006
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B 		0.070 AlteredExpression disease BEFREE Common variable immunodeficiency, CVID, is a primary antibody deficiency characterized by decreased levels of serum immunoglobulin G (IgG), decreased IgA and/or IgM and recurrent infections. 15963052 2005