Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 29851
Gene Symbol: ICOS
ICOS
0.800 GermlineCausalMutation disease ORPHANET
Entrez Id: 29851
Gene Symbol: ICOS
ICOS
0.800 Biomarker disease CTD_human
Entrez Id: 4791
Gene Symbol: NFKB2
NFKB2
0.780 Biomarker disease CTD_human
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
0.700 Biomarker disease CTD_human
Entrez Id: 115650
Gene Symbol: TNFRSF13C
TNFRSF13C
0.600 Biomarker disease CTD_human
Entrez Id: 1380
Gene Symbol: CR2
CR2
0.600 Biomarker disease CTD_human
Entrez Id: 930
Gene Symbol: CD19
CD19
0.600 GermlineCausalMutation disease ORPHANET
Entrez Id: 115650
Gene Symbol: TNFRSF13C
TNFRSF13C
0.600 GermlineCausalMutation disease ORPHANET
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1
0.560 Biomarker disease CTD_human
Entrez Id: 975
Gene Symbol: CD81
CD81
0.510 Biomarker disease CTD_human
Entrez Id: 931
Gene Symbol: MS4A1
MS4A1
0.510 Biomarker disease CTD_human
Entrez Id: 59067
Gene Symbol: IL21
IL21
0.350 Biomarker disease CTD_human
Entrez Id: 10320
Gene Symbol: IKZF1
IKZF1
0.330 Biomarker disease CTD_human
Entrez Id: 931
Gene Symbol: MS4A1
MS4A1
0.510 GermlineCausalMutation disease ORPHANET """A rose is a rose is a rose,"" but CVID is Not CVID common variable immune deficiency (CVID), what do we know in 2011?" 21970952 2011
Entrez Id: 975
Gene Symbol: CD81
CD81
0.510 GermlineCausalMutation disease ORPHANET """A rose is a rose is a rose,"" but CVID is Not CVID common variable immune deficiency (CVID), what do we know in 2011?" 21970952 2011
Entrez Id: 4791
Gene Symbol: NFKB2
NFKB2
0.780 Biomarker disease MGD "A novel mutation in the Nfkb2 gene generates an NF-kappa B2 ""super repressor""." 18025196 2007
Entrez Id: 1493
Gene Symbol: CTLA4
CTLA4
0.350 GeneticVariation disease BEFREE +49 A > G changes in exon 1 of CTLA-4 gene: GG and AG genotypes increase the risk of CVID development 1.32 and 2.18 fold, respectively. 22699762 2012
Entrez Id: 604
Gene Symbol: BCL6
BCL6
0.020 GeneticVariation disease BEFREE Common-variable immunodeficiency-related lymphomas associate with mutations and rearrangements of BCL-6: pathogenetic and histogenetic implications. 10923927 2000
Entrez Id: 3077
Gene Symbol: HFE
HFE
0.010 GeneticVariation disease BEFREE Common variable immunodeficiency and IgG subclass deficiency in central Alabama hemochromatosis probands homozygous for HFE C282Y. 12850493 2004
Entrez Id: 939
Gene Symbol: CD27
CD27
0.090 AlteredExpression disease BEFREE Common variable immune deficiency (CVID) is a primary immune deficiency characterized by low levels of serum immune globulins, lack of Ab, and reduced numbers of CD27+ memory B cells. 16424230 2006
Entrez Id: 54106
Gene Symbol: TLR9
TLR9
0.070 Biomarker disease BEFREE Common variable immune deficiency (CVID) B cells have impaired responses to TLR7 and TLR9 agonists including poor cell proliferation, loss of cytokine production, and failure to produce IgG or IgA. 22048980 2012
Entrez Id: 952
Gene Symbol: CD38
CD38
0.020 AlteredExpression disease BEFREE Common variable immunodeficiency is associated with impaired in-vitro development of peripheral blood mononuclear cells or purified B-cells into memory or CD38 B-cells following addition of IL-21. 24126614 2013
Entrez Id: 59067
Gene Symbol: IL21
IL21
0.350 AlteredExpression disease BEFREE Common variable immunodeficiency is associated with impaired in-vitro development of peripheral blood mononuclear cells or purified B-cells into memory or CD38 B-cells following addition of IL-21. 24126614 2013
Entrez Id: 1380
Gene Symbol: CR2
CR2
0.600 Biomarker disease BEFREE CVID is a multifactorial antibody deficiency that can be associated with autoimmunity, which some studies have proposed to be secondary to altered CD21 expression. 31089823 2019
Entrez Id: 7421
Gene Symbol: VDR
VDR
0.010 GeneticVariation disease BEFREE Vitamin D receptor and IL-6 alleles were associated with immunophenotypic abnormalities characteristic of more severe disease; and tumour necrosis factor and IL-10 alleles conferred susceptibility to the granulomatous form of CVID in an interacting fashion. 11196660 1999