rs886039326
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
Characterization of nine novel mutations in the CD40 ligand gene in patients with X-linked hyper IgM syndrome of various ancestry.
7717401
1995
rs886039326
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
CD40 ligand gene defects responsible for X-linked hyper-IgM syndrome.
7679801
1993
rs886039326
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
Signaling through CD40 rescues IgE but not IgG or IgA secretion in X-linked immunodeficiency with hyper-IgM.
7532185
1995
rs886039326
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
Mutation analysis in CD40 ligand deficiency leading to X-linked hypogammaglobulinemia with hyper IgM syndrome.
8889581
1996
rs886039326
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
Mutations of the CD40 ligand gene in 13 Japanese patients with X-linked hyper-IgM syndrome.
9150729
1997
rs886039326
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndrome.
7678782
1993
rs886039326
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
Integrin Binding to the Trimeric Interface of CD40L Plays a Critical Role in CD40/CD40L Signaling.
31331973
2019
rs886039326
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
CD40 ligand mutations in x-linked immunodeficiency with hyper-IgM.
8094231
1993
rs886039326
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
A single strand conformation polymorphism study of CD40 ligand. Efficient mutation analysis and carrier detection for X-linked hyper IgM syndrome.
8550833
1996
rs886039326
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
Mutations of the CD40 ligand gene and its effect on CD40 ligand expression in patients with X-linked hyper IgM syndrome.
9746782
1998
rs886039326
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients.
26545377
2016
rs886039326
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
Defective expression of T-cell CD40 ligand causes X-linked immunodeficiency with hyper-IgM.
7679206
1993
rs756468554
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
CD40 ligand gene defects responsible for X-linked hyper-IgM syndrome.
7679801
1993
rs756468554
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
A single strand conformation polymorphism study of CD40 ligand. Efficient mutation analysis and carrier detection for X-linked hyper IgM syndrome.
8550833
1996
rs756468554
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
CD40 ligand mutations in x-linked immunodeficiency with hyper-IgM.
8094231
1993
rs756468554
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
Mutations of the CD40 ligand gene and its effect on CD40 ligand expression in patients with X-linked hyper IgM syndrome.
9746782
1998
rs756468554
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients.
26545377
2016
rs756468554
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
Integrin Binding to the Trimeric Interface of CD40L Plays a Critical Role in CD40/CD40L Signaling.
31331973
2019
rs756468554
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
Mutations of the CD40 ligand gene in 13 Japanese patients with X-linked hyper-IgM syndrome.
9150729
1997
rs756468554
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
Signaling through CD40 rescues IgE but not IgG or IgA secretion in X-linked immunodeficiency with hyper-IgM.
7532185
1995
rs756468554
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
Mutation analysis in CD40 ligand deficiency leading to X-linked hypogammaglobulinemia with hyper IgM syndrome.
8889581
1996
rs756468554
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
Characterization of nine novel mutations in the CD40 ligand gene in patients with X-linked hyper IgM syndrome of various ancestry.
7717401
1995
rs756468554
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
Defective expression of T-cell CD40 ligand causes X-linked immunodeficiency with hyper-IgM.
7679206
1993
rs756468554
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Hyper-IgM Immunodeficiency Syndrome, Type 1
0.700
GeneticVariation
UNIPROT
The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndrome.
7678782
1993
rs3092936
×
Entrez Id:
959
Gene Symbol:
CD40LG
CD40LG
Acute GVH disease
0.010
GeneticVariation
BEFREE
Results The rs3092936 CC/CT genotype was associated with an increased risk of transplant-associated thrombotic microangiopathy ( P = .001), overall NRM ( P = .03), and NRM after acute graft-versus-host disease ( P = .01).
29369699
2018