Agammaglobulinemia Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores 2025
Category disease or phenotype associations
Type disease
Description A B cell deficiency that is caused by a reduction in all types of gamma globulins. (Human Disease Ontology, DOID_2583)
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Genes

16 genes involed in the disease Agammaglobulinemia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Symbol Name Standardized Value
IL21 interleukin 21 5.0
PRKCD protein kinase C, delta 5.0
LRBA LPS-responsive vesicle trafficking, beach and anchor containing 5.0
TNFRSF13C tumor necrosis factor receptor superfamily, member 13C 5.0
TNFRSF13B tumor necrosis factor receptor superfamily, member 13B 5.0
CD19 CD19 molecule 5.0
BTK Bruton agammaglobulinemia tyrosine kinase 5.0
CR2 complement component (3d/Epstein Barr virus) receptor 2 5.0
ICOS inducible T-cell co-stimulator 5.0
IKZF1 IKAROS family zinc finger 1 (Ikaros) 5.0
CD81 CD81 molecule 5.0
MS4A1 membrane-spanning 4-domains, subfamily A, member 1 5.0
NFKB2 nuclear factor of kappa light polypeptide gene enhancer in B-cells 2 (p49/p100) 5.0
NFKB1 nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 5.0
SAA2 serum amyloid A2 3.0
SAA1 serum amyloid A1 3.0