Agammaglobulinemia Gene Set

Dataset CTD Gene-Disease Associations
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D000361
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Genes

5 genes/proteins associated with the disease Agammaglobulinemia from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
IGLL1 immunoglobulin lambda-like polypeptide 1 2.88009
BTK Bruton agammaglobulinemia tyrosine kinase 2.88009
CD19 CD19 molecule 2.88009
LRRC8A leucine rich repeat containing 8 family, member A 2.88009
CD79A CD79a molecule, immunoglobulin-associated alpha 2.88009