b cell deficiency Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A primary immunnodeficiency disease that is caused by a lack of infection-fighting antibody producing B cells (immunoglobulins) or B cells that are not functioning properly. (Human Disease Ontology, DOID_2115)
Similar Terms
Downloads & Tools

Genes

12 genes involed in the disease b cell deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
BTK Bruton agammaglobulinemia tyrosine kinase
CD19 CD19 molecule
CD81 CD81 molecule
CR2 complement component (3d/Epstein Barr virus) receptor 2
ICOS inducible T-cell co-stimulator
LRBA LPS-responsive vesicle trafficking, beach and anchor containing
MS4A1 membrane-spanning 4-domains, subfamily A, member 1
NFKB2 nuclear factor of kappa light polypeptide gene enhancer in B-cells 2 (p49/p100)
PRKCD protein kinase C, delta
STAT3 signal transducer and activator of transcription 3 (acute-phase response factor)
TNFRSF13B tumor necrosis factor receptor superfamily, member 13B
TNFRSF13C tumor necrosis factor receptor superfamily, member 13C