abnormality of b cell number Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	A deviation from the normal count of B cells, i.e., the cells that are formed in the bone marrow, migrate to the peripheral lymphatic system, and mature into plasma cells or memory cells. (Human Phenotype Ontology, HP_0010975)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0010975
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Genes

9 genes associated with the abnormality of b cell number phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
ADA	adenosine deaminase
CASP10	caspase 10, apoptosis-related cysteine peptidase
DCLRE1C	DNA cross-link repair 1C
GFI1	growth factor independent 1 transcription repressor
ICOS	inducible T-cell co-stimulator
IGHM	immunoglobulin heavy constant mu
NBN	nibrin
RAG1	recombination activating gene 1
RAG2	recombination activating gene 2