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