panhypogammaglobulinemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003139
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Genes

10 genes associated with the panhypogammaglobulinemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BTK Bruton agammaglobulinemia tyrosine kinase
CIITA class II, major histocompatibility complex, transactivator
DCLRE1C DNA cross-link repair 1C
JAK3 Janus kinase 3
RAG1 recombination activating gene 1
RAG2 recombination activating gene 2
RFX5 regulatory factor X, 5 (influences HLA class II expression)
RFXANK regulatory factor X-associated ankyrin-containing protein
RFXAP regulatory factor X-associated protein
ZAP70 zeta-chain (TCR) associated protein kinase 70kDa