Immunologic Deficiency Syndromes Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

23 genes associated with the Immunologic Deficiency Syndromes phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
AICDA activation-induced cytidine deaminase
BRAF B-Raf proto-oncogene, serine/threonine kinase
BTK Bruton agammaglobulinemia tyrosine kinase
C5 complement component 5
CD40LG CD40 ligand
DCLRE1C DNA cross-link repair 1C
DNMT3B DNA (cytosine-5-)-methyltransferase 3 beta
FCGR3A Fc fragment of IgG, low affinity IIIa, receptor (CD16a)
IFNG interferon, gamma
IL2RG interleukin 2 receptor, gamma
JAK3 Janus kinase 3
KRAS Kirsten rat sarcoma viral oncogene homolog
LEPR leptin receptor
LIG4 ligase IV, DNA, ATP-dependent
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
RAG1 recombination activating gene 1
RAG2 recombination activating gene 2
SERPINA1 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 1
SH2D1A SH2 domain containing 1A
UNG uracil-DNA glycosylase
WAS Wiskott-Aldrich syndrome
XIAP X-linked inhibitor of apoptosis, E3 ubiquitin protein ligase
ZBTB24 zinc finger and BTB domain containing 24