abnormal lymphocyte count Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0040088
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Genes

23 genes associated with the abnormal lymphocyte count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACP5 acid phosphatase 5, tartrate resistant
ADA adenosine deaminase
ATM ATM serine/threonine kinase
CASP10 caspase 10, apoptosis-related cysteine peptidase
CD247 CD247 molecule
CD8A CD8a molecule
DCLRE1C DNA cross-link repair 1C
DNMT3B DNA (cytosine-5-)-methyltransferase 3 beta
EPG5 ectopic P-granules autophagy protein 5 homolog (C. elegans)
FAS Fas cell surface death receptor
FASLG Fas ligand (TNF superfamily, member 6)
GFI1 growth factor independent 1 transcription repressor
ICOS inducible T-cell co-stimulator
IGHM immunoglobulin heavy constant mu
IL2RA interleukin 2 receptor, alpha
IL2RG interleukin 2 receptor, gamma
IL7R interleukin 7 receptor
MAGT1 magnesium transporter 1
NBN nibrin
PTPRC protein tyrosine phosphatase, receptor type, C
RAG1 recombination activating gene 1
RAG2 recombination activating gene 2
WIPF1 WAS/WASL interacting protein family, member 1