abnormality of t cell number Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A deviation from the normal count of T cells. (Human Phenotype Ontology, HP_0011839)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011839
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
ACP5 acid phosphatase 5, tartrate resistant
ATM ATM serine/threonine kinase
CASP10 caspase 10, apoptosis-related cysteine peptidase
CD247 CD247 molecule
CD8A CD8a molecule
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)
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