abnormality of t cell physiology 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_0011840)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011840
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22 genes associated with the abnormality of t cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AK2 adenylate kinase 2
CASP10 caspase 10, apoptosis-related cysteine peptidase
CASP8 caspase 8, apoptosis-related cysteine peptidase
CD40LG CD40 ligand
CIITA class II, major histocompatibility complex, transactivator
COG6 component of oligomeric golgi complex 6
EPG5 ectopic P-granules autophagy protein 5 homolog (C. elegans)
FAS Fas cell surface death receptor
FASLG Fas ligand (TNF superfamily, member 6)
ICOS inducible T-cell co-stimulator
JAK3 Janus kinase 3
MAGT1 magnesium transporter 1
PNP purine nucleoside phosphorylase
RAB27A RAB27A, member RAS oncogene family
RFX5 regulatory factor X, 5 (influences HLA class II expression)
RFXANK regulatory factor X-associated ankyrin-containing protein
RFXAP regulatory factor X-associated protein
SLC39A4 solute carrier family 39 (zinc transporter), member 4
TBX1 T-box 1
TNFRSF13B tumor necrosis factor receptor superfamily, member 13B
UMPS uridine monophosphate synthetase
WAS Wiskott-Aldrich syndrome