impaired t cell function Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005435
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Genes

7 genes associated with the impaired t cell function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COG6 component of oligomeric golgi complex 6
ICOS inducible T-cell co-stimulator
PNP purine nucleoside phosphorylase
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