abnormal delayed hypersensitivity skin test Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Delay in cutaneous immune reaction to specific antigens mediated not by antibodies but by cells. The delayed hypersensitivity test is an immune function test measuring the presence of activated T cells that recognize a specific antigen and is performed by injecting a small amount of the antigen into the skin. The area of the injection is examined 48-72 hours thereafter. (Human Phenotype Ontology, HP_0002963)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002963
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Genes

11 genes associated with the abnormal delayed hypersensitivity skin test phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CASP10 caspase 10, apoptosis-related cysteine peptidase
CIITA class II, major histocompatibility complex, transactivator
EPG5 ectopic P-granules autophagy protein 5 homolog (C. elegans)
FAS Fas cell surface death receptor
FASLG Fas ligand (TNF superfamily, member 6)
JAK3 Janus kinase 3
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
WAS Wiskott-Aldrich syndrome