chronic mucocutaneous candidiasis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp. (Human Disease Ontology, DOID_2058)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002728
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Genes

12 genes associated with the chronic mucocutaneous candidiasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AIRE autoimmune regulator
CARD9 caspase recruitment domain family, member 9
CIITA class II, major histocompatibility complex, transactivator
CLEC7A C-type lectin domain family 7, member A
EPG5 ectopic P-granules autophagy protein 5 homolog (C. elegans)
IL17F interleukin 17F
IL17RA interleukin 17 receptor A
IL2RG interleukin 2 receptor, gamma
RFX5 regulatory factor X, 5 (influences HLA class II expression)
RFXANK regulatory factor X-associated ankyrin-containing protein
RFXAP regulatory factor X-associated protein
STAT1 signal transducer and activator of transcription 1, 91kDa