recurrent skin infections Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Infections of the skin that happen multiple times. (Human Phenotype Ontology, HP_0001581)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001581
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Genes

30 genes associated with the recurrent skin infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AIRE autoimmune regulator
BTD biotinidase
BTK Bruton agammaglobulinemia tyrosine kinase
CARD9 caspase recruitment domain family, member 9
CFI complement factor I
CHST14 carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 14
CIITA class II, major histocompatibility complex, transactivator
CLEC7A C-type lectin domain family 7, member A
CTSC cathepsin C
CYBA cytochrome b-245, alpha polypeptide
CYBB cytochrome b-245, beta polypeptide
DSG1 desmoglein 1
EPG5 ectopic P-granules autophagy protein 5 homolog (C. elegans)
GJB2 gap junction protein, beta 2, 26kDa
GJC2 gap junction protein, gamma 2, 47kDa
IL10RA interleukin 10 receptor, alpha
IL17F interleukin 17F
IL17RA interleukin 17 receptor A
IL2RG interleukin 2 receptor, gamma
LYST lysosomal trafficking regulator
MNX1 motor neuron and pancreas homeobox 1
NCF1 neutrophil cytosolic factor 1
NCF2 neutrophil cytosolic factor 2
PSEN1 presenilin 1
PSENEN presenilin enhancer gamma secretase subunit
PSTPIP1 proline-serine-threonine phosphatase interacting protein 1
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