Impetigo Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A pyoderma consisting of three forms of skin lesions having either a thick, adherent, recurrent, dirty yellow crust with an erythematous margin (common or superficial impetigo) or lessions which are superficial, thin-walled, and bullous as found in bullous impetigo. The lesions in bullous (staphylococcal) impetigo, which are always caused by S aureus, are superficial, thin-walled, and bullous. (Human Disease Ontology, DOID_8504)
External Link https://www.disgenet.org/browser/0/1/0/C0021099
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Genes

9 genes associated with the disease Impetigo in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
DSG1 desmoglein 1
EDNRA endothelin receptor type A
EDNRB endothelin receptor type B
GALNS galactosamine (N-acetyl)-6-sulfatase
GAST gastrin
PAGR1 PAXIP1 associated glutamate-rich protein 1
PLG plasminogen
SLC9A6 solute carrier family 9, subfamily A (NHE6, cation proton antiporter 6), member 6
SUMF2 sulfatase modifying factor 2