Kawasaki disease Gene Set

Dataset GWAS Catalog SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A lymphadenitis characterized by swelling of cervical lymph nodes in infants and young children and inflammation of medium-sized blood vessels located_in body, has_symptom fever, has_symptom congestion of ocular conjunctivae, has_symptom reddening of lips, has_symptom reddening of oral cavity, has_symptom protuberance of tongue papillae and has_symptom edema of extremities. (Human Disease Ontology, DOID_13378)
External Link https://www.ebi.ac.uk/gwas/search?query=Kawasaki disease
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Genes

10 genes associated with the Kawasaki disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
FCGR2A Fc fragment of IgG, low affinity IIa, receptor (CD32) 0.602611
CENPU centromere protein U 0.389385
TECRL trans-2,3-enoyl-CoA reductase-like 0.295129
MED30 mediator complex subunit 30 0.266721
NAALADL2 N-acetylated alpha-linked acidic dipeptidase-like 2 0.220915
PELI1 pellino E3 ubiquitin protein ligase 1 0.165905
ZFHX3 zinc finger homeobox 3 0.165905
IGH immunoglobulin heavy locus 0.057619
BTBD1 BTB (POZ) domain containing 1 0.057619
PPM1L protein phosphatase, Mg2+/Mn2+ dependent, 1L 0.042592