Legionnaires' Disease Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A legionellosis that is characterized by severe form of infection producing pneumonia. Symptoms include fever, chills, and cough. (Human Disease Ontology, DOID_10457)
External Link https://www.disgenet.org/browser/0/1/0/C0023241
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Genes

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

Symbol Name
CASP1 caspase 1, apoptosis-related cysteine peptidase
CRP C-reactive protein, pentraxin-related
IFNG interferon, gamma
MIP major intrinsic protein of lens fiber
MYD88 myeloid differentiation primary response 88
NAIP NLR family, apoptosis inhibitory protein
NFE2 nuclear factor, erythroid 2
NTAN1 N-terminal asparagine amidase
POMC proopiomelanocortin
PSMC5 proteasome (prosome, macropain) 26S subunit, ATPase, 5
SKP2 S-phase kinase-associated protein 2, E3 ubiquitin protein ligase
STING1 stimulator of interferon response cGAMP interactor 1
TLR1 toll-like receptor 1
TLR2 toll-like receptor 2
TLR4 toll-like receptor 4
TLR5 toll-like receptor 5
TLR6 toll-like receptor 6
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A
TNFRSF1B tumor necrosis factor receptor superfamily, member 1B
TOLLIP toll interacting protein