asthma Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing. The symptoms appear due to a variety of triggers such as allergens, irritants, respiratory infections, weather changes, exercise, stress, reflux disease, medications, foods and emotional anxiety. (Human Disease Ontology, DOID_2841)
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10 genes involed in the disease asthma from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ADAM33 ADAM metallopeptidase domain 33
CHI3L1 chitinase 3-like 1 (cartilage glycoprotein-39)
DPP10 dipeptidyl-peptidase 10 (non-functional)
IRAK3 interleukin-1 receptor-associated kinase 3
MUC7 mucin 7, secreted
NPSR1 neuropeptide S receptor 1
ORMDL3 ORMDL sphingolipid biosynthesis regulator 3
PLA2G7 phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma)
PTGDR prostaglandin D2 receptor (DP)
TBX21 T-box 21