Asthma Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores 2025
Category disease or phenotype associations
Type disease
Description A chronic respiratory disease manifested as difficulty breathing due to the narrowing of bronchial passageways.|Tendency of the smooth muscle of the tracheobronchial tree to contract more intensely in response to a given stimulus than it does in the response seen in normal individuals. This condition is present in virtually all symptomatic patients with asthma. The most prominent manifestation of this smooth muscle contraction is a decrease in airway caliber that can be readily measured in the pulmonary function laboratory.|A form of bronchial disorder with three distinct components: airway hyper-responsiveness (RESPIRATORY HYPERSENSITIVITY), airway INFLAMMATION, and intermittent AIRWAY OBSTRUCTION. It is characterized by spasmodic contraction of airway smooth muscle, WHEEZING, and dyspnea (DYSPNEA, PAROXYSMAL).|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 resulting in recurring periods of wheezing (a whistling sound while breathing), chest tightness, shortness of breath, mucus production and coughing. The symptoms appear due to a variety of triggers such as allergens, irritants, respiratory infections, weather changes, excercise, stress, reflux disease, medications, foods and emotional anxiety. (Experimental Factor Ontology, EFO_0000270)
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Genes

12 genes involed in the disease Asthma from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Symbol Name Standardized Value
PLA2G7 phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma) 4.0
TBX21 T-box 21 4.0
IRAK3 interleukin-1 receptor-associated kinase 3 4.0
NPSR1 neuropeptide S receptor 1 4.0
ADAM33 ADAM metallopeptidase domain 33 4.0
ORMDL3 ORMDL sphingolipid biosynthesis regulator 3 4.0
PTGDR prostaglandin D2 receptor (DP) 4.0
CDHR3 cadherin-related family member 3 4.0
CHI3L1 chitinase 3-like 1 (cartilage glycoprotein-39) 4.0
DENND1B DENN/MADD domain containing 1B 4.0
MUC7 mucin 7, secreted 4.0
DPP10 dipeptidyl-peptidase 10 (non-functional) 4.0