lung disease Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A lower respiratory tract disease in which the function of the lungs is adversely affected by narrowing or blockage of the airways resulting in poor air flow, a loss of elasticity in the lungs that produces a decrease in the total volume of air that the lungs are able to hold, and clotting, scarring, or inflammation of the blood vessels that affect the ability of the lungs to take up oxygen and to release carbon dioxide. (Human Disease Ontology, DOID_850)
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18 genes involed in the disease lung disease 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)
ELMOD2 ELMO/CED-12 domain containing 2
IRAK3 interleukin-1 receptor-associated kinase 3
MICA MHC class I polypeptide-related sequence A
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)
SFTPA1 surfactant protein A1
SFTPA2 surfactant protein A2
SFTPC surfactant protein C
TBX21 T-box 21
TERT telomerase reverse transcriptase
TSC1 tuberous sclerosis 1
TSC2 tuberous sclerosis 2