respiratory system disease Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A disease of anatomical entity that located_in the respiratory system which extends from the nasal sinuses to the diaphragm. (Human Disease Ontology, DOID_1579)
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Genes

19 genes involed in the disease respiratory system 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
FLCN folliculin
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