Respiratory Insufficiency Gene Set

Dataset	HuGE Navigator Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	Failure to adequately provide oxygen to cells of the body and to remove excess carbon dioxide. (Human Phenotype Ontology, HP_0002093)
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Genes

10 genes associated with the Respiratory Insufficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol	Name
ABCB1	ATP-binding cassette, sub-family B (MDR/TAP), member 1
ABO	ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase)
ACE	angiotensin I converting enzyme
ADRB2	adrenoceptor beta 2, surface
CFTR	cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
LTA	lymphotoxin alpha
OPRM1	opioid receptor, mu 1
SFTPB	surfactant protein B
SOD2	superoxide dismutase 2, mitochondrial
TNF	tumor necrosis factor