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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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