Hyperoxia Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description elevated concentration of O2 in the blood, alveoli or other tissues resulting in the increased pressure of this component of body gases (Mammalian Phenotype Ontology, MP_0002319)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D018496
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Genes

3 genes/proteins associated with the disease Hyperoxia from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1 2.88009
AHR aryl hydrocarbon receptor 2.88009
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A 2.88009