emphysema Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A subcategory of chronic obstructive pulmonary disease (COPD). It occurs in people who smoke and suffer from chronic bronchitis. It is characterized by inflation of the alveoli, alveolar wall damage, and reduction in the number of alveoli, resulting in difficulty breathing. (Experimental Factor Ontology, EFO_0000464)
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Genes

16 genes associated with the disease emphysema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ADARB2 adenosine deaminase, RNA-specific, B2 (non-functional)
BICD1 bicaudal D homolog 1 (Drosophila)
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1
CYP2A13 cytochrome P450, family 2, subfamily A, polypeptide 13
CYP2A6 cytochrome P450, family 2, subfamily A, polypeptide 6
CYP2E1 cytochrome P450, family 2, subfamily E, polypeptide 1
EPHX1 epoxide hydrolase 1, microsomal (xenobiotic)
GSTM1 glutathione S-transferase mu 1
GSTP1 glutathione S-transferase pi 1
GSTT1 glutathione S-transferase theta 1
HMOX1 heme oxygenase 1
MMP9 matrix metallopeptidase 9
SERPINE2 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 2
SFTPB surfactant protein B
TGFB1 transforming growth factor, beta 1
TNF tumor necrosis factor