hearing loss/deafness Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description disease cluster belonging to disease group other (Genetic Association Database)
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Genes

14 genes associated with the disease hearing loss/deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ESPN espin
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
GJB2 gap junction protein, beta 2, 26kDa
GJB6 gap junction protein, beta 6, 30kDa
ITGA1 integrin, alpha 1
ITGA3 integrin, alpha 3 (antigen CD49C, alpha 3 subunit of VLA-3 receptor)
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
PLAT plasminogen activator, tissue
PON1 paraoxonase 1
PON2 paraoxonase 2
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SOD2 superoxide dismutase 2, mitochondrial