deafness Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A decreased magnitude of the sensory perception of sound. (Human Phenotype Ontology, HP_0000365)
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10 genes associated with the disease deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
GJB2 gap junction protein, beta 2, 26kDa
GJB3 gap junction protein, beta 3, 31kDa
GJB6 gap junction protein, beta 6, 30kDa
MYH9 myosin, heavy chain 9, non-muscle
MYO6 myosin VI
POU3F4 POU class 3 homeobox 4
RNR1 RNA, ribosomal cluster 1
SLC26A4 solute carrier family 26 (anion exchanger), member 4
UCN urocortin