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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Genes

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
MT-TS1 tRNA
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