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 |
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 |