hearing impairment; hearing loss Gene Set

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

17 genes associated with the disease hearing impairment; hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
DFNB59 deafness, autosomal recessive 59
GJA1 gap junction protein, alpha 1, 43kDa
GJB2 gap junction protein, beta 2, 26kDa
GJB3 gap junction protein, beta 3, 31kDa
GJB4 gap junction protein, beta 4, 30.3kDa
GJB6 gap junction protein, beta 6, 30kDa
GJC3 gap junction protein, gamma 3, 30.2kDa
GSTM1 glutathione S-transferase mu 1
GSTT1 glutathione S-transferase theta 1
KCNE1 potassium channel, voltage gated subfamily E regulatory beta subunit 1
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
MT-TS1 tRNA
RNR1 RNA, ribosomal cluster 1
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SLC26A5 solute carrier family 26 (anion exchanger), member 5
SOD2 superoxide dismutase 2, mitochondrial
TECTA tectorin alpha