hearing loss, sensorineural; sensorineural 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

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

Symbol Name
APOE apolipoprotein E
CLDN23 claudin 23
DEFA3 defensin, alpha 3, neutrophil-specific
GJB2 gap junction protein, beta 2, 26kDa
GJB6 gap junction protein, beta 6, 30kDa
GJC3 gap junction protein, gamma 3, 30.2kDa
MRPS18CP2 mitochondrial ribosomal protein S18C pseudogene 2
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
RNR1 RNA, ribosomal cluster 1
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
TECTA tectorin alpha