Hearing Loss, Unilateral Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

4 genes associated with the Hearing Loss, Unilateral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
FOXI1 forkhead box I1
GJB2 gap junction protein, beta 2, 26kDa
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
SLC26A4 solute carrier family 26 (anion exchanger), member 4
Funding