Tinnitus Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Tinnitus is an auditory perception that can be described as the experience of sound, in the ear or in the head, in the absence of external acoustic stimulation. (Human Phenotype Ontology, HP_0000360)
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Genes

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

Symbol Name
KCNE1 potassium channel, voltage gated subfamily E regulatory beta subunit 1
KCNE3 potassium channel, voltage gated subfamily E regulatory beta subunit 3
SLC12A2 solute carrier family 12 (sodium/potassium/chloride transporter), member 2
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4