Deafness Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A decreased magnitude of the sensory perception of sound. (Human Phenotype Ontology, HP_0000365)
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33 genes associated with the Deafness phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ALMS1 Alstrom syndrome protein 1
CLDN14 claudin 14
EGR2 early growth response 2
ERBB4 erb-b2 receptor tyrosine kinase 4
FOXI1 forkhead box I1
GJB1 gap junction protein, beta 1, 32kDa
GJB2 gap junction protein, beta 2, 26kDa
GJB3 gap junction protein, beta 3, 31kDa
GJB6 gap junction protein, beta 6, 30kDa
GJE1 gap junction protein, epsilon 1, 23kDa
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
KCNQ4 potassium channel, voltage gated KQT-like subfamily Q, member 4
KIF1B kinesin family member 1B
LRTOMT leucine rich transmembrane and O-methyltransferase domain containing
MPZ myelin protein zero
MTMR2 myotubularin related protein 2
MTRNR2L1 MT-RNR2-like 1
MYH9 myosin, heavy chain 9, non-muscle
MYO7A myosin VIIA
NDRG1 N-myc downstream regulated 1
OTOF otoferlin
PDS5A PDS5 cohesin associated factor A
PMP22 peripheral myelin protein 22
PRPH peripherin
PRX periaxin
SLC26A4 solute carrier family 26 (anion exchanger), member 4
TJP2 tight junction protein 2
TMC1 transmembrane channel-like 1
TMIE transmembrane inner ear
TMPRSS3 transmembrane protease, serine 3
TYMP thymidine phosphorylase