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. 2015 Apr 17;20:383. doi: 10.11604/pamj.2015.20.383.5230

Table 2.

Genes implicated in cases of autosomal recessive non-syndromic hearing loss

Function Genes
Cochlear Homeostasis Gap Junctions: GJB2, GJB6, GJB3
Tight Junctions: CLDN14, TRIC
SLC26A4
Cellular Organization Myosins: MYO3A, MYO6, MYO7A, MYO15A
TRIOBP, WHRN, USH1C, CDH23
Tectorial Membranes Associated Proteins TECTA, COL11A2, STRC
Neural transmission OTOF, PJVK
Other or Unknown function TMC1, TMPRSS3, LOXHD1, PDZD7, GIPC3

Adapted from [57]