decreased endocochlear potential Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduction of the electrical potential difference between the endolymphatic and perilymphatic compartments of the cochlea (Mammalian Phenotype Ontology, MP_0004411)
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11 gene mutations causing the decreased endocochlear potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CLDN11 claudin 11
FBXO11 F-box protein 11
FGFR1 fibroblast growth factor receptor 1
GJB6 gap junction protein, beta 6, 30kDa
GRID1 glutamate receptor, ionotropic, delta 1
POU3F4 POU class 3 homeobox 4
SCARB2 scavenger receptor class B, member 2
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SLC4A11 solute carrier family 4, sodium borate transporter, member 11
TYRP1 tyrosinase-related protein 1