|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||absence or loss of motility of the cochlear OHCs in response to electrical stimulation (Mammalian Phenotype Ontology, MP_0004436)|
|Downloads & Tools|
1 gene mutations causing the absent cochlear outer hair cell electromotility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|SLC26A5||solute carrier family 26 (anion exchanger), member 5|