absent cochlear outer hair cell electromotility Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence or loss of motility of the cochlear OHCs in response to electrical stimulation (Mammalian Phenotype Ontology, MP_0004436)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004436
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Genes

1 gene mutations causing the absent cochlear outer hair cell electromotility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
SLC26A5 solute carrier family 26 (anion exchanger), member 5