absent cochlear microphonics Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence or loss of the bioelectric potentials produced by the hair cells of the organ of Corti in response to sound (Mammalian Phenotype Ontology, MP_0004413)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004413
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6 gene mutations causing the absent cochlear microphonics phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALG10 ALG10, alpha-1,2-glucosyltransferase
CHD7 chromodomain helicase DNA binding protein 7
ESPN espin
MYO7A myosin VIIA
SLC26A5 solute carrier family 26 (anion exchanger), member 5
USH1G Usher syndrome 1G (autosomal recessive)