increased cochlear nerve compound action potential Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater combined potentials resulting from activation of the auditory division of the eighth cranial nerve (Mammalian Phenotype Ontology, MP_0004767)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004767
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Genes

2 gene mutations causing the increased cochlear nerve compound action potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
MYO7A myosin VIIA
SLC26A5 solute carrier family 26 (anion exchanger), member 5