absent cochlear nerve compound action potential Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the combined potentials resulting from activation of the auditory division of the eighth cranial nerve (Mammalian Phenotype Ontology, MP_0004416)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004416
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5 gene mutations causing the absent cochlear nerve compound action potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ESPN espin
MIR96 microRNA 96
MYO6 myosin VI
SLC17A8 solute carrier family 17 (vesicular glutamate transporter), member 8
SOX2 SRY (sex determining region Y)-box 2