decreased cochlear nerve compound action potential Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduction of the combined potentials resulting from activation of the auditory division of the eighth cranial nerve (Mammalian Phenotype Ontology, MP_0004417)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004417
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Genes

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

Symbol Name
BSN bassoon presynaptic cytomatrix protein
CHD7 chromodomain helicase DNA binding protein 7
EMX2 empty spiracles homeobox 2
EPS8L2 EPS8-like 2
GRXCR1 glutaredoxin, cysteine rich 1
MIR96 microRNA 96
NFKB1 nuclear factor of kappa light polypeptide gene enhancer in B-cells 1
OTOS otospiralin
SLC26A5 solute carrier family 26 (anion exchanger), member 5
SOX2 SRY (sex determining region Y)-box 2
TECTA tectorin alpha
TECTB tectorin beta
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)