abnormal cochlear nerve compound action potential Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the combined potentials resulting from activation of the auditory division of the eighth cranial nerve; these potentials represent the summed activity of multiple cochlear afferent fibers discharging synchronously and thus assess the combined functional state of OHCs, IHCs, and their primary afferent innervation (Mammalian Phenotype Ontology, MP_0004415)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004415
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Genes

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

Symbol Name
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
BSN bassoon presynaptic cytomatrix protein
CDH23 cadherin-related 23
CHD7 chromodomain helicase DNA binding protein 7
CHRNA9 cholinergic receptor, nicotinic, alpha 9 (neuronal)
EMX2 empty spiracles homeobox 2
EPS8L2 EPS8-like 2
ESPN espin
FGFR1 fibroblast growth factor receptor 1
GRXCR1 glutaredoxin, cysteine rich 1
MIR96 microRNA 96
MYO6 myosin VI
MYO7A myosin VIIA
NFKB1 nuclear factor of kappa light polypeptide gene enhancer in B-cells 1
OTOA otoancorin
OTOS otospiralin
SLC17A8 solute carrier family 17 (vesicular glutamate transporter), member 8
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)
THRB thyroid hormone receptor, beta