abnormal cochlear ihc efferent innervation pattern Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any changes in the morphology of the normally dense plexus of efferent terminals that contact radial fibers of the spiral ganglion below cochlear IHCs or of the sparser plexus of terminals positioned around IHC somata; normally, lateral olivocochlear neurons, which are found in and/or around the lateral superior olive, project mainly to the ipsilateral cochlea and terminate mostly on dendritic fibers below IHCs (Mammalian Phenotype Ontology, MP_0004633)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004633
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7 gene mutations causing the abnormal cochlear ihc efferent innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
CHRNA10 cholinergic receptor, nicotinic, alpha 10 (neuronal)
CHRNA9 cholinergic receptor, nicotinic, alpha 9 (neuronal)
PAX8 paired box 8
PSAP prosaposin
SLC17A8 solute carrier family 17 (vesicular glutamate transporter), member 8
SLITRK6 SLIT and NTRK-like family, member 6