absent cochlear ganglion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the group of nerve cell bodies that conveys auditory sensation from the organ of Corti to the hindbrain and resides on the cochlear part of the vestibulocochlear nerve (eighth cranial nerve) (Mammalian Phenotype Ontology, MP_0003146)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003146
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Genes

5 gene mutations causing the absent cochlear ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADGRV1 adhesion G protein-coupled receptor V1
GBX2 gastrulation brain homeobox 2
HOXA1 homeobox A1
PAX2 paired box 2
SLC26A4 solute carrier family 26 (anion exchanger), member 4