abnormal cochlear nerve morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the part of the vestibulocochlear nerve [CN VIII] peripheral to the cochlear root; composed of the central nerve processes of the bipolar neurons of the spiral ganglion, which have their peripheral processes on the four rows of neuroepithelial cells (hair cells) of the spiral organ (Mammalian Phenotype Ontology, MP_0004716)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004716
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Genes

11 gene mutations causing the abnormal cochlear nerve morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADGRG6 adhesion G protein-coupled receptor G6
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
GABRB3 gamma-aminobutyric acid (GABA) A receptor, beta 3
HOXA1 homeobox A1
IGF1 insulin-like growth factor 1 (somatomedin C)
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
LAMA2 laminin, alpha 2
NTRK3 neurotrophic tyrosine kinase, receptor, type 3
PAX2 paired box 2
SOD1 superoxide dismutase 1, soluble