abnormal vestibulocochlear nerve morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the composite sensory nerve innervating the receptor cells of the membranous labyrinth; it consists of two major, anatomically and functionally distinct components, each of which have different central connections: the vestibular nerve and the cochlear nerve (Mammalian Phenotype Ontology, MP_0001072)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001072
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20 gene mutations causing the abnormal vestibulocochlear 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
BDNF brain-derived neurotrophic factor
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
CHD7 chromodomain helicase DNA binding protein 7
ERBB4 erb-b2 receptor tyrosine kinase 4
EYA1 EYA transcriptional coactivator and phosphatase 1
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
NRP1 neuropilin 1
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
NTRK3 neurotrophic tyrosine kinase, receptor, type 3
OTULIN OTU deubiquitinase with linear linkage specificity
PAX2 paired box 2
SOD1 superoxide dismutase 1, soluble
TBX1 T-box 1
TBX10 T-box 10