abnormal vestibulocochlear ganglion morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the group of neuron cell bodies associated with the eighth cranial nerve during embryogenesis; splits in later development to form the cochlear and vestibular ganglia (Mammalian Phenotype Ontology, MP_0003703)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003703
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15 gene mutations causing the abnormal vestibulocochlear ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALDH1A2 aldehyde dehydrogenase 1 family, member A2
CHD7 chromodomain helicase DNA binding protein 7
CHRD chordin
ERBB4 erb-b2 receptor tyrosine kinase 4
FGF3 fibroblast growth factor 3
FGFR2 fibroblast growth factor receptor 2
HOXA1 homeobox A1
MCOLN3 mucolipin 3
NTF3 neurotrophin 3
PAX2 paired box 2
POU4F3 POU class 4 homeobox 3
RDH10 retinol dehydrogenase 10 (all-trans)
SHH sonic hedgehog
SIX1 SIX homeobox 1
TBX1 T-box 1