absent vestibulocochlear ganglion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence 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_0004313)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004313
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2 gene mutations causing the absent vestibulocochlear ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
SHH sonic hedgehog
SIX1 SIX homeobox 1