cochlear ganglion hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or reduced size, usually due to a reduced number of cells, 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_0003637)
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10 gene mutations causing the cochlear ganglion hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDH23 cadherin-related 23
CYS1 cystin 1
FGF3 fibroblast growth factor 3
GABRB3 gamma-aminobutyric acid (GABA) A receptor, beta 3
HR hair growth associated
MPV17 MpV17 mitochondrial inner membrane protein
MYO15A myosin XVA
NTF3 neurotrophin 3
PCDH15 protocadherin-related 15
POU4F1 POU class 4 homeobox 1