small cochlear ganglion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced size of the cochlear ganglion or of the sensory neuron 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_0003986)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003986
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Genes

15 gene mutations causing the small cochlear ganglion 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
IGF1 insulin-like growth factor 1 (somatomedin C)
LHFPL5 lipoma HMGIC fusion partner-like 5
MPV17 MpV17 mitochondrial inner membrane protein
MYO15A myosin XVA
NTF3 neurotrophin 3
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
NTRK3 neurotrophic tyrosine kinase, receptor, type 3
PCDH15 protocadherin-related 15
POU4F1 POU class 4 homeobox 1
SLITRK6 SLIT and NTRK-like family, member 6