abnormal cochlear ohc afferent innervation pattern Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any changes in the morphology, placement or number of afferent terminals and/or their synapses in the cochlear OHC region (Mammalian Phenotype Ontology, MP_0004747)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004747
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Genes

2 gene mutations causing the abnormal cochlear ohc afferent innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BDNF brain-derived neurotrophic factor
NTRK2 neurotrophic tyrosine kinase, receptor, type 2