abnormal cochlear ihc afferent innervation pattern Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any changes in the placement, morphology or number of afferent terminals and/or their synapses in the cochlear IHC region (Mammalian Phenotype Ontology, MP_0004746)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004746
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Genes

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

Symbol Name
ACAN aggrecan
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
CALCB calcitonin-related polypeptide beta
ESR2 estrogen receptor 2 (ER beta)
GABRB3 gamma-aminobutyric acid (GABA) A receptor, beta 3
KCNMA1 potassium channel, calcium activated large conductance subfamily M alpha, member 1
NTRK3 neurotrophic tyrosine kinase, receptor, type 3
PSAP prosaposin
SLITRK6 SLIT and NTRK-like family, member 6