abnormal cochlear ohc efferent innervation pattern Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any changes in the morphology or number of efferent terminals, occurring as clusters, in the cochlear OHC region; normally, medial olivocochlear neurons, which are primarily found in rostral and ventral periolivary regions, project mainly to the contralateral cochlea, and terminate directly on OHCs (Mammalian Phenotype Ontology, MP_0004632)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004632
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Genes

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

Symbol Name
CHRNA10 cholinergic receptor, nicotinic, alpha 10 (neuronal)
CHRNA9 cholinergic receptor, nicotinic, alpha 9 (neuronal)
FGFR3 fibroblast growth factor receptor 3
GABRA5 gamma-aminobutyric acid (GABA) A receptor, alpha 5
GABRB2 gamma-aminobutyric acid (GABA) A receptor, beta 2
GABRB3 gamma-aminobutyric acid (GABA) A receptor, beta 3
GFI1 growth factor independent 1 transcription repressor
MYO7A myosin VIIA
PSAP prosaposin
SLITRK6 SLIT and NTRK-like family, member 6