abnormal cochlear inner hair cell physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly in processes pertinent to the function of cochlear IHCs which constitute the true sensory cell type sending impulses via the cochlear (auditory) nerve (Mammalian Phenotype Ontology, MP_0004433)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004433
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Genes

10 gene mutations causing the abnormal cochlear inner hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BSN bassoon presynaptic cytomatrix protein
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
CHRNA10 cholinergic receptor, nicotinic, alpha 10 (neuronal)
CHRNA9 cholinergic receptor, nicotinic, alpha 9 (neuronal)
HPN hepsin
KCNMA1 potassium channel, calcium activated large conductance subfamily M alpha, member 1
OTOF otoferlin
PAX8 paired box 8
SLC17A8 solute carrier family 17 (vesicular glutamate transporter), member 8
THRB thyroid hormone receptor, beta
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