abnormal cochlear frequency tuning Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the frequency resolution of the cochlea, normally determined by the passive mechanical properties of the basilar membrane and active feedback from the outer hair cells which detect and amplify sound-induced basilar membrane motions (Mammalian Phenotype Ontology, MP_0006383)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006383
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1 gene mutations causing the abnormal cochlear frequency tuning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
TECTB tectorin beta