abnormal basilar membrane morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the membrane extending from the bony spiral membrane to the basilar crest of the cochlea; it forms the greater part of the floor of the cochlear duct separating the latter from the scala tympani, and it supports the organ of Corti (Mammalian Phenotype Ontology, MP_0004308)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004308
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3 gene mutations causing the abnormal basilar membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APOE apolipoprotein E
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
POU4F3 POU class 4 homeobox 3