abnormal inner ear canal fusion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly or mistiming of the fusion of the canal primordia during development (Mammalian Phenotype Ontology, MP_0002859)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002859
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3 gene mutations causing the abnormal inner ear canal fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CHD7 chromodomain helicase DNA binding protein 7
HMX2 H6 family homeobox 2
NTN1 netrin 1