abnormal outer hair cell kinocilium morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the nonmotile primary cilium that is found at the apical surface of outer hair cells (Mammalian Phenotype Ontology, MP_0011062)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011062
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7 gene mutations causing the abnormal outer hair cell kinocilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDH23 cadherin-related 23
CELSR1 cadherin, EGF LAG seven-pass G-type receptor 1
MYO6 myosin VI
PCDH15 protocadherin-related 15
PDZD7 PDZ domain containing 7
PTK7 protein tyrosine kinase 7 (inactive)
USH1G Usher syndrome 1G (autosomal recessive)