abnormal inner 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 inner hair cells (Mammalian Phenotype Ontology, MP_0011061)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011061
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Genes

5 gene mutations causing the abnormal inner hair cell kinocilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDH23 cadherin-related 23
GRXCR1 glutaredoxin, cysteine rich 1
IGF1R insulin-like growth factor 1 receptor
MKKS McKusick-Kaufman syndrome
PCDH15 protocadherin-related 15