abnormal 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 auditory receptor cells (Mammalian Phenotype Ontology, MP_0011060)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011060
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14 gene mutations causing the abnormal 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
FGF10 fibroblast growth factor 10
GRXCR1 glutaredoxin, cysteine rich 1
IGF1R insulin-like growth factor 1 receptor
MKKS McKusick-Kaufman syndrome
MYO6 myosin VI
PAX8 paired box 8
PCDH15 protocadherin-related 15
PDZD7 PDZ domain containing 7
PTK7 protein tyrosine kinase 7 (inactive)
TMPRSS3 transmembrane protease, serine 3
USH1G Usher syndrome 1G (autosomal recessive)
WDPCP WD repeat containing planar cell polarity effector