abnormal orientation of inner hair cell stereociliary bundles Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	misorientation or rotation of inner hair cell (IHC) stereociliary bundles, resulting in defective planar cell polarity of the inner ear sensory epithelium (Mammalian Phenotype Ontology, MP_0004492)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004492
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Genes

12 gene mutations causing the abnormal orientation of inner hair cell stereociliary bundles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
CDH23	cadherin-related 23
FGFR1	fibroblast growth factor receptor 1
JAG2	jagged 2
MYO6	myosin VI
MYO7A	myosin VIIA
NR2F1	nuclear receptor subfamily 2, group F, member 1
PCDH15	protocadherin-related 15
PTK7	protein tyrosine kinase 7 (inactive)
PTPRQ	protein tyrosine phosphatase, receptor type, Q
SEC24B	SEC24 family member B
USH1C	Usher syndrome 1C (autosomal recessive, severe)
VANGL2	VANGL planar cell polarity protein 2