short outer hair cell stereocilia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced length of the nonmotile, actin-filled specialized microvilli (stereocilia) which are normally arrayed on cochlear outer hair cells (Mammalian Phenotype Ontology, MP_0004531)
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4 gene mutations causing the short outer hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DFNB31 deafness, autosomal recessive 31
MYO15A myosin XVA
PTPRQ protein tyrosine phosphatase, receptor type, Q
RDX radixin