fused inner hair cell stereocilia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description coalescence of the nonmotile, actin-filled specialized microvilli (stereocilia) normally arrayed on cochlear inner hair cells, often resulting in giant stereocilia (Mammalian Phenotype Ontology, MP_0004533)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004533
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Genes

7 gene mutations causing the fused inner hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
MYO6 myosin VI
MYO7A myosin VIIA
PTPRQ protein tyrosine phosphatase, receptor type, Q
RDX radixin
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SYNJ2 synaptojanin 2
TRIOBP TRIO and F-actin binding protein