short cochlear 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 inner and outer hair cells (Mammalian Phenotype Ontology, MP_0004524)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004524
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Genes

11 gene mutations causing the short cochlear hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DFNB31 deafness, autosomal recessive 31
EPS8 epidermal growth factor receptor pathway substrate 8
EPS8L2 EPS8-like 2
ESPN espin
GFI1 growth factor independent 1 transcription repressor
GRXCR1 glutaredoxin, cysteine rich 1
MYO15A myosin XVA
MYO7A myosin VIIA
PCDH15 protocadherin-related 15
PTPRQ protein tyrosine phosphatase, receptor type, Q
RDX radixin