absent outer hair cell stereocilia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description complete absence of the nonmotile, actin-filled specialized microvilli (stereocilia) which are normally arrayed on cochlear outer hair cells (Mammalian Phenotype Ontology, MP_0004530)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004530
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Genes

8 gene mutations causing the absent outer hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
CDH23 cadherin-related 23
CLDN14 claudin 14
GFI1 growth factor independent 1 transcription repressor
LOC102723475 putative uncharacterized protein LOC388820
MSRB3 methionine sulfoxide reductase B3
POU4F3 POU class 4 homeobox 3