vestibular hair cell degeneration Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	degeneration or loss of the sensory epithelial cells of the maculae and cristae of the membranous labyrinth of the inner ear which are normally in synaptic contact with the vestibular nerve (Mammalian Phenotype Ontology, MP_0004324)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004324
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Genes

12 gene mutations causing the vestibular hair cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
CLIC5	chloride intracellular channel 5
ESPN	espin
GRXCR1	glutaredoxin, cysteine rich 1
KCNJ10	potassium channel, inwardly rectifying subfamily J, member 10
KIT	v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
LOC102723475	putative uncharacterized protein LOC388820
MYO6	myosin VI
POU4F3	POU class 4 homeobox 3
SLC26A4	solute carrier family 26 (anion exchanger), member 4
TMPRSS3	transmembrane protease, serine 3
USH1C	Usher syndrome 1C (autosomal recessive, severe)
USH1G	Usher syndrome 1G (autosomal recessive)