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
Similar Terms
Downloads & Tools


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)