stria vascularis degeneration Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description degeneration or loss of the stratified, secretory epithelium which lines the upper part of the cochlear spiral ligament and maintains potassium ion homeostasis in the endolymph (Mammalian Phenotype Ontology, MP_0004363)
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12 gene mutations causing the stria vascularis degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDH23 cadherin-related 23
FZD4 frizzled class receptor 4
GRXCR1 glutaredoxin, cysteine rich 1
LAMA2 laminin, alpha 2
MPV17 MpV17 mitochondrial inner membrane protein
MYO6 myosin VI
MYO7A myosin VIIA
NDP Norrie disease (pseudoglioma)
POLG polymerase (DNA directed), gamma
POU4F3 POU class 4 homeobox 3
SCARB2 scavenger receptor class B, member 2
SLC26A4 solute carrier family 26 (anion exchanger), member 4