abnormal cochlear endolymph ionic homeostasis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the state of equilibrium in the cochlear endolymph with respect to charged molecules; cochlear endolymph is not only an unusual extracellular fluid for its high potassium ion and low sodium ion concentration but also for its low calcium ion concentration, high HCO3- concentration and low protein content (Mammalian Phenotype Ontology, MP_0006403)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006403
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Genes

3 gene mutations causing the abnormal cochlear endolymph ionic homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
GJB6 gap junction protein, beta 6, 30kDa
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
SLC26A4 solute carrier family 26 (anion exchanger), member 4