abnormal cochlear endolymph Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description change in the normal production (volume) or ionic homeostasis of the fluid contained within the cochlea of the inner ear (Mammalian Phenotype Ontology, MP_0006390)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006390
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Genes

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

Symbol Name
ATP6V0A4 ATPase, H+ transporting, lysosomal V0 subunit a4
CLDN11 claudin 11
ESPN espin
FBXO11 F-box protein 11
FGFR1 fibroblast growth factor receptor 1
FOXI1 forkhead box I1
GJB6 gap junction protein, beta 6, 30kDa
GRID1 glutamate receptor, ionotropic, delta 1
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
POU3F4 POU class 3 homeobox 4
SCARB2 scavenger receptor class B, member 2
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SLC4A11 solute carrier family 4, sodium borate transporter, member 11
TYRP1 tyrosinase-related protein 1