abnormal endolymph Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	any alteration in the normal production (volume) or ionic homeostasis of the fluid contained within the membranous labyrinth of the inner ear; unlike perilymph, endolymph resembles intracellular fluid in composition and has a high concentration of potassium ion and a low concentration of sodium ion (Mammalian Phenotype Ontology, MP_0004885)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004885
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Genes

17 gene mutations causing the abnormal 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
EFNB2	ephrin-B2
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