absent endocochlear potential Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the electrical potential difference between the endolymphatic and perilymphatic compartments of the cochlea, indicating a primary defect in fluid homeostasis of the inner ear (Mammalian Phenotype Ontology, MP_0004410)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004410
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Genes

7 gene mutations causing the absent endocochlear potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP6V0A4 ATPase, H+ transporting, lysosomal V0 subunit a4
FOXI1 forkhead box I1
GJB6 gap junction protein, beta 6, 30kDa
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
SCARB2 scavenger receptor class B, member 2
SLC26A4 solute carrier family 26 (anion exchanger), member 4