abnormal cochlear potential Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the evoked response of the cochlea (Mammalian Phenotype Ontology, MP_0006332)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006332
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14 gene mutations causing the abnormal cochlear potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALG10 ALG10, alpha-1,2-glucosyltransferase
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
CHD7 chromodomain helicase DNA binding protein 7
CLRN1 clarin 1
ESPN espin
GJB6 gap junction protein, beta 6, 30kDa
MYO7A myosin VIIA
OTOS otospiralin
PDZD7 PDZ domain containing 7
SLC26A5 solute carrier family 26 (anion exchanger), member 5
STRC stereocilin
TECTA tectorin alpha
THRB thyroid hormone receptor, beta
USH1G Usher syndrome 1G (autosomal recessive)