abnormal cochlear microphonics Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the bioelectric potentials produced by the hair cells of the organ of Corti in response to sound; the cochlear microphonic (CM) is an electric response dominated by OHC receptor potentials from the basal turn of the cochlea and provides a measure of transducer function in OHCs; in an active ear, CM waveforms show post-stimulus ringing (i.e. a cochlear echo) whereas in a passive ear system, CM decays at the cessation of the tone burst (Mammalian Phenotype Ontology, MP_0004412)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004412
Similar Terms
Downloads & Tools


13 gene mutations causing the abnormal cochlear microphonics 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
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)