short cochlear outer hair cells Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced height of the sensory cells of the organ of Corti which are in synaptic contact with sensory as well as efferent fibers of the auditory nerve (Mammalian Phenotype Ontology, MP_0004466)
External Link
Similar Terms
Downloads & Tools


5 gene mutations causing the short cochlear outer hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
MYO7A myosin VIIA
SLC26A5 solute carrier family 26 (anion exchanger), member 5
THRB thyroid hormone receptor, beta
UCN urocortin
USH1G Usher syndrome 1G (autosomal recessive)