|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||absence of the nonmotile primary cilium that is found at the apical surface of inner hair cells (Mammalian Phenotype Ontology, MP_0011063)|
|Downloads & Tools|
1 gene mutations causing the absent inner hair cell kinocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|GRXCR1||glutaredoxin, cysteine rich 1|