absent inner hair cell kinocilia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the nonmotile primary cilium that is found at the apical surface of inner hair cells (Mammalian Phenotype Ontology, MP_0011063)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011063
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Genes

1 gene mutations causing the absent inner hair cell kinocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
GRXCR1 glutaredoxin, cysteine rich 1