delayed inner ear development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description slowed progression to structurally mature components of the labyrinth, including the semicircular canals, vestibule and cochlea (Mammalian Phenotype Ontology, MP_0004664)
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6 gene mutations causing the delayed inner ear development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DUOX2 dual oxidase 2
GATA3 GATA binding protein 3
IGF1 insulin-like growth factor 1 (somatomedin C)
PAX8 paired box 8
THRB thyroid hormone receptor, beta
TPO thyroid peroxidase