abnormal inner ear development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description atypical initial production, differentiation, migration or maturation of the labyrinth, including the semicircular canals, vestibule and cochlea (Mammalian Phenotype Ontology, MP_0011238)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011238
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6 gene mutations causing the abnormal 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