absent inner ear Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of all components of the labyrinth, including the semicircular canals, vestibule and cochlea (Mammalian Phenotype Ontology, MP_0006285)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006285
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5 gene mutations causing the absent inner ear phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CHRD chordin
EYA1 EYA transcriptional coactivator and phosphatase 1
FOXI3 forkhead box I3
SIX1 SIX homeobox 1
TBX1 T-box 1