absent cochlea Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence or agenesis of the spiral-shaped bony canal in the inner ear containing the hair cells that transduce sound (Mammalian Phenotype Ontology, MP_0003147)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003147
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Genes

6 gene mutations causing the absent cochlea phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EYA1 EYA transcriptional coactivator and phosphatase 1
FOXI1 forkhead box I1
HOXA1 homeobox A1
PAX2 paired box 2
SIX1 SIX homeobox 1
TBX1 T-box 1