dilated cochlea Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description the luminal space of the cochlea is increased in volume or area, usually with an increase in contained fluid (Mammalian Phenotype Ontology, MP_0004493)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004493
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Genes

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

Symbol Name
FGF3 fibroblast growth factor 3
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SOX2 SRY (sex determining region Y)-box 2