abnormal patterning of the organ of corti Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the organization of the various cell types within the organ of Corti into a set number of distinct rows (Mammalian Phenotype Ontology, MP_0006331)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006331
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2 gene mutations causing the abnormal patterning of the organ of corti phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FGFR3 fibroblast growth factor receptor 3
SLC12A2 solute carrier family 12 (sodium/potassium/chloride transporter), member 2