abnormal organ of corti supporting cell differentiation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description atypical production of or inability to produce the highly differentiated epithelial cells with distinctive morphological features that surround the hair cells in the organ of Corti (Mammalian Phenotype Ontology, MP_0008304)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008304
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Genes

3 gene mutations causing the abnormal organ of corti supporting cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FGFR3 fibroblast growth factor receptor 3
NR2F1 nuclear receptor subfamily 2, group F, member 1
POU4F3 POU class 4 homeobox 3