absent organ of corti supporting cells Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the highly differentiated epithelial cells with distinctive morphological features that surround all hair cells in the organ of Corti (Mammalian Phenotype Ontology, MP_0004301)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004301
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Genes

5 gene mutations causing the absent organ of corti supporting cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
FGFR1 fibroblast growth factor receptor 1
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
POU4F3 POU class 4 homeobox 3
SLC12A2 solute carrier family 12 (sodium/potassium/chloride transporter), member 2