abnormal claudius cell morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the columnar cells located on the floor of the ductus cochlearis external to the spiral organ (also known as the organ of Corti) (Mammalian Phenotype Ontology, MP_0004430)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004430
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Genes

4 gene mutations causing the abnormal claudius cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FBXO2 F-box protein 2
SLC26A5 solute carrier family 26 (anion exchanger), member 5
SLC4A7 solute carrier family 4, sodium bicarbonate cotransporter, member 7
SPRY2 sprouty homolog 2 (Drosophila)