abnormal boettcher cell morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the polyhedral cells located on the basilar membrane beneath the Claudius cells in the basal turn of the cochlea, and considered supporting cells for the organ of Corti; Boettcher cells interweave with each other, project microvilli into the intercellular space, show high levels of calmodulin, and may be involved in mediating Ca(2+) regulation and ion transport (Mammalian Phenotype Ontology, MP_0011739)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011739
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Genes

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

Symbol Name
SLC12A2 solute carrier family 12 (sodium/potassium/chloride transporter), member 2