absent tunnel of corti Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description complete absence of the triangular, fluid-filled space normally found between the inner and outer rows of supporting pillar cells in the organ of Corti (Mammalian Phenotype Ontology, MP_0003151)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003151
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5 gene mutations causing the absent tunnel of corti phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
FGFR3 fibroblast growth factor receptor 3
POU4F3 POU class 4 homeobox 3
SLC12A2 solute carrier family 12 (sodium/potassium/chloride transporter), member 2
TUB tubby bipartite transcription factor