degeneration of organ of corti supporting cells Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description degeneration or loss of the highly differentiated epithelial cells with distinctive morphological features that surround all hair cells in the organ of Corti (Mammalian Phenotype Ontology, MP_0004465)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004465
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Genes

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

Symbol Name
ATP8B1 ATPase, aminophospholipid transporter, class I, type 8B, member 1
CLRN1 clarin 1
FBXO2 F-box protein 2
GATA3 GATA binding protein 3
GFI1 growth factor independent 1 transcription repressor
POU4F3 POU class 4 homeobox 3
SLC26A5 solute carrier family 26 (anion exchanger), member 5
SLC4A7 solute carrier family 4, sodium bicarbonate cotransporter, member 7
THRB thyroid hormone receptor, beta
TUB tubby bipartite transcription factor