absent organ of corti Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the highly specialized epithelium in the floor of the ductus cochlearis (Mammalian Phenotype Ontology, MP_0000044)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000044
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Genes

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

Symbol Name
EYA1 EYA transcriptional coactivator and phosphatase 1
LOC102723475 putative uncharacterized protein LOC388820
MYO6 myosin VI
PAX2 paired box 2
SLC12A7 solute carrier family 12 (potassium/chloride transporter), member 7