absent scala media Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description missing spiral tube within the cochlea that contains the organ of Corti, the neuroepithelial receptor organ for hearing (Mammalian Phenotype Ontology, MP_0000033)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000033
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5 gene mutations causing the absent scala media phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
GBX2 gastrulation brain homeobox 2
HOXA1 homeobox A1
SHH sonic hedgehog
SIX1 SIX homeobox 1
SLC12A2 solute carrier family 12 (sodium/potassium/chloride transporter), member 2