abnormal rosenthal canal morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the winding tube of the bony labyrinth that makes two and a half turns about the modiolus of the cochlea; it is divided incompletely into two compartments by a winding shelf of bone, the bony spiral lamina (Mammalian Phenotype Ontology, MP_0004305)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004305
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Genes

3 gene mutations causing the abnormal rosenthal canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
POU4F3 POU class 4 homeobox 3
S1PR2 sphingosine-1-phosphate receptor 2
TGFB2 transforming growth factor, beta 2