abnormal round window morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the opening on the medial wall of the middle ear leading into the cochlea, closed in life by the secondary tympanic membrane; serves to regulate fluid pressure in the inner ear (Mammalian Phenotype Ontology, MP_0004480)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004480
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4 gene mutations causing the abnormal round window morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CHD7 chromodomain helicase DNA binding protein 7
FGFR1 fibroblast growth factor receptor 1
PAX8 paired box 8
RPL38 ribosomal protein L38