absent tympanic ring Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description missing the bony ring at the ear canal to which the tympanic membrane is attached (Mammalian Phenotype Ontology, MP_0003138)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003138
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8 gene mutations causing the absent tympanic ring phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ECE1 endothelin converting enzyme 1
EDNRA endothelin receptor type A
FGFR1 fibroblast growth factor receptor 1
FOXI3 forkhead box I3
GLI2 GLI family zinc finger 2
GSC goosecoid homeobox
PRRX1 paired related homeobox 1
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)