absent middle ear ossicles Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Absence of the middle ear ossicles, malleus, incus, and stapes. (Human Phenotype Ontology, HP_0009910)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000040
Similar Terms
Downloads & Tools


4 gene mutations causing the absent middle ear ossicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ECE1 endothelin converting enzyme 1
FGFR1 fibroblast growth factor receptor 1
HOXA1 homeobox A1
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)