absent incus Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the middle of the three auditory ossicles (Mammalian Phenotype Ontology, MP_0004318)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004318
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6 gene mutations causing the absent incus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ECE1 endothelin converting enzyme 1
EDNRA endothelin receptor type A
EMX2 empty spiracles homeobox 2
FOXC2 forkhead box C2
FOXI3 forkhead box I3
SIX1 SIX homeobox 1