short endolymphatic duct Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description length reduction or truncation of the small membranous canal which connects with both saccule and utricle of the membranous labyrinth, passes through the aqueduct of vestibule, and terminates in the endolymphatic sac (Mammalian Phenotype Ontology, MP_0008065)
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6 gene mutations causing the short endolymphatic duct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DLX5 distal-less homeobox 5
EYA1 EYA transcriptional coactivator and phosphatase 1
FGF3 fibroblast growth factor 3
PAX2 paired box 2
PAX3 paired box 3
SIX1 SIX homeobox 1