absent endolymphatic duct Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description missing small membranous canal of the inner ear; connecting membranous labyrinth with the endolymphatic sac (Mammalian Phenotype Ontology, MP_0000041)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000041
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Genes

7 gene mutations causing the absent 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
GBX2 gastrulation brain homeobox 2
HOXA1 homeobox A1
MAFB v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog B
SHH sonic hedgehog