dilated endolymphatic duct Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description stretched or widened aperture of the luminal space of the endolymphatic duct (Mammalian Phenotype Ontology, MP_0006012)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006012
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10 gene mutations causing the dilated endolymphatic duct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP6V0A4 ATPase, H+ transporting, lysosomal V0 subunit a4
EFNB2 ephrin-B2
FOXI1 forkhead box I1
LMX1A LIM homeobox transcription factor 1, alpha
PAX2 paired box 2
POU3F4 POU class 3 homeobox 4
SIX1 SIX homeobox 1
SLC26A4 solute carrier family 26 (anion exchanger), member 4
TBX1 T-box 1
ZEB1 zinc finger E-box binding homeobox 1