absent otoliths Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the crystalline calciferous particles adhering to the otolithic membrane (Mammalian Phenotype Ontology, MP_0002978)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002978
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Genes

15 gene mutations causing the absent otoliths phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AP3D1 adaptor-related protein complex 3, delta 1 subunit
ATG4B autophagy related 4B, cysteine peptidase
ATG5 autophagy related 5
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
ATP6V0A4 ATPase, H+ transporting, lysosomal V0 subunit a4
BLOC1S5 biogenesis of lysosomal organelles complex-1, subunit 5, muted
CYBA cytochrome b-245, alpha polypeptide
FOXI1 forkhead box I1
LMX1A LIM homeobox transcription factor 1, alpha
NOX3 NADPH oxidase 3
NOXO1 NADPH oxidase organizer 1
OTOP1 otopetrin 1
SCARB2 scavenger receptor class B, member 2
SLC26A4 solute carrier family 26 (anion exchanger), member 4
ZEB1 zinc finger E-box binding homeobox 1