absent otoliths Gene Set
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
|
