brain vacuoles Gene Set
Genes
19 gene mutations causing the brain vacuoles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
ASPA
|
aspartoacylase
|
|
ATRN
|
attractin
|
|
CLCN2
|
chloride channel, voltage-sensitive 2
|
|
COQ9
|
coenzyme Q9
|
|
DCR
|
Down syndrome chromosome region
|
|
IDS
|
iduronate 2-sulfatase
|
|
LYNX1
|
Ly6/neurotoxin 1
|
|
MAN2C1
|
mannosidase, alpha, class 2C, member 1
|
|
MGRN1
|
mahogunin ring finger 1, E3 ubiquitin protein ligase
|
|
NDUFS4
|
NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase)
|
|
PARK2
|
parkin RBR E3 ubiquitin protein ligase
|
|
PDE4B
|
phosphodiesterase 4B, cAMP-specific
|
|
PDE6A
|
phosphodiesterase 6A, cGMP-specific, rod, alpha
|
|
PEPD
|
peptidase D
|
|
PIKFYVE
|
phosphoinositide kinase, FYVE finger containing
|
|
PRKAB1
|
protein kinase, AMP-activated, beta 1 non-catalytic subunit
|
|
PRNP
|
prion protein
|
|
SLC17A5
|
solute carrier family 17 (acidic sugar transporter), member 5
|
|
SOD2
|
superoxide dismutase 2, mitochondrial
|
