Learning Disturbance Gene Set
Genes
29 genes associated with the disease Learning Disturbance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
ACHE
|
acetylcholinesterase (Yt blood group)
|
|
APOD
|
apolipoprotein D
|
|
APP
|
amyloid beta (A4) precursor protein
|
|
BCL2
|
B-cell CLL/lymphoma 2
|
|
CAMKMT
|
calmodulin-lysine N-methyltransferase
|
|
GRIA1
|
glutamate receptor, ionotropic, AMPA 1
|
|
HMOX1
|
heme oxygenase 1
|
|
HTR1A
|
5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled
|
|
HTR7
|
5-hydroxytryptamine (serotonin) receptor 7, adenylate cyclase-coupled
|
|
IL1B
|
interleukin 1, beta
|
|
IL1RN
|
interleukin 1 receptor antagonist
|
|
KL
|
klotho
|
|
MAPT
|
microtubule-associated protein tau
|
|
MECP2
|
methyl CpG binding protein 2
|
|
MICU1
|
mitochondrial calcium uptake 1
|
|
NF1
|
neurofibromin 1
|
|
PARK2
|
parkin RBR E3 ubiquitin protein ligase
|
|
PDE1B
|
phosphodiesterase 1B, calmodulin-dependent
|
|
PNOC
|
prepronociceptin
|
|
POR
|
P450 (cytochrome) oxidoreductase
|
|
PSEN1
|
presenilin 1
|
|
SIGMAR1
|
sigma non-opioid intracellular receptor 1
|
|
SLC17A6
|
solute carrier family 17 (vesicular glutamate transporter), member 6
|
|
SLC17A7
|
solute carrier family 17 (vesicular glutamate transporter), member 7
|
|
SYP
|
synaptophysin
|
|
TH
|
tyrosine hydroxylase
|
|
TLR4
|
toll-like receptor 4
|
|
TRH
|
thyrotropin-releasing hormone
|
|
VEGFA
|
vascular endothelial growth factor A
|
