induced hyperactivity Gene Set
Genes
29 gene mutations causing the induced hyperactivity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
ADGRL3
|
adhesion G protein-coupled receptor L3
|
|
CACNA2D2
|
calcium channel, voltage-dependent, alpha 2/delta subunit 2
|
|
CARS2
|
cysteinyl-tRNA synthetase 2, mitochondrial (putative)
|
|
CCDC7
|
coiled-coil domain containing 7
|
|
CERS6
|
ceramide synthase 6
|
|
CPLX2
|
complexin 2
|
|
DCR
|
Down syndrome chromosome region
|
|
DDC
|
dopa decarboxylase (aromatic L-amino acid decarboxylase)
|
|
DISC1
|
disrupted in schizophrenia 1
|
|
DRD4
|
dopamine receptor D4
|
|
DRD5
|
dopamine receptor D5
|
|
EIF4H
|
eukaryotic translation initiation factor 4H
|
|
FABP7
|
fatty acid binding protein 7, brain
|
|
GRIA1
|
glutamate receptor, ionotropic, AMPA 1
|
|
GRIA4
|
glutamate receptor, ionotropic, AMPA 4
|
|
HFE
|
hemochromatosis
|
|
HTR6
|
5-hydroxytryptamine (serotonin) receptor 6, G protein-coupled
|
|
KCNJ6
|
potassium channel, inwardly rectifying subfamily J, member 6
|
|
LMO4
|
LIM domain only 4
|
|
OCA2
|
oculocutaneous albinism II
|
|
OPRM1
|
opioid receptor, mu 1
|
|
POMC
|
proopiomelanocortin
|
|
PPP1R1B
|
protein phosphatase 1, regulatory (inhibitor) subunit 1B
|
|
SHANK3
|
SH3 and multiple ankyrin repeat domains 3
|
|
SLC6A1
|
solute carrier family 6 (neurotransmitter transporter), member 1
|
|
SRGAP3
|
SLIT-ROBO Rho GTPase activating protein 3
|
|
SRR
|
serine racemase
|
|
TAAR1
|
trace amine associated receptor 1
|
|
TPH2
|
tryptophan hydroxylase 2
|
