induced hyperactivity Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increased physical activity following stimulation such as handling, touching or noise (Mammalian Phenotype Ontology, MP_0008911)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008911
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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