abnormal nmda-mediated synaptic currents Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description change in the measured amplitude, current density or duration of response to stimulation of NMDA receptors (Mammalian Phenotype Ontology, MP_0002888)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002888
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Genes

18 gene mutations causing the abnormal nmda-mediated synaptic currents phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNB3 calcium channel, voltage-dependent, beta 3 subunit
DAPK1 death-associated protein kinase 1
DLG4 discs, large homolog 4 (Drosophila)
DLGAP3 discs, large (Drosophila) homolog-associated protein 3
EPS8 epidermal growth factor receptor pathway substrate 8
FABP7 fatty acid binding protein 7, brain
FOSB FBJ murine osteosarcoma viral oncogene homolog B
GRIN1 glutamate receptor, ionotropic, N-methyl D-aspartate 1
GRIN2A glutamate receptor, ionotropic, N-methyl D-aspartate 2A
GRIN2B glutamate receptor, ionotropic, N-methyl D-aspartate 2B
GRIN2C glutamate receptor, ionotropic, N-methyl D-aspartate 2C
KIF17 kinesin family member 17
MAPK8IP1 mitogen-activated protein kinase 8 interacting protein 1
MAPK8IP2 mitogen-activated protein kinase 8 interacting protein 2
SERPINE2 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 2
SHANK3 SH3 and multiple ankyrin repeat domains 3
SLC6A9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9
WASF1 WAS protein family, member 1