Symbol Name ID |
Grin2a
glutamate receptor, ionotropic, NMDA2A (epsilon 1) MGI:95820 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Gliosis |
Cerebellar atrophy |
Neuronal loss in central nervous system |
Gait ataxia |
Bradykinesia |
Chorea |
EEG abnormality |
Depression |
Delusion |
Schizophrenia |
Hallucinations |
Negativism |
Personality changes |
Addictive alcohol use |
Dementia |
Social and occupational deterioration |
Hyperreflexia |
Seizure |
Disease(s) Associated with GRIN2A | ||||||||||||||||||
alcohol dependence | ||||||||||||||||||
Huntington's disease | ||||||||||||||||||
schizophrenia |
Mouse Phenotypes | nervous system phenotype |
decreased kindling response |
abnormal excitatory postsynaptic currents |
reduced NMDA-mediated synaptic currents |
reduced long-term potentiation |
abnormal miniature excitatory postsynaptic currents |
|
Availability | Mouse Genotype | ||||||
Grin2atm1.1Jpleo/Grin2atm1.1Jpleo | * | ||||||
Grin2atm1.1Ppao/Grin2atm1.1Ppao | |||||||
Grin2atm1.1Tnkw/Grin2atm1.1Tnkw | * | ||||||
Grin2atm1Mim/Grin2atm1Mim | |||||||
Grin2atm1Nak/Grin2atm1Nak | * | ||||||
Grin2atm1Rsp/Grin2atm1Rsp | * |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 08/02/2024 MGI 6.24 |
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