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Symbol
Name
ID
Grin2a
glutamate receptor, ionotropic, NMDA2A (epsilon 1)
MGI:95820
Phenotype annotations related to nervous system
*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 *

Contributing Projects:
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
The Jackson Laboratory