About   Help   FAQ
Symbol
Name
ID
Grin2a
glutamate receptor, ionotropic, NMDA2A (epsilon 1)
MGI:95820
Phenotype annotations related to behavior/neurological
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Attention deficit hyperactivity disorder
Behavioral abnormality
Disease(s) Associated with GRIN2A
Landau-Kleffner syndrome

Mouse Phenotypes
behavior/neurological phenotype
impaired contextual conditioning behavior
impaired cued conditioning behavior
abnormal long term object recognition memory
decreased exploration in new environment
abnormal spatial learning
abnormal spatial working memory
abnormal depression-related behavior
decreased anxiety-related response
increased startle reflex
impaired coordination
jumpy
decreased vertical activity
decreased chemical nociceptive threshold
decreased chemically-elicited antinociception
allodynia
decreased thermal nociceptive threshold
reduced kindling response
Availability Mouse Genotype
Grin2atm1.1Jpleo/Grin2atm1.1Jpleo
Grin2atm1.1Nhk/Grin2atm1.1Nhk
Grin2atm1.1Ppao/Grin2atm1.1Ppao *
Grin2atm1.1Tnkw/Grin2atm1.1Tnkw *
Grin2atm1Mim/Grin2atm1Mim
Grin2atm1Nak/Grin2atm1Nak *
Grin2atm1Rsp/Grin2atm1Rsp
Tg(Camk2a-Grin2a)1Jzt/?

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)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
12/03/2019
MGI 6.14
The Jackson Laboratory