Summary | Mutation origin | Mutation description | Expression | Phenotypes | Find Mice (IMSR) | References

Symbol:	Grin2atm1Nak
Name:	glutamate receptor, ionotropic, NMDA2A (epsilon 1); targeted mutation 1, Shigetada Nakanishi
MGI ID:	MGI:1928506
Synonyms:	NR2A -, NR2A KO
Gene:	Grin2a  Location: Chr16:9385762-9813424 bp, - strand  Genetic Position: Chr16, 5.28 cM
Alliance:	Grin2atm1Nak page

Germline Transmission:	Earliest citation of germline transmission: J:66455
Parent Cell Line:	CCE/EK.CCE (ES Cell)
Strain of Origin:	129S/SvEv-Gpi1c

Allele Type:    Targeted (Null/knockout) Mutations:    Insertion, Intragenic deletion   Mutation details: The region spanning the second transmembrane domain was deleted and replaced with a neomycin cassette. (J:66455)

View phenotypes and curated references for all genotypes (concatenated display).

In Mice Carrying this Mutation:

2 RNA-Seq or microarray experiment(s)

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 7 strains available      Cell Lines: 0 lines available
Carrying any Grin2a Mutation:	66 strains or lines available

Original:	J:66455 Kadotani H, et al., Motor discoordination results from combined gene disruption of the NMDA receptor NR2A and NR2C subunits, but not from single disruption of the NR2A or NR2C subunit. J Neurosci. 1996 Dec 15;16(24):7859-67
All:	16 reference(s)