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Grin2btm1.1Jwhe
Targeted Allele Detail
Summary
Symbol: Grin2btm1.1Jwhe
Name: glutamate receptor, ionotropic, NMDA2B (epsilon 2); targeted mutation 1.1, Johannes W Hell
MGI ID: MGI:5314923
Synonyms: GluN2B L1298A/R1300Q
Gene: Grin2b  Location: Chr6:135690231-136150509 bp, - strand  Genetic Position: Chr6, 66.38 cM
Alliance: Grin2btm1.1Jwhe page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:181943
Parent Cell Line:  E14 (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted (Not Applicable)
Mutations:    Insertion, Nucleotide substitutions
 
Mutation detailsExon 13 was replaced with one in which nucleotide substitutions (CTGCGCCGG to GCGCGCCAA) results in the amino acid substitution of alanine for leucine at positions 1298 (L1298A) and glutamine for arginine at position 1300 (Q1300R). Cre-mediated recombination removed the floxed neo cassette inserted downstream of the modified exon 13. (J:181943)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Grin2b Mutation:  99 strains or lines available
References
Original:  J:181943 Halt AR, et al., CaMKII binding to GluN2B is critical during memory consolidation. EMBO J. 2012 Mar 7;31(5):1203-16
All:  7 reference(s)

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
10/29/2024
MGI 6.24
The Jackson Laboratory