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Grin2btm1Mim
Targeted Allele Detail
Summary
Symbol: Grin2btm1Mim
Name: glutamate receptor, ionotropic, NMDA2B (epsilon 2); targeted mutation 1, Masayoshi Mishina
MGI ID: MGI:1928295
Synonyms: NMDA epsilon2 -
Gene: Grin2b  Location: Chr6:135690231-136150509 bp, - strand  Genetic Position: Chr6, 66.38 cM
Alliance: Grin2btm1Mim page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:31622
Parent Cell Line:  TT2 (ES Cell)
Strain of Origin:  (C57BL/6NCrlj x CBA/JNCrlj)F1
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Insertion
 
Mutation detailsDisruption by insertion of a neomycin cassette into the exon encoding the translation initiation site. (J:31622)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
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:  96 strains or lines available
References
Original:  J:31622 Kutsuwada T, et al., Impairment of suckling response, trigeminal neuronal pattern formation, and hippocampal LTD in NMDA receptor epsilon 2 subunit mutant mice. Neuron. 1996 Feb;16(2):333-44
All:  21 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
04/23/2024
MGI 6.23
The Jackson Laboratory