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Grin1tm2Blt
Targeted Allele Detail
Summary
Symbol: Grin1tm2Blt
Name: glutamate receptor, ionotropic, NMDA1 (zeta 1); targeted mutation 2, Horst Bluethmann
MGI ID: MGI:1928284
Synonyms: Grin1K483Q, Grin1tm2Jnck
Gene: Grin1  Location: Chr2:25181193-25209199 bp, - strand  Genetic Position: Chr2, 17.14 cM
Alliance: Grin1tm2Blt page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:62289
Parent Cell Line:  E14 (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted
Mutations:    Insertion, Nucleotide substitutions
 
Mutation detailsPoint mutations were introduced by homologous recombination which altered the sequence corresponding to codon 483 from lysine to glutamine. A loxP flanked neomycin/thymidine kinase cassette in intron 10 was removed by transient Cre recombinase expression, leaving one loxP site in the intron. (J:62289)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Grin1 Mutation:  67 strains or lines available
References
Original:  J:62289 Kew JN, et al., Functional consequences of reduction in NMDA receptor glycine affinity in mice carrying targeted point mutations in the glycine binding site. J Neurosci. 2000 Jun 1;20(11):4037-49
All:  3 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
12/10/2024
MGI 6.24
The Jackson Laboratory