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Grin1tm1.1Phs
Targeted Allele Detail
Summary
Symbol: Grin1tm1.1Phs
Name: glutamate receptor, ionotropic, NMDA1 (zeta 1); targeted mutation 1.1, Peter H Seeburg
MGI ID: MGI:2178082
Synonyms: NR1Q
Gene: Grin1  Location: Chr2:25181193-25209199 bp, - strand  Genetic Position: Chr2, 17.14 cM
Alliance: Grin1tm1.1Phs page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:75497
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted
Mutation:    Nucleotide substitutions
 
Mutation detailsThis allele is a derivative of Grin1tm1Phs. Point mutations were introduced that altered codon 598 in exon 15 from one encoding asparagine to one encoding glutamine. A loxP-flanked neomycin selection cassette in intron 18 was removed by transient Cre recombinase expression in ES cells prior to the production of chimeric mice. (J:75497)
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: 0 strains available      Cell Lines: 0 lines available
Carrying any Grin1 Mutation:  67 strains or lines available
References
Original:  J:75497 Single FN, et al., Dysfunctions in mice by NMDA receptor point mutations NR1(N598Q) and NR1(N598R). J Neurosci. 2000 Apr 1;20(7):2558-66
All:  2 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