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Phenotypes Associated with This Genotype
Genotype
MGI:5485189
Allelic
Composition
Grin1tm1c(EUCOMM)Wtsi/Grin1tm2.1Stl
Gt(ROSA)26Sortm14(CAG-tdTomato)Hze/Gt(ROSA)26Sor+
Tg(Slc6a4-cre)ET127Gsat/0
Genetic
Background
involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * FVB/N * SJL
Cell Lines EPD0469_5_C11
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Grin1tm1c(EUCOMM)Wtsi mutation (1 available); any Grin1 mutation (64 available)
Grin1tm2.1Stl mutation (0 available); any Grin1 mutation (64 available)
Gt(ROSA)26Sortm14(CAG-tdTomato)Hze mutation (8 available); any Gt(ROSA)26Sor mutation (1062 available)
Tg(Slc6a4-cre)ET127Gsat mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• disruption of somatic innervation during development in the absence of NMDARs at P14


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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Funding Information
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last database update
01/06/2026
MGI 6.24
The Jackson Laboratory