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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Grin2btm1.1(Grin2a)Bjha
targeted mutation 1.1, Benjamin J Hall
MGI:5307054
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Grin2btm1.1(Grin2a)Bjha/Grin2btm1.1(Grin2a)Bjha involves: 129S6/SvEvTac * C57BL/6 MGI:5307057


Genotype
MGI:5307057
hm1
Allelic
Composition
Grin2btm1.1(Grin2a)Bjha/Grin2btm1.1(Grin2a)Bjha
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Grin2btm1.1(Grin2a)Bjha mutation (1 available); any Grin2b mutation (96 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• only about 8% of mice survive past P0

behavior/neurological
• at P0 a decrease in the number of rhythmic mouth suckling movements in response to stimulation with a feeding needle is seen
• lack of milk in the stomach at P0
• increased spontaneous locomotion at P15-P21
• interact less frequently with their littermates than control animals
• in a social approach assay mice spend less time exploring the bottle containing the mouse

growth/size/body
• at P12-P16 but not at P0

nervous system
• significant increase in mean mEPSC amplitudes
• NMDA evoked currents in neurons are insensitive to ifenprodil and are more sensitive to zinc ions
• significantly faster decay times





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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
05/07/2024
MGI 6.23
The Jackson Laboratory