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Phenotypes Associated with This Genotype
Genotype
MGI:4360658
Allelic
Composition
Grin2btm1Mim/Grin2btm1Mim
Genetic
Background
involves: C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Grin2btm1Mim mutation (1 available); any Grin2b mutation (96 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die shortly after birth without feeding; these mice can survive as long as P6 if hand-fed

behavior/neurological
• unless hand-fed, mice do not have milk in stomachs up to 6-7 hours after birth
• sensory inputs do not induce the suckling response in mutant neonates

nervous system
• no clear barrelettes are seen at P0 and at P2
• the terminal arbors of the primary sensory neurons in the barrelette regions have a diffuse distribution pattern and no distinct clustering is seen, whereas in control mice, terminal clusters coincide with barellettes
• significant increase in mean mEPSC amplitudes
• in hippocampal CA1 slices, no NMDA component of EPSPs is detectable in mutant mice
• in hippocampal slices, no long lasting depression is observed in P2-P3 mutant mice


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