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Phenotypes Associated with This Genotype
Genotype
MGI:5307061
Allelic
Composition
Grin2btm1.1Jlbr/Grin2btm1.1Jlbr
Neurod6tm1(cre)Kan/Neurod6+
Genetic
Background
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Grin2btm1.1Jlbr mutation (0 available); any Grin2b mutation (100 available)
Neurod6tm1(cre)Kan mutation (0 available); any Neurod6 mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
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


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
03/18/2025
MGI 6.24
The Jackson Laboratory