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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cacng8tm1.1Mwa
targeted mutation 1.1, Masahiko Watanabe
MGI:3696717
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cacng8tm1.1Mwa/Cacng8tm1.1Mwa involves: C57BL/6 * C57BL/6N * CBA MGI:3696718


Genotype
MGI:3696718
hm1
Allelic
Composition
Cacng8tm1.1Mwa/Cacng8tm1.1Mwa
Genetic
Background
involves: C57BL/6 * C57BL/6N * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cacng8tm1.1Mwa mutation (0 available); any Cacng8 mutation (31 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• 8-11 week-old mutants have severe deficits of surface AMPA receptors on spines and dendrites, but not on somata in CA1 pyramidal cells





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