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Phenotypes Associated with This Genotype
Genotype
MGI:5569497
Allelic
Composition
Ssbtm1Rjma/Ssbtm2.1Rjma
Tg(Camk2a-cre)T29-1Stl/0
Genetic
Background
involves: 129S/SvEv * BALB/c * C57BL * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ssbtm1Rjma mutation (0 available); any Ssb mutation (32 available)
Ssbtm2.1Rjma mutation (0 available); any Ssb mutation (32 available)
Tg(Camk2a-cre)T29-1Stl mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• after 5 weeks
• rapid decline from 13 to 25 weeks, slowed decline afterward
• at 59 to 79 weeks
• postnatal loss of forebrain mass at 16 and 32 weeks
• progressive cell loss
• loss of cortical cytoarchitecture at 16 and 32 weeks
• progressive neurodegeneration in the cerebral cortex (starting at 16 weeks) and hippocampus starting
• severely diminished at 65 weeks
• decrease in neuronal density at 16 and 32 weeks
• in the CA1 and subiculum
• however, the CA3 and dentate gyrus are relatively spared
• progressive neurodegeneration in the cerebral cortex and hippocampus


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
06/16/2026
MGI 6.24
The Jackson Laboratory