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Phenotypes Associated with This Genotype
Genotype
MGI:3698949
Allelic
Composition
Surf1tm2.1Zev/Surf1tm2.1Zev
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Surf1tm2.1Zev mutation (0 available); any Surf1 mutation (14 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mutants show extended survival vs control value
• median survival is 793 days compared to 654 days reported for control laboratory mice

growth/size/body
• newborns are significantly smaller than littermates, but difference progressively disappears after weaning

nervous system
• after seizure induction by kainic acid injection, no CA1 and CA3 hippocampal cells damaged by Ca2+ excitotoxicity are detected in mutants compared to damage detected in these regions in all control mice
• in cultured cortical/hippocampal neurons, glutamate treatment to increase Ca2+ to levels resulting in cell death causes less neuronal cell death in mutant neurons compared to wild-type cells

behavior/neurological
• at 2 months of age, mutants show mildly decreased motor coordination based on rotating rod trials

homeostasis/metabolism
• after seizure induction by kainic acid injection, no CA1 and CA3 hippocampal cells damaged by Ca2+ excitotoxicity are detected in mutants compared to damage detected in these regions in all control mice
• in cultured cortical/hippocampal neurons, glutamate treatment to increase Ca2+ to levels resulting in cell death causes less neuronal cell death in mutant neurons compared to wild-type cells
• cytochrome C oxidase (COX) and intermediates are found at lower levels than in wild-type tissues

cellular
• after seizure induction by kainic acid injection, no CA1 and CA3 hippocampal cells damaged by Ca2+ excitotoxicity are detected in mutants compared to damage detected in these regions in all control mice
• in cultured cortical/hippocampal neurons, glutamate treatment to increase Ca2+ to levels resulting in cell death causes less neuronal cell death in mutant neurons compared to wild-type cells
• Ca2+ uptake by mutant mitochondria is reduced compared to controls without changing mitochondrial structure or membrane potential


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
03/25/2025
MGI 6.24
The Jackson Laboratory