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Phenotypes Associated with This Genotype
Genotype
MGI:5771812
Allelic
Composition
Slc1a2tm1.1Pros/Slc1a2tm1.1Pros
Tg(GFAP-cre/ERT2)13Kdmc/0
Genetic
Background
involves: 129S4/SvJae * 129S4/SvJaeSor * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Slc1a2tm1.1Pros mutation (1 available); any Slc1a2 mutation (40 available)
Tg(GFAP-cre/ERT2)13Kdmc mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• following postnatal tamoxifen treatment (P5-P9), mice die significantly earlier than control mice, with a median survival at 23 weeks of age

growth/size/body
• tamoxifen-treated mice gain significantly less weight than controls from 10 weeks of age

behavior/neurological
N
• at 28-67 weeks of age, tamoxifen-treated mice show no significant differences in total SHIRPA scores relative to control mice
• tamoxifen-treated mice show more electroencephalographic seizure events than controls
• however, no spontaneous clinical seizures are observed

nervous system
N
• at 14-19 weeks of age, tamoxifen-treated mice show only a minor, insignificant decrease in the uptake of L-[3H]glutamate (~15%) and D-[3H]aspartate (~13%) into crude forebrain synaptosomes relative to controls
• tamoxifen-treated mice show more electroencephalographic seizure events than controls
• however, no spontaneous clinical seizures are observed
• tamoxifen-treated mice show a significantly higher number of automatically detected spike-trains (electroencephalographic seizures) per 20 min of scalp EEG recording relative to controls (18.7 +/- 7.2 vs 1.9 +/- 0.5)


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
12/17/2024
MGI 6.24
The Jackson Laboratory