Research Models
Selected Results
1 Models
Name | Other Names | Strain Name | Genetic Background | Gene | Mutation | Modification Info | Modification | Disease | Neuropathology | Behavior/Cognition | Other Phenotype | Availability | Primary Paper | Visualization | |
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Mouse Models (1)
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B6(SJL)-Apoetm1.1(APOE*4)Adiuj Sorl1em1Adiuj Trem2em1Adiuj/J | C57BL/6J | Sorl1, APOE, Trem2 | TREM2 R47H, SORL1 A528T (SNP 13), APOE C130R (ApoE4) | CRISPR/cas9 was used to generate a knock-in A528T mutation of the Sorl1 gene of APOE4/Trem2*R47H mice—double-mutant mice with a humanized Apoe (ε4 allele) gene and the R47H point mutation knocked into the mouse Trem2 gene. | Sorl1: Knock-In; APOE: Knock-In; Trem2: Knock-In | Alzheimer's Disease | Unknown. | Unknown. | The Jackson Laboratory, Stock# 031940. Cryopreserved. | The Jackson Laboratory | Yes |
1 Visualizations
AD-related Research Models
Phenotypes Examined
- Plaques
- Tangles
- Neuronal Loss
- Gliosis
- Synaptic Loss
- Changes in LTP/LTD
- Cognitive Impairment
When visualized, these phenotypes will distributed over a 18 month timeline demarcated at the following intervals: 3mo, 6mo, 9mo, 1yr, 15mo, 18mo+.
Sorl1*A528T/APOE4/Trem2*R47H
Observed
Absent
No Data
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Plaques at
No data.
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Tangles at
No data.
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Neuronal Loss at
No data.
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Gliosis at
No data.
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Synaptic Loss at
No data.
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Synaptic Loss at
No data.
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Changes in LTP/LTD at
No data.
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Cognitive Impairment at
No data.
Genes | Mutations | Modification | Disease | Neuropathology | Behavior/Cognition |
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Sorl1, APOE, Trem2 | TREM2 R47H, SORL1 A528T (SNP 13), APOE C130R (ApoE4) | Sorl1: Knock-In; APOE: Knock-In; Trem2: Knock-In | Alzheimer's Disease | Unknown. |
Unknown. |