Symbol Name ID |
App
amyloid beta precursor protein MGI:88059 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Decreased circulating GABA concentration |
Cerebral amyloid angiopathy |
Disease(s) Associated with APP | ||
Alzheimer's disease 1 | ||
APP-related cerebral amyloid angiopathy |
Mouse Phenotypes | homeostasis/metabolism phenotype |
amyloidosis |
amyloid beta deposits |
increased blood urea nitrogen level |
increased circulating calcium level |
increased susceptibility to induced thrombosis |
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Availability | Mouse Genotype | ||||||
Apptm1.1Tcs/Apptm1.1Tcs | * | ||||||
Apptm1.1Wevn/Apptm1.1Wevn | |||||||
Apptm1Dbo/Apptm1Dbo | |||||||
Apptm2.1Tcs/Apptm2.1Tcs | |||||||
Apptm3.1Tcs/Apptm3.1Tcs | |||||||
Apptm1b(KOMP)Wtsi/App+ | |||||||
Apptm1Ini/App+ | |||||||
Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-APPSwInd)18Dbo/0 |
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Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-APPSwInd)107Dbo/0 |
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Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-APPSwInd)Dbo/0 |
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 07/05/2024 MGI 6.24 |
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