Symbol Name ID |
Notch3
notch 3 MGI:99460 |
Darker colors indicate more annotations |
Human Phenotypes | Hypercalcemia |
Keloids |
Chondrocalcinosis |
Disease(s) Associated with NOTCH3 | |||
infantile myofibromatosis | |||
lateral meningocele syndrome |
Mouse Phenotypes | abnormal brain thrombosis |
improved glucose tolerance |
increased susceptibility to ischemic brain injury |
increased cerebral infarct size |
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Availability | Mouse Genotype | ||||
Notch3Gt(PST033)Byg/Notch3Gt(PST033)Byg | |||||
Notch3tm1.1(KOMP)Vlcg/Notch3tm1.1(KOMP)Vlcg | |||||
Notch3tm1.1Dwr/Notch3tm1.1Dwr | |||||
Notch3tm1.1Dwr/Notch3+ |
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 04/23/2024 MGI 6.23 |
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