|
Symbol Name ID |
Notch2
notch 2 MGI:97364 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hepatomegaly |
Cirrhosis |
Reduced number of intrahepatic bile ducts |
Cholestasis |
Cholestatic liver disease |
Prolonged neonatal jaundice |
Hepatocellular carcinoma |
| Disease(s) Associated with NOTCH2 | |||||||
| Alagille syndrome |
| Mouse Phenotypes | focal hepatic necrosis |
abnormal bile duct morphology |
abnormal bile duct development |
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| Availability | Mouse Genotype | |||
| Notch2tm1Grid/Notch2tm1Grid | ||||
| Notch2tm2Grid/Notch2tm3Grid Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+ (conditional) |
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| Notch2tm3Grid/Notch2tm3.1Grid Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+ (conditional) |
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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 04/30/2024 MGI 6.23 |
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