Symbol Name ID |
Notch2
notch 2 MGI:97364 |
Darker colors indicate more annotations |
Human Phenotypes | Exocrine pancreatic insufficiency |
Papillary thyroid carcinoma |
Delayed puberty |
Disease(s) Associated with NOTCH2 | |||
Alagille syndrome |
Mouse Phenotypes | ovary hemorrhage |
abnormal bile duct morphology |
abnormal bile duct development |
small pituitary gland |
abnormal ovary morphology |
ovarian follicular cyst |
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Availability | Mouse Genotype | ||||||
Notch2tm1Grid/Notch2tm1Grid | |||||||
Notch2tm3Grid/Notch2tm3Grid Foxg1tm1(cre)Skm/Foxg1+ (conditional) |
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Notch2tm3Grid/Notch2tm3Grid Tg(Tpbpa-cre,-EGFP)5Jcc/0 (conditional) |
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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) |
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 09/03/2024 MGI 6.24 |
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