|
Symbol Name ID |
Notch2
notch 2 MGI:97364 |
| Darker colors indicate more annotations |
| Human Phenotypes | Short neck |
Hepatomegaly |
Inguinal hernia |
Umbilical hernia |
Delayed puberty |
Short stature |
Failure to thrive |
Intrauterine growth retardation |
| Disease(s) Associated with NOTCH2 | ||||||||
| Alagille syndrome | ||||||||
| Hajdu-Cheney syndrome |
| Mouse Phenotypes | abnormal tooth morphology |
abnormal olfactory epithelium morphology |
embryonic growth retardation |
ovarian follicular cyst |
abnormal body composition |
decreased body weight |
renal glomerulus cyst |
decreased body size |
increased spleen weight |
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| Availability | Mouse Genotype | |||||||||
| Notch2tm1Grid/Notch2tm1Grid | ||||||||||
| Notch2tm1Yha/Notch2tm1Yha | ||||||||||
| Notch2tm2Grid/Notch2tm2Grid | ||||||||||
| Notch2tm3.1Grid/Notch2tm3.1Grid | ||||||||||
| Notch2tm1.1Ecan/Notch2+ | ||||||||||
| Notch2tm1.1Hhtg/Notch2+ | ||||||||||
| Notch2tm3Grid/Notch2tm3Grid Foxg1tm1(cre)Skm/Foxg1+ (conditional) |
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| Notch2tm3Grid/Notch2tm3Grid Tg(Tpbpa-cre,-EGFP)5Jcc/0 (conditional) |
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| Gt(ROSA)26Sortm2(CAG-Notch2*)Uzs/Gt(ROSA)26Sor+ Cd19tm1(cre)Cgn/Cd19+ (conditional) |
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| Gt(ROSA)26Sortm2(Notch2)Ryn/Gt(ROSA)26Sor+ Six2tm1(tTA,tetO-EGFP/cre)Amc/Six2+ (conditional) |
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| Notch2tm2Grid/Notch2tm3Grid Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+ (conditional) |
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| Notch2tm3Grid/Notch2tm3.1Grid Pax3tm1(cre)Joe/Pax3+ (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 04/16/2024 MGI 6.23 |
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