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Symbol Name ID |
Notch1
notch 1 MGI:97363 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Low anterior hairline |
Calvarial skull defect |
Micrognathia |
Microcephaly |
Macrocephaly |
Encephalocele |
Cleft upper lip |
Cleft palate |
Bulbous nose |
Depressed nasal bridge |
Narrow palpebral fissure |
Short palpebral fissure |
| Disease(s) Associated with NOTCH1 | ||||||||||||
| Adams-Oliver syndrome |
| Mouse Phenotypes | craniofacial phenotype |
thick neurocranium |
small pharyngeal arch |
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| Availability | Mouse Genotype | |||
| Notch1sot/Notch1sot | ||||
| Notch1tm2Rko/Notch1tm2Rko H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
* | |||
| Gt(ROSA)26Sortm1(Notch1)Dam/Gt(ROSA)26Sor+ Tg(Col1a1-cre)1Kry/0 (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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