Symbol Name ID |
Notch3
notch 3 MGI:99460 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Pseudobulbar paralysis |
Urinary incontinence |
Atypical behavior |
Abulia |
Personality changes |
Hypernasal speech |
Disease(s) Associated with NOTCH3 | ||||||
CADASIL 1 | ||||||
lateral meningocele syndrome |
Mouse Phenotypes | behavior/neurological phenotype |
lethargy |
decreased exploration in new environment |
abnormal motor capabilities/coordination/movement |
ataxia |
hunched posture |
paresis |
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Availability | Mouse Genotype | |||||||
Notch3tm1.1Dwr/Notch3tm1.1Dwr | ||||||||
Notch3em1Ecan/Notch3+ | * | |||||||
Notch3tm1.1Dwr/Notch3+ | ||||||||
Tg(Lck-Notch3)#Issc/0 |
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 05/14/2024 MGI 6.23 |
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