Symbol Name ID |
Notch2
notch 2 MGI:97364 |
Darker colors indicate more annotations |
Human Phenotypes | Stroke |
Hydrocephalus |
Spina bifida occulta |
Delayed speech and language development |
Intellectual disability |
Intellectual disability, mild |
Areflexia |
Global developmental delay |
Severe global developmental delay |
Specific learning disability |
Disease(s) Associated with NOTCH2 | ||||||||||
Alagille syndrome | ||||||||||
Hajdu-Cheney syndrome |
Mouse Phenotypes | increased neuron apoptosis |
small pituitary gland |
increased neuronal precursor cell number |
abnormal sensory neuron morphology |
neuron degeneration |
abnormal nervous system physiology |
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Availability | Mouse Genotype | ||||||
Notch2tm3Grid/Notch2tm3Grid Foxg1tm1(cre)Skm/Foxg1+ (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 04/30/2024 MGI 6.23 |
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