Symbol Name ID |
Notch2
notch 2 MGI:97364 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal anterior chamber morphology |
Band keratopathy |
Posterior embryotoxon |
Microcornea |
Keratoconus |
Corneal dystrophy |
Cataract |
Abnormal pupil morphology |
Iris coloboma |
Axenfeld anomaly |
Chorioretinal atrophy |
Pigmentary retinopathy |
Deeply set eye |
Hypertelorism |
Strabismus |
Myopia |
Disease(s) Associated with NOTCH2 | ||||||||||||||||
Alagille syndrome | ||||||||||||||||
Hajdu-Cheney syndrome |
Mouse Phenotypes | abnormal hyaloid artery morphology |
abnormal eye morphology |
persistent hyperplastic primary vitreous |
microphthalmia |
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Availability | Mouse Genotype | ||||
Notch2tm1Grid/Notch2tm1Grid |
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 08/02/2024 MGI 6.24 |
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