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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 04/16/2024 MGI 6.23 |
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