|
Symbol Name ID |
Dll4
delta like canonical Notch ligand 4 MGI:1859388 |
| Darker colors indicate more annotations |
| Human Phenotypes | Cataract |
Developmental cataract |
Optic atrophy |
Hypertelorism |
Microphthalmia |
Strabismus |
Esotropia |
Visual impairment |
| Disease(s) Associated with DLL4 | ||||||||
| Adams-Oliver syndrome |
| Mouse Phenotypes | abnormal retina vasculature morphology |
abnormal induced retina neovascularization |
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| Availability | Mouse Genotype | ||
| Dll4tm1Nwg/Dll4+ | |||
| Dll4tm2.1Vlcg/Dll4tm2.1Vlcg Gt(ROSA)26Sortm3.1(cre/ERT2)Vlcg/Gt(ROSA)26Sor+ (conditional) |
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| Dll4tm2.1Vlcg/Dll4+ Gt(ROSA)26Sortm2(cre/ERT2)Brn/Gt(ROSA)26Sor+ (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 04/16/2024 MGI 6.23 |
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