Symbol Name ID |
Rax
retina and anterior neural fold homeobox MGI:109632 |
Darker colors indicate more annotations |
Human Phenotypes | Sclerocornea |
Anophthalmia |
Microphthalmia |
Disease(s) Associated with RAX | |||
isolated microphthalmia 3 |
Mouse Phenotypes | abnormal optic nerve morphology |
abnormal eye morphology |
abnormal lens morphology |
abnormal lens development |
small lens |
abnormal eye development |
abnormal optic cup morphology |
absent optic vesicle |
microphthalmia |
retina hypoplasia |
anophthalmia |
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Availability | Mouse Genotype | |||||||||||
Raxey1/Raxey1 | ||||||||||||
Raxtm1.2Lwd/Raxtm1.2Lwd | ||||||||||||
Raxtm1Lwd/Raxtm1Lwd | ||||||||||||
Raxtm1Mjam/Raxtm1Mjam | ||||||||||||
Raxey1/Rax+ | ||||||||||||
Raxtm1.1(rTA,tetO-cre)Lan/? | ||||||||||||
Raxtm1.1Lwd/Raxtm1.1Lwd Tg(rx3-icre)1Mjam/0 (conditional) |
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Raxtm1.1Tfur/Raxtm1.1Tfur Tg(Crx-cre/ERT2)1Tfur/0 (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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