Symbol Name ID |
Rab23
RAB23, member RAS oncogene family MGI:99833 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal cornea morphology |
Opacification of the corneal stroma |
Microcornea |
Optic atrophy |
Blue sclerae |
Hypertelorism |
Disease(s) Associated with RAB23 | ||||||
Carpenter syndrome |
Mouse Phenotypes | abnormal eye morphology |
abnormal lens induction |
abnormal lens vesicle development |
abnormal optic cup morphology |
abnormal retina neuronal layer morphology |
anophthalmia |
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Availability | Mouse Genotype | ||||||
Rab23opb2/Rab23opb2 | |||||||
Rab23opb/Rab23opb |
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 05/14/2024 MGI 6.23 |
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