Symbol Name ID |
Rarb
retinoic acid receptor, beta MGI:97857 |
Darker colors indicate more annotations |
Human Phenotypes | Anophthalmia |
Microphthalmia |
Disease(s) Associated with RARB | ||
syndromic microphthalmia 12 |
Mouse Phenotypes | absent metoptic pillar |
cataract |
persistent hyperplastic primary vitreous |
persistence of hyaloid vascular system |
narrow eye opening |
retina fold |
vitreous body deposition |
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Availability | Mouse Genotype | |||||||
Rarbtm1Ipc/Rarbtm1Ipc | ||||||||
Rarbtm1Mma/Rarbtm1Mma | ||||||||
Rarbtm2.1Ipc/Rarbtm2.1Ipc | ||||||||
Rarbtm1Mma/Rarb+ |
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 04/09/2024 MGI 6.23 |
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