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Symbol
Name
ID
Rarb
retinoic acid receptor, beta
MGI:97857
Phenotype annotations related to vision/eye
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
Availability Mouse Genotype
Rarbtm1Ipc/Rarbtm1Ipc
Rarbtm1Mma/Rarbtm1Mma
Rarbtm2.1Ipc/Rarbtm2.1Ipc
Rarbtm1Mma/Rarb+

Contributing Projects:
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
The Jackson Laboratory