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Symbol
Name
ID
Rarb
retinoic acid receptor, beta
MGI:97857
Phenotype annotations related to nervous system
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Intellectual disability
Disease(s) Associated with RARB
syndromic microphthalmia 12

Mouse Phenotypes
nervous system phenotype
abnormal excitatory postsynaptic potential
reduced long-term potentiation
absent long-term depression
Availability Mouse Genotype
Rarbtm1Mma/Rarbtm1Mma *
Rarbtm1Vgi/Rarbtm1Vgi

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
04/16/2024
MGI 6.23
The Jackson Laboratory