Symbol Name ID |
Rarb
retinoic acid receptor, beta MGI:97857 |
* | 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 |
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Availability | Mouse Genotype | ||||
Rarbtm1Mma/Rarbtm1Mma | * | ||||
Rarbtm1Vgi/Rarbtm1Vgi |
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 09/03/2024 MGI 6.24 |
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