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Symbol
Name
ID
Rorb
RAR-related orphan receptor beta
MGI:1343464
Phenotype annotations related to nervous system
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Myoclonus
Eyelid myoclonus
Behavioral abnormality
Aggressive behavior
Delayed speech and language development
Global developmental delay
Seizures
Absence seizure
Generalized tonic-clonic seizures
Disease(s) Associated with RORB
idiopathic generalized epilepsy 15

Mouse Phenotypes
nervous system phenotype
absent amacrine cells
decreased retinal rod cell number
absent retinal rod cells
increased retinal ganglion cell number
increased retinal cone cell number
absent horizontal cells
abnormal retinal ganglion cell morphology
absent photoreceptor inner segment
absent photoreceptor outer segment
abnormal retinal cone cell morphology
retinal photoreceptor degeneration
Availability Mouse Genotype
Rorbhstp/Rorbhstp
Rorbtm1.1Df/Rorbtm1.1Df
Rorbtm1Mba/Rorbtm1Mba *
Rorbtm2.1Df/Rorbtm2.1Df

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
11/12/2019
MGI 6.14
The Jackson Laboratory