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	Delayed speech and language development	Atypical behavior	Aggressive behavior	Global developmental delay	Seizure	Bilateral tonic-clonic seizure	Generalized non-motor (absence) seizure
Disease(s) Associated with RORB
idiopathic generalized epilepsy 15

Mouse Phenotypes

nervous system phenotype

abnormal neuron morphology

absent amacrine cells

decreased retina rod cell number

absent retina rod cells

increased retina ganglion cell number

increased retina cone cell number

abnormal retina ganglion cell morphology

absent retina horizontal cells

abnormal photoreceptor inner segment morphology

abnormal retina cone cell inner segment morphology

absent photoreceptor inner segment

disorganized photoreceptor inner segment

abnormal photoreceptor outer segment morphology

absent photoreceptor outer segment

abnormal retina cone cell outer segment morphology

disorganized photoreceptor outer segment

abnormal retina cone cell morphology

retina photoreceptor degeneration

Availability

Mouse Genotype

Rorb^hstp-2J/Rorb^hstp-2J

Rorb^hstp/Rorb^hstp

Rorb^tm1.1Df/Rorb^tm1.1Df

Rorb^tm1Mba/Rorb^tm1Mba

Rorb^tm2.1Df/Rorb^tm2.1Df

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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