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Symbol
Name
ID

Crbn
cereblon
MGI:1913277

Phenotype annotations related to nervous system

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Absent speech	Attention deficit hyperactivity disorder	Self-injurious behavior	Intellectual disability, mild	Intellectual disability, severe	Global developmental delay	Delayed ability to walk	Seizure
Disease(s) Associated with CRBN
autosomal recessive intellectual developmental disorder 2

Mouse Phenotypes		nervous system phenotype	abnormal synapse morphology	absent optic nerve	reduced long-term potentiation	decreased prepulse inhibition
Availability	Mouse Genotype	nervous system phenotype	abnormal synapse morphology	absent optic nerve	reduced long-term potentiation	decreased prepulse inhibition
	Crbn^tm1.2Jjh/Crbn^tm1.2Jjh	*
	Crbn^{tm1b(KOMP)Wtsi}/Crbn^{tm1b(KOMP)Wtsi}

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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