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Symbol
Name
ID

Jarid2
jumonji and AT-rich interaction domain containing 2
MGI:104813

Phenotype annotations related to nervous system

*	Aspects of the system are reported to show a normal phenotype.
!	Indicates phenotype varies with strain background.
	Darker colors indicate more annotations

Human Phenotypes	EEG abnormality	Abnormal nonverbal communicative behavior	Delayed speech and language development	Lack of spontaneous play	Impaired ability to form peer relationships	Autism	Inflexible adherence to routines	Motor stereotypy	Restrictive behavior	Intellectual disability	Seizure
Disease(s) Associated with JARID2
autistic disorder

Mouse Phenotypes		nervous system phenotype	abnormal neural plate morphology	abnormal neural tube morphology	abnormal neural tube closure	delayed neural tube closure	incomplete rostral neuropore closure	abnormal nervous system development
Availability	Mouse Genotype	nervous system phenotype	abnormal neural plate morphology	abnormal neural tube morphology	abnormal neural tube closure	delayed neural tube closure	incomplete rostral neuropore closure	abnormal nervous system development
	Jarid2^{Gt(pGT1.8geo)6Pgr}/Jarid2^{Gt(pGT1.8geo)6Pgr}
	Jarid2^jumonji/Jarid2^jumonji	*!		!				!

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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