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Symbol
Name
ID

Nr2f1
nuclear receptor subfamily 2, group F, member 1
MGI:1352451

Phenotype annotations related to behavior/neurological

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

Human Phenotypes	Feeding difficulties	Autistic behavior	Autism	Compulsive behaviors	Attention deficit hyperactivity disorder	Repetitive compulsive behavior
Disease(s) Associated with NR2F1
Bosch-Boonstra-Schaaf optic atrophy syndrome

Mouse Phenotypes		behavior/neurological phenotype	no swallowing reflex	slow extinction of fear memory	impaired righting response	decreased startle reflex	decreased grip strength
Availability	Mouse Genotype	behavior/neurological phenotype	no swallowing reflex	slow extinction of fear memory	impaired righting response	decreased startle reflex	decreased grip strength
	Nr2f1^tm1Mjts/Nr2f1^tm1Mjts
	Nr2f1^tm1Mjts/Nr2f1⁺	*

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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