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Symbol
Name
ID

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

Phenotype annotations related to vision/eye

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

Human Phenotypes

Keratoconus

Optic atrophy

Optic disc pallor

Optic disc hypoplasia

Optic nerve hypoplasia

Strabismus

Esotropia

Exotropia

Nystagmus

Hypermetropia

Myopia

Cerebral visual impairment

Reduced visual acuity

Amblyopia

Visual field defect

Disease(s) Associated with NR2F1

Bosch-Boonstra-Schaaf optic atrophy syndrome

Mouse Phenotypes		vision/eye phenotype	persistence of hyaloid vascular system
Availability	Mouse Genotype	vision/eye phenotype	persistence of hyaloid vascular system
	Nr2f1^{tm1.1(KOMP)Mbp}/Nr2f1⁺
	Nr2f1^tm1Mjts/Nr2f1⁺	*
	Nr2f1^tm2.1Mjts/Nr2f1^tm2.1Mjts Tg(rx3-icre)1Mjam/0 (conditional)	*

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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