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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Nr2f1
nuclear receptor subfamily 2, group F, member 1
MGI:1352451
16 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
\Mctp1dwnd/\Nr2f1tm1.1(KOMP)Mbp
involves: C57BL/6J * C57BL/6NJ * C57BL/10SnJ 		abnormal cochlear hair cell morphology J:264553
abnormal cochlear inner hair cell morphology J:264553
abnormal cochlear outer hair cell morphology J:264553
abnormal utricular macula morphology J:264553
abnormal vestibular saccular macula morphology J:264553
fused vestibular saccule and utricle J:264553
impaired hearing J:264553
increased or absent threshold for auditory brainstem response J:264553
short scala media J:264553
\Nr2f1tm2.1Mjts/\Nr2f1+
\Nr2f2tm2.1Tsa/\Nr2f2tm2.1Tsa
\Tg(rx3-icre)1Mjam/0
involves: 129S7/SvEvBrd 		abnormal optic fissure closure J:157924
coloboma J:157924
\Nr2f1tm2.1Mjts/\Nr2f1tm2.1Mjts
\Nr2f2tm2.1Tsa/\Nr2f2+
\Tg(rx3-icre)1Mjam/0
involves: 129S7/SvEvBrd 		abnormal optic fissure closure J:157924
coloboma J:157924
\Nr2f1tm2.1Mjts/\Nr2f1tm2.1Mjts
\Nr2f2tm2.1Tsa/\Nr2f2tm2.1Tsa
\Tg(rx3-icre)1Mjam/0
involves: 129S7/SvEvBrd 		abnormal eye development J:157924
abnormal optic stalk morphology J:157924
abnormal retina pigment epithelium morphology J:157924
absent optic disk J:157924
coloboma J:157924
microphthalmia J:157924
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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Send questions and comments to User Support. 		last database update
03/25/2025
MGI 6.24 		The Jackson Laboratory