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Symbol
Name
ID
Nr2f1
nuclear receptor subfamily 2, group F, member 1
MGI:1352451
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Spasticity
Hypotonia
Disease(s) Associated with NR2F1
Bosch-Boonstra-Schaaf optic atrophy syndrome

Mouse Phenotypes
hypotonia
Availability Mouse Genotype
Nr2f1tm1Mjts/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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory