Symbol Name ID |
Nr2f1
nuclear receptor subfamily 2, group F, member 1 MGI:1352451 |
Darker colors indicate more annotations |
Human Phenotypes | Spasticity |
Hypotonia |
Disease(s) Associated with NR2F1 | ||
Bosch-Boonstra-Schaaf optic atrophy syndrome |
Mouse Phenotypes | hypotonia |
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Availability | Mouse Genotype | |
Nr2f1tm1Mjts/Nr2f1+ |
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 05/14/2024 MGI 6.23 |
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