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Symbol Name ID |
Nr2f2
nuclear receptor subfamily 2, group F, member 2 MGI:1352452 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Mouse Phenotypes | embryo phenotype |
abnormal placental labyrinth vasculature morphology |
abnormal embryo turning |
embryonic growth retardation |
incomplete somite formation |
increased trophoblast giant cell number |
abnormal maternal decidual layer morphology |
decreased spongiotrophoblast cell number |
absent placental labyrinth |
abnormal placenta development |
abnormal vitelline vascular remodeling |
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| Availability | Mouse Genotype | |||||||||||
| Nr2f2tm1Tsa/Nr2f2tm1Tsa | * | |||||||||||
| Tg(Tek-Nr2f2)1Tsa/0 | ||||||||||||
| Amhr2tm3(cre)Bhr/Amhr2+ Nr2f2tm2.1Tsa/Nr2f2tm2.1Tsa (conditional) |
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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 |
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