Symbol Name ID |
Nr5a1
nuclear receptor subfamily 5, group A, member 1 MGI:1346833 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Death in infancy |
Disease(s) Associated with NR5A1 | |
Zellweger syndrome |
Mouse Phenotypes | mortality/aging |
premature death |
perinatal lethality, complete penetrance |
postnatal lethality, complete penetrance |
postnatal lethality, incomplete penetrance |
|
Availability | Mouse Genotype | |||||
Nr5a1em1Kemi/Nr5a1em1Kemi | ||||||
Nr5a1tm1.1Hain/Nr5a1tm1.1Hain | * | |||||
Nr5a1tm1Enl/Nr5a1tm1Enl | ||||||
Nr5a1tm1Jmi/Nr5a1tm1Jmi | ||||||
Nr5a1tm1Klp/Nr5a1tm1Klp | ||||||
Nr5a1tm2.1Klp/Nr5a1tm2.1Klp | ||||||
Nr5a1tm3Klp/Nr5a1tm3Klp | ||||||
Nr5a1em1Kemi/Nr5a1+ | * |
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 06/12/2024 MGI 6.13 |
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