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Symbol
Name
ID

Nr5a1
nuclear receptor subfamily 5, group A, member 1
MGI:1346833

Phenotype annotations related to mortality/aging

*	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	Death in infancy
Zellweger syndrome

Mouse Phenotypes		mortality/aging	premature death	perinatal lethality, complete penetrance	postnatal lethality, complete penetrance	postnatal lethality, incomplete penetrance
Availability	Mouse Genotype	mortality/aging	premature death	perinatal lethality, complete penetrance	postnatal lethality, complete penetrance	postnatal lethality, incomplete penetrance
	Nr5a1^em1Kemi/Nr5a1^em1Kemi
	Nr5a1^tm1.1Hain/Nr5a1^tm1.1Hain	*
	Nr5a1^tm1Enl/Nr5a1^tm1Enl
	Nr5a1^tm1Jmi/Nr5a1^tm1Jmi
	Nr5a1^tm1Klp/Nr5a1^tm1Klp
	Nr5a1^tm2.1Klp/Nr5a1^tm2.1Klp
	Nr5a1^tm3Klp/Nr5a1^tm3Klp
	Nr5a1^em1Kemi/Nr5a1⁺	*

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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