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Symbol
Name
ID

Ppil1
peptidylprolyl isomerase (cyclophilin)-like 1
MGI:1916066

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 PPIL1	Death in infancy
pontocerebellar hypoplasia type 14

Mouse Phenotypes		mortality/aging	neonatal lethality, complete penetrance	perinatal lethality, complete penetrance	embryonic lethality prior to organogenesis	embryonic lethality, complete penetrance	preweaning lethality, complete penetrance
Availability	Mouse Genotype	mortality/aging	neonatal lethality, complete penetrance	perinatal lethality, complete penetrance	embryonic lethality prior to organogenesis	embryonic lethality, complete penetrance	preweaning lethality, complete penetrance
	Ppil1^em1(IMPC)Mbp/Ppil1^em1(IMPC)Mbp
	Ppil1^em2Jgg/Ppil1^em2Jgg
	Ppil1^em3Jgg/Ppil1^em3Jgg
	Ppil1^em4Jgg/Ppil1^em4Jgg
	Ppil1^em5Jgg/Ppil1^em5Jgg	*

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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