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Symbol
Name
ID

Psap
prosaposin
MGI:97783

Phenotype annotations related to mortality/aging

Darker colors indicate more annotations

Human Phenotypes	Death in infancy
Disease(s) Associated with PSAP	Death in infancy
combined saposin deficiency

Mouse Phenotypes		lethality at weaning, complete penetrance	premature death	neonatal lethality, incomplete penetrance	prenatal lethality, incomplete penetrance
Availability	Mouse Genotype	lethality at weaning, complete penetrance	premature death	neonatal lethality, incomplete penetrance	prenatal lethality, incomplete penetrance
	Psap^tm1Ggb/Psap^tm1Ggb
	Psap^tm1Juma/Psap^tm1Juma
	Psap^tm1Suz/Psap^tm1Suz
	Psap^tm2Ggb/Psap^tm2Ggb
	Psap^tm2Suz/Psap^tm2Suz
	Psap^tm4.1Ggb/Psap^tm4.1Ggb

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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