About Help FAQ

Symbol
Name
ID

Psap
prosaposin
MGI:97783

Phenotype annotations related to hematopoietic system

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Anemia	Thrombocytopenia	Splenomegaly	Hypersplenism
Disease(s) Associated with PSAP	Anemia	Thrombocytopenia	Splenomegaly	Hypersplenism
atypical Gaucher's disease due to saposin c deficiency
combined saposin deficiency

Mouse Phenotypes		hematopoietic system phenotype	abnormal macrophage morphology	microgliosis	abnormal spleen morphology	decreased spleen weight	abnormal microglial cell physiology
Availability	Mouse Genotype	hematopoietic system phenotype	abnormal macrophage morphology	microgliosis	abnormal spleen morphology	decreased spleen weight	abnormal microglial cell physiology
	Psap^tm1Ggb/Psap^tm1Ggb
	Psap^tm1Juma/Psap^tm1Juma
	Psap^tm1Suz/Psap^tm1Suz
	Psap^tm2.1Juma/Psap^tm2.1Juma	*
	Psap^tm2Ggb/Psap^tm2Ggb
	Psap^tm2Suz/Psap^tm2Suz
	Psap^tm4.1Ggb/Psap^tm4.1Ggb
	Psap^tm1Suz/Psap^tm2.1Juma	*

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/23/2024 MGI 6.23