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Symbol
Name
ID
Psap
prosaposin
MGI:97783
Phenotype annotations related to liver/biliary system
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Hepatomegaly
Disease(s) Associated with PSAP
atypical Gaucher's disease due to saposin c deficiency
combined saposin deficiency

Mouse Phenotypes
liver/biliary system phenotype
abnormal liver morphology
abnormal hepatocyte morphology
decreased liver weight
Availability Mouse Genotype
Psaptm1Suz/Psaptm1Suz
Psaptm2.1Juma/Psaptm2.1Juma *
Psaptm2Suz/Psaptm2Suz
Psaptm4.1Ggb/Psaptm4.1Ggb
Psaptm1Suz/Psaptm2.1Juma *

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)
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last database update
05/21/2024
MGI 6.23
The Jackson Laboratory