Symbol Name ID |
Psap
prosaposin MGI:97783 |
* | 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 | * |
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 |
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