Symbol Name ID |
Psap
prosaposin MGI:97783 |
Darker colors indicate more annotations |
Human Phenotypes | Splenomegaly |
Hepatomegaly |
Weight loss |
Disease(s) Associated with PSAP | |||
atypical Gaucher's disease due to saposin c deficiency | |||
combined saposin deficiency | |||
late onset Parkinson's disease |
Mouse Phenotypes | decreased body weight |
slow postnatal weight gain |
weight loss |
decreased body size |
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Availability | Mouse Genotype | ||||
Psaptm1Ggb/Psaptm1Ggb | |||||
Psaptm1Suz/Psaptm1Suz | |||||
Psaptm2Ggb/Psaptm2Ggb | |||||
Psaptm4.1Ggb/Psaptm4.1Ggb |
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 04/23/2024 MGI 6.23 |
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