Symbol Name ID |
Psap
prosaposin MGI:97783 |
Darker colors indicate more annotations |
Human Phenotypes | Splenomegaly |
Hypersplenism |
Recurrent respiratory infections |
Disease(s) Associated with PSAP | |||
atypical Gaucher's disease due to saposin c deficiency | |||
combined saposin deficiency |
Mouse Phenotypes | abnormal macrophage morphology |
microgliosis |
abnormal spleen morphology |
decreased spleen weight |
abnormal microglial cell physiology |
CNS inflammation |
kidney inflammation |
|
Availability | Mouse Genotype | |||||||
Psaptm1Ggb/Psaptm1Ggb | ||||||||
Psaptm1Juma/Psaptm1Juma | ||||||||
Psaptm1Suz/Psaptm1Suz | ||||||||
Psaptm2Ggb/Psaptm2Ggb | ||||||||
Psaptm2Suz/Psaptm2Suz | ||||||||
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 07/05/2024 MGI 6.24 |
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