Symbol Name ID |
Psap
prosaposin MGI:97783 |
Darker colors indicate more annotations |
Human Phenotypes | Orthostatic hypotension due to autonomic dysfunction |
Splenomegaly |
Hypersplenism |
Disease(s) Associated with PSAP | |||
atypical Gaucher's disease due to saposin c deficiency | |||
combined saposin deficiency | |||
late onset Parkinson's disease |
Mouse Phenotypes | abnormal vascular endothelial cell morphology |
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Availability | Mouse Genotype | |
Psaptm1Suz/Psaptm1Suz | ||
Psaptm2.1Juma/Psaptm2.1Juma | ||
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 04/23/2024 MGI 6.23 |
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