Symbol Name ID |
Psap
prosaposin MGI:97783 |
Darker colors indicate more annotations |
Human Phenotypes | Hypomimic face |
Rigidity |
Hypotonia |
Frequent falls |
Muscle spasm |
Disease(s) Associated with PSAP | |||||
combined saposin deficiency | |||||
late onset Parkinson's disease |
Mouse Phenotypes | abnormal intestinal peristalsis |
abnormal muscle fiber morphology |
muscular atrophy |
muscle weakness |
progressive muscle weakness |
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Availability | Mouse Genotype | |||||
Psaptm1Suz/Psaptm1Suz | ||||||
Psaptm2Suz/Psaptm2Suz |
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 04/16/2024 MGI 6.23 |
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