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Symbol
Name
ID
Psap
prosaposin
MGI:97783
Phenotype annotations related to muscle
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
Availability Mouse Genotype
Psaptm1Suz/Psaptm1Suz
Psaptm2Suz/Psaptm2Suz

Contributing Projects:
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
The Jackson Laboratory