Title : A mutation in the saposin C domain of the sphingolipid activator protein (Prosaposin) gene causes neurodegenerative disease in mice.

Pub. Date : 2010 Aug 1

PMID : 20175216






3 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 A mutation in the saposin C domain of the sphingolipid activator protein (Prosaposin) gene causes neurodegenerative disease in mice. Sphingolipids prosaposin Mus musculus
2 Saposins A, B, C, and D are small amphiphatic glycoproteins that are encoded in tandem within a precursor protein (prosaposin, PSAP), and are required for in vivo degradation of sphingolipids. Sphingolipids prosaposin Mus musculus
3 Saposins A, B, C, and D are small amphiphatic glycoproteins that are encoded in tandem within a precursor protein (prosaposin, PSAP), and are required for in vivo degradation of sphingolipids. Sphingolipids prosaposin Mus musculus