5uph | pdb_00005uph
From Proteopedia
Lipids bound lysosomal integral membrane protein 2
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Structural highlights
Disease[SCRB2_HUMAN] Unverricht-Lundborg disease;Gaucher disease type 1;Action myoclonus - renal failure syndrome. The disease is caused by mutations affecting the gene represented in this entry. Genetic variants in SCARB2 can act as modifier of the phenotypic expression and severity of Gaucher disease. Function[SCRB2_HUMAN] Acts as a lysosomal receptor for glucosylceramidase (GBA) targeting.[1] References
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This page was last modified 06:57, 13 December 2017.