disease:Defects in SCARB2 are the cause of action myoclonus-renal failure syndrome (AMRF) [MIM:254900]; also known as myoclonus-nephropathy syndrome. AMRF is an autosomal recessive progressive myoclonic epilepsy associated with renal failure. Myoclonus is a brief, involuntary twitching of a muscle or a group of muscles. Cognitive function is preserved.,function:May act as a lysosomal receptor.,mass spectrometry: PubMed:11840567,similarity:Belongs to the CD36 family.,
Lysosome membrane ; Multi-pass membrane protein .
Cerebellum,Eye,Liver,Mammary cancer,
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