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An endoplasmic reticulum-resident membrane protein (398 aa), that is N-glycosylated and proteolytically cleaved into N- and C-terminal fragments. Highly expressed in the nervous system. Seipin mutations are involved in various disorders including congenital lipodystrophy type 2, Silver's syndrome/spastic paraplegia 17, and distal hereditary motor neuropathy type V.

Subjects: Medicine and Health.

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