This gene encodes an endoplasmic reticulum membrane protein that is required for utilization of the mannose donor mannose-P-dolichol in the synthesis of lipid-linked oligosaccharides and glycosylphosphatidylinositols. Mutations in this gene result in congenital disorder of glycosylation type If. Alternative splicing results in multiple transcript variants.
HBeAg-binding protein 2 binding protein A; Mannose-P-dolichol utilization defect 1 protein; SL15; Suppressor of Lec15 and Lec35 glycosylation mutation homolog; suppressor of Lec15 homolog (C.griseus)
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