Structural highlights
Disease
GDE_HUMAN Glycogen storage disease due to glycogen debranching enzyme deficiency. The disease is caused by variants affecting the gene represented in this entry.
Function
GDE_HUMAN Multifunctional enzyme acting as 1,4-alpha-D-glucan:1,4-alpha-D-glucan 4-alpha-D-glycosyltransferase and amylo-1,6-glucosidase in glycogen degradation.