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AGL

This gene encodes the glycogen debrancher enzyme which is involved in glycogen degradation. This enzyme has two independent catalytic activities which occur at different sites on the protein: a 4-alpha-glucotransferase activity and a amylo-1,6-glucosidase activity. Mutations in this gene are associated with glycogen storage disease although a wide range of enzymatic and clinical variability occurs which may be due to tissue-specific alternative splicing. Alternatively spliced transcripts encoding different isoforms have been described.
Protein class

Disease related genes, Enzymes, Human disease related genes, Metabolic proteins, Plasma proteins, Potential drug targets

Predicted location

Membrane

Single cell type specificity

Cell type enhanced (Muller glia cells, Theca cells)

Immune cell specificity

Low immune cell specificity

Cell line specificity

Low cell line specificity

Interaction

Monomer. Interacts with NHLRC1/malin.

Molecular function

Glycosidase, Glycosyltransferase, Hydrolase, Multifunctional enzyme, Transferase

More Types Infomation

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For Research Use Only. Not For Clinical Use.

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