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AGL (NM_000028) - amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase
Glycogen Debranching Enzyme Isoform 1
Legend
Mutation impacts
direct
network-rewiring
motif-changing
proximal
distal
none
Sites
multiple types
acetylation
methylation
succinylation
sumoylation
ubiquitination
glycosylation
- C-linked
- N-linked
- O-linked
- S-linked
phosphorylation
- SARS-CoV-2
Others
Exact position of a PTM site
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Mutations Visualisation
Protein summary
This is preferred isoform of AGL protein.
View all 6 isoforms
AGL:
glycogen debranching enzyme isoform 1
Description:
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. [provided by RefSeq, Jul 2008].
- Strand
- +
- Chromosome
- 1
- Protein
- 1532 residues
- All mutations
- 473
- PTM sites
- 31
- CDS
- 100,316,598 - 100,387,207
- Transcription
- 100,316,044 - 100,389,579
External references
Mappings retrieved from NCBI & UniProt.