Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 178
MIM: 610860
HGNC: 321
Ensembl: ENSG00000162688
Variants:
dbSNP: 178
ClinVar: 178
TCGA: ENSG00000162688
COSMIC: AGL
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 32222031 | 2020 | Spectrum of amyloglucosidase mutations in Asian Indian patients with Glycogen storage disease type III. | 5 |
| 32222031 | 2020 | Spectrum of amyloglucosidase mutations in Asian Indian patients with Glycogen storage disease type III. | 5 |
| 31028654 | 2019 | Intron retention is among six unreported AGL mutations identified in Malaysian GSD III patients. | 1 |
| 31028654 | 2019 | Intron retention is among six unreported AGL mutations identified in Malaysian GSD III patients. | 1 |
| 29794575 | 2018 | Distinct Clinical and Genetic Findings in Iranian Patients With Glycogen Storage Disease Type 3. | 5 |
| 29794575 | 2018 | Distinct Clinical and Genetic Findings in Iranian Patients With Glycogen Storage Disease Type 3. | 5 |
| 26490312 | 2016 | Loss of Glycogen Debranching Enzyme AGL Drives Bladder Tumor Growth via Induction of Hyaluronic Acid Synthesis. | 19 |
| 26975021 | 2016 | Metabolic phenotype of bladder cancer. | 132 |
| 26984562 | 2016 | Spectrum of AGL mutations in Chinese patients with glycogen storage disease type III: identification of 31 novel mutations. | 10 |
| 26490312 | 2016 | Loss of Glycogen Debranching Enzyme AGL Drives Bladder Tumor Growth via Induction of Hyaluronic Acid Synthesis. | 19 |
| 26975021 | 2016 | Metabolic phenotype of bladder cancer. | 132 |
| 26984562 | 2016 | Spectrum of AGL mutations in Chinese patients with glycogen storage disease type III: identification of 31 novel mutations. | 10 |
| 25451950 | 2015 | Molecular and clinical delineation of 12 patients with glycogen storage disease type III in Western Turkey. | 1 |
| 25602008 | 2015 | A founder AGL mutation causing glycogen storage disease type IIIa in Inuit identified through whole-exome sequencing: a case series. | 9 |
| 26252094 | 2015 | [Analysis of clinical features and AGL gene mutations in a family with glycogen storage disease type IIIa]. | 1 |
Citation
Dessen P
AGL (amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase)
Atlas Genet Cytogenet Oncol Haematol. 2016-08-01
Online version: http://atlasgeneticsoncology.org/gene/55879/agl-(amylo-alpha-1-6-glucosidase-4-alpha-glucanotransferase)
