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: 79053
MIM: 608103
HGNC: 23161
Ensembl: ENSG00000159063
Variants:
dbSNP: 79053
ClinVar: 79053
TCGA: ENSG00000159063
COSMIC: ALG8
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 36574950 | 2023 | Individuals heterozygous for ALG8 protein-truncating variants are at increased risk of a mild cystic kidney disease. | 8 |
| 36574950 | 2023 | Individuals heterozygous for ALG8 protein-truncating variants are at increased risk of a mild cystic kidney disease. | 8 |
| 36454274 | 2022 | ALG8 Fuels Stemness Through Glycosylation of the WNT/Beta-Catenin Signaling Pathway in Colon Cancer. | 2 |
| 36454274 | 2022 | ALG8 Fuels Stemness Through Glycosylation of the WNT/Beta-Catenin Signaling Pathway in Colon Cancer. | 2 |
| 30420707 | 2019 | Wide clinical spectrum in ALG8-CDG: clues from molecular findings suggest an explanation for a milder phenotype in the first-described patient. | 4 |
| 30420707 | 2019 | Wide clinical spectrum in ALG8-CDG: clues from molecular findings suggest an explanation for a milder phenotype in the first-described patient. | 4 |
| 28375157 | 2017 | Isolated polycystic liver disease genes define effectors of polycystin-1 function. | 68 |
| 28375157 | 2017 | Isolated polycystic liver disease genes define effectors of polycystin-1 function. | 68 |
| 26066342 | 2015 | ALG8-CDG: novel patients and review of the literature. | 23 |
| 26066342 | 2015 | ALG8-CDG: novel patients and review of the literature. | 23 |
| 24555185 | 2014 | Wrinkled skin and fat pads in patients with ALG8-CDG: revisiting skin manifestations in congenital disorders of glycosylation. | 5 |
| 24555185 | 2014 | Wrinkled skin and fat pads in patients with ALG8-CDG: revisiting skin manifestations in congenital disorders of glycosylation. | 5 |
| 22306853 | 2012 | Severe ALG8-CDG (CDG-Ih) associated with homozygosity for two novel missense mutations detected by exome sequencing of candidate genes. | 2 |
| 22306853 | 2012 | Severe ALG8-CDG (CDG-Ih) associated with homozygosity for two novel missense mutations detected by exome sequencing of candidate genes. | 2 |
| 20379614 | 2010 | Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. | 78 |
Citation
Dessen P
ALG8 (ALG8 alpha-1,3-glucosyltransferase)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/60255/alg8-(alg8-alpha-1-3-glucosyltransferase)
