Identity
HGNC
LOCATION
11q23.1
LOCUSID
ALIAS
CDG1L,DIBD1,GIKANIS,LOH11CR1J
FUSION GENES
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: 79796
MIM: 606941
HGNC: 15672
Ensembl: ENSG00000086848
Variants:
dbSNP: 79796
ClinVar: 79796
TCGA: ENSG00000086848
COSMIC: ALG9
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37761895 | 2023 | Heterozygosity of ALG9 in Association with Autosomal Dominant Polycystic Liver Disease. | 0 |
| 37761895 | 2023 | Heterozygosity of ALG9 in Association with Autosomal Dominant Polycystic Liver Disease. | 0 |
| 35839600 | 2022 | Missense variant c.1460 T > C (p.L487P) enhances protein degradation of ER mannosyltransferase ALG9 in two new ALG9-CDG patients presenting with West syndrome and review of the literature. | 3 |
| 35839600 | 2022 | Missense variant c.1460 T > C (p.L487P) enhances protein degradation of ER mannosyltransferase ALG9 in two new ALG9-CDG patients presenting with West syndrome and review of the literature. | 3 |
| 32359033 | 2020 | LncRNA MEG3 contributes to drug resistance in acute myeloid leukemia by positively regulating ALG9 through sponging miR-155. | 22 |
| 32359033 | 2020 | LncRNA MEG3 contributes to drug resistance in acute myeloid leukemia by positively regulating ALG9 through sponging miR-155. | 22 |
| 31395617 | 2019 | ALG9 Mutation Carriers Develop Kidney and Liver Cysts. | 56 |
| 31395617 | 2019 | ALG9 Mutation Carriers Develop Kidney and Liver Cysts. | 56 |
| 25966638 | 2016 | A novel phenotype in N-glycosylation disorders: Gillessen-Kaesbach-Nishimura skeletal dysplasia due to pathogenic variants in ALG9. | 13 |
| 26733289 | 2016 | Classical galactosaemia: novel insights in IgG N-glycosylation and N-glycan biosynthesis. | 21 |
| 25966638 | 2016 | A novel phenotype in N-glycosylation disorders: Gillessen-Kaesbach-Nishimura skeletal dysplasia due to pathogenic variants in ALG9. | 13 |
| 26733289 | 2016 | Classical galactosaemia: novel insights in IgG N-glycosylation and N-glycan biosynthesis. | 21 |
| 19451548 | 2009 | Quality control of glycoproteins bearing truncated glycans in an ALG9-defective (CDG-IL) patient. | 10 |
| 19451548 | 2009 | Quality control of glycoproteins bearing truncated glycans in an ALG9-defective (CDG-IL) patient. | 10 |
| 16859551 | 2006 | Common variations in ALG9 are not associated with bipolar I disorder: a family-based study. | 2 |
Citation
Dessen P
ALG9 (ALG9 alpha-1,2-mannosyltransferase)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/60256/alg9-(alg9-alpha-1-2-mannosyltransferase)
