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: 4122
MIM: 600988
HGNC: 6825
Ensembl: ENSG00000196547
Variants:
dbSNP: 4122
ClinVar: 4122
TCGA: ENSG00000196547
COSMIC: MAN2A2
RNA/Proteins
Expression (GTEx)
Pathways
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 36357165 | 2023 | Homozygous truncating variant in MAN2A2 causes a novel congenital disorder of glycosylation with neurological involvement. | 1 |
| 36357165 | 2023 | Homozygous truncating variant in MAN2A2 causes a novel congenital disorder of glycosylation with neurological involvement. | 1 |
| 33141432 | 2021 | High glucose-ROS conditions enhance the progression in cholangiocarcinoma via upregulation of MAN2A2 and CHD8. | 6 |
| 33141432 | 2021 | High glucose-ROS conditions enhance the progression in cholangiocarcinoma via upregulation of MAN2A2 and CHD8. | 6 |
Citation
Dessen P
MAN2A2 (mannosidase alpha class 2A member 2)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/68779/man2a2-(mannosidase-alpha-class-2a-member-2)
