ALG11 (ALG11 alpha-1,2-mannosyltransferase)

2014-11-01  

Identity

HGNC
LOCATION
13q14.3
LOCUSID
ALIAS
CDG1P,GT8
FUSION GENES

Other Information

Locus ID:

NCBI: 440138
MIM: 613666
HGNC: 32456
Ensembl: ENSG00000253710

Variants:

dbSNP: 440138
ClinVar: 440138
TCGA: ENSG00000253710
COSMIC: ALG11

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000253710ENST00000521508Q2TAA5
ENSG00000253710ENST00000523764Q5TAP0
ENSG00000253710ENST00000616513A0A087WYL8
ENSG00000253710ENST00000649340A0A3B3IS90
ENSG00000253710ENST00000649708A0A3B3ISU2
ENSG00000253710ENST00000650049A0A3B3ISP7

Expression (GTEx)

0
1
2
3
4
5

Pathways

PathwaySourceExternal ID
N-Glycan biosynthesisKEGGko00510
N-Glycan biosynthesisKEGGhsa00510
Metabolic pathwaysKEGGhsa01100
N-glycan precursor biosynthesisKEGGhsa_M00055
N-glycan precursor biosynthesisKEGGM00055
Metabolism of proteinsREACTOMER-HSA-392499
Post-translational protein modificationREACTOMER-HSA-597592
Asparagine N-linked glycosylationREACTOMER-HSA-446203
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent proteinREACTOMER-HSA-446193

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
250368262014Cloning and transcriptional expression of mouse mannosyltransferase IV/V cDNA, which is involved in the synthesis of lipid-linked oligosaccharides.0
250368262014Cloning and transcriptional expression of mouse mannosyltransferase IV/V cDNA, which is involved in the synthesis of lipid-linked oligosaccharides.0
222131322012Improved diagnostics lead to identification of three new patients with congenital disorder of glycosylation-Ip.14
222131322012Improved diagnostics lead to identification of three new patients with congenital disorder of glycosylation-Ip.14
200809372010A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip.18
200809372010A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip.18

Citation

Dessen P

ALG11 (ALG11 alpha-1,2-mannosyltransferase)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/60248/alg11-(alg11-alpha-1-2-mannosyltransferase)