The ALG2 gene homepage

General information
Gene symbol ALG2
Gene name ALG2, alpha-1,3/1,6-mannosyltransferase
Chromosome 9
Chromosomal band q31.1
Imprinted Unknown
Genomic reference NG_008928.1
Transcript reference NM_033087.3
Associated with diseases CDG-1I, CMS-14, ID
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 25
Unique public DNA variants reported 6
Individuals with public variants 22
Hidden variants 2
Date created November 30, -0001
Date last updated September 28, 2016
Version ALG2:160928

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
External URL List of LSDBs for this gene
The reference LOVD for this gene, if available
HGNC HGNC:23159
Entrez Gene 85365
PubMed articles ALG2
OMIM - Gene 607905
OMIM - Diseases CDG-1I (glycosylation, congenital disorder of, type Ii (CDG-1I))
CMS-14 (myasthenic syndrome, congenital, type 14, with tubular aggregates (CMS-14))


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00028174 9 transcript variant 1 NM_033087.3 NP_149078.1 25