The ALG2 gene homepage

General information
Gene symbol ALG2
Gene name asparagine-linked glycosylation 2, alpha-1,3-mannosyltransferase homolog (S. cerevisiae)
Chromosome 9
Chromosomal band q31.1
Imprinted Unknown
Genomic reference NG_008928.1
Transcript reference NM_033087.3
Exon/intron information NM_033087.3 exon/intron table
Associated with diseases CDG1I, CMS14, ID
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Gert Matthijs
Total number of public variants reported 15
Unique public DNA variants reported 14
Individuals with public variants 2
Hidden variants 2
Download all this gene's data Download all data
Notes The establishment of this gene variant database (LSDB) was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement 200754 - the GEN2PHEN project.
Date created April 29, 2010
Date last updated September 17, 2021
Version ALG2:210917

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_033087.3.
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
Homepage URL
External URL Congenital Disorders of Glycosylation pages
HGNC 23159
Entrez Gene 85365
PubMed articles ALG2
OMIM - Gene 607905
OMIM - Diseases CDG1I (glycosylation, congenital disorder of, type Ii (CDG-1I))
CMS14 (myasthenic syndrome, congenital, type 14, with tubular aggregates (CMS-14))
GeneCards ALG2
GeneTests ALG2
Orphanet ALG2

Active transcripts




NCBI ID     

NCBI Protein ID     

00002370 9 transcript variant 1 NM_033087.3 NP_149078.1 15

Copyright & disclaimer
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