The ALG12 gene homepage

General information
Gene symbol ALG12
Gene name ALG12, alpha-1,6-mannosyltransferase
Chromosome 22
Chromosomal band q13.33
Imprinted Unknown
Genomic reference NG_008927.1
Transcript reference NM_024105.3
Associated with diseases CDG-1G, ID
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 355
Unique public DNA variants reported 47
Individuals with public variants 35
Hidden variants -
Date created November 30, -0001
Date last updated September 28, 2016
Version ALG12:160928

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:19358
Entrez Gene 79087
PubMed articles ALG12
OMIM - Gene 607144
OMIM - Diseases CDG-1G (glycosylation, congenital disorder of, type Ig (CDG-1G))


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00009932 22 ALG12, alpha-1,6-mannosyltransferase NM_024105.3 NP_077010.1 355