Alg2 Gene Summary [Mouse]

Predicted to enable GDP-Man:Man1GlcNAc2-PP-Dol alpha-1,3-mannosyltransferase activity and GDP-Man:Man2GlcNAc2-PP-dolichol alpha-1,6-mannosyltransferase activity. Predicted to be involved in dolichol-linked oligosaccharide biosynthetic process. Predicted to act upstream of with a positive effect on protein N-linked glycosylation. Predicted to be active in cytoplasmic side of endoplasmic reticulum membrane. Is expressed in several structures, including alimentary system; brain; genitourinary system; hemolymphoid system; and sensory organ. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation Ii and congenital myasthenic syndrome 14. Orthologous to human ALG2 (ALG2 alpha-1,3/1,6-mannosyltransferase). [provided by Alliance of Genome Resources, Apr 2025]

Details

Type
Processed Transcript
Official Symbol
Alg2
Official Name
asparagine-linked glycosylation 2 (alpha-1,3-mannosyltransferase) [Source:MGI Symbol;Acc:MGI:1914731]
Ensembl ID
ENSMUSG00000039740
Bio databases IDs NCBI: 56737 Ensembl: ENSMUSG00000039740
Aliases asparagine-linked glycosylation 2 (alpha-1,3-mannosyltransferase)
Synonyms 1110018A23Rik, 1300013N08RIK, ALG2 alpha-1,3/1,6-mannosyltransferase, ALG2, alpha-1,3/1,6-mannosyltransferase, ALG2 α-1,3/1,6-mannosyltransferase, ALG2, α-1,3/1,6-mannosyltransferase, ALPG2, CDG1I, CDGIi, CMS14, CMSTA3, hALPG2, MNCb-5081, NET38
Species
Mouse, Mus musculus
OrthologiesHumanRat

Protein Domains

A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in mouse Alg2 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • glycolipid 3-alpha-mannosyltransferase
  • glycosyltransferase family 1 and related proteins with GTB topology
  • alpha-1,3-mannosyltransferase
  • alpha-1,6-mannosyltransferase
  • Glycosyl transferase 4-like domain
  • enzyme
  • protein binding
  • glycolipid mannosyltransferase
  • Glycosyl transferases group 1
  • Glycosyltransferase Family 4

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • Alzheimer disease
  • adenoma formation
  • congenital disorder of glycosylation type 1i
  • aldosterone producing adrenocortical adenoma
  • congenital myasthenic syndrome type 14
  • early onset hypertension
regulated by
  • benzo(a)pyrene
  • heavy metal
  • XBP1
  • beta-estradiol
  • Ca2+
  • HIVEP3
  • medroxyprogesterone acetate
  • 8-bromo-cAMP
  • RYR1
regulates
role in cell
  • expression in
  • differentiation
  • survival
  • maturation
  • chondrogenesis in
  • biosynthesis in
  • endoplasmic reticulum-associated degradation in

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Cytoplasm
  • cellular membrane
  • endoplasmic reticulum membrane

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the mouse Alg2 gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • oligosaccharide-lipid intermediate biosynthetic process
  • protein glycosylation
  • protein N-linked glycosylation
  • dolichol-linked oligosaccharide biosynthetic process

Cellular Component

Where in the cell the gene product is active
  • endoplasmic reticulum membrane
  • membrane

Molecular Function

What the gene product does at the molecular level
  • alpha-1,3-mannosyltransferase activity
  • protein binding
  • GDP-Man:Man1GlcNAc2-PP-Dol alpha-1,3-mannosyltransferase activity

Gene-Specific Assays for Results You Can Trust

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.