Alg14 Gene Summary [Mouse]

Predicted to enable protein-membrane adaptor 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 part of UDP-N-acetylglucosamine transferase complex. Predicted to be active in cytoplasmic side of endoplasmic reticulum membrane. Is expressed in several structures, including early conceptus; gallbladder; genitourinary system; gut gland; and nervous system. Human ortholog(s) of this gene implicated in congenital myasthenic syndrome 15. Orthologous to human ALG14 (ALG14 UDP-N-acetylglucosaminyltransferase subunit). [provided by Alliance of Genome Resources, Apr 2025]

Details

Type
Protein Coding
Official Symbol
Alg14
Official Name
asparagine-linked glycosylation 14 [Source:MGI Symbol;Acc:MGI:1914039]
Ensembl ID
ENSMUSG00000039887
Bio databases IDs NCBI: 66789 Ensembl: ENSMUSG00000039887
Aliases asparagine-linked glycosylation 14
Synonyms 5430428G01Rik, ALG14 UDP-N-acetylglucosaminyltransferase subunit, ALG14, UDP-N-acetylglucosaminyltransferase subunit, asparagine-linked glycosylation 14, CMS15, IDDEBF, MEPCA, RGD1312003
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 Alg14 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • glycosyltransferase family 1 and related proteins with GTB topology
  • protein binding activity, bridging
  • protein binding

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • pneumonia
  • nonalcoholic fatty liver disease
  • myopathy, epilepsy, and progressive cerebral atrophy
  • congenital myopathy
  • congenital myasthenic syndrome type 15
  • intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies
  • aldosterone producing adrenocortical adenoma
  • adenoma formation
  • congenital disorders of glycosylation
  • productive infection by HIV-1
regulated by
regulates
  • oligosaccharide-diphosphodolichol
  • Carboxypeptidase Y
role in cell
  • growth

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
  • endoplasmic reticulum membrane

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the mouse Alg14 gene, providing context for its role in the cell.

Biological Process

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

Cellular Component

Where in the cell the gene product is active
  • endoplasmic reticulum membrane
  • UDP-N-acetylglucosamine transferase complex

Molecular Function

What the gene product does at the molecular level
  • protein binding
  • protein anchor
  • N-acetylglucosaminyldiphosphodolichol N-acetylglucosaminyltransferase 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.