St3gal3 Gene Summary [Rat]

Predicted to enable beta-galactoside (CMP) alpha-2,3-sialyltransferase activity. Predicted to be involved in ganglioside biosynthetic process via lactosylceramide and protein glycosylation. Predicted to be located in Golgi cisterna membrane; Golgi membrane; and extracellular region. Human ortholog(s) of this gene implicated in autosomal recessive intellectual developmental disorder 12 and developmental and epileptic encephalopathy 15. Orthologous to human ST3GAL3 (ST3 beta-galactoside alpha-2,3-sialyltransferase 3). [provided by Alliance of Genome Resources, Apr 2025]

Details

Type
Protein Coding
Official Symbol
St3gal3
Official Name
ST3 beta-galactoside alpha-2,3-sialyltransferase 3 [Source:RGD Symbol;Acc:68414]
Ensembl ID
ENSRNOG00000019843
Bio databases IDs NCBI: 64445 Ensembl: ENSRNOG00000019843
Aliases ST3 beta-galactoside alpha-2,3-sialyltransferase 3
Synonyms DEE15, EIEE15, MRT12, Siat3, SIAT6, ST3 beta-galactoside alpha-2,3-sialyltransferase 3, ST3GALII, ST3Gal III, ST3N, ST3 β-galactoside α-2,3-sialyltransferase 3
Species
Rat, Rattus norvegicus
OrthologiesHumanMouse

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 rat St3gal3 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 29 (sialyltransferase)
  • glycosyltransferase family 29
  • N-acetyllactosaminide alpha-2,3-sialyltransferase
  • sialyltransferase
  • enzyme
  • 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
  • Alzheimer disease
  • coronary artery disease
  • Ohtahara syndrome
  • schizophrenia
  • autosomal recessive mental retardation type 12
  • attention deficit hyperactivity disorder
  • hereditary disorder
  • early infantile epileptic encephalopathy type 15
  • nonlobar intracerebral hemorrhage
  • amyotrophic lateral sclerosis
regulated by
regulates
  • oligosaccharide
  • glycosphingolipid
  • sialyl 6-sulfo Lewis X
  • Alpha1-3-gt
  • O-glycan
  • keratan sulfate
role in cell
  • apoptosis
  • antigenicity
  • reverse transcription
  • reverse transcription in
  • cytolysis

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
  • Extracellular Space
  • cellular membrane
  • Golgi membrane
  • trans Golgi network
  • trans Golgi cisternae

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the rat St3gal3 gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • ganglioside biosynthetic process via lactosylceramide
  • viral protein processing
  • protein glycosylation
  • oligosaccharide biosynthetic process
  • keratan sulfate biosynthetic process
  • O-glycan processing
  • glycosphingolipid biosynthetic process

Cellular Component

Where in the cell the gene product is active
  • Golgi cisterna membrane
  • Golgi membrane
  • extracellular region

Molecular Function

What the gene product does at the molecular level
  • protein binding
  • sialyltransferase activity
  • beta-galactoside (CMP) alpha-2,3-sialyltransferase activity
  • N-acetyllactosaminide alpha-2,3-sialyltransferase 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.