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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
ST3 beta-galactoside alpha-2,3-sialyltransferase 5
Summary
- Gene Symbol
-
- ST3GAL5
- Aliases
-
- SIATGM3S
- ST3GalV
- ganglioside GM3 synthase
- lactosylceramide alpha-2,3-sialyltransferase
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Disulfide bond
- Epilepsy
- Glycoprotein
- Glycosyltransferase
- Golgi apparatus
- Intellectual disability
- Lipid metabolism
- Reference proteome
- Signal-anchor
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| Q9UNP4 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| glycosphingolipid biosynthetic process | ||
| protein glycosylation | ||
| ganglioside biosynthetic process |
GO Hierarchy
biological process
metabolic process [inference]
nitrogen compound metabolic process [inference]
biosynthetic process [inference]
cellular metabolic process [inference]
primary metabolic process [inference]
organic substance metabolic process [inference]
cellular process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| membrane | ||
| Golgi membrane |
| GO Term | Evidence Code | PMID |
|---|---|---|
| lactosylceramide alpha-2,3-sialyltransferase activity | ||
| beta-galactoside (CMP) alpha-2,3-sialyltransferase activity | ||
| sialyltransferase activity |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
GlycoGene Database (GGDB)
- GGDB ID
- gg052
- Gene Symbol
-
- ST3GAL5
- Reactions
G84224TW
G91237TK
- Orthologous Gene
| Species | Protein | mRNA |
|---|---|---|
| Rattus norvegicus | NP_112627 | NM_031337 |
| Mus musculus | NP_035505 | NM_011375 |
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:12359 | endocrine exophthalmos | |
| DOID:12697 | locked-in syndrome | |
| DOID:12835 | quadriplegia | |
| DOID:12918 | thromboangiitis obliterans | |
| DOID:13174 | dissociated nystagmus | |
| DOID:1432 | blindness | |
| DOID:14504 | Niemann-Pick disease | |
| DOID:1824 | status epilepticus | |
| DOID:1969 | cerebral palsy | |
| DOID:2303 | stereotypic movement disorder |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003623 | Neonatal onset |
| HP:0006834 | Developmental stagnation at onset of seizures |
| HP:0008872 | Feeding difficulties in infancy |
| HP:0010841 | Multifocal epileptiform discharges |
| HP:0012391 | Hyporeflexia of upper limbs |
| HP:0100704 | Cerebral visual impairment |
| Disease ID | Disease Name |
|---|---|
| OMIM:609056 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP000401
- Gene Name
- ST3 beta-galactoside alpha-2,3-sialyltransferase 5
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 100974771 | PANPA25225 | ||
| 459371 | PANTR28085 | ||
| 100458488 | PONAB22826 | ||
| 612022 | CANLF05162 | ||
| 112916669 | VULVU09296 | ||
| 123799693 | URSAM11834 | ||
| 100469790 | AILME03105 | ||
| 101679411 | MUSPF17886 | ||
| 101092099 | FELCA06498 | ||
| 122216282 | PANLE01489 |
