Identity
HGNC
LOCATION
1p34.1
LOCUSID
ALIAS
DEE15,EIEE15,MRT12,SIAT6,ST3GALII,ST3Gal
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 6487
MIM: 606494
HGNC: 10866
Ensembl: ENSG00000126091
Variants:
dbSNP: 6487
ClinVar: 6487
TCGA: ENSG00000126091
COSMIC: ST3GAL3
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38602029 | 2024 | Human ST3Gal II and ST6GalNAc IV genes increase human serum-mediated cytotoxicity to xenogeneic cells. | 0 |
| 38602029 | 2024 | Human ST3Gal II and ST6GalNAc IV genes increase human serum-mediated cytotoxicity to xenogeneic cells. | 0 |
| 37067065 | 2023 | The epilepsy phenotype of ST3GAL3-related developmental and epileptic encephalopathy. | 2 |
| 37067065 | 2023 | The epilepsy phenotype of ST3GAL3-related developmental and epileptic encephalopathy. | 2 |
| 36405992 | 2022 | ST3GAL3 Promotes the Inflammatory Response of Fibroblast-Like Synoviocytes in Rheumatoid Arthritis by Activating the TLR9/MyD88 Pathway. | 0 |
| 36405992 | 2022 | ST3GAL3 Promotes the Inflammatory Response of Fibroblast-Like Synoviocytes in Rheumatoid Arthritis by Activating the TLR9/MyD88 Pathway. | 0 |
| 31584066 | 2020 | A novel nonsense and inactivating variant of ST3GAL3 in two infant siblings suffering severe epilepsy and expressing circulating CA19.9. | 14 |
| 31914669 | 2020 | ST3GAL3, ST3GAL4, and ST3GAL6 differ in their regulation of biological functions via the specificities for the α2,3-sialylation of target proteins. | 29 |
| 32046534 | 2020 | Contribution of Intellectual Disability-Related Genes to ADHD Risk and to Locomotor Activity in Drosophila. | 13 |
| 32666583 | 2020 | A novel variant of ST3GAL3 causes non-syndromic autosomal recessive intellectual disability in Iranian patients. | 3 |
| 31584066 | 2020 | A novel nonsense and inactivating variant of ST3GAL3 in two infant siblings suffering severe epilepsy and expressing circulating CA19.9. | 14 |
| 31914669 | 2020 | ST3GAL3, ST3GAL4, and ST3GAL6 differ in their regulation of biological functions via the specificities for the α2,3-sialylation of target proteins. | 29 |
| 32046534 | 2020 | Contribution of Intellectual Disability-Related Genes to ADHD Risk and to Locomotor Activity in Drosophila. | 13 |
| 32666583 | 2020 | A novel variant of ST3GAL3 causes non-syndromic autosomal recessive intellectual disability in Iranian patients. | 3 |
| 31702036 | 2019 | ST3Gal3 confers paclitaxel‑mediated chemoresistance in ovarian cancer cells by attenuating caspase‑8/3 signaling. | 10 |
Citation
Dessen P
ST3GAL3 (ST3 beta-galactoside alpha-2,3-sialyltransferase 3)
Atlas Genet Cytogenet Oncol Haematol. 2007-02-01
Online version: http://atlasgeneticsoncology.org/gene/46012/st3gal3-(st3-beta-galactoside-alpha-2-3-sialyltransferase-3)
