Identity
HGNC
LOCATION
2p11.2
LOCUSID
ALIAS
SATI,SIAT9,SIATGM3S,SPDRS,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: 8869
MIM: 604402
HGNC: 10872
Ensembl: ENSG00000115525
Variants:
dbSNP: 8869
ClinVar: 8869
TCGA: ENSG00000115525
COSMIC: ST3GAL5
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 36690566 | 2023 | Neurological insights on two siblings with GM3 synthase deficiency due to novel compound heterozygous ST3GAL5 variants. | 2 |
| 37676252 | 2023 | Neural-specific alterations in glycosphingolipid biosynthesis and cell signaling associated with two human ganglioside GM3 synthase deficiency variants. | 0 |
| 36690566 | 2023 | Neurological insights on two siblings with GM3 synthase deficiency due to novel compound heterozygous ST3GAL5 variants. | 2 |
| 37676252 | 2023 | Neural-specific alterations in glycosphingolipid biosynthesis and cell signaling associated with two human ganglioside GM3 synthase deficiency variants. | 0 |
| 36172374 | 2022 | Identification of ST3GAL5 as a prognostic biomarker correlating with CD8(+) T cell exhaustion in clear cell renal cell carcinoma. | 10 |
| 36172374 | 2022 | Identification of ST3GAL5 as a prognostic biomarker correlating with CD8(+) T cell exhaustion in clear cell renal cell carcinoma. | 10 |
| 30576498 | 2019 | Total loss of GM3 synthase activity by a normally processed enzyme in a novel variant and in all ST3GAL5 variants reported to cause a distinct congenital disorder of glycosylation. | 16 |
| 30576498 | 2019 | Total loss of GM3 synthase activity by a normally processed enzyme in a novel variant and in all ST3GAL5 variants reported to cause a distinct congenital disorder of glycosylation. | 16 |
| 29983310 | 2018 | Diseases of ganglioside biosynthesis: An expanding group of congenital disorders of glycosylation. | 21 |
| 30185102 | 2018 | ST3GAL5-Related Disorders: A Deficiency in Ganglioside Metabolism and a Genetic Cause of Intellectual Disability and Choreoathetosis. | 10 |
| 29983310 | 2018 | Diseases of ganglioside biosynthesis: An expanding group of congenital disorders of glycosylation. | 21 |
| 30185102 | 2018 | ST3GAL5-Related Disorders: A Deficiency in Ganglioside Metabolism and a Genetic Cause of Intellectual Disability and Choreoathetosis. | 10 |
| 28218742 | 2017 | MiRNA expression profiles reveal the involvement of miR-26a, miR-548l and miR-34a in hepatocellular carcinoma progression through regulation of ST3GAL5. | 25 |
| 28698248 | 2017 | Ganglioside glycosyltransferases are S-acylated at conserved cysteine residues involved in homodimerisation. | 2 |
| 29047240 | 2017 | Identification and Functional Characterization of ST3GAL5 and ST8SIA1 Variants in Patients with Thyroid-Associated Ophthalmopathy. | 6 |
Citation
Dessen P
ST3GAL5 (ST3 beta-galactoside alpha-2,3-sialyltransferase 5)
Atlas Genet Cytogenet Oncol Haematol. 2010-03-01
Online version: http://atlasgeneticsoncology.org/gene/51375/st3gal5
