EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   2.4.99.2 | (n-acetylneuraminyl)-galactosylglucosylceramide n-acetylgalactosaminyltransferase deficiency |
27232954 |
GM3 synthase deficiency due to ST3GAL5 variants in two Korean female siblings: Masquerading as Rett syndrome-like phenotype. |
causal interaction
diagnostic usage
unassigned |
3
3
0 |
| 2.4.99.2 | (n-acetylneuraminyl)-galactosylglucosylceramide n-acetylgalactosaminyltransferase deficiency |
30185102 |
ST3GAL5-Related Disorders: A Deficiency in Ganglioside Metabolism and a Genetic Cause of Intellectual Disability and Choreoathetosis. |
causal interaction
unassigned |
4
0 |
| 2.4.99.2 | Adenocarcinoma |
32872308 |
Knockdown of ?2,3-Sialyltransferases Impairs Pancreatic Cancer Cell Migration, Invasion and E-selectin-Dependent Adhesion. |
causal interaction
therapeutic application
unassigned |
4
4
0 |
| 2.4.99.2 | alpha-n-acetylgalactosaminide alpha-2,6-sialyltransferase deficiency |
12068010 |
Genetically altered mice with different sialyltransferase deficiencies show tissue-specific alterations in sialylation and sialic acid 9-O-acetylation. |
causal interaction
ongoing research
unassigned |
2
3
0 |
| 2.4.99.2 | Atherosclerosis |
27584569 |
Association of Single Nucleotide Polymorphisms in the ST3GAL4 Gene with VWF Antigen and Factor VIII Activity. |
causal interaction
diagnostic usage
ongoing research
unassigned |
1
4
2
0 |
| 2.4.99.2 | beta-d-galactosyl-(1->3)-n-acetyl-beta-d-galactosaminide alpha-2,3-sialyltransferase deficiency |
12068010 |
Genetically altered mice with different sialyltransferase deficiencies show tissue-specific alterations in sialylation and sialic acid 9-O-acetylation. |
causal interaction
ongoing research
unassigned |
2
3
0 |
| 2.4.99.2 | beta-d-galactosyl-(1->3)-n-acetyl-beta-d-galactosaminide alpha-2,3-sialyltransferase deficiency |
16751387 |
The sialyltransferase ST3Gal-I is not required for regulation of CD8-class I MHC binding during T cell development. |
causal interaction
ongoing research
unassigned |
4
1
0 |
| 2.4.99.2 | beta-d-galactosyl-(1->3)-n-acetyl-beta-d-galactosaminide alpha-2,3-sialyltransferase deficiency |
29983310 |
Diseases of ganglioside biosynthesis: An expanding group of congenital disorders of glycosylation. |
causal interaction
therapeutic application
unassigned |
3
1
0 |
| 2.4.99.2 | beta-d-galactosyl-(1->3)-n-acetyl-beta-d-galactosaminide alpha-2,3-sialyltransferase deficiency |
32664815 |
Enhanced Susceptibility to Chemoconvulsant-Induced Seizures in Ganglioside GM3 Synthase Knockout Mice. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
3
3
3
1 |
| 2.4.99.2 | Breast Neoplasms |
9751611 |
Multiplex reverse transcription polymerase chain reaction assessment of sialyltransferase expression in human breast cancer. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
4
3
0 |
