EC Number |
Protein Variants |
Reference |
---|
2.4.1.150 | A169T |
naturally occuring mutation in the GCNT2 gene causing blood group I and cataract formation phenotype |
759326 |
2.4.1.150 | G310D |
naturally occuring mutation in the GCNT2 gene causing blood group I and cataract formation phenotype |
759326 |
2.4.1.150 | G334R |
naturally occuring mutation in the GCNT2 gene causing blood group I and cataract formation phenotype |
759326 |
2.4.1.150 | G348E |
naturally occuring mutation in the GCNT2 gene causing blood group I and cataract formation phenotype |
759326 |
2.4.1.150 | more |
CRISPR-mediated knockout of GCNT3 in pancreatic cancer cells |
758993 |
2.4.1.150 | more |
CRISPR-mediated knockout of GCNT3 in pancreatic cancer cells. A significant increase in pancreas weight is observed in Kras mice compared with wild-type mice. Only 6% of the pancreata from Kras mice are free from PanIN lesions and PDAC, whereas 100% of pancreata are normal in wild-type mice |
-, 758993 |
2.4.1.150 | more |
GCNT3 downregulation by shGCNT3 7. GCNT3 overexpression reduces 5-fluorouracil resistance in colorectal cancer (CRC) cells. GCNT3 overexpression reduces proliferation, invasion and changes metabolic capacities of CRC cells. Genomic analysis of GCNT3 overexpression, overview |
760171 |
2.4.1.150 | more |
knockdown of GCNT3 using GCNT3-specific small interfering RNAs: siGCNT3-1 (GCUACUGCGAGCUGUGUAUTT), and siGCNT3-2 (GCUCAGUGCCGUGGAAAUATT). Reduction of the expression of endogenous GCNT3 by siRNA transfection in SGC7901 and BGC823 cells. Epstein-Barr virus (EBV) miRNA miR-BART1-5p specifically targets GCNT3. miR-BART1-5p suppresses GCNT3 expression, cell proliferation, and migration in EBVnGC, and the MiR-BART1-5p inhibitor increases GCNT3 expression, cell proliferation, and migration in transfected GT39 and GT38 cells. NF-kappaB can activate the expression of multiple miR-BARTs, including miR-BART1-5p |
760226 |
2.4.1.150 | more |
mutation experiments at the GT boxes of the promoters of IGnT A and B genes |
638562 |
2.4.1.150 | N388R |
homozygous frameshift mutation c.1163_1166delATCA, p.(Asn388Argfs*20) is the cause of congenital cataract in two affected siblings, pleiotropic effect of the mutation causing congenital cataract and adult I blood group phenotype, overview |
759326 |