EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   2.4.1.150 | Breast Neoplasms |
21750175 |
Engagement of I-Branching {beta}-1, 6-N-Acetylglucosaminyltransferase 2 in Breast Cancer Metastasis and TGF-{beta} Signaling. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
4
3
4
2 |
| 2.4.1.150 | Breast Neoplasms |
26678556 |
I-branching N-acetylglucosaminyltransferase regulates prostate cancer invasiveness by enhancing ?5?1 integrin signaling. |
unassigned |
0 |
| 2.4.1.150 | Carcinoma |
30575058 |
GCNT2 induces epithelial-mesenchymal transition and promotes migration and invasion in esophageal squamous cell carcinoma cells. |
causal interaction
diagnostic usage
unassigned |
4
1
0 |
| 2.4.1.150 | Cataract |
15161861 |
A nonsense mutation in the glucosaminyl (N-acetyl) transferase 2 gene (GCNT2): association with autosomal recessive congenital cataracts. |
causal interaction
unassigned |
3
0 |
| 2.4.1.150 | Cataract |
18703362 |
Scanning 17 candidate genes for association with primary cataracts in the wire-haired Dachshund. |
diagnostic usage
ongoing research
unassigned |
1
1
0 |
| 2.4.1.150 | Cataract |
21761136 |
An Alu repeat-mediated genomic GCNT2 deletion underlies congenital cataracts and adult i blood group. |
causal interaction
ongoing research
therapeutic application
unassigned |
4
2
1
0 |
| 2.4.1.150 | Cataract |
26622071 |
Phenotypes of Recessive Pediatric Cataract in a Cohort of Children with Identified Homozygous Gene Mutations (An American Ophthalmological Society Thesis). |
unassigned |
0 |
| 2.4.1.150 | Cataract |
27609212 |
Case report of homozygous deletion involving the first coding exons of GCNT2 isoforms A and B and part of the upstream region of TFAP2A in congenital cataract. |
causal interaction
unassigned |
4
0 |
| 2.4.1.150 | Cataract |
27936067 |
Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts. |
causal interaction
unassigned |
4
0 |
| 2.4.1.150 | Cataract |
28278293 |
Correction: Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts. |
causal interaction
unassigned |
3
0 |
