EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   2.4.1.224 | Carcinoma |
33314711 |
Exostosin1 as a novel prognostic and predictive biomarker for squamous cell lung carcinoma: A study based on bioinformatics analysis. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
1
4
3
2 |
| 2.4.1.224 | Diabetes Mellitus |
23871501 |
Lack of replication of common EXT2 gene variants with susceptibility to type 2 diabetes in Lebanese Arabs. |
causal interaction
therapeutic application
unassigned |
1
1
0 |
| 2.4.1.224 | Diabetes Mellitus, Type 2 |
23871501 |
Lack of replication of common EXT2 gene variants with susceptibility to type 2 diabetes in Lebanese Arabs. |
causal interaction
therapeutic application
unassigned |
1
1
0 |
| 2.4.1.224 | Exostoses |
10806213 |
Structural analysis of glycosaminoglycans in animals bearing mutations in sugarless, sulfateless, and tout-velu. Drosophila homologues of vertebrate genes encoding glycosaminoglycan biosynthetic enzymes. |
unassigned |
0 |
| 2.4.1.224 | Exostoses |
26246518 |
Old gene, new phenotype: mutations in heparan sulfate synthesis enzyme, EXT2 leads to seizure and developmental disorder, no exostoses. |
causal interaction
unassigned |
2
0 |
| 2.4.1.224 | Exostoses |
32818603 |
Heparan sulfate deficiency leads to hypertrophic chondrocytes by increasing bone morphogenetic protein signaling. |
causal interaction
ongoing research
unassigned |
2
1
0 |
| 2.4.1.224 | Exostoses, Multiple Hereditary |
11391482 |
Etiological point mutations in the hereditary multiple exostoses gene EXT1: a functional analysis of heparan sulfate polymerase activity. |
causal interaction
diagnostic usage
unassigned |
1
2
0 |
| 2.4.1.224 | Exostoses, Multiple Hereditary |
18216313 |
Familial nephropathy and multiple exostoses with exostosin-1 (EXT1) gene mutation. |
causal interaction
unassigned |
2
0 |
| 2.4.1.224 | Exostoses, Multiple Hereditary |
20233460 |
Multiple osteochondromas: clinicopathological and genetic spectrum and suggestions for clinical management. |
causal interaction
therapeutic application
unassigned |
2
1
0 |
| 2.4.1.224 | Exostoses, Multiple Hereditary |
22037484 |
Identification and functional characterization of the human EXT1 promoter region. |
causal interaction
unassigned |
1
0 |
