| GO ID | GO name | Interaction type | Reference |
|---|---|---|---|
| GO:0006805 | Xenobiotic metabolic process | Decreases phenotype | PMID:30545405 |
| GO:0010718 | Positive regulation of epithelial to mesenchymal transition | Increases phenotype | PMID:26310382 |
| GO:0030520 | Intracellular estrogen receptor signaling pathway | Affects phenotype | PMID:39365753 |
| GO:0030521 | Androgen receptor signaling pathway | Affects phenotype | PMID:39365753 |
| GO:1901671 | Positive regulation of superoxide dismutase activity | Decreases phenotype | PMID:26310382 |
| GO:1904480 | Positive regulation of intestinal absorption | Increases phenotype | PMID:30545405 |
| GO:2000491 | Positive regulation of hepatic stellate cell activation | Increases phenotype | PMID:26310382 |
We have built a comprehensive resource which compiles potential endocrine disrupting chemicals (EDCs) based on the observed adverse effects or endocrine-mediated endpoints in published experiments on humans or rodents to support basic research. We are not responsible for any errors or omissions in the published research articles or supporting literature on potential EDCs compiled in this resource. Users are advised to exercise their own judgement on the weight of evidence for potential EDCs compiled in this resource. Importantly, our sole goal to build this resource on potential EDCs is to enable future basic research towards better understanding of the systems-level perturbations upon chemical exposure rather than influencing regulatory advice on chemical use.