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. 2015 Jun 19;124(3):380–387. doi: 10.1289/ehp.1408409

Table 4.

Gene ontology (GO) biological processes among genes predicted in silico to be targeted by miRNAs associated with EDC burden (miR-185, miR-142-3p, miR-15a-5p).

GO term Annotated Significant Expected p‑Value FDR q‑value
Ubiquitin-dependent protein catabolic process 403 39 17.43 3.50E-06 0.08
Regulation of protein serine/threonine kinase activity 366 35 15.83 1.90E-05 0.22
Positive regulation of small GTPase mediated signal transduction 30 8 1.3 2.90E-05 0.22
Positive regulation of protein insertion into mitochondrial membrane involved in apoptotic signaling pathway 26 7 1.12 8.80E-05 0.51
Heterophilic cell–cell adhesion 29 7 1.25 1.90E-04 0.88
Insulin-like growth factor receptor signaling pathway 32 8 1.38 2.60E-04 0.93
Axonal fasciculation 15 5 0.65 3.10E-04 0.93
Negative regulation of cellular macromolecule biosynthetic process 948 64 41 3.20E-04 0.93
Cellular response to insulin stimulus 207 20 8.95 5.40E-04 1.00
Regulation of sodium ion transmembrane transport 25 6 1.08 5.60E-04 1.00
Regulation of translational elongation 10 4 0.43 5.90E-04 1.00
Protein dephosphorylation 140 16 6.05 6.20E-04 1.00
Metencephalon development 84 13 3.63 6.20E-04 1.00
Embryonic epithelial tube formation 106 13 4.58 6.50E-04 1.00
Positive regulation of mesenchymal cell proliferation 36 7 1.56 7.60E-04 1.00
Platelet-derived growth factor receptor signaling pathway 36 7 1.56 7.60E-04 1.00
Smooth muscle tissue development 18 5 0.78 8.00E-04 1.00
Negative regulation of cell proliferation 529 39 22.88 9.80E-04 1.00
Neuron projection guidance 347 30 15.01 9.90E-04 1.00
FDR, false discovery rate.
HHS Vulnerability Disclosure