This regulatory network was inferred from the input dataset. The miRNAs and mRNAs are
presented as round and rectangle nodes respectively. The numerical value popped up upon mouse over the gene node is the log2 transformed fold-change of the gene expression between the two groups. All of the nodes are clickable, and the detailed information of the miRNAs/mRNAs and related cancer pathway will be displayed in another window. The edges between nodes are supported by both interactions (predicted or experimentally verified) and correlations learnt from cancer dataset. The numerical value popped up upon mouse over the edge is the correlation beat value (effect size) between the two nodes. The experimental evidences of the edges reported in previous cancer studies are highlighted by red/orange color. All of these information can be accessed by the "mouse-over" action. This network shows a full map of the miRNA-mRNA regulation of the input gene list(s), and the hub miRNAs (with the high network degree/betweenness centrality) would be the potential cancer drivers or tumor suppressors. The full result table can be accessed in the "Regulations" tab.
"miRNACancerMAP" is also a network visualization tool for users to draw their regulatory network by personal customization. Users can set the complexity of the network by limiting the number of nodes or edges. And the color of the nodes can be defined by different categories of the mRNAs and miRNAs, such as Gene-Ontology, pathway, and expression status. Users can also select to use network degree or network betweenness centrality to define the node size. And edges can be black or colored by the correlation. Purple edge means negative correlation (mostly found between miRNA and mRNA), and blue edge means positive correlation (found in PPI or miRNA-miRNA sponge effect). We can also add the protein-protein interactions (PPI) into the network. This result will show the cluster of genes regulated by some specific miRNAs. Additionally, miRNA-miRNA edges can be added by the "miRNA sponge" button, presenting some clusters of miRNAs that have the interactions via sponge effect.
Num | microRNA | Gene | miRNA log2FC | miRNA pvalue | Gene log2FC | Gene pvalue | Interaction | Correlation beta | Correlation P-value | PMID | Reported in cancer studies |
---|---|---|---|---|---|---|---|---|---|---|---|
1 | hsa-miR-128-3p | ABL1 | 0.98 | 6.0E-5 | -0.96 | 0 | MirTarget | -0.16 | 0.00096 | NA | |
2 | hsa-miR-141-3p | ABL1 | 1.46 | 0.00116 | -0.96 | 0 | MirTarget | -0.19 | 0 | NA | |
3 | hsa-miR-142-5p | ABL1 | 1.56 | 1.0E-5 | -0.96 | 0 | MirTarget | -0.17 | 0 | NA | |
4 | hsa-miR-15b-3p | ABL1 | 1.76 | 0 | -0.96 | 0 | MirTarget | -0.15 | 4.0E-5 | NA | |
5 | hsa-miR-15b-5p | ABL1 | 1.62 | 0 | -0.96 | 0 | mirMAP | -0.2 | 0 | NA | |
6 | hsa-miR-16-5p | ABL1 | 1.01 | 1.0E-5 | -0.96 | 0 | mirMAP | -0.28 | 0 | NA | |
7 | hsa-miR-19a-3p | ABL1 | 1.27 | 0.00011 | -0.96 | 0 | mirMAP | -0.16 | 2.0E-5 | NA | |
8 | hsa-miR-200a-3p | ABL1 | 0.72 | 0.19391 | -0.96 | 0 | MirTarget | -0.12 | 0 | NA | |
9 | hsa-miR-29a-5p | ABL1 | 0.59 | 0.02301 | -0.96 | 0 | MirTarget | -0.13 | 0.00827 | NA | |
10 | hsa-miR-30b-5p | ABL1 | -0.43 | 0.05936 | -0.96 | 0 | MirTarget; miRNATAP | -0.14 | 0.0083 | NA | |
11 | hsa-miR-30e-5p | ABL1 | -0.57 | 0.01125 | -0.96 | 0 | MirTarget; miRNATAP | -0.15 | 0.00794 | NA | |
12 | hsa-miR-330-5p | ABL1 | 0.49 | 0.05122 | -0.96 | 0 | MirTarget | -0.24 | 0 | NA | |
13 | hsa-miR-423-5p | ABL1 | 0.83 | 0.00079 | -0.96 | 0 | MirTarget | -0.15 | 0.00245 | NA | |
14 | hsa-miR-484 | ABL1 | 0.71 | 0.00234 | -0.96 | 0 | miRNAWalker2 validate | -0.26 | 0 | NA | |
15 | hsa-miR-503-5p | ABL1 | 1.89 | 0 | -0.96 | 0 | mirMAP | -0.1 | 0.00051 | NA | |
16 | hsa-miR-30a-3p | ANAPC10 | -1.73 | 0 | 0.45 | 0.00577 | MirTarget; miRNATAP | -0.13 | 8.0E-5 | NA | |
17 | hsa-miR-139-5p | ANAPC7 | -1.83 | 0 | 0.58 | 0.00037 | miRanda | -0.1 | 0.00535 | NA | |
18 | hsa-miR-30c-2-3p | ANAPC7 | -1.14 | 0.00085 | 0.58 | 0.00037 | MirTarget | -0.12 | 0.00048 | NA | |
19 | hsa-miR-125a-3p | ATM | 1.2 | 0.00164 | -0.39 | 0.08341 | miRanda | -0.13 | 0.00188 | NA | |
20 | hsa-miR-203a-3p | ATM | 1.45 | 0.03941 | -0.39 | 0.08341 | MirTarget | -0.14 | 0 | 24145123; 27542403 | miR 203 induces oxaliplatin resistance in colorectal cancer cells by negatively regulating ATM kinase; In silico analysis identified ataxia telangiectasia mutated ATM a primary mediator of the DNA damage response as a potential target of miR-203; Using TCGA database we identified a significant reverse correlation of miR-203 and ATM expression in CRC tissues; We validated ATM as a bona fide target of miR-203 in CRC cells; Mutation of the putative miR-203 binding site in the 3' untranslated region 3'UTR of the ATM mRNA abolished the inhibitory effect of miR-203 on ATM;MiR 203 inhibits tumor invasion and metastasis in gastric cancer by ATM; Our results showed that miR-203 was significantly downregulated in gastric cancer tissues and cells while ataxia telangiectasia mutated kinase ATM was upregulated in gastric cancer tissues and cells and was directly regulated by miR-203; ATM knockdown phenocopied the effect of miR-203 overexpression |
21 | hsa-miR-590-5p | ATM | 1.04 | 0.00027 | -0.39 | 0.08341 | mirMAP | -0.17 | 0.00247 | NA | |
22 | hsa-miR-30b-5p | ATR | -0.43 | 0.05936 | 0.73 | 0.00017 | mirMAP | -0.19 | 0.00265 | NA | |
23 | hsa-miR-139-5p | BUB1 | -1.83 | 0 | 3.99 | 0 | miRanda | -0.52 | 0 | NA | |
24 | hsa-miR-139-5p | BUB3 | -1.83 | 0 | 0.88 | 0 | miRanda | -0.16 | 0 | NA | |
25 | hsa-miR-107 | CCNA1 | 0.9 | 5.0E-5 | 1.85 | 0.16644 | miRanda | -2.11 | 0 | NA | |
26 | hsa-miR-30a-5p | CCNA1 | -1.72 | 0 | 1.85 | 0.16644 | MirTarget | -0.88 | 0.00139 | NA | |
27 | hsa-miR-30b-5p | CCNA1 | -0.43 | 0.05936 | 1.85 | 0.16644 | MirTarget | -1.24 | 0.00319 | NA | |
28 | hsa-miR-30d-5p | CCNA1 | -0.55 | 0.01401 | 1.85 | 0.16644 | MirTarget | -2.13 | 0 | NA | |
29 | hsa-miR-335-5p | CCNA1 | 1.6 | 6.0E-5 | 1.85 | 0.16644 | miRNAWalker2 validate | -1.05 | 1.0E-5 | NA | |
30 | hsa-miR-129-5p | CCNA2 | -2.57 | 0 | 2.9 | 0 | miRanda | -0.17 | 7.0E-5 | NA | |
31 | hsa-miR-218-5p | CCNA2 | -0.99 | 0.01083 | 2.9 | 0 | MirTarget | -0.16 | 0.00836 | NA | |
32 | hsa-miR-29c-3p | CCNA2 | -1.62 | 0 | 2.9 | 0 | MirTarget | -0.44 | 0 | NA | |
33 | hsa-miR-139-5p | CCNB1 | -1.83 | 0 | 2.86 | 0 | miRanda | -0.49 | 0 | NA | |
34 | hsa-miR-338-3p | CCND1 | -0.96 | 0.01915 | 0.62 | 0.1312 | miRNAWalker2 validate; miRTarBase; miRanda | -0.24 | 0.00086 | NA | |
35 | hsa-let-7a-3p | CCND2 | 0.5 | 0.04111 | -0.5 | 0.3 | mirMAP | -0.54 | 0.0001 | 20418948 | MicroRNA let 7a inhibits proliferation of human prostate cancer cells in vitro and in vivo by targeting E2F2 and CCND2 |
36 | hsa-let-7b-3p | CCND2 | 0.22 | 0.29604 | -0.5 | 0.3 | mirMAP | -0.46 | 0.00588 | NA | |
37 | hsa-miR-106b-5p | CCND2 | 1.71 | 0 | -0.5 | 0.3 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.42 | 9.0E-5 | NA | |
38 | hsa-miR-130b-5p | CCND2 | 0.7 | 0.05101 | -0.5 | 0.3 | mirMAP | -0.39 | 2.0E-5 | NA | |
39 | hsa-miR-141-3p | CCND2 | 1.46 | 0.00116 | -0.5 | 0.3 | MirTarget; TargetScan | -0.21 | 0.00436 | NA | |
40 | hsa-miR-15b-5p | CCND2 | 1.62 | 0 | -0.5 | 0.3 | miRNATAP | -0.44 | 0.00021 | NA | |
41 | hsa-miR-16-2-3p | CCND2 | 1.8 | 0 | -0.5 | 0.3 | mirMAP | -0.55 | 0 | NA | |
42 | hsa-miR-16-5p | CCND2 | 1.01 | 1.0E-5 | -0.5 | 0.3 | miRNAWalker2 validate; miRNATAP | -0.67 | 1.0E-5 | NA | |
43 | hsa-miR-181a-2-3p | CCND2 | 0.9 | 0.00083 | -0.5 | 0.3 | mirMAP | -0.38 | 0.00236 | NA | |
44 | hsa-miR-182-5p | CCND2 | 0.89 | 0.03106 | -0.5 | 0.3 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.32 | 9.0E-5 | NA | |
45 | hsa-miR-183-5p | CCND2 | 1.66 | 0.00052 | -0.5 | 0.3 | miRNATAP | -0.29 | 2.0E-5 | NA | |
46 | hsa-miR-19b-3p | CCND2 | 0.76 | 0.00653 | -0.5 | 0.3 | miRNAWalker2 validate; MirTarget; miRNATAP | -0.32 | 0.00853 | NA | |
47 | hsa-miR-21-3p | CCND2 | 1.75 | 0 | -0.5 | 0.3 | mirMAP | -0.33 | 0.0051 | NA | |
48 | hsa-miR-224-3p | CCND2 | 1.52 | 0.0065 | -0.5 | 0.3 | mirMAP | -0.27 | 4.0E-5 | NA | |
49 | hsa-miR-26b-5p | CCND2 | -0.3 | 0.16008 | -0.5 | 0.3 | mirMAP; miRNATAP | -0.58 | 0.00034 | NA | |
50 | hsa-miR-301a-3p | CCND2 | 1.45 | 1.0E-5 | -0.5 | 0.3 | miRNAWalker2 validate | -0.38 | 0.0002 | NA | |
51 | hsa-miR-3065-3p | CCND2 | -1.04 | 0.02184 | -0.5 | 0.3 | MirTarget; miRNATAP | -0.2 | 0.00685 | NA | |
52 | hsa-miR-3065-5p | CCND2 | -0.24 | 0.63312 | -0.5 | 0.3 | mirMAP | -0.24 | 0.00057 | NA | |
53 | hsa-miR-424-5p | CCND2 | 1.09 | 0.00042 | -0.5 | 0.3 | miRNATAP | -0.39 | 0.0003 | NA | |
54 | hsa-miR-429 | CCND2 | 1.4 | 0.009 | -0.5 | 0.3 | miRNATAP | -0.19 | 0.002 | NA | |
55 | hsa-miR-450b-5p | CCND2 | 0.46 | 0.13274 | -0.5 | 0.3 | MirTarget; PITA; miRNATAP | -0.32 | 0.00413 | NA | |
56 | hsa-miR-590-3p | CCND2 | 1.12 | 0.00016 | -0.5 | 0.3 | miRanda; mirMAP | -0.33 | 0.00348 | NA | |
57 | hsa-miR-590-5p | CCND2 | 1.04 | 0.00027 | -0.5 | 0.3 | mirMAP | -0.41 | 0.00055 | NA | |
58 | hsa-miR-9-3p | CCND2 | 0.33 | 0.54111 | -0.5 | 0.3 | MirTarget; mirMAP; miRNATAP | -0.19 | 0.00361 | NA | |
59 | hsa-miR-93-5p | CCND2 | 1.75 | 0 | -0.5 | 0.3 | miRNATAP | -0.32 | 0.00244 | NA | |
60 | hsa-miR-96-5p | CCND2 | 1.14 | 0.00943 | -0.5 | 0.3 | TargetScan; miRNATAP | -0.33 | 3.0E-5 | NA | |
61 | hsa-miR-96-5p | CCND3 | 1.14 | 0.00943 | 0.04 | 0.88352 | TargetScan | -0.12 | 0.00328 | NA | |
62 | hsa-miR-125b-5p | CCNE1 | -0.51 | 0.13327 | 2.19 | 0 | miRNAWalker2 validate | -0.26 | 0.00155 | NA | |
63 | hsa-miR-195-5p | CCNE1 | -0.91 | 0.00151 | 2.19 | 0 | miRNAWalker2 validate; MirTarget; miRNATAP | -0.43 | 1.0E-5 | 24402230 | Furthermore through qPCR and western blot assays we showed that overexpression of miR-195-5p reduced CCNE1 mRNA and protein levels respectively |
64 | hsa-miR-497-5p | CCNE1 | -0.8 | 0.0036 | 2.19 | 0 | MirTarget; miRNATAP | -0.43 | 2.0E-5 | 24112607; 25909221; 24909281 | Western blot assays confirmed that overexpression of miR-497 reduced cyclin E1 protein levels; Inhibited cellular growth suppressed cellular migration and invasion and G1 cell cycle arrest were observed upon overexpression of miR-497 in cells possibly by targeting cyclin E1;The effect of simultaneous overexpression of miR-497 and miR-34a on the inhibition of cell proliferation colony formation and tumor growth and the downregulation of cyclin E1 was stronger than the effect of each miRNA alone; The synergistic actions of miR-497 and miR-34a partly correlated with cyclin E1 levels; These results indicate cyclin E1 is downregulated by both miR-497 and miR-34a which synergistically retard the growth of human lung cancer cells;miR 497 suppresses proliferation of human cervical carcinoma HeLa cells by targeting cyclin E1; Furthermore the target effect of miR-497 on the CCNE1 was identified by dual-luciferase reporter assay system qRT-PCR and Western blotting; Over-expressed miR-497 in HeLa cells could suppress cell proliferation by targeting CCNE1 |
65 | hsa-miR-26a-5p | CCNE2 | -0.38 | 0.04425 | 1.36 | 0 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.44 | 0.0001 | 24116110; 21901171 | The loss of miR 26a mediated post transcriptional regulation of cyclin E2 in pancreatic cancer cell proliferation and decreased patient survival; The in vitro and in vivo assays showed that overexpression of miR-26a resulted in cell cycle arrest inhibited cell proliferation and decreased tumor growth which was associated with cyclin E2 downregulation;We also show that enforced expression of miR-26a in AML cells is able to inhibit cell cycle progression by downregulating cyclin E2 expression |
66 | hsa-miR-30a-5p | CCNE2 | -1.72 | 0 | 1.36 | 0 | miRNATAP | -0.22 | 0.00034 | NA | |
67 | hsa-miR-23b-3p | CCNH | -0.29 | 0.18665 | -0.18 | 0.23096 | MirTarget | -0.18 | 0.00023 | NA | |
68 | hsa-let-7a-3p | CDC14A | 0.5 | 0.04111 | -0.72 | 0.0057 | mirMAP | -0.25 | 0.00105 | NA | |
69 | hsa-let-7b-3p | CDC14A | 0.22 | 0.29604 | -0.72 | 0.0057 | mirMAP | -0.4 | 1.0E-5 | NA | |
70 | hsa-let-7f-1-3p | CDC14A | 1.29 | 0 | -0.72 | 0.0057 | mirMAP | -0.28 | 5.0E-5 | NA | |
71 | hsa-let-7a-3p | CDC14B | 0.5 | 0.04111 | -0.81 | 0.00843 | miRNATAP | -0.37 | 3.0E-5 | NA | |
72 | hsa-let-7b-3p | CDC14B | 0.22 | 0.29604 | -0.81 | 0.00843 | miRNATAP | -0.36 | 0.0007 | NA | |
73 | hsa-miR-193a-5p | CDC14B | 0.07 | 0.76855 | -0.81 | 0.00843 | miRNATAP | -0.47 | 0 | NA | |
74 | hsa-miR-27a-3p | CDC14B | 1.3 | 0 | -0.81 | 0.00843 | miRNATAP | -0.55 | 0 | NA | |
75 | hsa-miR-27b-3p | CDC14B | 0.08 | 0.72527 | -0.81 | 0.00843 | miRNATAP | -0.4 | 1.0E-5 | NA | |
76 | hsa-miR-944 | CDC14B | 3.33 | 0.01778 | -0.81 | 0.00843 | PITA; mirMAP; miRNATAP | -0.14 | 0 | NA | |
77 | hsa-miR-30a-5p | CDC20 | -1.72 | 0 | 3.92 | 0 | miRNAWalker2 validate | -0.48 | 0 | NA | |
78 | hsa-miR-29c-3p | CDC23 | -1.62 | 0 | 0.35 | 0.01053 | miRNAWalker2 validate | -0.14 | 0 | NA | |
79 | hsa-let-7c-5p | CDC25A | -0.5 | 0.20685 | 2.07 | 0 | MirTarget | -0.21 | 0.00039 | 25909324 | MicroRNA let 7c Inhibits Cell Proliferation and Induces Cell Cycle Arrest by Targeting CDC25A in Human Hepatocellular Carcinoma; The aim of the present study was to determine whether the cell cycle regulator CDC25A is involved in the antitumor effect of let-7c in HCC; The luciferase reporter assay showed that CDC25A was a direct target of let-7c and that let-7c inhibited the expression of CDC25A protein by directly targeting its 3' UTR; In conclusion this study indicates that let-7c suppresses HCC progression possibly by directly targeting the cell cycle regulator CDC25A and indirectly affecting its downstream target molecules |
80 | hsa-miR-195-5p | CDC25A | -0.91 | 0.00151 | 2.07 | 0 | MirTarget; miRNATAP | -0.37 | 0 | NA | |
81 | hsa-miR-497-5p | CDC25A | -0.8 | 0.0036 | 2.07 | 0 | MirTarget; miRNATAP | -0.39 | 0 | NA | |
82 | hsa-miR-148a-3p | CDC25B | -1.54 | 4.0E-5 | 2.46 | 0 | miRNAWalker2 validate; miRNATAP | -0.19 | 0.00242 | 25341915 | Gene CDC25B might be the target gene of miR-148a according to the results of targetscan; CDC25B may be the target gene of miR-148a that plays a role in tumor suppressor |
83 | hsa-miR-107 | CDC27 | 0.9 | 5.0E-5 | 0.38 | 0.0058 | miRanda; miRNATAP | -0.15 | 0.00056 | NA | |
84 | hsa-miR-195-5p | CDC27 | -0.91 | 0.00151 | 0.38 | 0.0058 | miRNATAP | -0.22 | 0 | NA | |
85 | hsa-miR-32-5p | CDC27 | 0.42 | 0.10646 | 0.38 | 0.0058 | miRNAWalker2 validate | -0.15 | 5.0E-5 | NA | |
86 | hsa-miR-326 | CDC27 | -0.43 | 0.26299 | 0.38 | 0.0058 | miRanda | -0.12 | 0 | NA | |
87 | hsa-miR-335-5p | CDC27 | 1.6 | 6.0E-5 | 0.38 | 0.0058 | miRNATAP | -0.1 | 1.0E-5 | NA | |
88 | hsa-miR-497-5p | CDC27 | -0.8 | 0.0036 | 0.38 | 0.0058 | miRNATAP | -0.16 | 1.0E-5 | NA | |
89 | hsa-miR-338-5p | CDC7 | -1.2 | 0.01003 | 1.75 | 0 | mirMAP | -0.16 | 0.0001 | NA | |
90 | hsa-miR-145-5p | CDK4 | -1.75 | 2.0E-5 | 1.16 | 0 | miRNAWalker2 validate; miRTarBase | -0.13 | 0.00065 | 21092188 | Furthermore we found that CDK4 was regulated by miR-145 in cell cycle control |
91 | hsa-miR-195-5p | CDK4 | -0.91 | 0.00151 | 1.16 | 0 | miRNAWalker2 validate; miRTarBase | -0.16 | 0.00344 | NA | |
92 | hsa-miR-101-3p | CDK6 | -0.45 | 0.02834 | 0.3 | 0.4008 | mirMAP | -0.39 | 0.00173 | NA | |
93 | hsa-miR-129-5p | CDK6 | -2.57 | 0 | 0.3 | 0.4008 | miRNAWalker2 validate | -0.13 | 0.00427 | 24055727 | Interestingly we showed that cyclin dependent kinase 6 CDK6 a cell cycle-associated protein involved in G1-S transition was a target of miR-129 |
94 | hsa-miR-30d-3p | CDK6 | -0.55 | 0.04337 | 0.3 | 0.4008 | mirMAP | -0.28 | 0.00298 | NA | |
95 | hsa-miR-30d-5p | CDK6 | -0.55 | 0.01401 | 0.3 | 0.4008 | mirMAP | -0.44 | 9.0E-5 | NA | |
96 | hsa-miR-139-5p | CDK7 | -1.83 | 0 | 0.5 | 0.00793 | miRanda | -0.13 | 0.00188 | NA | |
97 | hsa-miR-199a-5p | CDK7 | 0.37 | 0.23266 | 0.5 | 0.00793 | miRanda | -0.13 | 0.00271 | NA | |
98 | hsa-let-7d-5p | CDKN1A | 0.98 | 0 | -0.53 | 0.09948 | MirTarget | -0.4 | 0.00048 | NA | |
99 | hsa-let-7g-5p | CDKN1A | 0.33 | 0.24114 | -0.53 | 0.09948 | MirTarget | -0.31 | 0.00013 | NA | |
100 | hsa-let-7i-5p | CDKN1A | 0.8 | 3.0E-5 | -0.53 | 0.09948 | MirTarget | -0.32 | 0.00701 | NA | |
101 | hsa-miR-101-3p | CDKN1A | -0.45 | 0.02834 | -0.53 | 0.09948 | MirTarget | -0.45 | 6.0E-5 | NA | |
102 | hsa-miR-106b-5p | CDKN1A | 1.71 | 0 | -0.53 | 0.09948 | miRNAWalker2 validate; miRTarBase; MirTarget; miRNATAP | -0.32 | 1.0E-5 | NA | |
103 | hsa-miR-146a-5p | CDKN1A | 1.82 | 2.0E-5 | -0.53 | 0.09948 | miRNAWalker2 validate | -0.18 | 0.00045 | NA | |
104 | hsa-miR-17-5p | CDKN1A | 1.66 | 0 | -0.53 | 0.09948 | miRNAWalker2 validate; miRTarBase; MirTarget; TargetScan; miRNATAP | -0.26 | 0.00022 | 26482648; 24989082 | The low expressions of miR-17 and miR-92 families can maintain cisplatin resistance through the regulation of CDKN1A and RAD21;According to PicTar and Miranda algorithms which predicted CDKN1A p21 as a putative target of miR-17 a luciferase assay was performed and revealed that miR-17 directly targets the 3'-UTR of p21 mRNA |
105 | hsa-miR-20a-5p | CDKN1A | 1.45 | 0 | -0.53 | 0.09948 | miRNAWalker2 validate; miRTarBase; MirTarget; miRNATAP | -0.31 | 4.0E-5 | 26012475 | Using the poorly tumorigenic and TGF-β-sensitive FET cell line that expresses low miR-20a levels we first confirmed that miR-20a downmodulated CDKN1A expression both at mRNA and protein level through direct binding to its 3'-UTR; Moreover besides modulating CDKN1A miR-20a blocked TGF-β-induced transactivation of its promoter without affecting the post-receptor activation of Smad3/4 effectors directly; Finally miR-20a abrogated the TGF-β-mediated c-Myc repression a direct inhibitor of the CDKN1A promoter activation most likely by reducing the expression of specific MYC-regulating genes from the Smad/E2F-based core repressor complex |
106 | hsa-miR-30b-3p | CDKN1A | -0.27 | 0.40085 | -0.53 | 0.09948 | MirTarget | -0.23 | 0.00125 | NA | |
107 | hsa-miR-335-5p | CDKN1A | 1.6 | 6.0E-5 | -0.53 | 0.09948 | miRNAWalker2 validate | -0.32 | 0 | NA | |
108 | hsa-miR-345-5p | CDKN1A | 1.84 | 0 | -0.53 | 0.09948 | miRNAWalker2 validate; miRTarBase; MirTarget | -0.24 | 0.00033 | NA | |
109 | hsa-miR-423-3p | CDKN1A | 0.82 | 0.00026 | -0.53 | 0.09948 | miRNAWalker2 validate; miRTarBase | -0.32 | 0.00138 | NA | |
110 | hsa-miR-423-5p | CDKN1A | 0.83 | 0.00079 | -0.53 | 0.09948 | MirTarget | -0.41 | 0 | NA | |
111 | hsa-miR-429 | CDKN1A | 1.4 | 0.009 | -0.53 | 0.09948 | miRNATAP | -0.13 | 0.00128 | NA | |
112 | hsa-miR-93-5p | CDKN1A | 1.75 | 0 | -0.53 | 0.09948 | miRNAWalker2 validate; miRTarBase; MirTarget; miRNATAP | -0.32 | 1.0E-5 | 25633810 | MicroRNA 93 activates c Met/PI3K/Akt pathway activity in hepatocellular carcinoma by directly inhibiting PTEN and CDKN1A; We confirmed that miR-93 directly bound with the 3' untranslated regions of the tumor-suppressor genes PTEN and CDKN1A respectivelyand inhibited their expression; We concluded that miR-93 stimulated cell proliferation migration and invasion through the oncogenic c-Met/PI3K/Akt pathway and also inhibited apoptosis by directly inhibiting PTEN and CDKN1A expression in human HCC |
113 | hsa-miR-942-5p | CDKN1A | 1.91 | 0 | -0.53 | 0.09948 | miRNAWalker2 validate | -0.18 | 0.00704 | NA | |
114 | hsa-miR-24-3p | CDKN1B | 1.09 | 0 | 0.16 | 0.36377 | miRNAWalker2 validate; miRNATAP | -0.15 | 0.00772 | 26847530; 26044523 | The biological significance of miR-24 expression in prostate cancer cells was assessed by a series of in vitro bioassays and the effect on proposed targets p27 CDKN1B and p16 CDK2NA was investigated;With the bioinformatic method we further identified that p27Kip1 is a direct target of miR-24-3p and its protein level was negatively regulated by miR-24-3p |
115 | hsa-miR-221-3p | CDKN1C | 1.33 | 0 | -1.65 | 3.0E-5 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.32 | 0.00244 | 20461750 | miR-221 and miR-222 negatively regulate expression of CDKN1B p27 and CDKN1C p57 two cell cycle regulators expressed in ovarian surface epithelium and down-regulated in ovarian carcinomas; Higher miR-222 and miR-221 expression were significantly associated with decreased CDKN1C expression P = 0.009 and 0.01 |
116 | hsa-miR-222-3p | CDKN1C | 1.39 | 0 | -1.65 | 3.0E-5 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.37 | 0.00017 | 20461750 | miR-221 and miR-222 negatively regulate expression of CDKN1B p27 and CDKN1C p57 two cell cycle regulators expressed in ovarian surface epithelium and down-regulated in ovarian carcinomas; Higher miR-222 and miR-221 expression were significantly associated with decreased CDKN1C expression P = 0.009 and 0.01 |
117 | hsa-miR-92a-3p | CDKN1C | 1.22 | 1.0E-5 | -1.65 | 3.0E-5 | MirTarget; miRNATAP | -0.27 | 0.01 | NA | |
118 | hsa-miR-125b-5p | CDKN2A | -0.51 | 0.13327 | 1.06 | 0.26133 | miRNAWalker2 validate | -0.58 | 0.00347 | 23585871 | In this study we further extend our studies by showing that miR-125b represses the protein product of the ink4a/ARF locus p14ARF in two prostate cancer cell lines LNCaP wild type-p53 and 22Rv1 both wild type and mutant p53 as well as in the PC-346C prostate cancer xenograft model that lentivirally overexpressed miR-125b; Conversely treatment of prostate cancer cells with an inhibitor of miR-125b anti-miR-125b resulted in increased expression of p14ARF decreased level of Mdm2 and induction of apoptosis; In addition overexpression of miR-125b in p53-deficient PC3 cells induced down-regulation of p14ARF which leads to increased cell proliferation through a p53-independent manner |
119 | hsa-miR-365a-3p | CDKN2A | -0.89 | 0.00255 | 1.06 | 0.26133 | MirTarget | -0.76 | 0.00074 | NA | |
120 | hsa-miR-9-3p | CDKN2B | 0.33 | 0.54111 | -0.03 | 0.96549 | mirMAP | -0.29 | 0.00089 | NA | |
121 | hsa-miR-192-5p | CDKN2D | 0.08 | 0.94106 | 0.86 | 0.00075 | miRNAWalker2 validate | -0.11 | 0 | NA | |
122 | hsa-miR-362-3p | CDKN2D | -0.03 | 0.91378 | 0.86 | 0.00075 | MirTarget; PITA; miRanda; miRNATAP | -0.16 | 0.00453 | NA | |
123 | hsa-miR-129-5p | CHEK1 | -2.57 | 0 | 2.16 | 0 | miRanda | -0.14 | 0.00016 | NA | |
124 | hsa-miR-139-5p | CHEK1 | -1.83 | 0 | 2.16 | 0 | miRanda | -0.39 | 0 | NA | |
125 | hsa-miR-195-5p | CHEK1 | -0.91 | 0.00151 | 2.16 | 0 | MirTarget; miRNATAP | -0.34 | 0 | 25840419 | MiR 195 suppresses non small cell lung cancer by targeting CHEK1; We discovered that CHEK1 was a direct target of miR-195 which decreased CHEK1 expression in lung cancer cells |
126 | hsa-miR-497-5p | CHEK1 | -0.8 | 0.0036 | 2.16 | 0 | MirTarget; miRNATAP | -0.35 | 0 | 24464213 | Checkpoint kinase 1 is negatively regulated by miR 497 in hepatocellular carcinoma; In silico analysis showed that CHEK1 was a candidate target of miR-497 which was previously found to be downregulated in HCC by us; To test whether miR-497 could bind to 3'untranslated region 3'UTR of CHEK1 luciferase reporter assay was conducted; The result revealed that miR-497 could bind to the 3'untranslated region 3'UTR of CHEK1 mRNA; Western blot showed that ectopic expression of miR-497 suppressed the CHEK1 expression and inhibition of miR-497 led to significant upregulation of CHEK1; Finally miR-497 expression was measured in the same 30 HCC samples and the correlation between miR-497 and CHEK1 was analyzed; The results indicated that miR-497 was downregulated in HCC and had a significant negative correlation with CHEK1; Taken together these results demonstrated that CHEK1 was negatively regulated by miR-497 and the overexpressed CHEK1 was resulted from the downregulated miR-497 in HCC which provided a potential molecular target for HCC therapy |
127 | hsa-miR-186-5p | CREBBP | 0.15 | 0.43471 | -0.11 | 0.45436 | mirMAP; miRNATAP | -0.14 | 0.00768 | NA | |
128 | hsa-miR-195-3p | DBF4 | -1.35 | 2.0E-5 | 1.68 | 0 | mirMAP | -0.23 | 8.0E-5 | NA | |
129 | hsa-miR-30a-5p | DBF4 | -1.72 | 0 | 1.68 | 0 | MirTarget | -0.17 | 0.00221 | NA | |
130 | hsa-miR-10a-5p | E2F1 | -0.47 | 0.1488 | 1.94 | 0 | miRNAWalker2 validate | -0.16 | 0.00697 | NA | |
131 | hsa-miR-125a-5p | E2F2 | -0.88 | 0.00021 | 2.79 | 0 | MirTarget | -0.4 | 0.00032 | NA | |
132 | hsa-miR-125b-5p | E2F2 | -0.51 | 0.13327 | 2.79 | 0 | miRNAWalker2 validate; miRTarBase; MirTarget; miRNATAP | -0.22 | 0.00603 | 22999819 | miR 125b regulates the proliferation of glioblastoma stem cells by targeting E2F2; This study demonstrated that miR-125b plays important roles in regulating the proliferation of GSCs by directly targeting E2F2 |
133 | hsa-miR-101-3p | E2F3 | -0.45 | 0.02834 | 1.26 | 0 | miRNAWalker2 validate | -0.24 | 0.00078 | NA | |
134 | hsa-miR-10a-5p | E2F3 | -0.47 | 0.1488 | 1.26 | 0 | miRNATAP | -0.12 | 0.00663 | NA | |
135 | hsa-miR-145-5p | E2F3 | -1.75 | 2.0E-5 | 1.26 | 0 | miRNATAP | -0.14 | 3.0E-5 | 25762621 | miR 145 mediates the antiproliferative and gene regulatory effects of vitamin D3 by directly targeting E2F3 in gastric cancer cells; Furthermore miR-145 expression was lower in tumors compared with matched normal samples and correlated with increased the E2F3 transcription factor protein staining |
136 | hsa-miR-195-5p | E2F3 | -0.91 | 0.00151 | 1.26 | 0 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.23 | 0 | 22217655 | We identified E2F3 and CCND3 as functional downstream targets of miR-195 in glioblastoma cells |
137 | hsa-miR-497-5p | E2F3 | -0.8 | 0.0036 | 1.26 | 0 | miRNATAP | -0.18 | 0.00065 | NA | |
138 | hsa-let-7a-2-3p | E2F5 | 0.2 | 0.64356 | 0.53 | 0.22286 | MirTarget | -0.24 | 0.00118 | NA | |
139 | hsa-let-7b-5p | E2F5 | 0.06 | 0.7814 | 0.53 | 0.22286 | miRNAWalker2 validate; MirTarget; miRNATAP | -0.71 | 0 | NA | |
140 | hsa-let-7c-5p | E2F5 | -0.5 | 0.20685 | 0.53 | 0.22286 | MirTarget | -0.22 | 0.00545 | NA | |
141 | hsa-miR-1-3p | E2F5 | -2.66 | 2.0E-5 | 0.53 | 0.22286 | MirTarget | -0.13 | 0.00626 | NA | |
142 | hsa-miR-1271-5p | E2F5 | 1.16 | 0.00208 | 0.53 | 0.22286 | MirTarget | -0.27 | 0.00093 | NA | |
143 | hsa-miR-199a-5p | E2F5 | 0.37 | 0.23266 | 0.53 | 0.22286 | miRanda | -0.37 | 0.00018 | NA | |
144 | hsa-miR-199b-5p | E2F5 | 0.12 | 0.67816 | 0.53 | 0.22286 | miRanda | -0.28 | 0.00597 | NA | |
145 | hsa-miR-205-5p | E2F5 | 3.14 | 0.02932 | 0.53 | 0.22286 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.16 | 0 | 21454583 | The expression levels of E2F1 and E2F5 were correlated inversely with that of miR-205 in melanoma cell lines; miR-205 significantly suppressed the luciferase activity of reporter plasmids containing the 3'-UTR sequences complementary to either E2F1 or E2F5; Overexpression of miR-205 in melanoma cells reduced E2F1 and E2F5 protein levels |
146 | hsa-miR-337-3p | E2F5 | -0.72 | 0.03374 | 0.53 | 0.22286 | MirTarget; PITA | -0.31 | 0.00051 | NA | |
147 | hsa-miR-34c-5p | E2F5 | 2.21 | 0.00038 | 0.53 | 0.22286 | MirTarget; PITA; miRanda; miRNATAP | -0.28 | 0 | NA | |
148 | hsa-miR-106b-5p | EP300 | 1.71 | 0 | 0.03 | 0.83304 | miRNATAP | -0.1 | 0.00164 | NA | |
149 | hsa-miR-212-3p | EP300 | 0.96 | 0.00133 | 0.03 | 0.83304 | MirTarget; miRNATAP | -0.12 | 0.00033 | NA | |
150 | hsa-miR-26a-5p | EP300 | -0.38 | 0.04425 | 0.03 | 0.83304 | miRNATAP | -0.19 | 0.00038 | NA |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | CELL CYCLE | 69 | 1316 | 1.025e-68 | 4.768e-65 |
2 | CELL CYCLE PROCESS | 64 | 1081 | 3.025e-65 | 7.038e-62 |
3 | REGULATION OF CELL CYCLE | 61 | 949 | 1.944e-63 | 3.015e-60 |
4 | MITOTIC CELL CYCLE | 57 | 766 | 6.94e-62 | 8.073e-59 |
5 | REGULATION OF MITOTIC CELL CYCLE | 42 | 468 | 8.984e-47 | 8.361e-44 |
6 | REGULATION OF CELL CYCLE PHASE TRANSITION | 36 | 321 | 4.087e-43 | 2.717e-40 |
7 | NEGATIVE REGULATION OF CELL CYCLE | 39 | 433 | 3.596e-43 | 2.717e-40 |
8 | CELL CYCLE PHASE TRANSITION | 33 | 255 | 1.89e-41 | 1.099e-38 |
9 | REGULATION OF CELL CYCLE PROCESS | 40 | 558 | 2.338e-40 | 1.209e-37 |
10 | CELL CYCLE CHECKPOINT | 29 | 194 | 3.828e-38 | 1.781e-35 |
11 | NEGATIVE REGULATION OF MITOTIC CELL CYCLE | 27 | 199 | 3.043e-34 | 1.287e-31 |
12 | REGULATION OF PROTEIN MODIFICATION PROCESS | 51 | 1710 | 4.535e-34 | 1.758e-31 |
13 | REGULATION OF TRANSFERASE ACTIVITY | 42 | 946 | 6.208e-34 | 2.222e-31 |
14 | NEGATIVE REGULATION OF CELL CYCLE PROCESS | 27 | 214 | 2.381e-33 | 7.914e-31 |
15 | MITOTIC CELL CYCLE CHECKPOINT | 24 | 139 | 4.694e-33 | 1.456e-30 |
16 | CELL DIVISION | 33 | 460 | 8.818e-33 | 2.564e-30 |
17 | POSITIVE REGULATION OF CELL CYCLE | 29 | 332 | 4.02e-31 | 1.1e-28 |
18 | CELL CYCLE G1 S PHASE TRANSITION | 21 | 111 | 8.056e-30 | 1.973e-27 |
19 | G1 S TRANSITION OF MITOTIC CELL CYCLE | 21 | 111 | 8.056e-30 | 1.973e-27 |
20 | NEGATIVE REGULATION OF CELL CYCLE PHASE TRANSITION | 22 | 146 | 6.688e-29 | 1.556e-26 |
21 | POSITIVE REGULATION OF CELL CYCLE PROCESS | 24 | 247 | 8.832e-27 | 1.957e-24 |
22 | DNA INTEGRITY CHECKPOINT | 20 | 146 | 2.037e-25 | 4.309e-23 |
23 | NEGATIVE REGULATION OF PROTEIN METABOLIC PROCESS | 37 | 1087 | 2.402e-25 | 4.859e-23 |
24 | NEGATIVE REGULATION OF PROTEIN MODIFICATION PROCESS | 30 | 616 | 1.122e-24 | 2.176e-22 |
25 | REGULATION OF PHOSPHORUS METABOLIC PROCESS | 42 | 1618 | 1.389e-24 | 2.585e-22 |
26 | POSITIVE REGULATION OF PROTEIN METABOLIC PROCESS | 40 | 1492 | 9.383e-24 | 1.679e-21 |
27 | REGULATION OF KINASE ACTIVITY | 31 | 776 | 5.701e-23 | 9.825e-21 |
28 | MITOTIC NUCLEAR DIVISION | 24 | 361 | 8.386e-23 | 1.394e-20 |
29 | POSITIVE REGULATION OF PROTEIN MODIFICATION PROCESS | 35 | 1135 | 1.986e-22 | 3.187e-20 |
30 | REGULATION OF ORGANELLE ORGANIZATION | 35 | 1178 | 6.708e-22 | 1.04e-19 |
31 | REGULATION OF CYCLIN DEPENDENT PROTEIN KINASE ACTIVITY | 16 | 97 | 8.259e-22 | 1.24e-19 |
32 | NEGATIVE REGULATION OF CELL CYCLE G1 S PHASE TRANSITION | 16 | 98 | 9.839e-22 | 1.431e-19 |
33 | CELLULAR RESPONSE TO DNA DAMAGE STIMULUS | 29 | 720 | 1.621e-21 | 2.285e-19 |
34 | REGULATION OF CELL DIVISION | 21 | 272 | 2.56e-21 | 3.503e-19 |
35 | REGULATION OF CELL CYCLE ARREST | 16 | 108 | 5.122e-21 | 6.809e-19 |
36 | ORGANELLE FISSION | 25 | 496 | 8.155e-21 | 1.054e-18 |
37 | REGULATION OF CELL CYCLE G1 S PHASE TRANSITION | 17 | 147 | 2.226e-20 | 2.8e-18 |
38 | NEGATIVE REGULATION OF TRANSFERASE ACTIVITY | 22 | 351 | 2.396e-20 | 2.933e-18 |
39 | G1 DNA DAMAGE CHECKPOINT | 14 | 73 | 3.601e-20 | 4.296e-18 |
40 | SIGNAL TRANSDUCTION IN RESPONSE TO DNA DAMAGE | 15 | 96 | 4.052e-20 | 4.714e-18 |
41 | REGULATION OF PROTEIN SERINE THREONINE KINASE ACTIVITY | 24 | 470 | 4.163e-20 | 4.725e-18 |
42 | CELL CYCLE ARREST | 17 | 154 | 5.028e-20 | 5.57e-18 |
43 | MITOTIC DNA INTEGRITY CHECKPOINT | 15 | 100 | 7.749e-20 | 8.385e-18 |
44 | POSITIVE REGULATION OF TRANSFERASE ACTIVITY | 26 | 616 | 9.877e-20 | 1.044e-17 |
45 | REGULATION OF NUCLEAR DIVISION | 17 | 163 | 1.353e-19 | 1.399e-17 |
46 | REGULATION OF CELL PROLIFERATION | 36 | 1496 | 1.519e-19 | 1.536e-17 |
47 | REGULATION OF PROTEIN CATABOLIC PROCESS | 22 | 393 | 2.74e-19 | 2.713e-17 |
48 | POSITIVE REGULATION OF CELL CYCLE ARREST | 14 | 85 | 3.562e-19 | 3.453e-17 |
49 | POSITIVE REGULATION OF PROTEOLYSIS | 21 | 363 | 1.027e-18 | 9.749e-17 |
50 | CHROMOSOME ORGANIZATION | 30 | 1009 | 1.43e-18 | 1.331e-16 |
51 | REGULATION OF CELLULAR PROTEIN CATABOLIC PROCESS | 19 | 274 | 1.927e-18 | 1.758e-16 |
52 | REGULATION OF PROTEOLYSIS | 26 | 711 | 3.395e-18 | 3.037e-16 |
53 | CELL CYCLE G2 M PHASE TRANSITION | 15 | 138 | 1.181e-17 | 1.037e-15 |
54 | POSITIVE REGULATION OF CELL DEATH | 24 | 605 | 1.388e-17 | 1.196e-15 |
55 | REGULATION OF SISTER CHROMATID SEGREGATION | 12 | 67 | 4.878e-17 | 4.127e-15 |
56 | CELLULAR RESPONSE TO STRESS | 34 | 1565 | 5.42e-17 | 4.503e-15 |
57 | REGULATION OF CHROMOSOME ORGANIZATION | 18 | 278 | 5.699e-17 | 4.652e-15 |
58 | REGULATION OF CELL DEATH | 33 | 1472 | 7.471e-17 | 5.994e-15 |
59 | POSITIVE REGULATION OF MITOTIC CELL CYCLE | 14 | 123 | 8.013e-17 | 6.32e-15 |
60 | NEGATIVE REGULATION OF CATALYTIC ACTIVITY | 26 | 829 | 1.413e-16 | 1.096e-14 |
61 | REGULATION OF LIGASE ACTIVITY | 14 | 130 | 1.775e-16 | 1.354e-14 |
62 | POSITIVE REGULATION OF CATALYTIC ACTIVITY | 33 | 1518 | 1.854e-16 | 1.391e-14 |
63 | NEGATIVE REGULATION OF PHOSPHORUS METABOLIC PROCESS | 22 | 541 | 2.372e-16 | 1.712e-14 |
64 | RESPONSE TO ABIOTIC STIMULUS | 28 | 1024 | 2.392e-16 | 1.712e-14 |
65 | NEGATIVE REGULATION OF PHOSPHATE METABOLIC PROCESS | 22 | 541 | 2.372e-16 | 1.712e-14 |
66 | POSITIVE REGULATION OF BIOSYNTHETIC PROCESS | 35 | 1805 | 5.262e-16 | 3.71e-14 |
67 | NEGATIVE REGULATION OF MOLECULAR FUNCTION | 28 | 1079 | 9.075e-16 | 6.302e-14 |
68 | REGULATION OF CATABOLIC PROCESS | 24 | 731 | 9.823e-16 | 6.722e-14 |
69 | POSITIVE REGULATION OF CELL PROLIFERATION | 25 | 814 | 1.012e-15 | 6.727e-14 |
70 | REGULATION OF CHROMOSOME SEGREGATION | 12 | 85 | 1.009e-15 | 6.727e-14 |
71 | POSITIVE REGULATION OF GENE EXPRESSION | 34 | 1733 | 1.176e-15 | 7.709e-14 |
72 | POSITIVE REGULATION OF CELLULAR PROTEIN CATABOLIC PROCESS | 15 | 192 | 1.772e-15 | 1.145e-13 |
73 | POSITIVE REGULATION OF MOLECULAR FUNCTION | 34 | 1791 | 3.142e-15 | 1.979e-13 |
74 | PROTEIN PHOSPHORYLATION | 26 | 944 | 3.147e-15 | 1.979e-13 |
75 | SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR | 13 | 127 | 4.488e-15 | 2.784e-13 |
76 | POSITIVE REGULATION OF CELLULAR PROTEIN LOCALIZATION | 18 | 360 | 5.29e-15 | 3.239e-13 |
77 | NEGATIVE REGULATION OF PHOSPHORYLATION | 19 | 422 | 5.648e-15 | 3.413e-13 |
78 | RESPONSE TO OXYGEN LEVELS | 17 | 311 | 7.649e-15 | 4.563e-13 |
79 | POSITIVE REGULATION OF PROTEIN CATABOLIC PROCESS | 16 | 263 | 9.735e-15 | 5.734e-13 |
80 | REGULATION OF PROTEIN UBIQUITINATION INVOLVED IN UBIQUITIN DEPENDENT PROTEIN CATABOLIC PROCESS | 12 | 103 | 1.107e-14 | 6.437e-13 |
81 | SISTER CHROMATID SEGREGATION | 14 | 176 | 1.294e-14 | 7.435e-13 |
82 | ANAPHASE PROMOTING COMPLEX DEPENDENT CATABOLIC PROCESS | 11 | 77 | 1.474e-14 | 8.365e-13 |
83 | CHROMOSOME SEGREGATION | 16 | 272 | 1.647e-14 | 9.233e-13 |
84 | NUCLEAR CHROMOSOME SEGREGATION | 15 | 228 | 2.279e-14 | 1.263e-12 |
85 | DNA METABOLIC PROCESS | 23 | 758 | 2.35e-14 | 1.286e-12 |
86 | POSITIVE REGULATION OF LIGASE ACTIVITY | 12 | 110 | 2.488e-14 | 1.346e-12 |
87 | POSITIVE REGULATION OF PROTEIN MODIFICATION BY SMALL PROTEIN CONJUGATION OR REMOVAL | 14 | 196 | 5.791e-14 | 3.097e-12 |
88 | REGULATION OF CELLULAR PROTEIN LOCALIZATION | 20 | 552 | 5.925e-14 | 3.133e-12 |
89 | POSITIVE REGULATION OF ORGANELLE ORGANIZATION | 20 | 573 | 1.189e-13 | 6.214e-12 |
90 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 32 | 1784 | 1.4e-13 | 7.238e-12 |
91 | POSITIVE REGULATION OF CELL CYCLE PHASE TRANSITION | 10 | 68 | 1.826e-13 | 9.338e-12 |
92 | PROTEIN UBIQUITINATION INVOLVED IN UBIQUITIN DEPENDENT PROTEIN CATABOLIC PROCESS | 12 | 134 | 2.757e-13 | 1.395e-11 |
93 | POSITIVE REGULATION OF CELLULAR COMPONENT ORGANIZATION | 26 | 1152 | 3.297e-13 | 1.65e-11 |
94 | REGULATION OF PROTEIN MODIFICATION BY SMALL PROTEIN CONJUGATION OR REMOVAL | 15 | 280 | 4.604e-13 | 2.279e-11 |
95 | POSITIVE REGULATION OF FIBROBLAST PROLIFERATION | 9 | 53 | 7.977e-13 | 3.907e-11 |
96 | REGULATION OF PROTEASOMAL UBIQUITIN DEPENDENT PROTEIN CATABOLIC PROCESS | 12 | 148 | 9.12e-13 | 4.421e-11 |
97 | CELL DEATH | 24 | 1001 | 9.421e-13 | 4.519e-11 |
98 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 24 | 1004 | 1.004e-12 | 4.768e-11 |
99 | PHOSPHORYLATION | 26 | 1228 | 1.423e-12 | 6.688e-11 |
100 | INTRACELLULAR SIGNAL TRANSDUCTION | 29 | 1572 | 1.508e-12 | 7.019e-11 |
101 | POSITIVE REGULATION OF MITOCHONDRIAL OUTER MEMBRANE PERMEABILIZATION INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 8 | 36 | 1.551e-12 | 7.146e-11 |
102 | NEGATIVE REGULATION OF KINASE ACTIVITY | 14 | 250 | 1.632e-12 | 7.443e-11 |
103 | RESPONSE TO UV | 11 | 126 | 3.819e-12 | 1.709e-10 |
104 | NEGATIVE REGULATION OF PROTEIN SERINE THREONINE KINASE ACTIVITY | 11 | 126 | 3.819e-12 | 1.709e-10 |
105 | PROTEASOMAL PROTEIN CATABOLIC PROCESS | 14 | 271 | 4.858e-12 | 2.153e-10 |
106 | POSITIVE REGULATION OF CATABOLIC PROCESS | 16 | 395 | 5.042e-12 | 2.213e-10 |
107 | CELLULAR RESPONSE TO UV | 9 | 66 | 6.384e-12 | 2.776e-10 |
108 | POSITIVE REGULATION OF RESPONSE TO STIMULUS | 31 | 1929 | 7.137e-12 | 3.075e-10 |
109 | REGULATION OF MITOCHONDRIAL OUTER MEMBRANE PERMEABILIZATION INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 8 | 43 | 7.263e-12 | 3.101e-10 |
110 | DNA REPAIR | 17 | 480 | 8.465e-12 | 3.581e-10 |
111 | CELLULAR RESPONSE TO RADIATION | 11 | 137 | 9.601e-12 | 4.024e-10 |
112 | RESPONSE TO RADIATION | 16 | 413 | 9.85e-12 | 4.071e-10 |
113 | NEGATIVE REGULATION OF CELL PROLIFERATION | 19 | 643 | 9.887e-12 | 4.071e-10 |
114 | REGULATION OF PROTEASOMAL PROTEIN CATABOLIC PROCESS | 12 | 181 | 9.988e-12 | 4.077e-10 |
115 | NEGATIVE REGULATION OF PROTEIN MODIFICATION BY SMALL PROTEIN CONJUGATION OR REMOVAL | 11 | 139 | 1.125e-11 | 4.554e-10 |
116 | POSITIVE REGULATION OF PHOSPHATE METABOLIC PROCESS | 23 | 1036 | 1.5e-11 | 5.966e-10 |
117 | POSITIVE REGULATION OF PHOSPHORUS METABOLIC PROCESS | 23 | 1036 | 1.5e-11 | 5.966e-10 |
118 | NEGATIVE REGULATION OF CHROMOSOME SEGREGATION | 7 | 28 | 1.656e-11 | 6.53e-10 |
119 | REGULATION OF PROTEIN INSERTION INTO MITOCHONDRIAL MEMBRANE INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 7 | 29 | 2.176e-11 | 8.436e-10 |
120 | POSITIVE REGULATION OF PROTEIN INSERTION INTO MITOCHONDRIAL MEMBRANE INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 7 | 29 | 2.176e-11 | 8.436e-10 |
121 | POSITIVE REGULATION OF INTRACELLULAR TRANSPORT | 15 | 370 | 2.485e-11 | 9.555e-10 |
122 | POSITIVE REGULATION OF STEM CELL DIFFERENTIATION | 8 | 50 | 2.628e-11 | 1.002e-09 |
123 | SISTER CHROMATID COHESION | 10 | 111 | 2.811e-11 | 1.063e-09 |
124 | POSITIVE REGULATION OF CELL COMMUNICATION | 27 | 1532 | 3.306e-11 | 1.241e-09 |
125 | REGULATION OF CELLULAR RESPONSE TO STRESS | 19 | 691 | 3.413e-11 | 1.271e-09 |
126 | REGULATION OF FIBROBLAST PROLIFERATION | 9 | 81 | 4.282e-11 | 1.581e-09 |
127 | RESPONSE TO LIPID | 21 | 888 | 4.367e-11 | 1.6e-09 |
128 | POSITIVE REGULATION OF EPITHELIAL TO MESENCHYMAL TRANSITION | 7 | 34 | 7.377e-11 | 2.661e-09 |
129 | NEGATIVE REGULATION OF MITOTIC NUCLEAR DIVISION | 7 | 34 | 7.377e-11 | 2.661e-09 |
130 | NEGATIVE REGULATION OF CELL DIVISION | 8 | 60 | 1.212e-10 | 4.337e-09 |
131 | CELLULAR RESPONSE TO LIGHT STIMULUS | 9 | 91 | 1.245e-10 | 4.388e-09 |
132 | MITOTIC SISTER CHROMATID SEGREGATION | 9 | 91 | 1.245e-10 | 4.388e-09 |
133 | PEPTIDYL AMINO ACID MODIFICATION | 20 | 841 | 1.26e-10 | 4.408e-09 |
134 | REGULATION OF PROTEIN LOCALIZATION | 21 | 950 | 1.517e-10 | 5.267e-09 |
135 | NEGATIVE REGULATION OF NITROGEN COMPOUND METABOLIC PROCESS | 26 | 1517 | 1.589e-10 | 5.478e-09 |
136 | PROTEIN MODIFICATION BY SMALL PROTEIN CONJUGATION OR REMOVAL | 20 | 873 | 2.431e-10 | 8.319e-09 |
137 | POSITIVE REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION | 16 | 514 | 2.513e-10 | 8.537e-09 |
138 | PHOSPHATE CONTAINING COMPOUND METABOLIC PROCESS | 29 | 1977 | 3.968e-10 | 1.338e-08 |
139 | REGULATION OF MEMBRANE PERMEABILITY | 8 | 70 | 4.326e-10 | 1.448e-08 |
140 | REGULATION OF INTRACELLULAR TRANSPORT | 17 | 621 | 4.628e-10 | 1.538e-08 |
141 | DIGESTIVE SYSTEM DEVELOPMENT | 10 | 148 | 4.918e-10 | 1.623e-08 |
142 | POSITIVE REGULATION OF CHROMOSOME ORGANIZATION | 10 | 150 | 5.611e-10 | 1.839e-08 |
143 | RESPONSE TO ORGANIC CYCLIC COMPOUND | 20 | 917 | 5.741e-10 | 1.868e-08 |
144 | NEGATIVE REGULATION OF PROTEIN CATABOLIC PROCESS | 9 | 109 | 6.382e-10 | 2.062e-08 |
145 | SPINDLE CHECKPOINT | 6 | 25 | 6.562e-10 | 2.106e-08 |
146 | NEGATIVE REGULATION OF NUCLEAR DIVISION | 7 | 46 | 7.056e-10 | 2.249e-08 |
147 | CELLULAR RESPONSE TO ABIOTIC STIMULUS | 12 | 263 | 7.622e-10 | 2.413e-08 |
148 | REPLICATIVE SENESCENCE | 5 | 12 | 7.927e-10 | 2.492e-08 |
149 | DNA REPLICATION | 11 | 208 | 8.676e-10 | 2.709e-08 |
150 | REGULATION OF DNA METABOLIC PROCESS | 13 | 340 | 1.224e-09 | 3.798e-08 |
151 | PROTEIN CATABOLIC PROCESS | 16 | 579 | 1.412e-09 | 4.35e-08 |
152 | CELL PROLIFERATION | 17 | 672 | 1.534e-09 | 4.695e-08 |
153 | POSITIVE REGULATION OF APOPTOTIC SIGNALING PATHWAY | 10 | 171 | 2.017e-09 | 6.135e-08 |
154 | RESPONSE TO DRUG | 14 | 431 | 2.187e-09 | 6.608e-08 |
155 | ACTIVATION OF ANAPHASE PROMOTING COMPLEX ACTIVITY | 5 | 15 | 2.977e-09 | 8.937e-08 |
156 | NEGATIVE REGULATION OF GENE EXPRESSION | 24 | 1493 | 3.563e-09 | 1.063e-07 |
157 | MITOCHONDRIAL MEMBRANE ORGANIZATION | 8 | 92 | 3.967e-09 | 1.176e-07 |
158 | G2 DNA DAMAGE CHECKPOINT | 6 | 33 | 3.998e-09 | 1.177e-07 |
159 | REGULATION OF CELL CYCLE G2 M PHASE TRANSITION | 7 | 59 | 4.309e-09 | 1.261e-07 |
160 | CELLULAR RESPONSE TO ORGANIC CYCLIC COMPOUND | 14 | 465 | 5.765e-09 | 1.676e-07 |
161 | POSITIVE REGULATION OF CYCLIN DEPENDENT PROTEIN KINASE ACTIVITY | 6 | 36 | 6.963e-09 | 2.012e-07 |
162 | NEGATIVE REGULATION OF CELLULAR PROTEIN CATABOLIC PROCESS | 7 | 64 | 7.719e-09 | 2.205e-07 |
163 | POSITIVE REGULATION OF TRANSMEMBRANE RECEPTOR PROTEIN SERINE THREONINE KINASE SIGNALING PATHWAY | 8 | 100 | 7.724e-09 | 2.205e-07 |
164 | REGULATION OF RESPONSE TO DNA DAMAGE STIMULUS | 9 | 145 | 8.057e-09 | 2.286e-07 |
165 | POSITIVE REGULATION OF KINASE ACTIVITY | 14 | 482 | 9.085e-09 | 2.562e-07 |
166 | REGULATION OF EPITHELIAL TO MESENCHYMAL TRANSITION | 7 | 67 | 1.07e-08 | 2.999e-07 |
167 | NEGATIVE REGULATION OF CELL DEATH | 18 | 872 | 1.145e-08 | 3.19e-07 |
168 | REGULATION OF TRANSMEMBRANE RECEPTOR PROTEIN SERINE THREONINE KINASE SIGNALING PATHWAY | 10 | 207 | 1.27e-08 | 3.516e-07 |
169 | RESPONSE TO STEROID HORMONE | 14 | 497 | 1.337e-08 | 3.681e-07 |
170 | RESPONSE TO LIGHT STIMULUS | 11 | 280 | 1.933e-08 | 5.291e-07 |
171 | REGULATION OF STEM CELL DIFFERENTIATION | 8 | 113 | 2.035e-08 | 5.537e-07 |
172 | REGULATION OF PROTEIN LOCALIZATION TO NUCLEUS | 10 | 218 | 2.078e-08 | 5.623e-07 |
173 | POSITIVE REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 9 | 162 | 2.123e-08 | 5.71e-07 |
174 | REGULATION OF BINDING | 11 | 283 | 2.157e-08 | 5.768e-07 |
175 | APOPTOTIC SIGNALING PATHWAY | 11 | 289 | 2.675e-08 | 7.112e-07 |
176 | RESPONSE TO ALCOHOL | 12 | 362 | 2.738e-08 | 7.238e-07 |
177 | REGULATION OF CELLULAR LOCALIZATION | 21 | 1277 | 2.951e-08 | 7.757e-07 |
178 | PROTEIN UBIQUITINATION | 15 | 629 | 3.499e-08 | 9.146e-07 |
179 | RHYTHMIC PROCESS | 11 | 298 | 3.661e-08 | 9.516e-07 |
180 | NEGATIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 16 | 740 | 4.486e-08 | 1.16e-06 |
181 | POSITIVE REGULATION OF CHROMOSOME SEGREGATION | 5 | 25 | 5.1e-08 | 1.311e-06 |
182 | RESPONSE TO ENDOGENOUS STIMULUS | 22 | 1450 | 5.367e-08 | 1.372e-06 |
183 | REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION TO MITOCHONDRION | 8 | 128 | 5.411e-08 | 1.376e-06 |
184 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO NUCLEUS | 8 | 129 | 5.75e-08 | 1.454e-06 |
185 | REGULATION OF MICROTUBULE BASED PROCESS | 10 | 243 | 5.794e-08 | 1.457e-06 |
186 | RESPONSE TO GROWTH FACTOR | 13 | 475 | 6.52e-08 | 1.631e-06 |
187 | REGULATION OF RESPONSE TO STRESS | 22 | 1468 | 6.677e-08 | 1.661e-06 |
188 | POSITIVE REGULATION OF CELL DIVISION | 8 | 132 | 6.878e-08 | 1.702e-06 |
189 | MEIOTIC CELL CYCLE | 9 | 186 | 7.005e-08 | 1.725e-06 |
190 | PROTEIN K11 LINKED UBIQUITINATION | 5 | 27 | 7.7e-08 | 1.876e-06 |
191 | REGULATION OF TRANSCRIPTION INVOLVED IN G1 S TRANSITION OF MITOTIC CELL CYCLE | 5 | 27 | 7.7e-08 | 1.876e-06 |
192 | NEGATIVE REGULATION OF PROTEOLYSIS | 11 | 329 | 9.997e-08 | 2.423e-06 |
193 | CELLULAR RESPONSE TO ENDOGENOUS STIMULUS | 18 | 1008 | 1.038e-07 | 2.503e-06 |
194 | NEGATIVE REGULATION OF CELLULAR COMPONENT ORGANIZATION | 15 | 684 | 1.045e-07 | 2.506e-06 |
195 | SMAD PROTEIN SIGNAL TRANSDUCTION | 6 | 56 | 1.087e-07 | 2.595e-06 |
196 | DNA REPLICATION INITIATION | 5 | 29 | 1.126e-07 | 2.672e-06 |
197 | REGULATION OF CYTOSKELETON ORGANIZATION | 13 | 502 | 1.236e-07 | 2.92e-06 |
198 | NEGATIVE REGULATION OF CHROMOSOME ORGANIZATION | 7 | 96 | 1.333e-07 | 3.133e-06 |
199 | NEGATIVE REGULATION OF CATABOLIC PROCESS | 9 | 203 | 1.48e-07 | 3.46e-06 |
200 | REGULATION OF TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 7 | 99 | 1.649e-07 | 3.817e-06 |
201 | REGULATION OF CELLULAR RESPONSE TO TRANSFORMING GROWTH FACTOR BETA STIMULUS | 7 | 99 | 1.649e-07 | 3.817e-06 |
202 | MACROMOLECULE CATABOLIC PROCESS | 17 | 926 | 1.69e-07 | 3.894e-06 |
203 | MITOTIC CELL CYCLE ARREST | 4 | 13 | 1.824e-07 | 4.182e-06 |
204 | NEGATIVE REGULATION OF CYCLIN DEPENDENT PROTEIN KINASE ACTIVITY | 5 | 32 | 1.89e-07 | 4.311e-06 |
205 | INTRINSIC APOPTOTIC SIGNALING PATHWAY | 8 | 152 | 2.049e-07 | 4.651e-06 |
206 | REGULATION OF CELL AGING | 5 | 33 | 2.221e-07 | 5.016e-06 |
207 | POSITIVE REGULATION OF MITOTIC SISTER CHROMATID SEPARATION | 4 | 14 | 2.546e-07 | 5.662e-06 |
208 | POSITIVE REGULATION OF MITOTIC METAPHASE ANAPHASE TRANSITION | 4 | 14 | 2.546e-07 | 5.662e-06 |
209 | REGULATION OF EPITHELIAL CELL PROLIFERATION | 10 | 285 | 2.555e-07 | 5.662e-06 |
210 | POSITIVE REGULATION OF METAPHASE ANAPHASE TRANSITION OF CELL CYCLE | 4 | 14 | 2.546e-07 | 5.662e-06 |
211 | REGULATION OF APOPTOTIC SIGNALING PATHWAY | 11 | 363 | 2.68e-07 | 5.91e-06 |
212 | REGULATION OF MITOCHONDRION ORGANIZATION | 9 | 218 | 2.709e-07 | 5.917e-06 |
213 | RESPONSE TO ESTROGEN | 9 | 218 | 2.709e-07 | 5.917e-06 |
214 | CHROMATIN MODIFICATION | 13 | 539 | 2.793e-07 | 6.072e-06 |
215 | POSITIVE REGULATION OF PROTEIN SERINE THREONINE KINASE ACTIVITY | 10 | 289 | 2.905e-07 | 6.288e-06 |
216 | REGULATION OF NUCLEOCYTOPLASMIC TRANSPORT | 9 | 220 | 2.926e-07 | 6.303e-06 |
217 | PROTEOLYSIS | 19 | 1208 | 3.092e-07 | 6.631e-06 |
218 | REGULATION OF DNA REPLICATION | 8 | 161 | 3.185e-07 | 6.799e-06 |
219 | REGULATION OF SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR | 8 | 162 | 3.34e-07 | 7.096e-06 |
220 | POSITIVE REGULATION OF MITOCHONDRION ORGANIZATION | 8 | 167 | 4.212e-07 | 8.909e-06 |
221 | NEGATIVE REGULATION OF EPITHELIAL CELL PROLIFERATION | 7 | 115 | 4.604e-07 | 9.567e-06 |
222 | INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO DNA DAMAGE | 6 | 71 | 4.568e-07 | 9.567e-06 |
223 | PROTEIN SUMOYLATION | 7 | 115 | 4.604e-07 | 9.567e-06 |
224 | CHROMATIN ORGANIZATION | 14 | 663 | 4.626e-07 | 9.567e-06 |
225 | MESENCHYME MORPHOGENESIS | 5 | 38 | 4.622e-07 | 9.567e-06 |
226 | NEGATIVE REGULATION OF CELL GROWTH | 8 | 170 | 4.824e-07 | 9.932e-06 |
227 | NEGATIVE REGULATION OF ORGANELLE ORGANIZATION | 11 | 387 | 5.057e-07 | 1.037e-05 |
228 | RESPONSE TO OXYGEN CONTAINING COMPOUND | 20 | 1381 | 5.27e-07 | 1.075e-05 |
229 | REGULATION OF CELL GROWTH | 11 | 391 | 5.597e-07 | 1.137e-05 |
230 | RESPONSE TO HORMONE | 16 | 893 | 5.718e-07 | 1.157e-05 |
231 | NEGATIVE REGULATION OF CELL AGING | 4 | 17 | 5.997e-07 | 1.208e-05 |
232 | GLAND DEVELOPMENT | 11 | 395 | 6.187e-07 | 1.241e-05 |
233 | MITOCHONDRIAL TRANSPORT | 8 | 177 | 6.554e-07 | 1.298e-05 |
234 | POSITIVE REGULATION OF NUCLEOCYTOPLASMIC TRANSPORT | 7 | 121 | 6.505e-07 | 1.298e-05 |
235 | POSITIVE REGULATION OF DEVELOPMENTAL PROCESS | 18 | 1142 | 6.543e-07 | 1.298e-05 |
236 | PROTEIN POLYUBIQUITINATION | 9 | 243 | 6.743e-07 | 1.329e-05 |
237 | REGULATION OF CELLULAR RESPONSE TO HEAT | 6 | 76 | 6.86e-07 | 1.341e-05 |
238 | REGULATION OF MICROTUBULE POLYMERIZATION OR DEPOLYMERIZATION | 8 | 178 | 6.84e-07 | 1.341e-05 |
239 | REGULATION OF UBIQUITIN PROTEIN LIGASE ACTIVITY | 4 | 18 | 7.687e-07 | 1.497e-05 |
240 | NEGATIVE REGULATION OF DEVELOPMENTAL PROCESS | 15 | 801 | 7.831e-07 | 1.518e-05 |
241 | RESPONSE TO KETONE | 8 | 182 | 8.092e-07 | 1.562e-05 |
242 | REPRODUCTION | 19 | 1297 | 9.109e-07 | 1.751e-05 |
243 | POSITIVE REGULATION OF DNA METABOLIC PROCESS | 8 | 185 | 9.155e-07 | 1.753e-05 |
244 | POSITIVE REGULATION OF TRANSPORT | 16 | 936 | 1.064e-06 | 2.028e-05 |
245 | ORGAN REGENERATION | 6 | 83 | 1.158e-06 | 2.199e-05 |
246 | REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 10 | 337 | 1.179e-06 | 2.231e-05 |
247 | EPITHELIUM DEVELOPMENT | 16 | 945 | 1.206e-06 | 2.271e-05 |
248 | AGING | 9 | 264 | 1.343e-06 | 2.519e-05 |
249 | POSITIVE REGULATION OF PATHWAY RESTRICTED SMAD PROTEIN PHOSPHORYLATION | 5 | 48 | 1.527e-06 | 2.853e-05 |
250 | MEIOSIS I | 6 | 88 | 1.635e-06 | 3.044e-05 |
251 | REGULATION OF GROWTH | 13 | 633 | 1.698e-06 | 3.147e-05 |
252 | REGULATION OF CELL DIFFERENTIATION | 20 | 1492 | 1.765e-06 | 3.259e-05 |
253 | CELLULAR RESPONSE TO OXYGEN LEVELS | 7 | 143 | 2.003e-06 | 3.684e-05 |
254 | POSITIVE REGULATION OF MITOTIC NUCLEAR DIVISION | 5 | 51 | 2.075e-06 | 3.8e-05 |
255 | RESPONSE TO TRANSFORMING GROWTH FACTOR BETA | 7 | 144 | 2.099e-06 | 3.83e-05 |
256 | RESPONSE TO IONIZING RADIATION | 7 | 145 | 2.198e-06 | 3.964e-05 |
257 | POSITIVE REGULATION OF MULTICELLULAR ORGANISMAL METABOLIC PROCESS | 4 | 23 | 2.19e-06 | 3.964e-05 |
258 | POSITIVE REGULATION OF COLLAGEN METABOLIC PROCESS | 4 | 23 | 2.19e-06 | 3.964e-05 |
259 | TISSUE DEVELOPMENT | 20 | 1518 | 2.303e-06 | 4.138e-05 |
260 | PEPTIDYL SERINE MODIFICATION | 7 | 148 | 2.52e-06 | 4.509e-05 |
261 | CELLULAR RESPONSE TO LIPID | 11 | 457 | 2.557e-06 | 4.553e-05 |
262 | TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 6 | 95 | 2.563e-06 | 4.553e-05 |
263 | REGULATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY | 8 | 213 | 2.631e-06 | 4.655e-05 |
264 | INTERSPECIES INTERACTION BETWEEN ORGANISMS | 13 | 662 | 2.78e-06 | 4.881e-05 |
265 | SYMBIOSIS ENCOMPASSING MUTUALISM THROUGH PARASITISM | 13 | 662 | 2.78e-06 | 4.881e-05 |
266 | MEIOTIC CELL CYCLE PROCESS | 7 | 152 | 3.009e-06 | 5.263e-05 |
267 | NEGATIVE REGULATION OF DNA REPLICATION | 5 | 55 | 3.033e-06 | 5.286e-05 |
268 | POSITIVE REGULATION OF PROTEASOMAL PROTEIN CATABOLIC PROCESS | 6 | 98 | 3.075e-06 | 5.338e-05 |
269 | DNA DEPENDENT DNA REPLICATION | 6 | 99 | 3.262e-06 | 5.643e-05 |
270 | CELLULAR RESPONSE TO ORGANIC SUBSTANCE | 22 | 1848 | 3.385e-06 | 5.834e-05 |
271 | NEGATIVE REGULATION OF CELLULAR CATABOLIC PROCESS | 7 | 156 | 3.574e-06 | 6.137e-05 |
272 | REGULATION OF CELLULAR SENESCENCE | 4 | 26 | 3.663e-06 | 6.266e-05 |
273 | RESPONSE TO INORGANIC SUBSTANCE | 11 | 479 | 4.012e-06 | 6.838e-05 |
274 | CELLULAR RESPONSE TO REACTIVE OXYGEN SPECIES | 6 | 104 | 4.346e-06 | 7.381e-05 |
275 | REGENERATION | 7 | 161 | 4.404e-06 | 7.452e-05 |
276 | REGULATION OF CELLULAR RESPONSE TO GROWTH FACTOR STIMULUS | 8 | 229 | 4.497e-06 | 7.582e-05 |
277 | REGULATION OF PATHWAY RESTRICTED SMAD PROTEIN PHOSPHORYLATION | 5 | 60 | 4.686e-06 | 7.872e-05 |
278 | REGULATION OF DNA DAMAGE RESPONSE SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR | 4 | 28 | 4.985e-06 | 8.344e-05 |
279 | CELLULAR RESPONSE TO HYDROGEN PEROXIDE | 5 | 61 | 5.088e-06 | 8.486e-05 |
280 | PEPTIDYL LYSINE MODIFICATION | 9 | 312 | 5.265e-06 | 8.738e-05 |
281 | SENSORY ORGAN DEVELOPMENT | 11 | 493 | 5.277e-06 | 8.738e-05 |
282 | SOMITOGENESIS | 5 | 62 | 5.517e-06 | 9.071e-05 |
283 | POSITIVE REGULATION OF NUCLEAR DIVISION | 5 | 62 | 5.517e-06 | 9.071e-05 |
284 | NEGATIVE REGULATION OF GROWTH | 8 | 236 | 5.612e-06 | 9.195e-05 |
285 | NEGATIVE REGULATION OF PRODUCTION OF MOLECULAR MEDIATOR OF IMMUNE RESPONSE | 4 | 29 | 5.765e-06 | 9.347e-05 |
286 | REGULATION OF EXTRACELLULAR MATRIX ORGANIZATION | 4 | 29 | 5.765e-06 | 9.347e-05 |
287 | REGULATION OF HEART MORPHOGENESIS | 4 | 29 | 5.765e-06 | 9.347e-05 |
288 | NEGATIVE REGULATION OF DNA METABOLIC PROCESS | 6 | 111 | 6.34e-06 | 0.0001024 |
289 | REGULATION OF PROTEIN ACETYLATION | 5 | 64 | 6.459e-06 | 0.0001036 |
290 | POSITIVE REGULATION OF RESPONSE TO DNA DAMAGE STIMULUS | 5 | 64 | 6.459e-06 | 0.0001036 |
291 | GROWTH | 10 | 410 | 6.748e-06 | 0.0001079 |
292 | NOTCH SIGNALING PATHWAY | 6 | 114 | 7.394e-06 | 0.0001178 |
293 | NEGATIVE REGULATION OF RESPONSE TO STIMULUS | 18 | 1360 | 7.754e-06 | 0.0001231 |
294 | CELL AGING | 5 | 67 | 8.103e-06 | 0.0001282 |
295 | DEVELOPMENTAL GROWTH | 9 | 333 | 8.895e-06 | 0.0001403 |
296 | RESPONSE TO NITROGEN COMPOUND | 14 | 859 | 9.48e-06 | 0.000149 |
297 | PROTEIN COMPLEX SUBUNIT ORGANIZATION | 19 | 1527 | 9.977e-06 | 0.0001563 |
298 | REGULATION OF PROTEIN IMPORT | 7 | 183 | 1.021e-05 | 0.0001594 |
299 | NEGATIVE REGULATION OF CELLULAR SENESCENCE | 3 | 11 | 1.07e-05 | 0.000166 |
300 | ACTIVATION OF MAPKKK ACTIVITY | 3 | 11 | 1.07e-05 | 0.000166 |
301 | PROTEIN DESTABILIZATION | 4 | 34 | 1.108e-05 | 0.0001713 |
302 | MACROMOLECULAR COMPLEX ASSEMBLY | 18 | 1398 | 1.131e-05 | 0.0001743 |
303 | TRANSCRIPTION COUPLED NUCLEOTIDE EXCISION REPAIR | 5 | 73 | 1.236e-05 | 0.0001898 |
304 | RESPONSE TO MINERALOCORTICOID | 4 | 35 | 1.247e-05 | 0.0001903 |
305 | RESPONSE TO IRON ION | 4 | 35 | 1.247e-05 | 0.0001903 |
306 | CELLULAR RESPONSE TO EXTERNAL STIMULUS | 8 | 264 | 1.271e-05 | 0.0001933 |
307 | MESENCHYME DEVELOPMENT | 7 | 190 | 1.303e-05 | 0.0001975 |
308 | REGULATION OF MACROPHAGE CYTOKINE PRODUCTION | 3 | 12 | 1.423e-05 | 0.0002143 |
309 | POSITIVE REGULATION OF SMAD PROTEIN IMPORT INTO NUCLEUS | 3 | 12 | 1.423e-05 | 0.0002143 |
310 | TUBE DEVELOPMENT | 11 | 552 | 1.525e-05 | 0.0002282 |
311 | REGULATION OF CELL MORPHOGENESIS | 11 | 552 | 1.525e-05 | 0.0002282 |
312 | SOMITE DEVELOPMENT | 5 | 78 | 1.71e-05 | 0.000255 |
313 | REGULATION OF MULTICELLULAR ORGANISMAL METABOLIC PROCESS | 4 | 38 | 1.742e-05 | 0.000259 |
314 | POSITIVE REGULATION OF DNA DAMAGE RESPONSE SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR | 3 | 13 | 1.844e-05 | 0.0002733 |
315 | POSITIVE REGULATION OF CYTOPLASMIC TRANSPORT | 8 | 282 | 2.044e-05 | 0.0003011 |
316 | HEART DEVELOPMENT | 10 | 466 | 2.045e-05 | 0.0003011 |
317 | CELLULAR CATABOLIC PROCESS | 17 | 1322 | 2.114e-05 | 0.0003103 |
318 | NEGATIVE REGULATION OF CELL COMMUNICATION | 16 | 1192 | 2.292e-05 | 0.0003353 |
319 | POSITIVE REGULATION OF P38MAPK CASCADE | 3 | 14 | 2.34e-05 | 0.0003414 |
320 | IMMUNE SYSTEM DEVELOPMENT | 11 | 582 | 2.485e-05 | 0.0003614 |
321 | REGULATION OF INTRACELLULAR PROTEIN TRANSPORT | 9 | 381 | 2.586e-05 | 0.0003749 |
322 | POSITIVE REGULATION OF CHROMATIN MODIFICATION | 5 | 85 | 2.598e-05 | 0.0003754 |
323 | REGULATION OF CYTOPLASMIC TRANSPORT | 10 | 481 | 2.68e-05 | 0.0003861 |
324 | POSITIVE REGULATION OF DNA REPLICATION | 5 | 86 | 2.749e-05 | 0.0003949 |
325 | BETA CATENIN TCF COMPLEX ASSEMBLY | 4 | 43 | 2.868e-05 | 0.0004106 |
326 | RESPONSE TO ESTRADIOL | 6 | 146 | 3.029e-05 | 0.0004323 |
327 | REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 19 | 1656 | 3.115e-05 | 0.0004433 |
328 | CELLULAR RESPONSE TO STEROID HORMONE STIMULUS | 7 | 218 | 3.157e-05 | 0.0004478 |
329 | SEGMENTATION | 5 | 89 | 3.246e-05 | 0.000459 |
330 | PROTEIN LOCALIZATION TO CHROMOSOME | 4 | 45 | 3.441e-05 | 0.0004827 |
331 | REGULATION OF PROTEIN STABILITY | 7 | 221 | 3.444e-05 | 0.0004827 |
332 | MESONEPHROS DEVELOPMENT | 5 | 90 | 3.426e-05 | 0.0004827 |
333 | CHROMATIN REMODELING | 6 | 150 | 3.526e-05 | 0.0004927 |
334 | REGULATION OF SMAD PROTEIN IMPORT INTO NUCLEUS | 3 | 16 | 3.579e-05 | 0.0004928 |
335 | REGULATION OF EXIT FROM MITOSIS | 3 | 16 | 3.579e-05 | 0.0004928 |
336 | REGULATION OF MULTICELLULAR ORGANISMAL DEVELOPMENT | 19 | 1672 | 3.557e-05 | 0.0004928 |
337 | ORGAN MORPHOGENESIS | 13 | 841 | 3.561e-05 | 0.0004928 |
338 | CELLULAR RESPONSE TO ANTIBIOTIC | 3 | 16 | 3.579e-05 | 0.0004928 |
339 | REGULATION OF PROTEIN TARGETING | 8 | 307 | 3.745e-05 | 0.0005141 |
340 | NEGATIVE REGULATION OF CELL DIFFERENTIATION | 11 | 609 | 3.76e-05 | 0.0005146 |
341 | REGULATION OF CHROMATIN ORGANIZATION | 6 | 152 | 3.798e-05 | 0.0005183 |
342 | CELLULAR RESPONSE TO NITROGEN COMPOUND | 10 | 505 | 4.047e-05 | 0.0005506 |
343 | POSITIVE REGULATION OF MULTICELLULAR ORGANISMAL PROCESS | 17 | 1395 | 4.189e-05 | 0.0005682 |
344 | REGULATION OF DNA BIOSYNTHETIC PROCESS | 5 | 94 | 4.224e-05 | 0.0005713 |
345 | POSITIVE REGULATION OF CELLULAR COMPONENT BIOGENESIS | 9 | 406 | 4.244e-05 | 0.0005724 |
346 | POSITIVE REGULATION OF SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR | 3 | 17 | 4.334e-05 | 0.0005794 |
347 | POSITIVE REGULATION OF EXTRACELLULAR MATRIX ORGANIZATION | 3 | 17 | 4.334e-05 | 0.0005794 |
348 | REGULATION OF SISTER CHROMATID COHESION | 3 | 17 | 4.334e-05 | 0.0005794 |
349 | REGULATION OF LIPID KINASE ACTIVITY | 4 | 48 | 4.452e-05 | 0.0005935 |
350 | HEMATOPOIETIC PROGENITOR CELL DIFFERENTIATION | 5 | 98 | 5.159e-05 | 0.000684 |
351 | RESPONSE TO VITAMIN | 5 | 98 | 5.159e-05 | 0.000684 |
352 | POSITIVE REGULATION OF CELL CYCLE G2 M PHASE TRANSITION | 3 | 18 | 5.185e-05 | 0.0006854 |
353 | RESPONSE TO PROGESTERONE | 4 | 50 | 5.236e-05 | 0.0006882 |
354 | RESPONSE TO GAMMA RADIATION | 4 | 50 | 5.236e-05 | 0.0006882 |
355 | CELL DEVELOPMENT | 17 | 1426 | 5.518e-05 | 0.0007232 |
356 | RESPONSE TO AMMONIUM ION | 4 | 51 | 5.664e-05 | 0.0007403 |
357 | EYE DEVELOPMENT | 8 | 326 | 5.719e-05 | 0.0007453 |
358 | CELLULAR RESPONSE TO IONIZING RADIATION | 4 | 52 | 6.117e-05 | 0.000795 |
359 | NEGATIVE REGULATION OF TRANSMEMBRANE RECEPTOR PROTEIN SERINE THREONINE KINASE SIGNALING PATHWAY | 5 | 102 | 6.248e-05 | 0.0008097 |
360 | REGULATION OF CELLULAR COMPONENT BIOGENESIS | 12 | 767 | 6.543e-05 | 0.0008457 |
361 | INTRINSIC APOPTOTIC SIGNALING PATHWAY BY P53 CLASS MEDIATOR | 4 | 53 | 6.596e-05 | 0.0008501 |
362 | RESPONSE TO METAL ION | 8 | 333 | 6.636e-05 | 0.0008529 |
363 | EMBRYO DEVELOPMENT | 13 | 894 | 6.659e-05 | 0.0008536 |
364 | POSITIVE REGULATION OF PROTEIN IMPORT | 5 | 104 | 6.854e-05 | 0.0008761 |
365 | NEGATIVE REGULATION OF CELL CYCLE ARREST | 3 | 20 | 7.201e-05 | 0.000918 |
366 | CRANIAL SKELETAL SYSTEM DEVELOPMENT | 4 | 55 | 7.635e-05 | 0.0009706 |
367 | LYMPHOCYTE ACTIVATION | 8 | 342 | 7.992e-05 | 0.001013 |
368 | EPITHELIAL TO MESENCHYMAL TRANSITION | 4 | 56 | 8.196e-05 | 0.001036 |
369 | COVALENT CHROMATIN MODIFICATION | 8 | 345 | 8.492e-05 | 0.001071 |
370 | RESPONSE TO HYDROGEN PEROXIDE | 5 | 109 | 8.569e-05 | 0.001078 |
371 | MICROTUBULE CYTOSKELETON ORGANIZATION | 8 | 348 | 9.018e-05 | 0.001131 |
372 | POSITIVE REGULATION OF INTRACELLULAR PROTEIN TRANSPORT | 7 | 258 | 9.142e-05 | 0.001143 |
373 | NEGATIVE REGULATION OF CYTOKINE PRODUCTION INVOLVED IN IMMUNE RESPONSE | 3 | 22 | 9.67e-05 | 0.001203 |
374 | ENDOCARDIAL CUSHION MORPHOGENESIS | 3 | 22 | 9.67e-05 | 0.001203 |
375 | REGULATION OF CYTOKINE PRODUCTION | 10 | 563 | 1e-04 | 0.001241 |
376 | POSITIVE REGULATION OF DNA BIOSYNTHETIC PROCESS | 4 | 59 | 0.0001006 | 0.001245 |
377 | NUCLEOTIDE EXCISION REPAIR | 5 | 113 | 0.0001016 | 0.001255 |
378 | CELL ACTIVATION | 10 | 568 | 0.0001076 | 0.001324 |
379 | CELLULAR RESPONSE TO OXIDATIVE STRESS | 6 | 184 | 0.0001096 | 0.001346 |
380 | RESPONSE TO INCREASED OXYGEN LEVELS | 3 | 23 | 0.0001109 | 0.001354 |
381 | RESPONSE TO HYPEROXIA | 3 | 23 | 0.0001109 | 0.001354 |
382 | EMBRYONIC DIGIT MORPHOGENESIS | 4 | 61 | 0.0001147 | 0.001397 |
383 | POSITIVE REGULATION OF CELLULAR RESPONSE TO TRANSFORMING GROWTH FACTOR BETA STIMULUS | 3 | 24 | 0.0001263 | 0.001531 |
384 | POSITIVE REGULATION OF TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 3 | 24 | 0.0001263 | 0.001531 |
385 | POSITIVE REGULATION OF CELL DIFFERENTIATION | 12 | 823 | 0.0001275 | 0.001541 |
386 | TRANSMEMBRANE RECEPTOR PROTEIN SERINE THREONINE KINASE SIGNALING PATHWAY | 6 | 190 | 0.0001307 | 0.001575 |
387 | CELLULAR MACROMOLECULE LOCALIZATION | 15 | 1234 | 0.0001312 | 0.001578 |
388 | POSITIVE REGULATION OF CELL DEVELOPMENT | 9 | 472 | 0.0001341 | 0.001604 |
389 | RESPONSE TO NUTRIENT | 6 | 191 | 0.0001345 | 0.001604 |
390 | RESPONSE TO REACTIVE OXYGEN SPECIES | 6 | 191 | 0.0001345 | 0.001604 |
391 | LENS FIBER CELL DIFFERENTIATION | 3 | 25 | 0.0001431 | 0.001669 |
392 | NEGATIVE REGULATION OF CELLULAR RESPONSE TO GROWTH FACTOR STIMULUS | 5 | 121 | 0.0001403 | 0.001669 |
393 | CELLULAR RESPONSE TO TOXIC SUBSTANCE | 3 | 25 | 0.0001431 | 0.001669 |
394 | REGULATION OF TRANSFORMING GROWTH FACTOR BETA PRODUCTION | 3 | 25 | 0.0001431 | 0.001669 |
395 | POSITIVE REGULATION OF PEPTIDYL THREONINE PHOSPHORYLATION | 3 | 25 | 0.0001431 | 0.001669 |
396 | EPITHELIAL CELL APOPTOTIC PROCESS | 3 | 25 | 0.0001431 | 0.001669 |
397 | NEGATIVE REGULATION OF IMMUNE SYSTEM PROCESS | 8 | 372 | 0.0001428 | 0.001669 |
398 | HISTONE PHOSPHORYLATION | 3 | 25 | 0.0001431 | 0.001669 |
399 | DEVELOPMENTAL MATURATION | 6 | 193 | 0.0001423 | 0.001669 |
400 | HEAD DEVELOPMENT | 11 | 709 | 0.0001458 | 0.001696 |
401 | ANTERIOR POSTERIOR PATTERN SPECIFICATION | 6 | 194 | 0.0001464 | 0.001699 |
402 | REGULATION OF CELL DEVELOPMENT | 12 | 836 | 0.0001476 | 0.001708 |
403 | NEGATIVE REGULATION OF CELLULAR RESPONSE TO TRANSFORMING GROWTH FACTOR BETA STIMULUS | 4 | 66 | 0.0001559 | 0.001791 |
404 | NEGATIVE REGULATION OF TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 4 | 66 | 0.0001559 | 0.001791 |
405 | LENS DEVELOPMENT IN CAMERA TYPE EYE | 4 | 66 | 0.0001559 | 0.001791 |
406 | RESPONSE TO CORTICOSTERONE | 3 | 26 | 0.0001613 | 0.001845 |
407 | REGULATION OF P38MAPK CASCADE | 3 | 26 | 0.0001613 | 0.001845 |
408 | KIDNEY EPITHELIUM DEVELOPMENT | 5 | 125 | 0.0001635 | 0.001864 |
409 | POSITIVE REGULATION OF NEURON DEATH | 4 | 67 | 0.0001653 | 0.001876 |
410 | REGULATION OF DNA TEMPLATED TRANSCRIPTION IN RESPONSE TO STRESS | 4 | 67 | 0.0001653 | 0.001876 |
411 | TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 11 | 724 | 0.000175 | 0.001981 |
412 | POSITIVE REGULATION OF BINDING | 5 | 127 | 0.0001761 | 0.001988 |
413 | MITOTIC SPINDLE ORGANIZATION | 4 | 69 | 0.0001853 | 0.002087 |
414 | PROTEIN COMPLEX BIOGENESIS | 14 | 1132 | 0.0001896 | 0.002126 |
415 | PROTEIN COMPLEX ASSEMBLY | 14 | 1132 | 0.0001896 | 0.002126 |
416 | EPITHELIAL CELL DIFFERENTIATION | 9 | 495 | 0.0001914 | 0.002141 |
417 | CELL MATURATION | 5 | 131 | 0.0002035 | 0.00227 |
418 | REGULATION OF PEPTIDASE ACTIVITY | 8 | 392 | 0.0002041 | 0.002272 |
419 | ENDODERM DEVELOPMENT | 4 | 71 | 0.0002069 | 0.002298 |
420 | LYMPHOCYTE DIFFERENTIATION | 6 | 209 | 0.0002193 | 0.002429 |
421 | NUCLEOTIDE EXCISION REPAIR PREINCISION COMPLEX ASSEMBLY | 3 | 29 | 0.0002247 | 0.002484 |
422 | POSITIVE REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 12 | 876 | 0.0002274 | 0.002508 |
423 | CATABOLIC PROCESS | 18 | 1773 | 0.0002495 | 0.002744 |
424 | CIRCADIAN RHYTHM | 5 | 137 | 0.0002506 | 0.00275 |
425 | PROTEIN TARGETING | 8 | 406 | 0.0002587 | 0.002832 |
426 | REGULATION OF PROTEIN COMPLEX DISASSEMBLY | 6 | 217 | 0.0002684 | 0.002931 |
427 | MULTICELLULAR ORGANISM REPRODUCTION | 11 | 768 | 0.0002908 | 0.003168 |
428 | LEUKOCYTE ACTIVATION | 8 | 414 | 0.0002949 | 0.003206 |
429 | SALIVARY GLAND DEVELOPMENT | 3 | 32 | 0.0003024 | 0.003264 |
430 | ENDOCARDIAL CUSHION DEVELOPMENT | 3 | 32 | 0.0003024 | 0.003264 |
431 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER IN RESPONSE TO HYPOXIA | 3 | 32 | 0.0003024 | 0.003264 |
432 | REGULATION OF TRANSPORT | 18 | 1804 | 0.0003087 | 0.003325 |
433 | REGULATION OF PROTEIN EXPORT FROM NUCLEUS | 3 | 33 | 0.0003316 | 0.003564 |
434 | RESPONSE TO ACID CHEMICAL | 7 | 319 | 0.000336 | 0.003602 |
435 | RESPONSE TO EXTERNAL STIMULUS | 18 | 1821 | 0.0003461 | 0.003702 |
436 | RESPONSE TO TRANSITION METAL NANOPARTICLE | 5 | 148 | 0.0003579 | 0.003811 |
437 | REGULATION OF GENE EXPRESSION EPIGENETIC | 6 | 229 | 0.0003578 | 0.003811 |
438 | HEART VALVE DEVELOPMENT | 3 | 34 | 0.0003627 | 0.003853 |
439 | RESPONSE TO MONOAMINE | 3 | 35 | 0.0003955 | 0.004182 |
440 | POSITIVE REGULATION OF OSSIFICATION | 4 | 84 | 0.0003947 | 0.004182 |
441 | CELLULAR RESPONSE TO OXYGEN CONTAINING COMPOUND | 11 | 799 | 0.0004067 | 0.004291 |
442 | TRANSCRIPTION INITIATION FROM RNA POLYMERASE II PROMOTER | 5 | 153 | 0.0004169 | 0.004388 |
443 | CELLULAR RESPONSE TO HORMONE STIMULUS | 9 | 552 | 0.000426 | 0.004475 |
444 | POSITIVE REGULATION OF PROTEIN ACETYLATION | 3 | 36 | 0.0004302 | 0.004498 |
445 | HEAD MORPHOGENESIS | 3 | 36 | 0.0004302 | 0.004498 |
446 | EMBRYO DEVELOPMENT ENDING IN BIRTH OR EGG HATCHING | 9 | 554 | 0.0004373 | 0.004563 |
447 | RESPONSE TO EXTRACELLULAR STIMULUS | 8 | 441 | 0.0004492 | 0.004666 |
448 | PROTEIN LOCALIZATION TO ORGANELLE | 9 | 556 | 0.0004489 | 0.004666 |
449 | TISSUE REMODELING | 4 | 87 | 0.0004511 | 0.004675 |
450 | REGULATION OF PEPTIDYL THREONINE PHOSPHORYLATION | 3 | 37 | 0.0004668 | 0.004826 |
451 | OVULATION CYCLE PROCESS | 4 | 88 | 0.0004711 | 0.004839 |
452 | NEGATIVE REGULATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY | 4 | 88 | 0.0004711 | 0.004839 |
453 | RESPONSE TO TOXIC SUBSTANCE | 6 | 241 | 0.0004692 | 0.004839 |
454 | REGULATION OF ORGAN MORPHOGENESIS | 6 | 242 | 0.0004795 | 0.004915 |
455 | REGULATION OF DEPHOSPHORYLATION | 5 | 158 | 0.0004829 | 0.004938 |
456 | B CELL DIFFERENTIATION | 4 | 89 | 0.0004918 | 0.005018 |
457 | POSTTRANSCRIPTIONAL REGULATION OF GENE EXPRESSION | 8 | 448 | 0.0004984 | 0.005075 |
458 | POSITIVE REGULATION OF BIOMINERAL TISSUE DEVELOPMENT | 3 | 38 | 0.0005053 | 0.005122 |
459 | OOCYTE DIFFERENTIATION | 3 | 38 | 0.0005053 | 0.005122 |
460 | REGULATION OF CELL MATRIX ADHESION | 4 | 90 | 0.0005131 | 0.00519 |
461 | REGULATION OF IMMUNE SYSTEM PROCESS | 15 | 1403 | 0.0005226 | 0.005275 |
462 | CELLULAR RESPONSE TO NUTRIENT | 3 | 39 | 0.0005458 | 0.005485 |
463 | SPLEEN DEVELOPMENT | 3 | 39 | 0.0005458 | 0.005485 |
464 | REGULATION OF DNA BINDING | 4 | 93 | 0.0005808 | 0.005825 |
465 | POSITIVE REGULATION OF CELL MATRIX ADHESION | 3 | 40 | 0.0005883 | 0.005886 |
466 | REGULATION OF DNA DEPENDENT DNA REPLICATION | 3 | 41 | 0.0006328 | 0.006279 |
467 | NEGATIVE REGULATION OF FAT CELL DIFFERENTIATION | 3 | 41 | 0.0006328 | 0.006279 |
468 | LEUKOCYTE CELL CELL ADHESION | 6 | 255 | 0.0006314 | 0.006279 |
469 | ANDROGEN RECEPTOR SIGNALING PATHWAY | 3 | 41 | 0.0006328 | 0.006279 |
470 | RESPONSE TO CARBOHYDRATE | 5 | 168 | 0.0006381 | 0.006317 |
471 | NEGATIVE REGULATION OF PROTEIN COMPLEX DISASSEMBLY | 5 | 170 | 0.0006732 | 0.006651 |
472 | WOUND HEALING | 8 | 470 | 0.0006823 | 0.006726 |
473 | MITOCHONDRION ORGANIZATION | 9 | 594 | 0.0007209 | 0.007092 |
474 | EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 4 | 99 | 0.0007351 | 0.007216 |
475 | MODIFICATION OF MORPHOLOGY OR PHYSIOLOGY OF OTHER ORGANISM | 4 | 100 | 0.0007633 | 0.007446 |
476 | REGULATION OF SMOOTH MUSCLE CELL PROLIFERATION | 4 | 100 | 0.0007633 | 0.007446 |
477 | PEPTIDYL TYROSINE DEPHOSPHORYLATION | 4 | 100 | 0.0007633 | 0.007446 |
478 | BODY MORPHOGENESIS | 3 | 44 | 0.0007793 | 0.007586 |
479 | RESPONSE TO CORTICOSTEROID | 5 | 176 | 0.0007871 | 0.007646 |
480 | DEVELOPMENTAL PROCESS INVOLVED IN REPRODUCTION | 9 | 602 | 0.0007926 | 0.007667 |
481 | REGULATION OF PRODUCTION OF MOLECULAR MEDIATOR OF IMMUNE RESPONSE | 4 | 101 | 0.0007923 | 0.007667 |
482 | POSITIVE REGULATION OF CYTOKINE PRODUCTION | 7 | 370 | 0.0008105 | 0.007824 |
483 | NEGATIVE REGULATION OF IMMUNE EFFECTOR PROCESS | 4 | 102 | 0.0008221 | 0.00792 |
484 | REGULATION OF OSSIFICATION | 5 | 178 | 0.0008281 | 0.007961 |
485 | EXOCRINE SYSTEM DEVELOPMENT | 3 | 45 | 0.0008325 | 0.007987 |
486 | RESPONSE TO COCAINE | 3 | 46 | 0.000888 | 0.00845 |
487 | REGULATION OF MITOTIC SPINDLE CHECKPOINT | 2 | 11 | 0.0008917 | 0.00845 |
488 | REGULATION OF EXTRACELLULAR MATRIX ASSEMBLY | 2 | 11 | 0.0008917 | 0.00845 |
489 | POSITIVE REGULATION OF RECEPTOR BIOSYNTHETIC PROCESS | 2 | 11 | 0.0008917 | 0.00845 |
490 | REGULATION OF MITOTIC CELL CYCLE SPINDLE ASSEMBLY CHECKPOINT | 2 | 11 | 0.0008917 | 0.00845 |
491 | EMBRYONIC CRANIAL SKELETON MORPHOGENESIS | 3 | 46 | 0.000888 | 0.00845 |
492 | REGULATION OF ANATOMICAL STRUCTURE MORPHOGENESIS | 12 | 1021 | 0.0008949 | 0.008463 |
493 | ODONTOGENESIS | 4 | 105 | 0.0009163 | 0.008648 |
494 | RESPONSE TO ANTIBIOTIC | 3 | 47 | 0.0009457 | 0.00889 |
495 | POSITIVE REGULATION OF NEURON APOPTOTIC PROCESS | 3 | 47 | 0.0009457 | 0.00889 |
496 | HOMOLOGOUS CHROMOSOME SEGREGATION | 3 | 48 | 0.001006 | 0.009431 |
497 | ACTIVATION OF PROTEIN KINASE ACTIVITY | 6 | 279 | 0.001007 | 0.009431 |
498 | CELLULAR RESPONSE TO EXTRACELLULAR STIMULUS | 5 | 188 | 0.001058 | 0.009881 |
499 | MITOTIC SISTER CHROMATID COHESION | 2 | 12 | 0.001067 | 0.009951 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | CYCLIN DEPENDENT PROTEIN SERINE THREONINE KINASE REGULATOR ACTIVITY | 11 | 28 | 5.56e-20 | 5.165e-17 |
2 | ENZYME BINDING | 37 | 1737 | 2.243e-18 | 1.042e-15 |
3 | KINASE BINDING | 22 | 606 | 2.492e-15 | 7.716e-13 |
4 | TRANSCRIPTION FACTOR BINDING | 20 | 524 | 2.234e-14 | 5.189e-12 |
5 | KINASE REGULATOR ACTIVITY | 13 | 186 | 6.504e-13 | 1.209e-10 |
6 | PROTEIN KINASE ACTIVITY | 20 | 640 | 9.178e-13 | 1.421e-10 |
7 | PROTEIN COMPLEX BINDING | 23 | 935 | 1.86e-12 | 2.468e-10 |
8 | CYCLIN DEPENDENT PROTEIN SERINE THREONINE KINASE INHIBITOR ACTIVITY | 6 | 12 | 3.572e-12 | 4.148e-10 |
9 | KINASE ACTIVITY | 21 | 842 | 1.621e-11 | 1.673e-09 |
10 | PROTEIN SERINE THREONINE KINASE INHIBITOR ACTIVITY | 7 | 30 | 2.829e-11 | 2.324e-09 |
11 | PROTEIN SERINE THREONINE KINASE ACTIVITY | 16 | 445 | 3.002e-11 | 2.324e-09 |
12 | MACROMOLECULAR COMPLEX BINDING | 26 | 1399 | 2.671e-11 | 2.324e-09 |
13 | TRANSFERASE ACTIVITY TRANSFERRING PHOSPHORUS CONTAINING GROUPS | 21 | 992 | 3.344e-10 | 2.389e-08 |
14 | RNA POLYMERASE II TRANSCRIPTION FACTOR BINDING | 8 | 104 | 1.055e-08 | 7.002e-07 |
15 | KINASE INHIBITOR ACTIVITY | 7 | 89 | 7.886e-08 | 4.884e-06 |
16 | ACTIVATING TRANSCRIPTION FACTOR BINDING | 6 | 57 | 1.211e-07 | 7.034e-06 |
17 | NF KAPPAB BINDING | 5 | 30 | 1.346e-07 | 7.357e-06 |
18 | CORE PROMOTER BINDING | 8 | 152 | 2.049e-07 | 1.058e-05 |
19 | CYCLIN DEPENDENT PROTEIN KINASE ACTIVITY | 5 | 34 | 2.595e-07 | 1.269e-05 |
20 | ENZYME REGULATOR ACTIVITY | 17 | 959 | 2.774e-07 | 1.289e-05 |
21 | UBIQUITIN LIKE PROTEIN LIGASE BINDING | 9 | 264 | 1.343e-06 | 5.94e-05 |
22 | TRANSFORMING GROWTH FACTOR BETA RECEPTOR BINDING | 5 | 50 | 1.877e-06 | 7.927e-05 |
23 | TRANSCRIPTION FACTOR ACTIVITY PROTEIN BINDING | 12 | 588 | 4.731e-06 | 0.0001911 |
24 | MOLECULAR FUNCTION REGULATOR | 18 | 1353 | 7.222e-06 | 0.0002796 |
25 | P53 BINDING | 5 | 67 | 8.103e-06 | 0.0003011 |
26 | SMAD BINDING | 5 | 72 | 1.155e-05 | 0.0003975 |
27 | CHROMATIN BINDING | 10 | 435 | 1.13e-05 | 0.0003975 |
28 | RNA POLYMERASE II ACTIVATING TRANSCRIPTION FACTOR BINDING | 4 | 36 | 1.399e-05 | 0.0004642 |
29 | ANDROGEN RECEPTOR BINDING | 4 | 39 | 1.935e-05 | 0.0006199 |
30 | STEROID HORMONE RECEPTOR BINDING | 5 | 81 | 2.055e-05 | 0.0006365 |
31 | LIGASE REGULATOR ACTIVITY | 3 | 14 | 2.34e-05 | 0.0007014 |
32 | NUCLEIC ACID BINDING TRANSCRIPTION FACTOR ACTIVITY | 16 | 1199 | 2.462e-05 | 0.0007147 |
33 | REGULATORY REGION NUCLEIC ACID BINDING | 13 | 818 | 2.671e-05 | 0.0007519 |
34 | PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR BINDING | 3 | 15 | 2.917e-05 | 0.000797 |
35 | CYCLIN BINDING | 3 | 19 | 6.139e-05 | 0.001629 |
36 | HISTONE DEACETYLASE BINDING | 5 | 105 | 7.174e-05 | 0.001851 |
37 | PROTEIN C TERMINUS BINDING | 6 | 186 | 0.0001163 | 0.002771 |
38 | R SMAD BINDING | 3 | 23 | 0.0001109 | 0.002771 |
39 | ADENYL NUCLEOTIDE BINDING | 17 | 1514 | 0.0001155 | 0.002771 |
40 | CORE PROMOTER PROXIMAL REGION DNA BINDING | 8 | 371 | 0.0001402 | 0.003256 |
41 | BHLH TRANSCRIPTION FACTOR BINDING | 3 | 28 | 0.0002021 | 0.004579 |
42 | RNA POLYMERASE II TRANSCRIPTION FACTOR ACTIVITY SEQUENCE SPECIFIC DNA BINDING | 10 | 629 | 0.0002457 | 0.005436 |
43 | DOUBLE STRANDED DNA BINDING | 11 | 764 | 0.0002781 | 0.005983 |
44 | RECEPTOR BINDING | 16 | 1476 | 0.0002834 | 0.005983 |
45 | CHROMATIN DNA BINDING | 4 | 80 | 0.0003276 | 0.006763 |
46 | BETA CATENIN BINDING | 4 | 84 | 0.0003947 | 0.007971 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | CHROMOSOME | 28 | 880 | 4.783e-18 | 2.793e-15 |
2 | TRANSCRIPTION FACTOR COMPLEX | 18 | 298 | 1.945e-16 | 5.679e-14 |
3 | TRANSFERASE COMPLEX | 23 | 703 | 4.752e-15 | 6.937e-13 |
4 | CYCLIN DEPENDENT PROTEIN KINASE HOLOENZYME COMPLEX | 9 | 31 | 3.902e-15 | 6.937e-13 |
5 | CHROMATIN | 18 | 441 | 1.723e-13 | 2.013e-11 |
6 | NUCLEAR CHROMOSOME | 19 | 523 | 2.651e-13 | 2.58e-11 |
7 | CHROMOSOMAL REGION | 16 | 330 | 3.277e-13 | 2.734e-11 |
8 | CATALYTIC COMPLEX | 24 | 1038 | 2.041e-12 | 1.49e-10 |
9 | PROTEIN KINASE COMPLEX | 10 | 90 | 3.343e-12 | 2.169e-10 |
10 | ANAPHASE PROMOTING COMPLEX | 6 | 22 | 2.792e-10 | 1.63e-08 |
11 | NUCLEAR UBIQUITIN LIGASE COMPLEX | 7 | 42 | 3.603e-10 | 1.913e-08 |
12 | CULLIN RING UBIQUITIN LIGASE COMPLEX | 10 | 150 | 5.611e-10 | 2.731e-08 |
13 | MICROTUBULE CYTOSKELETON | 20 | 1068 | 7.834e-09 | 3.519e-07 |
14 | SPINDLE | 11 | 289 | 2.675e-08 | 1.116e-06 |
15 | CHROMOSOME CENTROMERIC REGION | 9 | 174 | 3.944e-08 | 1.536e-06 |
16 | TRANSFERASE COMPLEX TRANSFERRING PHOSPHORUS CONTAINING GROUPS | 10 | 237 | 4.58e-08 | 1.672e-06 |
17 | UBIQUITIN LIGASE COMPLEX | 10 | 262 | 1.171e-07 | 4.024e-06 |
18 | CENTROSOME | 12 | 487 | 6.704e-07 | 2.175e-05 |
19 | CONDENSED NUCLEAR CHROMOSOME | 6 | 85 | 1.333e-06 | 3.973e-05 |
20 | CONDENSED CHROMOSOME | 8 | 195 | 1.361e-06 | 3.973e-05 |
21 | RNA POLYMERASE II TRANSCRIPTION FACTOR COMPLEX | 6 | 101 | 3.666e-06 | 0.0001019 |
22 | CONDENSED CHROMOSOME CENTROMERIC REGION | 6 | 102 | 3.882e-06 | 0.0001031 |
23 | CHROMOSOME TELOMERIC REGION | 7 | 162 | 4.588e-06 | 0.0001165 |
24 | NUCLEOLUS | 14 | 848 | 8.192e-06 | 0.0001984 |
25 | MICROTUBULE ORGANIZING CENTER | 12 | 623 | 8.494e-06 | 0.0001984 |
26 | CYTOSKELETON | 22 | 1967 | 9.294e-06 | 0.0002088 |
27 | KINETOCHORE | 6 | 120 | 9.932e-06 | 0.0002148 |
28 | SPINDLE POLE | 6 | 126 | 1.313e-05 | 0.0002739 |
29 | NUCLEAR TRANSCRIPTION FACTOR COMPLEX | 6 | 127 | 1.374e-05 | 0.0002767 |
30 | CONDENSED CHROMOSOME OUTER KINETOCHORE | 3 | 12 | 1.423e-05 | 0.000277 |
31 | NUCLEAR CHROMOSOME TELOMERIC REGION | 6 | 132 | 1.712e-05 | 0.0003225 |
32 | CONDENSED NUCLEAR CHROMOSOME CENTROMERIC REGION | 3 | 18 | 5.185e-05 | 0.0009463 |
33 | CYTOSKELETAL PART | 17 | 1436 | 6.02e-05 | 0.001065 |
34 | CARBOXY TERMINAL DOMAIN PROTEIN KINASE COMPLEX | 3 | 22 | 9.67e-05 | 0.001661 |
35 | NUCLEAR CHROMATIN | 7 | 291 | 0.0001923 | 0.003209 |
36 | TRANSCRIPTIONAL REPRESSOR COMPLEX | 4 | 74 | 0.0002428 | 0.003939 |
37 | SCF UBIQUITIN LIGASE COMPLEX | 3 | 34 | 0.0003627 | 0.005724 |
38 | NUCLEOPLASM PART | 10 | 708 | 0.0006228 | 0.009572 |
Num | Pathway | Pathview | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|---|
1 | hsa04110_Cell_cycle | 82 | 128 | 1.711e-195 | 3.08e-193 | |
2 | hsa04114_Oocyte_meiosis | 20 | 114 | 1.058e-27 | 9.523e-26 | |
3 | hsa04115_p53_signaling_pathway | 17 | 69 | 2.25e-26 | 1.35e-24 | |
4 | hsa04350_TGF.beta_signaling_pathway | 16 | 85 | 8.506e-23 | 3.828e-21 | |
5 | hsa04390_Hippo_signaling_pathway | 16 | 154 | 1.86e-18 | 6.697e-17 | |
6 | hsa04914_Progesterone.mediated_oocyte_maturation | 13 | 87 | 2.746e-17 | 8.238e-16 | |
7 | hsa04151_PI3K_AKT_signaling_pathway | 18 | 351 | 3.41e-15 | 8.768e-14 | |
8 | hsa04310_Wnt_signaling_pathway | 12 | 151 | 1.16e-12 | 2.61e-11 | |
9 | hsa04120_Ubiquitin_mediated_proteolysis | 10 | 139 | 2.65e-10 | 5.3e-09 | |
10 | hsa04722_Neurotrophin_signaling_pathway | 7 | 127 | 9.027e-07 | 1.625e-05 | |
11 | hsa04520_Adherens_junction | 5 | 73 | 1.236e-05 | 0.0002023 | |
12 | hsa04010_MAPK_signaling_pathway | 8 | 268 | 1.417e-05 | 0.0002126 | |
13 | hsa04012_ErbB_signaling_pathway | 5 | 87 | 2.908e-05 | 0.0004026 | |
14 | hsa03420_Nucleotide_excision_repair | 4 | 45 | 3.441e-05 | 0.0004424 | |
15 | hsa04330_Notch_signaling_pathway | 4 | 47 | 4.093e-05 | 0.0004767 | |
16 | hsa04630_Jak.STAT_signaling_pathway | 6 | 155 | 4.238e-05 | 0.0004767 | |
17 | hsa04144_Endocytosis | 6 | 203 | 0.0001873 | 0.001983 | |
18 | hsa03030_DNA_replication | 3 | 36 | 0.0004302 | 0.004302 | |
19 | hsa04710_Circadian_rhythm_._mammal | 2 | 23 | 0.003973 | 0.03764 | |
20 | hsa04916_Melanogenesis | 3 | 101 | 0.008296 | 0.07467 | |
21 | hsa04510_Focal_adhesion | 4 | 200 | 0.009253 | 0.07931 | |
22 | hsa04720_Long.term_potentiation | 2 | 70 | 0.03351 | 0.2741 | |
23 | hsa04660_T_cell_receptor_signaling_pathway | 2 | 108 | 0.07262 | 0.5447 | |
24 | hsa04380_Osteoclast_differentiation | 2 | 128 | 0.09703 | 0.6639 | |
25 | hsa04360_Axon_guidance | 2 | 130 | 0.09959 | 0.6639 | |
26 | hsa04141_Protein_processing_in_endoplasmic_reticulum | 2 | 168 | 0.1512 | 0.9387 |
Num | lncRNA | miRNAs | miRNAs count | Gene | Sponge regulatory network | lncRNA log2FC | lncRNA pvalue | Gene log2FC | Gene pvalue | lncRNA-gene Pearson correlation |
---|---|---|---|---|---|---|---|---|---|---|
1 | PCA3 | hsa-let-7a-3p;hsa-let-7b-3p;hsa-miR-106b-5p;hsa-miR-130b-5p;hsa-miR-141-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-181a-2-3p;hsa-miR-182-5p;hsa-miR-183-5p;hsa-miR-19b-3p;hsa-miR-224-3p;hsa-miR-301a-3p;hsa-miR-3065-3p;hsa-miR-424-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-93-5p;hsa-miR-96-5p | 20 | CCND2 | Sponge network | -2.778 | 8.0E-5 | -0.496 | 0.3 | 0.318 |