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-106b-5p | BMP2 | 0.5 | 1.0E-5 | 0.81 | 0.0004 | miRNATAP | -0.34 | 7.0E-5 | NA | |
2 | hsa-miR-335-3p | BMP2 | 0.34 | 0.05424 | 0.81 | 0.0004 | mirMAP | -0.31 | 0 | NA | |
3 | hsa-miR-335-5p | BMP2 | -1.17 | 0 | 0.81 | 0.0004 | miRNAWalker2 validate | -0.36 | 0 | NA | |
4 | hsa-miR-374b-5p | BMP2 | -0.29 | 0.00415 | 0.81 | 0.0004 | miRNATAP | -0.42 | 3.0E-5 | NA | |
5 | hsa-miR-378c | BMP2 | -1.83 | 0 | 0.81 | 0.0004 | miRNATAP | -0.21 | 2.0E-5 | NA | |
6 | hsa-miR-429 | BMP2 | 0.56 | 0.00564 | 0.81 | 0.0004 | miRNATAP | -0.29 | 0 | NA | |
7 | hsa-miR-125a-3p | BMP7 | 0.12 | 0.44483 | -0.21 | 0.49209 | miRanda | -0.41 | 0 | NA | |
8 | hsa-miR-338-3p | BMP7 | -0.95 | 0 | -0.21 | 0.49209 | miRanda | -0.21 | 0.00394 | NA | |
9 | hsa-miR-455-5p | BMP7 | 1.41 | 0 | -0.21 | 0.49209 | miRanda | -0.34 | 9.0E-5 | NA | |
10 | hsa-miR-495-3p | BMP7 | -1.48 | 0 | -0.21 | 0.49209 | MirTarget | -0.17 | 0.0081 | NA | |
11 | hsa-miR-542-3p | BMP7 | 0.64 | 0 | -0.21 | 0.49209 | miRanda; miRNATAP | -0.31 | 0.00166 | NA | |
12 | hsa-let-7a-3p | CTNNB1 | 0.1 | 0.42376 | -0.3 | 0.00164 | MirTarget; miRNATAP | -0.13 | 0.00011 | NA | |
13 | hsa-miR-320a | CTNNB1 | 0.8 | 0 | -0.3 | 0.00164 | PITA; miRanda; miRNATAP | -0.13 | 2.0E-5 | NA | |
14 | hsa-miR-532-3p | CTNNB1 | 0.8 | 0 | -0.3 | 0.00164 | miRNAWalker2 validate | -0.14 | 0 | NA | |
15 | hsa-miR-7-1-3p | CTNNB1 | 1.14 | 0 | -0.3 | 0.00164 | mirMAP | -0.13 | 0 | NA | |
16 | hsa-miR-15a-5p | EPB41L5 | 0.78 | 0 | -0.49 | 9.0E-5 | MirTarget | -0.26 | 0 | NA | |
17 | hsa-miR-15b-5p | EPB41L5 | 0.85 | 0 | -0.49 | 9.0E-5 | MirTarget | -0.13 | 0.00377 | NA | |
18 | hsa-miR-16-1-3p | EPB41L5 | 0.96 | 0 | -0.49 | 9.0E-5 | mirMAP | -0.1 | 0.00499 | NA | |
19 | hsa-miR-16-2-3p | EPB41L5 | 1.16 | 0 | -0.49 | 9.0E-5 | mirMAP | -0.11 | 0.00161 | NA | |
20 | hsa-miR-17-5p | EPB41L5 | 1.42 | 0 | -0.49 | 9.0E-5 | miRNAWalker2 validate | -0.11 | 0.00058 | NA | |
21 | hsa-miR-181a-2-3p | EPB41L5 | 0.56 | 5.0E-5 | -0.49 | 9.0E-5 | MirTarget | -0.14 | 0.00037 | NA | |
22 | hsa-miR-186-5p | EPB41L5 | 0.35 | 0.00015 | -0.49 | 9.0E-5 | mirMAP | -0.21 | 0.00046 | NA | |
23 | hsa-miR-19a-3p | EPB41L5 | 1.36 | 0 | -0.49 | 9.0E-5 | MirTarget; mirMAP | -0.1 | 0.00017 | NA | |
24 | hsa-miR-19b-3p | EPB41L5 | 0.54 | 0.00062 | -0.49 | 9.0E-5 | MirTarget; mirMAP | -0.13 | 0.00019 | NA | |
25 | hsa-miR-26b-5p | EPB41L5 | -0.25 | 0.02852 | -0.49 | 9.0E-5 | mirMAP | -0.14 | 0.00319 | NA | |
26 | hsa-miR-424-5p | EPB41L5 | 1.48 | 0 | -0.49 | 9.0E-5 | MirTarget | -0.11 | 0.00078 | NA | |
27 | hsa-miR-505-5p | EPB41L5 | 1.26 | 0 | -0.49 | 9.0E-5 | MirTarget | -0.12 | 4.0E-5 | NA | |
28 | hsa-miR-576-5p | EPB41L5 | 0.94 | 0 | -0.49 | 9.0E-5 | MirTarget; PITA | -0.13 | 0.00059 | NA | |
29 | hsa-let-7a-3p | FGFR2 | 0.1 | 0.42376 | -0.69 | 0.00028 | miRNATAP | -0.19 | 0.0051 | NA | |
30 | hsa-miR-146b-5p | FGFR2 | 0.92 | 0 | -0.69 | 0.00028 | miRanda | -0.32 | 0 | NA | |
31 | hsa-miR-186-5p | FGFR2 | 0.35 | 0.00015 | -0.69 | 0.00028 | miRNAWalker2 validate | -0.39 | 1.0E-5 | NA | |
32 | hsa-miR-193a-3p | FGFR2 | 0.22 | 0.11183 | -0.69 | 0.00028 | miRanda | -0.36 | 0 | NA | |
33 | hsa-miR-330-5p | FGFR2 | 0.94 | 0 | -0.69 | 0.00028 | miRanda | -0.21 | 0.00057 | NA | |
34 | hsa-miR-338-3p | FGFR2 | -0.95 | 0 | -0.69 | 0.00028 | miRanda; miRNATAP | -0.18 | 0.00015 | NA | |
35 | hsa-miR-542-3p | FGFR2 | 0.64 | 0 | -0.69 | 0.00028 | miRanda | -0.36 | 0 | NA | |
36 | hsa-miR-200b-3p | FOXF2 | 0.07 | 0.68286 | 1.77 | 0 | TargetScan | -0.28 | 0 | 25798833 | The miR 200 family and the miR 183~96~182 cluster target Foxf2 to inhibit invasion and metastasis in lung cancers; We therefore identified a novel mechanism whereby the miR-200 family and the miR-183~96~182 cluster inhibit lung cancer invasion and metastasis by targeting Foxf2 |
37 | hsa-miR-26b-5p | FOXF2 | -0.25 | 0.02852 | 1.77 | 0 | miRNAWalker2 validate | -0.32 | 3.0E-5 | NA | |
38 | hsa-miR-429 | FOXF2 | 0.56 | 0.00564 | 1.77 | 0 | PITA; miRanda; miRNATAP | -0.16 | 0.00032 | NA | |
39 | hsa-miR-146b-5p | GSK3B | 0.92 | 0 | 0.34 | 0.00016 | miRanda | -0.13 | 0 | NA | |
40 | hsa-miR-155-5p | GSK3B | 0.53 | 0.00249 | 0.34 | 0.00016 | miRNAWalker2 validate; miRNATAP | -0.13 | 0 | NA | |
41 | hsa-miR-181a-5p | GSK3B | 0.82 | 0 | 0.34 | 0.00016 | mirMAP | -0.13 | 0.00022 | NA | |
42 | hsa-miR-181c-5p | GSK3B | -0.17 | 0.19695 | 0.34 | 0.00016 | mirMAP | -0.1 | 0.00092 | NA | |
43 | hsa-miR-19b-3p | GSK3B | 0.54 | 0.00062 | 0.34 | 0.00016 | mirMAP | -0.15 | 0 | NA | |
44 | hsa-miR-26b-5p | GSK3B | -0.25 | 0.02852 | 0.34 | 0.00016 | miRNATAP | -0.18 | 0 | NA | |
45 | hsa-miR-29b-3p | GSK3B | -0.11 | 0.51126 | 0.34 | 0.00016 | miRTarBase; miRNATAP | -0.16 | 0 | NA | |
46 | hsa-miR-30d-3p | GSK3B | -0.58 | 0 | 0.34 | 0.00016 | miRNATAP | -0.13 | 5.0E-5 | NA | |
47 | hsa-miR-320a | GSK3B | 0.8 | 0 | 0.34 | 0.00016 | miRanda; mirMAP | -0.12 | 3.0E-5 | NA | |
48 | hsa-miR-342-3p | GSK3B | 1 | 0 | 0.34 | 0.00016 | miRanda | -0.15 | 0 | NA | |
49 | hsa-miR-362-5p | GSK3B | 0.41 | 0.04043 | 0.34 | 0.00016 | miRNATAP | -0.13 | 0 | NA | |
50 | hsa-miR-374a-5p | GSK3B | -0.62 | 0 | 0.34 | 0.00016 | mirMAP | -0.15 | 0.00067 | NA | |
51 | hsa-miR-374b-5p | GSK3B | -0.29 | 0.00415 | 0.34 | 0.00016 | mirMAP | -0.23 | 0 | NA | |
52 | hsa-miR-664a-3p | GSK3B | -0.26 | 0.05132 | 0.34 | 0.00016 | mirMAP | -0.16 | 0 | NA | |
53 | hsa-let-7a-3p | HGF | 0.1 | 0.42376 | -0.63 | 0.02489 | mirMAP | -0.68 | 0 | NA | |
54 | hsa-miR-141-3p | HGF | 0.73 | 0.00012 | -0.63 | 0.02489 | MirTarget; TargetScan | -0.56 | 0 | NA | |
55 | hsa-miR-200a-3p | HGF | 0.61 | 0.0029 | -0.63 | 0.02489 | MirTarget | -0.46 | 0 | NA | |
56 | hsa-miR-203a-3p | HGF | 0.04 | 0.88046 | -0.63 | 0.02489 | MirTarget | -0.32 | 0 | NA | |
57 | hsa-miR-224-3p | HGF | 0.5 | 0.00811 | -0.63 | 0.02489 | mirMAP | -0.38 | 0 | NA | |
58 | hsa-miR-26b-5p | HGF | -0.25 | 0.02852 | -0.63 | 0.02489 | MirTarget; miRNATAP | -0.29 | 0.00556 | NA | |
59 | hsa-miR-29a-5p | HGF | 0.32 | 0.03704 | -0.63 | 0.02489 | mirMAP | -0.34 | 2.0E-5 | NA | |
60 | hsa-miR-30b-5p | HGF | -0.4 | 0.00347 | -0.63 | 0.02489 | mirMAP | -0.34 | 0.00014 | NA | |
61 | hsa-miR-30c-5p | HGF | 0.02 | 0.88637 | -0.63 | 0.02489 | mirMAP | -0.36 | 1.0E-5 | NA | |
62 | hsa-miR-33a-3p | HGF | 0.2 | 0.21234 | -0.63 | 0.02489 | mirMAP | -0.25 | 0.00127 | NA | |
63 | hsa-miR-429 | HGF | 0.56 | 0.00564 | -0.63 | 0.02489 | miRanda | -0.41 | 0 | NA | |
64 | hsa-miR-590-5p | HGF | 0.76 | 0 | -0.63 | 0.02489 | miRanda | -0.58 | 0 | NA | |
65 | hsa-miR-651-5p | HGF | 0.5 | 0.00156 | -0.63 | 0.02489 | MirTarget | -0.32 | 2.0E-5 | NA | |
66 | hsa-miR-7-1-3p | HGF | 1.14 | 0 | -0.63 | 0.02489 | mirMAP | -0.28 | 0.00052 | NA | |
67 | hsa-miR-944 | HGF | 1.47 | 0 | -0.63 | 0.02489 | mirMAP | -0.33 | 0 | NA | |
68 | hsa-miR-106a-5p | HIF1A | 0.68 | 0.00222 | 0.67 | 0 | MirTarget | -0.14 | 0 | NA | |
69 | hsa-miR-106b-5p | HIF1A | 0.5 | 1.0E-5 | 0.67 | 0 | MirTarget | -0.22 | 4.0E-5 | NA | |
70 | hsa-miR-139-5p | HIF1A | -1.46 | 0 | 0.67 | 0 | miRanda | -0.15 | 0.00022 | NA | |
71 | hsa-miR-155-5p | HIF1A | 0.53 | 0.00249 | 0.67 | 0 | MirTarget | -0.17 | 0 | NA | |
72 | hsa-miR-16-2-3p | HIF1A | 1.16 | 0 | 0.67 | 0 | MirTarget; mirMAP | -0.16 | 0.00019 | NA | |
73 | hsa-miR-195-3p | HIF1A | -0.62 | 0.00016 | 0.67 | 0 | MirTarget | -0.18 | 0 | NA | |
74 | hsa-miR-199b-5p | HIF1A | -1.08 | 0 | 0.67 | 0 | miRNAWalker2 validate; miRTarBase; MirTarget; PITA; miRanda | -0.11 | 0.00129 | NA | |
75 | hsa-miR-20a-5p | HIF1A | 1.15 | 0 | 0.67 | 0 | miRNAWalker2 validate; miRTarBase; MirTarget | -0.12 | 0.00162 | 22901144 | Correlation analysis showed that the key miRNAs miR-20a and miR-20b negatively correlated with the target proteins VEGF-A and HIF-1alpha |
76 | hsa-miR-20b-5p | HIF1A | 0.35 | 0.23201 | 0.67 | 0 | miRNAWalker2 validate; miRTarBase; MirTarget | -0.15 | 0 | 22901144 | Correlation analysis showed that the key miRNAs miR-20a and miR-20b negatively correlated with the target proteins VEGF-A and HIF-1alpha |
77 | hsa-miR-217 | HIF1A | -1.35 | 0 | 0.67 | 0 | miRanda | -0.18 | 0 | NA | |
78 | hsa-miR-320a | HIF1A | 0.8 | 0 | 0.67 | 0 | miRanda | -0.23 | 0 | NA | |
79 | hsa-miR-338-3p | HIF1A | -0.95 | 0 | 0.67 | 0 | MirTarget; PITA; miRanda | -0.19 | 0 | NA | |
80 | hsa-miR-582-3p | HIF1A | -0.25 | 0.1438 | 0.67 | 0 | PITA | -0.23 | 0 | NA | |
81 | hsa-miR-582-5p | HIF1A | -0.04 | 0.82183 | 0.67 | 0 | MirTarget; PITA; miRNATAP | -0.22 | 0 | NA | |
82 | hsa-miR-660-5p | HIF1A | -0.2 | 0.10109 | 0.67 | 0 | MirTarget | -0.3 | 0 | NA | |
83 | hsa-miR-93-5p | HIF1A | 1.61 | 0 | 0.67 | 0 | MirTarget | -0.14 | 0.00035 | NA | |
84 | hsa-let-7a-5p | HMGA2 | -0.44 | 3.0E-5 | 4.46 | 0 | miRNAWalker2 validate; miRTarBase; MirTarget; TargetScan | -0.77 | 1.0E-5 | 20949044; 18413822; 23073586; 21598109; 24612219; 23134218; 23700794; 21412931 | Since let-7 miRNAs generally play a tumor-suppressive role as targeting oncogenes such as RAS and HMGA2 our results suggest that AZ-P7a cells release let-7 miRNAs via exosomes into the extracellular environment to maintain their oncogenesis;Recent studies report that HMGA2 is negatively regulated by the let-7 microRNA miRNA family; However no studies have examined the clinical significance of HMGA2 and its relationship to the let-7 miRNA family in gastric cancer; We also did an association study comparing HMGA2 expression and let-7 miRNA family expression in gastric cancer; An inverse correlation between HMGA2 and let-7a was found in gastric cancer cell lines P = 0.08; Furthermore our findings suggest that HMGA2 is negatively regulated by the let-7 miRNA family in human gastric cancer;HMGA2 mRNA and let-7 family microRNA were detected by real time fluorescent quantitative reverse transcription polymerase chain reaction in the corresponding frozen tissues; All let-7 family members were detectable in all ovarian cancer samples and their expression were inversely correlated with HMGA2 mRNA expression r=-0.305P<0.05; The downregulation of let-7 is but not the only mechanism of HMGA2 overexpression in serous ovarian cancer;Role of microRNA let 7 and effect to HMGA2 in esophageal squamous cell carcinoma; To investigated the role of microRNA miRNA let-7 and its regulation on high mobility group A2 HMGA2 protein expression in esophageal squamous cell carcinoma ESCC; To evaluate the role of let-7 and HMGA2 cell proliferations were analyzed with synthetic let-7 mimics- or its inhibitor-transfected cells; The transcription of let-7 inversely correlated with HMGA2 protein; The present results demonstrated that let-7 and HMGA2 involved in ESCC carcinogenesis;HMGA2 is down regulated by microRNA let 7 and associated with epithelial mesenchymal transition in oesophageal squamous cell carcinomas of Kazakhs; To investigate the expression of let-7 and its regulation of high-mobility group A2 protein HMGA2 and to verify the relationship between let-7 HMGA2 and the process of epithelial-mesenchymal transition EMT in oesophageal squamous cell carcinomas OSCC of Kazakh patients; Let-7 could repress expression of HMGA2 after co-transfection with let-7 and HMGA2 P = 0.002; Moreover let-7 expression was observed less frequently P = 2.0 × 10-8 and HMGA2 expression more frequently P = 1.0 × 10-10 in OSCC than in normal adjacent tissues; and let-7 expression was observed less frequently in OSCC from Kazakh patients than in those from Han and Uygur patients P = 0.041; There was a reverse correlation between expression of let-7 and HMGA2 P = 0.018; Expression of let-7 can suppress cell proliferation by acting directly on regulation of HMGA2 in OSCC;MicroRNA let 7a inhibits the proliferation and invasion of nonsmall cell lung cancer cell line 95D by regulating K Ras and HMGA2 gene expression; K-RAS and HMGA2 mRNA levels were significantly higher in the let-7a overexpressed group than those in the let-7a inhibited group p < 0.05; However the protein levels of K-RAS and HMGA2 were significantly lower in the let-7a overexpressed group than those in the let-7a inhibited group p < 0.05; We suppose that let-7a inhibits the proliferation and invasion of the cell line 95D by regulating the translation of K-RAS and HMGA2 mRNA not the transcription of the mRNA itself;MiR-98 a member in the let-7 family acts as a negative regulator in the expression of HMGA2 high mobility group A2 oncogene and it has been shown to have a nearly 3-fold decrease in A549/DDP cells;Let 7 microRNA and HMGA2 levels of expression are not inversely linked in adipocytic tumors: analysis of 56 lipomas and liposarcomas with molecular cytogenetic data; The aim of our study was first to assess the role of HMGA2 expression in the pathogenesis of adipocytic tumors AT and second to seek a potential correlation between overexpression of HMGA2 and let-7 expression inhibition by analyzing a series of 56 benign and malignant AT with molecular cytogenetic data; We measured the levels of expression of HMGA2 mRNA and of eight members of the let-7 microRNA family using quantitative RT-PCR and expression of HMGA2 protein using immunohistochemistry; Although overexpression of both HMGA2 mRNA and protein in a majority of ordinary lipomas without HMGA2 structural rearrangement may have suggested a potential role for let-7 microRNAs we did not observe a significant link with let-7 inhibition in such cases |
85 | hsa-let-7b-5p | HMGA2 | -0.25 | 0.02114 | 4.46 | 0 | miRNAWalker2 validate; miRTarBase; MirTarget | -0.69 | 4.0E-5 | 20949044; 18413822; 23073586; 21598109; 24612219; 23700794; 21412931 | Since let-7 miRNAs generally play a tumor-suppressive role as targeting oncogenes such as RAS and HMGA2 our results suggest that AZ-P7a cells release let-7 miRNAs via exosomes into the extracellular environment to maintain their oncogenesis;Recent studies report that HMGA2 is negatively regulated by the let-7 microRNA miRNA family; However no studies have examined the clinical significance of HMGA2 and its relationship to the let-7 miRNA family in gastric cancer; We also did an association study comparing HMGA2 expression and let-7 miRNA family expression in gastric cancer; Furthermore our findings suggest that HMGA2 is negatively regulated by the let-7 miRNA family in human gastric cancer;HMGA2 mRNA and let-7 family microRNA were detected by real time fluorescent quantitative reverse transcription polymerase chain reaction in the corresponding frozen tissues; All let-7 family members were detectable in all ovarian cancer samples and their expression were inversely correlated with HMGA2 mRNA expression r=-0.305P<0.05; The downregulation of let-7 is but not the only mechanism of HMGA2 overexpression in serous ovarian cancer;Role of microRNA let 7 and effect to HMGA2 in esophageal squamous cell carcinoma; To investigated the role of microRNA miRNA let-7 and its regulation on high mobility group A2 HMGA2 protein expression in esophageal squamous cell carcinoma ESCC; To evaluate the role of let-7 and HMGA2 cell proliferations were analyzed with synthetic let-7 mimics- or its inhibitor-transfected cells; The transcription of let-7 inversely correlated with HMGA2 protein; The present results demonstrated that let-7 and HMGA2 involved in ESCC carcinogenesis;HMGA2 is down regulated by microRNA let 7 and associated with epithelial mesenchymal transition in oesophageal squamous cell carcinomas of Kazakhs; To investigate the expression of let-7 and its regulation of high-mobility group A2 protein HMGA2 and to verify the relationship between let-7 HMGA2 and the process of epithelial-mesenchymal transition EMT in oesophageal squamous cell carcinomas OSCC of Kazakh patients; Let-7 could repress expression of HMGA2 after co-transfection with let-7 and HMGA2 P = 0.002; Moreover let-7 expression was observed less frequently P = 2.0 × 10-8 and HMGA2 expression more frequently P = 1.0 × 10-10 in OSCC than in normal adjacent tissues; and let-7 expression was observed less frequently in OSCC from Kazakh patients than in those from Han and Uygur patients P = 0.041; There was a reverse correlation between expression of let-7 and HMGA2 P = 0.018; Expression of let-7 can suppress cell proliferation by acting directly on regulation of HMGA2 in OSCC;MiR-98 a member in the let-7 family acts as a negative regulator in the expression of HMGA2 high mobility group A2 oncogene and it has been shown to have a nearly 3-fold decrease in A549/DDP cells;Let 7 microRNA and HMGA2 levels of expression are not inversely linked in adipocytic tumors: analysis of 56 lipomas and liposarcomas with molecular cytogenetic data; The aim of our study was first to assess the role of HMGA2 expression in the pathogenesis of adipocytic tumors AT and second to seek a potential correlation between overexpression of HMGA2 and let-7 expression inhibition by analyzing a series of 56 benign and malignant AT with molecular cytogenetic data; We measured the levels of expression of HMGA2 mRNA and of eight members of the let-7 microRNA family using quantitative RT-PCR and expression of HMGA2 protein using immunohistochemistry; Although overexpression of both HMGA2 mRNA and protein in a majority of ordinary lipomas without HMGA2 structural rearrangement may have suggested a potential role for let-7 microRNAs we did not observe a significant link with let-7 inhibition in such cases |
86 | hsa-let-7c-5p | HMGA2 | -2.08 | 0 | 4.46 | 0 | miRNAWalker2 validate; miRTarBase; MirTarget | -0.81 | 0 | NA | |
87 | hsa-let-7f-5p | HMGA2 | -0.44 | 0.00243 | 4.46 | 0 | miRNAWalker2 validate; MirTarget | -0.35 | 0.00531 | NA | |
88 | hsa-let-7g-5p | HMGA2 | -0.25 | 0.0094 | 4.46 | 0 | miRNAWalker2 validate; miRTarBase; MirTarget | -0.75 | 8.0E-5 | 21472347; 18308936 | Furthermore K-Ras and HMGA2 are well known as targets of let-7g; In this study we evaluated the potential role of precursor pre-let-7g in lung cancer cell metastasis focusing on the two targets of let-7g HMGA2 and K-Ras;In let-7g expressing tumors reductions in Ras family and HMGA2 protein levels were detected; Ectopic expression of K-RasG12D largely rescued let-7g mediated tumor suppression whereas ectopic expression of HMGA2 was less effective |
89 | hsa-miR-125b-2-3p | HMGA2 | -1.88 | 0 | 4.46 | 0 | mirMAP | -0.6 | 0 | NA | |
90 | hsa-miR-125b-5p | HMGA2 | -0.99 | 0 | 4.46 | 0 | miRNAWalker2 validate; miRTarBase | -0.87 | 0 | NA | |
91 | hsa-miR-148a-5p | HMGA2 | -1 | 0 | 4.46 | 0 | mirMAP | -0.52 | 0 | NA | |
92 | hsa-miR-195-3p | HMGA2 | -0.62 | 0.00016 | 4.46 | 0 | mirMAP | -0.73 | 0 | NA | |
93 | hsa-miR-195-5p | HMGA2 | -1.84 | 0 | 4.46 | 0 | MirTarget | -0.82 | 0 | NA | |
94 | hsa-miR-199a-5p | HMGA2 | -0.36 | 0.04351 | 4.46 | 0 | miRanda | -0.28 | 0.00611 | NA | |
95 | hsa-miR-199b-5p | HMGA2 | -1.08 | 0 | 4.46 | 0 | miRanda | -0.41 | 6.0E-5 | NA | |
96 | hsa-miR-20b-5p | HMGA2 | 0.35 | 0.23201 | 4.46 | 0 | miRNATAP | -0.31 | 0 | NA | |
97 | hsa-miR-23b-3p | HMGA2 | -0.5 | 3.0E-5 | 4.46 | 0 | mirMAP | -1.07 | 0 | NA | |
98 | hsa-miR-26a-5p | HMGA2 | -1.09 | 0 | 4.46 | 0 | miRNAWalker2 validate; miRTarBase; miRNATAP | -1.05 | 0 | 24682444 | Furthermore we demonstrated that high mobility group AT-hook 2 HMGA2 was a direct target of miR-26a; The results showed that HMGA2 mRNA levels and miR-26a levels were negatively correlated; In addition we confirmed that reintroduction of HMGA2 antagonized the inhibition of miR-26a to GBC cell proliferation and all these effects were achieved through the cell cycle; Together all these results suggest that miR-26a expression contributes to GBC proliferation by targeting HMGA2 miR-26a shows promise as a prognosis factor and therapeutic target of GBC patients |
99 | hsa-miR-29b-2-5p | HMGA2 | -0.5 | 0.00073 | 4.46 | 0 | mirMAP | -0.58 | 0 | NA | |
100 | hsa-miR-30a-3p | HMGA2 | -2.26 | 0 | 4.46 | 0 | MirTarget | -0.51 | 0 | NA | |
101 | hsa-miR-30a-5p | HMGA2 | -1.8 | 0 | 4.46 | 0 | mirMAP | -0.62 | 0 | NA | |
102 | hsa-miR-30b-5p | HMGA2 | -0.4 | 0.00347 | 4.46 | 0 | mirMAP | -0.39 | 0.00312 | NA | |
103 | hsa-miR-30d-3p | HMGA2 | -0.58 | 0 | 4.46 | 0 | MirTarget | -0.58 | 0.0001 | NA | |
104 | hsa-miR-30d-5p | HMGA2 | -0.38 | 0.00017 | 4.46 | 0 | mirMAP | -0.92 | 0 | NA | |
105 | hsa-miR-30e-3p | HMGA2 | -0.89 | 0 | 4.46 | 0 | MirTarget | -1.38 | 0 | NA | |
106 | hsa-miR-30e-5p | HMGA2 | -1.02 | 0 | 4.46 | 0 | mirMAP | -1.28 | 0 | NA | |
107 | hsa-miR-337-3p | HMGA2 | -1.7 | 0 | 4.46 | 0 | MirTarget; PITA | -0.22 | 0.00394 | NA | |
108 | hsa-miR-340-5p | HMGA2 | -0.61 | 4.0E-5 | 4.46 | 0 | mirMAP | -0.34 | 0.00498 | NA | |
109 | hsa-miR-34a-5p | HMGA2 | -0.12 | 0.364 | 4.46 | 0 | miRNAWalker2 validate | -0.56 | 6.0E-5 | 18803879 | miR-34 targets Notch HMGA2 and Bcl-2 genes involved in the self-renewal and survival of cancer stem cells; Human gastric cancer Kato III cells with miR-34 restoration reduced the expression of target genes Bcl-2 Notch and HMGA2; The mechanism of miR-34-mediated suppression of self-renewal appears to be related to the direct modulation of downstream targets Bcl-2 Notch and HMGA2 indicating that miR-34 may be involved in gastric cancer stem cell self-renewal/differentiation decision-making |
110 | hsa-miR-381-3p | HMGA2 | -2.21 | 0 | 4.46 | 0 | mirMAP | -0.23 | 0.0037 | NA | |
111 | hsa-miR-491-5p | HMGA2 | -0.54 | 0.00136 | 4.46 | 0 | PITA; miRanda | -0.33 | 0.00326 | NA | |
112 | hsa-miR-497-5p | HMGA2 | -0.97 | 0 | 4.46 | 0 | MirTarget | -0.94 | 0 | NA | |
113 | hsa-miR-532-5p | HMGA2 | -0.02 | 0.83099 | 4.46 | 0 | mirMAP | -0.58 | 0.00111 | NA | |
114 | hsa-miR-664a-3p | HMGA2 | -0.26 | 0.05132 | 4.46 | 0 | mirMAP | -0.48 | 0.00049 | NA | |
115 | hsa-miR-664a-5p | HMGA2 | -0.87 | 0 | 4.46 | 0 | MirTarget | -0.56 | 0 | NA | |
116 | hsa-let-7a-3p | LEF1 | 0.1 | 0.42376 | 0.49 | 0.01109 | miRNATAP | -0.28 | 7.0E-5 | NA | |
117 | hsa-miR-193b-3p | LEF1 | 1.73 | 0 | 0.49 | 0.01109 | miRNAWalker2 validate | -0.31 | 0 | NA | |
118 | hsa-miR-455-5p | LEF1 | 1.41 | 0 | 0.49 | 0.01109 | miRanda | -0.21 | 0.00012 | NA | |
119 | hsa-let-7a-3p | LIMS1 | 0.1 | 0.42376 | 0.2 | 0.25634 | mirMAP | -0.33 | 0 | NA | |
120 | hsa-miR-140-5p | LIMS1 | -0.41 | 0.00014 | 0.2 | 0.25634 | miRanda | -0.2 | 0.00499 | NA | |
121 | hsa-miR-148b-5p | LIMS1 | 1.15 | 0 | 0.2 | 0.25634 | MirTarget | -0.31 | 0 | NA | |
122 | hsa-miR-182-5p | LIMS1 | 1.15 | 0 | 0.2 | 0.25634 | MirTarget; miRNATAP | -0.17 | 2.0E-5 | NA | |
123 | hsa-miR-186-5p | LIMS1 | 0.35 | 0.00015 | 0.2 | 0.25634 | mirMAP | -0.5 | 0 | NA | |
124 | hsa-miR-18a-3p | LIMS1 | 1.83 | 0 | 0.2 | 0.25634 | miRNAWalker2 validate | -0.15 | 3.0E-5 | NA | |
125 | hsa-miR-193a-3p | LIMS1 | 0.22 | 0.11183 | 0.2 | 0.25634 | MirTarget; miRanda | -0.16 | 0.00379 | NA | |
126 | hsa-miR-205-3p | LIMS1 | 1.3 | 0 | 0.2 | 0.25634 | MirTarget | -0.11 | 0.00249 | NA | |
127 | hsa-miR-222-3p | LIMS1 | 1.08 | 0 | 0.2 | 0.25634 | MirTarget | -0.21 | 7.0E-5 | NA | |
128 | hsa-miR-29b-3p | LIMS1 | -0.11 | 0.51126 | 0.2 | 0.25634 | MirTarget; miRNATAP | -0.44 | 0 | NA | |
129 | hsa-miR-30a-5p | LIMS1 | -1.8 | 0 | 0.2 | 0.25634 | MirTarget | -0.19 | 1.0E-5 | NA | |
130 | hsa-miR-30b-5p | LIMS1 | -0.4 | 0.00347 | 0.2 | 0.25634 | MirTarget | -0.52 | 0 | NA | |
131 | hsa-miR-30c-5p | LIMS1 | 0.02 | 0.88637 | 0.2 | 0.25634 | MirTarget | -0.53 | 0 | NA | |
132 | hsa-miR-30d-3p | LIMS1 | -0.58 | 0 | 0.2 | 0.25634 | mirMAP | -0.42 | 0 | NA | |
133 | hsa-miR-30e-5p | LIMS1 | -1.02 | 0 | 0.2 | 0.25634 | MirTarget | -0.26 | 1.0E-5 | NA | |
134 | hsa-miR-3607-3p | LIMS1 | 1.01 | 9.0E-5 | 0.2 | 0.25634 | mirMAP | -0.2 | 0 | NA | |
135 | hsa-miR-374a-3p | LIMS1 | -0.3 | 0.00683 | 0.2 | 0.25634 | mirMAP | -0.31 | 0 | NA | |
136 | hsa-miR-429 | LIMS1 | 0.56 | 0.00564 | 0.2 | 0.25634 | miRanda; miRNATAP | -0.25 | 0 | NA | |
137 | hsa-miR-505-3p | LIMS1 | 0.91 | 0 | 0.2 | 0.25634 | miRNAWalker2 validate; MirTarget | -0.29 | 0 | NA | |
138 | hsa-miR-576-5p | LIMS1 | 0.94 | 0 | 0.2 | 0.25634 | mirMAP | -0.41 | 0 | NA | |
139 | hsa-miR-590-3p | LIMS1 | 0.22 | 0.09659 | 0.2 | 0.25634 | miRNAWalker2 validate; miRanda | -0.2 | 0.00035 | NA | |
140 | hsa-miR-7-1-3p | LIMS1 | 1.14 | 0 | 0.2 | 0.25634 | mirMAP | -0.28 | 0 | NA | |
141 | hsa-miR-96-5p | LIMS1 | 1.42 | 0 | 0.2 | 0.25634 | TargetScan; miRNATAP | -0.19 | 0 | NA | |
142 | hsa-miR-338-3p | LOXL2 | -0.95 | 0 | 3.12 | 0 | miRanda | -0.33 | 0 | NA | |
143 | hsa-miR-362-5p | LOXL3 | 0.41 | 0.04043 | 1.33 | 0 | TargetScan | -0.12 | 0.00271 | NA | |
144 | hsa-miR-148a-3p | NOG | -0.43 | 0.00954 | -0.81 | 0.02813 | MirTarget; miRNATAP | -0.34 | 0.00046 | NA | |
145 | hsa-miR-148b-3p | NOG | 0.39 | 0 | -0.81 | 0.02813 | MirTarget | -0.76 | 8.0E-5 | NA | |
146 | hsa-miR-200b-3p | NOG | 0.07 | 0.68286 | -0.81 | 0.02813 | MirTarget; TargetScan | -0.8 | 0 | NA | |
147 | hsa-miR-200c-3p | NOG | 0.63 | 0.00013 | -0.81 | 0.02813 | MirTarget; miRNATAP | -0.7 | 0 | NA | |
148 | hsa-miR-429 | NOG | 0.56 | 0.00564 | -0.81 | 0.02813 | MirTarget; PITA; miRanda; miRNATAP | -0.54 | 0 | NA | |
149 | hsa-miR-18a-3p | NOTCH1 | 1.83 | 0 | -0.1 | 0.54477 | MirTarget | -0.11 | 0.00052 | NA | |
150 | hsa-miR-199b-5p | NOTCH1 | -1.08 | 0 | -0.1 | 0.54477 | miRanda | -0.11 | 0.00583 | 24659709 | Epigenetic silencing of microRNA 199b 5p is associated with acquired chemoresistance via activation of JAG1 Notch1 signaling in ovarian cancer; Here we report that the loss of miR-199b-5p due to progressive epigenetic silencing leads to the activation of the JAG1-mediated Notch1 signaling cascade thereby leading to the development of acquired chemoresistance in ovarian cancer |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | EPITHELIAL TO MESENCHYMAL TRANSITION | 27 | 56 | 6.097e-73 | 2.837e-69 |
2 | MESENCHYMAL CELL DIFFERENTIATION | 27 | 134 | 1.232e-60 | 2.866e-57 |
3 | MESENCHYME DEVELOPMENT | 27 | 190 | 3.662e-56 | 4.26e-53 |
4 | STEM CELL DIFFERENTIATION | 27 | 190 | 3.662e-56 | 4.26e-53 |
5 | CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 27 | 513 | 5.631e-44 | 5.24e-41 |
6 | CELLULAR COMPONENT MORPHOGENESIS | 27 | 900 | 2.974e-37 | 2.306e-34 |
7 | CELL DEVELOPMENT | 27 | 1426 | 8.58e-32 | 5.703e-29 |
8 | TISSUE DEVELOPMENT | 27 | 1518 | 4.711e-31 | 2.74e-28 |
9 | TISSUE MORPHOGENESIS | 21 | 533 | 1.505e-28 | 7.782e-26 |
10 | RESPONSE TO GROWTH FACTOR | 19 | 475 | 1.791e-25 | 8.334e-23 |
11 | MORPHOGENESIS OF AN EPITHELIUM | 18 | 400 | 7.124e-25 | 3.013e-22 |
12 | GLAND DEVELOPMENT | 17 | 395 | 5.294e-23 | 1.971e-20 |
13 | REGULATION OF STEM CELL DIFFERENTIATION | 13 | 113 | 5.506e-23 | 1.971e-20 |
14 | REGULATION OF ANATOMICAL STRUCTURE MORPHOGENESIS | 21 | 1021 | 1.338e-22 | 4.445e-20 |
15 | ORGAN MORPHOGENESIS | 20 | 841 | 1.613e-22 | 5.004e-20 |
16 | REGULATION OF OSSIFICATION | 14 | 178 | 2.111e-22 | 6.139e-20 |
17 | POSITIVE REGULATION OF DEVELOPMENTAL PROCESS | 21 | 1142 | 1.385e-21 | 3.583e-19 |
18 | MESENCHYME MORPHOGENESIS | 10 | 38 | 1.386e-21 | 3.583e-19 |
19 | REGULATION OF CARTILAGE DEVELOPMENT | 11 | 63 | 1.51e-21 | 3.699e-19 |
20 | ANATOMICAL STRUCTURE FORMATION INVOLVED IN MORPHOGENESIS | 20 | 957 | 2.111e-21 | 4.911e-19 |
21 | EMBRYONIC ORGAN DEVELOPMENT | 16 | 406 | 6.594e-21 | 1.461e-18 |
22 | NEGATIVE REGULATION OF GENE EXPRESSION | 22 | 1493 | 7.81e-21 | 1.58e-18 |
23 | REGULATION OF CELL DIFFERENTIATION | 22 | 1492 | 7.697e-21 | 1.58e-18 |
24 | EMBRYONIC MORPHOGENESIS | 17 | 539 | 1.07e-20 | 2.075e-18 |
25 | REGULATION OF ORGAN MORPHOGENESIS | 14 | 242 | 1.723e-20 | 3.208e-18 |
26 | EMBRYO DEVELOPMENT | 19 | 894 | 2.983e-20 | 5.143e-18 |
27 | POSITIVE REGULATION OF STEM CELL DIFFERENTIATION | 10 | 50 | 2.984e-20 | 5.143e-18 |
28 | EPITHELIUM DEVELOPMENT | 19 | 945 | 8.476e-20 | 1.36e-17 |
29 | POSITIVE REGULATION OF CELLULAR COMPONENT ORGANIZATION | 20 | 1152 | 8.325e-20 | 1.36e-17 |
30 | REGULATION OF CELLULAR COMPONENT MOVEMENT | 18 | 771 | 9.857e-20 | 1.529e-17 |
31 | REGULATION OF EPITHELIAL CELL PROLIFERATION | 14 | 285 | 1.757e-19 | 2.638e-17 |
32 | POSITIVE REGULATION OF GENE EXPRESSION | 22 | 1733 | 1.992e-19 | 2.896e-17 |
33 | CELLULAR RESPONSE TO ENDOGENOUS STIMULUS | 19 | 1008 | 2.85e-19 | 4.018e-17 |
34 | POSITIVE REGULATION OF CELL DIFFERENTIATION | 18 | 823 | 3.159e-19 | 4.323e-17 |
35 | REGULATION OF CELL DEVELOPMENT | 18 | 836 | 4.176e-19 | 5.552e-17 |
36 | NEGATIVE REGULATION OF NITROGEN COMPOUND METABOLIC PROCESS | 21 | 1517 | 5.028e-19 | 6.498e-17 |
37 | TUBE DEVELOPMENT | 16 | 552 | 9.014e-19 | 1.134e-16 |
38 | TUBE MORPHOGENESIS | 14 | 323 | 1.029e-18 | 1.26e-16 |
39 | NEGATIVE REGULATION OF RESPONSE TO STIMULUS | 20 | 1360 | 2.194e-18 | 2.617e-16 |
40 | SKELETAL SYSTEM DEVELOPMENT | 15 | 455 | 2.439e-18 | 2.837e-16 |
41 | REGULATION OF MULTICELLULAR ORGANISMAL DEVELOPMENT | 21 | 1672 | 3.745e-18 | 4.25e-16 |
42 | NEGATIVE REGULATION OF CELL COMMUNICATION | 19 | 1192 | 6.574e-18 | 7.283e-16 |
43 | CONNECTIVE TISSUE DEVELOPMENT | 12 | 194 | 7.535e-18 | 7.969e-16 |
44 | NEGATIVE REGULATION OF MULTICELLULAR ORGANISMAL PROCESS | 18 | 983 | 7.424e-18 | 7.969e-16 |
45 | NEGATIVE REGULATION OF DEVELOPMENTAL PROCESS | 17 | 801 | 8.613e-18 | 8.906e-16 |
46 | REGULATION OF CELL DEATH | 20 | 1472 | 1.037e-17 | 1.049e-15 |
47 | REGULATION OF STEM CELL PROLIFERATION | 10 | 88 | 1.273e-17 | 1.26e-15 |
48 | REGULATION OF MORPHOGENESIS OF A BRANCHING STRUCTURE | 9 | 53 | 1.423e-17 | 1.352e-15 |
49 | REGULATION OF CELL PROLIFERATION | 20 | 1496 | 1.424e-17 | 1.352e-15 |
50 | POSITIVE REGULATION OF BIOSYNTHETIC PROCESS | 21 | 1805 | 1.809e-17 | 1.684e-15 |
51 | HEART MORPHOGENESIS | 12 | 212 | 2.224e-17 | 2.029e-15 |
52 | UROGENITAL SYSTEM DEVELOPMENT | 13 | 299 | 2.388e-17 | 2.137e-15 |
53 | CARTILAGE DEVELOPMENT | 11 | 147 | 2.726e-17 | 2.394e-15 |
54 | CELLULAR RESPONSE TO ORGANIC SUBSTANCE | 21 | 1848 | 2.935e-17 | 2.529e-15 |
55 | NEGATIVE REGULATION OF CELL DEATH | 17 | 872 | 3.574e-17 | 3.024e-15 |
56 | POSITIVE REGULATION OF LOCOMOTION | 14 | 420 | 4.094e-17 | 3.402e-15 |
57 | POSITIVE REGULATION OF EPITHELIAL TO MESENCHYMAL TRANSITION | 8 | 34 | 6.219e-17 | 5.077e-15 |
58 | LOCOMOTION | 18 | 1114 | 6.779e-17 | 5.438e-15 |
59 | MORPHOGENESIS OF A BRANCHING STRUCTURE | 11 | 167 | 1.145e-16 | 9.033e-15 |
60 | MESODERM MORPHOGENESIS | 9 | 66 | 1.176e-16 | 9.12e-15 |
61 | POSITIVE REGULATION OF MULTICELLULAR ORGANISMAL PROCESS | 19 | 1395 | 1.227e-16 | 9.362e-15 |
62 | FORMATION OF PRIMARY GERM LAYER | 10 | 110 | 1.3e-16 | 9.76e-15 |
63 | REGULATION OF EPITHELIAL TO MESENCHYMAL TRANSITION | 9 | 67 | 1.357e-16 | 1.003e-14 |
64 | POSITIVE REGULATION OF CELL DEVELOPMENT | 14 | 472 | 2.082e-16 | 1.514e-14 |
65 | RESPONSE TO ENDOGENOUS STIMULUS | 19 | 1450 | 2.514e-16 | 1.8e-14 |
66 | SENSORY ORGAN DEVELOPMENT | 14 | 493 | 3.812e-16 | 2.687e-14 |
67 | KIDNEY EPITHELIUM DEVELOPMENT | 10 | 125 | 4.861e-16 | 3.376e-14 |
68 | CELL MOTILITY | 16 | 835 | 6.276e-16 | 4.232e-14 |
69 | LOCALIZATION OF CELL | 16 | 835 | 6.276e-16 | 4.232e-14 |
70 | MOVEMENT OF CELL OR SUBCELLULAR COMPONENT | 18 | 1275 | 7.285e-16 | 4.813e-14 |
71 | REGULATION OF BINDING | 12 | 283 | 7.344e-16 | 4.813e-14 |
72 | BRANCHING MORPHOGENESIS OF AN EPITHELIAL TUBE | 10 | 131 | 7.868e-16 | 5.085e-14 |
73 | CELL PROLIFERATION | 15 | 672 | 8.055e-16 | 5.135e-14 |
74 | CARDIAC EPITHELIAL TO MESENCHYMAL TRANSITION | 7 | 24 | 1.194e-15 | 7.505e-14 |
75 | REPRODUCTIVE SYSTEM DEVELOPMENT | 13 | 408 | 1.357e-15 | 8.421e-14 |
76 | EMBRYO DEVELOPMENT ENDING IN BIRTH OR EGG HATCHING | 14 | 554 | 1.918e-15 | 1.174e-13 |
77 | MESONEPHROS DEVELOPMENT | 9 | 90 | 2.201e-15 | 1.33e-13 |
78 | NEGATIVE REGULATION OF CARTILAGE DEVELOPMENT | 7 | 26 | 2.264e-15 | 1.351e-13 |
79 | DIGESTIVE SYSTEM DEVELOPMENT | 10 | 148 | 2.742e-15 | 1.615e-13 |
80 | POSITIVE REGULATION OF EPITHELIAL CELL PROLIFERATION | 10 | 154 | 4.111e-15 | 2.391e-13 |
81 | GLAND MORPHOGENESIS | 9 | 97 | 4.428e-15 | 2.513e-13 |
82 | GASTRULATION | 10 | 155 | 4.391e-15 | 2.513e-13 |
83 | REGULATION OF CANONICAL WNT SIGNALING PATHWAY | 11 | 236 | 5.399e-15 | 3.027e-13 |
84 | REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 12 | 337 | 5.974e-15 | 3.306e-13 |
85 | DEVELOPMENTAL PROCESS INVOLVED IN REPRODUCTION | 14 | 602 | 6.039e-15 | 3.306e-13 |
86 | NEGATIVE REGULATION OF CANONICAL WNT SIGNALING PATHWAY | 10 | 162 | 6.882e-15 | 3.681e-13 |
87 | POSITIVE REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 10 | 162 | 6.882e-15 | 3.681e-13 |
88 | NEGATIVE REGULATION OF CELL DIFFERENTIATION | 14 | 609 | 7.081e-15 | 3.744e-13 |
89 | HEART DEVELOPMENT | 13 | 466 | 7.533e-15 | 3.939e-13 |
90 | CARDIOVASCULAR SYSTEM DEVELOPMENT | 15 | 788 | 8.4e-15 | 4.295e-13 |
91 | CIRCULATORY SYSTEM DEVELOPMENT | 15 | 788 | 8.4e-15 | 4.295e-13 |
92 | REGULATION OF CELL ADHESION | 14 | 629 | 1.105e-14 | 5.587e-13 |
93 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 16 | 1004 | 1.121e-14 | 5.606e-13 |
94 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 19 | 1784 | 1.151e-14 | 5.695e-13 |
95 | POSITIVE REGULATION OF CELL PROLIFERATION | 15 | 814 | 1.352e-14 | 6.623e-13 |
96 | NEGATIVE REGULATION OF CELL PROLIFERATION | 14 | 643 | 1.495e-14 | 7.247e-13 |
97 | EPITHELIAL CELL DIFFERENTIATION | 13 | 495 | 1.636e-14 | 7.848e-13 |
98 | REGULATION OF OSTEOBLAST DIFFERENTIATION | 9 | 112 | 1.682e-14 | 7.985e-13 |
99 | MESODERM DEVELOPMENT | 9 | 118 | 2.723e-14 | 1.28e-12 |
100 | EMBRYONIC ORGAN MORPHOGENESIS | 11 | 279 | 3.421e-14 | 1.592e-12 |
101 | NEGATIVE REGULATION OF WNT SIGNALING PATHWAY | 10 | 197 | 4.984e-14 | 2.296e-12 |
102 | GROWTH | 12 | 410 | 6.184e-14 | 2.821e-12 |
103 | PATTERN SPECIFICATION PROCESS | 12 | 418 | 7.778e-14 | 3.514e-12 |
104 | NEUROGENESIS | 17 | 1402 | 9.338e-14 | 4.178e-12 |
105 | REGULATION OF WNT SIGNALING PATHWAY | 11 | 310 | 1.087e-13 | 4.817e-12 |
106 | IN UTERO EMBRYONIC DEVELOPMENT | 11 | 311 | 1.126e-13 | 4.943e-12 |
107 | POSITIVE REGULATION OF OSSIFICATION | 8 | 84 | 1.431e-13 | 6.225e-12 |
108 | PALATE DEVELOPMENT | 8 | 85 | 1.579e-13 | 6.802e-12 |
109 | REGULATION OF CELLULAR COMPONENT BIOGENESIS | 14 | 767 | 1.672e-13 | 7.137e-12 |
110 | RESPONSE TO TRANSFORMING GROWTH FACTOR BETA | 9 | 144 | 1.695e-13 | 7.171e-12 |
111 | CELL FATE COMMITMENT | 10 | 227 | 2.073e-13 | 8.689e-12 |
112 | REGULATION OF CELLULAR RESPONSE TO GROWTH FACTOR STIMULUS | 10 | 229 | 2.263e-13 | 9.403e-12 |
113 | ENDOCARDIAL CUSHION MORPHOGENESIS | 6 | 22 | 2.451e-13 | 1.009e-11 |
114 | DIGESTIVE TRACT MORPHOGENESIS | 7 | 48 | 2.486e-13 | 1.015e-11 |
115 | OSSIFICATION | 10 | 251 | 5.667e-13 | 2.293e-11 |
116 | DEVELOPMENTAL GROWTH INVOLVED IN MORPHOGENESIS | 8 | 104 | 8.315e-13 | 3.335e-11 |
117 | POSITIVE REGULATION OF RESPONSE TO STIMULUS | 18 | 1929 | 9.688e-13 | 3.82e-11 |
118 | AXIS ELONGATION | 6 | 27 | 9.68e-13 | 3.82e-11 |
119 | NEURON DIFFERENTIATION | 14 | 874 | 9.87e-13 | 3.859e-11 |
120 | COLUMNAR CUBOIDAL EPITHELIAL CELL DIFFERENTIATION | 8 | 111 | 1.417e-12 | 5.494e-11 |
121 | POSITIVE REGULATION OF STEM CELL PROLIFERATION | 7 | 61 | 1.456e-12 | 5.601e-11 |
122 | REGULATION OF HEART MORPHOGENESIS | 6 | 29 | 1.551e-12 | 5.914e-11 |
123 | NEGATIVE REGULATION OF EPITHELIAL CELL PROLIFERATION | 8 | 115 | 1.892e-12 | 7.099e-11 |
124 | NEPHRON DEVELOPMENT | 8 | 115 | 1.892e-12 | 7.099e-11 |
125 | REGULATION OF CELL MORPHOGENESIS | 12 | 552 | 2.069e-12 | 7.702e-11 |
126 | NEGATIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 13 | 740 | 2.728e-12 | 1.007e-10 |
127 | ENDOCARDIAL CUSHION DEVELOPMENT | 6 | 32 | 2.95e-12 | 1.081e-10 |
128 | PATHWAY RESTRICTED SMAD PROTEIN PHOSPHORYLATION | 5 | 13 | 3.87e-12 | 1.407e-10 |
129 | REGULATION OF TRANSMEMBRANE RECEPTOR PROTEIN SERINE THREONINE KINASE SIGNALING PATHWAY | 9 | 207 | 4.566e-12 | 1.647e-10 |
130 | REGIONALIZATION | 10 | 311 | 4.778e-12 | 1.71e-10 |
131 | REGULATION OF REPRODUCTIVE PROCESS | 8 | 129 | 4.817e-12 | 1.711e-10 |
132 | POSITIVE REGULATION OF CELL DEATH | 12 | 605 | 6.052e-12 | 2.133e-10 |
133 | MORPHOGENESIS OF EMBRYONIC EPITHELIUM | 8 | 134 | 6.557e-12 | 2.294e-10 |
134 | POSITIVE REGULATION OF CELL COMMUNICATION | 16 | 1532 | 7.549e-12 | 2.621e-10 |
135 | RENAL TUBULE DEVELOPMENT | 7 | 78 | 8.689e-12 | 2.995e-10 |
136 | DEVELOPMENTAL GROWTH | 10 | 333 | 9.394e-12 | 3.214e-10 |
137 | REGULATION OF GROWTH | 12 | 633 | 1.026e-11 | 3.484e-10 |
138 | REPRODUCTION | 15 | 1297 | 1.156e-11 | 3.898e-10 |
139 | PROSTATE GLAND DEVELOPMENT | 6 | 41 | 1.452e-11 | 4.86e-10 |
140 | FOREBRAIN DEVELOPMENT | 10 | 357 | 1.866e-11 | 6.202e-10 |
141 | REGULATION OF APOPTOTIC SIGNALING PATHWAY | 10 | 363 | 2.199e-11 | 7.256e-10 |
142 | REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 16 | 1656 | 2.462e-11 | 8.066e-10 |
143 | RESPONSE TO LIPID | 13 | 888 | 2.689e-11 | 8.75e-10 |
144 | NEPHRON EPITHELIUM DEVELOPMENT | 7 | 93 | 3.075e-11 | 9.937e-10 |
145 | CANONICAL WNT SIGNALING PATHWAY | 7 | 95 | 3.581e-11 | 1.149e-09 |
146 | HEAD DEVELOPMENT | 12 | 709 | 3.832e-11 | 1.221e-09 |
147 | REGULATION OF PROTEIN BINDING | 8 | 168 | 4.063e-11 | 1.286e-09 |
148 | APPENDAGE DEVELOPMENT | 8 | 169 | 4.261e-11 | 1.331e-09 |
149 | LIMB DEVELOPMENT | 8 | 169 | 4.261e-11 | 1.331e-09 |
150 | POSITIVE REGULATION OF TRANSMEMBRANE RECEPTOR PROTEIN SERINE THREONINE KINASE SIGNALING PATHWAY | 7 | 100 | 5.164e-11 | 1.602e-09 |
151 | REGULATION OF MUSCLE TISSUE DEVELOPMENT | 7 | 103 | 6.375e-11 | 1.952e-09 |
152 | REGULATION OF MUSCLE ORGAN DEVELOPMENT | 7 | 103 | 6.375e-11 | 1.952e-09 |
153 | POSITIVE REGULATION OF CELLULAR COMPONENT BIOGENESIS | 10 | 406 | 6.6e-11 | 2.007e-09 |
154 | MESONEPHRIC TUBULE MORPHOGENESIS | 6 | 53 | 7.334e-11 | 2.216e-09 |
155 | REGULATION OF KIDNEY DEVELOPMENT | 6 | 55 | 9.244e-11 | 2.775e-09 |
156 | TRANSMEMBRANE RECEPTOR PROTEIN SERINE THREONINE KINASE SIGNALING PATHWAY | 8 | 190 | 1.089e-10 | 3.247e-09 |
157 | MUSCLE STRUCTURE DEVELOPMENT | 10 | 432 | 1.211e-10 | 3.589e-09 |
158 | ANTERIOR POSTERIOR PATTERN SPECIFICATION | 8 | 194 | 1.286e-10 | 3.786e-09 |
159 | NEGATIVE REGULATION OF CELL DEVELOPMENT | 9 | 303 | 1.378e-10 | 4.032e-09 |
160 | RESPIRATORY SYSTEM DEVELOPMENT | 8 | 197 | 1.453e-10 | 4.226e-09 |
161 | STEM CELL PROLIFERATION | 6 | 60 | 1.589e-10 | 4.481e-09 |
162 | REGULATION OF FIBROBLAST GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 5 | 25 | 1.58e-10 | 4.481e-09 |
163 | REGULATION OF PATHWAY RESTRICTED SMAD PROTEIN PHOSPHORYLATION | 6 | 60 | 1.589e-10 | 4.481e-09 |
164 | MAMMARY GLAND DEVELOPMENT | 7 | 117 | 1.576e-10 | 4.481e-09 |
165 | RESPONSE TO ABIOTIC STIMULUS | 13 | 1024 | 1.582e-10 | 4.481e-09 |
166 | NEGATIVE REGULATION OF APOPTOTIC SIGNALING PATHWAY | 8 | 200 | 1.639e-10 | 4.595e-09 |
167 | SKELETAL SYSTEM MORPHOGENESIS | 8 | 201 | 1.706e-10 | 4.753e-09 |
168 | RESPONSE TO OXYGEN LEVELS | 9 | 311 | 1.736e-10 | 4.808e-09 |
169 | POSITIVE REGULATION OF PHOSPHATE METABOLIC PROCESS | 13 | 1036 | 1.827e-10 | 5.001e-09 |
170 | POSITIVE REGULATION OF PHOSPHORUS METABOLIC PROCESS | 13 | 1036 | 1.827e-10 | 5.001e-09 |
171 | NEGATIVE REGULATION OF CELLULAR RESPONSE TO GROWTH FACTOR STIMULUS | 7 | 121 | 2e-10 | 5.441e-09 |
172 | EMBRYONIC SKELETAL SYSTEM DEVELOPMENT | 7 | 122 | 2.12e-10 | 5.734e-09 |
173 | ENDOCRINE SYSTEM DEVELOPMENT | 7 | 123 | 2.246e-10 | 6.04e-09 |
174 | SKIN DEVELOPMENT | 8 | 211 | 2.511e-10 | 6.716e-09 |
175 | EYE DEVELOPMENT | 9 | 326 | 2.635e-10 | 7.005e-09 |
176 | POSITIVE REGULATION OF BINDING | 7 | 127 | 2.815e-10 | 7.443e-09 |
177 | TUBE FORMATION | 7 | 129 | 3.143e-10 | 8.263e-09 |
178 | EPIDERMIS MORPHOGENESIS | 5 | 29 | 3.519e-10 | 9.198e-09 |
179 | CENTRAL NERVOUS SYSTEM DEVELOPMENT | 12 | 872 | 4.157e-10 | 1.081e-08 |
180 | SKIN EPIDERMIS DEVELOPMENT | 6 | 71 | 4.501e-10 | 1.157e-08 |
181 | ENDODERM DEVELOPMENT | 6 | 71 | 4.501e-10 | 1.157e-08 |
182 | POSITIVE REGULATION OF PROTEIN MODIFICATION PROCESS | 13 | 1135 | 5.631e-10 | 1.44e-08 |
183 | ENZYME LINKED RECEPTOR PROTEIN SIGNALING PATHWAY | 11 | 689 | 5.908e-10 | 1.502e-08 |
184 | REGULATION OF ORGAN FORMATION | 5 | 32 | 5.95e-10 | 1.505e-08 |
185 | REGULATION OF CELLULAR RESPONSE TO STRESS | 11 | 691 | 6.092e-10 | 1.532e-08 |
186 | REGULATION OF BIOMINERAL TISSUE DEVELOPMENT | 6 | 75 | 6.306e-10 | 1.577e-08 |
187 | SENSORY ORGAN MORPHOGENESIS | 8 | 239 | 6.751e-10 | 1.68e-08 |
188 | BLOOD VESSEL MORPHOGENESIS | 9 | 364 | 6.969e-10 | 1.725e-08 |
189 | REGULATION OF MESENCHYMAL CELL PROLIFERATION | 5 | 34 | 8.207e-10 | 2.02e-08 |
190 | POSITIVE REGULATION OF CELL ADHESION | 9 | 376 | 9.27e-10 | 2.27e-08 |
191 | REGULATION OF CELL CELL ADHESION | 9 | 380 | 1.017e-09 | 2.478e-08 |
192 | PROTEIN PHOSPHORYLATION | 12 | 944 | 1.029e-09 | 2.493e-08 |
193 | AMEBOIDAL TYPE CELL MIGRATION | 7 | 154 | 1.092e-09 | 2.607e-08 |
194 | REGULATION OF CELL CYCLE | 12 | 949 | 1.092e-09 | 2.607e-08 |
195 | KIDNEY MORPHOGENESIS | 6 | 82 | 1.09e-09 | 2.607e-08 |
196 | POSITIVE REGULATION OF MOLECULAR FUNCTION | 15 | 1791 | 1.11e-09 | 2.635e-08 |
197 | HAIR CYCLE | 6 | 83 | 1.174e-09 | 2.758e-08 |
198 | MOLTING CYCLE | 6 | 83 | 1.174e-09 | 2.758e-08 |
199 | NEGATIVE REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 8 | 262 | 1.395e-09 | 3.256e-08 |
200 | RESPONSE TO EXTERNAL STIMULUS | 15 | 1821 | 1.4e-09 | 3.256e-08 |
201 | REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 11 | 750 | 1.444e-09 | 3.343e-08 |
202 | GLANDULAR EPITHELIAL CELL DIFFERENTIATION | 5 | 39 | 1.69e-09 | 3.894e-08 |
203 | REGULATION OF EPITHELIAL CELL MIGRATION | 7 | 166 | 1.846e-09 | 4.23e-08 |
204 | MESENCHYMAL CELL PROLIFERATION | 4 | 13 | 1.867e-09 | 4.259e-08 |
205 | IMMUNE SYSTEM DEVELOPMENT | 10 | 582 | 2.178e-09 | 4.943e-08 |
206 | ANGIOGENESIS | 8 | 293 | 3.363e-09 | 7.596e-08 |
207 | EXOCRINE SYSTEM DEVELOPMENT | 5 | 45 | 3.567e-09 | 7.981e-08 |
208 | REGULATION OF PHOSPHORUS METABOLIC PROCESS | 14 | 1618 | 3.568e-09 | 7.981e-08 |
209 | CAMERA TYPE EYE MORPHOGENESIS | 6 | 101 | 3.877e-09 | 8.631e-08 |
210 | REGULATION OF CHONDROCYTE DIFFERENTIATION | 5 | 46 | 3.999e-09 | 8.86e-08 |
211 | EPITHELIAL CELL DEVELOPMENT | 7 | 186 | 4.077e-09 | 8.992e-08 |
212 | NEGATIVE REGULATION OF TRANSMEMBRANE RECEPTOR PROTEIN SERINE THREONINE KINASE SIGNALING PATHWAY | 6 | 102 | 4.115e-09 | 9.033e-08 |
213 | POSITIVE REGULATION OF EPITHELIAL CELL MIGRATION | 6 | 103 | 4.366e-09 | 9.538e-08 |
214 | CARDIAC CHAMBER MORPHOGENESIS | 6 | 104 | 4.629e-09 | 1.007e-07 |
215 | PARAXIAL MESODERM DEVELOPMENT | 4 | 16 | 4.74e-09 | 1.021e-07 |
216 | CELL SURFACE RECEPTOR SIGNALING PATHWAY INVOLVED IN HEART DEVELOPMENT | 4 | 16 | 4.74e-09 | 1.021e-07 |
217 | ODONTOGENESIS | 6 | 105 | 4.905e-09 | 1.052e-07 |
218 | REGULATION OF CARDIAC MUSCLE TISSUE DEVELOPMENT | 5 | 48 | 4.986e-09 | 1.059e-07 |
219 | POSITIVE REGULATION OF PATHWAY RESTRICTED SMAD PROTEIN PHOSPHORYLATION | 5 | 48 | 4.986e-09 | 1.059e-07 |
220 | CARDIAC VENTRICLE DEVELOPMENT | 6 | 106 | 5.195e-09 | 1.099e-07 |
221 | EAR DEVELOPMENT | 7 | 195 | 5.661e-09 | 1.192e-07 |
222 | BRANCH ELONGATION OF AN EPITHELIUM | 4 | 17 | 6.193e-09 | 1.281e-07 |
223 | NEGATIVE REGULATION OF ALCOHOL BIOSYNTHETIC PROCESS | 4 | 17 | 6.193e-09 | 1.281e-07 |
224 | NEGATIVE REGULATION OF STEM CELL PROLIFERATION | 4 | 17 | 6.193e-09 | 1.281e-07 |
225 | FACE DEVELOPMENT | 5 | 50 | 6.158e-09 | 1.281e-07 |
226 | VASCULATURE DEVELOPMENT | 9 | 469 | 6.398e-09 | 1.317e-07 |
227 | REGULATION OF MAPK CASCADE | 10 | 660 | 7.267e-09 | 1.487e-07 |
228 | POSITIVE REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 11 | 876 | 7.32e-09 | 1.487e-07 |
229 | REGULATION OF PROTEIN MODIFICATION PROCESS | 14 | 1710 | 7.308e-09 | 1.487e-07 |
230 | NOTOCHORD DEVELOPMENT | 4 | 18 | 7.955e-09 | 1.609e-07 |
231 | NOTCH SIGNALING PATHWAY | 6 | 114 | 8.063e-09 | 1.617e-07 |
232 | REGULATION OF EMBRYONIC DEVELOPMENT | 6 | 114 | 8.063e-09 | 1.617e-07 |
233 | MAMMARY GLAND EPITHELIUM DEVELOPMENT | 5 | 53 | 8.317e-09 | 1.661e-07 |
234 | CARDIAC MUSCLE TISSUE MORPHOGENESIS | 5 | 54 | 9.158e-09 | 1.821e-07 |
235 | RESPONSE TO STEROID HORMONE | 9 | 497 | 1.058e-08 | 2.095e-07 |
236 | RESPONSE TO ORGANIC CYCLIC COMPOUND | 11 | 917 | 1.177e-08 | 2.32e-07 |
237 | REGULATION OF PROTEIN LOCALIZATION TO NUCLEUS | 7 | 218 | 1.225e-08 | 2.405e-07 |
238 | REGULATION OF ORGANELLE ORGANIZATION | 12 | 1178 | 1.255e-08 | 2.448e-07 |
239 | NEGATIVE REGULATION OF CHONDROCYTE DIFFERENTIATION | 4 | 20 | 1.257e-08 | 2.448e-07 |
240 | REGULATION OF RESPONSE TO STRESS | 13 | 1468 | 1.289e-08 | 2.499e-07 |
241 | EMBRYONIC PATTERN SPECIFICATION | 5 | 58 | 1.322e-08 | 2.552e-07 |
242 | OSTEOBLAST DIFFERENTIATION | 6 | 126 | 1.473e-08 | 2.832e-07 |
243 | POSITIVE REGULATION OF PROTEIN METABOLIC PROCESS | 13 | 1492 | 1.567e-08 | 2.999e-07 |
244 | POSITIVE REGULATION OF OSTEOBLAST DIFFERENTIATION | 5 | 60 | 1.573e-08 | 2.999e-07 |
245 | HEPATICOBILIARY SYSTEM DEVELOPMENT | 6 | 128 | 1.619e-08 | 3.075e-07 |
246 | REGULATION OF PROTEIN LOCALIZATION | 11 | 950 | 1.697e-08 | 3.209e-07 |
247 | SOMATIC STEM CELL DIVISION | 4 | 22 | 1.895e-08 | 3.569e-07 |
248 | POSITIVE REGULATION OF CATALYTIC ACTIVITY | 13 | 1518 | 1.928e-08 | 3.617e-07 |
249 | REGULATION OF VASCULATURE DEVELOPMENT | 7 | 233 | 1.938e-08 | 3.622e-07 |
250 | PHOSPHORYLATION | 12 | 1228 | 1.998e-08 | 3.718e-07 |
251 | NEUROEPITHELIAL CELL DIFFERENTIATION | 5 | 63 | 2.019e-08 | 3.742e-07 |
252 | MUSCLE CELL DIFFERENTIATION | 7 | 237 | 2.179e-08 | 4.024e-07 |
253 | PROSTATE GLAND MORPHOGENESIS | 4 | 23 | 2.291e-08 | 4.214e-07 |
254 | EYE MORPHOGENESIS | 6 | 136 | 2.329e-08 | 4.267e-07 |
255 | REGULATION OF CELLULAR PROTEIN LOCALIZATION | 9 | 552 | 2.62e-08 | 4.78e-07 |
256 | NEGATIVE REGULATION OF STEROID METABOLIC PROCESS | 4 | 24 | 2.747e-08 | 4.993e-07 |
257 | CARDIAC MUSCLE TISSUE DEVELOPMENT | 6 | 140 | 2.771e-08 | 5.016e-07 |
258 | REGULATION OF CELL JUNCTION ASSEMBLY | 5 | 68 | 2.98e-08 | 5.354e-07 |
259 | ORGAN GROWTH | 5 | 68 | 2.98e-08 | 5.354e-07 |
260 | REGULATION OF CYTOKINE PRODUCTION | 9 | 563 | 3.104e-08 | 5.556e-07 |
261 | NEGATIVE REGULATION OF OSSIFICATION | 5 | 69 | 3.21e-08 | 5.722e-07 |
262 | CARDIAC CHAMBER DEVELOPMENT | 6 | 144 | 3.279e-08 | 5.801e-07 |
263 | POSITIVE REGULATION OF PEPTIDYL THREONINE PHOSPHORYLATION | 4 | 25 | 3.267e-08 | 5.801e-07 |
264 | EPIDERMIS DEVELOPMENT | 7 | 253 | 3.414e-08 | 6.017e-07 |
265 | MUSCLE ORGAN MORPHOGENESIS | 5 | 70 | 3.454e-08 | 6.064e-07 |
266 | RESPONSE TO ESTRADIOL | 6 | 146 | 3.561e-08 | 6.228e-07 |
267 | POSITIVE REGULATION OF ORGANELLE ORGANIZATION | 9 | 573 | 3.612e-08 | 6.294e-07 |
268 | NEGATIVE REGULATION OF EMBRYONIC DEVELOPMENT | 4 | 26 | 3.858e-08 | 6.698e-07 |
269 | EMBRYONIC HEART TUBE DEVELOPMENT | 5 | 73 | 4.274e-08 | 7.366e-07 |
270 | REGULATION OF NEURAL PRECURSOR CELL PROLIFERATION | 5 | 73 | 4.274e-08 | 7.366e-07 |
271 | NEGATIVE REGULATION OF LOCOMOTION | 7 | 263 | 4.453e-08 | 7.646e-07 |
272 | DEVELOPMENTAL INDUCTION | 4 | 27 | 4.525e-08 | 7.69e-07 |
273 | REGULATION OF MUSCLE CELL DIFFERENTIATION | 6 | 152 | 4.528e-08 | 7.69e-07 |
274 | POSITIVE REGULATION OF MESENCHYMAL CELL PROLIFERATION | 4 | 27 | 4.525e-08 | 7.69e-07 |
275 | VENTRICULAR SEPTUM MORPHOGENESIS | 4 | 28 | 5.274e-08 | 8.859e-07 |
276 | REGULATION OF NEUROBLAST PROLIFERATION | 4 | 28 | 5.274e-08 | 8.859e-07 |
277 | MAMMARY GLAND DUCT MORPHOGENESIS | 4 | 28 | 5.274e-08 | 8.859e-07 |
278 | DIENCEPHALON DEVELOPMENT | 5 | 77 | 5.602e-08 | 9.376e-07 |
279 | SOMITE DEVELOPMENT | 5 | 78 | 5.98e-08 | 9.973e-07 |
280 | MUSCLE TISSUE DEVELOPMENT | 7 | 275 | 6.043e-08 | 1.004e-06 |
281 | REGULATION OF EXTRACELLULAR MATRIX ORGANIZATION | 4 | 29 | 6.112e-08 | 1.005e-06 |
282 | STEM CELL DIVISION | 4 | 29 | 6.112e-08 | 1.005e-06 |
283 | POSITIVE REGULATION OF CARTILAGE DEVELOPMENT | 4 | 29 | 6.112e-08 | 1.005e-06 |
284 | SMOOTH MUSCLE CELL DIFFERENTIATION | 4 | 30 | 7.046e-08 | 1.154e-06 |
285 | RESPONSE TO OXYGEN CONTAINING COMPOUND | 12 | 1381 | 7.352e-08 | 1.2e-06 |
286 | POSITIVE REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 8 | 437 | 7.516e-08 | 1.223e-06 |
287 | ORGAN REGENERATION | 5 | 83 | 8.187e-08 | 1.323e-06 |
288 | EMBRYONIC PLACENTA DEVELOPMENT | 5 | 83 | 8.187e-08 | 1.323e-06 |
289 | SALIVARY GLAND DEVELOPMENT | 4 | 32 | 9.228e-08 | 1.486e-06 |
290 | GLIOGENESIS | 6 | 175 | 1.047e-07 | 1.679e-06 |
291 | CELLULAR RESPONSE TO LIPID | 8 | 457 | 1.06e-07 | 1.695e-06 |
292 | HEART VALVE DEVELOPMENT | 4 | 34 | 1.188e-07 | 1.893e-06 |
293 | RESPONSE TO HORMONE | 10 | 893 | 1.263e-07 | 2.006e-06 |
294 | POSITIVE REGULATION OF MAPK CASCADE | 8 | 470 | 1.314e-07 | 2.08e-06 |
295 | REGULATION OF PROTEIN IMPORT | 6 | 183 | 1.364e-07 | 2.151e-06 |
296 | EMBRYONIC SKELETAL SYSTEM MORPHOGENESIS | 5 | 93 | 1.452e-07 | 2.279e-06 |
297 | CELL JUNCTION ORGANIZATION | 6 | 185 | 1.455e-07 | 2.279e-06 |
298 | NEGATIVE REGULATION OF MUSCLE ORGAN DEVELOPMENT | 4 | 36 | 1.506e-07 | 2.336e-06 |
299 | NEGATIVE REGULATION OF MUSCLE TISSUE DEVELOPMENT | 4 | 36 | 1.506e-07 | 2.336e-06 |
300 | HEAD MORPHOGENESIS | 4 | 36 | 1.506e-07 | 2.336e-06 |
301 | RESPONSE TO BMP | 5 | 94 | 1.532e-07 | 2.361e-06 |
302 | CELLULAR RESPONSE TO BMP STIMULUS | 5 | 94 | 1.532e-07 | 2.361e-06 |
303 | REGULATION OF MAP KINASE ACTIVITY | 7 | 319 | 1.66e-07 | 2.55e-06 |
304 | REGULATION OF PEPTIDYL THREONINE PHOSPHORYLATION | 4 | 37 | 1.687e-07 | 2.574e-06 |
305 | NEGATIVE REGULATION OF EPITHELIAL CELL DIFFERENTIATION | 4 | 37 | 1.687e-07 | 2.574e-06 |
306 | POSITIVE REGULATION OF BIOMINERAL TISSUE DEVELOPMENT | 4 | 38 | 1.884e-07 | 2.865e-06 |
307 | WNT SIGNALING PATHWAY CALCIUM MODULATING PATHWAY | 4 | 39 | 2.097e-07 | 3.179e-06 |
308 | REGULATION OF TRANSFERASE ACTIVITY | 10 | 946 | 2.161e-07 | 3.265e-06 |
309 | POSITIVE REGULATION OF CELL CYCLE | 7 | 332 | 2.177e-07 | 3.278e-06 |
310 | MAMMARY GLAND MORPHOGENESIS | 4 | 40 | 2.328e-07 | 3.483e-06 |
311 | POSITIVE REGULATION OF CELL MATRIX ADHESION | 4 | 40 | 2.328e-07 | 3.483e-06 |
312 | POSITIVE REGULATION OF KIDNEY DEVELOPMENT | 4 | 41 | 2.577e-07 | 3.844e-06 |
313 | PITUITARY GLAND DEVELOPMENT | 4 | 42 | 2.846e-07 | 4.231e-06 |
314 | WNT SIGNALING PATHWAY | 7 | 351 | 3.171e-07 | 4.699e-06 |
315 | BODY MORPHOGENESIS | 4 | 44 | 3.445e-07 | 5.057e-06 |
316 | NEGATIVE REGULATION OF LIPID BIOSYNTHETIC PROCESS | 4 | 44 | 3.445e-07 | 5.057e-06 |
317 | BRANCHING INVOLVED IN URETERIC BUD MORPHOGENESIS | 4 | 44 | 3.445e-07 | 5.057e-06 |
318 | REGULATION OF CELLULAR LOCALIZATION | 11 | 1277 | 3.468e-07 | 5.075e-06 |
319 | REGULATION OF EXTRACELLULAR MATRIX ASSEMBLY | 3 | 11 | 3.594e-07 | 5.21e-06 |
320 | EPITHELIAL TO MESENCHYMAL TRANSITION INVOLVED IN ENDOCARDIAL CUSHION FORMATION | 3 | 11 | 3.594e-07 | 5.21e-06 |
321 | EPITHELIAL CELL DIFFERENTIATION INVOLVED IN PROSTATE GLAND DEVELOPMENT | 3 | 11 | 3.594e-07 | 5.21e-06 |
322 | LUNG MORPHOGENESIS | 4 | 45 | 3.778e-07 | 5.443e-06 |
323 | REGULATION OF ALCOHOL BIOSYNTHETIC PROCESS | 4 | 45 | 3.778e-07 | 5.443e-06 |
324 | RESPONSE TO ESTROGEN | 6 | 218 | 3.827e-07 | 5.497e-06 |
325 | RESPONSE TO ALCOHOL | 7 | 362 | 3.904e-07 | 5.59e-06 |
326 | REGULATION OF NUCLEOCYTOPLASMIC TRANSPORT | 6 | 220 | 4.038e-07 | 5.764e-06 |
327 | CELL MORPHOGENESIS INVOLVED IN NEURON DIFFERENTIATION | 7 | 368 | 4.362e-07 | 6.184e-06 |
328 | NEGATIVE REGULATION OF CELL ADHESION | 6 | 223 | 4.372e-07 | 6.184e-06 |
329 | MULTICELLULAR ORGANISM REPRODUCTION | 9 | 768 | 4.357e-07 | 6.184e-06 |
330 | REGULATION OF NEURON DIFFERENTIATION | 8 | 554 | 4.597e-07 | 6.482e-06 |
331 | REGULATION OF KINASE ACTIVITY | 9 | 776 | 4.753e-07 | 6.682e-06 |
332 | REGULATION OF MESENCHYMAL CELL APOPTOTIC PROCESS | 3 | 12 | 4.788e-07 | 6.69e-06 |
333 | REGULATION OF MACROPHAGE CYTOKINE PRODUCTION | 3 | 12 | 4.788e-07 | 6.69e-06 |
334 | REGULATION OF CELL CYCLE PROCESS | 8 | 558 | 4.854e-07 | 6.763e-06 |
335 | TELENCEPHALON DEVELOPMENT | 6 | 228 | 4.979e-07 | 6.916e-06 |
336 | REGULATION OF STEROID BIOSYNTHETIC PROCESS | 4 | 49 | 5.353e-07 | 7.391e-06 |
337 | CARDIAC SEPTUM MORPHOGENESIS | 4 | 49 | 5.353e-07 | 7.391e-06 |
338 | NEGATIVE REGULATION OF GROWTH | 6 | 236 | 6.094e-07 | 8.389e-06 |
339 | POSITIVE REGULATION OF GROWTH | 6 | 238 | 6.402e-07 | 8.787e-06 |
340 | REGULATION OF CELL GROWTH | 7 | 391 | 6.555e-07 | 8.971e-06 |
341 | POSITIVE REGULATION OF REPRODUCTIVE PROCESS | 4 | 52 | 6.821e-07 | 9.307e-06 |
342 | NEGATIVE REGULATION OF REPRODUCTIVE PROCESS | 4 | 54 | 7.953e-07 | 1.066e-05 |
343 | CELL MIGRATION INVOLVED IN GASTRULATION | 3 | 14 | 7.908e-07 | 1.066e-05 |
344 | NEURON PROJECTION MORPHOGENESIS | 7 | 402 | 7.895e-07 | 1.066e-05 |
345 | EMBRYONIC SKELETAL JOINT DEVELOPMENT | 3 | 14 | 7.908e-07 | 1.066e-05 |
346 | VENTRICULAR SEPTUM DEVELOPMENT | 4 | 54 | 7.953e-07 | 1.066e-05 |
347 | CONVERGENT EXTENSION | 3 | 14 | 7.908e-07 | 1.066e-05 |
348 | NEGATIVE REGULATION OF BINDING | 5 | 131 | 8.029e-07 | 1.074e-05 |
349 | POSITIVE REGULATION OF CELL DIVISION | 5 | 132 | 8.338e-07 | 1.112e-05 |
350 | NEGATIVE REGULATION OF MUSCLE CELL DIFFERENTIATION | 4 | 55 | 8.569e-07 | 1.136e-05 |
351 | CRANIAL SKELETAL SYSTEM DEVELOPMENT | 4 | 55 | 8.569e-07 | 1.136e-05 |
352 | SMAD PROTEIN SIGNAL TRANSDUCTION | 4 | 56 | 9.22e-07 | 1.212e-05 |
353 | POSITIVE REGULATION OF MUSCLE TISSUE DEVELOPMENT | 4 | 56 | 9.22e-07 | 1.212e-05 |
354 | OUTFLOW TRACT MORPHOGENESIS | 4 | 56 | 9.22e-07 | 1.212e-05 |
355 | CELL GROWTH | 5 | 135 | 9.32e-07 | 1.222e-05 |
356 | GLIAL CELL DIFFERENTIATION | 5 | 136 | 9.666e-07 | 1.263e-05 |
357 | ENDOCARDIAL CUSHION FORMATION | 3 | 15 | 9.876e-07 | 1.276e-05 |
358 | MORPHOGENESIS OF AN EPITHELIAL FOLD | 3 | 15 | 9.876e-07 | 1.276e-05 |
359 | REGULATION OF CELL PROLIFERATION INVOLVED IN HEART MORPHOGENESIS | 3 | 15 | 9.876e-07 | 1.276e-05 |
360 | STRIATED MUSCLE CELL PROLIFERATION | 3 | 15 | 9.876e-07 | 1.276e-05 |
361 | POSITIVE REGULATION OF TRANSFERASE ACTIVITY | 8 | 616 | 1.023e-06 | 1.319e-05 |
362 | NEGATIVE REGULATION OF CELL CELL ADHESION | 5 | 138 | 1.039e-06 | 1.332e-05 |
363 | PLACENTA DEVELOPMENT | 5 | 138 | 1.039e-06 | 1.332e-05 |
364 | NON CANONICAL WNT SIGNALING PATHWAY | 5 | 140 | 1.116e-06 | 1.426e-05 |
365 | REGULATION OF GLIAL CELL DIFFERENTIATION | 4 | 59 | 1.139e-06 | 1.452e-05 |
366 | CHONDROCYTE DIFFERENTIATION | 4 | 60 | 1.22e-06 | 1.55e-05 |
367 | SEX DIFFERENTIATION | 6 | 266 | 1.225e-06 | 1.553e-05 |
368 | NEGATIVE REGULATION OF CELL CYCLE | 7 | 433 | 1.297e-06 | 1.64e-05 |
369 | EMBRYONIC DIGIT MORPHOGENESIS | 4 | 61 | 1.304e-06 | 1.644e-05 |
370 | CARDIAC VENTRICLE MORPHOGENESIS | 4 | 62 | 1.393e-06 | 1.749e-05 |
371 | REGULATION OF CELL DIVISION | 6 | 272 | 1.394e-06 | 1.749e-05 |
372 | MALE SEX DIFFERENTIATION | 5 | 148 | 1.468e-06 | 1.836e-05 |
373 | POSITIVE REGULATION OF EXTRACELLULAR MATRIX ORGANIZATION | 3 | 17 | 1.473e-06 | 1.838e-05 |
374 | ACTIVATION OF PROTEIN KINASE ACTIVITY | 6 | 279 | 1.616e-06 | 2.01e-05 |
375 | REGULATION OF HORMONE BIOSYNTHETIC PROCESS | 3 | 18 | 1.766e-06 | 2.18e-05 |
376 | PERICARDIUM DEVELOPMENT | 3 | 18 | 1.766e-06 | 2.18e-05 |
377 | NEPHRON TUBULE FORMATION | 3 | 18 | 1.766e-06 | 2.18e-05 |
378 | LENS DEVELOPMENT IN CAMERA TYPE EYE | 4 | 66 | 1.793e-06 | 2.207e-05 |
379 | PROTEIN LOCALIZATION TO NUCLEUS | 5 | 156 | 1.903e-06 | 2.336e-05 |
380 | POSITIVE REGULATION OF ENDOTHELIAL CELL PROLIFERATION | 4 | 68 | 2.022e-06 | 2.476e-05 |
381 | CELLULAR RESPONSE TO ORGANIC CYCLIC COMPOUND | 7 | 465 | 2.083e-06 | 2.544e-05 |
382 | MUSCLE CELL PROLIFERATION | 3 | 19 | 2.096e-06 | 2.553e-05 |
383 | REGENERATION | 5 | 161 | 2.222e-06 | 2.7e-05 |
384 | WOUND HEALING | 7 | 470 | 2.236e-06 | 2.703e-05 |
385 | REGULATION OF PROTEIN SERINE THREONINE KINASE ACTIVITY | 7 | 470 | 2.236e-06 | 2.703e-05 |
386 | TRACHEA DEVELOPMENT | 3 | 20 | 2.463e-06 | 2.962e-05 |
387 | BRANCHING INVOLVED IN MAMMARY GLAND DUCT MORPHOGENESIS | 3 | 20 | 2.463e-06 | 2.962e-05 |
388 | POSITIVE REGULATION OF KINASE ACTIVITY | 7 | 482 | 2.643e-06 | 3.169e-05 |
389 | EXTRACELLULAR STRUCTURE ORGANIZATION | 6 | 304 | 2.655e-06 | 3.176e-05 |
390 | POSITIVE REGULATION OF PROTEIN BINDING | 4 | 73 | 2.69e-06 | 3.209e-05 |
391 | REGULATION OF PROTEIN TARGETING | 6 | 307 | 2.81e-06 | 3.344e-05 |
392 | REGULATION OF STEROID METABOLIC PROCESS | 4 | 74 | 2.841e-06 | 3.372e-05 |
393 | POSITIVE REGULATION OF NEUROBLAST PROLIFERATION | 3 | 21 | 2.871e-06 | 3.382e-05 |
394 | LEFT RIGHT PATTERN FORMATION | 3 | 21 | 2.871e-06 | 3.382e-05 |
395 | POSITIVE REGULATION OF ADHERENS JUNCTION ORGANIZATION | 3 | 21 | 2.871e-06 | 3.382e-05 |
396 | ODONTOGENESIS OF DENTIN CONTAINING TOOTH | 4 | 75 | 2.998e-06 | 3.514e-05 |
397 | NEURAL CREST CELL DIFFERENTIATION | 4 | 75 | 2.998e-06 | 3.514e-05 |
398 | REGULATION OF CELL SUBSTRATE ADHESION | 5 | 173 | 3.162e-06 | 3.697e-05 |
399 | EMBRYONIC PLACENTA MORPHOGENESIS | 3 | 22 | 3.322e-06 | 3.864e-05 |
400 | POSITIVE REGULATION OF MESONEPHROS DEVELOPMENT | 3 | 22 | 3.322e-06 | 3.864e-05 |
401 | RESPONSE TO ACID CHEMICAL | 6 | 319 | 3.506e-06 | 4.068e-05 |
402 | PHOSPHATE CONTAINING COMPOUND METABOLIC PROCESS | 12 | 1977 | 3.546e-06 | 4.104e-05 |
403 | IMMUNE SYSTEM PROCESS | 12 | 1984 | 3.68e-06 | 4.249e-05 |
404 | NEGATIVE REGULATION OF PROTEIN BINDING | 4 | 79 | 3.693e-06 | 4.253e-05 |
405 | NEGATIVE REGULATION OF LIPID METABOLIC PROCESS | 4 | 80 | 3.883e-06 | 4.45e-05 |
406 | CELLULAR RESPONSE TO MECHANICAL STIMULUS | 4 | 80 | 3.883e-06 | 4.45e-05 |
407 | POSITIVE REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION | 7 | 514 | 4.039e-06 | 4.618e-05 |
408 | METANEPHROS DEVELOPMENT | 4 | 81 | 4.081e-06 | 4.654e-05 |
409 | EMBRYONIC CAMERA TYPE EYE MORPHOGENESIS | 3 | 24 | 4.358e-06 | 4.933e-05 |
410 | POSITIVE REGULATION OF CELL JUNCTION ASSEMBLY | 3 | 24 | 4.358e-06 | 4.933e-05 |
411 | NEGATIVE REGULATION OF MYOBLAST DIFFERENTIATION | 3 | 24 | 4.358e-06 | 4.933e-05 |
412 | POSITIVE REGULATION OF DNA METABOLIC PROCESS | 5 | 185 | 4.39e-06 | 4.958e-05 |
413 | RESPONSE TO METAL ION | 6 | 333 | 4.488e-06 | 5.056e-05 |
414 | REGULATION OF HYDROLASE ACTIVITY | 10 | 1327 | 4.75e-06 | 5.339e-05 |
415 | CARDIAC SEPTUM DEVELOPMENT | 4 | 85 | 4.949e-06 | 5.509e-05 |
416 | EPITHELIAL TUBE BRANCHING INVOLVED IN LUNG MORPHOGENESIS | 3 | 25 | 4.947e-06 | 5.509e-05 |
417 | REGULATION OF TRANSFORMING GROWTH FACTOR BETA PRODUCTION | 3 | 25 | 4.947e-06 | 5.509e-05 |
418 | POSITIVE REGULATION OF CHROMATIN MODIFICATION | 4 | 85 | 4.949e-06 | 5.509e-05 |
419 | REGULATION OF DNA METABOLIC PROCESS | 6 | 340 | 5.057e-06 | 5.616e-05 |
420 | NEGATIVE REGULATION OF NEURON DIFFERENTIATION | 5 | 191 | 5.13e-06 | 5.684e-05 |
421 | CELL CELL SIGNALING | 8 | 767 | 5.236e-06 | 5.787e-05 |
422 | TISSUE REMODELING | 4 | 87 | 5.43e-06 | 5.987e-05 |
423 | NEGATIVE REGULATION OF GLIAL CELL DIFFERENTIATION | 3 | 26 | 5.588e-06 | 6.103e-05 |
424 | REGULATION OF MESONEPHROS DEVELOPMENT | 3 | 26 | 5.588e-06 | 6.103e-05 |
425 | HEART GROWTH | 3 | 26 | 5.588e-06 | 6.103e-05 |
426 | REGULATION OF HORMONE METABOLIC PROCESS | 3 | 26 | 5.588e-06 | 6.103e-05 |
427 | NEURON PROJECTION DEVELOPMENT | 7 | 545 | 5.934e-06 | 6.464e-05 |
428 | EPITHELIAL CELL PROLIFERATION | 4 | 89 | 5.946e-06 | 6.464e-05 |
429 | AXIS SPECIFICATION | 4 | 90 | 6.216e-06 | 6.711e-05 |
430 | REGULATION OF CELL MATRIX ADHESION | 4 | 90 | 6.216e-06 | 6.711e-05 |
431 | REGULATION OF GLIOGENESIS | 4 | 90 | 6.216e-06 | 6.711e-05 |
432 | REGULATION OF ASTROCYTE DIFFERENTIATION | 3 | 27 | 6.28e-06 | 6.733e-05 |
433 | RESPONSE TO LITHIUM ION | 3 | 27 | 6.28e-06 | 6.733e-05 |
434 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER INVOLVED IN CELLULAR RESPONSE TO CHEMICAL STIMULUS | 3 | 27 | 6.28e-06 | 6.733e-05 |
435 | DOPAMINERGIC NEURON DIFFERENTIATION | 3 | 28 | 7.028e-06 | 7.5e-05 |
436 | METANEPHROS MORPHOGENESIS | 3 | 28 | 7.028e-06 | 7.5e-05 |
437 | REGULATION OF DNA BINDING | 4 | 93 | 7.084e-06 | 7.542e-05 |
438 | NEGATIVE REGULATION OF MOLECULAR FUNCTION | 9 | 1079 | 7.257e-06 | 7.709e-05 |
439 | RESPONSE TO WOUNDING | 7 | 563 | 7.341e-06 | 7.781e-05 |
440 | TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 4 | 95 | 7.709e-06 | 8.153e-05 |
441 | REGULATION OF CARDIAC MUSCLE CELL PROLIFERATION | 3 | 29 | 7.832e-06 | 8.245e-05 |
442 | POSITIVE REGULATION OF CARDIAC MUSCLE TISSUE DEVELOPMENT | 3 | 29 | 7.832e-06 | 8.245e-05 |
443 | POSITIVE REGULATION OF CYTOKINE PRODUCTION | 6 | 370 | 8.203e-06 | 8.616e-05 |
444 | NEGATIVE REGULATION OF CYTOKINE PRODUCTION | 5 | 211 | 8.329e-06 | 8.728e-05 |
445 | REGULATION OF ENDOTHELIAL CELL PROLIFERATION | 4 | 98 | 8.724e-06 | 9.121e-05 |
446 | POSITIVE REGULATION OF CELL SUBSTRATE ADHESION | 4 | 99 | 9.082e-06 | 9.476e-05 |
447 | REGULATION OF SMOOTH MUSCLE CELL PROLIFERATION | 4 | 100 | 9.452e-06 | 9.839e-05 |
448 | REGULATION OF INTRACELLULAR PROTEIN TRANSPORT | 6 | 381 | 9.693e-06 | 0.0001007 |
449 | REGULATION OF TRANSPORT | 11 | 1804 | 1.04e-05 | 0.0001078 |
450 | PROTEIN LOCALIZATION | 11 | 1805 | 1.046e-05 | 0.0001081 |
451 | EMBRYONIC AXIS SPECIFICATION | 3 | 33 | 1.165e-05 | 0.0001194 |
452 | REGULATION OF T CELL APOPTOTIC PROCESS | 3 | 33 | 1.165e-05 | 0.0001194 |
453 | EMBRYONIC DIGESTIVE TRACT DEVELOPMENT | 3 | 33 | 1.165e-05 | 0.0001194 |
454 | EMBRYONIC EYE MORPHOGENESIS | 3 | 33 | 1.165e-05 | 0.0001194 |
455 | REGULATION OF FAT CELL DIFFERENTIATION | 4 | 106 | 1.191e-05 | 0.0001218 |
456 | ORGAN FORMATION | 3 | 34 | 1.277e-05 | 0.0001303 |
457 | NEGATIVE REGULATION OF PROTEIN MODIFICATION PROCESS | 7 | 616 | 1.319e-05 | 0.0001343 |
458 | SIGNAL TRANSDUCTION BY PROTEIN PHOSPHORYLATION | 6 | 404 | 1.352e-05 | 0.0001374 |
459 | EMBRYONIC CAMERA TYPE EYE DEVELOPMENT | 3 | 35 | 1.395e-05 | 0.0001414 |
460 | EAR MORPHOGENESIS | 4 | 112 | 1.481e-05 | 0.0001498 |
461 | REGULATION OF TRANSCRIPTION REGULATORY REGION DNA BINDING | 3 | 36 | 1.521e-05 | 0.0001535 |
462 | MULTI ORGANISM REPRODUCTIVE PROCESS | 8 | 891 | 1.567e-05 | 0.0001578 |
463 | CELL PART MORPHOGENESIS | 7 | 633 | 1.573e-05 | 0.0001581 |
464 | PROTEIN COMPLEX SUBUNIT ORGANIZATION | 10 | 1527 | 1.649e-05 | 0.0001654 |
465 | NEGATIVE REGULATION OF GLIOGENESIS | 3 | 37 | 1.653e-05 | 0.0001654 |
466 | RESPONSE TO FIBROBLAST GROWTH FACTOR | 4 | 116 | 1.701e-05 | 0.0001698 |
467 | NEGATIVE REGULATION OF CYTOPLASMIC TRANSPORT | 4 | 117 | 1.759e-05 | 0.0001749 |
468 | NEGATIVE REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 4 | 117 | 1.759e-05 | 0.0001749 |
469 | POSITIVE REGULATION OF CELL CYCLE PROCESS | 5 | 247 | 1.784e-05 | 0.000177 |
470 | COLLAGEN FIBRIL ORGANIZATION | 3 | 38 | 1.794e-05 | 0.0001772 |
471 | BONE MINERALIZATION | 3 | 38 | 1.794e-05 | 0.0001772 |
472 | REGULATION OF PEPTIDYL SERINE PHOSPHORYLATION | 4 | 118 | 1.819e-05 | 0.0001794 |
473 | POSITIVE REGULATION OF NUCLEOCYTOPLASMIC TRANSPORT | 4 | 121 | 2.009e-05 | 0.0001976 |
474 | REGULATION OF EPITHELIAL CELL DIFFERENTIATION | 4 | 122 | 2.075e-05 | 0.0002037 |
475 | LEUKOCYTE CELL CELL ADHESION | 5 | 255 | 2.079e-05 | 0.0002037 |
476 | NEGATIVE REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 6 | 437 | 2.108e-05 | 0.0002061 |
477 | CELLULAR MACROMOLECULE LOCALIZATION | 9 | 1234 | 2.139e-05 | 0.0002086 |
478 | T CELL DIFFERENTIATION | 4 | 123 | 2.143e-05 | 0.0002086 |
479 | CELLULAR RESPONSE TO ABIOTIC STIMULUS | 5 | 263 | 2.411e-05 | 0.0002342 |
480 | NEGATIVE REGULATION OF BMP SIGNALING PATHWAY | 3 | 42 | 2.432e-05 | 0.0002343 |
481 | POSITIVE REGULATION OF NEURAL PRECURSOR CELL PROLIFERATION | 3 | 42 | 2.432e-05 | 0.0002343 |
482 | REGULATION OF HEART GROWTH | 3 | 42 | 2.432e-05 | 0.0002343 |
483 | GENITALIA DEVELOPMENT | 3 | 42 | 2.432e-05 | 0.0002343 |
484 | CELLULAR RESPONSE TO EXTERNAL STIMULUS | 5 | 264 | 2.456e-05 | 0.0002356 |
485 | AGING | 5 | 264 | 2.456e-05 | 0.0002356 |
486 | REGULATION OF LIPID BIOSYNTHETIC PROCESS | 4 | 128 | 2.506e-05 | 0.0002399 |
487 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO NUCLEUS | 4 | 129 | 2.584e-05 | 0.0002469 |
488 | NEGATIVE REGULATION OF CELLULAR COMPONENT ORGANIZATION | 7 | 684 | 2.592e-05 | 0.0002471 |
489 | NEGATIVE REGULATION OF STEM CELL DIFFERENTIATION | 3 | 43 | 2.612e-05 | 0.0002485 |
490 | NEURON DEVELOPMENT | 7 | 687 | 2.666e-05 | 0.0002531 |
491 | SINGLE ORGANISM CELL ADHESION | 6 | 459 | 2.779e-05 | 0.0002634 |
492 | MAINTENANCE OF CELL NUMBER | 4 | 132 | 2.828e-05 | 0.0002675 |
493 | NEGATIVE REGULATION OF RESPONSE TO EXTERNAL STIMULUS | 5 | 274 | 2.934e-05 | 0.000277 |
494 | TAXIS | 6 | 464 | 2.953e-05 | 0.0002782 |
495 | SPROUTING ANGIOGENESIS | 3 | 45 | 2.998e-05 | 0.0002812 |
496 | VENTRICULAR CARDIAC MUSCLE TISSUE DEVELOPMENT | 3 | 45 | 2.998e-05 | 0.0002812 |
497 | MUSCLE ORGAN DEVELOPMENT | 5 | 277 | 3.091e-05 | 0.0002888 |
498 | NEGATIVE REGULATION OF CELLULAR PROTEIN LOCALIZATION | 4 | 135 | 3.089e-05 | 0.0002888 |
499 | EMBRYONIC CRANIAL SKELETON MORPHOGENESIS | 3 | 46 | 3.204e-05 | 0.0002988 |
500 | REGULATION OF PHOSPHATIDYLINOSITOL 3 KINASE SIGNALING | 4 | 138 | 3.366e-05 | 0.0003127 |
501 | REGULATION OF LIPID METABOLIC PROCESS | 5 | 282 | 3.367e-05 | 0.0003127 |
502 | POSITIVE REGULATION OF NEURON APOPTOTIC PROCESS | 3 | 47 | 3.42e-05 | 0.000317 |
503 | RESPONSE TO INORGANIC SUBSTANCE | 6 | 479 | 3.53e-05 | 0.0003265 |
504 | REGULATION OF CYTOPLASMIC TRANSPORT | 6 | 481 | 3.613e-05 | 0.0003335 |
505 | CELL DEATH | 8 | 1001 | 3.625e-05 | 0.000334 |
506 | REGULATION OF MYOBLAST DIFFERENTIATION | 3 | 48 | 3.644e-05 | 0.0003345 |
507 | ANTERIOR POSTERIOR AXIS SPECIFICATION | 3 | 48 | 3.644e-05 | 0.0003345 |
508 | TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 7 | 724 | 3.729e-05 | 0.0003415 |
509 | REGULATION OF DEVELOPMENTAL GROWTH | 5 | 289 | 3.785e-05 | 0.000346 |
510 | NEGATIVE REGULATION OF INTRACELLULAR TRANSPORT | 4 | 143 | 3.87e-05 | 0.0003531 |
511 | REGULATION OF RESPONSE TO DNA DAMAGE STIMULUS | 4 | 145 | 4.086e-05 | 0.000372 |
512 | REGULATION OF ADHERENS JUNCTION ORGANIZATION | 3 | 50 | 4.122e-05 | 0.0003739 |
513 | ENDODERM FORMATION | 3 | 50 | 4.122e-05 | 0.0003739 |
514 | ARTERY MORPHOGENESIS | 3 | 51 | 4.376e-05 | 0.0003961 |
515 | POSITIVE REGULATION OF CELL GROWTH | 4 | 148 | 4.426e-05 | 0.0003999 |
516 | BIOLOGICAL ADHESION | 8 | 1032 | 4.507e-05 | 0.0004064 |
517 | NEURAL TUBE DEVELOPMENT | 4 | 149 | 4.544e-05 | 0.0004089 |
518 | NEGATIVE REGULATION OF RESPONSE TO DNA DAMAGE STIMULUS | 3 | 52 | 4.64e-05 | 0.0004168 |
519 | POSITIVE REGULATION OF CHROMOSOME ORGANIZATION | 4 | 150 | 4.664e-05 | 0.0004181 |
520 | POSITIVE REGULATION OF CELL PROJECTION ORGANIZATION | 5 | 303 | 4.741e-05 | 0.0004243 |
521 | REGULATION OF CHROMATIN ORGANIZATION | 4 | 152 | 4.911e-05 | 0.0004378 |
522 | POSITIVE REGULATION OF WNT SIGNALING PATHWAY | 4 | 152 | 4.911e-05 | 0.0004378 |
523 | POSITIVE REGULATION OF NEURON DIFFERENTIATION | 5 | 306 | 4.969e-05 | 0.0004421 |
524 | REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 4 | 153 | 5.039e-05 | 0.0004466 |
525 | PALLIUM DEVELOPMENT | 4 | 153 | 5.039e-05 | 0.0004466 |
526 | REGULATION OF LYMPHOCYTE APOPTOTIC PROCESS | 3 | 54 | 5.198e-05 | 0.0004598 |
527 | BONE DEVELOPMENT | 4 | 156 | 5.435e-05 | 0.0004789 |
528 | CELLULAR RESPONSE TO INORGANIC SUBSTANCE | 4 | 156 | 5.435e-05 | 0.0004789 |
529 | REGULATION OF HEMOPOIESIS | 5 | 314 | 5.616e-05 | 0.000494 |
530 | POSITIVE REGULATION OF EPITHELIAL CELL DIFFERENTIATION | 3 | 57 | 6.115e-05 | 0.0005359 |
531 | REGULATION OF CYTOKINE PRODUCTION INVOLVED IN IMMUNE RESPONSE | 3 | 57 | 6.115e-05 | 0.0005359 |
532 | REGULATION OF NUCLEAR DIVISION | 4 | 163 | 6.447e-05 | 0.0005628 |
533 | CELLULAR RESPONSE TO BIOTIC STIMULUS | 4 | 163 | 6.447e-05 | 0.0005628 |
534 | NEGATIVE REGULATION OF PROTEIN METABOLIC PROCESS | 8 | 1087 | 6.516e-05 | 0.0005678 |
535 | POSITIVE REGULATION OF DNA BIOSYNTHETIC PROCESS | 3 | 59 | 6.782e-05 | 0.0005899 |
536 | CHROMATIN MODIFICATION | 6 | 539 | 6.808e-05 | 0.000591 |
537 | NEGATIVE REGULATION OF PHOSPHORUS METABOLIC PROCESS | 6 | 541 | 6.949e-05 | 0.000601 |
538 | NEGATIVE REGULATION OF PHOSPHATE METABOLIC PROCESS | 6 | 541 | 6.949e-05 | 0.000601 |
539 | CELLULAR RESPONSE TO OXYGEN CONTAINING COMPOUND | 7 | 799 | 6.971e-05 | 0.0006017 |
540 | POSITIVE REGULATION OF SMOOTH MUSCLE CELL PROLIFERATION | 3 | 60 | 7.133e-05 | 0.0006135 |
541 | OLIGODENDROCYTE DIFFERENTIATION | 3 | 60 | 7.133e-05 | 0.0006135 |
542 | REGULATION OF VIRAL TRANSCRIPTION | 3 | 61 | 7.495e-05 | 0.0006434 |
543 | NEGATIVE REGULATION OF CELL GROWTH | 4 | 170 | 7.59e-05 | 0.0006504 |
544 | CELLULAR RESPONSE TO HORMONE STIMULUS | 6 | 552 | 7.767e-05 | 0.0006643 |
545 | SOMITOGENESIS | 3 | 62 | 7.869e-05 | 0.0006681 |
546 | POSITIVE REGULATION OF NUCLEAR DIVISION | 3 | 62 | 7.869e-05 | 0.0006681 |
547 | POSITIVE REGULATION OF PHOSPHATIDYLINOSITOL 3 KINASE SIGNALING | 3 | 62 | 7.869e-05 | 0.0006681 |
548 | EMBRYONIC HEART TUBE MORPHOGENESIS | 3 | 62 | 7.869e-05 | 0.0006681 |
549 | PROTEIN LOCALIZATION TO ORGANELLE | 6 | 556 | 8.083e-05 | 0.0006851 |
550 | CELLULAR RESPONSE TO ACID CHEMICAL | 4 | 175 | 8.493e-05 | 0.0007172 |
551 | HOMEOSTASIS OF NUMBER OF CELLS | 4 | 175 | 8.493e-05 | 0.0007172 |
552 | RESPONSE TO CORTICOSTEROID | 4 | 176 | 8.683e-05 | 0.0007319 |
553 | CELLULAR RESPONSE TO RETINOIC ACID | 3 | 65 | 9.064e-05 | 0.0007599 |
554 | REGULATION OF CHEMOKINE PRODUCTION | 3 | 65 | 9.064e-05 | 0.0007599 |
555 | REGULATION OF RESPONSE TO OXIDATIVE STRESS | 3 | 65 | 9.064e-05 | 0.0007599 |
556 | NEGATIVE REGULATION OF CELLULAR RESPONSE TO TRANSFORMING GROWTH FACTOR BETA STIMULUS | 3 | 66 | 9.487e-05 | 0.0007911 |
557 | FOREBRAIN GENERATION OF NEURONS | 3 | 66 | 9.487e-05 | 0.0007911 |
558 | NEGATIVE REGULATION OF TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 3 | 66 | 9.487e-05 | 0.0007911 |
559 | POSITIVE REGULATION OF HORMONE METABOLIC PROCESS | 2 | 11 | 9.581e-05 | 0.0007918 |
560 | NEGATIVE REGULATION OF FIBROBLAST GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 2 | 11 | 9.581e-05 | 0.0007918 |
561 | RESPONSE TO FOLLICLE STIMULATING HORMONE | 2 | 11 | 9.581e-05 | 0.0007918 |
562 | PROSTATE GLAND GROWTH | 2 | 11 | 9.581e-05 | 0.0007918 |
563 | PROSTATE GLANDULAR ACINUS DEVELOPMENT | 2 | 11 | 9.581e-05 | 0.0007918 |
564 | RESPONSE TO KETONE | 4 | 182 | 9.885e-05 | 0.0008155 |
565 | POSITIVE REGULATION OF NEURON DEATH | 3 | 67 | 9.922e-05 | 0.0008157 |
566 | NEURON FATE COMMITMENT | 3 | 67 | 9.922e-05 | 0.0008157 |
567 | POSITIVE REGULATION OF CELLULAR PROTEIN LOCALIZATION | 5 | 360 | 0.0001071 | 0.0008787 |
568 | RESPONSE TO ACTIVITY | 3 | 69 | 0.0001083 | 0.0008874 |
569 | CARTILAGE MORPHOGENESIS | 2 | 12 | 0.0001149 | 0.0009296 |
570 | REGULATION OF VITAMIN METABOLIC PROCESS | 2 | 12 | 0.0001149 | 0.0009296 |
571 | REGULATION OF THYMOCYTE APOPTOTIC PROCESS | 2 | 12 | 0.0001149 | 0.0009296 |
572 | POSITIVE REGULATION OF SMAD PROTEIN IMPORT INTO NUCLEUS | 2 | 12 | 0.0001149 | 0.0009296 |
573 | MYELOID CELL DIFFERENTIATION | 4 | 189 | 0.0001144 | 0.0009296 |
574 | POSITIVE REGULATION OF ASTROCYTE DIFFERENTIATION | 2 | 12 | 0.0001149 | 0.0009296 |
575 | NEGATIVE REGULATION OF RECEPTOR BINDING | 2 | 12 | 0.0001149 | 0.0009296 |
576 | GAMETE GENERATION | 6 | 595 | 0.0001174 | 0.0009481 |
577 | NEGATIVE REGULATION OF NUCLEOCYTOPLASMIC TRANSPORT | 3 | 71 | 0.000118 | 0.0009496 |
578 | CELL FATE SPECIFICATION | 3 | 71 | 0.000118 | 0.0009496 |
579 | REGULATION OF NEURON APOPTOTIC PROCESS | 4 | 192 | 0.0001215 | 0.0009766 |
580 | DEVELOPMENTAL MATURATION | 4 | 193 | 0.000124 | 0.0009946 |
581 | NEGATIVE REGULATION OF IMMUNE SYSTEM PROCESS | 5 | 372 | 0.0001249 | 0.001 |
582 | PANCREAS DEVELOPMENT | 3 | 73 | 0.0001281 | 0.001023 |
583 | REGULATION OF ORGAN GROWTH | 3 | 73 | 0.0001281 | 0.001023 |
584 | CELL CELL ADHESION | 6 | 608 | 0.0001321 | 0.001053 |
585 | NEURONAL STEM CELL DIVISION | 2 | 13 | 0.0001356 | 0.001059 |
586 | NEGATIVE REGULATION OF OLIGODENDROCYTE DIFFERENTIATION | 2 | 13 | 0.0001356 | 0.001059 |
587 | REGULATION OF STRESS ACTIVATED PROTEIN KINASE SIGNALING CASCADE | 4 | 197 | 0.0001342 | 0.001059 |
588 | LEFT RIGHT AXIS SPECIFICATION | 2 | 13 | 0.0001356 | 0.001059 |
589 | CELLULAR RESPONSE TO HEPATOCYTE GROWTH FACTOR STIMULUS | 2 | 13 | 0.0001356 | 0.001059 |
590 | HEART VALVE FORMATION | 2 | 13 | 0.0001356 | 0.001059 |
591 | CARDIOBLAST DIFFERENTIATION | 2 | 13 | 0.0001356 | 0.001059 |
592 | RESPONSE TO HEPATOCYTE GROWTH FACTOR | 2 | 13 | 0.0001356 | 0.001059 |
593 | NEUROBLAST DIVISION | 2 | 13 | 0.0001356 | 0.001059 |
594 | GLIAL CELL FATE COMMITMENT | 2 | 13 | 0.0001356 | 0.001059 |
595 | REGULATION OF BICELLULAR TIGHT JUNCTION ASSEMBLY | 2 | 13 | 0.0001356 | 0.001059 |
596 | NEGATIVE REGULATION OF DNA DAMAGE RESPONSE SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR | 2 | 13 | 0.0001356 | 0.001059 |
597 | ARTERY DEVELOPMENT | 3 | 75 | 0.0001389 | 0.00108 |
598 | BIOMINERAL TISSUE DEVELOPMENT | 3 | 75 | 0.0001389 | 0.00108 |
599 | NEGATIVE REGULATION OF MITOTIC CELL CYCLE | 4 | 199 | 0.0001395 | 0.001084 |
600 | REGULATION OF INTRACELLULAR TRANSPORT | 6 | 621 | 0.0001483 | 0.00115 |
601 | CELL PROJECTION ORGANIZATION | 7 | 902 | 0.0001489 | 0.001153 |
602 | REGULATION OF BMP SIGNALING PATHWAY | 3 | 77 | 0.0001502 | 0.001161 |
603 | POSITIVE REGULATION OF HYDROLASE ACTIVITY | 7 | 905 | 0.0001521 | 0.001173 |
604 | CELL MIGRATION INVOLVED IN HEART DEVELOPMENT | 2 | 14 | 0.0001581 | 0.001196 |
605 | RENAL VESICLE DEVELOPMENT | 2 | 14 | 0.0001581 | 0.001196 |
606 | POSITIVE REGULATION OF MEIOTIC CELL CYCLE | 2 | 14 | 0.0001581 | 0.001196 |
607 | REGULATION OF SYMBIOSIS ENCOMPASSING MUTUALISM THROUGH PARASITISM | 4 | 205 | 0.0001564 | 0.001196 |
608 | REGULATION OF GLOMERULUS DEVELOPMENT | 2 | 14 | 0.0001581 | 0.001196 |
609 | METANEPHRIC MESENCHYME DEVELOPMENT | 2 | 14 | 0.0001581 | 0.001196 |
610 | POSITIVE REGULATION OF TRANSCRIPTION REGULATORY REGION DNA BINDING | 2 | 14 | 0.0001581 | 0.001196 |
611 | REGULATION OF PROTEIN KINASE C SIGNALING | 2 | 14 | 0.0001581 | 0.001196 |
612 | NEURON PROJECTION GUIDANCE | 4 | 205 | 0.0001564 | 0.001196 |
613 | REGULATION OF EXTRACELLULAR MATRIX DISASSEMBLY | 2 | 14 | 0.0001581 | 0.001196 |
614 | ADENOHYPOPHYSIS DEVELOPMENT | 2 | 14 | 0.0001581 | 0.001196 |
615 | MIDGUT DEVELOPMENT | 2 | 14 | 0.0001581 | 0.001196 |
616 | REGULATION OF LEUKOCYTE APOPTOTIC PROCESS | 3 | 79 | 0.000162 | 0.001222 |
617 | BONE MORPHOGENESIS | 3 | 79 | 0.000162 | 0.001222 |
618 | POSITIVE REGULATION OF MAP KINASE ACTIVITY | 4 | 207 | 0.0001623 | 0.001222 |
619 | NEGATIVE REGULATION OF VASCULATURE DEVELOPMENT | 3 | 80 | 0.0001682 | 0.001264 |
620 | LYMPHOCYTE DIFFERENTIATION | 4 | 209 | 0.0001684 | 0.001264 |
621 | RESPONSE TO MECHANICAL STIMULUS | 4 | 210 | 0.0001715 | 0.001285 |
622 | POSITIVE REGULATION OF PROTEIN SECRETION | 4 | 211 | 0.0001747 | 0.001305 |
623 | REGULATION OF FIBROBLAST PROLIFERATION | 3 | 81 | 0.0001745 | 0.001305 |
624 | REGULATION OF RESPONSE TO EXTERNAL STIMULUS | 7 | 926 | 0.0001753 | 0.001307 |
625 | MULTI MULTICELLULAR ORGANISM PROCESS | 4 | 213 | 0.0001811 | 0.001348 |
626 | POSITIVE REGULATION OF ENDOTHELIAL CELL DIFFERENTIATION | 2 | 15 | 0.0001823 | 0.001351 |
627 | OTIC VESICLE DEVELOPMENT | 2 | 15 | 0.0001823 | 0.001351 |
628 | POSITIVE REGULATION OF T CELL APOPTOTIC PROCESS | 2 | 15 | 0.0001823 | 0.001351 |
629 | RESPONSE TO PEPTIDE | 5 | 404 | 0.0001836 | 0.001358 |
630 | POSITIVE REGULATION OF TRANSPORT | 7 | 936 | 0.0001873 | 0.001384 |
631 | POSITIVE REGULATION OF HOMEOSTATIC PROCESS | 4 | 216 | 0.0001911 | 0.001407 |
632 | DEVELOPMENT OF PRIMARY SEXUAL CHARACTERISTICS | 4 | 216 | 0.0001911 | 0.001407 |
633 | TISSUE MIGRATION | 3 | 84 | 0.0001944 | 0.001429 |
634 | CELLULAR RESPONSE TO STEROID HORMONE STIMULUS | 4 | 218 | 0.0001979 | 0.001453 |
635 | REGULATION OF STRIATED MUSCLE CELL DIFFERENTIATION | 3 | 85 | 0.0002013 | 0.001475 |
636 | REGULATION OF SMAD PROTEIN IMPORT INTO NUCLEUS | 2 | 16 | 0.0002082 | 0.001511 |
637 | MORPHOGENESIS OF AN ENDOTHELIUM | 2 | 16 | 0.0002082 | 0.001511 |
638 | ORGAN INDUCTION | 2 | 16 | 0.0002082 | 0.001511 |
639 | APOPTOTIC PROCESS INVOLVED IN MORPHOGENESIS | 2 | 16 | 0.0002082 | 0.001511 |
640 | ATRIOVENTRICULAR VALVE MORPHOGENESIS | 2 | 16 | 0.0002082 | 0.001511 |
641 | BRANCHING INVOLVED IN SALIVARY GLAND MORPHOGENESIS | 2 | 16 | 0.0002082 | 0.001511 |
642 | CHROMATIN ORGANIZATION | 6 | 663 | 0.0002117 | 0.001534 |
643 | LEUKOCYTE PROLIFERATION | 3 | 88 | 0.000223 | 0.001612 |
644 | POSITIVE REGULATION OF PEPTIDYL SERINE PHOSPHORYLATION | 3 | 88 | 0.000223 | 0.001612 |
645 | NEGATIVE REGULATION OF PHOSPHORYLATION | 5 | 422 | 0.0002247 | 0.001621 |
646 | REGULATION OF GTPASE ACTIVITY | 6 | 673 | 0.0002295 | 0.001653 |
647 | SEGMENTATION | 3 | 89 | 0.0002306 | 0.001659 |
648 | NEGATIVE REGULATION OF KIDNEY DEVELOPMENT | 2 | 17 | 0.0002357 | 0.001677 |
649 | CELLULAR RESPONSE TO LITHIUM ION | 2 | 17 | 0.0002357 | 0.001677 |
650 | REGULATION OF RECEPTOR BINDING | 2 | 17 | 0.0002357 | 0.001677 |
651 | ESTABLISHMENT OF TISSUE POLARITY | 2 | 17 | 0.0002357 | 0.001677 |
652 | NEGATIVE REGULATION OF ANOIKIS | 2 | 17 | 0.0002357 | 0.001677 |
653 | REGULATION OF STEM CELL POPULATION MAINTENANCE | 2 | 17 | 0.0002357 | 0.001677 |
654 | NEGATIVE REGULATION OF CARDIAC MUSCLE TISSUE DEVELOPMENT | 2 | 17 | 0.0002357 | 0.001677 |
655 | NEGATIVE REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY | 3 | 90 | 0.0002384 | 0.001691 |
656 | MIDBRAIN DEVELOPMENT | 3 | 90 | 0.0002384 | 0.001691 |
657 | RESPONSE TO DRUG | 5 | 431 | 0.0002478 | 0.001755 |
658 | POSITIVE REGULATION OF NEURON PROJECTION DEVELOPMENT | 4 | 232 | 0.0002511 | 0.001775 |
659 | INNER EAR MORPHOGENESIS | 3 | 92 | 0.0002543 | 0.001796 |
660 | KIDNEY MESENCHYME DEVELOPMENT | 2 | 18 | 0.000265 | 0.001868 |
661 | REGULATION OF DNA BIOSYNTHETIC PROCESS | 3 | 94 | 0.000271 | 0.001905 |
662 | NEURAL TUBE FORMATION | 3 | 94 | 0.000271 | 0.001905 |
663 | NEGATIVE REGULATION OF INTRACELLULAR PROTEIN TRANSPORT | 3 | 95 | 0.0002796 | 0.001959 |
664 | REGULATION OF TRANSCRIPTION FACTOR IMPORT INTO NUCLEUS | 3 | 95 | 0.0002796 | 0.001959 |
665 | MYELOID LEUKOCYTE DIFFERENTIATION | 3 | 96 | 0.0002883 | 0.002014 |
666 | CARDIOCYTE DIFFERENTIATION | 3 | 96 | 0.0002883 | 0.002014 |
667 | REGULATION OF CARDIAC MUSCLE CELL DIFFERENTIATION | 2 | 19 | 0.0002959 | 0.002055 |
668 | POSITIVE REGULATION OF CARDIAC MUSCLE CELL PROLIFERATION | 2 | 19 | 0.0002959 | 0.002055 |
669 | ATRIOVENTRICULAR VALVE DEVELOPMENT | 2 | 19 | 0.0002959 | 0.002055 |
670 | POSITIVE REGULATION OF CHONDROCYTE DIFFERENTIATION | 2 | 19 | 0.0002959 | 0.002055 |
671 | POSITIVE REGULATION OF CELL CELL ADHESION | 4 | 243 | 0.0002995 | 0.002077 |
672 | NEGATIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 3 | 98 | 0.0003064 | 0.002121 |
673 | EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 3 | 99 | 0.0003157 | 0.002173 |
674 | REGULATION OF TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 3 | 99 | 0.0003157 | 0.002173 |
675 | REGULATION OF CELLULAR RESPONSE TO TRANSFORMING GROWTH FACTOR BETA STIMULUS | 3 | 99 | 0.0003157 | 0.002173 |
676 | RESPONSE TO CYTOKINE | 6 | 714 | 0.0003156 | 0.002173 |
677 | MODIFICATION OF MORPHOLOGY OR PHYSIOLOGY OF OTHER ORGANISM | 3 | 100 | 0.0003251 | 0.002231 |
678 | LIMBIC SYSTEM DEVELOPMENT | 3 | 100 | 0.0003251 | 0.002231 |
679 | POSITIVE REGULATION OF LYMPHOCYTE APOPTOTIC PROCESS | 2 | 20 | 0.0003285 | 0.002235 |
680 | NEGATIVE REGULATION OF BIOMINERAL TISSUE DEVELOPMENT | 2 | 20 | 0.0003285 | 0.002235 |
681 | METANEPHRIC EPITHELIUM DEVELOPMENT | 2 | 20 | 0.0003285 | 0.002235 |
682 | REGULATION OF SMOOTH MUSCLE CELL DIFFERENTIATION | 2 | 20 | 0.0003285 | 0.002235 |
683 | TONGUE DEVELOPMENT | 2 | 20 | 0.0003285 | 0.002235 |
684 | NEGATIVE REGULATION OF TRANSPORT | 5 | 458 | 0.000328 | 0.002235 |
685 | CELL DIVISION | 5 | 460 | 0.0003346 | 0.002271 |
686 | REGULATION OF PRODUCTION OF MOLECULAR MEDIATOR OF IMMUNE RESPONSE | 3 | 101 | 0.0003348 | 0.002271 |
687 | CELLULAR PROCESS INVOLVED IN REPRODUCTION IN MULTICELLULAR ORGANISM | 4 | 252 | 0.0003438 | 0.002325 |
688 | REGULATION OF NEURON DEATH | 4 | 252 | 0.0003438 | 0.002325 |
689 | SEXUAL REPRODUCTION | 6 | 730 | 0.0003555 | 0.0024 |
690 | METANEPHRIC NEPHRON MORPHOGENESIS | 2 | 21 | 0.0003628 | 0.002425 |
691 | ECTODERM DEVELOPMENT | 2 | 21 | 0.0003628 | 0.002425 |
692 | CELL AGGREGATION | 2 | 21 | 0.0003628 | 0.002425 |
693 | APOPTOTIC PROCESS INVOLVED IN DEVELOPMENT | 2 | 21 | 0.0003628 | 0.002425 |
694 | COCHLEA MORPHOGENESIS | 2 | 21 | 0.0003628 | 0.002425 |
695 | NEGATIVE REGULATION OF NEURAL PRECURSOR CELL PROLIFERATION | 2 | 21 | 0.0003628 | 0.002425 |
696 | CARTILAGE CONDENSATION | 2 | 21 | 0.0003628 | 0.002425 |
697 | POSITIVE REGULATION OF PROTEIN IMPORT | 3 | 104 | 0.0003648 | 0.002436 |
698 | MACROMOLECULAR COMPLEX ASSEMBLY | 8 | 1398 | 0.000373 | 0.002487 |
699 | CEREBRAL CORTEX DEVELOPMENT | 3 | 105 | 0.0003752 | 0.002498 |
700 | POSITIVE REGULATION OF INTRACELLULAR PROTEIN TRANSPORT | 4 | 258 | 0.0003759 | 0.002498 |
701 | REGULATION OF IMMUNE SYSTEM PROCESS | 8 | 1403 | 0.0003822 | 0.002537 |
702 | FAT CELL DIFFERENTIATION | 3 | 106 | 0.0003858 | 0.002557 |
703 | NEGATIVE REGULATION OF CYTOKINE PRODUCTION INVOLVED IN IMMUNE RESPONSE | 2 | 22 | 0.0003987 | 0.002617 |
704 | SEX DETERMINATION | 2 | 22 | 0.0003987 | 0.002617 |
705 | BETA CATENIN DESTRUCTION COMPLEX DISASSEMBLY | 2 | 22 | 0.0003987 | 0.002617 |
706 | MODULATION OF TRANSCRIPTION IN OTHER ORGANISM INVOLVED IN SYMBIOTIC INTERACTION | 2 | 22 | 0.0003987 | 0.002617 |
707 | PROTEIN LOCALIZATION TO CELL SURFACE | 2 | 22 | 0.0003987 | 0.002617 |
708 | RESPONSE TO RETINOIC ACID | 3 | 107 | 0.0003966 | 0.002617 |
709 | PLATELET DEGRANULATION | 3 | 107 | 0.0003966 | 0.002617 |
710 | POSITIVE REGULATION OF MULTICELLULAR ORGANISMAL METABOLIC PROCESS | 2 | 23 | 0.0004363 | 0.00284 |
711 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER IN RESPONSE TO STRESS | 2 | 23 | 0.0004363 | 0.00284 |
712 | REGULATION OF OSTEOBLAST PROLIFERATION | 2 | 23 | 0.0004363 | 0.00284 |
713 | ADRENAL GLAND DEVELOPMENT | 2 | 23 | 0.0004363 | 0.00284 |
714 | REGULATION OF SUPEROXIDE METABOLIC PROCESS | 2 | 23 | 0.0004363 | 0.00284 |
715 | POSITIVE REGULATION OF COLLAGEN METABOLIC PROCESS | 2 | 23 | 0.0004363 | 0.00284 |
716 | NEGATIVE REGULATION OF DNA METABOLIC PROCESS | 3 | 111 | 0.0004416 | 0.00287 |
717 | CELL CYCLE PROCESS | 7 | 1081 | 0.0004519 | 0.002932 |
718 | NEGATIVE REGULATION OF BLOOD VESSEL ENDOTHELIAL CELL MIGRATION | 2 | 24 | 0.0004756 | 0.003069 |
719 | RESPONSE TO STEROL | 2 | 24 | 0.0004756 | 0.003069 |
720 | REGULATION OF ODONTOGENESIS | 2 | 24 | 0.0004756 | 0.003069 |
721 | REGULATION OF ANOIKIS | 2 | 24 | 0.0004756 | 0.003069 |
722 | REGULATION OF ENDOTHELIAL CELL MIGRATION | 3 | 114 | 0.0004775 | 0.003077 |
723 | TRANSMEMBRANE RECEPTOR PROTEIN TYROSINE KINASE SIGNALING PATHWAY | 5 | 498 | 0.0004812 | 0.003097 |
724 | REGULATION OF CHROMOSOME ORGANIZATION | 4 | 278 | 0.0004983 | 0.003202 |
725 | REGULATION OF CYTOSKELETON ORGANIZATION | 5 | 502 | 0.0004991 | 0.003203 |
726 | CELLULAR RESPONSE TO EPIDERMAL GROWTH FACTOR STIMULUS | 2 | 25 | 0.0005165 | 0.003301 |
727 | LUNG CELL DIFFERENTIATION | 2 | 25 | 0.0005165 | 0.003301 |
728 | SPECIFICATION OF SYMMETRY | 3 | 117 | 0.0005151 | 0.003301 |
729 | POSITIVE REGULATION OF CYTOPLASMIC TRANSPORT | 4 | 282 | 0.0005258 | 0.003356 |
730 | DEVELOPMENTAL PROGRAMMED CELL DEATH | 2 | 26 | 0.0005591 | 0.003535 |
731 | NEGATIVE REGULATION OF STRIATED MUSCLE CELL DIFFERENTIATION | 2 | 26 | 0.0005591 | 0.003535 |
732 | HEART TRABECULA MORPHOGENESIS | 2 | 26 | 0.0005591 | 0.003535 |
733 | CYTOKINE PRODUCTION | 3 | 120 | 0.0005546 | 0.003535 |
734 | MESODERMAL CELL DIFFERENTIATION | 2 | 26 | 0.0005591 | 0.003535 |
735 | REGULATION OF P38MAPK CASCADE | 2 | 26 | 0.0005591 | 0.003535 |
736 | POSITIVE REGULATION OF VASCULAR ENDOTHELIAL GROWTH FACTOR PRODUCTION | 2 | 26 | 0.0005591 | 0.003535 |
737 | POSITIVE REGULATION OF PROTEIN SERINE THREONINE KINASE ACTIVITY | 4 | 289 | 0.0005766 | 0.00364 |
738 | PROTEIN COMPLEX BIOGENESIS | 7 | 1132 | 0.0005964 | 0.003755 |
739 | PROTEIN COMPLEX ASSEMBLY | 7 | 1132 | 0.0005964 | 0.003755 |
740 | REGULATION OF ENDOTHELIAL CELL DIFFERENTIATION | 2 | 27 | 0.0006033 | 0.003768 |
741 | POSITIVE REGULATION OF HEART GROWTH | 2 | 27 | 0.0006033 | 0.003768 |
742 | NEGATIVE REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO DNA DAMAGE | 2 | 27 | 0.0006033 | 0.003768 |
743 | LEUKOCYTE DIFFERENTIATION | 4 | 292 | 0.0005993 | 0.003768 |
744 | NEGATIVE REGULATION OF SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR | 2 | 27 | 0.0006033 | 0.003768 |
745 | SUBSTRATE DEPENDENT CELL MIGRATION | 2 | 27 | 0.0006033 | 0.003768 |
746 | STEROID HORMONE MEDIATED SIGNALING PATHWAY | 3 | 125 | 0.0006247 | 0.003897 |
747 | POSITIVE REGULATION OF LEUKOCYTE APOPTOTIC PROCESS | 2 | 28 | 0.0006492 | 0.004022 |
748 | GASTRULATION WITH MOUTH FORMING SECOND | 2 | 28 | 0.0006492 | 0.004022 |
749 | REGULATION OF DNA DAMAGE RESPONSE SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR | 2 | 28 | 0.0006492 | 0.004022 |
750 | MORPHOGENESIS OF A POLARIZED EPITHELIUM | 2 | 28 | 0.0006492 | 0.004022 |
751 | RESPONSE TO GONADOTROPIN | 2 | 28 | 0.0006492 | 0.004022 |
752 | NUCLEAR IMPORT | 3 | 129 | 0.0006847 | 0.004231 |
753 | CELL JUNCTION ASSEMBLY | 3 | 129 | 0.0006847 | 0.004231 |
754 | REGULATION OF MEIOTIC NUCLEAR DIVISION | 2 | 29 | 0.0006967 | 0.004277 |
755 | NEGATIVE REGULATION OF PRODUCTION OF MOLECULAR MEDIATOR OF IMMUNE RESPONSE | 2 | 29 | 0.0006967 | 0.004277 |
756 | EMBRYONIC HINDLIMB MORPHOGENESIS | 2 | 29 | 0.0006967 | 0.004277 |
757 | REGULATION OF OLIGODENDROCYTE DIFFERENTIATION | 2 | 29 | 0.0006967 | 0.004277 |
758 | NEUROBLAST PROLIFERATION | 2 | 29 | 0.0006967 | 0.004277 |
759 | NEGATIVE REGULATION OF CATALYTIC ACTIVITY | 6 | 829 | 0.0006979 | 0.004279 |
760 | PROTEIN EXPORT FROM NUCLEUS | 2 | 30 | 0.0007459 | 0.004548 |
761 | ESTABLISHMENT OR MAINTENANCE OF EPITHELIAL CELL APICAL BASAL POLARITY | 2 | 30 | 0.0007459 | 0.004548 |
762 | RESPONSE TO EPIDERMAL GROWTH FACTOR | 2 | 30 | 0.0007459 | 0.004548 |
763 | NEGATIVE REGULATION OF MUSCLE CELL APOPTOTIC PROCESS | 2 | 30 | 0.0007459 | 0.004548 |
764 | POSITIVE REGULATION OF VASCULATURE DEVELOPMENT | 3 | 133 | 0.0007482 | 0.004557 |
765 | PEPTIDYL AMINO ACID MODIFICATION | 6 | 841 | 0.0007527 | 0.004578 |
766 | REGULATION OF ACTIN FILAMENT BASED PROCESS | 4 | 312 | 0.000768 | 0.004665 |
767 | POSITIVE REGULATION OF STRESS ACTIVATED PROTEIN KINASE SIGNALING CASCADE | 3 | 135 | 0.0007813 | 0.00474 |
768 | HYALURONAN METABOLIC PROCESS | 2 | 31 | 0.0007966 | 0.004808 |
769 | CARDIAC ATRIUM DEVELOPMENT | 2 | 31 | 0.0007966 | 0.004808 |
770 | REGULATION OF VASCULAR ENDOTHELIAL GROWTH FACTOR PRODUCTION | 2 | 31 | 0.0007966 | 0.004808 |
771 | CELLULAR RESPONSE TO STRESS | 8 | 1565 | 0.000795 | 0.004808 |
772 | REGULATION OF CELL PROJECTION ORGANIZATION | 5 | 558 | 0.0008058 | 0.004857 |
773 | HINDBRAIN DEVELOPMENT | 3 | 137 | 0.0008154 | 0.004902 |
774 | ACTIVATION OF MAPK ACTIVITY | 3 | 137 | 0.0008154 | 0.004902 |
775 | INTRACELLULAR SIGNAL TRANSDUCTION | 8 | 1572 | 0.0008188 | 0.004916 |
776 | RESPONSE TO NITROGEN COMPOUND | 6 | 859 | 0.0008409 | 0.005042 |
777 | POSITIVE REGULATION OF GLIAL CELL DIFFERENTIATION | 2 | 32 | 0.000849 | 0.005058 |
778 | PATTERNING OF BLOOD VESSELS | 2 | 32 | 0.000849 | 0.005058 |
779 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER IN RESPONSE TO HYPOXIA | 2 | 32 | 0.000849 | 0.005058 |
780 | POSITIVE REGULATION OF EPIDERMIS DEVELOPMENT | 2 | 32 | 0.000849 | 0.005058 |
781 | METANEPHRIC NEPHRON DEVELOPMENT | 2 | 32 | 0.000849 | 0.005058 |
782 | RESPONSE TO MOLECULE OF BACTERIAL ORIGIN | 4 | 321 | 0.0008538 | 0.00508 |
783 | CELL ACTIVATION | 5 | 568 | 0.0008728 | 0.005187 |
784 | ESTABLISHMENT OR MAINTENANCE OF CELL POLARITY | 3 | 141 | 0.0008863 | 0.00526 |
785 | REGULATION OF MYELINATION | 2 | 33 | 0.0009031 | 0.005332 |
786 | RESPONSE TO VITAMIN D | 2 | 33 | 0.0009031 | 0.005332 |
787 | POSITIVE REGULATION OF RESPONSE TO CYTOKINE STIMULUS | 2 | 33 | 0.0009031 | 0.005332 |
788 | POSITIVE REGULATION OF EMBRYONIC DEVELOPMENT | 2 | 33 | 0.0009031 | 0.005332 |
789 | EPIDERMAL CELL DIFFERENTIATION | 3 | 142 | 0.0009046 | 0.005335 |
790 | CELLULAR RESPONSE TO OXYGEN LEVELS | 3 | 143 | 0.0009231 | 0.005437 |
791 | FOREBRAIN NEURON DEVELOPMENT | 2 | 34 | 0.0009587 | 0.005625 |
792 | PROTEIN KINASE B SIGNALING | 2 | 34 | 0.0009587 | 0.005625 |
793 | REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO DNA DAMAGE | 2 | 34 | 0.0009587 | 0.005625 |
794 | REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY | 3 | 145 | 0.000961 | 0.005632 |
795 | RESPONSE TO BIOTIC STIMULUS | 6 | 886 | 0.0009883 | 0.005784 |
796 | NEGATIVE REGULATION OF RESPONSE TO OXIDATIVE STRESS | 2 | 35 | 0.001016 | 0.005909 |
797 | BONE REMODELING | 2 | 35 | 0.001016 | 0.005909 |
798 | HAIR CELL DIFFERENTIATION | 2 | 35 | 0.001016 | 0.005909 |
799 | NEGATIVE REGULATION OF CELLULAR RESPONSE TO OXIDATIVE STRESS | 2 | 35 | 0.001016 | 0.005909 |
800 | REGULATION OF RESPONSE TO REACTIVE OXYGEN SPECIES | 2 | 35 | 0.001016 | 0.005909 |
801 | PEPTIDYL SERINE MODIFICATION | 3 | 148 | 0.00102 | 0.005915 |
802 | SECRETION | 5 | 588 | 0.001019 | 0.005915 |
803 | CHROMATIN REMODELING | 3 | 150 | 0.00106 | 0.006141 |
804 | CELL DIFFERENTIATION INVOLVED IN KIDNEY DEVELOPMENT | 2 | 36 | 0.001075 | 0.006205 |
805 | POSITIVE REGULATION OF PROTEIN ACETYLATION | 2 | 36 | 0.001075 | 0.006205 |
806 | POSITIVE CHEMOTAXIS | 2 | 36 | 0.001075 | 0.006205 |
807 | LYMPHOCYTE ACTIVATION | 4 | 342 | 0.00108 | 0.006229 |
808 | REGULATION OF REACTIVE OXYGEN SPECIES METABOLIC PROCESS | 3 | 152 | 0.001101 | 0.006341 |
809 | HINDLIMB MORPHOGENESIS | 2 | 37 | 0.001135 | 0.006498 |
810 | MYOBLAST DIFFERENTIATION | 2 | 37 | 0.001135 | 0.006498 |
811 | GLIAL CELL MIGRATION | 2 | 37 | 0.001135 | 0.006498 |
812 | ESTABLISHMENT OR MAINTENANCE OF APICAL BASAL CELL POLARITY | 2 | 37 | 0.001135 | 0.006498 |
813 | ESTABLISHMENT OR MAINTENANCE OF BIPOLAR CELL POLARITY | 2 | 37 | 0.001135 | 0.006498 |
814 | CELL CYCLE ARREST | 3 | 154 | 0.001143 | 0.006536 |
815 | PROTEIN IMPORT | 3 | 155 | 0.001165 | 0.00665 |
816 | CELLULAR RESPONSE TO CYTOKINE STIMULUS | 5 | 606 | 0.001166 | 0.00665 |
817 | POSITIVE REGULATION OF DEVELOPMENTAL GROWTH | 3 | 156 | 0.001187 | 0.006758 |
818 | OOCYTE DIFFERENTIATION | 2 | 38 | 0.001197 | 0.006794 |
819 | POSITIVE REGULATION OF ORGAN GROWTH | 2 | 38 | 0.001197 | 0.006794 |
820 | REGULATION OF MULTICELLULAR ORGANISMAL METABOLIC PROCESS | 2 | 38 | 0.001197 | 0.006794 |
821 | HORMONE MEDIATED SIGNALING PATHWAY | 3 | 158 | 0.001231 | 0.006968 |
822 | REGULATION OF DEPHOSPHORYLATION | 3 | 158 | 0.001231 | 0.006968 |
823 | NUCLEAR TRANSPORT | 4 | 355 | 0.00124 | 0.007011 |
824 | POSITIVE REGULATION OF VIRAL TRANSCRIPTION | 2 | 39 | 0.001261 | 0.007061 |
825 | NEGATIVE REGULATION OF TRANSCRIPTION FACTOR IMPORT INTO NUCLEUS | 2 | 39 | 0.001261 | 0.007061 |
826 | ANATOMICAL STRUCTURE MATURATION | 2 | 39 | 0.001261 | 0.007061 |
827 | TRABECULA MORPHOGENESIS | 2 | 39 | 0.001261 | 0.007061 |
828 | REGULATION OF CELL ADHESION MEDIATED BY INTEGRIN | 2 | 39 | 0.001261 | 0.007061 |
829 | ASTROCYTE DIFFERENTIATION | 2 | 39 | 0.001261 | 0.007061 |
830 | COCHLEA DEVELOPMENT | 2 | 39 | 0.001261 | 0.007061 |
831 | NEGATIVE REGULATION OF ENDOTHELIAL CELL MIGRATION | 2 | 39 | 0.001261 | 0.007061 |
832 | CELL CHEMOTAXIS | 3 | 162 | 0.001323 | 0.007382 |
833 | REGULATION OF MEIOTIC CELL CYCLE | 2 | 40 | 0.001326 | 0.007382 |
834 | ENDOCRINE PANCREAS DEVELOPMENT | 2 | 40 | 0.001326 | 0.007382 |
835 | ENDODERMAL CELL DIFFERENTIATION | 2 | 40 | 0.001326 | 0.007382 |
836 | NEGATIVE REGULATION OF OSTEOBLAST DIFFERENTIATION | 2 | 40 | 0.001326 | 0.007382 |
837 | POSITIVE REGULATION OF HEMOPOIESIS | 3 | 163 | 0.001346 | 0.007485 |
838 | REGULATION OF SEQUENCE SPECIFIC DNA BINDING TRANSCRIPTION FACTOR ACTIVITY | 4 | 365 | 0.001374 | 0.007628 |
839 | NEGATIVE REGULATION OF FAT CELL DIFFERENTIATION | 2 | 41 | 0.001393 | 0.007717 |
840 | LUNG ALVEOLUS DEVELOPMENT | 2 | 41 | 0.001393 | 0.007717 |
841 | CENTRAL NERVOUS SYSTEM NEURON DIFFERENTIATION | 3 | 166 | 0.001419 | 0.007849 |
842 | POSITIVE REGULATION OF INTRACELLULAR TRANSPORT | 4 | 370 | 0.001444 | 0.007972 |
843 | POSITIVE REGULATION OF SECRETION | 4 | 370 | 0.001444 | 0.007972 |
844 | CELL CYCLE | 7 | 1316 | 0.001452 | 0.008006 |
845 | POSITIVE REGULATION OF DNA BINDING | 2 | 42 | 0.001462 | 0.008039 |
846 | EPITHELIAL CELL MORPHOGENESIS | 2 | 42 | 0.001462 | 0.008039 |
847 | REGULATION OF MUSCLE CELL APOPTOTIC PROCESS | 2 | 43 | 0.001532 | 0.008384 |
848 | MORPHOGENESIS OF AN EPITHELIAL SHEET | 2 | 43 | 0.001532 | 0.008384 |
849 | REGULATION OF POLYSACCHARIDE METABOLIC PROCESS | 2 | 43 | 0.001532 | 0.008384 |
850 | BETA CATENIN TCF COMPLEX ASSEMBLY | 2 | 43 | 0.001532 | 0.008384 |
851 | POSITIVE REGULATION OF APOPTOTIC SIGNALING PATHWAY | 3 | 171 | 0.001545 | 0.008446 |
852 | REGULATION OF CARBOHYDRATE METABOLIC PROCESS | 3 | 172 | 0.001571 | 0.008568 |
853 | REGULATION OF CELL SIZE | 3 | 172 | 0.001571 | 0.008568 |
854 | STRIATED MUSCLE CELL DIFFERENTIATION | 3 | 173 | 0.001597 | 0.008701 |
855 | LABYRINTHINE LAYER DEVELOPMENT | 2 | 44 | 0.001603 | 0.008725 |
856 | THYMOCYTE AGGREGATION | 2 | 45 | 0.001676 | 0.009102 |
857 | T CELL DIFFERENTIATION IN THYMUS | 2 | 45 | 0.001676 | 0.009102 |
858 | REGULATION OF PROTEIN SECRETION | 4 | 389 | 0.001735 | 0.009411 |
859 | NEGATIVE REGULATION OF DNA BINDING | 2 | 46 | 0.001751 | 0.009453 |
860 | PEPTIDYL THREONINE MODIFICATION | 2 | 46 | 0.001751 | 0.009453 |
861 | REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 2 | 46 | 0.001751 | 0.009453 |
862 | REGULATION OF OXIDATIVE STRESS INDUCED CELL DEATH | 2 | 46 | 0.001751 | 0.009453 |
863 | REGULATION OF CHEMOTAXIS | 3 | 180 | 0.001789 | 0.009644 |
864 | THYMUS DEVELOPMENT | 2 | 47 | 0.001827 | 0.009819 |
865 | POSITIVE REGULATION OF DEPHOSPHORYLATION | 2 | 47 | 0.001827 | 0.009819 |
866 | POSITIVE REGULATION OF GLIOGENESIS | 2 | 47 | 0.001827 | 0.009819 |
867 | POSITIVE REGULATION OF CATABOLIC PROCESS | 4 | 395 | 0.001835 | 0.009849 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | TRANSFORMING GROWTH FACTOR BETA RECEPTOR BINDING | 6 | 50 | 5.09e-11 | 3.387e-08 |
2 | RECEPTOR BINDING | 15 | 1476 | 7.291e-11 | 3.387e-08 |
3 | SMAD BINDING | 5 | 72 | 3.985e-08 | 1.234e-05 |
4 | CHROMATIN BINDING | 8 | 435 | 7.255e-08 | 1.576e-05 |
5 | MACROMOLECULAR COMPLEX BINDING | 12 | 1399 | 8.481e-08 | 1.576e-05 |
6 | TRANSCRIPTION FACTOR ACTIVITY RNA POLYMERASE II DISTAL ENHANCER SEQUENCE SPECIFIC BINDING | 5 | 90 | 1.231e-07 | 1.906e-05 |
7 | NUCLEIC ACID BINDING TRANSCRIPTION FACTOR ACTIVITY | 11 | 1199 | 1.836e-07 | 2.437e-05 |
8 | REGULATORY REGION NUCLEIC ACID BINDING | 9 | 818 | 7.393e-07 | 8.585e-05 |
9 | PROTEIN KINASE ACTIVITY | 8 | 640 | 1.363e-06 | 0.0001268 |
10 | CYTOKINE RECEPTOR BINDING | 6 | 271 | 1.365e-06 | 0.0001268 |
11 | PROTEIN HETERODIMERIZATION ACTIVITY | 7 | 468 | 2.174e-06 | 0.0001683 |
12 | GROWTH FACTOR ACTIVITY | 5 | 160 | 2.155e-06 | 0.0001683 |
13 | TRANSCRIPTION FACTOR ACTIVITY RNA POLYMERASE II CORE PROMOTER PROXIMAL REGION SEQUENCE SPECIFIC BINDING | 6 | 328 | 4.114e-06 | 0.000294 |
14 | TRANSCRIPTION FACTOR BINDING | 7 | 524 | 4.585e-06 | 0.0003043 |
15 | SEQUENCE SPECIFIC DNA BINDING | 9 | 1037 | 5.252e-06 | 0.0003253 |
16 | KINASE ACTIVITY | 8 | 842 | 1.038e-05 | 0.0005358 |
17 | TRANSCRIPTION FACTOR ACTIVITY PROTEIN BINDING | 7 | 588 | 9.747e-06 | 0.0005358 |
18 | CYTOKINE ACTIVITY | 5 | 219 | 9.976e-06 | 0.0005358 |
19 | PROTEIN DIMERIZATION ACTIVITY | 9 | 1149 | 1.207e-05 | 0.0005901 |
20 | RNA POLYMERASE II TRANSCRIPTION FACTOR ACTIVITY SEQUENCE SPECIFIC DNA BINDING | 7 | 629 | 1.51e-05 | 0.0006727 |
21 | FRIZZLED BINDING | 3 | 36 | 1.521e-05 | 0.0006727 |
22 | TRANSFERASE ACTIVITY TRANSFERRING PHOSPHORUS CONTAINING GROUPS | 8 | 992 | 3.398e-05 | 0.001435 |
23 | ENZYME BINDING | 10 | 1737 | 5.049e-05 | 0.002039 |
24 | TRANSCRIPTIONAL ACTIVATOR ACTIVITY RNA POLYMERASE II TRANSCRIPTION REGULATORY REGION SEQUENCE SPECIFIC BINDING | 5 | 315 | 5.702e-05 | 0.002207 |
25 | I SMAD BINDING | 2 | 11 | 9.581e-05 | 0.00356 |
26 | KINASE BINDING | 6 | 606 | 0.0001298 | 0.004636 |
27 | PROTEIN DOMAIN SPECIFIC BINDING | 6 | 624 | 0.0001522 | 0.005238 |
28 | C2H2 ZINC FINGER DOMAIN BINDING | 2 | 14 | 0.0001581 | 0.005246 |
29 | TRANSMEMBRANE RECEPTOR PROTEIN KINASE ACTIVITY | 3 | 81 | 0.0001745 | 0.005292 |
30 | RECEPTOR SERINE THREONINE KINASE BINDING | 2 | 15 | 0.0001823 | 0.005292 |
31 | PROTEIN KINASE A CATALYTIC SUBUNIT BINDING | 2 | 15 | 0.0001823 | 0.005292 |
32 | OXIDOREDUCTASE ACTIVITY ACTING ON THE CH NH2 GROUP OF DONORS OXYGEN AS ACCEPTOR | 2 | 15 | 0.0001823 | 0.005292 |
33 | BETA CATENIN BINDING | 3 | 84 | 0.0001944 | 0.005472 |
34 | TRANSFORMING GROWTH FACTOR BETA BINDING | 2 | 16 | 0.0002082 | 0.005525 |
35 | RECEPTOR AGONIST ACTIVITY | 2 | 16 | 0.0002082 | 0.005525 |
36 | TRANSCRIPTIONAL ACTIVATOR ACTIVITY RNA POLYMERASE II CORE PROMOTER PROXIMAL REGION SEQUENCE SPECIFIC BINDING | 4 | 226 | 0.0002272 | 0.005862 |
37 | TRANSMEMBRANE RECEPTOR PROTEIN SERINE THREONINE KINASE ACTIVITY | 2 | 17 | 0.0002357 | 0.005919 |
38 | CYTOKINE BINDING | 3 | 92 | 0.0002543 | 0.006218 |
39 | MOLECULAR FUNCTION REGULATOR | 8 | 1353 | 0.0002986 | 0.006765 |
40 | OXIDOREDUCTASE ACTIVITY ACTING ON THE CH NH2 GROUP OF DONORS | 2 | 19 | 0.0002959 | 0.006765 |
41 | PROTEIN SERINE THREONINE KINASE ACTIVITY | 5 | 445 | 0.0002872 | 0.006765 |
42 | DNA BINDING BENDING | 2 | 20 | 0.0003285 | 0.007266 |
43 | TRANSCRIPTIONAL REPRESSOR ACTIVITY RNA POLYMERASE II CORE PROMOTER PROXIMAL REGION SEQUENCE SPECIFIC BINDING | 3 | 105 | 0.0003752 | 0.008107 |
44 | IONOTROPIC GLUTAMATE RECEPTOR BINDING | 2 | 23 | 0.0004363 | 0.009008 |
45 | FIBROBLAST GROWTH FACTOR BINDING | 2 | 23 | 0.0004363 | 0.009008 |
46 | DOUBLE STRANDED DNA BINDING | 6 | 764 | 0.0004532 | 0.009152 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | EXTRACELLULAR MATRIX | 9 | 426 | 2.768e-09 | 1.617e-06 |
2 | EXTRACELLULAR SPACE | 12 | 1376 | 7.064e-08 | 2.063e-05 |
3 | NUCLEAR TRANSCRIPTION FACTOR COMPLEX | 5 | 127 | 6.884e-07 | 0.000134 |
4 | TRANSCRIPTION FACTOR COMPLEX | 6 | 298 | 2.367e-06 | 0.0003455 |
5 | CELL SURFACE | 8 | 757 | 4.753e-06 | 0.0005551 |
6 | PROTEINACEOUS EXTRACELLULAR MATRIX | 6 | 356 | 6.581e-06 | 0.0006405 |
7 | RNA POLYMERASE II TRANSCRIPTION FACTOR COMPLEX | 4 | 101 | 9.833e-06 | 0.0008203 |
8 | PLATELET ALPHA GRANULE LUMEN | 3 | 55 | 5.493e-05 | 0.00401 |
9 | WNT SIGNALOSOME | 2 | 11 | 9.581e-05 | 0.006217 |
10 | PLATELET ALPHA GRANULE | 3 | 75 | 0.0001389 | 0.008109 |
11 | BETA CATENIN DESTRUCTION COMPLEX | 2 | 14 | 0.0001581 | 0.008395 |
12 | SECRETORY GRANULE LUMEN | 3 | 85 | 0.0002013 | 0.009796 |
Num | Pathway | Pathview | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|---|
1 | hsa04390_Hippo_signaling_pathway | 12 | 154 | 4.422e-19 | 7.96e-17 | |
2 | hsa04340_Hedgehog_signaling_pathway | 6 | 56 | 1.034e-10 | 9.309e-09 | |
3 | hsa04350_TGF.beta_signaling_pathway | 6 | 85 | 1.357e-09 | 8.144e-08 | |
4 | hsa04916_Melanogenesis | 6 | 101 | 3.877e-09 | 1.745e-07 | |
5 | hsa04520_Adherens_junction | 5 | 73 | 4.274e-08 | 1.306e-06 | |
6 | hsa04310_Wnt_signaling_pathway | 6 | 151 | 4.353e-08 | 1.306e-06 | |
7 | hsa04144_Endocytosis | 4 | 203 | 0.0001506 | 0.003872 | |
8 | hsa04010_MAPK_signaling_pathway | 4 | 268 | 0.000434 | 0.009765 | |
9 | hsa04110_Cell_cycle | 3 | 128 | 0.0006694 | 0.01205 | |
10 | hsa04380_Osteoclast_differentiation | 3 | 128 | 0.0006694 | 0.01205 | |
11 | hsa04510_Focal_adhesion | 3 | 200 | 0.002414 | 0.0395 | |
12 | hsa04151_PI3K_AKT_signaling_pathway | 3 | 351 | 0.01147 | 0.1721 | |
13 | hsa04014_Ras_signaling_pathway | 2 | 236 | 0.04011 | 0.5156 |
Num | lncRNA | miRNAs | miRNAs count | Gene | Sponge regulatory network | lncRNA log2FC | lncRNA pvalue | Gene log2FC | Gene pvalue | lncRNA-gene Pearson correlation |
---|---|---|---|---|---|---|---|---|---|---|
1 | LINC00941 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-3p;hsa-miR-195-5p;hsa-miR-199b-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-340-5p;hsa-miR-497-5p;hsa-miR-532-5p | 17 | HMGA2 | Sponge network | 4.292 | 0 | 4.457 | 0 | 0.69 |
2 | MAGI2-AS3 |
hsa-let-7a-3p;hsa-miR-141-3p;hsa-miR-200a-3p;hsa-miR-224-3p;hsa-miR-26b-5p;hsa-miR-29a-5p;hsa-miR-30c-5p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-651-5p;hsa-miR-7-1-3p;hsa-miR-944 | 12 | HGF | Sponge network | -0.939 | 4.0E-5 | -0.629 | 0.02489 | 0.681 |
3 | RP11-221N13.3 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-3p;hsa-miR-20b-5p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30d-3p;hsa-miR-30e-3p;hsa-miR-664a-5p | 15 | HMGA2 | Sponge network | 5.876 | 0 | 4.457 | 0 | 0.612 |
4 | AC007879.7 | hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-148a-5p;hsa-miR-195-3p;hsa-miR-195-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30d-3p;hsa-miR-30e-3p;hsa-miR-340-5p | 15 | HMGA2 | Sponge network | 2.7 | 0 | 4.457 | 0 | 0.545 |
5 | DNM3OS | hsa-let-7a-3p;hsa-miR-141-3p;hsa-miR-200a-3p;hsa-miR-224-3p;hsa-miR-26b-5p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-590-5p;hsa-miR-651-5p;hsa-miR-7-1-3p;hsa-miR-944 | 11 | HGF | Sponge network | 0.932 | 0.00442 | -0.629 | 0.02489 | 0.521 |
6 | RP11-462L8.1 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-148a-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-30a-3p;hsa-miR-34a-5p;hsa-miR-532-5p | 11 | HMGA2 | Sponge network | 4.262 | 0 | 4.457 | 0 | 0.518 |
7 | RP11-218E20.3 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-3p;hsa-miR-195-5p;hsa-miR-199b-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30b-5p;hsa-miR-30d-3p;hsa-miR-30d-5p;hsa-miR-30e-3p;hsa-miR-30e-5p;hsa-miR-337-3p;hsa-miR-381-3p;hsa-miR-491-5p;hsa-miR-497-5p;hsa-miR-532-5p | 26 | HMGA2 | Sponge network | 4.613 | 0 | 4.457 | 0 | 0.517 |
8 | RP11-166D19.1 |
hsa-let-7a-3p;hsa-miR-141-3p;hsa-miR-200a-3p;hsa-miR-224-3p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-590-5p;hsa-miR-651-5p;hsa-miR-7-1-3p;hsa-miR-944 | 10 | HGF | Sponge network | -0.882 | 5.0E-5 | -0.629 | 0.02489 | 0.51 |
9 | RP11-445F12.1 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7g-5p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-340-5p;hsa-miR-491-5p;hsa-miR-497-5p;hsa-miR-664a-5p | 15 | HMGA2 | Sponge network | 7.107 | 0 | 4.457 | 0 | 0.508 |
10 | TPTEP1 | hsa-miR-15a-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-181b-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-29a-5p;hsa-miR-339-5p;hsa-miR-424-5p;hsa-miR-455-5p;hsa-miR-484;hsa-miR-589-3p;hsa-miR-590-5p;hsa-miR-944 | 18 | TGFBR3 | Sponge network | -2.193 | 0 | -2.338 | 0 | 0.503 |
11 | RP11-890B15.2 | hsa-let-7c-5p;hsa-let-7g-5p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30d-3p;hsa-miR-30e-3p;hsa-miR-34a-5p;hsa-miR-497-5p;hsa-miR-532-5p | 16 | HMGA2 | Sponge network | 4.029 | 0 | 4.457 | 0 | 0.474 |
12 | CTD-2587H24.5 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-5p;hsa-miR-23b-3p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30d-3p;hsa-miR-30e-3p;hsa-miR-491-5p;hsa-miR-497-5p;hsa-miR-664a-5p | 16 | HMGA2 | Sponge network | 7.138 | 0 | 4.457 | 0 | 0.472 |
13 | LINC00704 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-148a-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30e-3p;hsa-miR-491-5p;hsa-miR-532-5p;hsa-miR-664a-5p | 15 | HMGA2 | Sponge network | 2.465 | 0 | 4.457 | 0 | 0.464 |
14 | SNHG14 | hsa-miR-15a-5p;hsa-miR-16-2-3p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-339-5p;hsa-miR-455-5p;hsa-miR-484;hsa-miR-589-3p;hsa-miR-944 | 13 | TGFBR3 | Sponge network | -1.125 | 0.0001 | -2.338 | 0 | 0.457 |
15 | RP11-417E7.1 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7g-5p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-5p;hsa-miR-20b-5p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-491-5p;hsa-miR-532-5p | 13 | HMGA2 | Sponge network | 3.987 | 0 | 4.457 | 0 | 0.455 |
16 | CTD-2357A8.3 | hsa-let-7c-5p;hsa-let-7g-5p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-199b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-34a-5p | 10 | HMGA2 | Sponge network | 7.162 | 0 | 4.457 | 0 | 0.455 |
17 | LINC00911 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-20b-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-491-5p | 11 | HMGA2 | Sponge network | 4.956 | 0 | 4.457 | 0 | 0.454 |
18 | TTLL11-IT1 | hsa-let-7c-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-199b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p | 10 | HMGA2 | Sponge network | 5.5 | 0 | 4.457 | 0 | 0.454 |
19 | APCDD1L-AS1 |
hsa-miR-107;hsa-miR-126-5p;hsa-miR-140-5p;hsa-miR-148b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-330-3p;hsa-miR-335-3p;hsa-miR-375;hsa-miR-532-5p;hsa-miR-9-5p | 11 | SNAI2 | Sponge network | 2.077 | 0 | 1.574 | 0 | 0.453 |
20 | RP11-346D19.1 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7g-5p;hsa-miR-148a-5p;hsa-miR-195-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-340-5p | 11 | HMGA2 | Sponge network | 6.549 | 0 | 4.457 | 0 | 0.453 |
21 | VPS9D1-AS1 | hsa-let-7c-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-30a-3p;hsa-miR-497-5p | 10 | HMGA2 | Sponge network | 1.07 | 1.0E-5 | 4.457 | 0 | 0.453 |
22 | RP5-884M6.1 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-3p;hsa-miR-195-5p;hsa-miR-199b-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-337-3p;hsa-miR-381-3p;hsa-miR-664a-5p | 18 | HMGA2 | Sponge network | 6.548 | 0 | 4.457 | 0 | 0.452 |
23 | LINC00460 | hsa-let-7c-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-148a-5p;hsa-miR-195-5p;hsa-miR-199b-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30d-3p;hsa-miR-30e-3p;hsa-miR-491-5p;hsa-miR-497-5p;hsa-miR-532-5p;hsa-miR-664a-5p | 17 | HMGA2 | Sponge network | 7.222 | 0 | 4.457 | 0 | 0.45 |
24 | MAGI2-AS3 |
hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-29a-5p;hsa-miR-339-5p;hsa-miR-3607-3p;hsa-miR-424-5p;hsa-miR-455-5p;hsa-miR-589-3p;hsa-miR-7-1-3p;hsa-miR-944 | 19 | TGFBR3 | Sponge network | -0.939 | 4.0E-5 | -2.338 | 0 | 0.449 |
25 | RAMP2-AS1 | hsa-miR-181b-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-29a-5p;hsa-miR-339-5p;hsa-miR-424-5p;hsa-miR-455-5p;hsa-miR-484;hsa-miR-589-3p | 13 | TGFBR3 | Sponge network | -1.258 | 0.00026 | -2.338 | 0 | 0.448 |
26 | RP13-463N16.6 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-148a-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p | 10 | HMGA2 | Sponge network | 3.312 | 0 | 4.457 | 0 | 0.446 |
27 | RP11-30P6.6 | hsa-let-7c-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30b-5p;hsa-miR-30d-3p;hsa-miR-30d-5p;hsa-miR-30e-3p;hsa-miR-30e-5p;hsa-miR-491-5p | 17 | HMGA2 | Sponge network | 2.847 | 0 | 4.457 | 0 | 0.439 |
28 | RP1-193H18.2 | hsa-miR-181b-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-424-5p;hsa-miR-450b-5p;hsa-miR-589-3p;hsa-miR-944 | 11 | TGFBR3 | Sponge network | -1.539 | 0 | -2.338 | 0 | 0.438 |
29 | AC005682.5 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-3p;hsa-miR-195-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30e-3p;hsa-miR-340-5p;hsa-miR-664a-5p | 15 | HMGA2 | Sponge network | 1.074 | 0 | 4.457 | 0 | 0.434 |
30 | RP11-150O12.1 | hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30d-5p;hsa-miR-30e-5p;hsa-miR-532-5p;hsa-miR-664a-5p | 16 | HMGA2 | Sponge network | 1.523 | 0 | 4.457 | 0 | 0.432 |
31 | SH3RF3-AS1 |
hsa-let-7a-3p;hsa-miR-148b-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-193a-3p;hsa-miR-205-3p;hsa-miR-222-3p;hsa-miR-29b-3p;hsa-miR-30b-5p;hsa-miR-30c-5p;hsa-miR-576-5p;hsa-miR-7-1-3p | 13 | LIMS1 | Sponge network | -0.175 | 0.58985 | 0.197 | 0.25634 | 0.431 |
32 | MAGI2-AS3 |
hsa-miR-141-3p;hsa-miR-142-3p;hsa-miR-149-5p;hsa-miR-200a-3p;hsa-miR-29b-3p;hsa-miR-33a-3p;hsa-miR-362-5p;hsa-miR-429;hsa-miR-454-3p;hsa-miR-500a-5p;hsa-miR-500b-5p;hsa-miR-589-3p;hsa-miR-944 | 13 | TGFB2 | Sponge network | -0.939 | 4.0E-5 | 0.078 | 0.72302 | 0.43 |
33 | RP11-879F14.2 | hsa-let-7a-5p;hsa-let-7b-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30e-3p | 15 | HMGA2 | Sponge network | 1.149 | 9.0E-5 | 4.457 | 0 | 0.422 |
34 | RP11-1020M18.10 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-195-5p;hsa-miR-20b-5p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-497-5p;hsa-miR-664a-5p | 12 | HMGA2 | Sponge network | 6.911 | 0 | 4.457 | 0 | 0.415 |
35 | ZNF667-AS1 | hsa-miR-15a-5p;hsa-miR-16-2-3p;hsa-miR-181b-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-339-5p;hsa-miR-424-5p;hsa-miR-484;hsa-miR-589-3p;hsa-miR-590-5p | 14 | TGFBR3 | Sponge network | -1.395 | 0 | -2.338 | 0 | 0.412 |
36 | LINC00958 | hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-148a-5p;hsa-miR-195-5p;hsa-miR-20b-5p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-340-5p;hsa-miR-497-5p;hsa-miR-664a-5p | 13 | HMGA2 | Sponge network | 1.836 | 0 | 4.457 | 0 | 0.41 |
37 | LINC00518 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-664a-5p | 14 | HMGA2 | Sponge network | 2.747 | 4.0E-5 | 4.457 | 0 | 0.41 |
38 | KTN1-AS1 | hsa-let-7c-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-3p;hsa-miR-195-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30d-3p;hsa-miR-30e-3p;hsa-miR-34a-5p;hsa-miR-532-5p | 16 | HMGA2 | Sponge network | 1.107 | 0 | 4.457 | 0 | 0.408 |
39 | AC007743.1 | hsa-miR-15a-5p;hsa-miR-16-2-3p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-29a-5p;hsa-miR-339-5p;hsa-miR-424-5p;hsa-miR-455-5p;hsa-miR-589-3p;hsa-miR-590-5p;hsa-miR-7-1-3p | 16 | TGFBR3 | Sponge network | -1.053 | 0.00923 | -2.338 | 0 | 0.405 |
40 | CTD-2066L21.3 | hsa-let-7c-5p;hsa-let-7g-5p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30b-5p;hsa-miR-30d-3p;hsa-miR-30d-5p;hsa-miR-30e-3p;hsa-miR-30e-5p | 15 | HMGA2 | Sponge network | 5.449 | 0 | 4.457 | 0 | 0.402 |
41 | RP11-13K12.5 | hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-29a-5p;hsa-miR-339-5p;hsa-miR-424-5p;hsa-miR-589-3p | 10 | TGFBR3 | Sponge network | -0.552 | 0.43847 | -2.338 | 0 | 0.399 |
42 | RP4-798P15.3 |
hsa-let-7a-3p;hsa-miR-148b-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-193a-3p;hsa-miR-205-3p;hsa-miR-222-3p;hsa-miR-576-5p;hsa-miR-7-1-3p;hsa-miR-96-5p | 11 | LIMS1 | Sponge network | -1.213 | 0.00098 | 0.197 | 0.25634 | 0.399 |
43 | LINC01018 | hsa-miR-15a-5p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-29a-5p;hsa-miR-424-5p;hsa-miR-450b-5p;hsa-miR-944 | 11 | TGFBR3 | Sponge network | -1.613 | 0.00396 | -2.338 | 0 | 0.398 |
44 | AL035610.1 | hsa-miR-15a-5p;hsa-miR-16-2-3p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-29a-5p;hsa-miR-424-5p | 12 | TGFBR3 | Sponge network | -5.893 | 0 | -2.338 | 0 | 0.398 |
45 | CTD-2555C10.3 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-30a-5p;hsa-miR-30d-5p;hsa-miR-30e-5p;hsa-miR-491-5p;hsa-miR-664a-3p | 16 | HMGA2 | Sponge network | 1.037 | 0.0004 | 4.457 | 0 | 0.397 |
46 | LINC00702 |
hsa-miR-141-3p;hsa-miR-142-3p;hsa-miR-149-5p;hsa-miR-200a-3p;hsa-miR-33a-3p;hsa-miR-454-3p;hsa-miR-500a-5p;hsa-miR-500b-5p;hsa-miR-589-3p;hsa-miR-590-5p | 10 | TGFB2 | Sponge network | -0.573 | 0.0699 | 0.078 | 0.72302 | 0.396 |
47 | PWAR6 | hsa-miR-15a-5p;hsa-miR-16-2-3p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-339-5p;hsa-miR-455-5p;hsa-miR-589-3p;hsa-miR-944 | 12 | TGFBR3 | Sponge network | -1.629 | 0 | -2.338 | 0 | 0.395 |
48 | NOP14-AS1 | hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-3p;hsa-miR-195-5p;hsa-miR-199b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30b-5p;hsa-miR-30d-3p;hsa-miR-30d-5p;hsa-miR-30e-3p;hsa-miR-30e-5p;hsa-miR-340-5p;hsa-miR-34a-5p;hsa-miR-491-5p;hsa-miR-497-5p;hsa-miR-664a-5p | 24 | HMGA2 | Sponge network | 0.939 | 0 | 4.457 | 0 | 0.392 |
49 | SOX21-AS1 | hsa-miR-15a-5p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-29a-5p;hsa-miR-424-5p;hsa-miR-455-5p | 11 | TGFBR3 | Sponge network | -1.061 | 0.01562 | -2.338 | 0 | 0.391 |
50 | MAGI2-AS3 |
hsa-let-7a-3p;hsa-miR-148b-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-193a-3p;hsa-miR-205-3p;hsa-miR-222-3p;hsa-miR-29b-3p;hsa-miR-30c-5p;hsa-miR-3607-3p;hsa-miR-429;hsa-miR-505-3p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-7-1-3p | 16 | LIMS1 | Sponge network | -0.939 | 4.0E-5 | 0.197 | 0.25634 | 0.387 |
51 | CASC15 |
hsa-miR-142-3p;hsa-miR-155-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-205-3p;hsa-miR-26b-5p;hsa-miR-30b-5p;hsa-miR-30d-3p;hsa-miR-30e-3p;hsa-miR-30e-5p;hsa-miR-582-5p;hsa-miR-590-3p;hsa-miR-7-1-3p | 14 | WNT5A | Sponge network | 1.485 | 0 | 0.23 | 0.27604 | 0.383 |
52 | LINC00707 | hsa-let-7c-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-3p;hsa-miR-195-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30b-5p;hsa-miR-30d-3p;hsa-miR-30d-5p;hsa-miR-30e-3p;hsa-miR-30e-5p;hsa-miR-340-5p;hsa-miR-34a-5p;hsa-miR-491-5p;hsa-miR-497-5p;hsa-miR-664a-3p;hsa-miR-664a-5p | 24 | HMGA2 | Sponge network | 2.018 | 1.0E-5 | 4.457 | 0 | 0.383 |
53 | RP11-297P16.4 | hsa-let-7a-5p;hsa-let-7b-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-3p;hsa-miR-195-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p | 15 | HMGA2 | Sponge network | 7.048 | 0 | 4.457 | 0 | 0.379 |
54 | AC108142.1 | hsa-let-7c-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-148a-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30d-3p;hsa-miR-30e-3p;hsa-miR-34a-5p;hsa-miR-664a-5p | 12 | HMGA2 | Sponge network | 2.31 | 0 | 4.457 | 0 | 0.378 |
55 | CTD-2015G9.2 |
hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-505-5p;hsa-miR-576-5p | 10 | EPB41L5 | Sponge network | -3.112 | 5.0E-5 | -0.492 | 9.0E-5 | 0.378 |
56 | XXyac-YX65C7_A.3 | hsa-let-7c-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-195-3p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30b-5p;hsa-miR-30d-5p;hsa-miR-30e-5p | 14 | HMGA2 | Sponge network | 6.112 | 0 | 4.457 | 0 | 0.374 |
57 | RP11-42I10.1 | hsa-let-7c-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p | 11 | HMGA2 | Sponge network | 2.1 | 0 | 4.457 | 0 | 0.374 |
58 | CTD-2269F5.1 |
hsa-miR-142-3p;hsa-miR-155-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-205-3p;hsa-miR-29a-5p;hsa-miR-576-5p;hsa-miR-7-1-3p;hsa-miR-92a-3p | 11 | WNT5A | Sponge network | -0.168 | 0.67173 | 0.23 | 0.27604 | 0.371 |
59 | KB-1732A1.1 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-148a-5p;hsa-miR-195-3p;hsa-miR-195-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30d-3p;hsa-miR-30e-3p;hsa-miR-491-5p;hsa-miR-497-5p | 16 | HMGA2 | Sponge network | 1.697 | 0 | 4.457 | 0 | 0.366 |
60 | CTD-2354A18.1 | hsa-let-7c-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-195-3p;hsa-miR-195-5p;hsa-miR-199a-5p;hsa-miR-199b-5p;hsa-miR-26a-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30e-3p;hsa-miR-34a-5p;hsa-miR-381-3p | 13 | HMGA2 | Sponge network | 4.214 | 0 | 4.457 | 0 | 0.364 |
61 | RP11-366H4.1 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-195-5p;hsa-miR-20b-5p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-340-5p;hsa-miR-497-5p;hsa-miR-664a-5p | 13 | HMGA2 | Sponge network | 4.872 | 0 | 4.457 | 0 | 0.363 |
62 | CTD-2171N6.1 | hsa-let-7c-5p;hsa-miR-125b-2-3p;hsa-miR-148a-5p;hsa-miR-195-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30b-5p;hsa-miR-30d-3p;hsa-miR-30d-5p;hsa-miR-30e-3p;hsa-miR-30e-5p;hsa-miR-34a-5p;hsa-miR-497-5p | 17 | HMGA2 | Sponge network | 5.89 | 0 | 4.457 | 0 | 0.363 |
63 | RP11-863P13.3 | hsa-let-7c-5p;hsa-miR-125b-2-3p;hsa-miR-148a-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30d-3p;hsa-miR-30e-3p | 11 | HMGA2 | Sponge network | 4.189 | 0 | 4.457 | 0 | 0.361 |
64 | SH3RF3-AS1 |
hsa-let-7a-3p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-205-3p;hsa-miR-26b-5p;hsa-miR-29a-5p;hsa-miR-30b-5p;hsa-miR-30c-5p;hsa-miR-576-5p;hsa-miR-582-5p;hsa-miR-7-1-3p | 13 | WNT5A | Sponge network | -0.175 | 0.58985 | 0.23 | 0.27604 | 0.358 |
65 | RP11-357H14.17 | hsa-let-7c-5p;hsa-miR-125b-2-3p;hsa-miR-195-3p;hsa-miR-195-5p;hsa-miR-199b-5p;hsa-miR-23b-3p;hsa-miR-30a-3p;hsa-miR-30d-3p;hsa-miR-30e-3p;hsa-miR-497-5p | 10 | HMGA2 | Sponge network | 8.011 | 0 | 4.457 | 0 | 0.357 |
66 | FZD10-AS1 |
hsa-let-7a-3p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-205-3p;hsa-miR-26b-5p;hsa-miR-29a-5p;hsa-miR-330-5p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-92a-3p | 13 | WNT5A | Sponge network | -0.218 | 0.34607 | 0.23 | 0.27604 | 0.354 |
67 | RP11-321G12.1 | hsa-miR-15a-5p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-484;hsa-miR-589-3p | 11 | TGFBR3 | Sponge network | -3.552 | 0 | -2.338 | 0 | 0.352 |
68 | RP4-798P15.3 |
hsa-miR-15a-5p;hsa-miR-16-2-3p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-29a-5p;hsa-miR-339-5p;hsa-miR-455-5p;hsa-miR-484;hsa-miR-589-3p;hsa-miR-590-5p;hsa-miR-7-1-3p;hsa-miR-944 | 16 | TGFBR3 | Sponge network | -1.213 | 0.00098 | -2.338 | 0 | 0.35 |
69 | LINC00152 | hsa-let-7c-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30b-5p;hsa-miR-30d-3p;hsa-miR-30d-5p;hsa-miR-30e-3p;hsa-miR-30e-5p;hsa-miR-497-5p;hsa-miR-532-5p | 15 | HMGA2 | Sponge network | 1.218 | 0 | 4.457 | 0 | 0.349 |
70 | MIR4435-1HG | hsa-let-7c-5p;hsa-miR-125b-2-3p;hsa-miR-148a-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30d-3p;hsa-miR-30e-3p;hsa-miR-497-5p;hsa-miR-532-5p | 10 | HMGA2 | Sponge network | 1.225 | 0 | 4.457 | 0 | 0.343 |
71 | AC011738.4 | hsa-let-7c-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-34a-5p;hsa-miR-497-5p;hsa-miR-532-5p;hsa-miR-664a-3p;hsa-miR-664a-5p | 15 | HMGA2 | Sponge network | 3.153 | 0 | 4.457 | 0 | 0.342 |
72 | LINC00284 | hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-424-5p;hsa-miR-455-5p;hsa-miR-589-3p;hsa-miR-590-5p;hsa-miR-944 | 13 | TGFBR3 | Sponge network | -4.159 | 0 | -2.338 | 0 | 0.341 |
73 | CTD-2554C21.3 | hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-455-5p | 10 | TGFBR3 | Sponge network | -2.118 | 6.0E-5 | -2.338 | 0 | 0.34 |
74 | RP11-384L8.1 | hsa-miR-15a-5p;hsa-miR-16-5p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-29a-5p;hsa-miR-424-5p;hsa-miR-484 | 13 | TGFBR3 | Sponge network | -1.152 | 0.00016 | -2.338 | 0 | 0.339 |
75 | FAM66C | hsa-miR-15a-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-424-5p;hsa-miR-484;hsa-miR-944 | 10 | TGFBR3 | Sponge network | -0.798 | 0.00038 | -2.338 | 0 | 0.338 |
76 | RP11-479G22.8 | hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30d-3p;hsa-miR-30e-3p | 11 | HMGA2 | Sponge network | 0.955 | 0 | 4.457 | 0 | 0.335 |
77 | CTD-2008P7.9 |
hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-181a-2-3p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-424-5p;hsa-miR-576-5p | 11 | EPB41L5 | Sponge network | -1.202 | 0.00093 | -0.492 | 9.0E-5 | 0.334 |
78 | DLGAP1-AS5 | hsa-miR-15a-5p;hsa-miR-181b-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-424-5p;hsa-miR-450b-5p;hsa-miR-455-5p;hsa-miR-484;hsa-miR-589-3p;hsa-miR-944 | 12 | TGFBR3 | Sponge network | -6.207 | 0 | -2.338 | 0 | 0.331 |
79 | AC003090.1 |
hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-424-5p;hsa-miR-590-5p;hsa-miR-7-1-3p | 13 | TGFBR3 | Sponge network | -4.323 | 0 | -2.338 | 0 | 0.331 |
80 | RP11-483L5.1 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-148a-5p;hsa-miR-195-3p;hsa-miR-195-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-497-5p | 10 | HMGA2 | Sponge network | 2.236 | 1.0E-5 | 4.457 | 0 | 0.33 |
81 | RP11-297P16.3 | hsa-let-7a-5p;hsa-let-7b-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30d-5p;hsa-miR-30e-5p;hsa-miR-340-5p | 15 | HMGA2 | Sponge network | 6.381 | 0 | 4.457 | 0 | 0.328 |
82 | HOTAIR | hsa-let-7c-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-195-5p;hsa-miR-199b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30b-5p;hsa-miR-30d-5p;hsa-miR-30e-5p;hsa-miR-337-3p | 14 | HMGA2 | Sponge network | 7 | 0 | 4.457 | 0 | 0.326 |
83 | LINC00639 | hsa-miR-15a-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-27a-3p;hsa-miR-339-5p;hsa-miR-424-5p;hsa-miR-484;hsa-miR-589-3p | 10 | TGFBR3 | Sponge network | -0.91 | 0.00848 | -2.338 | 0 | 0.325 |
84 | RP11-161I6.2 | hsa-let-7c-5p;hsa-miR-148a-5p;hsa-miR-26a-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30d-3p;hsa-miR-30e-3p;hsa-miR-30e-5p;hsa-miR-340-5p;hsa-miR-664a-5p | 10 | HMGA2 | Sponge network | 3.332 | 0 | 4.457 | 0 | 0.323 |
85 | CTA-384D8.35 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30d-3p;hsa-miR-30e-3p;hsa-miR-664a-5p | 12 | HMGA2 | Sponge network | 3.12 | 0 | 4.457 | 0 | 0.319 |
86 | RP11-386G11.5 | hsa-let-7c-5p;hsa-miR-125b-5p;hsa-miR-195-5p;hsa-miR-199b-5p;hsa-miR-26a-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30e-3p;hsa-miR-337-3p;hsa-miR-381-3p | 10 | HMGA2 | Sponge network | 4.247 | 0 | 4.457 | 0 | 0.319 |
87 | AC005042.4 | hsa-miR-15a-5p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-424-5p;hsa-miR-450b-5p;hsa-miR-455-5p | 10 | TGFBR3 | Sponge network | -0.876 | 0.0183 | -2.338 | 0 | 0.319 |
88 | HHIP-AS1 |
hsa-let-7a-3p;hsa-miR-142-3p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-205-3p;hsa-miR-29a-5p;hsa-miR-330-5p;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-92a-3p | 12 | WNT5A | Sponge network | -1.293 | 0.01561 | 0.23 | 0.27604 | 0.315 |
89 | RP11-227H15.4 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7g-5p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30d-3p;hsa-miR-30e-3p;hsa-miR-34a-5p;hsa-miR-497-5p | 16 | HMGA2 | Sponge network | 4.405 | 0 | 4.457 | 0 | 0.315 |
90 | LINC00520 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-3p;hsa-miR-195-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-497-5p | 13 | HMGA2 | Sponge network | 3.383 | 0 | 4.457 | 0 | 0.313 |
91 | RP11-78C3.1 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-3p;hsa-miR-195-5p;hsa-miR-199a-5p;hsa-miR-199b-5p;hsa-miR-20b-5p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30d-3p;hsa-miR-30e-3p;hsa-miR-337-3p | 18 | HMGA2 | Sponge network | 5.978 | 0 | 4.457 | 0 | 0.311 |
92 | RP11-285E9.6 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-5p;hsa-miR-199a-5p;hsa-miR-199b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-30a-3p;hsa-miR-491-5p;hsa-miR-497-5p;hsa-miR-664a-5p | 15 | HMGA2 | Sponge network | 1.44 | 1.0E-5 | 4.457 | 0 | 0.308 |
93 | PART1 | hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-29a-5p;hsa-miR-424-5p;hsa-miR-450b-5p;hsa-miR-455-5p | 10 | TGFBR3 | Sponge network | -3.265 | 0 | -2.338 | 0 | 0.306 |
94 | SSTR5-AS1 | hsa-miR-15a-5p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-484 | 10 | TGFBR3 | Sponge network | -1.443 | 0.04871 | -2.338 | 0 | 0.303 |
95 | FLG-AS1 | hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-424-5p;hsa-miR-450b-5p;hsa-miR-7-1-3p | 11 | TGFBR3 | Sponge network | -1.901 | 0 | -2.338 | 0 | 0.302 |
96 | RP11-783K16.13 | hsa-let-7a-5p;hsa-let-7b-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-23b-3p;hsa-miR-30a-3p;hsa-miR-491-5p | 10 | HMGA2 | Sponge network | 0.411 | 0.01987 | 4.457 | 0 | 0.302 |
97 | ADIRF-AS1 | hsa-let-7a-5p;hsa-let-7b-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-3p;hsa-miR-195-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-30a-3p;hsa-miR-30e-3p;hsa-miR-664a-5p | 15 | HMGA2 | Sponge network | 1.011 | 0 | 4.457 | 0 | 0.299 |
98 | RP11-774O3.3 | hsa-miR-15a-5p;hsa-miR-16-2-3p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-424-5p;hsa-miR-589-3p;hsa-miR-7-1-3p;hsa-miR-944 | 12 | TGFBR3 | Sponge network | -1.712 | 0 | -2.338 | 0 | 0.298 |
99 | RP5-1185I7.1 | hsa-miR-15a-5p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-29a-5p;hsa-miR-424-5p | 10 | TGFBR3 | Sponge network | -1.805 | 0.01092 | -2.338 | 0 | 0.296 |
100 | LINC00957 | hsa-miR-15a-5p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-424-5p;hsa-miR-450b-5p;hsa-miR-455-5p;hsa-miR-484 | 11 | TGFBR3 | Sponge network | -0.677 | 2.0E-5 | -2.338 | 0 | 0.294 |
101 | LINC00900 |
hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-339-5p;hsa-miR-424-5p;hsa-miR-455-5p;hsa-miR-589-3p;hsa-miR-590-5p;hsa-miR-7-1-3p | 15 | TGFBR3 | Sponge network | -1.803 | 0 | -2.338 | 0 | 0.294 |
102 | RP11-815I9.4 | hsa-miR-15a-5p;hsa-miR-181b-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-29a-5p;hsa-miR-589-3p;hsa-miR-590-5p | 10 | TGFBR3 | Sponge network | 0.004 | 0.98116 | -2.338 | 0 | 0.293 |
103 | AC108676.1 | hsa-let-7c-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-195-5p;hsa-miR-199b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-30a-3p;hsa-miR-30e-3p;hsa-miR-381-3p;hsa-miR-497-5p | 11 | HMGA2 | Sponge network | 7.672 | 0 | 4.457 | 0 | 0.292 |
104 | RP6-91H8.3 | hsa-let-7c-5p;hsa-miR-125b-2-3p;hsa-miR-148a-5p;hsa-miR-195-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-30b-5p;hsa-miR-30d-3p;hsa-miR-30d-5p;hsa-miR-30e-3p;hsa-miR-30e-5p;hsa-miR-497-5p;hsa-miR-532-5p | 13 | HMGA2 | Sponge network | 3.796 | 0 | 4.457 | 0 | 0.292 |
105 | MAGI2-AS3 |
hsa-let-7a-3p;hsa-miR-142-3p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-205-3p;hsa-miR-26b-5p;hsa-miR-29a-5p;hsa-miR-30c-5p;hsa-miR-330-5p;hsa-miR-576-5p;hsa-miR-582-5p;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-92a-3p | 16 | WNT5A | Sponge network | -0.939 | 4.0E-5 | 0.23 | 0.27604 | 0.291 |
106 | HCG22 | hsa-miR-15b-5p;hsa-miR-181b-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-424-5p;hsa-miR-450b-5p;hsa-miR-455-5p;hsa-miR-7-1-3p | 10 | TGFBR3 | Sponge network | -4.567 | 0 | -2.338 | 0 | 0.286 |
107 | RP11-379B18.5 | hsa-let-7a-5p;hsa-let-7b-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30d-5p;hsa-miR-30e-3p;hsa-miR-30e-5p;hsa-miR-381-3p;hsa-miR-664a-5p | 18 | HMGA2 | Sponge network | 1.569 | 0 | 4.457 | 0 | 0.285 |
108 | FOXD2-AS1 | hsa-let-7b-5p;hsa-let-7c-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-5p;hsa-miR-199b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-30a-3p | 10 | HMGA2 | Sponge network | 2.446 | 0 | 4.457 | 0 | 0.276 |
109 | RP11-757G1.6 | hsa-miR-15a-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-339-5p;hsa-miR-424-5p;hsa-miR-589-3p;hsa-miR-944 | 11 | TGFBR3 | Sponge network | -1.346 | 0.00088 | -2.338 | 0 | 0.276 |
110 | RP11-598F7.6 | hsa-let-7c-5p;hsa-miR-125b-5p;hsa-miR-195-5p;hsa-miR-199b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-497-5p | 10 | HMGA2 | Sponge network | 4.086 | 0 | 4.457 | 0 | 0.273 |
111 | AC006262.4 | hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-195-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-497-5p | 13 | HMGA2 | Sponge network | 1.721 | 0.01526 | 4.457 | 0 | 0.271 |
112 | RP11-848P1.4 | hsa-let-7a-5p;hsa-let-7b-5p;hsa-let-7c-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-26a-5p;hsa-miR-30a-3p;hsa-miR-30a-5p | 10 | HMGA2 | Sponge network | 2.864 | 0 | 4.457 | 0 | 0.268 |
113 | RP11-166D19.1 |
hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-27a-3p;hsa-miR-339-5p;hsa-miR-484;hsa-miR-589-3p;hsa-miR-590-5p;hsa-miR-7-1-3p;hsa-miR-944 | 15 | TGFBR3 | Sponge network | -0.882 | 5.0E-5 | -2.338 | 0 | 0.267 |
114 | AC144831.1 | hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-3p;hsa-miR-21-5p;hsa-miR-424-5p;hsa-miR-450b-5p;hsa-miR-7-1-3p | 10 | TGFBR3 | Sponge network | -1.546 | 0 | -2.338 | 0 | 0.266 |
115 | HHIP-AS1 |
hsa-miR-15a-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-29a-5p;hsa-miR-455-5p;hsa-miR-7-1-3p;hsa-miR-944 | 10 | TGFBR3 | Sponge network | -1.293 | 0.01561 | -2.338 | 0 | 0.264 |
116 | LINC00865 | hsa-miR-15a-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-27a-3p;hsa-miR-29a-5p;hsa-miR-339-5p;hsa-miR-424-5p | 10 | TGFBR3 | Sponge network | -0.336 | 0.22355 | -2.338 | 0 | 0.259 |
117 | APCDD1L-AS1 |
hsa-let-7c-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-125b-5p;hsa-miR-148a-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-497-5p;hsa-miR-532-5p;hsa-miR-664a-5p | 13 | HMGA2 | Sponge network | 2.077 | 0 | 4.457 | 0 | 0.256 |
118 | LUCAT1 | hsa-let-7a-5p;hsa-let-7c-5p;hsa-let-7g-5p;hsa-miR-125b-2-3p;hsa-miR-148a-5p;hsa-miR-195-3p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-26a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-532-5p | 13 | HMGA2 | Sponge network | 1.475 | 0 | 4.457 | 0 | 0.25 |