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-125b-5p | AKT1 | -0.35 | 0.0042 | 0.07 | 0.42433 | miRNAWalker2 validate; miRTarBase | -0.1 | 0.00717 | NA | |
2 | hsa-let-7a-5p | AKT2 | -0.64 | 0 | 0.65 | 0 | TargetScan | -0.33 | 0 | NA | |
3 | hsa-let-7b-3p | AKT2 | -0.4 | 0.00233 | 0.65 | 0 | MirTarget | -0.11 | 0.01121 | NA | |
4 | hsa-let-7f-1-3p | AKT2 | 0.02 | 0.90939 | 0.65 | 0 | MirTarget | -0.1 | 0.01135 | NA | |
5 | hsa-miR-140-5p | AKT2 | -0.62 | 0 | 0.65 | 0 | mirMAP | -0.11 | 0.03688 | NA | |
6 | hsa-miR-1976 | AKT2 | -1.14 | 0 | 0.65 | 0 | miRNATAP | -0.11 | 0.01016 | NA | |
7 | hsa-miR-22-3p | AKT2 | -0.49 | 0 | 0.65 | 0 | mirMAP | -0.19 | 0.00177 | NA | |
8 | hsa-miR-29a-3p | AKT2 | -1.03 | 0 | 0.65 | 0 | MirTarget | -0.13 | 0.00232 | 24076586 | Furthermore a feed-back loop comprising of c-Myc miR-29 family and Akt2 were found in myeloid leukemogenesis |
9 | hsa-miR-30e-3p | AKT2 | -0.57 | 0 | 0.65 | 0 | mirMAP | -0.12 | 0.01888 | NA | |
10 | hsa-miR-106b-5p | AKT3 | 0.77 | 0 | -1.05 | 0 | miRNATAP | -0.3 | 0.00047 | NA | |
11 | hsa-miR-15b-5p | AKT3 | 0.58 | 1.0E-5 | -1.05 | 0 | miRNATAP | -0.23 | 0.01218 | NA | |
12 | hsa-miR-17-5p | AKT3 | 1.27 | 0 | -1.05 | 0 | TargetScan; miRNATAP | -0.18 | 0.00931 | NA | |
13 | hsa-miR-362-5p | AKT3 | 0.26 | 0.18295 | -1.05 | 0 | PITA; TargetScan; miRNATAP | -0.16 | 0.00916 | NA | |
14 | hsa-miR-421 | AKT3 | 1.17 | 0 | -1.05 | 0 | miRanda; mirMAP | -0.28 | 3.0E-5 | NA | |
15 | hsa-miR-424-5p | AKT3 | 1.51 | 0 | -1.05 | 0 | miRNATAP | -0.16 | 0.01623 | 26315541 | Silencing Akt3 and E2F3 by siRNA pheno-copied the effect of ectopic miR-424 on HCC growth; Whereas overexpression of Akt3 and E2F3 attenuated the effect of miR-424 on HCC growth |
16 | hsa-miR-502-5p | AKT3 | 0.38 | 0.08522 | -1.05 | 0 | PITA; miRNATAP | -0.17 | 0.00244 | NA | |
17 | hsa-miR-505-3p | AKT3 | 1.03 | 0 | -1.05 | 0 | mirMAP | -0.17 | 0.03471 | 22051041 | We also find that Akt3 correlate inversely with miR-505 modulates drug sensitivity in MCF7-ADR |
18 | hsa-miR-548v | AKT3 | 1.38 | 0 | -1.05 | 0 | miRNATAP | -0.21 | 0.0001 | NA | |
19 | hsa-miR-616-5p | AKT3 | 2.36 | 0 | -1.05 | 0 | mirMAP | -0.18 | 0.00016 | NA | |
20 | hsa-miR-93-5p | AKT3 | 1.27 | 0 | -1.05 | 0 | miRNATAP | -0.18 | 0.00772 | NA | |
21 | hsa-miR-129-5p | ANGPT1 | 2.04 | 0 | -3.64 | 0 | miRanda; mirMAP | -0.16 | 7.0E-5 | NA | |
22 | hsa-miR-429 | ANGPT1 | 1.44 | 0 | -3.64 | 0 | miRanda | -0.36 | 0 | NA | |
23 | hsa-miR-590-3p | ANGPT1 | 0.92 | 0 | -3.64 | 0 | PITA; miRanda; mirMAP | -0.63 | 0 | NA | |
24 | hsa-miR-944 | ANGPT1 | 6.31 | 0 | -3.64 | 0 | PITA; mirMAP | -0.35 | 0 | NA | |
25 | hsa-miR-186-5p | ANGPT2 | 0.44 | 6.0E-5 | -0.31 | 0.10237 | MirTarget; mirMAP | -0.21 | 0.01831 | NA | |
26 | hsa-miR-19a-3p | ANGPT2 | 1.29 | 0 | -0.31 | 0.10237 | MirTarget | -0.14 | 0.00335 | NA | |
27 | hsa-miR-19b-3p | ANGPT2 | 0.79 | 0 | -0.31 | 0.10237 | MirTarget | -0.18 | 0.00259 | NA | |
28 | hsa-miR-33a-3p | ANGPT2 | 0.54 | 0.00271 | -0.31 | 0.10237 | mirMAP | -0.11 | 0.04544 | NA | |
29 | hsa-miR-374a-5p | ANGPT2 | -0.37 | 4.0E-5 | -0.31 | 0.10237 | mirMAP | -0.29 | 0.00762 | NA | |
30 | hsa-miR-374b-5p | ANGPT2 | -0.49 | 0 | -0.31 | 0.10237 | mirMAP | -0.33 | 0.00048 | NA | |
31 | hsa-miR-429 | ANGPT2 | 1.44 | 0 | -0.31 | 0.10237 | miRanda | -0.12 | 0.0082 | NA | |
32 | hsa-miR-576-5p | ANGPT2 | 0.99 | 0 | -0.31 | 0.10237 | mirMAP | -0.14 | 0.02034 | NA | |
33 | hsa-miR-582-5p | ANGPT2 | -0.01 | 0.93969 | -0.31 | 0.10237 | mirMAP | -0.12 | 0.03523 | NA | |
34 | hsa-miR-590-3p | ANGPT2 | 0.92 | 0 | -0.31 | 0.10237 | miRanda | -0.15 | 0.03063 | NA | |
35 | hsa-miR-628-3p | ANGPT2 | 0.96 | 0 | -0.31 | 0.10237 | mirMAP | -0.19 | 6.0E-5 | NA | |
36 | hsa-miR-140-3p | ATF2 | -1.57 | 0 | 0.03 | 0.68356 | MirTarget; PITA; miRNATAP | -0.13 | 2.0E-5 | NA | |
37 | hsa-miR-15a-5p | ATF2 | -0.25 | 0.02536 | 0.03 | 0.68356 | miRNAWalker2 validate | -0.15 | 6.0E-5 | NA | |
38 | hsa-miR-26a-5p | ATF2 | -0.93 | 0 | 0.03 | 0.68356 | MirTarget; miRNATAP | -0.15 | 0.00039 | NA | |
39 | hsa-miR-26b-5p | ATF2 | -0.02 | 0.8823 | 0.03 | 0.68356 | MirTarget; miRNATAP | -0.12 | 0.0003 | 21901137 | Coordinated regulation of ATF2 by miR 26b in γ irradiated lung cancer cells; Concurrent analysis of time-series mRNA and microRNA profiles uncovered that expression of miR-26b was down regulated and its target activating transcription factor 2 ATF2 mRNA was up regulated in γ-irradiated H1299 cells; IR in miR-26b overexpressed H1299 cells could not induce expression of ATF2; From these results we concluded that IR-induced up-regulation of ATF2 was coordinately enhanced by suppression of miR-26b in lung cancer cells which may enhance the effect of IR in the MAPK signaling pathway |
40 | hsa-miR-30b-5p | ATF2 | -1.5 | 0 | 0.03 | 0.68356 | mirMAP | -0.13 | 0 | NA | |
41 | hsa-miR-30c-5p | ATF2 | -0.43 | 0.00403 | 0.03 | 0.68356 | mirMAP | -0.1 | 0.00026 | NA | |
42 | hsa-miR-374b-5p | ATF2 | -0.49 | 0 | 0.03 | 0.68356 | miRNAWalker2 validate; mirMAP; miRNATAP | -0.11 | 0.0112 | NA | |
43 | hsa-miR-21-5p | BCL2 | 1.07 | 0 | -0.13 | 0.58174 | miRNAWalker2 validate; miRTarBase | -0.47 | 2.0E-5 | 22964582; 21468550; 25994220; 25381586; 26555418; 23359184; 21376256 | Tumors harvested from these lungs have elevated levels of oncogenic miRNAs miR-21 and miR-155; are deficient for p53-regulated miRNAs; and have heightened expression of miR-34 target genes such as Met and Bcl-2;BCL-2 up-regulation could be achieved by miR-21 overexpression which prevented T24 cells from apoptosis induced by doxorubicin; Furthermore the miR-21 induced BCL-2 up-regulation could be cancelled by the PI3K inhibitor LY294002;Meanwhile miR-21 loss reduced STAT3 and Bcl-2 activation causing an increase in the apoptosis of tumour cells in CAC mice;Changes in the sensitivity of osteosarcoma cells to CDDP were examined after transfection with miR-21 mimics or anti-miR-21 or bcl-2 siRNA in combination with CDDP;The expression of Bax Bcl-2 and miR-21 in parental and paclitaxel-resistant cells was detected by RT-PCR and Western blotting;Resveratrol induces apoptosis of pancreatic cancers cells by inhibiting miR 21 regulation of BCL 2 expression; We also used Western blot to measure BCL-2 protein levels after down-regulation of miR-21 expression; Besides down-regulation of miR-21 expression can inhibit BCL-2 expression in PANC-1 CFPAC-1 and MIA Paca-2 cells; Over-expression of miR-21 expression can reverse down-regulation of BCL-2 expression and apoptosis induced by resveratrol; In this study we demonstrated that the effect of resveratrol on apoptosis is due to inhibiting miR-21 regulation of BCL-2 expression;Bcl 2 upregulation induced by miR 21 via a direct interaction is associated with apoptosis and chemoresistance in MIA PaCa 2 pancreatic cancer cells; However the roles and mechanisms of miRNA miR-21 in regulation of Bcl-2 in pancreatic cancer remain to be elucidated; Then luciferase activity was observed after miR-21 mimics and pRL-TK plasmids containing wild-type and mutant 3'UTRs of Bcl-2 mRNA were co-transfected; Cells transfected with miR-21 inhibitor revealed an opposite trend. There was a significant increase in luciferase activity in the cells transfected with the wild-type pRL-TK plasmid in contrast to those transfected with the mutant one indicating that miR-21 promotes Bcl-2 expression by binding directly to the 3'UTR of Bcl-2 mRNA; Upregulation of Bcl-2 directly induced by miR-21 is associated with apoptosis chemoresistance and proliferation of MIA PaCa-2 pancreatic cancer cells |
44 | hsa-miR-24-2-5p | BCL2 | 0.71 | 0 | -0.13 | 0.58174 | miRNAWalker2 validate; miRTarBase | -0.27 | 0.00158 | NA | |
45 | hsa-miR-29a-3p | BCL2 | -1.03 | 0 | -0.13 | 0.58174 | miRNAWalker2 validate; miRTarBase | -0.19 | 0.03427 | 20041405 | Subsequent investigation characterized two antiapoptotic molecules Bcl-2 and Mcl-1 as direct targets of miR-29; Furthermore silencing of Bcl-2 and Mcl-1 phenocopied the proapoptotic effect of miR-29 whereas overexpression of these proteins attenuated the effect of miR-29 |
46 | hsa-miR-29a-5p | BCL2 | 0.14 | 0.31145 | -0.13 | 0.58174 | mirMAP | -0.18 | 0.03245 | 20041405 | Subsequent investigation characterized two antiapoptotic molecules Bcl-2 and Mcl-1 as direct targets of miR-29; Furthermore silencing of Bcl-2 and Mcl-1 phenocopied the proapoptotic effect of miR-29 whereas overexpression of these proteins attenuated the effect of miR-29 |
47 | hsa-miR-3065-5p | BCL2 | -0.96 | 0.0001 | -0.13 | 0.58174 | mirMAP | -0.15 | 0.00136 | NA | |
48 | hsa-miR-365a-3p | BCL2 | 0.79 | 0 | -0.13 | 0.58174 | miRNAWalker2 validate; miRTarBase | -0.41 | 0 | NA | |
49 | hsa-miR-409-3p | BCL2 | 1.5 | 0 | -0.13 | 0.58174 | mirMAP | -0.19 | 0.00025 | NA | |
50 | hsa-miR-582-5p | BCL2 | -0.01 | 0.93969 | -0.13 | 0.58174 | PITA | -0.19 | 0.00404 | NA | |
51 | hsa-miR-7-5p | BCL2 | 2.15 | 0 | -0.13 | 0.58174 | miRNAWalker2 validate; miRTarBase; mirMAP | -0.11 | 0.01667 | 26464649; 25862909; 21750649 | Western blotting was used to evaluate the effect of miR-7 on Bcl2 in A549 and H460 cells; Moreover subsequent experiments showed that BCL-2 was downregulated by miR-7 at both transcriptional and translational levels; This study further extends the biological role of miR-7 in NSCLC A549 and H460 cells and identifies BCL-2 as a novel target possibly involved in miR-7-mediated growth suppression and apoptosis induction of NSCLC cells;miR-7 overexpression correlated with diminished BCL2 expression but there was no relationship between miR-7 and EGFR expression neither in tumour samples nor in the cell lines; Of the two postulated miR-7 target genes we examined BCL2 but not EGFR seems to be a possible miR-7 target in OC;Bioinformatics predictions revealed a potential binding site of miR-7 on 3'UTR of BCL-2 and it was further confirmed by luciferase assay; Moreover subsequent experiments showed that BCL-2 was downregulated by miR-7 at both transcriptional and translational levels; These results suggest that miR-7 regulates the expression of BCL-2 through direct 3'UTR interactions |
52 | hsa-let-7i-5p | BCL2L1 | 0.14 | 0.09018 | -0.41 | 0.00013 | miRNATAP | -0.23 | 0.00062 | NA | |
53 | hsa-miR-23b-3p | BCL2L1 | -0.3 | 0.00433 | -0.41 | 0.00013 | miRNAWalker2 validate | -0.17 | 0.00091 | NA | |
54 | hsa-miR-342-5p | BCL2L1 | 0.05 | 0.67349 | -0.41 | 0.00013 | miRNATAP | -0.12 | 0.0063 | NA | |
55 | hsa-miR-140-5p | BCL2L11 | -0.62 | 0 | 0.77 | 0 | miRanda | -0.13 | 0.0054 | NA | |
56 | hsa-miR-195-5p | BCL2L11 | -1.62 | 0 | 0.77 | 0 | miRNAWalker2 validate | -0.11 | 0.00055 | NA | |
57 | hsa-miR-221-3p | BCL2L11 | -0.38 | 0.00383 | 0.77 | 0 | miRNAWalker2 validate | -0.14 | 0.00025 | 26503209 | Knockdown of miR 221 promotes the cisplatin inducing apoptosis by targeting the BIM Bax/Bak axis in breast cancer |
58 | hsa-miR-3065-5p | BCL2L11 | -0.96 | 0.0001 | 0.77 | 0 | mirMAP | -0.11 | 0 | NA | |
59 | hsa-miR-30a-5p | BCL2L11 | -2.99 | 0 | 0.77 | 0 | miRNATAP | -0.14 | 0 | NA | |
60 | hsa-miR-30b-5p | BCL2L11 | -1.5 | 0 | 0.77 | 0 | miRNATAP | -0.17 | 0 | NA | |
61 | hsa-miR-30d-5p | BCL2L11 | -2.07 | 0 | 0.77 | 0 | miRNATAP | -0.19 | 0 | NA | |
62 | hsa-miR-338-5p | BCL2L11 | -3 | 0 | 0.77 | 0 | PITA | -0.12 | 0 | NA | |
63 | hsa-miR-136-5p | BDNF | 1.45 | 0 | -1.92 | 0 | mirMAP | -0.23 | 0.00353 | NA | |
64 | hsa-miR-155-5p | BDNF | 0.46 | 0.00515 | -1.92 | 0 | miRNATAP | -0.31 | 0.00235 | NA | |
65 | hsa-miR-191-5p | BDNF | 0.87 | 0 | -1.92 | 0 | miRNATAP | -0.48 | 0.00032 | NA | |
66 | hsa-miR-210-3p | BDNF | 4.69 | 0 | -1.92 | 0 | miRNAWalker2 validate; miRTarBase | -0.18 | 0.00071 | NA | |
67 | hsa-miR-29b-1-5p | BDNF | 0.59 | 0.00038 | -1.92 | 0 | mirMAP | -0.3 | 0.00352 | NA | |
68 | hsa-miR-330-3p | BDNF | 0.01 | 0.95128 | -1.92 | 0 | MirTarget | -0.33 | 0.0054 | NA | |
69 | hsa-miR-382-5p | BDNF | 0.8 | 5.0E-5 | -1.92 | 0 | MirTarget; miRNATAP | -0.22 | 0.01106 | NA | |
70 | hsa-miR-3913-5p | BDNF | -0.2 | 0.15226 | -1.92 | 0 | mirMAP | -0.34 | 0.00416 | NA | |
71 | hsa-miR-424-5p | BDNF | 1.51 | 0 | -1.92 | 0 | MirTarget; miRNATAP | -0.37 | 0.00015 | NA | |
72 | hsa-miR-589-3p | BDNF | 1.64 | 0 | -1.92 | 0 | MirTarget | -0.27 | 0.0008 | NA | |
73 | hsa-miR-7-1-3p | BDNF | 1.23 | 0 | -1.92 | 0 | MirTarget | -0.23 | 0.04324 | NA | |
74 | hsa-miR-125a-3p | BRCA1 | -0.49 | 0.00629 | 1.95 | 0 | MirTarget; PITA; miRanda; miRNATAP | -0.25 | 0 | 27693788 | From a mechanistic standpoint hsa-miR-125a-3p directly targeted 3'-untranslated regions 3'-UTRs of breast cancer early onset gene 1 BRCA1 and inhibits its protein expression via translational repression mechanism; In addition suppression of BRCA1 expression by siRNA treatment effectively improved hsa-miR-125a-3p deficiency-triggered chemoresistance in BCa cells; Collectively these findings suggest that hsa-miR-125a-3p may function as a tumor suppressor by regulating the BRCA1 signaling and reintroduction of hsa-miR-125a-3p analogs could be a potential adjunct therapy for advanced/chemoresistant BCa |
75 | hsa-miR-146b-5p | BRCA1 | -0.43 | 0.00592 | 1.95 | 0 | miRanda | -0.19 | 0.0007 | 21472990 | We report here the involvement of miR-146a and miR-146b-5p that bind to the same site in the 3'UTR of BRCA1 and down-regulate its expression as demonstrated using reporter assays; Furthermore we showed that the highest levels of miR-146a and/or miR-146b-5p are found in basal-like mammary tumour epithelial cell lines and in triple negative breast tumours which are the closest to tumours arising in carriers of BRCA1 mutations |
76 | hsa-miR-181a-5p | BRCA1 | -1.32 | 0 | 1.95 | 0 | miRNAWalker2 validate | -0.5 | 0 | NA | |
77 | hsa-miR-199a-5p | BRCA1 | 0.13 | 0.39843 | 1.95 | 0 | miRanda | -0.21 | 0.00039 | NA | |
78 | hsa-miR-199b-5p | BRCA1 | -0.12 | 0.44661 | 1.95 | 0 | miRanda | -0.23 | 8.0E-5 | NA | |
79 | hsa-miR-34c-5p | BRCA1 | -1.65 | 0 | 1.95 | 0 | miRanda | -0.14 | 0 | NA | |
80 | hsa-miR-99b-3p | BRCA1 | -0.26 | 0.1241 | 1.95 | 0 | miRNAWalker2 validate | -0.18 | 0.00065 | NA | |
81 | hsa-let-7g-5p | CCND1 | 0.09 | 0.32216 | -0.64 | 0.01031 | miRNATAP | -0.41 | 0.00606 | NA | |
82 | hsa-miR-106a-5p | CCND1 | 0.89 | 3.0E-5 | -0.64 | 0.01031 | MirTarget; miRNATAP | -0.22 | 0.00028 | NA | |
83 | hsa-miR-106b-5p | CCND1 | 0.77 | 0 | -0.64 | 0.01031 | miRNAWalker2 validate; miRTarBase; MirTarget; miRNATAP | -0.32 | 0.00062 | NA | |
84 | hsa-miR-15b-5p | CCND1 | 0.58 | 1.0E-5 | -0.64 | 0.01031 | miRNAWalker2 validate; miRTarBase; MirTarget; miRNATAP | -0.24 | 0.01303 | NA | |
85 | hsa-miR-17-5p | CCND1 | 1.27 | 0 | -0.64 | 0.01031 | miRNAWalker2 validate; MirTarget; TargetScan; miRNATAP | -0.23 | 0.0014 | 26431674 | Bioinformatics Prediction and In Vitro Analysis Revealed That miR 17 Targets Cyclin D1 mRNA in Triple Negative Breast Cancer Cells; In this study using bioinformatic analyses miR-17 was selected as it targets the 3'UTR of CCND1 gene with the highest score; After lentiviral transduction of miR-17 to the target cells gene expression analysis showed decreased expression of CCND1 gene |
86 | hsa-miR-183-5p | CCND1 | 2.81 | 0 | -0.64 | 0.01031 | miRNAWalker2 validate | -0.24 | 1.0E-5 | NA | |
87 | hsa-miR-186-5p | CCND1 | 0.44 | 6.0E-5 | -0.64 | 0.01031 | mirMAP | -0.35 | 0.00274 | NA | |
88 | hsa-miR-19a-3p | CCND1 | 1.29 | 0 | -0.64 | 0.01031 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.18 | 0.00437 | 25985117 | Moreover miR-19a might play inhibitory roles in HCC malignancy via regulating Cyclin D1 expression |
89 | hsa-miR-19b-3p | CCND1 | 0.79 | 0 | -0.64 | 0.01031 | miRNATAP | -0.2 | 0.00837 | NA | |
90 | hsa-miR-20a-5p | CCND1 | 0.76 | 3.0E-5 | -0.64 | 0.01031 | miRNAWalker2 validate; miRTarBase; MirTarget; miRNATAP | -0.16 | 0.02112 | NA | |
91 | hsa-miR-20b-5p | CCND1 | 0.4 | 0.19401 | -0.64 | 0.01031 | MirTarget; miRNATAP | -0.13 | 0.00127 | NA | |
92 | hsa-miR-340-5p | CCND1 | 0.17 | 0.17644 | -0.64 | 0.01031 | mirMAP | -0.34 | 0.00068 | NA | |
93 | hsa-miR-374b-5p | CCND1 | -0.49 | 0 | -0.64 | 0.01031 | miRNAWalker2 validate; MirTarget | -0.25 | 0.0454 | NA | |
94 | hsa-miR-425-5p | CCND1 | 0.85 | 0 | -0.64 | 0.01031 | miRNAWalker2 validate | -0.33 | 1.0E-5 | NA | |
95 | hsa-miR-503-5p | CCND1 | 2.45 | 0 | -0.64 | 0.01031 | miRNAWalker2 validate; miRTarBase; MirTarget | -0.11 | 0.04336 | 26047605; 23731275 | MiR 503 inhibited cell proliferation of human breast cancer cells by suppressing CCND1 expression; Overexpression of miR-503 in breast cancer cell lines reduced cell proliferation through inducing G0/G1 cell cycle arrest by targeting CCND1;MicroRNA 503 suppresses proliferation and cell cycle progression of endometrioid endometrial cancer by negatively regulating cyclin D1; CCND1 has a binding sequence of miR-503 within its 3' untranslated region and was confirmed to be a direct target of miR-503 by the fluorescent reporter assays; Increasing the miR-503 level in EEC cells suppressed cell viability colon formation activity and cell-cycle progression and the inhibited oncogenic phenotypes induced by miR-503 were alleviated by ectopic expression of CCND1 without the untranslated region sequence; Collectively this study suggested that miR-503 plays a tumor-suppressor role by targeting CCND1; Abnormal suppression of miR-503 leads to an increase in the CCND1 level which may promote carcinogenesis and progression of EEC |
96 | hsa-miR-589-3p | CCND1 | 1.64 | 0 | -0.64 | 0.01031 | MirTarget | -0.22 | 0.00038 | NA | |
97 | hsa-miR-590-3p | CCND1 | 0.92 | 0 | -0.64 | 0.01031 | mirMAP | -0.29 | 0.00105 | NA | |
98 | hsa-miR-7-1-3p | CCND1 | 1.23 | 0 | -0.64 | 0.01031 | mirMAP | -0.22 | 0.01076 | NA | |
99 | hsa-miR-769-3p | CCND1 | 1.7 | 0 | -0.64 | 0.01031 | mirMAP | -0.29 | 0 | NA | |
100 | hsa-miR-9-5p | CCND1 | 4.98 | 0 | -0.64 | 0.01031 | miRNAWalker2 validate | -0.14 | 0 | NA | |
101 | hsa-miR-93-5p | CCND1 | 1.27 | 0 | -0.64 | 0.01031 | miRNAWalker2 validate; MirTarget; miRNATAP | -0.25 | 0.00081 | NA | |
102 | hsa-miR-942-5p | CCND1 | 0.71 | 2.0E-5 | -0.64 | 0.01031 | MirTarget | -0.18 | 0.01967 | NA | |
103 | hsa-miR-141-3p | CCND2 | 1.97 | 0 | -0.7 | 0.01609 | MirTarget; TargetScan | -0.14 | 0.04579 | NA | |
104 | hsa-miR-17-5p | CCND2 | 1.27 | 0 | -0.7 | 0.01609 | miRNAWalker2 validate; miRTarBase; TargetScan; miRNATAP | -0.2 | 0.01613 | NA | |
105 | hsa-miR-19a-3p | CCND2 | 1.29 | 0 | -0.7 | 0.01609 | MirTarget; miRNATAP | -0.17 | 0.02171 | NA | |
106 | hsa-miR-20a-5p | CCND2 | 0.76 | 3.0E-5 | -0.7 | 0.01609 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.23 | 0.005 | NA | |
107 | hsa-miR-21-3p | CCND2 | 0.92 | 0 | -0.7 | 0.01609 | mirMAP | -0.31 | 0.00339 | NA | |
108 | hsa-miR-301a-3p | CCND2 | 1.24 | 0 | -0.7 | 0.01609 | miRNAWalker2 validate | -0.2 | 0.01072 | NA | |
109 | hsa-miR-550a-5p | CCND2 | 0.76 | 2.0E-5 | -0.7 | 0.01609 | MirTarget | -0.18 | 0.02539 | NA | |
110 | hsa-miR-589-3p | CCND2 | 1.64 | 0 | -0.7 | 0.01609 | mirMAP | -0.22 | 0.00216 | NA | |
111 | hsa-miR-590-5p | CCND2 | 1.23 | 0 | -0.7 | 0.01609 | mirMAP | -0.25 | 0.00893 | NA | |
112 | hsa-miR-616-5p | CCND2 | 2.36 | 0 | -0.7 | 0.01609 | mirMAP | -0.14 | 0.01968 | NA | |
113 | hsa-miR-7-1-3p | CCND2 | 1.23 | 0 | -0.7 | 0.01609 | mirMAP | -0.24 | 0.01647 | NA | |
114 | hsa-miR-877-5p | CCND2 | 2.9 | 0 | -0.7 | 0.01609 | miRNAWalker2 validate | -0.14 | 0.0158 | NA | |
115 | hsa-miR-15b-5p | CCND3 | 0.58 | 1.0E-5 | -1.55 | 0 | miRNATAP | -0.18 | 0.00191 | NA | |
116 | hsa-miR-27b-3p | CCND3 | 0.08 | 0.45554 | -1.55 | 0 | miRNAWalker2 validate | -0.26 | 0.00043 | NA | |
117 | hsa-miR-28-5p | CCND3 | 0.19 | 0.02781 | -1.55 | 0 | miRNATAP | -0.25 | 0.00658 | NA | |
118 | hsa-miR-320b | CCND3 | 1.16 | 0 | -1.55 | 0 | miRanda | -0.15 | 0.00033 | NA | |
119 | hsa-miR-324-5p | CCND3 | 1.22 | 0 | -1.55 | 0 | miRNAWalker2 validate | -0.22 | 0 | NA | |
120 | hsa-miR-409-5p | CCND3 | 1.56 | 0 | -1.55 | 0 | miRNATAP | -0.17 | 0 | NA | |
121 | hsa-miR-421 | CCND3 | 1.17 | 0 | -1.55 | 0 | PITA; miRanda | -0.13 | 0.00217 | NA | |
122 | hsa-miR-424-5p | CCND3 | 1.51 | 0 | -1.55 | 0 | miRNAWalker2 validate; miRTarBase | -0.18 | 7.0E-5 | NA | |
123 | hsa-miR-429 | CCND3 | 1.44 | 0 | -1.55 | 0 | miRNATAP | -0.2 | 0 | NA | |
124 | hsa-miR-454-3p | CCND3 | 0.94 | 0 | -1.55 | 0 | miRNATAP | -0.16 | 0.00095 | NA | |
125 | hsa-miR-940 | CCND3 | 1.92 | 0 | -1.55 | 0 | MirTarget; miRNATAP | -0.19 | 0 | NA | |
126 | hsa-miR-96-5p | CCND3 | 2.81 | 0 | -1.55 | 0 | TargetScan | -0.23 | 0 | NA | |
127 | hsa-miR-125b-5p | CCNE1 | -0.35 | 0.0042 | 3.92 | 0 | miRNAWalker2 validate | -0.58 | 0 | NA | |
128 | hsa-miR-138-5p | CCNE1 | -1.37 | 0 | 3.92 | 0 | MirTarget; miRNATAP | -0.31 | 0 | NA | |
129 | hsa-miR-195-5p | CCNE1 | -1.62 | 0 | 3.92 | 0 | miRNAWalker2 validate; MirTarget; miRNATAP | -0.92 | 0 | 24402230 | Furthermore through qPCR and western blot assays we showed that overexpression of miR-195-5p reduced CCNE1 mRNA and protein levels respectively |
130 | hsa-miR-26a-5p | CCNE1 | -0.93 | 0 | 3.92 | 0 | miRNAWalker2 validate; miRTarBase; miRNATAP | -1.32 | 0 | 22094936 | Cell cycle regulation and CCNE1 and CDC2 were the only significant overlapping pathway and genes differentially expressed between tumors with high and low levels of miR-26a and EZH2 respectively; Low mRNA levels of EZH2 CCNE1 and CDC2 and high levels of miR-26a are associated with favorable outcome on tamoxifen |
131 | hsa-miR-497-5p | CCNE1 | -1.37 | 0 | 3.92 | 0 | MirTarget; miRNATAP | -0.87 | 0 | 25909221; 24112607; 24909281 | The effect of simultaneous overexpression of miR-497 and miR-34a on the inhibition of cell proliferation colony formation and tumor growth and the downregulation of cyclin E1 was stronger than the effect of each miRNA alone; The synergistic actions of miR-497 and miR-34a partly correlated with cyclin E1 levels; These results indicate cyclin E1 is downregulated by both miR-497 and miR-34a which synergistically retard the growth of human lung cancer cells;Western blot assays confirmed that overexpression of miR-497 reduced cyclin E1 protein levels; Inhibited cellular growth suppressed cellular migration and invasion and G1 cell cycle arrest were observed upon overexpression of miR-497 in cells possibly by targeting cyclin E1;miR 497 suppresses proliferation of human cervical carcinoma HeLa cells by targeting cyclin E1; Furthermore the target effect of miR-497 on the CCNE1 was identified by dual-luciferase reporter assay system qRT-PCR and Western blotting; Over-expressed miR-497 in HeLa cells could suppress cell proliferation by targeting CCNE1 |
132 | hsa-let-7b-3p | CCNE2 | -0.4 | 0.00233 | 2.53 | 0 | mirMAP | -0.3 | 0.00016 | NA | |
133 | hsa-miR-126-3p | CCNE2 | -1.53 | 0 | 2.53 | 0 | miRNAWalker2 validate | -0.41 | 0 | NA | |
134 | hsa-miR-140-5p | CCNE2 | -0.62 | 0 | 2.53 | 0 | miRanda | -0.5 | 0 | NA | |
135 | hsa-miR-26a-5p | CCNE2 | -0.93 | 0 | 2.53 | 0 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.94 | 0 | 24116110; 21901171 | The loss of miR 26a mediated post transcriptional regulation of cyclin E2 in pancreatic cancer cell proliferation and decreased patient survival; The in vitro and in vivo assays showed that overexpression of miR-26a resulted in cell cycle arrest inhibited cell proliferation and decreased tumor growth which was associated with cyclin E2 downregulation;We also show that enforced expression of miR-26a in AML cells is able to inhibit cell cycle progression by downregulating cyclin E2 expression |
136 | hsa-miR-3065-5p | CCNE2 | -0.96 | 0.0001 | 2.53 | 0 | mirMAP | -0.12 | 0.00406 | NA | |
137 | hsa-miR-30a-5p | CCNE2 | -2.99 | 0 | 2.53 | 0 | miRNATAP | -0.53 | 0 | NA | |
138 | hsa-miR-30b-5p | CCNE2 | -1.5 | 0 | 2.53 | 0 | miRNAWalker2 validate; miRTarBase | -0.39 | 0 | 22384020 | A luciferase-based reporter assay demonstrated that miR-30b post-transcriptionally reduced 27% p = 0.005 of the gene expression by interacting with two binding sites in the 3'-UTR of CCNE2; The upregulation of miR-30b by trastuzumab may play a biological role in trastuzumab-induced cell growth inhibition by targeting CCNE2 |
139 | hsa-miR-30c-5p | CCNE2 | -0.43 | 0.00403 | 2.53 | 0 | miRNATAP | -0.21 | 0.00294 | NA | |
140 | hsa-miR-30d-5p | CCNE2 | -2.07 | 0 | 2.53 | 0 | miRNATAP | -0.54 | 0 | 25843294 | MicroRNA 30d 5p inhibits tumour cell proliferation and motility by directly targeting CCNE2 in non small cell lung cancer; In addition the re-introduction of CCNE2 expression antagonised the inhibitory effects of miR-30d-5p on the capacity of NSCLC cells for proliferation and motility |
141 | hsa-miR-34a-5p | CCNE2 | -0.44 | 0.00012 | 2.53 | 0 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.28 | 0.00211 | NA | |
142 | hsa-miR-34b-5p | CCNE2 | -1.07 | 0.00216 | 2.53 | 0 | miRNAWalker2 validate; miRTarBase | -0.11 | 0.00016 | NA | |
143 | hsa-miR-34c-5p | CCNE2 | -1.65 | 0 | 2.53 | 0 | miRNAWalker2 validate; miRTarBase; PITA; miRanda; miRNATAP | -0.14 | 0 | NA | |
144 | hsa-miR-140-5p | CDK2 | -0.62 | 0 | 0.97 | 0 | miRanda | -0.25 | 0 | NA | |
145 | hsa-miR-145-5p | CDK4 | -1.08 | 0 | 1.34 | 0 | miRNAWalker2 validate; miRTarBase | -0.28 | 0 | 21092188 | Furthermore we found that CDK4 was regulated by miR-145 in cell cycle control |
146 | hsa-miR-195-5p | CDK4 | -1.62 | 0 | 1.34 | 0 | miRNAWalker2 validate; miRTarBase | -0.31 | 0 | NA | |
147 | hsa-miR-34a-5p | CDK4 | -0.44 | 0.00012 | 1.34 | 0 | miRNAWalker2 validate; miRTarBase | -0.21 | 5.0E-5 | 25789847 | Real-time PCR and western blot analysis of extracted RNA and total protein revealed artemsinin and artesunate increased miR-34a expression in a dose-dependent manner correlating with down-regulation of the miR-34a target gene CDK4; Phytochemical treatments inhibited the luciferase activity of a construct containing the wild-type 3'UTR of CDK4 but not those with a mutated miR-34a binding site whereas transfection of miR-34a inhibitors ablated the phytochemical mediated down-regulation of CDK4 and induction of cell cycle arrest |
148 | hsa-miR-486-5p | CDK4 | -3.31 | 0 | 1.34 | 0 | miRanda; miRNATAP | -0.15 | 0 | 27049724 | Direct repression of the oncogene CDK4 by the tumor suppressor miR 486 5p in non small cell lung cancer; Additionally we showed that CDK4 an oncogene that plays an important role in cell cycle G1/S phase progression was directly targeted by miR-486-5p; Collectively our results suggest that miR-486-5p could not only inhibit NSCLC by downregulating the expression of CDK4 but also be as a promising and potent therapy in the near future |
149 | hsa-miR-101-3p | CDK6 | -2.02 | 0 | 1.06 | 0 | mirMAP | -0.3 | 0 | NA | |
150 | hsa-miR-107 | CDK6 | -0.46 | 1.0E-5 | 1.06 | 0 | miRNAWalker2 validate; miRTarBase; PITA; miRNATAP | -0.18 | 0.0351 | 19407485; 22491216; 21264532; 19688090 | Enforced expression of miR-107 in MiaPACA-2 and PANC-1 cells downregulated in vitro growth and this was associated with repression of the putative miR-107 target cyclin-dependent kinase 6 thereby providing a functional basis for the epigenetic inactivation of this miRNA in pancreatic cancer;Levels of known miR-107 targets protein kinase Cε PKCε cyclin-dependent kinase 6 CDK6 and hypoxia-inducible factor 1-β HIF1-β decreased following NP/pre-miR-107 treatment;We have identified miR-107 as a potential regulator of CDK6 expression; A bioinformatics search revealed a putative target site for miR-107 within the CDK6 3' untranslated region; Expression of miR-107 in gastric cancer cell lines was found inversely correlated with CDK6 expression; miR-107 could significantly suppress CDK6 3' UTR luciferase reporter activity and this effect was not detectable when the putative 3' UTR target site was mutated; Consistent with the results of the reporter assay ectopic expression of miR-107 reduced both mRNA and protein expression levels of CDK6 inhibited proliferation induced G1 cell cycle arrest and blocked invasion of the gastric cancer cells; Our results suggest that miR-107 may have a tumor suppressor function by directly targeting CDK6 to inhibit the proliferation and invasion activities of gastric cancer cells;Using miRNA-target prediction analyses and the array data we listed up a set of likely targets of miR-107 and miR-185 for G1 cell cycle arrest and validate a subset of them using real-time RT-PCR and immunoblotting for CDK6 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | REGULATION OF PHOSPHORUS METABOLIC PROCESS | 128 | 1618 | 9.418e-73 | 4.382e-69 |
2 | TRANSMEMBRANE RECEPTOR PROTEIN TYROSINE KINASE SIGNALING PATHWAY | 80 | 498 | 1.233e-66 | 2.869e-63 |
3 | REGULATION OF PROTEIN MODIFICATION PROCESS | 124 | 1710 | 1.498e-65 | 2.324e-62 |
4 | POSITIVE REGULATION OF PHOSPHATE METABOLIC PROCESS | 100 | 1036 | 1.151e-62 | 9.286e-60 |
5 | CELLULAR RESPONSE TO ORGANIC SUBSTANCE | 125 | 1848 | 1.197e-62 | 9.286e-60 |
6 | POSITIVE REGULATION OF PHOSPHORUS METABOLIC PROCESS | 100 | 1036 | 1.151e-62 | 9.286e-60 |
7 | REGULATION OF KINASE ACTIVITY | 87 | 776 | 3.502e-59 | 2.328e-56 |
8 | ENZYME LINKED RECEPTOR PROTEIN SIGNALING PATHWAY | 83 | 689 | 8.681e-59 | 5.049e-56 |
9 | POSITIVE REGULATION OF RESPONSE TO STIMULUS | 123 | 1929 | 1.691e-58 | 8.745e-56 |
10 | POSITIVE REGULATION OF PROTEIN MODIFICATION PROCESS | 98 | 1135 | 1.068e-56 | 4.971e-54 |
11 | PROTEIN PHOSPHORYLATION | 91 | 944 | 2.393e-56 | 1.012e-53 |
12 | POSITIVE REGULATION OF PROTEIN METABOLIC PROCESS | 108 | 1492 | 1.569e-55 | 6.084e-53 |
13 | REGULATION OF PHOSPHATIDYLINOSITOL 3 KINASE SIGNALING | 47 | 138 | 2.962e-55 | 1.06e-52 |
14 | POSITIVE REGULATION OF CELL PROLIFERATION | 85 | 814 | 3.925e-55 | 1.305e-52 |
15 | POSITIVE REGULATION OF KINASE ACTIVITY | 70 | 482 | 1.039e-54 | 3.224e-52 |
16 | INTRACELLULAR SIGNAL TRANSDUCTION | 109 | 1572 | 3.073e-54 | 8.423e-52 |
17 | POSITIVE REGULATION OF MOLECULAR FUNCTION | 115 | 1791 | 3.077e-54 | 8.423e-52 |
18 | REGULATION OF TRANSFERASE ACTIVITY | 89 | 946 | 4.473e-54 | 1.156e-51 |
19 | REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 111 | 1656 | 6.693e-54 | 1.639e-51 |
20 | REGULATION OF CELL PROLIFERATION | 106 | 1496 | 2.021e-53 | 4.702e-51 |
21 | POSITIVE REGULATION OF CELL COMMUNICATION | 107 | 1532 | 2.18e-53 | 4.829e-51 |
22 | POSITIVE REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 84 | 876 | 2.03e-51 | 4.293e-49 |
23 | PHOSPHORYLATION | 95 | 1228 | 1.783e-50 | 3.607e-48 |
24 | LOCOMOTION | 91 | 1114 | 4.122e-50 | 7.991e-48 |
25 | REGULATION OF MAPK CASCADE | 74 | 660 | 1.036e-49 | 1.929e-47 |
26 | EXTRACELLULAR STRUCTURE ORGANIZATION | 56 | 304 | 2.307e-49 | 4.128e-47 |
27 | POSITIVE REGULATION OF MAPK CASCADE | 65 | 470 | 3.131e-49 | 5.395e-47 |
28 | POSITIVE REGULATION OF CATALYTIC ACTIVITY | 102 | 1518 | 6.249e-49 | 1.038e-46 |
29 | POSITIVE REGULATION OF TRANSFERASE ACTIVITY | 71 | 616 | 2.074e-48 | 3.327e-46 |
30 | RESPONSE TO ENDOGENOUS STIMULUS | 99 | 1450 | 6.582e-48 | 1.021e-45 |
31 | REGULATION OF CELLULAR COMPONENT MOVEMENT | 75 | 771 | 6.079e-46 | 9.125e-44 |
32 | CELLULAR RESPONSE TO ENDOGENOUS STIMULUS | 83 | 1008 | 1.53e-45 | 2.225e-43 |
33 | REGULATION OF MULTICELLULAR ORGANISMAL DEVELOPMENT | 102 | 1672 | 4.835e-45 | 6.818e-43 |
34 | POSITIVE REGULATION OF LOCOMOTION | 58 | 420 | 1.028e-43 | 1.407e-41 |
35 | REGULATION OF PROTEIN SERINE THREONINE KINASE ACTIVITY | 60 | 470 | 3.19e-43 | 4.241e-41 |
36 | CELL MOTILITY | 74 | 835 | 1.932e-42 | 2.429e-40 |
37 | LOCALIZATION OF CELL | 74 | 835 | 1.932e-42 | 2.429e-40 |
38 | MOVEMENT OF CELL OR SUBCELLULAR COMPONENT | 88 | 1275 | 2.543e-42 | 3.114e-40 |
39 | REGULATION OF CELL DEATH | 93 | 1472 | 8.779e-42 | 1.047e-39 |
40 | POSITIVE REGULATION OF PROTEIN SERINE THREONINE KINASE ACTIVITY | 49 | 289 | 2.947e-41 | 3.428e-39 |
41 | INOSITOL LIPID MEDIATED SIGNALING | 37 | 124 | 5.039e-41 | 5.719e-39 |
42 | PEPTIDYL TYROSINE MODIFICATION | 42 | 186 | 7.139e-41 | 7.909e-39 |
43 | PHOSPHATE CONTAINING COMPOUND METABOLIC PROCESS | 104 | 1977 | 3.964e-40 | 4.29e-38 |
44 | POSITIVE REGULATION OF MULTICELLULAR ORGANISMAL PROCESS | 89 | 1395 | 4.185e-40 | 4.425e-38 |
45 | RESPONSE TO OXYGEN CONTAINING COMPOUND | 88 | 1381 | 1.467e-39 | 1.517e-37 |
46 | RESPONSE TO EXTERNAL STIMULUS | 99 | 1821 | 4.059e-39 | 4.106e-37 |
47 | RESPONSE TO GROWTH FACTOR | 56 | 475 | 2.366e-38 | 2.342e-36 |
48 | NEGATIVE REGULATION OF CELL DEATH | 71 | 872 | 3.646e-38 | 3.534e-36 |
49 | POSITIVE REGULATION OF DEVELOPMENTAL PROCESS | 78 | 1142 | 9.539e-37 | 9.058e-35 |
50 | REGULATION OF MAP KINASE ACTIVITY | 47 | 319 | 1.254e-36 | 1.167e-34 |
51 | RESPONSE TO HORMONE | 70 | 893 | 1.588e-36 | 1.448e-34 |
52 | TISSUE DEVELOPMENT | 88 | 1518 | 2.399e-36 | 2.147e-34 |
53 | POSITIVE REGULATION OF MAP KINASE ACTIVITY | 39 | 207 | 1.072e-34 | 9.412e-33 |
54 | BIOLOGICAL ADHESION | 72 | 1032 | 2.607e-34 | 2.246e-32 |
55 | REGULATION OF PEPTIDYL TYROSINE PHOSPHORYLATION | 39 | 213 | 3.444e-34 | 2.913e-32 |
56 | RESPONSE TO NITROGEN COMPOUND | 66 | 859 | 8.481e-34 | 7.047e-32 |
57 | REGULATION OF HYDROLASE ACTIVITY | 79 | 1327 | 4.669e-33 | 3.812e-31 |
58 | SIGNAL TRANSDUCTION BY PROTEIN PHOSPHORYLATION | 48 | 404 | 5.958e-33 | 4.779e-31 |
59 | CELLULAR RESPONSE TO OXYGEN CONTAINING COMPOUND | 63 | 799 | 7.691e-33 | 6.066e-31 |
60 | CELLULAR RESPONSE TO NITROGEN COMPOUND | 51 | 505 | 1.487e-31 | 1.153e-29 |
61 | CARDIOVASCULAR SYSTEM DEVELOPMENT | 61 | 788 | 2.611e-31 | 1.959e-29 |
62 | CIRCULATORY SYSTEM DEVELOPMENT | 61 | 788 | 2.611e-31 | 1.959e-29 |
63 | VASCULATURE DEVELOPMENT | 49 | 469 | 5.398e-31 | 3.987e-29 |
64 | PEPTIDYL AMINO ACID MODIFICATION | 62 | 841 | 1.206e-30 | 8.766e-29 |
65 | LIPID PHOSPHORYLATION | 28 | 99 | 1.831e-30 | 1.31e-28 |
66 | TAXIS | 48 | 464 | 3.687e-30 | 2.599e-28 |
67 | REGULATION OF CELL ADHESION | 54 | 629 | 7.452e-30 | 5.175e-28 |
68 | REGULATION OF CELL DIFFERENTIATION | 79 | 1492 | 1.427e-29 | 9.762e-28 |
69 | ACTIVATION OF PROTEIN KINASE ACTIVITY | 39 | 279 | 1.621e-29 | 1.093e-27 |
70 | POSITIVE REGULATION OF PEPTIDYL TYROSINE PHOSPHORYLATION | 32 | 162 | 2.939e-29 | 1.953e-27 |
71 | ANGIOGENESIS | 39 | 293 | 1.087e-28 | 7.121e-27 |
72 | ANATOMICAL STRUCTURE FORMATION INVOLVED IN MORPHOGENESIS | 63 | 957 | 2.215e-28 | 1.431e-26 |
73 | CELL SUBSTRATE ADHESION | 31 | 164 | 9.603e-28 | 6.121e-26 |
74 | CELLULAR RESPONSE TO HORMONE STIMULUS | 49 | 552 | 1.022e-27 | 6.427e-26 |
75 | RESPONSE TO PEPTIDE | 43 | 404 | 1.575e-27 | 9.773e-26 |
76 | BLOOD VESSEL MORPHOGENESIS | 41 | 364 | 3.129e-27 | 1.916e-25 |
77 | CELL DEVELOPMENT | 74 | 1426 | 5.376e-27 | 3.249e-25 |
78 | POSITIVE REGULATION OF PHOSPHATIDYLINOSITOL 3 KINASE SIGNALING | 22 | 62 | 1.171e-26 | 6.983e-25 |
79 | CELL DEATH | 62 | 1001 | 1.817e-26 | 1.07e-24 |
80 | ORGAN MORPHOGENESIS | 57 | 841 | 3.147e-26 | 1.83e-24 |
81 | LEUKOCYTE MIGRATION | 35 | 259 | 4.984e-26 | 2.863e-24 |
82 | REGULATION OF ANATOMICAL STRUCTURE MORPHOGENESIS | 62 | 1021 | 5.297e-26 | 3.006e-24 |
83 | IMMUNE SYSTEM PROCESS | 85 | 1984 | 1.585e-25 | 8.885e-24 |
84 | PHOSPHATIDYLINOSITOL METABOLIC PROCESS | 31 | 193 | 1.773e-25 | 9.821e-24 |
85 | POSITIVE REGULATION OF HYDROLASE ACTIVITY | 58 | 905 | 1.865e-25 | 1.021e-23 |
86 | POSITIVE REGULATION OF GENE EXPRESSION | 79 | 1733 | 2.876e-25 | 1.556e-23 |
87 | POSITIVE REGULATION OF BIOSYNTHETIC PROCESS | 80 | 1805 | 8.063e-25 | 4.312e-23 |
88 | POSITIVE REGULATION OF CELLULAR COMPONENT ORGANIZATION | 64 | 1152 | 9.589e-25 | 5.07e-23 |
89 | REGULATION OF EPITHELIAL CELL PROLIFERATION | 35 | 285 | 1.353e-24 | 7.072e-23 |
90 | POSITIVE REGULATION OF ERK1 AND ERK2 CASCADE | 29 | 172 | 1.632e-24 | 8.436e-23 |
91 | RESPONSE TO WOUNDING | 46 | 563 | 1.738e-24 | 8.885e-23 |
92 | PROTEIN AUTOPHOSPHORYLATION | 30 | 192 | 2.57e-24 | 1.3e-22 |
93 | REGULATION OF LIPID KINASE ACTIVITY | 19 | 48 | 2.907e-24 | 1.455e-22 |
94 | RESPONSE TO LIPID | 56 | 888 | 3.264e-24 | 1.616e-22 |
95 | CELLULAR RESPONSE TO PEPTIDE | 34 | 274 | 4.623e-24 | 2.264e-22 |
96 | PHOSPHATIDYLINOSITOL 3 PHOSPHATE BIOSYNTHETIC PROCESS | 19 | 49 | 4.696e-24 | 2.276e-22 |
97 | CELL PROLIFERATION | 49 | 672 | 6.914e-24 | 3.317e-22 |
98 | REGULATION OF ERK1 AND ERK2 CASCADE | 32 | 238 | 8.671e-24 | 4.117e-22 |
99 | REGULATION OF IMMUNE SYSTEM PROCESS | 69 | 1403 | 1.053e-23 | 4.951e-22 |
100 | RESPONSE TO ABIOTIC STIMULUS | 59 | 1024 | 1.539e-23 | 7.161e-22 |
101 | POSITIVE REGULATION OF EPITHELIAL CELL PROLIFERATION | 27 | 154 | 2.33e-23 | 1.073e-21 |
102 | POSITIVE REGULATION OF CELL DIFFERENTIATION | 53 | 823 | 2.576e-23 | 1.175e-21 |
103 | LIPID MODIFICATION | 30 | 210 | 3.861e-23 | 1.744e-21 |
104 | NEUROGENESIS | 68 | 1402 | 5.318e-23 | 2.379e-21 |
105 | CELL ACTIVATION | 44 | 568 | 1.681e-22 | 7.447e-21 |
106 | REGULATION OF PHOSPHATIDYLINOSITOL 3 KINASE ACTIVITY | 17 | 40 | 1.763e-22 | 7.739e-21 |
107 | CELL MATRIX ADHESION | 24 | 119 | 2.113e-22 | 9.187e-21 |
108 | INTEGRIN MEDIATED SIGNALING PATHWAY | 21 | 82 | 4.325e-22 | 1.863e-20 |
109 | REGULATION OF VASCULATURE DEVELOPMENT | 30 | 233 | 8.524e-22 | 3.639e-20 |
110 | REGULATION OF LIPID METABOLIC PROCESS | 32 | 282 | 1.755e-21 | 7.424e-20 |
111 | REGULATION OF RESPONSE TO STRESS | 67 | 1468 | 3.386e-21 | 1.419e-19 |
112 | RESPONSE TO ORGANIC CYCLIC COMPOUND | 53 | 917 | 3.673e-21 | 1.526e-19 |
113 | WOUND HEALING | 39 | 470 | 4.762e-21 | 1.961e-19 |
114 | REGULATION OF NEURON DEATH | 30 | 252 | 8.5e-21 | 3.469e-19 |
115 | POSITIVE REGULATION OF IMMUNE SYSTEM PROCESS | 51 | 867 | 1.086e-20 | 4.393e-19 |
116 | CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 40 | 513 | 1.364e-20 | 5.473e-19 |
117 | POSITIVE REGULATION OF CELL ADHESION | 35 | 376 | 1.441e-20 | 5.731e-19 |
118 | REGULATION OF PHOSPHOLIPID METABOLIC PROCESS | 18 | 61 | 2.437e-20 | 9.61e-19 |
119 | REGULATION OF TRANSPORT | 73 | 1804 | 3.593e-20 | 1.405e-18 |
120 | EMBRYO DEVELOPMENT | 51 | 894 | 4.124e-20 | 1.599e-18 |
121 | GLYCEROPHOSPHOLIPID METABOLIC PROCESS | 31 | 297 | 9.276e-20 | 3.567e-18 |
122 | PHOSPHATIDYLINOSITOL BIOSYNTHETIC PROCESS | 22 | 120 | 1.138e-19 | 4.341e-18 |
123 | REGULATION OF GTPASE ACTIVITY | 44 | 673 | 1.291e-19 | 4.883e-18 |
124 | GLYCEROLIPID METABOLIC PROCESS | 33 | 356 | 2.225e-19 | 8.348e-18 |
125 | PLATELET ACTIVATION | 23 | 142 | 3.063e-19 | 1.14e-17 |
126 | REGULATION OF CELL CYCLE | 51 | 949 | 5.377e-19 | 1.986e-17 |
127 | REGULATION OF ENDOTHELIAL CELL MIGRATION | 21 | 114 | 7.136e-19 | 2.615e-17 |
128 | REGULATION OF EPITHELIAL CELL MIGRATION | 24 | 166 | 7.813e-19 | 2.84e-17 |
129 | POSITIVE REGULATION OF CELL DIVISION | 22 | 132 | 9.896e-19 | 3.569e-17 |
130 | REGULATION OF RESPONSE TO EXTERNAL STIMULUS | 50 | 926 | 1.039e-18 | 3.72e-17 |
131 | RESPONSE TO CYTOKINE | 44 | 714 | 1.235e-18 | 4.386e-17 |
132 | POSITIVE REGULATION OF TRANSPORT | 50 | 936 | 1.628e-18 | 5.739e-17 |
133 | CELLULAR COMPONENT MORPHOGENESIS | 49 | 900 | 1.745e-18 | 6.105e-17 |
134 | POSITIVE REGULATION OF CELL DEATH | 40 | 605 | 4.837e-18 | 1.679e-16 |
135 | RESPONSE TO ACID CHEMICAL | 30 | 319 | 7.174e-18 | 2.473e-16 |
136 | POSITIVE REGULATION OF RESPONSE TO EXTERNAL STIMULUS | 29 | 296 | 8.661e-18 | 2.963e-16 |
137 | TUBE DEVELOPMENT | 38 | 552 | 9.39e-18 | 3.189e-16 |
138 | RESPONSE TO STEROID HORMONE | 36 | 497 | 1.471e-17 | 4.959e-16 |
139 | NEGATIVE REGULATION OF RESPONSE TO STIMULUS | 59 | 1360 | 1.538e-17 | 5.147e-16 |
140 | POSITIVE REGULATION OF VASCULATURE DEVELOPMENT | 21 | 133 | 1.983e-17 | 6.589e-16 |
141 | POSITIVE REGULATION OF CELL CYCLE | 30 | 332 | 2.186e-17 | 7.214e-16 |
142 | REGULATION OF BODY FLUID LEVELS | 36 | 506 | 2.61e-17 | 8.553e-16 |
143 | PHOSPHOLIPID METABOLIC PROCESS | 31 | 364 | 3.352e-17 | 1.091e-15 |
144 | ACTIVATION OF MAPK ACTIVITY | 21 | 137 | 3.721e-17 | 1.202e-15 |
145 | POSITIVE REGULATION OF CHEMOTAXIS | 20 | 120 | 3.92e-17 | 1.258e-15 |
146 | NEURON PROJECTION DEVELOPMENT | 37 | 545 | 4.16e-17 | 1.317e-15 |
147 | REGULATION OF IMMUNE RESPONSE | 46 | 858 | 4.144e-17 | 1.317e-15 |
148 | EPITHELIUM DEVELOPMENT | 48 | 945 | 6.554e-17 | 2.06e-15 |
149 | REGULATION OF CHEMOTAXIS | 23 | 180 | 7.146e-17 | 2.232e-15 |
150 | FORMATION OF PRIMARY GERM LAYER | 19 | 110 | 1.226e-16 | 3.802e-15 |
151 | POSITIVE REGULATION OF CELLULAR PROTEIN LOCALIZATION | 30 | 360 | 2.041e-16 | 6.288e-15 |
152 | REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 42 | 750 | 2.542e-16 | 7.78e-15 |
153 | REGULATION OF NEURON APOPTOTIC PROCESS | 23 | 192 | 3.041e-16 | 9.247e-15 |
154 | REGULATION OF CELL SUBSTRATE ADHESION | 22 | 173 | 3.83e-16 | 1.157e-14 |
155 | NEURON PROJECTION MORPHOGENESIS | 31 | 402 | 5.483e-16 | 1.646e-14 |
156 | POSITIVE REGULATION OF EPITHELIAL CELL MIGRATION | 18 | 103 | 6.405e-16 | 1.911e-14 |
157 | REGULATION OF PROTEIN KINASE B SIGNALING | 19 | 121 | 7.777e-16 | 2.305e-14 |
158 | POSITIVE REGULATION OF SMALL GTPASE MEDIATED SIGNAL TRANSDUCTION | 13 | 39 | 8.098e-16 | 2.385e-14 |
159 | CELLULAR RESPONSE TO CYTOKINE STIMULUS | 37 | 606 | 1.25e-15 | 3.658e-14 |
160 | RESPONSE TO INSULIN | 23 | 205 | 1.302e-15 | 3.786e-14 |
161 | POSITIVE REGULATION OF CELL PROJECTION ORGANIZATION | 27 | 303 | 1.354e-15 | 3.914e-14 |
162 | CELL PROJECTION ORGANIZATION | 45 | 902 | 1.383e-15 | 3.973e-14 |
163 | NEGATIVE REGULATION OF MULTICELLULAR ORGANISMAL PROCESS | 47 | 983 | 1.471e-15 | 4.199e-14 |
164 | POSITIVE REGULATION OF DNA METABOLIC PROCESS | 22 | 185 | 1.612e-15 | 4.575e-14 |
165 | RESPONSE TO ALCOHOL | 29 | 362 | 1.89e-15 | 5.33e-14 |
166 | POSITIVE REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION | 34 | 514 | 1.908e-15 | 5.347e-14 |
167 | POSITIVE REGULATION OF LIPID KINASE ACTIVITY | 12 | 32 | 2.021e-15 | 5.628e-14 |
168 | REGULATION OF APOPTOTIC SIGNALING PATHWAY | 29 | 363 | 2.032e-15 | 5.628e-14 |
169 | NEURON DEVELOPMENT | 39 | 687 | 2.165e-15 | 5.961e-14 |
170 | GLYCEROLIPID BIOSYNTHETIC PROCESS | 23 | 211 | 2.457e-15 | 6.726e-14 |
171 | REGULATION OF CELLULAR PROTEIN LOCALIZATION | 35 | 552 | 2.557e-15 | 6.958e-14 |
172 | RESPONSE TO OXYGEN LEVELS | 27 | 311 | 2.589e-15 | 6.962e-14 |
173 | HEMOSTASIS | 27 | 311 | 2.589e-15 | 6.962e-14 |
174 | PEPTIDYL SERINE MODIFICATION | 20 | 148 | 2.661e-15 | 7.115e-14 |
175 | REGULATION OF NEURON DIFFERENTIATION | 35 | 554 | 2.852e-15 | 7.583e-14 |
176 | SINGLE ORGANISM CELL ADHESION | 32 | 459 | 3.157e-15 | 8.345e-14 |
177 | REGULATION OF CELL PROJECTION ORGANIZATION | 35 | 558 | 3.543e-15 | 9.313e-14 |
178 | POSITIVE REGULATION OF ENDOTHELIAL CELL MIGRATION | 15 | 67 | 3.617e-15 | 9.455e-14 |
179 | APOPTOTIC SIGNALING PATHWAY | 26 | 289 | 3.722e-15 | 9.674e-14 |
180 | REGULATION OF REACTIVE OXYGEN SPECIES METABOLIC PROCESS | 20 | 152 | 4.503e-15 | 1.164e-13 |
181 | REGULATION OF GROWTH | 37 | 633 | 4.934e-15 | 1.268e-13 |
182 | POSITIVE REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 31 | 437 | 5.502e-15 | 1.407e-13 |
183 | RESPONSE TO FIBROBLAST GROWTH FACTOR | 18 | 116 | 5.679e-15 | 1.444e-13 |
184 | REPRODUCTIVE SYSTEM DEVELOPMENT | 30 | 408 | 6.016e-15 | 1.515e-13 |
185 | REGULATION OF CELLULAR LOCALIZATION | 53 | 1277 | 6.022e-15 | 1.515e-13 |
186 | UROGENITAL SYSTEM DEVELOPMENT | 26 | 299 | 8.407e-15 | 2.103e-13 |
187 | CELLULAR RESPONSE TO STRESS | 59 | 1565 | 9.067e-15 | 2.256e-13 |
188 | REGULATION OF PROTEIN LOCALIZATION | 45 | 950 | 9.124e-15 | 2.258e-13 |
189 | NEURON DIFFERENTIATION | 43 | 874 | 1.058e-14 | 2.604e-13 |
190 | REGULATION OF CELL DEVELOPMENT | 42 | 836 | 1.106e-14 | 2.708e-13 |
191 | REGULATION OF PHOSPHOPROTEIN PHOSPHATASE ACTIVITY | 14 | 60 | 1.643e-14 | 4.002e-13 |
192 | VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 15 | 74 | 1.765e-14 | 4.279e-13 |
193 | GLAND DEVELOPMENT | 29 | 395 | 1.829e-14 | 4.408e-13 |
194 | REGULATION OF DNA METABOLIC PROCESS | 27 | 340 | 2.317e-14 | 5.558e-13 |
195 | REGULATION OF DEVELOPMENTAL GROWTH | 25 | 289 | 3.193e-14 | 7.619e-13 |
196 | DEVELOPMENTAL PROCESS INVOLVED IN REPRODUCTION | 35 | 602 | 3.41e-14 | 8.096e-13 |
197 | REGULATION OF NEURON PROJECTION DEVELOPMENT | 29 | 408 | 4.201e-14 | 9.922e-13 |
198 | POSITIVE REGULATION OF CELL DEVELOPMENT | 31 | 472 | 4.454e-14 | 1.047e-12 |
199 | NEGATIVE REGULATION OF NEURON DEATH | 20 | 171 | 4.477e-14 | 1.047e-12 |
200 | GROWTH | 29 | 410 | 4.761e-14 | 1.108e-12 |
201 | NEGATIVE REGULATION OF DEVELOPMENTAL PROCESS | 40 | 801 | 6.296e-14 | 1.457e-12 |
202 | CELL SUBSTRATE JUNCTION ASSEMBLY | 12 | 41 | 6.402e-14 | 1.475e-12 |
203 | GASTRULATION | 19 | 155 | 8.299e-14 | 1.902e-12 |
204 | REGULATION OF ENDOTHELIAL CELL PROLIFERATION | 16 | 98 | 8.36e-14 | 1.907e-12 |
205 | REGULATION OF INTRACELLULAR TRANSPORT | 35 | 621 | 8.51e-14 | 1.932e-12 |
206 | POSITIVE REGULATION OF PHOSPHOLIPID METABOLIC PROCESS | 12 | 42 | 8.864e-14 | 2.002e-12 |
207 | FIBROBLAST GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 15 | 84 | 1.283e-13 | 2.884e-12 |
208 | REGULATION OF PROTEIN PHOSPHATASE TYPE 2A ACTIVITY | 10 | 24 | 1.308e-13 | 2.927e-12 |
209 | HOMEOSTATIC PROCESS | 52 | 1337 | 1.507e-13 | 3.354e-12 |
210 | CELL MORPHOGENESIS INVOLVED IN NEURON DIFFERENTIATION | 27 | 368 | 1.57e-13 | 3.478e-12 |
211 | POSITIVE REGULATION OF INTRACELLULAR TRANSPORT | 27 | 370 | 1.788e-13 | 3.942e-12 |
212 | POSITIVE REGULATION OF NEURON PROJECTION DEVELOPMENT | 22 | 232 | 1.834e-13 | 4.026e-12 |
213 | POSITIVE REGULATION OF DNA REPLICATION | 15 | 86 | 1.846e-13 | 4.032e-12 |
214 | CELL CHEMOTAXIS | 19 | 162 | 1.872e-13 | 4.071e-12 |
215 | CENTRAL NERVOUS SYSTEM DEVELOPMENT | 41 | 872 | 2.138e-13 | 4.628e-12 |
216 | CELLULAR LIPID METABOLIC PROCESS | 42 | 913 | 2.164e-13 | 4.661e-12 |
217 | PHOSPHOLIPID BIOSYNTHETIC PROCESS | 22 | 235 | 2.387e-13 | 5.117e-12 |
218 | EMBRYONIC MORPHOGENESIS | 32 | 539 | 2.682e-13 | 5.726e-12 |
219 | REGULATION OF CELL MATRIX ADHESION | 15 | 90 | 3.712e-13 | 7.887e-12 |
220 | IMMUNE SYSTEM DEVELOPMENT | 33 | 582 | 3.951e-13 | 8.356e-12 |
221 | POSITIVE REGULATION OF LIPID METABOLIC PROCESS | 17 | 128 | 4.608e-13 | 9.702e-12 |
222 | RESPONSE TO ESTROGEN | 21 | 218 | 4.877e-13 | 1.022e-11 |
223 | REGULATION OF CELL DIVISION | 23 | 272 | 5.755e-13 | 1.201e-11 |
224 | MULTICELLULAR ORGANISM METABOLIC PROCESS | 15 | 93 | 6.125e-13 | 1.272e-11 |
225 | CELLULAR RESPONSE TO LIPID | 29 | 457 | 7.382e-13 | 1.527e-11 |
226 | REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 18 | 153 | 7.809e-13 | 1.608e-11 |
227 | HEAD DEVELOPMENT | 36 | 709 | 8.056e-13 | 1.651e-11 |
228 | SUBSTRATE ADHESION DEPENDENT CELL SPREADING | 11 | 38 | 8.346e-13 | 1.703e-11 |
229 | STAT CASCADE | 12 | 50 | 8.908e-13 | 1.802e-11 |
230 | JAK STAT CASCADE | 12 | 50 | 8.908e-13 | 1.802e-11 |
231 | POSITIVE REGULATION OF NEURON DIFFERENTIATION | 24 | 306 | 9.039e-13 | 1.821e-11 |
232 | MULTICELLULAR ORGANISMAL MACROMOLECULE METABOLIC PROCESS | 14 | 79 | 9.546e-13 | 1.914e-11 |
233 | REGULATION OF ORGANELLE ORGANIZATION | 47 | 1178 | 1.135e-12 | 2.267e-11 |
234 | NEGATIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 15 | 98 | 1.355e-12 | 2.695e-11 |
235 | POSITIVE REGULATION OF PROTEIN KINASE B SIGNALING | 14 | 81 | 1.368e-12 | 2.709e-11 |
236 | POSITIVE REGULATION OF ORGANELLE ORGANIZATION | 32 | 573 | 1.39e-12 | 2.741e-11 |
237 | NEURON PROJECTION GUIDANCE | 20 | 205 | 1.409e-12 | 2.766e-11 |
238 | ENDODERMAL CELL DIFFERENTIATION | 11 | 40 | 1.569e-12 | 3.067e-11 |
239 | EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 15 | 99 | 1.58e-12 | 3.076e-11 |
240 | REGULATION OF CELLULAR RESPONSE TO STRESS | 35 | 691 | 1.859e-12 | 3.604e-11 |
241 | CELLULAR RESPONSE TO VASCULAR ENDOTHELIAL GROWTH FACTOR STIMULUS | 10 | 30 | 1.877e-12 | 3.623e-11 |
242 | POSITIVE REGULATION OF PHOSPHOLIPASE ACTIVITY | 12 | 53 | 1.894e-12 | 3.626e-11 |
243 | POSITIVE REGULATION OF FIBROBLAST PROLIFERATION | 12 | 53 | 1.894e-12 | 3.626e-11 |
244 | POSITIVE REGULATION OF ENDOTHELIAL CELL PROLIFERATION | 13 | 68 | 2.269e-12 | 4.327e-11 |
245 | REGULATION OF RESPONSE TO WOUNDING | 27 | 413 | 2.409e-12 | 4.575e-11 |
246 | REGULATION OF CELL ACTIVATION | 29 | 484 | 3.059e-12 | 5.785e-11 |
247 | POSITIVE REGULATION OF REACTIVE OXYGEN SPECIES METABOLIC PROCESS | 14 | 86 | 3.222e-12 | 6.07e-11 |
248 | CYTOKINE MEDIATED SIGNALING PATHWAY | 28 | 452 | 3.366e-12 | 6.315e-11 |
249 | REGULATION OF POLYSACCHARIDE METABOLIC PROCESS | 11 | 43 | 3.776e-12 | 7.056e-11 |
250 | RESPONSE TO ESTRADIOL | 17 | 146 | 4.076e-12 | 7.555e-11 |
251 | CELLULAR RESPONSE TO INSULIN STIMULUS | 17 | 146 | 4.076e-12 | 7.555e-11 |
252 | SENSORY ORGAN DEVELOPMENT | 29 | 493 | 4.806e-12 | 8.874e-11 |
253 | POSITIVE REGULATION OF STAT CASCADE | 13 | 73 | 5.904e-12 | 1.082e-10 |
254 | POSITIVE REGULATION OF JAK STAT CASCADE | 13 | 73 | 5.904e-12 | 1.082e-10 |
255 | NEGATIVE REGULATION OF CELL CYCLE | 27 | 433 | 7.227e-12 | 1.319e-10 |
256 | CELLULAR RESPONSE TO ACID CHEMICAL | 18 | 175 | 7.867e-12 | 1.419e-10 |
257 | GLIOGENESIS | 18 | 175 | 7.867e-12 | 1.419e-10 |
258 | HOMEOSTASIS OF NUMBER OF CELLS | 18 | 175 | 7.867e-12 | 1.419e-10 |
259 | REGULATION OF GLUCOSE IMPORT | 12 | 60 | 9.195e-12 | 1.645e-10 |
260 | POSITIVE REGULATION OF SMOOTH MUSCLE CELL PROLIFERATION | 12 | 60 | 9.195e-12 | 1.645e-10 |
261 | POSITIVE REGULATION OF CELL ACTIVATION | 23 | 311 | 9.228e-12 | 1.645e-10 |
262 | RESPONSE TO AMINO ACID | 15 | 112 | 9.97e-12 | 1.771e-10 |
263 | RESPONSE TO EXTRACELLULAR STIMULUS | 27 | 441 | 1.102e-11 | 1.95e-10 |
264 | PHOSPHATIDYLINOSITOL 3 KINASE SIGNALING | 9 | 25 | 1.107e-11 | 1.951e-10 |
265 | REGULATION OF HEMOPOIESIS | 23 | 314 | 1.122e-11 | 1.971e-10 |
266 | NEGATIVE REGULATION OF ANOIKIS | 8 | 17 | 1.176e-11 | 2.049e-10 |
267 | REGULATION OF ENDOTHELIAL CELL CHEMOTAXIS | 8 | 17 | 1.176e-11 | 2.049e-10 |
268 | POSITIVE REGULATION OF DEVELOPMENTAL GROWTH | 17 | 156 | 1.2e-11 | 2.083e-10 |
269 | GLIAL CELL DIFFERENTIATION | 16 | 136 | 1.513e-11 | 2.617e-10 |
270 | ERBB SIGNALING PATHWAY | 13 | 79 | 1.69e-11 | 2.913e-10 |
271 | CELL PART MORPHOGENESIS | 32 | 633 | 1.909e-11 | 3.277e-10 |
272 | CELLULAR RESPONSE TO EXTERNAL STIMULUS | 21 | 264 | 1.953e-11 | 3.341e-10 |
273 | REGULATION OF DNA REPLICATION | 17 | 161 | 1.998e-11 | 3.406e-10 |
274 | REGULATION OF PHOSPHOLIPASE ACTIVITY | 12 | 64 | 2.065e-11 | 3.506e-10 |
275 | REGULATION OF PEPTIDYL SERINE PHOSPHORYLATION | 15 | 118 | 2.15e-11 | 3.637e-10 |
276 | POSITIVE REGULATION OF GROWTH | 20 | 238 | 2.219e-11 | 3.741e-10 |
277 | ENDODERM FORMATION | 11 | 50 | 2.27e-11 | 3.814e-10 |
278 | REGULATION OF FIBROBLAST PROLIFERATION | 13 | 81 | 2.352e-11 | 3.936e-10 |
279 | REGULATION OF BLOOD VESSEL ENDOTHELIAL CELL MIGRATION | 11 | 51 | 2.863e-11 | 4.775e-10 |
280 | POSITIVE REGULATION OF LIPASE ACTIVITY | 12 | 66 | 3.027e-11 | 5.031e-10 |
281 | TISSUE MORPHOGENESIS | 29 | 533 | 3.179e-11 | 5.263e-10 |
282 | LIPID METABOLIC PROCESS | 44 | 1158 | 3.363e-11 | 5.55e-10 |
283 | ERBB2 SIGNALING PATHWAY | 10 | 39 | 3.598e-11 | 5.895e-10 |
284 | MORPHOGENESIS OF A BRANCHING STRUCTURE | 17 | 167 | 3.598e-11 | 5.895e-10 |
285 | CELLULAR RESPONSE TO ORGANIC CYCLIC COMPOUND | 27 | 465 | 3.696e-11 | 6.034e-10 |
286 | POSITIVE REGULATION OF MITOTIC CELL CYCLE | 15 | 123 | 3.943e-11 | 6.414e-10 |
287 | REGULATION OF MITOTIC CELL CYCLE | 27 | 468 | 4.276e-11 | 6.933e-10 |
288 | REGULATION OF TYROSINE PHOSPHORYLATION OF STAT PROTEIN | 12 | 68 | 4.38e-11 | 7.077e-10 |
289 | POSITIVE REGULATION OF APOPTOTIC SIGNALING PATHWAY | 17 | 171 | 5.253e-11 | 8.457e-10 |
290 | RESPIRATORY SYSTEM DEVELOPMENT | 18 | 197 | 5.766e-11 | 9.251e-10 |
291 | OSSIFICATION | 20 | 251 | 5.815e-11 | 9.297e-10 |
292 | CELLULAR RESPONSE TO GROWTH HORMONE STIMULUS | 8 | 20 | 5.898e-11 | 9.398e-10 |
293 | REGULATION OF MEMBRANE PERMEABILITY | 12 | 70 | 6.26e-11 | 9.941e-10 |
294 | REGULATION OF PHOSPHATASE ACTIVITY | 15 | 128 | 7.03e-11 | 1.113e-09 |
295 | RESPONSE TO GROWTH HORMONE | 9 | 30 | 7.342e-11 | 1.158e-09 |
296 | ENDODERM DEVELOPMENT | 12 | 71 | 7.451e-11 | 1.171e-09 |
297 | CHEMICAL HOMEOSTASIS | 37 | 874 | 7.629e-11 | 1.195e-09 |
298 | CELL JUNCTION ASSEMBLY | 15 | 129 | 7.868e-11 | 1.228e-09 |
299 | NEGATIVE REGULATION OF CELL COMMUNICATION | 44 | 1192 | 8.568e-11 | 1.333e-09 |
300 | REGULATION OF CELL CELL ADHESION | 24 | 380 | 8.7e-11 | 1.349e-09 |
301 | REGULATION OF LEUKOCYTE DIFFERENTIATION | 19 | 232 | 1.114e-10 | 1.723e-09 |
302 | REPRODUCTION | 46 | 1297 | 1.118e-10 | 1.723e-09 |
303 | FC RECEPTOR SIGNALING PATHWAY | 18 | 206 | 1.209e-10 | 1.856e-09 |
304 | IMMUNE RESPONSE REGULATING CELL SURFACE RECEPTOR SIGNALING PATHWAY | 22 | 323 | 1.31e-10 | 2.006e-09 |
305 | REGULATION OF TYROSINE PHOSPHORYLATION OF STAT3 PROTEIN | 10 | 44 | 1.329e-10 | 2.028e-09 |
306 | CELLULAR RESPONSE TO ABIOTIC STIMULUS | 20 | 263 | 1.344e-10 | 2.043e-09 |
307 | VASCULAR ENDOTHELIAL GROWTH FACTOR SIGNALING PATHWAY | 7 | 14 | 1.397e-10 | 2.117e-09 |
308 | CELL CELL SIGNALING | 34 | 767 | 1.462e-10 | 2.208e-09 |
309 | REGULATION OF DEPHOSPHORYLATION | 16 | 158 | 1.49e-10 | 2.244e-09 |
310 | NEGATIVE REGULATION OF NEURON APOPTOTIC PROCESS | 15 | 135 | 1.514e-10 | 2.272e-09 |
311 | RESPONSE TO MECHANICAL STIMULUS | 18 | 210 | 1.66e-10 | 2.483e-09 |
312 | SPROUTING ANGIOGENESIS | 10 | 45 | 1.691e-10 | 2.521e-09 |
313 | CELL JUNCTION ORGANIZATION | 17 | 185 | 1.827e-10 | 2.716e-09 |
314 | NEPHRON DEVELOPMENT | 14 | 115 | 1.833e-10 | 2.716e-09 |
315 | REGENERATION | 16 | 161 | 1.977e-10 | 2.921e-09 |
316 | LIPID BIOSYNTHETIC PROCESS | 28 | 539 | 2.064e-10 | 3.038e-09 |
317 | RESPONSE TO DRUG | 25 | 431 | 2.096e-10 | 3.077e-09 |
318 | MAMMARY GLAND DEVELOPMENT | 14 | 117 | 2.316e-10 | 3.389e-09 |
319 | POSITIVE REGULATION OF CELL CELL ADHESION | 19 | 243 | 2.464e-10 | 3.594e-09 |
320 | PLATELET DERIVED GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 9 | 34 | 2.577e-10 | 3.747e-09 |
321 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 39 | 1004 | 2.755e-10 | 3.993e-09 |
322 | REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 22 | 337 | 2.945e-10 | 4.256e-09 |
323 | REGULATION OF PROTEIN LOCALIZATION TO NUCLEUS | 18 | 218 | 3.062e-10 | 4.411e-09 |
324 | FC EPSILON RECEPTOR SIGNALING PATHWAY | 15 | 142 | 3.116e-10 | 4.475e-09 |
325 | MYELOID LEUKOCYTE MIGRATION | 13 | 99 | 3.176e-10 | 4.519e-09 |
326 | INSULIN RECEPTOR SIGNALING PATHWAY | 12 | 80 | 3.175e-10 | 4.519e-09 |
327 | POSITIVE REGULATION OF CELL SUBSTRATE ADHESION | 13 | 99 | 3.176e-10 | 4.519e-09 |
328 | POSITIVE REGULATION OF CELL CYCLE PROCESS | 19 | 247 | 3.253e-10 | 4.615e-09 |
329 | REGULATION OF ANOIKIS | 8 | 24 | 3.298e-10 | 4.664e-09 |
330 | REGULATION OF CELL MORPHOGENESIS | 28 | 552 | 3.547e-10 | 5.001e-09 |
331 | REGULATION OF SMOOTH MUSCLE CELL PROLIFERATION | 13 | 100 | 3.61e-10 | 5.075e-09 |
332 | POSITIVE REGULATION OF NUCLEOCYTOPLASMIC TRANSPORT | 14 | 121 | 3.647e-10 | 5.112e-09 |
333 | REGULATION OF AXONOGENESIS | 16 | 168 | 3.737e-10 | 5.221e-09 |
334 | REGULATION OF JAK STAT CASCADE | 15 | 144 | 3.801e-10 | 5.279e-09 |
335 | REGULATION OF STAT CASCADE | 15 | 144 | 3.801e-10 | 5.279e-09 |
336 | GLUCOSE HOMEOSTASIS | 16 | 170 | 4.457e-10 | 6.153e-09 |
337 | CARBOHYDRATE HOMEOSTASIS | 16 | 170 | 4.457e-10 | 6.153e-09 |
338 | POSITIVE REGULATION OF MITOCHONDRIAL OUTER MEMBRANE PERMEABILIZATION INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 9 | 36 | 4.526e-10 | 6.212e-09 |
339 | POSITIVE CHEMOTAXIS | 9 | 36 | 4.526e-10 | 6.212e-09 |
340 | RESPONSE TO RADIATION | 24 | 413 | 4.739e-10 | 6.485e-09 |
341 | POSITIVE REGULATION OF BLOOD VESSEL ENDOTHELIAL CELL MIGRATION | 8 | 25 | 4.797e-10 | 6.546e-09 |
342 | REGULATION OF LIPASE ACTIVITY | 12 | 83 | 4.937e-10 | 6.717e-09 |
343 | POSITIVE REGULATION OF IMMUNE RESPONSE | 28 | 563 | 5.538e-10 | 7.513e-09 |
344 | POSITIVE REGULATION OF TYROSINE PHOSPHORYLATION OF STAT3 PROTEIN | 9 | 37 | 5.916e-10 | 8.002e-09 |
345 | POSITIVE REGULATION OF NEURON DEATH | 11 | 67 | 6.478e-10 | 8.737e-09 |
346 | NEGATIVE REGULATION OF CELL DIFFERENTIATION | 29 | 609 | 7.282e-10 | 9.792e-09 |
347 | REGULATION OF GLUCOSE IMPORT IN RESPONSE TO INSULIN STIMULUS | 7 | 17 | 7.665e-10 | 1.028e-08 |
348 | INTRINSIC APOPTOTIC SIGNALING PATHWAY | 15 | 152 | 8.155e-10 | 1.09e-08 |
349 | LEUKOCYTE DIFFERENTIATION | 20 | 292 | 8.511e-10 | 1.132e-08 |
350 | PLATELET DEGRANULATION | 13 | 107 | 8.512e-10 | 1.132e-08 |
351 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO NUCLEUS | 14 | 129 | 8.602e-10 | 1.14e-08 |
352 | REGULATION OF CARBOHYDRATE BIOSYNTHETIC PROCESS | 12 | 87 | 8.651e-10 | 1.144e-08 |
353 | POSITIVE REGULATION OF AXONOGENESIS | 11 | 69 | 8.994e-10 | 1.182e-08 |
354 | RESPONSE TO ACTIVITY | 11 | 69 | 8.994e-10 | 1.182e-08 |
355 | ACTIVATION OF IMMUNE RESPONSE | 24 | 427 | 9.245e-10 | 1.212e-08 |
356 | MAMMARY GLAND EPITHELIUM DEVELOPMENT | 10 | 53 | 9.466e-10 | 1.234e-08 |
357 | CELLULAR RESPONSE TO AMINO ACID STIMULUS | 10 | 53 | 9.466e-10 | 1.234e-08 |
358 | AMEBOIDAL TYPE CELL MIGRATION | 15 | 154 | 9.798e-10 | 1.273e-08 |
359 | REGULATION OF PHOSPHOLIPASE C ACTIVITY | 9 | 39 | 9.86e-10 | 1.274e-08 |
360 | PEPTIDYL TYROSINE AUTOPHOSPHORYLATION | 9 | 39 | 9.86e-10 | 1.274e-08 |
361 | POSITIVE REGULATION OF PEPTIDYL SERINE PHOSPHORYLATION | 12 | 88 | 9.907e-10 | 1.277e-08 |
362 | BRANCHING MORPHOGENESIS OF AN EPITHELIAL TUBE | 14 | 131 | 1.056e-09 | 1.357e-08 |
363 | HEART DEVELOPMENT | 25 | 466 | 1.06e-09 | 1.358e-08 |
364 | REGULATION OF GENERATION OF PRECURSOR METABOLITES AND ENERGY | 12 | 89 | 1.133e-09 | 1.448e-08 |
365 | RESPONSE TO KETONE | 16 | 182 | 1.221e-09 | 1.556e-08 |
366 | INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO DNA DAMAGE | 11 | 71 | 1.235e-09 | 1.57e-08 |
367 | REGULATION OF PROTEIN IMPORT | 16 | 183 | 1.323e-09 | 1.673e-08 |
368 | REGULATION OF SEQUENCE SPECIFIC DNA BINDING TRANSCRIPTION FACTOR ACTIVITY | 22 | 365 | 1.321e-09 | 1.673e-08 |
369 | EPIDERMAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 10 | 55 | 1.389e-09 | 1.752e-08 |
370 | POSITIVE REGULATION OF ENDOTHELIAL CELL CHEMOTAXIS | 6 | 11 | 1.575e-09 | 1.976e-08 |
371 | CELL GROWTH | 14 | 135 | 1.573e-09 | 1.976e-08 |
372 | MITOCHONDRIAL MEMBRANE ORGANIZATION | 12 | 92 | 1.675e-09 | 2.095e-08 |
373 | REGULATION OF PROTEIN INSERTION INTO MITOCHONDRIAL MEMBRANE INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 8 | 29 | 1.823e-09 | 2.268e-08 |
374 | POSITIVE REGULATION OF PROTEIN INSERTION INTO MITOCHONDRIAL MEMBRANE INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 8 | 29 | 1.823e-09 | 2.268e-08 |
375 | POSITIVE REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 15 | 162 | 1.987e-09 | 2.465e-08 |
376 | POSITIVE REGULATION OF GLUCOSE TRANSPORT | 9 | 42 | 2.008e-09 | 2.485e-08 |
377 | REGULATION OF CYTOPLASMIC TRANSPORT | 25 | 481 | 2.024e-09 | 2.499e-08 |
378 | POSITIVE REGULATION OF HEMOPOIESIS | 15 | 163 | 2.164e-09 | 2.664e-08 |
379 | POSITIVE REGULATION OF CARBOHYDRATE METABOLIC PROCESS | 11 | 75 | 2.261e-09 | 2.776e-08 |
380 | LYMPHOCYTE ACTIVATION | 21 | 342 | 2.287e-09 | 2.801e-08 |
381 | POSITIVE REGULATION OF SMOOTH MUSCLE CELL MIGRATION | 8 | 30 | 2.46e-09 | 3.004e-08 |
382 | REGULATION OF MITOCHONDRIAL OUTER MEMBRANE PERMEABILIZATION INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 9 | 43 | 2.512e-09 | 3.06e-08 |
383 | LEUKOCYTE CHEMOTAXIS | 13 | 117 | 2.604e-09 | 3.164e-08 |
384 | REGULATION OF NUCLEOCYTOPLASMIC TRANSPORT | 17 | 220 | 2.668e-09 | 3.225e-08 |
385 | RESPONSE TO LIGHT STIMULUS | 19 | 280 | 2.663e-09 | 3.225e-08 |
386 | COGNITION | 18 | 251 | 2.959e-09 | 3.567e-08 |
387 | CONNECTIVE TISSUE DEVELOPMENT | 16 | 194 | 3.1e-09 | 3.727e-08 |
388 | HEMIDESMOSOME ASSEMBLY | 6 | 12 | 3.118e-09 | 3.729e-08 |
389 | INFLAMMATORY RESPONSE | 24 | 454 | 3.11e-09 | 3.729e-08 |
390 | SINGLE ORGANISM BEHAVIOR | 22 | 384 | 3.378e-09 | 4.03e-08 |
391 | MEMORY | 12 | 98 | 3.509e-09 | 4.176e-08 |
392 | NEGATIVE REGULATION OF TRANSPORT | 24 | 458 | 3.694e-09 | 4.384e-08 |
393 | REGULATION OF STRESS ACTIVATED PROTEIN KINASE SIGNALING CASCADE | 16 | 197 | 3.871e-09 | 4.583e-08 |
394 | REGULATION OF GLUCOSE TRANSPORT | 12 | 100 | 4.439e-09 | 5.242e-08 |
395 | REGULATION OF CARBOHYDRATE METABOLIC PROCESS | 15 | 172 | 4.546e-09 | 5.341e-08 |
396 | REGULATION OF CELL SIZE | 15 | 172 | 4.546e-09 | 5.341e-08 |
397 | POSITIVE REGULATION OF SEQUENCE SPECIFIC DNA BINDING TRANSCRIPTION FACTOR ACTIVITY | 17 | 228 | 4.585e-09 | 5.374e-08 |
398 | NEGATIVE REGULATION OF APOPTOTIC SIGNALING PATHWAY | 16 | 200 | 4.815e-09 | 5.629e-08 |
399 | REGULATION OF CELLULAR RESPONSE TO GROWTH FACTOR STIMULUS | 17 | 229 | 4.898e-09 | 5.712e-08 |
400 | SIGNAL TRANSDUCTION IN ABSENCE OF LIGAND | 8 | 33 | 5.649e-09 | 6.554e-08 |
401 | EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 8 | 33 | 5.649e-09 | 6.554e-08 |
402 | CELL CYCLE | 43 | 1316 | 5.978e-09 | 6.92e-08 |
403 | ERK1 AND ERK2 CASCADE | 7 | 22 | 6.372e-09 | 7.357e-08 |
404 | POSITIVE REGULATION OF PROTEIN IMPORT | 12 | 104 | 6.99e-09 | 8.051e-08 |
405 | POSITIVE REGULATION OF REACTIVE OXYGEN SPECIES BIOSYNTHETIC PROCESS | 9 | 48 | 7.075e-09 | 8.109e-08 |
406 | RESPONSE TO GLUCAGON | 9 | 48 | 7.075e-09 | 8.109e-08 |
407 | MORPHOGENESIS OF AN EPITHELIUM | 22 | 400 | 7.123e-09 | 8.143e-08 |
408 | PROTEIN KINASE B SIGNALING | 8 | 34 | 7.307e-09 | 8.334e-08 |
409 | RHYTHMIC PROCESS | 19 | 298 | 7.405e-09 | 8.425e-08 |
410 | CELL CYCLE PROCESS | 38 | 1081 | 7.554e-09 | 8.573e-08 |
411 | TISSUE MIGRATION | 11 | 84 | 7.767e-09 | 8.793e-08 |
412 | DEVELOPMENTAL GROWTH | 20 | 333 | 8.132e-09 | 9.184e-08 |
413 | GLOMERULUS DEVELOPMENT | 9 | 49 | 8.573e-09 | 9.636e-08 |
414 | REGULATION OF SMOOTH MUSCLE CELL MIGRATION | 9 | 49 | 8.573e-09 | 9.636e-08 |
415 | CELL CYCLE ARREST | 14 | 154 | 8.802e-09 | 9.869e-08 |
416 | REGULATION OF CELLULAR COMPONENT BIOGENESIS | 31 | 767 | 9.084e-09 | 1.016e-07 |
417 | POSITIVE REGULATION OF CELLULAR COMPONENT BIOGENESIS | 22 | 406 | 9.33e-09 | 1.041e-07 |
418 | REGULATION OF GLYCOGEN METABOLIC PROCESS | 8 | 35 | 9.371e-09 | 1.043e-07 |
419 | INSULIN LIKE GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 6 | 14 | 9.922e-09 | 1.102e-07 |
420 | POSITIVE REGULATION OF LEUKOCYTE DIFFERENTIATION | 13 | 131 | 1.047e-08 | 1.16e-07 |
421 | REGULATION OF HOMEOSTATIC PROCESS | 23 | 447 | 1.117e-08 | 1.235e-07 |
422 | REGULATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY | 16 | 213 | 1.187e-08 | 1.308e-07 |
423 | POSITIVE REGULATION OF CYCLIN DEPENDENT PROTEIN KINASE ACTIVITY | 8 | 36 | 1.192e-08 | 1.311e-07 |
424 | REGULATION OF HOMOTYPIC CELL CELL ADHESION | 19 | 307 | 1.2e-08 | 1.317e-07 |
425 | CELLULAR RESPONSE TO PROSTAGLANDIN STIMULUS | 7 | 24 | 1.266e-08 | 1.383e-07 |
426 | REGULATION OF POSITIVE CHEMOTAXIS | 7 | 24 | 1.266e-08 | 1.383e-07 |
427 | CELL CELL ADHESION | 27 | 608 | 1.284e-08 | 1.4e-07 |
428 | LEUKOCYTE ACTIVATION | 22 | 414 | 1.327e-08 | 1.442e-07 |
429 | DEVELOPMENT OF PRIMARY SEXUAL CHARACTERISTICS | 16 | 216 | 1.447e-08 | 1.57e-07 |
430 | CELL CYCLE G1 S PHASE TRANSITION | 12 | 111 | 1.476e-08 | 1.594e-07 |
431 | G1 S TRANSITION OF MITOTIC CELL CYCLE | 12 | 111 | 1.476e-08 | 1.594e-07 |
432 | JAK STAT CASCADE INVOLVED IN GROWTH HORMONE SIGNALING PATHWAY | 6 | 15 | 1.636e-08 | 1.762e-07 |
433 | REGULATION OF NITRIC OXIDE BIOSYNTHETIC PROCESS | 9 | 53 | 1.771e-08 | 1.903e-07 |
434 | CELLULAR RESPONSE TO GLUCAGON STIMULUS | 8 | 38 | 1.885e-08 | 2.021e-07 |
435 | RESPONSE TO BIOTIC STIMULUS | 33 | 886 | 2.099e-08 | 2.246e-07 |
436 | NEGATIVE REGULATION OF PHOSPHORUS METABOLIC PROCESS | 25 | 541 | 2.118e-08 | 2.255e-07 |
437 | NEGATIVE REGULATION OF PHOSPHATE METABOLIC PROCESS | 25 | 541 | 2.118e-08 | 2.255e-07 |
438 | ASTROCYTE DIFFERENTIATION | 8 | 39 | 2.346e-08 | 2.49e-07 |
439 | MESODERMAL CELL DIFFERENTIATION | 7 | 26 | 2.355e-08 | 2.49e-07 |
440 | NEGATIVE REGULATION OF LIPID TRANSPORT | 7 | 26 | 2.355e-08 | 2.49e-07 |
441 | REGULATION OF CELL GROWTH | 21 | 391 | 2.396e-08 | 2.528e-07 |
442 | REGULATED EXOCYTOSIS | 16 | 224 | 2.42e-08 | 2.548e-07 |
443 | LEUKOCYTE CELL CELL ADHESION | 17 | 255 | 2.434e-08 | 2.556e-07 |
444 | REGULATION OF DNA BIOSYNTHETIC PROCESS | 11 | 94 | 2.587e-08 | 2.709e-07 |
445 | POSITIVE REGULATION OF VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 6 | 16 | 2.591e-08 | 2.709e-07 |
446 | POSITIVE REGULATION OF CELL MATRIX ADHESION | 8 | 40 | 2.901e-08 | 3.027e-07 |
447 | MESODERM DEVELOPMENT | 12 | 118 | 2.957e-08 | 3.078e-07 |
448 | REGULATION OF METAL ION TRANSPORT | 19 | 325 | 2.997e-08 | 3.113e-07 |
449 | REGULATION OF ION TRANSPORT | 26 | 592 | 3.037e-08 | 3.147e-07 |
450 | REGULATION OF VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 7 | 27 | 3.146e-08 | 3.245e-07 |
451 | HETEROTYPIC CELL CELL ADHESION | 7 | 27 | 3.146e-08 | 3.245e-07 |
452 | ENDOTHELIAL CELL MIGRATION | 9 | 57 | 3.441e-08 | 3.543e-07 |
453 | GLIAL CELL DEVELOPMENT | 10 | 76 | 3.603e-08 | 3.7e-07 |
454 | BEHAVIOR | 24 | 516 | 3.649e-08 | 3.74e-07 |
455 | REGULATION OF SYNAPSE STRUCTURE OR ACTIVITY | 16 | 232 | 3.959e-08 | 4.043e-07 |
456 | POSITIVE REGULATION OF GLYCOGEN METABOLIC PROCESS | 6 | 17 | 3.962e-08 | 4.043e-07 |
457 | NEGATIVE REGULATION OF CELL PROLIFERATION | 27 | 643 | 4.087e-08 | 4.162e-07 |
458 | REGULATION OF CELLULAR RESPONSE TO INSULIN STIMULUS | 9 | 59 | 4.703e-08 | 4.778e-07 |
459 | RESPONSE TO CORTICOSTEROID | 14 | 176 | 4.838e-08 | 4.905e-07 |
460 | LEUKOCYTE HOMEOSTASIS | 9 | 60 | 5.474e-08 | 5.537e-07 |
461 | ORGANOPHOSPHATE BIOSYNTHETIC PROCESS | 22 | 450 | 5.839e-08 | 5.894e-07 |
462 | CELLULAR RESPONSE TO PROSTAGLANDIN E STIMULUS | 6 | 18 | 5.881e-08 | 5.923e-07 |
463 | NEGATIVE REGULATION OF LIPID METABOLIC PROCESS | 10 | 80 | 5.948e-08 | 5.965e-07 |
464 | CELLULAR RESPONSE TO MECHANICAL STIMULUS | 10 | 80 | 5.948e-08 | 5.965e-07 |
465 | LYMPHOCYTE DIFFERENTIATION | 15 | 209 | 6.285e-08 | 6.289e-07 |
466 | RESPONSE TO TOXIC SUBSTANCE | 16 | 241 | 6.721e-08 | 6.711e-07 |
467 | PALLIUM DEVELOPMENT | 13 | 153 | 6.764e-08 | 6.74e-07 |
468 | REGULATION OF LIPID BIOSYNTHETIC PROCESS | 12 | 128 | 7.364e-08 | 7.321e-07 |
469 | DEFENSE RESPONSE | 39 | 1231 | 7.695e-08 | 7.634e-07 |
470 | ODONTOGENESIS | 11 | 105 | 8.272e-08 | 8.189e-07 |
471 | REGULATION OF RAS PROTEIN SIGNAL TRANSDUCTION | 14 | 184 | 8.449e-08 | 8.347e-07 |
472 | ORGAN REGENERATION | 10 | 83 | 8.504e-08 | 8.383e-07 |
473 | NEGATIVE REGULATION OF PROTEIN METABOLIC PROCESS | 36 | 1087 | 8.814e-08 | 8.671e-07 |
474 | REGULATION OF PLATELET ACTIVATION | 7 | 31 | 8.926e-08 | 8.762e-07 |
475 | REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 8 | 46 | 9.227e-08 | 9.039e-07 |
476 | REGULATION OF DEFENSE RESPONSE | 29 | 759 | 9.513e-08 | 9.299e-07 |
477 | RESPONSE TO OXIDATIVE STRESS | 19 | 352 | 1.055e-07 | 1.029e-06 |
478 | SECRETION | 25 | 588 | 1.059e-07 | 1.03e-06 |
479 | POSITIVE REGULATION OF NEURON APOPTOTIC PROCESS | 8 | 47 | 1.1e-07 | 1.069e-06 |
480 | REGULATION OF CELL CYCLE ARREST | 11 | 108 | 1.108e-07 | 1.074e-06 |
481 | REGULATION OF REACTIVE OXYGEN SPECIES BIOSYNTHETIC PROCESS | 9 | 65 | 1.121e-07 | 1.084e-06 |
482 | POSITIVE REGULATION OF LEUKOCYTE MIGRATION | 11 | 109 | 1.219e-07 | 1.177e-06 |
483 | INTERACTION WITH HOST | 12 | 134 | 1.224e-07 | 1.179e-06 |
484 | REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION TO PLASMA MEMBRANE | 8 | 48 | 1.306e-07 | 1.255e-06 |
485 | RESPONSE TO MOLECULE OF BACTERIAL ORIGIN | 18 | 321 | 1.31e-07 | 1.256e-06 |
486 | RESPONSE TO NUTRIENT | 14 | 191 | 1.344e-07 | 1.287e-06 |
487 | CELLULAR RESPONSE TO BIOTIC STIMULUS | 13 | 163 | 1.426e-07 | 1.362e-06 |
488 | RESPONSE TO ETHANOL | 12 | 136 | 1.441e-07 | 1.369e-06 |
489 | POSITIVE REGULATION OF LEUKOCYTE PROLIFERATION | 12 | 136 | 1.441e-07 | 1.369e-06 |
490 | TUBE MORPHOGENESIS | 18 | 323 | 1.437e-07 | 1.369e-06 |
491 | CELL CYCLE PHASE TRANSITION | 16 | 255 | 1.462e-07 | 1.385e-06 |
492 | OVULATION CYCLE PROCESS | 10 | 88 | 1.494e-07 | 1.413e-06 |
493 | REGULATION OF CELL CYCLE PROCESS | 24 | 558 | 1.563e-07 | 1.475e-06 |
494 | NEGATIVE REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 21 | 437 | 1.577e-07 | 1.485e-06 |
495 | EYE DEVELOPMENT | 18 | 326 | 1.649e-07 | 1.55e-06 |
496 | REGULATION OF PROTEIN IMPORT INTO NUCLEUS TRANSLOCATION | 6 | 21 | 1.666e-07 | 1.556e-06 |
497 | RESPONSE TO HEAT | 10 | 89 | 1.665e-07 | 1.556e-06 |
498 | EPITHELIAL CELL PROLIFERATION | 10 | 89 | 1.665e-07 | 1.556e-06 |
499 | POSITIVE REGULATION OF INTRACELLULAR PROTEIN TRANSPORT | 16 | 258 | 1.714e-07 | 1.599e-06 |
500 | RESPONSE TO INORGANIC SUBSTANCE | 22 | 479 | 1.727e-07 | 1.608e-06 |
501 | ANTIGEN RECEPTOR MEDIATED SIGNALING PATHWAY | 14 | 195 | 1.737e-07 | 1.613e-06 |
502 | RESPONSE TO PROSTAGLANDIN | 7 | 34 | 1.769e-07 | 1.639e-06 |
503 | REGULATION OF ADHERENS JUNCTION ORGANIZATION | 8 | 50 | 1.818e-07 | 1.682e-06 |
504 | TELENCEPHALON DEVELOPMENT | 15 | 228 | 1.962e-07 | 1.811e-06 |
505 | EMBRYONIC ORGAN DEVELOPMENT | 20 | 406 | 2.121e-07 | 1.954e-06 |
506 | POSITIVE REGULATION OF MITOTIC NUCLEAR DIVISION | 8 | 51 | 2.134e-07 | 1.962e-06 |
507 | CELL ADHESION MEDIATED BY INTEGRIN | 5 | 12 | 2.162e-07 | 1.976e-06 |
508 | ACTIVATION OF TRANSMEMBRANE RECEPTOR PROTEIN TYROSINE KINASE ACTIVITY | 5 | 12 | 2.162e-07 | 1.976e-06 |
509 | POSITIVE REGULATION OF GLUCOSE IMPORT IN RESPONSE TO INSULIN STIMULUS | 5 | 12 | 2.162e-07 | 1.976e-06 |
510 | SECRETION BY CELL | 22 | 486 | 2.215e-07 | 2.021e-06 |
511 | NEGATIVE REGULATION OF MOLECULAR FUNCTION | 35 | 1079 | 2.236e-07 | 2.036e-06 |
512 | POSITIVE REGULATION OF PROTEIN AUTOPHOSPHORYLATION | 6 | 22 | 2.267e-07 | 2.06e-06 |
513 | ORGANOPHOSPHATE METABOLIC PROCESS | 31 | 885 | 2.282e-07 | 2.069e-06 |
514 | FEMALE SEX DIFFERENTIATION | 11 | 116 | 2.313e-07 | 2.094e-06 |
515 | SEX DIFFERENTIATION | 16 | 266 | 2.595e-07 | 2.344e-06 |
516 | INTERSPECIES INTERACTION BETWEEN ORGANISMS | 26 | 662 | 2.719e-07 | 2.447e-06 |
517 | SYMBIOSIS ENCOMPASSING MUTUALISM THROUGH PARASITISM | 26 | 662 | 2.719e-07 | 2.447e-06 |
518 | REGULATION OF MORPHOGENESIS OF A BRANCHING STRUCTURE | 8 | 53 | 2.906e-07 | 2.611e-06 |
519 | POSITIVE REGULATION OF CELLULAR RESPONSE TO INSULIN STIMULUS | 6 | 23 | 3.035e-07 | 2.715e-06 |
520 | NEUROTROPHIN SIGNALING PATHWAY | 6 | 23 | 3.035e-07 | 2.715e-06 |
521 | SKELETAL SYSTEM DEVELOPMENT | 21 | 455 | 3.074e-07 | 2.745e-06 |
522 | FC GAMMA RECEPTOR SIGNALING PATHWAY | 10 | 95 | 3.099e-07 | 2.762e-06 |
523 | REGULATION OF ORGAN GROWTH | 9 | 73 | 3.121e-07 | 2.777e-06 |
524 | T CELL RECEPTOR SIGNALING PATHWAY | 12 | 146 | 3.133e-07 | 2.782e-06 |
525 | REGULATION OF PROTEIN AUTOPHOSPHORYLATION | 7 | 37 | 3.278e-07 | 2.905e-06 |
526 | POSITIVE REGULATION OF PROTEIN IMPORT INTO NUCLEUS TRANSLOCATION | 5 | 13 | 3.477e-07 | 3.076e-06 |
527 | REGULATION OF PROTEIN TARGETING | 17 | 307 | 3.522e-07 | 3.11e-06 |
528 | REGULATION OF INTRACELLULAR PROTEIN TRANSPORT | 19 | 381 | 3.577e-07 | 3.152e-06 |
529 | DIGESTIVE SYSTEM DEVELOPMENT | 12 | 148 | 3.632e-07 | 3.188e-06 |
530 | RESPONSE TO TEMPERATURE STIMULUS | 12 | 148 | 3.632e-07 | 3.188e-06 |
531 | MITOCHONDRIAL TRANSPORT | 13 | 177 | 3.711e-07 | 3.251e-06 |
532 | GLAND MORPHOGENESIS | 10 | 97 | 3.773e-07 | 3.294e-06 |
533 | REGULATION OF CYCLIN DEPENDENT PROTEIN KINASE ACTIVITY | 10 | 97 | 3.773e-07 | 3.294e-06 |
534 | NEGATIVE REGULATION OF PHOSPHORYLATION | 20 | 422 | 3.918e-07 | 3.414e-06 |
535 | CELLULAR HOMEOSTASIS | 26 | 676 | 4.055e-07 | 3.527e-06 |
536 | POSITIVE REGULATION OF MUSCLE TISSUE DEVELOPMENT | 8 | 56 | 4.51e-07 | 3.915e-06 |
537 | REGULATION OF SYSTEM PROCESS | 22 | 507 | 4.543e-07 | 3.936e-06 |
538 | SKIN DEVELOPMENT | 14 | 211 | 4.554e-07 | 3.939e-06 |
539 | REGULATION OF SMALL GTPASE MEDIATED SIGNAL TRANSDUCTION | 16 | 278 | 4.696e-07 | 4.054e-06 |
540 | MULTI MULTICELLULAR ORGANISM PROCESS | 14 | 213 | 5.105e-07 | 4.399e-06 |
541 | RESPONSE TO PROSTAGLANDIN E | 6 | 25 | 5.213e-07 | 4.476e-06 |
542 | CELLULAR EXTRAVASATION | 6 | 25 | 5.213e-07 | 4.476e-06 |
543 | REGULATION OF CATABOLIC PROCESS | 27 | 731 | 5.283e-07 | 4.527e-06 |
544 | REGULATION OF WOUND HEALING | 11 | 126 | 5.356e-07 | 4.582e-06 |
545 | POSITIVE REGULATION OF CYTOPLASMIC TRANSPORT | 16 | 282 | 5.682e-07 | 4.851e-06 |
546 | DEVELOPMENTAL PROGRAMMED CELL DEATH | 6 | 26 | 6.707e-07 | 5.716e-06 |
547 | REGULATION OF MITOCHONDRION ORGANIZATION | 14 | 218 | 6.753e-07 | 5.744e-06 |
548 | REGULATION OF EPITHELIAL CELL APOPTOTIC PROCESS | 8 | 59 | 6.817e-07 | 5.777e-06 |
549 | POSITIVE REGULATION OF DNA BIOSYNTHETIC PROCESS | 8 | 59 | 6.817e-07 | 5.777e-06 |
550 | POSITIVE REGULATION OF LYMPHOCYTE DIFFERENTIATION | 9 | 80 | 6.91e-07 | 5.846e-06 |
551 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 47 | 1784 | 7.231e-07 | 6.107e-06 |
552 | SYSTEM PROCESS | 47 | 1785 | 7.347e-07 | 6.193e-06 |
553 | CELLULAR RESPONSE TO EXTRACELLULAR STIMULUS | 13 | 188 | 7.393e-07 | 6.221e-06 |
554 | MATERNAL PROCESS INVOLVED IN FEMALE PREGNANCY | 8 | 60 | 7.781e-07 | 6.535e-06 |
555 | CELL MIGRATION INVOLVED IN SPROUTING ANGIOGENESIS | 5 | 15 | 7.949e-07 | 6.641e-06 |
556 | CEREBRAL CORTEX DEVELOPMENT | 10 | 105 | 7.931e-07 | 6.641e-06 |
557 | NEUROTROPHIN TRK RECEPTOR SIGNALING PATHWAY | 5 | 15 | 7.949e-07 | 6.641e-06 |
558 | POSITIVE REGULATION OF DEFENSE RESPONSE | 18 | 364 | 8.279e-07 | 6.904e-06 |
559 | B CELL ACTIVATION | 11 | 132 | 8.544e-07 | 7.086e-06 |
560 | REGULATION OF LYMPHOCYTE DIFFERENTIATION | 11 | 132 | 8.544e-07 | 7.086e-06 |
561 | POSITIVE REGULATION OF MESENCHYMAL CELL PROLIFERATION | 6 | 27 | 8.533e-07 | 7.086e-06 |
562 | CELLULAR CHEMICAL HOMEOSTASIS | 23 | 570 | 8.696e-07 | 7.2e-06 |
563 | OVARIAN FOLLICLE DEVELOPMENT | 8 | 61 | 8.86e-07 | 7.309e-06 |
564 | POSITIVE REGULATION OF STEM CELL PROLIFERATION | 8 | 61 | 8.86e-07 | 7.309e-06 |
565 | REGULATION OF T CELL DIFFERENTIATION | 10 | 107 | 9.451e-07 | 7.784e-06 |
566 | POSITIVE REGULATION OF NUCLEAR DIVISION | 8 | 62 | 1.006e-06 | 8.273e-06 |
567 | POSITIVE REGULATION OF CYTOKINE PRODUCTION | 18 | 370 | 1.047e-06 | 8.592e-06 |
568 | EAR DEVELOPMENT | 13 | 195 | 1.118e-06 | 9.159e-06 |
569 | NEGATIVE REGULATION OF LIPID BIOSYNTHETIC PROCESS | 7 | 44 | 1.133e-06 | 9.261e-06 |
570 | EPHRIN RECEPTOR SIGNALING PATHWAY | 9 | 85 | 1.162e-06 | 9.486e-06 |
571 | EPITHELIAL CELL DIFFERENTIATION | 21 | 495 | 1.203e-06 | 9.8e-06 |
572 | AGING | 15 | 264 | 1.268e-06 | 1.031e-05 |
573 | POSITIVE REGULATION OF CELLULAR AMIDE METABOLIC PROCESS | 10 | 111 | 1.327e-06 | 1.076e-05 |
574 | LUNG MORPHOGENESIS | 7 | 45 | 1.327e-06 | 1.076e-05 |
575 | PLACENTA DEVELOPMENT | 11 | 138 | 1.33e-06 | 1.076e-05 |
576 | RESPONSE TO ENDOPLASMIC RETICULUM STRESS | 14 | 233 | 1.494e-06 | 1.207e-05 |
577 | REGULATION OF SYNAPTIC PLASTICITY | 11 | 140 | 1.533e-06 | 1.236e-05 |
578 | PEPTIDYL THREONINE MODIFICATION | 7 | 46 | 1.549e-06 | 1.247e-05 |
579 | REGULATION OF COAGULATION | 9 | 88 | 1.561e-06 | 1.252e-05 |
580 | NEGATIVE REGULATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY | 9 | 88 | 1.561e-06 | 1.252e-05 |
581 | OVULATION CYCLE | 10 | 113 | 1.564e-06 | 1.253e-05 |
582 | MESODERM MORPHOGENESIS | 8 | 66 | 1.638e-06 | 1.309e-05 |
583 | RESPONSE TO EPIDERMAL GROWTH FACTOR | 6 | 30 | 1.659e-06 | 1.324e-05 |
584 | TISSUE HOMEOSTASIS | 12 | 171 | 1.7e-06 | 1.354e-05 |
585 | RESPONSE TO ANTIBIOTIC | 7 | 47 | 1.8e-06 | 1.432e-05 |
586 | NEGATIVE REGULATION OF CATALYTIC ACTIVITY | 28 | 829 | 1.871e-06 | 1.485e-05 |
587 | CELLULAR RESPONSE TO OXYGEN LEVELS | 11 | 143 | 1.889e-06 | 1.495e-05 |
588 | RAS PROTEIN SIGNAL TRANSDUCTION | 11 | 143 | 1.889e-06 | 1.495e-05 |
589 | EXOCYTOSIS | 16 | 310 | 1.972e-06 | 1.558e-05 |
590 | SENSORY ORGAN MORPHOGENESIS | 14 | 239 | 2.016e-06 | 1.59e-05 |
591 | NEGATIVE REGULATION OF CELL PROJECTION ORGANIZATION | 11 | 144 | 2.023e-06 | 1.593e-05 |
592 | LIPOPOLYSACCHARIDE MEDIATED SIGNALING PATHWAY | 6 | 31 | 2.035e-06 | 1.597e-05 |
593 | HOMEOSTASIS OF NUMBER OF CELLS WITHIN A TISSUE | 6 | 31 | 2.035e-06 | 1.597e-05 |
594 | REGULATION OF CELL JUNCTION ASSEMBLY | 8 | 68 | 2.063e-06 | 1.61e-05 |
595 | MULTICELLULAR ORGANISMAL RESPONSE TO STRESS | 8 | 68 | 2.063e-06 | 1.61e-05 |
596 | REGULATION OF NEUROLOGICAL SYSTEM PROCESS | 8 | 68 | 2.063e-06 | 1.61e-05 |
597 | REGULATION OF LEUKOCYTE PROLIFERATION | 13 | 206 | 2.067e-06 | 1.611e-05 |
598 | NEGATIVE REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 10 | 117 | 2.151e-06 | 1.674e-05 |
599 | REGULATION OF ANATOMICAL STRUCTURE SIZE | 20 | 472 | 2.218e-06 | 1.723e-05 |
600 | MUSCLE STRUCTURE DEVELOPMENT | 19 | 432 | 2.334e-06 | 1.81e-05 |
601 | REGULATION OF PEPTIDASE ACTIVITY | 18 | 392 | 2.376e-06 | 1.839e-05 |
602 | CARTILAGE DEVELOPMENT | 11 | 147 | 2.477e-06 | 1.903e-05 |
603 | NEGATIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 6 | 32 | 2.479e-06 | 1.903e-05 |
604 | REGULATION OF CELL CYCLE G1 S PHASE TRANSITION | 11 | 147 | 2.477e-06 | 1.903e-05 |
605 | REGULATION OF ACTIN CYTOSKELETON REORGANIZATION | 6 | 32 | 2.479e-06 | 1.903e-05 |
606 | NEGATIVE REGULATION OF SIGNAL TRANSDUCTION IN ABSENCE OF LIGAND | 6 | 32 | 2.479e-06 | 1.903e-05 |
607 | REGULATION OF CELLULAR AMIDE METABOLIC PROCESS | 17 | 354 | 2.504e-06 | 1.919e-05 |
608 | REGULATION OF CYTOKINE PRODUCTION | 22 | 563 | 2.563e-06 | 1.962e-05 |
609 | POSITIVE REGULATION OF CELL GROWTH | 11 | 148 | 2.646e-06 | 2.022e-05 |
610 | REGULATION OF DENDRITE DEVELOPMENT | 10 | 120 | 2.709e-06 | 2.066e-05 |
611 | LYMPHOCYTE HOMEOSTASIS | 7 | 50 | 2.77e-06 | 2.109e-05 |
612 | REGULATION OF INNATE IMMUNE RESPONSE | 17 | 357 | 2.805e-06 | 2.129e-05 |
613 | FOREBRAIN DEVELOPMENT | 17 | 357 | 2.805e-06 | 2.129e-05 |
614 | REGULATION OF LEUKOCYTE MIGRATION | 11 | 149 | 2.826e-06 | 2.142e-05 |
615 | KIDNEY VASCULATURE DEVELOPMENT | 5 | 19 | 2.955e-06 | 2.228e-05 |
616 | RENAL SYSTEM VASCULATURE DEVELOPMENT | 5 | 19 | 2.955e-06 | 2.228e-05 |
617 | ASTROCYTE DEVELOPMENT | 5 | 19 | 2.955e-06 | 2.228e-05 |
618 | REGULATION OF MYELINATION | 6 | 33 | 2.998e-06 | 2.258e-05 |
619 | NEGATIVE REGULATION OF CELL CYCLE PROCESS | 13 | 214 | 3.151e-06 | 2.369e-05 |
620 | CELLULAR RESPONSE TO FATTY ACID | 7 | 51 | 3.176e-06 | 2.384e-05 |
621 | ENDOCRINE SYSTEM DEVELOPMENT | 10 | 123 | 3.389e-06 | 2.539e-05 |
622 | REGULATION OF MYELOID CELL DIFFERENTIATION | 12 | 183 | 3.452e-06 | 2.578e-05 |
623 | IMMUNE EFFECTOR PROCESS | 20 | 486 | 3.448e-06 | 2.578e-05 |
624 | REGULATION OF PLASMA MEMBRANE ORGANIZATION | 8 | 73 | 3.555e-06 | 2.651e-05 |
625 | T CELL HOMEOSTASIS | 6 | 34 | 3.603e-06 | 2.678e-05 |
626 | REGULATION OF MESENCHYMAL CELL PROLIFERATION | 6 | 34 | 3.603e-06 | 2.678e-05 |
627 | ACTIVATION OF MAPKK ACTIVITY | 7 | 52 | 3.631e-06 | 2.695e-05 |
628 | CELLULAR RESPONSE TO OXIDATIVE STRESS | 12 | 184 | 3.652e-06 | 2.706e-05 |
629 | ION HOMEOSTASIS | 22 | 576 | 3.701e-06 | 2.738e-05 |
630 | NEGATIVE REGULATION OF CELL CYCLE G1 S PHASE TRANSITION | 9 | 98 | 3.857e-06 | 2.844e-05 |
631 | RESPONSE TO VITAMIN | 9 | 98 | 3.857e-06 | 2.844e-05 |
632 | REGULATION OF NEURON PROJECTION REGENERATION | 5 | 20 | 3.899e-06 | 2.871e-05 |
633 | CIRCULATORY SYSTEM PROCESS | 17 | 366 | 3.913e-06 | 2.874e-05 |
634 | EPIDERMIS DEVELOPMENT | 14 | 253 | 3.916e-06 | 2.874e-05 |
635 | MITOTIC CELL CYCLE | 26 | 766 | 4.091e-06 | 2.998e-05 |
636 | PROTEIN IMPORT | 11 | 155 | 4.147e-06 | 3.034e-05 |
637 | OSTEOBLAST DIFFERENTIATION | 10 | 126 | 4.212e-06 | 3.072e-05 |
638 | RESPONSE TO UV | 10 | 126 | 4.212e-06 | 3.072e-05 |
639 | CELLULAR RESPONSE TO DNA DAMAGE STIMULUS | 25 | 720 | 4.271e-06 | 3.11e-05 |
640 | PROTEIN LOCALIZATION TO NUCLEUS | 11 | 156 | 4.413e-06 | 3.208e-05 |
641 | SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR | 10 | 127 | 4.522e-06 | 3.283e-05 |
642 | LIMBIC SYSTEM DEVELOPMENT | 9 | 100 | 4.563e-06 | 3.307e-05 |
643 | TYROSINE PHOSPHORYLATION OF STAT PROTEIN | 4 | 10 | 4.718e-06 | 3.414e-05 |
644 | NEGATIVE REGULATION OF CELL ADHESION | 13 | 223 | 4.95e-06 | 3.576e-05 |
645 | MESENCHYME DEVELOPMENT | 12 | 190 | 5.084e-06 | 3.656e-05 |
646 | STEM CELL DIFFERENTIATION | 12 | 190 | 5.084e-06 | 3.656e-05 |
647 | PHAGOCYTOSIS | 12 | 190 | 5.084e-06 | 3.656e-05 |
648 | NEUROMUSCULAR JUNCTION DEVELOPMENT | 6 | 36 | 5.11e-06 | 3.664e-05 |
649 | POSITIVE REGULATION OF GLUCOSE METABOLIC PROCESS | 6 | 36 | 5.11e-06 | 3.664e-05 |
650 | NUCLEAR IMPORT | 10 | 129 | 5.203e-06 | 3.725e-05 |
651 | RESPONSE TO REACTIVE OXYGEN SPECIES | 12 | 191 | 5.366e-06 | 3.835e-05 |
652 | REGULATION OF CYTOSKELETON ORGANIZATION | 20 | 502 | 5.589e-06 | 3.988e-05 |
653 | NEGATIVE REGULATION OF CELLULAR COMPONENT ORGANIZATION | 24 | 684 | 5.628e-06 | 4.011e-05 |
654 | REGULATION OF CELLULAR COMPONENT SIZE | 16 | 337 | 5.743e-06 | 4.086e-05 |
655 | REGULATION OF MUSCLE ORGAN DEVELOPMENT | 9 | 103 | 5.827e-06 | 4.14e-05 |
656 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO CELL PERIPHERY | 6 | 37 | 6.036e-06 | 4.275e-05 |
657 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO PLASMA MEMBRANE | 6 | 37 | 6.036e-06 | 4.275e-05 |
658 | REGULATION OF VESICLE MEDIATED TRANSPORT | 19 | 462 | 6.151e-06 | 4.35e-05 |
659 | CELL CYCLE CHECKPOINT | 12 | 194 | 6.294e-06 | 4.444e-05 |
660 | DEVELOPMENTAL GROWTH INVOLVED IN MORPHOGENESIS | 9 | 104 | 6.311e-06 | 4.449e-05 |
661 | MODULATION OF SYNAPTIC TRANSMISSION | 15 | 301 | 6.333e-06 | 4.458e-05 |
662 | POSITIVE REGULATION OF RESPONSE TO WOUNDING | 11 | 162 | 6.345e-06 | 4.46e-05 |
663 | PROTEIN COMPLEX SUBUNIT ORGANIZATION | 40 | 1527 | 6.424e-06 | 4.508e-05 |
664 | REGULATION OF MUSCLE SYSTEM PROCESS | 12 | 195 | 6.634e-06 | 4.649e-05 |
665 | APOPTOTIC MITOCHONDRIAL CHANGES | 7 | 57 | 6.805e-06 | 4.762e-05 |
666 | NEGATIVE REGULATION OF CELL DEVELOPMENT | 15 | 303 | 6.858e-06 | 4.791e-05 |
667 | EMBRYO DEVELOPMENT ENDING IN BIRTH OR EGG HATCHING | 21 | 554 | 6.964e-06 | 4.858e-05 |
668 | POSITIVE REGULATION OF ORGAN GROWTH | 6 | 38 | 7.093e-06 | 4.933e-05 |
669 | REGULATION OF MULTICELLULAR ORGANISMAL METABOLIC PROCESS | 6 | 38 | 7.093e-06 | 4.933e-05 |
670 | NEGATIVE REGULATION OF VASCULATURE DEVELOPMENT | 8 | 80 | 7.11e-06 | 4.938e-05 |
671 | MESENCHYMAL CELL DIFFERENTIATION | 10 | 134 | 7.306e-06 | 5.066e-05 |
672 | REGULATION OF GLUCOSE METABOLIC PROCESS | 9 | 106 | 7.381e-06 | 5.111e-05 |
673 | REGULATION OF TRANSMEMBRANE TRANSPORT | 18 | 426 | 7.519e-06 | 5.198e-05 |
674 | NEGATIVE REGULATION OF MITOTIC CELL CYCLE | 12 | 199 | 8.158e-06 | 5.632e-05 |
675 | POSITIVE REGULATION OF NEUROLOGICAL SYSTEM PROCESS | 5 | 23 | 8.207e-06 | 5.649e-05 |
676 | LEUKOCYTE APOPTOTIC PROCESS | 5 | 23 | 8.207e-06 | 5.649e-05 |
677 | RESPONSE TO ALKALOID | 10 | 137 | 8.892e-06 | 6.112e-05 |
678 | POSITIVE REGULATION OF ION TRANSPORT | 13 | 236 | 9.14e-06 | 6.273e-05 |
679 | REGULATION OF MONOOXYGENASE ACTIVITY | 7 | 60 | 9.629e-06 | 6.589e-05 |
680 | CHONDROCYTE DIFFERENTIATION | 7 | 60 | 9.629e-06 | 6.589e-05 |
681 | NEGATIVE REGULATION OF RESPONSE TO EXTERNAL STIMULUS | 14 | 274 | 9.758e-06 | 6.667e-05 |
682 | NEURON MIGRATION | 9 | 110 | 9.995e-06 | 6.819e-05 |
683 | MITOTIC CELL CYCLE CHECKPOINT | 10 | 139 | 1.011e-05 | 6.886e-05 |
684 | AXON REGENERATION | 5 | 24 | 1.026e-05 | 6.971e-05 |
685 | BLOOD VESSEL ENDOTHELIAL CELL MIGRATION | 5 | 24 | 1.026e-05 | 6.971e-05 |
686 | POSITIVE REGULATION OF CATABOLIC PROCESS | 17 | 395 | 1.067e-05 | 7.234e-05 |
687 | NEGATIVE REGULATION OF PROTEIN MODIFICATION PROCESS | 22 | 616 | 1.068e-05 | 7.234e-05 |
688 | COLUMNAR CUBOIDAL EPITHELIAL CELL DIFFERENTIATION | 9 | 111 | 1.076e-05 | 7.277e-05 |
689 | REGULATION OF GOLGI ORGANIZATION | 4 | 12 | 1.09e-05 | 7.353e-05 |
690 | TRACHEA MORPHOGENESIS | 4 | 12 | 1.09e-05 | 7.353e-05 |
691 | POSITIVE REGULATION OF KIDNEY DEVELOPMENT | 6 | 41 | 1.12e-05 | 7.528e-05 |
692 | POSITIVE REGULATION OF CELL CYCLE ARREST | 8 | 85 | 1.119e-05 | 7.528e-05 |
693 | SINGLE ORGANISM BIOSYNTHETIC PROCESS | 36 | 1340 | 1.151e-05 | 7.727e-05 |
694 | RESPONSE TO BACTERIUM | 20 | 528 | 1.172e-05 | 7.857e-05 |
695 | REGULATION OF ORGAN MORPHOGENESIS | 13 | 242 | 1.196e-05 | 8.006e-05 |
696 | CELLULAR MACROMOLECULE LOCALIZATION | 34 | 1234 | 1.229e-05 | 8.217e-05 |
697 | HISTONE PHOSPHORYLATION | 5 | 25 | 1.27e-05 | 8.476e-05 |
698 | MULTICELLULAR ORGANISM REPRODUCTION | 25 | 768 | 1.293e-05 | 8.621e-05 |
699 | MOVEMENT IN ENVIRONMENT OF OTHER ORGANISM INVOLVED IN SYMBIOTIC INTERACTION | 8 | 87 | 1.329e-05 | 8.775e-05 |
700 | ENTRY INTO CELL OF OTHER ORGANISM INVOLVED IN SYMBIOTIC INTERACTION | 8 | 87 | 1.329e-05 | 8.775e-05 |
701 | VIRAL ENTRY INTO HOST CELL | 8 | 87 | 1.329e-05 | 8.775e-05 |
702 | ENTRY INTO OTHER ORGANISM INVOLVED IN SYMBIOTIC INTERACTION | 8 | 87 | 1.329e-05 | 8.775e-05 |
703 | MOVEMENT IN HOST ENVIRONMENT | 8 | 87 | 1.329e-05 | 8.775e-05 |
704 | ENTRY INTO HOST | 8 | 87 | 1.329e-05 | 8.775e-05 |
705 | ENTRY INTO HOST CELL | 8 | 87 | 1.329e-05 | 8.775e-05 |
706 | VESICLE MEDIATED TRANSPORT | 34 | 1239 | 1.337e-05 | 8.808e-05 |
707 | REGULATION OF CALCIUM ION TRANSPORT | 12 | 209 | 1.338e-05 | 8.808e-05 |
708 | PROTEIN COMPLEX BIOGENESIS | 32 | 1132 | 1.369e-05 | 8.983e-05 |
709 | PROTEIN COMPLEX ASSEMBLY | 32 | 1132 | 1.369e-05 | 8.983e-05 |
710 | RESPONSE TO TRANSFORMING GROWTH FACTOR BETA | 10 | 144 | 1.379e-05 | 9.038e-05 |
711 | LEUKOCYTE PROLIFERATION | 8 | 88 | 1.447e-05 | 9.455e-05 |
712 | REGULATION OF STEM CELL PROLIFERATION | 8 | 88 | 1.447e-05 | 9.455e-05 |
713 | POSITIVE REGULATION OF PROTEOLYSIS | 16 | 363 | 1.452e-05 | 9.474e-05 |
714 | RESPONSE TO IONIZING RADIATION | 10 | 145 | 1.465e-05 | 9.548e-05 |
715 | POSTTRANSCRIPTIONAL REGULATION OF GENE EXPRESSION | 18 | 448 | 1.485e-05 | 9.661e-05 |
716 | CEREBRAL CORTEX CELL MIGRATION | 6 | 43 | 1.487e-05 | 9.661e-05 |
717 | REPLACEMENT OSSIFICATION | 5 | 26 | 1.556e-05 | 0.0001008 |
718 | ENDOCHONDRAL OSSIFICATION | 5 | 26 | 1.556e-05 | 0.0001008 |
719 | REGULATION OF CELL PROLIFERATION INVOLVED IN KIDNEY DEVELOPMENT | 4 | 13 | 1.56e-05 | 0.0001009 |
720 | B CELL DIFFERENTIATION | 8 | 89 | 1.573e-05 | 0.0001016 |
721 | REGULATION OF AUTOPHAGY | 13 | 249 | 1.619e-05 | 0.0001045 |
722 | REGULATION OF RELEASE OF CYTOCHROME C FROM MITOCHONDRIA | 6 | 44 | 1.703e-05 | 0.0001098 |
723 | MIDBRAIN DEVELOPMENT | 8 | 90 | 1.708e-05 | 0.0001099 |
724 | MALE SEX DIFFERENTIATION | 10 | 148 | 1.752e-05 | 0.0001126 |
725 | REGULATION OF CYTOKINE SECRETION | 10 | 149 | 1.858e-05 | 0.0001192 |
726 | POSITIVE REGULATION OF HEART GROWTH | 5 | 27 | 1.89e-05 | 0.0001212 |
727 | EXOCRINE SYSTEM DEVELOPMENT | 6 | 45 | 1.945e-05 | 0.0001245 |
728 | IMMUNE RESPONSE | 31 | 1100 | 2.004e-05 | 0.0001281 |
729 | CELLULAR RESPONSE TO STEROID HORMONE STIMULUS | 12 | 218 | 2.038e-05 | 0.0001301 |
730 | POSITIVE REGULATION OF METANEPHROS DEVELOPMENT | 4 | 14 | 2.162e-05 | 0.0001371 |
731 | POSITIVE REGULATION OF RHO PROTEIN SIGNAL TRANSDUCTION | 4 | 14 | 2.162e-05 | 0.0001371 |
732 | POSITIVE REGULATION OF NITRIC OXIDE SYNTHASE BIOSYNTHETIC PROCESS | 4 | 14 | 2.162e-05 | 0.0001371 |
733 | PROTEIN HETEROTRIMERIZATION | 4 | 14 | 2.162e-05 | 0.0001371 |
734 | POSITIVE REGULATION OF SPROUTING ANGIOGENESIS | 4 | 14 | 2.162e-05 | 0.0001371 |
735 | ORGAN GROWTH | 7 | 68 | 2.22e-05 | 0.0001404 |
736 | REGULATION OF TOR SIGNALING | 7 | 68 | 2.22e-05 | 0.0001404 |
737 | LONG TERM MEMORY | 5 | 28 | 2.278e-05 | 0.0001436 |
738 | REGULATION OF SPROUTING ANGIOGENESIS | 5 | 28 | 2.278e-05 | 0.0001436 |
739 | ENDOCYTOSIS | 19 | 509 | 2.383e-05 | 0.00015 |
740 | MEMBRANE ORGANIZATION | 27 | 899 | 2.403e-05 | 0.0001511 |
741 | T CELL DIFFERENTIATION | 9 | 123 | 2.461e-05 | 0.0001545 |
742 | POSITIVE REGULATION OF PEPTIDASE ACTIVITY | 10 | 154 | 2.472e-05 | 0.000155 |
743 | THYMUS DEVELOPMENT | 6 | 47 | 2.511e-05 | 0.0001573 |
744 | ACTIVATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY | 8 | 95 | 2.538e-05 | 0.0001585 |
745 | REGULATION OF LIPID TRANSPORT | 8 | 95 | 2.538e-05 | 0.0001585 |
746 | POSITIVE REGULATION OF CARDIAC MUSCLE TISSUE DEVELOPMENT | 5 | 29 | 2.724e-05 | 0.0001699 |
747 | SIGNAL TRANSDUCTION IN RESPONSE TO DNA DAMAGE | 8 | 96 | 2.739e-05 | 0.0001704 |
748 | CARDIOCYTE DIFFERENTIATION | 8 | 96 | 2.739e-05 | 0.0001704 |
749 | BONE DEVELOPMENT | 10 | 156 | 2.763e-05 | 0.0001714 |
750 | NEGATIVE REGULATION OF RESPONSE TO WOUNDING | 10 | 156 | 2.763e-05 | 0.0001714 |
751 | RESPONSE TO AXON INJURY | 6 | 48 | 2.84e-05 | 0.000176 |
752 | PROTEIN LOCALIZATION | 43 | 1805 | 2.849e-05 | 0.0001763 |
753 | NEGATIVE REGULATION OF DENDRITE MORPHOGENESIS | 4 | 15 | 2.919e-05 | 0.0001801 |
754 | T CELL APOPTOTIC PROCESS | 4 | 15 | 2.919e-05 | 0.0001801 |
755 | NEGATIVE REGULATION OF NEURON DIFFERENTIATION | 11 | 191 | 2.983e-05 | 0.0001838 |
756 | RESPONSE TO PURINE CONTAINING COMPOUND | 10 | 158 | 3.082e-05 | 0.0001897 |
757 | NEGATIVE REGULATION OF ION TRANSPORT | 9 | 127 | 3.174e-05 | 0.0001951 |
758 | REGULATION OF NITRIC OXIDE SYNTHASE ACTIVITY | 6 | 49 | 3.203e-05 | 0.0001964 |
759 | POSITIVE REGULATION OF CHEMOKINE PRODUCTION | 6 | 49 | 3.203e-05 | 0.0001964 |
760 | REGULATION OF PROTEOLYSIS | 23 | 711 | 3.213e-05 | 0.0001967 |
761 | REGULATION OF PROTEIN SECRETION | 16 | 389 | 3.368e-05 | 0.000206 |
762 | HIPPOCAMPUS DEVELOPMENT | 7 | 73 | 3.539e-05 | 0.0002156 |
763 | G1 DNA DAMAGE CHECKPOINT | 7 | 73 | 3.539e-05 | 0.0002156 |
764 | CELLULAR RESPONSE TO KETONE | 7 | 73 | 3.539e-05 | 0.0002156 |
765 | MITOTIC DNA INTEGRITY CHECKPOINT | 8 | 100 | 3.683e-05 | 0.000224 |
766 | POSITIVE REGULATION OF ACTIN CYTOSKELETON REORGANIZATION | 4 | 16 | 3.854e-05 | 0.0002323 |
767 | REGULATION OF EARLY ENDOSOME TO LATE ENDOSOME TRANSPORT | 4 | 16 | 3.854e-05 | 0.0002323 |
768 | TOR SIGNALING | 4 | 16 | 3.854e-05 | 0.0002323 |
769 | POSITIVE REGULATION OF TYROSINE PHOSPHORYLATION OF STAT5 PROTEIN | 4 | 16 | 3.854e-05 | 0.0002323 |
770 | BRANCHING INVOLVED IN SALIVARY GLAND MORPHOGENESIS | 4 | 16 | 3.854e-05 | 0.0002323 |
771 | REGULATION OF DEVELOPMENTAL PIGMENTATION | 4 | 16 | 3.854e-05 | 0.0002323 |
772 | REGULATION OF FATTY ACID BETA OXIDATION | 4 | 16 | 3.854e-05 | 0.0002323 |
773 | REGULATION OF DENDRITE MORPHOGENESIS | 7 | 74 | 3.868e-05 | 0.0002328 |
774 | SMALL GTPASE MEDIATED SIGNAL TRANSDUCTION | 15 | 352 | 3.971e-05 | 0.0002387 |
775 | IN UTERO EMBRYONIC DEVELOPMENT | 14 | 311 | 3.979e-05 | 0.0002389 |
776 | MULTICELLULAR ORGANISMAL HOMEOSTASIS | 13 | 272 | 4.073e-05 | 0.0002442 |
777 | REGULATION OF TRANSPORTER ACTIVITY | 11 | 198 | 4.149e-05 | 0.0002485 |
778 | GRANULOCYTE MIGRATION | 7 | 75 | 4.221e-05 | 0.0002524 |
779 | NEGATIVE REGULATION OF GROWTH | 12 | 236 | 4.439e-05 | 0.0002651 |
780 | SALIVARY GLAND DEVELOPMENT | 5 | 32 | 4.481e-05 | 0.0002673 |
781 | REGULATION OF LIPID CATABOLIC PROCESS | 6 | 52 | 4.519e-05 | 0.0002693 |
782 | REGULATION OF MUSCLE TISSUE DEVELOPMENT | 8 | 103 | 4.557e-05 | 0.0002711 |
783 | REGULATION OF CELLULAR RESPONSE TO HEAT | 7 | 76 | 4.6e-05 | 0.0002734 |
784 | POSITIVE REGULATION OF MITOCHONDRION ORGANIZATION | 10 | 167 | 4.942e-05 | 0.0002933 |
785 | NEGATIVE REGULATION OF PLATELET ACTIVATION | 4 | 17 | 4.991e-05 | 0.0002943 |
786 | POSITIVE REGULATION OF NUCLEOTIDE CATABOLIC PROCESS | 4 | 17 | 4.991e-05 | 0.0002943 |
787 | NEGATIVE REGULATION OF RELEASE OF CYTOCHROME C FROM MITOCHONDRIA | 4 | 17 | 4.991e-05 | 0.0002943 |
788 | MAMMARY GLAND ALVEOLUS DEVELOPMENT | 4 | 17 | 4.991e-05 | 0.0002943 |
789 | MAMMARY GLAND LOBULE DEVELOPMENT | 4 | 17 | 4.991e-05 | 0.0002943 |
790 | REGULATION OF SODIUM ION TRANSPORT | 7 | 77 | 5.007e-05 | 0.0002949 |
791 | NEGATIVE REGULATION OF CELL SUBSTRATE ADHESION | 6 | 53 | 5.044e-05 | 0.0002963 |
792 | NEGATIVE REGULATION OF AUTOPHAGY | 6 | 53 | 5.044e-05 | 0.0002963 |
793 | RESPONSE TO CARBOHYDRATE | 10 | 168 | 5.198e-05 | 0.000305 |
794 | RESPONSE TO VITAMIN D | 5 | 33 | 5.227e-05 | 0.000306 |
795 | NEURON PROJECTION REGENERATION | 5 | 33 | 5.227e-05 | 0.000306 |
796 | ACTIVATION OF INNATE IMMUNE RESPONSE | 11 | 204 | 5.442e-05 | 0.0003181 |
797 | FAT CELL DIFFERENTIATION | 8 | 106 | 5.597e-05 | 0.0003268 |
798 | REGULATION OF MITOCHONDRIAL MEMBRANE POTENTIAL | 6 | 54 | 5.615e-05 | 0.0003274 |
799 | CELLULAR RESPONSE TO RADIATION | 9 | 137 | 5.759e-05 | 0.0003354 |
800 | POSITIVE REGULATION OF SODIUM ION TRANSPORT | 5 | 34 | 6.067e-05 | 0.0003524 |
801 | ORGAN FORMATION | 5 | 34 | 6.067e-05 | 0.0003524 |
802 | REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY VIA DEATH DOMAIN RECEPTORS | 6 | 55 | 6.237e-05 | 0.0003614 |
803 | REGULATION OF KIDNEY DEVELOPMENT | 6 | 55 | 6.237e-05 | 0.0003614 |
804 | REGULATION OF MITOCHONDRIAL DEPOLARIZATION | 4 | 18 | 6.354e-05 | 0.0003659 |
805 | POSITIVE REGULATION OF SYNAPTIC TRANSMISSION GLUTAMATERGIC | 4 | 18 | 6.354e-05 | 0.0003659 |
806 | REGULATION OF CELL MATURATION | 4 | 18 | 6.354e-05 | 0.0003659 |
807 | REGULATION OF COLLATERAL SPROUTING | 4 | 18 | 6.354e-05 | 0.0003659 |
808 | LYMPHOCYTE APOPTOTIC PROCESS | 4 | 18 | 6.354e-05 | 0.0003659 |
809 | REGULATION OF MYELOID LEUKOCYTE DIFFERENTIATION | 8 | 108 | 6.395e-05 | 0.0003678 |
810 | REGULATION OF CELL SHAPE | 9 | 139 | 6.446e-05 | 0.0003703 |
811 | ANATOMICAL STRUCTURE HOMEOSTASIS | 13 | 285 | 6.566e-05 | 0.0003767 |
812 | STRIATED MUSCLE CELL DIFFERENTIATION | 10 | 173 | 6.655e-05 | 0.0003813 |
813 | REGULATION OF RHO PROTEIN SIGNAL TRANSDUCTION | 8 | 109 | 6.828e-05 | 0.0003903 |
814 | RESPONSE TO HYDROGEN PEROXIDE | 8 | 109 | 6.828e-05 | 0.0003903 |
815 | POSITIVE REGULATION OF LEUKOCYTE CHEMOTAXIS | 7 | 81 | 6.94e-05 | 0.0003962 |
816 | NEGATIVE REGULATION OF EPITHELIAL CELL APOPTOTIC PROCESS | 5 | 35 | 7.006e-05 | 0.0003995 |
817 | POSITIVE REGULATION OF SYNAPTIC TRANSMISSION | 8 | 110 | 7.285e-05 | 0.0004149 |
818 | HEART MORPHOGENESIS | 11 | 212 | 7.694e-05 | 0.0004377 |
819 | NEGATIVE REGULATION OF KINASE ACTIVITY | 12 | 250 | 7.726e-05 | 0.0004389 |
820 | REGULATION OF NITRIC OXIDE SYNTHASE BIOSYNTHETIC PROCESS | 4 | 19 | 7.969e-05 | 0.0004517 |
821 | POSITIVE REGULATION OF CARDIAC MUSCLE CELL PROLIFERATION | 4 | 19 | 7.969e-05 | 0.0004517 |
822 | REGULATION OF NUCLEOTIDE CATABOLIC PROCESS | 5 | 36 | 8.053e-05 | 0.0004553 |
823 | POSITIVE REGULATION OF ERBB SIGNALING PATHWAY | 5 | 36 | 8.053e-05 | 0.0004553 |
824 | REGULATION OF ERBB SIGNALING PATHWAY | 7 | 83 | 8.113e-05 | 0.0004576 |
825 | RESPONSE TO FATTY ACID | 7 | 83 | 8.113e-05 | 0.0004576 |
826 | EAR MORPHOGENESIS | 8 | 112 | 8.276e-05 | 0.0004651 |
827 | REGULATION OF OSTEOBLAST DIFFERENTIATION | 8 | 112 | 8.276e-05 | 0.0004651 |
828 | ZYMOGEN ACTIVATION | 8 | 112 | 8.276e-05 | 0.0004651 |
829 | CELLULAR PROCESS INVOLVED IN REPRODUCTION IN MULTICELLULAR ORGANISM | 12 | 252 | 8.335e-05 | 0.0004678 |
830 | REGULATION OF OSSIFICATION | 10 | 178 | 8.444e-05 | 0.0004734 |
831 | REGULATION OF SYNAPSE ORGANIZATION | 8 | 113 | 8.812e-05 | 0.0004928 |
832 | POSITIVE REGULATION OF INFLAMMATORY RESPONSE | 8 | 113 | 8.812e-05 | 0.0004928 |
833 | SYNAPSE ORGANIZATION | 9 | 145 | 8.937e-05 | 0.0004992 |
834 | REGULATION OF INFLAMMATORY RESPONSE | 13 | 294 | 8.986e-05 | 0.0005014 |
835 | POSITIVE REGULATION OF PROTEIN TYROSINE KINASE ACTIVITY | 5 | 37 | 9.218e-05 | 0.0005136 |
836 | VASCULOGENESIS | 6 | 59 | 9.299e-05 | 0.0005176 |
837 | ESTABLISHMENT OF PROTEIN LOCALIZATION | 35 | 1423 | 9.364e-05 | 0.0005206 |
838 | REGULATION OF EMBRYONIC DEVELOPMENT | 8 | 114 | 9.376e-05 | 0.0005206 |
839 | NEGATIVE REGULATION OF CELL CYCLE PHASE TRANSITION | 9 | 146 | 9.422e-05 | 0.0005219 |
840 | DNA INTEGRITY CHECKPOINT | 9 | 146 | 9.422e-05 | 0.0005219 |
841 | EMBRYONIC HEMOPOIESIS | 4 | 20 | 9.864e-05 | 0.0005438 |
842 | TRACHEA DEVELOPMENT | 4 | 20 | 9.864e-05 | 0.0005438 |
843 | AMELOGENESIS | 4 | 20 | 9.864e-05 | 0.0005438 |
844 | REGULATION OF TYROSINE PHOSPHORYLATION OF STAT5 PROTEIN | 4 | 20 | 9.864e-05 | 0.0005438 |
845 | CELLULAR RESPONSE TO ALCOHOL | 8 | 115 | 9.97e-05 | 0.000549 |
846 | POSITIVE REGULATION OF B CELL ACTIVATION | 7 | 86 | 0.0001017 | 0.0005594 |
847 | NEGATIVE REGULATION OF TRANSMEMBRANE TRANSPORT | 7 | 87 | 0.0001094 | 0.0006013 |
848 | DIVALENT INORGANIC CATION HOMEOSTASIS | 14 | 343 | 0.0001133 | 0.0006217 |
849 | REGULATION OF CELL ADHESION MEDIATED BY INTEGRIN | 5 | 39 | 0.0001193 | 0.0006538 |
850 | B CELL HOMEOSTASIS | 4 | 21 | 0.0001207 | 0.0006597 |
851 | POSITIVE REGULATION OF ADHERENS JUNCTION ORGANIZATION | 4 | 21 | 0.0001207 | 0.0006597 |
852 | EPITHELIAL CELL DEVELOPMENT | 10 | 186 | 0.0001215 | 0.0006637 |
853 | FOREBRAIN CELL MIGRATION | 6 | 62 | 0.000123 | 0.0006708 |
854 | REGULATION OF MUSCLE ADAPTATION | 6 | 63 | 0.0001345 | 0.000732 |
855 | RESPONSE TO OSMOTIC STRESS | 6 | 63 | 0.0001345 | 0.000732 |
856 | ENDOCRINE PANCREAS DEVELOPMENT | 5 | 40 | 0.000135 | 0.0007336 |
857 | REGULATION OF OXIDOREDUCTASE ACTIVITY | 7 | 90 | 0.0001356 | 0.0007352 |
858 | MESONEPHROS DEVELOPMENT | 7 | 90 | 0.0001356 | 0.0007352 |
859 | MULTI ORGANISM REPRODUCTIVE PROCESS | 25 | 891 | 0.000143 | 0.0007748 |
860 | NEGATIVE REGULATION OF TRANSFERASE ACTIVITY | 14 | 351 | 0.0001442 | 0.00078 |
861 | CELLULAR RESPONSE TO LIGHT STIMULUS | 7 | 91 | 0.0001453 | 0.0007854 |
862 | SOMATIC STEM CELL DIVISION | 4 | 22 | 0.000146 | 0.0007873 |
863 | ACTIVATION OF PROTEIN KINASE B ACTIVITY | 4 | 22 | 0.000146 | 0.0007873 |
864 | SENSORY PERCEPTION OF MECHANICAL STIMULUS | 9 | 155 | 0.0001487 | 0.0008008 |
865 | REGULATION OF MEMBRANE DEPOLARIZATION | 5 | 41 | 0.0001522 | 0.0008175 |
866 | PROSTATE GLAND DEVELOPMENT | 5 | 41 | 0.0001522 | 0.0008175 |
867 | REGULATION OF CHEMOKINE PRODUCTION | 6 | 65 | 0.0001602 | 0.0008595 |
868 | REGULATION OF ACTIN FILAMENT BASED PROCESS | 13 | 312 | 0.0001622 | 0.0008694 |
869 | REGULATION OF ENDOTHELIAL CELL APOPTOTIC PROCESS | 5 | 42 | 0.000171 | 0.0009123 |
870 | REGULATION OF CELLULAR CARBOHYDRATE CATABOLIC PROCESS | 5 | 42 | 0.000171 | 0.0009123 |
871 | REGULATION OF HEART GROWTH | 5 | 42 | 0.000171 | 0.0009123 |
872 | REGULATION OF CARBOHYDRATE CATABOLIC PROCESS | 5 | 42 | 0.000171 | 0.0009123 |
873 | REGULATION OF MULTICELLULAR ORGANISM GROWTH | 6 | 66 | 0.0001743 | 0.0009282 |
874 | NEURAL NUCLEUS DEVELOPMENT | 6 | 66 | 0.0001743 | 0.0009282 |
875 | RESPONSE TO INCREASED OXYGEN LEVELS | 4 | 23 | 0.000175 | 0.0009287 |
876 | REGULATION OF METANEPHROS DEVELOPMENT | 4 | 23 | 0.000175 | 0.0009287 |
877 | RESPONSE TO HYPEROXIA | 4 | 23 | 0.000175 | 0.0009287 |
878 | KIDNEY EPITHELIUM DEVELOPMENT | 8 | 125 | 0.0001782 | 0.0009441 |
879 | REGULATION OF JNK CASCADE | 9 | 159 | 0.0001802 | 0.000954 |
880 | MITOCHONDRION ORGANIZATION | 19 | 594 | 0.0001833 | 0.0009691 |
881 | NEUROLOGICAL SYSTEM PROCESS | 31 | 1242 | 0.0001883 | 0.0009945 |
882 | CELL AGING | 6 | 67 | 0.0001895 | 0.0009998 |
883 | REGULATION OF TRANSCRIPTION FACTOR IMPORT INTO NUCLEUS | 7 | 95 | 0.0001902 | 0.001002 |
884 | RESPONSE TO ELECTRICAL STIMULUS | 5 | 43 | 0.0001915 | 0.001007 |
885 | MYELOID LEUKOCYTE MEDIATED IMMUNITY | 5 | 43 | 0.0001915 | 0.001007 |
886 | PROTEIN TARGETING | 15 | 406 | 0.0001938 | 0.001018 |
887 | POSITIVE REGULATION OF PROTEIN COMPLEX ASSEMBLY | 10 | 197 | 0.0001943 | 0.001019 |
888 | REGULATION OF SECRETION | 21 | 699 | 0.000199 | 0.001043 |
889 | MYELOID LEUKOCYTE DIFFERENTIATION | 7 | 96 | 0.000203 | 0.001061 |
890 | REGULATION OF LEUKOCYTE CHEMOTAXIS | 7 | 96 | 0.000203 | 0.001061 |
891 | MUSCLE CELL DIFFERENTIATION | 11 | 237 | 0.0002054 | 0.001072 |
892 | POSITIVE REGULATION OF NUCLEOSIDE METABOLIC PROCESS | 4 | 24 | 0.000208 | 0.001081 |
893 | POSITIVE REGULATION OF CELL JUNCTION ASSEMBLY | 4 | 24 | 0.000208 | 0.001081 |
894 | POSITIVE REGULATION OF RECEPTOR INTERNALIZATION | 4 | 24 | 0.000208 | 0.001081 |
895 | POSITIVE REGULATION OF ATP METABOLIC PROCESS | 4 | 24 | 0.000208 | 0.001081 |
896 | REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION TO MITOCHONDRION | 8 | 128 | 0.0002097 | 0.001089 |
897 | REGULATION OF ENDOCYTOSIS | 10 | 199 | 0.0002108 | 0.001094 |
898 | BRANCHING INVOLVED IN URETERIC BUD MORPHOGENESIS | 5 | 44 | 0.0002139 | 0.001108 |
899 | REGULATION OF NUCLEAR DIVISION | 9 | 163 | 0.0002171 | 0.001124 |
900 | PERIPHERAL NERVOUS SYSTEM DEVELOPMENT | 6 | 69 | 0.000223 | 0.001153 |
901 | MODIFICATION BY SYMBIONT OF HOST MORPHOLOGY OR PHYSIOLOGY | 5 | 45 | 0.0002382 | 0.001227 |
902 | SUBSTANTIA NIGRA DEVELOPMENT | 5 | 45 | 0.0002382 | 0.001227 |
903 | ENDOCHONDRAL BONE MORPHOGENESIS | 5 | 45 | 0.0002382 | 0.001227 |
904 | CENTRAL NERVOUS SYSTEM NEURON DEVELOPMENT | 6 | 70 | 0.0002413 | 0.001242 |
905 | ESTABLISHMENT OF LOCALIZATION IN CELL | 38 | 1676 | 0.0002439 | 0.001254 |
906 | CELLULAR RESPONSE TO EPIDERMAL GROWTH FACTOR STIMULUS | 4 | 25 | 0.0002452 | 0.001257 |
907 | DETECTION OF MECHANICAL STIMULUS INVOLVED IN SENSORY PERCEPTION | 4 | 25 | 0.0002452 | 0.001257 |
908 | THYROID GLAND DEVELOPMENT | 4 | 25 | 0.0002452 | 0.001257 |
909 | LEARNING | 8 | 131 | 0.0002458 | 0.001258 |
910 | REGULATION OF CYTOSOLIC CALCIUM ION CONCENTRATION | 10 | 203 | 0.0002475 | 0.001264 |
911 | NEGATIVE REGULATION OF CATABOLIC PROCESS | 10 | 203 | 0.0002475 | 0.001264 |
912 | POSITIVE REGULATION OF NF KAPPAB TRANSCRIPTION FACTOR ACTIVITY | 8 | 132 | 0.0002588 | 0.001321 |
913 | SKIN EPIDERMIS DEVELOPMENT | 6 | 71 | 0.0002609 | 0.00133 |
914 | NEGATIVE REGULATION OF IMMUNE SYSTEM PROCESS | 14 | 372 | 0.000262 | 0.001334 |
915 | REGULATION OF ALPHA BETA T CELL DIFFERENTIATION | 5 | 46 | 0.0002645 | 0.001344 |
916 | REGULATION OF OXIDATIVE STRESS INDUCED CELL DEATH | 5 | 46 | 0.0002645 | 0.001344 |
917 | NEGATIVE REGULATION OF PEPTIDASE ACTIVITY | 11 | 245 | 0.0002733 | 0.001387 |
918 | REGULATION OF EXTENT OF CELL GROWTH | 7 | 101 | 0.0002779 | 0.001408 |
919 | ENERGY RESERVE METABOLIC PROCESS | 6 | 72 | 0.0002817 | 0.001426 |
920 | POSITIVE REGULATION OF INNATE IMMUNE RESPONSE | 11 | 246 | 0.000283 | 0.001431 |
921 | REGULATION OF T HELPER CELL DIFFERENTIATION | 4 | 26 | 0.000287 | 0.001448 |
922 | SCHWANN CELL DEVELOPMENT | 4 | 26 | 0.000287 | 0.001448 |
923 | POSITIVE REGULATION OF DEPHOSPHORYLATION | 5 | 47 | 0.000293 | 0.001477 |
924 | PROSTATE GLAND GROWTH | 3 | 11 | 0.0002957 | 0.001487 |
925 | LYMPHOID PROGENITOR CELL DIFFERENTIATION | 3 | 11 | 0.0002957 | 0.001487 |
926 | NEGATIVE REGULATION OF CELL GROWTH | 9 | 170 | 0.0002968 | 0.001491 |
927 | ASSOCIATIVE LEARNING | 6 | 73 | 0.0003037 | 0.001523 |
928 | PANCREAS DEVELOPMENT | 6 | 73 | 0.0003037 | 0.001523 |
929 | REGULATION OF IMMUNE EFFECTOR PROCESS | 15 | 424 | 0.000308 | 0.001543 |
930 | REGULATION OF CARDIAC MUSCLE TISSUE DEVELOPMENT | 5 | 48 | 0.0003238 | 0.001618 |
931 | COLUMNAR CUBOIDAL EPITHELIAL CELL DEVELOPMENT | 5 | 48 | 0.0003238 | 0.001618 |
932 | CARDIAC MUSCLE CELL DIFFERENTIATION | 6 | 74 | 0.0003271 | 0.001633 |
933 | REGULATION OF LAMELLIPODIUM ASSEMBLY | 4 | 27 | 0.0003336 | 0.001658 |
934 | REGULATION OF FATTY ACID TRANSPORT | 4 | 27 | 0.0003336 | 0.001658 |
935 | SUBSTRATE DEPENDENT CELL MIGRATION | 4 | 27 | 0.0003336 | 0.001658 |
936 | CELLULAR RESPONSE TO REACTIVE OXYGEN SPECIES | 7 | 104 | 0.0003325 | 0.001658 |
937 | REGULATION OF NUCLEOTIDE METABOLIC PROCESS | 10 | 211 | 0.0003369 | 0.001671 |
938 | NEGATIVE REGULATION OF CYTOKINE PRODUCTION | 10 | 211 | 0.0003369 | 0.001671 |
939 | INTRACELLULAR PROTEIN TRANSPORT | 22 | 781 | 0.0003431 | 0.0017 |
940 | BIOMINERAL TISSUE DEVELOPMENT | 6 | 75 | 0.0003519 | 0.001738 |
941 | ODONTOGENESIS OF DENTIN CONTAINING TOOTH | 6 | 75 | 0.0003519 | 0.001738 |
942 | POSITIVE REGULATION OF AUTOPHAGY | 6 | 75 | 0.0003519 | 0.001738 |
943 | REGULATION OF NUCLEOSIDE METABOLIC PROCESS | 5 | 49 | 0.0003569 | 0.001758 |
944 | REGULATION OF STEROID BIOSYNTHETIC PROCESS | 5 | 49 | 0.0003569 | 0.001758 |
945 | REGULATION OF ATP METABOLIC PROCESS | 5 | 49 | 0.0003569 | 0.001758 |
946 | INNATE IMMUNE RESPONSE ACTIVATING CELL SURFACE RECEPTOR SIGNALING PATHWAY | 7 | 106 | 0.0003735 | 0.001837 |
947 | EXTRACELLULAR MATRIX DISASSEMBLY | 6 | 76 | 0.0003781 | 0.001858 |
948 | REGULATION OF FIBROBLAST MIGRATION | 4 | 28 | 0.0003854 | 0.001874 |
949 | POSITIVE REGULATION OF ACUTE INFLAMMATORY RESPONSE | 4 | 28 | 0.0003854 | 0.001874 |
950 | REGULATION OF MACROPHAGE DERIVED FOAM CELL DIFFERENTIATION | 4 | 28 | 0.0003854 | 0.001874 |
951 | PLACENTA BLOOD VESSEL DEVELOPMENT | 4 | 28 | 0.0003854 | 0.001874 |
952 | NEGATIVE REGULATION OF DENDRITE DEVELOPMENT | 4 | 28 | 0.0003854 | 0.001874 |
953 | CARDIAC MUSCLE TISSUE DEVELOPMENT | 8 | 140 | 0.0003853 | 0.001874 |
954 | POSITIVE REGULATION OF ACTIVATED T CELL PROLIFERATION | 4 | 28 | 0.0003854 | 0.001874 |
955 | REGULATION OF FATTY ACID OXIDATION | 4 | 28 | 0.0003854 | 0.001874 |
956 | MAMMARY GLAND DUCT MORPHOGENESIS | 4 | 28 | 0.0003854 | 0.001874 |
957 | POSITIVE REGULATION OF PHOSPHATASE ACTIVITY | 4 | 28 | 0.0003854 | 0.001874 |
958 | PRODUCTION OF MOLECULAR MEDIATOR INVOLVED IN INFLAMMATORY RESPONSE | 3 | 12 | 0.0003906 | 0.001893 |
959 | MYELIN MAINTENANCE | 3 | 12 | 0.0003906 | 0.001893 |
960 | MAMMARY GLAND EPITHELIAL CELL PROLIFERATION | 3 | 12 | 0.0003906 | 0.001893 |
961 | REGULATION OF COENZYME METABOLIC PROCESS | 5 | 50 | 0.0003926 | 0.001893 |
962 | FACE DEVELOPMENT | 5 | 50 | 0.0003926 | 0.001893 |
963 | RESPONSE TO GAMMA RADIATION | 5 | 50 | 0.0003926 | 0.001893 |
964 | VISUAL BEHAVIOR | 5 | 50 | 0.0003926 | 0.001893 |
965 | REGULATION OF COFACTOR METABOLIC PROCESS | 5 | 50 | 0.0003926 | 0.001893 |
966 | SINGLE ORGANISM CELLULAR LOCALIZATION | 24 | 898 | 0.0003965 | 0.00191 |
967 | POSITIVE REGULATION OF TRANSCRIPTION FACTOR IMPORT INTO NUCLEUS | 5 | 51 | 0.0004309 | 0.002069 |
968 | RESPONSE TO NICOTINE | 5 | 51 | 0.0004309 | 0.002069 |
969 | REGULATION OF INTERLEUKIN 12 PRODUCTION | 5 | 51 | 0.0004309 | 0.002069 |
970 | LYMPHOCYTE COSTIMULATION | 6 | 78 | 0.0004351 | 0.002083 |
971 | REGULATION OF RECEPTOR MEDIATED ENDOCYTOSIS | 6 | 78 | 0.0004351 | 0.002083 |
972 | RENAL TUBULE DEVELOPMENT | 6 | 78 | 0.0004351 | 0.002083 |
973 | REGULATION OF CARDIAC MUSCLE CELL PROLIFERATION | 4 | 29 | 0.0004427 | 0.00211 |
974 | REGULATION OF VACUOLAR TRANSPORT | 4 | 29 | 0.0004427 | 0.00211 |
975 | STEM CELL DIVISION | 4 | 29 | 0.0004427 | 0.00211 |
976 | RESPONSE TO PAIN | 4 | 29 | 0.0004427 | 0.00211 |
977 | REGULATION OF SYNAPSE ASSEMBLY | 6 | 79 | 0.000466 | 0.002215 |
978 | BONE MORPHOGENESIS | 6 | 79 | 0.000466 | 0.002215 |
979 | REGULATION OF RESPONSE TO CYTOKINE STIMULUS | 8 | 144 | 0.0004653 | 0.002215 |
980 | POSITIVE REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY | 5 | 52 | 0.0004719 | 0.002241 |
981 | NEGATIVE REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 11 | 262 | 0.0004822 | 0.002287 |
982 | NEURONAL STEM CELL DIVISION | 3 | 13 | 0.0005031 | 0.002362 |
983 | INDUCTION OF POSITIVE CHEMOTAXIS | 3 | 13 | 0.0005031 | 0.002362 |
984 | WNT SIGNALING PATHWAY | 13 | 351 | 0.0005028 | 0.002362 |
985 | BEHAVIORAL RESPONSE TO PAIN | 3 | 13 | 0.0005031 | 0.002362 |
986 | LEUKOCYTE TETHERING OR ROLLING | 3 | 13 | 0.0005031 | 0.002362 |
987 | CELLULAR RESPONSE TO HEPATOCYTE GROWTH FACTOR STIMULUS | 3 | 13 | 0.0005031 | 0.002362 |
988 | RESPONSE TO HEPATOCYTE GROWTH FACTOR | 3 | 13 | 0.0005031 | 0.002362 |
989 | LEUKOCYTE ADHESION TO VASCULAR ENDOTHELIAL CELL | 3 | 13 | 0.0005031 | 0.002362 |
990 | NEGATIVE REGULATION OF HYDROLASE ACTIVITY | 14 | 397 | 0.0005024 | 0.002362 |
991 | NEUROBLAST DIVISION | 3 | 13 | 0.0005031 | 0.002362 |
992 | INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO DNA DAMAGE BY P53 CLASS MEDIATOR | 4 | 30 | 0.0005058 | 0.002365 |
993 | NEGATIVE REGULATION OF MUSCLE CELL APOPTOTIC PROCESS | 4 | 30 | 0.0005058 | 0.002365 |
994 | NEGATIVE REGULATION OF TOR SIGNALING | 4 | 30 | 0.0005058 | 0.002365 |
995 | REGULATION OF ANION TRANSMEMBRANE TRANSPORT | 4 | 30 | 0.0005058 | 0.002365 |
996 | MESONEPHRIC TUBULE MORPHOGENESIS | 5 | 53 | 0.0005158 | 0.002407 |
997 | INTRINSIC APOPTOTIC SIGNALING PATHWAY BY P53 CLASS MEDIATOR | 5 | 53 | 0.0005158 | 0.002407 |
998 | METANEPHROS DEVELOPMENT | 6 | 81 | 0.000533 | 0.002482 |
999 | POSITIVE REGULATION OF MYELOID CELL DIFFERENTIATION | 6 | 81 | 0.000533 | 0.002482 |
1000 | PROTEIN HETEROOLIGOMERIZATION | 7 | 113 | 0.0005499 | 0.002558 |
1001 | REGULATION OF WNT SIGNALING PATHWAY | 12 | 310 | 0.000558 | 0.002592 |
1002 | RESPONSE TO TRANSITION METAL NANOPARTICLE | 8 | 148 | 0.0005582 | 0.002592 |
1003 | NUCLEAR TRANSPORT | 13 | 355 | 0.0005591 | 0.002594 |
1004 | KIDNEY MORPHOGENESIS | 6 | 82 | 0.0005691 | 0.002638 |
1005 | ACTIN FILAMENT BASED PROCESS | 15 | 450 | 0.000573 | 0.002653 |
1006 | SCHWANN CELL DIFFERENTIATION | 4 | 31 | 0.0005751 | 0.002655 |
1007 | CELLULAR RESPONSE TO GLUCOSE STARVATION | 4 | 31 | 0.0005751 | 0.002655 |
1008 | MATERNAL PLACENTA DEVELOPMENT | 4 | 31 | 0.0005751 | 0.002655 |
1009 | POSITIVE REGULATION OF ENDOCYTOSIS | 7 | 114 | 0.0005797 | 0.002673 |
1010 | HAIR CYCLE | 6 | 83 | 0.0006071 | 0.002792 |
1011 | EMBRYONIC PLACENTA DEVELOPMENT | 6 | 83 | 0.0006071 | 0.002792 |
1012 | MOLTING CYCLE | 6 | 83 | 0.0006071 | 0.002792 |
1013 | NEGATIVE REGULATION OF EPITHELIAL CELL PROLIFERATION | 7 | 115 | 0.0006108 | 0.002806 |
1014 | REGULATION OF FIBROBLAST APOPTOTIC PROCESS | 3 | 14 | 0.0006344 | 0.002905 |
1015 | REGULATION OF GLOMERULUS DEVELOPMENT | 3 | 14 | 0.0006344 | 0.002905 |
1016 | T CELL MIGRATION | 3 | 14 | 0.0006344 | 0.002905 |
1017 | METANEPHRIC NEPHRON DEVELOPMENT | 4 | 32 | 0.0006508 | 0.002978 |
1018 | ESTABLISHMENT OF PROTEIN LOCALIZATION TO ORGANELLE | 13 | 361 | 0.0006534 | 0.002986 |
1019 | REGULATION OF DENDRITIC SPINE DEVELOPMENT | 5 | 56 | 0.0006661 | 0.00304 |
1020 | PROTEIN DEPHOSPHORYLATION | 9 | 190 | 0.0006664 | 0.00304 |
1021 | MACROMOLECULAR COMPLEX ASSEMBLY | 32 | 1398 | 0.0006709 | 0.003058 |
1022 | DETECTION OF ABIOTIC STIMULUS | 7 | 117 | 0.000677 | 0.003082 |
1023 | CELL DIVISION | 15 | 460 | 0.0007173 | 0.003263 |
1024 | MUSCLE TISSUE DEVELOPMENT | 11 | 275 | 0.0007205 | 0.003274 |
1025 | POSITIVE REGULATION OF TUMOR NECROSIS FACTOR SUPERFAMILY CYTOKINE PRODUCTION | 5 | 57 | 0.0007227 | 0.003281 |
1026 | RESPONSE TO TUMOR NECROSIS FACTOR | 10 | 233 | 0.0007309 | 0.003315 |
1027 | CELLULAR SENESCENCE | 4 | 33 | 0.0007334 | 0.003316 |
1028 | NEGATIVE REGULATION OF ANION TRANSPORT | 4 | 33 | 0.0007334 | 0.003316 |
1029 | REGULATION OF BONE RESORPTION | 4 | 33 | 0.0007334 | 0.003316 |
1030 | GLUCOSE METABOLIC PROCESS | 7 | 119 | 0.0007488 | 0.003382 |
1031 | REGULATION OF CELL CYCLE PHASE TRANSITION | 12 | 321 | 0.0007576 | 0.003419 |
1032 | REGULATION OF FATTY ACID METABOLIC PROCESS | 6 | 87 | 0.0007793 | 0.00351 |
1033 | TISSUE REMODELING | 6 | 87 | 0.0007793 | 0.00351 |
1034 | POSITIVE REGULATION OF CREB TRANSCRIPTION FACTOR ACTIVITY | 3 | 15 | 0.0007857 | 0.003522 |
1035 | NEGATIVE REGULATION OF WOUND HEALING | 5 | 58 | 0.000783 | 0.003522 |
1036 | NEGATIVE REGULATION OF INTERLEUKIN 12 PRODUCTION | 3 | 15 | 0.0007857 | 0.003522 |
1037 | RESPONSE TO VITAMIN E | 3 | 15 | 0.0007857 | 0.003522 |
1038 | T CELL LINEAGE COMMITMENT | 3 | 15 | 0.0007857 | 0.003522 |
1039 | NEGATIVE REGULATION OF CELLULAR CATABOLIC PROCESS | 8 | 156 | 0.0007889 | 0.00353 |
1040 | REGULATION OF LEUKOCYTE MEDIATED IMMUNITY | 8 | 156 | 0.0007889 | 0.00353 |
1041 | EMBRYONIC ORGAN MORPHOGENESIS | 11 | 279 | 0.000811 | 0.003625 |
1042 | NEGATIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY VIA DEATH DOMAIN RECEPTORS | 4 | 34 | 0.0008231 | 0.003675 |
1043 | REGULATION OF B CELL ACTIVATION | 7 | 121 | 0.0008264 | 0.003687 |
1044 | HORMONE MEDIATED SIGNALING PATHWAY | 8 | 158 | 0.0008572 | 0.00382 |
1045 | REGULATION OF BINDING | 11 | 283 | 0.0009107 | 0.004055 |
1046 | NEGATIVE REGULATION OF RESPONSE TO OXIDATIVE STRESS | 4 | 35 | 0.0009202 | 0.004082 |
1047 | BONE REMODELING | 4 | 35 | 0.0009202 | 0.004082 |
1048 | RESPONSE TO MINERALOCORTICOID | 4 | 35 | 0.0009202 | 0.004082 |
1049 | NEGATIVE REGULATION OF CELLULAR RESPONSE TO OXIDATIVE STRESS | 4 | 35 | 0.0009202 | 0.004082 |
1050 | REGULATION OF PROTEIN COMPLEX ASSEMBLY | 13 | 375 | 0.0009267 | 0.004107 |
1051 | MAMMARY GLAND EPITHELIAL CELL DIFFERENTIATION | 3 | 16 | 0.0009581 | 0.004221 |
1052 | REGULATION OF GENE EXPRESSION BY GENETIC IMPRINTING | 3 | 16 | 0.0009581 | 0.004221 |
1053 | POSITIVE REGULATION OF PHOSPHOPROTEIN PHOSPHATASE ACTIVITY | 3 | 16 | 0.0009581 | 0.004221 |
1054 | POSITIVE REGULATION OF LAMELLIPODIUM ASSEMBLY | 3 | 16 | 0.0009581 | 0.004221 |
1055 | RETINA VASCULATURE DEVELOPMENT IN CAMERA TYPE EYE | 3 | 16 | 0.0009581 | 0.004221 |
1056 | RESPONSE TO UV B | 3 | 16 | 0.0009581 | 0.004221 |
1057 | REGULATION OF PROTEIN TYROSINE KINASE ACTIVITY | 5 | 61 | 0.0009862 | 0.004333 |
1058 | POSITIVE REGULATION OF SYNAPSE ASSEMBLY | 5 | 61 | 0.0009862 | 0.004333 |
1059 | ENSHEATHMENT OF NEURONS | 6 | 91 | 0.000987 | 0.004333 |
1060 | AXON ENSHEATHMENT | 6 | 91 | 0.000987 | 0.004333 |
1061 | STEROID HORMONE MEDIATED SIGNALING PATHWAY | 7 | 125 | 0.001001 | 0.004389 |
1062 | T CELL SELECTION | 4 | 36 | 0.001025 | 0.004492 |
1063 | RESPONSE TO METAL ION | 12 | 333 | 0.00104 | 0.004553 |
1064 | INNER EAR MORPHOGENESIS | 6 | 92 | 0.001045 | 0.00457 |
1065 | RESPONSE TO TOPOLOGICALLY INCORRECT PROTEIN | 8 | 163 | 0.001049 | 0.004578 |
1066 | VASCULAR PROCESS IN CIRCULATORY SYSTEM | 8 | 163 | 0.001049 | 0.004578 |
1067 | REGULATION OF TISSUE REMODELING | 5 | 62 | 0.001062 | 0.004631 |
1068 | NEPHRON EPITHELIUM DEVELOPMENT | 6 | 93 | 0.001106 | 0.004817 |
1069 | POSITIVE REGULATION OF B CELL PROLIFERATION | 4 | 37 | 0.001138 | 0.004922 |
1070 | RESPONSE TO NERVE GROWTH FACTOR | 4 | 37 | 0.001138 | 0.004922 |
1071 | REGULATION OF RECEPTOR INTERNALIZATION | 4 | 37 | 0.001138 | 0.004922 |
1072 | REGULATION OF MUSCLE HYPERTROPHY | 4 | 37 | 0.001138 | 0.004922 |
1073 | MODULATION BY VIRUS OF HOST MORPHOLOGY OR PHYSIOLOGY | 4 | 37 | 0.001138 | 0.004922 |
1074 | REGULATION OF LAMELLIPODIUM ORGANIZATION | 4 | 37 | 0.001138 | 0.004922 |
1075 | REGULATION OF PEPTIDYL THREONINE PHOSPHORYLATION | 4 | 37 | 0.001138 | 0.004922 |
1076 | POSITIVE REGULATION OF ALPHA BETA T CELL DIFFERENTIATION | 4 | 37 | 0.001138 | 0.004922 |
1077 | REGULATION OF OSTEOCLAST DIFFERENTIATION | 5 | 63 | 0.001142 | 0.004933 |
1078 | BRANCH ELONGATION OF AN EPITHELIUM | 3 | 17 | 0.001153 | 0.004966 |
1079 | REGULATION OF DNA METHYLATION | 3 | 17 | 0.001153 | 0.004966 |
1080 | NEGATIVE REGULATION OF LIPID STORAGE | 3 | 17 | 0.001153 | 0.004966 |
1081 | REGULATION OF REPRODUCTIVE PROCESS | 7 | 129 | 0.001203 | 0.005177 |
1082 | POSITIVE REGULATION OF T CELL PROLIFERATION | 6 | 95 | 0.001235 | 0.0053 |
1083 | CANONICAL WNT SIGNALING PATHWAY | 6 | 95 | 0.001235 | 0.0053 |
1084 | TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 6 | 95 | 0.001235 | 0.0053 |
1085 | COLLAGEN FIBRIL ORGANIZATION | 4 | 38 | 0.00126 | 0.005393 |
1086 | BONE MINERALIZATION | 4 | 38 | 0.00126 | 0.005393 |
1087 | REGULATION OF CD4 POSITIVE ALPHA BETA T CELL ACTIVATION | 4 | 38 | 0.00126 | 0.005393 |
1088 | REGULATION OF PROTEIN BINDING | 8 | 168 | 0.001273 | 0.00544 |
1089 | INTRACELLULAR RECEPTOR SIGNALING PATHWAY | 8 | 168 | 0.001273 | 0.00544 |
1090 | NEGATIVE REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION | 9 | 209 | 0.001305 | 0.005564 |
1091 | GERM CELL DEVELOPMENT | 9 | 209 | 0.001305 | 0.005564 |
1092 | REGULATION OF RESPONSE TO OXIDATIVE STRESS | 5 | 65 | 0.001315 | 0.005593 |
1093 | RETINA DEVELOPMENT IN CAMERA TYPE EYE | 7 | 131 | 0.001315 | 0.005593 |
1094 | NEGATIVE REGULATION OF AXONOGENESIS | 5 | 65 | 0.001315 | 0.005593 |
1095 | REGULATION OF MEMBRANE POTENTIAL | 12 | 343 | 0.001338 | 0.005687 |
1096 | NEGATIVE REGULATION OF RESPONSE TO REACTIVE OXYGEN SPECIES | 3 | 18 | 0.00137 | 0.005781 |
1097 | OVULATION | 3 | 18 | 0.00137 | 0.005781 |
1098 | RESPONSE TO PLATELET DERIVED GROWTH FACTOR | 3 | 18 | 0.00137 | 0.005781 |
1099 | RESPONSE TO CAFFEINE | 3 | 18 | 0.00137 | 0.005781 |
1100 | POSITIVE REGULATION OF T HELPER CELL DIFFERENTIATION | 3 | 18 | 0.00137 | 0.005781 |
1101 | MAST CELL MEDIATED IMMUNITY | 3 | 18 | 0.00137 | 0.005781 |
1102 | NEGATIVE REGULATION OF ORGANIC ACID TRANSPORT | 3 | 18 | 0.00137 | 0.005781 |
1103 | NOTOCHORD DEVELOPMENT | 3 | 18 | 0.00137 | 0.005781 |
1104 | EXTRINSIC APOPTOTIC SIGNALING PATHWAY VIA DEATH DOMAIN RECEPTORS | 4 | 39 | 0.00139 | 0.005828 |
1105 | CELLULAR RESPONSE TO NUTRIENT | 4 | 39 | 0.00139 | 0.005828 |
1106 | LONG TERM SYNAPTIC POTENTIATION | 4 | 39 | 0.00139 | 0.005828 |
1107 | PLATELET AGGREGATION | 4 | 39 | 0.00139 | 0.005828 |
1108 | NEGATIVE CHEMOTAXIS | 4 | 39 | 0.00139 | 0.005828 |
1109 | NEGATIVE REGULATION OF MITOCHONDRION ORGANIZATION | 4 | 39 | 0.00139 | 0.005828 |
1110 | GLANDULAR EPITHELIAL CELL DIFFERENTIATION | 4 | 39 | 0.00139 | 0.005828 |
1111 | POSITIVE REGULATION OF PROTEIN SECRETION | 9 | 211 | 0.001394 | 0.005836 |
1112 | CELLULAR RESPONSE TO UV | 5 | 66 | 0.001409 | 0.005894 |
1113 | AUTOPHAGY | 13 | 394 | 0.001446 | 0.006044 |
1114 | MYELOID LEUKOCYTE ACTIVATION | 6 | 98 | 0.00145 | 0.006056 |
1115 | MAMMARY GLAND MORPHOGENESIS | 4 | 40 | 0.00153 | 0.006372 |
1116 | REGULATION OF ACTIVATED T CELL PROLIFERATION | 4 | 40 | 0.00153 | 0.006372 |
1117 | PROTEIN TRIMERIZATION | 4 | 40 | 0.00153 | 0.006372 |
1118 | REGULATION OF CELLULAR KETONE METABOLIC PROCESS | 8 | 173 | 0.001534 | 0.006385 |
1119 | REGULATION OF ALPHA BETA T CELL ACTIVATION | 5 | 68 | 0.00161 | 0.006681 |
1120 | REGULATION OF HYDROGEN PEROXIDE INDUCED CELL DEATH | 3 | 19 | 0.001613 | 0.006681 |
1121 | CELLULAR SODIUM ION HOMEOSTASIS | 3 | 19 | 0.001613 | 0.006681 |
1122 | MACROPHAGE DIFFERENTIATION | 3 | 19 | 0.001613 | 0.006681 |
1123 | POSITIVE REGULATION OF INTERLEUKIN 6 PRODUCTION | 5 | 68 | 0.00161 | 0.006681 |
1124 | POSITIVE REGULATION OF CYTOSKELETON ORGANIZATION | 8 | 175 | 0.00165 | 0.00683 |
1125 | REGULATION OF LIPID STORAGE | 4 | 41 | 0.001679 | 0.006924 |
1126 | ANION HOMEOSTASIS | 4 | 41 | 0.001679 | 0.006924 |
1127 | MYELOID CELL ACTIVATION INVOLVED IN IMMUNE RESPONSE | 4 | 41 | 0.001679 | 0.006924 |
1128 | MONOCYTE CHEMOTAXIS | 4 | 41 | 0.001679 | 0.006924 |
1129 | REGULATION OF TUMOR NECROSIS FACTOR SUPERFAMILY CYTOKINE PRODUCTION | 6 | 101 | 0.001692 | 0.006975 |
1130 | CIRCADIAN RHYTHM | 7 | 137 | 0.001702 | 0.007008 |
1131 | NEGATIVE REGULATION OF IMMUNE EFFECTOR PROCESS | 6 | 102 | 0.00178 | 0.007322 |
1132 | POSITIVE REGULATION OF TYPE I INTERFERON PRODUCTION | 5 | 70 | 0.001832 | 0.007526 |
1133 | POSITIVE REGULATION OF DNA BINDING | 4 | 42 | 0.001837 | 0.007526 |
1134 | DETECTION OF MECHANICAL STIMULUS | 4 | 42 | 0.001837 | 0.007526 |
1135 | EYE PHOTORECEPTOR CELL DIFFERENTIATION | 4 | 42 | 0.001837 | 0.007526 |
1136 | REGULATION OF BONE REMODELING | 4 | 42 | 0.001837 | 0.007526 |
1137 | RESPONSE TO ORGANOPHOSPHORUS | 7 | 139 | 0.001849 | 0.007565 |
1138 | REGULATION OF SMOOTH MUSCLE CELL DIFFERENTIATION | 3 | 20 | 0.00188 | 0.007659 |
1139 | RESPONSE TO PROTOZOAN | 3 | 20 | 0.00188 | 0.007659 |
1140 | GENETIC IMPRINTING | 3 | 20 | 0.00188 | 0.007659 |
1141 | RESPONSE TO MUSCLE ACTIVITY | 3 | 20 | 0.00188 | 0.007659 |
1142 | LYMPH VESSEL DEVELOPMENT | 3 | 20 | 0.00188 | 0.007659 |
1143 | REGULATION OF INTERLEUKIN 6 PRODUCTION | 6 | 104 | 0.001965 | 0.007998 |
1144 | REGULATION OF GLYCOPROTEIN METABOLIC PROCESS | 4 | 43 | 0.002006 | 0.008152 |
1145 | REGULATION OF MUSCLE CELL APOPTOTIC PROCESS | 4 | 43 | 0.002006 | 0.008152 |
1146 | POSITIVE REGULATION OF CALCIUM ION TRANSPORT | 6 | 106 | 0.002164 | 0.008784 |
1147 | MAST CELL ACTIVATION | 3 | 21 | 0.002173 | 0.008784 |
1148 | POSITIVE T CELL SELECTION | 3 | 21 | 0.002173 | 0.008784 |
1149 | POSITIVE REGULATION OF EXCITATORY POSTSYNAPTIC POTENTIAL | 3 | 21 | 0.002173 | 0.008784 |
1150 | NEGATIVE REGULATION OF LIPID CATABOLIC PROCESS | 3 | 21 | 0.002173 | 0.008784 |
1151 | RUFFLE ORGANIZATION | 3 | 21 | 0.002173 | 0.008784 |
1152 | LABYRINTHINE LAYER DEVELOPMENT | 4 | 44 | 0.002185 | 0.008827 |
1153 | REGULATION OF STEROID METABOLIC PROCESS | 5 | 74 | 0.002342 | 0.009452 |
1154 | NEGATIVE REGULATION OF MAPK CASCADE | 7 | 145 | 0.002349 | 0.009462 |
1155 | REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY | 7 | 145 | 0.002349 | 0.009462 |
1156 | POSITIVE REGULATION OF RECEPTOR ACTIVITY | 4 | 45 | 0.002375 | 0.009561 |
1157 | MYELINATION IN PERIPHERAL NERVOUS SYSTEM | 3 | 22 | 0.002493 | 0.009974 |
1158 | POSITIVE REGULATION OF TRANSLATIONAL INITIATION | 3 | 22 | 0.002493 | 0.009974 |
1159 | SENSORY PERCEPTION OF PAIN | 5 | 75 | 0.002484 | 0.009974 |
1160 | POSITIVE REGULATION OF MUSCLE HYPERTROPHY | 3 | 22 | 0.002493 | 0.009974 |
1161 | PERIPHERAL NERVOUS SYSTEM AXON ENSHEATHMENT | 3 | 22 | 0.002493 | 0.009974 |
1162 | POSITIVE REGULATION OF CARDIAC MUSCLE HYPERTROPHY | 3 | 22 | 0.002493 | 0.009974 |
1163 | CELLULAR RESPONSE TO INTERLEUKIN 6 | 3 | 22 | 0.002493 | 0.009974 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | KINASE ACTIVITY | 77 | 842 | 2.769e-45 | 1.286e-42 |
2 | RECEPTOR BINDING | 97 | 1476 | 2.454e-45 | 1.286e-42 |
3 | TRANSFERASE ACTIVITY TRANSFERRING PHOSPHORUS CONTAINING GROUPS | 78 | 992 | 4.106e-41 | 1.272e-38 |
4 | PROTEIN KINASE ACTIVITY | 64 | 640 | 1.376e-39 | 3.196e-37 |
5 | PHOSPHATIDYLINOSITOL 3 KINASE ACTIVITY | 29 | 70 | 3.172e-37 | 5.893e-35 |
6 | PROTEIN TYROSINE KINASE ACTIVITY | 37 | 176 | 8.411e-35 | 1.302e-32 |
7 | GROWTH FACTOR BINDING | 31 | 123 | 6.587e-32 | 8.741e-30 |
8 | MOLECULAR FUNCTION REGULATOR | 78 | 1353 | 1.195e-31 | 1.388e-29 |
9 | GROWTH FACTOR ACTIVITY | 32 | 160 | 1.93e-29 | 1.992e-27 |
10 | TRANSMEMBRANE RECEPTOR PROTEIN TYROSINE KINASE ACTIVITY | 22 | 64 | 2.681e-26 | 2.491e-24 |
11 | GROWTH FACTOR RECEPTOR BINDING | 27 | 129 | 1.542e-25 | 1.303e-23 |
12 | X1 PHOSPHATIDYLINOSITOL 3 KINASE ACTIVITY | 19 | 43 | 2.131e-25 | 1.65e-23 |
13 | TRANSMEMBRANE RECEPTOR PROTEIN KINASE ACTIVITY | 22 | 81 | 1.03e-23 | 7.358e-22 |
14 | PHOSPHATIDYLINOSITOL KINASE ACTIVITY | 19 | 51 | 1.181e-23 | 7.836e-22 |
15 | RAS GUANYL NUCLEOTIDE EXCHANGE FACTOR ACTIVITY | 31 | 228 | 3.215e-23 | 1.991e-21 |
16 | ENZYME BINDING | 76 | 1737 | 4.018e-23 | 2.333e-21 |
17 | SIGNAL TRANSDUCER ACTIVITY | 75 | 1731 | 1.55e-22 | 8.469e-21 |
18 | PROTEIN COMPLEX BINDING | 53 | 935 | 8.836e-21 | 4.56e-19 |
19 | KINASE BINDING | 43 | 606 | 1.589e-20 | 7.77e-19 |
20 | MACROMOLECULAR COMPLEX BINDING | 63 | 1399 | 1.402e-19 | 6.512e-18 |
21 | GUANYL NUCLEOTIDE EXCHANGE FACTOR ACTIVITY | 31 | 303 | 1.671e-19 | 7.392e-18 |
22 | PLATELET DERIVED GROWTH FACTOR RECEPTOR BINDING | 10 | 15 | 2.211e-16 | 9.337e-15 |
23 | PLATELET DERIVED GROWTH FACTOR BINDING | 9 | 11 | 3.472e-16 | 1.402e-14 |
24 | PROTEIN PHOSPHATASE BINDING | 19 | 120 | 6.629e-16 | 2.566e-14 |
25 | PHOSPHATASE BINDING | 21 | 162 | 1.238e-15 | 4.601e-14 |
26 | INTEGRIN BINDING | 17 | 105 | 1.585e-14 | 5.663e-13 |
27 | KINASE REGULATOR ACTIVITY | 21 | 186 | 2.073e-14 | 6.878e-13 |
28 | CELL ADHESION MOLECULE BINDING | 21 | 186 | 2.073e-14 | 6.878e-13 |
29 | PROTEIN PHOSPHATASE TYPE 2A REGULATOR ACTIVITY | 10 | 21 | 2.432e-14 | 7.79e-13 |
30 | EXTRACELLULAR MATRIX STRUCTURAL CONSTITUENT | 15 | 76 | 2.689e-14 | 8.328e-13 |
31 | ENZYME REGULATOR ACTIVITY | 43 | 959 | 2.559e-13 | 7.669e-12 |
32 | RECEPTOR ACTIVITY | 58 | 1649 | 3.156e-13 | 9.163e-12 |
33 | RIBONUCLEOTIDE BINDING | 62 | 1860 | 4.165e-13 | 1.138e-11 |
34 | ADENYL NUCLEOTIDE BINDING | 55 | 1514 | 4.145e-13 | 1.138e-11 |
35 | SIGNALING RECEPTOR ACTIVITY | 52 | 1393 | 7.406e-13 | 1.966e-11 |
36 | COLLAGEN BINDING | 13 | 65 | 1.228e-12 | 3.169e-11 |
37 | PROTEIN SERINE THREONINE KINASE ACTIVITY | 28 | 445 | 2.315e-12 | 5.814e-11 |
38 | CYTOKINE RECEPTOR ACTIVITY | 14 | 89 | 5.242e-12 | 1.281e-10 |
39 | CYTOKINE RECEPTOR BINDING | 21 | 271 | 3.201e-11 | 7.624e-10 |
40 | FIBROBLAST GROWTH FACTOR RECEPTOR BINDING | 9 | 28 | 3.623e-11 | 8.414e-10 |
41 | CYTOKINE BINDING | 13 | 92 | 1.238e-10 | 2.806e-09 |
42 | HEPARIN BINDING | 16 | 157 | 1.354e-10 | 2.995e-09 |
43 | NEUROTROPHIN RECEPTOR BINDING | 7 | 14 | 1.397e-10 | 3.017e-09 |
44 | INSULIN LIKE GROWTH FACTOR RECEPTOR BINDING | 7 | 15 | 2.591e-10 | 5.47e-09 |
45 | GLYCOSAMINOGLYCAN BINDING | 17 | 205 | 9.045e-10 | 1.867e-08 |
46 | PROTEIN HETERODIMERIZATION ACTIVITY | 25 | 468 | 1.157e-09 | 2.287e-08 |
47 | PROTEIN DIMERIZATION ACTIVITY | 41 | 1149 | 1.137e-09 | 2.287e-08 |
48 | IDENTICAL PROTEIN BINDING | 42 | 1209 | 1.539e-09 | 2.978e-08 |
49 | INSULIN RECEPTOR SUBSTRATE BINDING | 6 | 11 | 1.575e-09 | 2.987e-08 |
50 | SULFUR COMPOUND BINDING | 17 | 234 | 6.779e-09 | 1.26e-07 |
51 | EXTRACELLULAR MATRIX BINDING | 9 | 51 | 1.242e-08 | 2.263e-07 |
52 | CHEMOATTRACTANT ACTIVITY | 7 | 27 | 3.146e-08 | 5.62e-07 |
53 | FIBRONECTIN BINDING | 7 | 28 | 4.15e-08 | 7.274e-07 |
54 | PHOSPHATIDYLINOSITOL 3 KINASE BINDING | 7 | 30 | 6.984e-08 | 1.202e-06 |
55 | KINASE ACTIVATOR ACTIVITY | 9 | 62 | 7.35e-08 | 1.241e-06 |
56 | PROTEIN DOMAIN SPECIFIC BINDING | 26 | 624 | 8.629e-08 | 1.431e-06 |
57 | PHOSPHATASE REGULATOR ACTIVITY | 10 | 87 | 1.339e-07 | 2.182e-06 |
58 | PROTEIN TYROSINE KINASE BINDING | 8 | 54 | 3.375e-07 | 5.406e-06 |
59 | PROTEIN SERINE THREONINE TYROSINE KINASE ACTIVITY | 7 | 39 | 4.794e-07 | 7.549e-06 |
60 | CYCLIN DEPENDENT PROTEIN SERINE THREONINE KINASE REGULATOR ACTIVITY | 6 | 28 | 1.075e-06 | 1.637e-05 |
61 | PROTEIN PHOSPHATASE 2A BINDING | 6 | 28 | 1.075e-06 | 1.637e-05 |
62 | PROTEIN BINDING INVOLVED IN CELL ADHESION | 5 | 17 | 1.605e-06 | 2.405e-05 |
63 | INSULIN RECEPTOR BINDING | 6 | 32 | 2.479e-06 | 3.599e-05 |
64 | SODIUM CHANNEL REGULATOR ACTIVITY | 6 | 32 | 2.479e-06 | 3.599e-05 |
65 | VIRUS RECEPTOR ACTIVITY | 8 | 70 | 2.578e-06 | 3.685e-05 |
66 | HISTONE KINASE ACTIVITY | 5 | 19 | 2.955e-06 | 4.159e-05 |
67 | PROTEASE BINDING | 9 | 104 | 6.311e-06 | 8.75e-05 |
68 | FIBROBLAST GROWTH FACTOR BINDING | 5 | 23 | 8.207e-06 | 0.0001121 |
69 | EPHRIN RECEPTOR BINDING | 5 | 24 | 1.026e-05 | 0.0001382 |
70 | RECEPTOR SIGNALING PROTEIN ACTIVITY | 11 | 172 | 1.122e-05 | 0.0001489 |
71 | PROTEIN HOMODIMERIZATION ACTIVITY | 24 | 722 | 1.381e-05 | 0.0001807 |
72 | CAMP RESPONSE ELEMENT BINDING | 4 | 13 | 1.56e-05 | 0.0002012 |
73 | LAMININ BINDING | 5 | 30 | 3.236e-05 | 0.0004118 |
74 | PHOSPHATIDYLINOSITOL PHOSPHATE KINASE ACTIVITY | 4 | 16 | 3.854e-05 | 0.0004839 |
75 | CYCLIN BINDING | 4 | 19 | 7.969e-05 | 0.0009592 |
76 | X14 3 3 PROTEIN BINDING | 4 | 19 | 7.969e-05 | 0.0009592 |
77 | PEPTIDE HORMONE BINDING | 5 | 36 | 8.053e-05 | 0.0009592 |
78 | EPHRIN RECEPTOR ACTIVITY | 4 | 19 | 7.969e-05 | 0.0009592 |
79 | ENZYME ACTIVATOR ACTIVITY | 17 | 471 | 9.688e-05 | 0.001139 |
80 | CHEMOKINE BINDING | 4 | 21 | 0.0001207 | 0.001401 |
81 | CHANNEL REGULATOR ACTIVITY | 8 | 131 | 0.0002458 | 0.002819 |
82 | NON MEMBRANE SPANNING PROTEIN TYROSINE KINASE ACTIVITY | 5 | 46 | 0.0002645 | 0.002997 |
83 | STRUCTURAL MOLECULE ACTIVITY | 21 | 732 | 0.0003685 | 0.004124 |
84 | PROTEIN KINASE C BINDING | 5 | 50 | 0.0003926 | 0.004291 |
85 | TAU PROTEIN BINDING | 3 | 12 | 0.0003906 | 0.004291 |
86 | CYTOKINE ACTIVITY | 10 | 219 | 0.0004518 | 0.004881 |
87 | UBIQUITIN LIKE PROTEIN LIGASE BINDING | 11 | 264 | 0.0005138 | 0.005487 |
88 | RECEPTOR ACTIVATOR ACTIVITY | 4 | 32 | 0.0006508 | 0.006871 |
89 | CYCLIN DEPENDENT PROTEIN KINASE ACTIVITY | 4 | 34 | 0.0008231 | 0.008592 |
90 | TRANSCRIPTION FACTOR BINDING | 16 | 524 | 0.0009656 | 0.009857 |
91 | CHLORIDE CHANNEL REGULATOR ACTIVITY | 3 | 16 | 0.0009581 | 0.009857 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | PROTEIN COMPLEX INVOLVED IN CELL ADHESION | 19 | 30 | 1.679e-29 | 9.804e-27 |
2 | EXTRACELLULAR MATRIX | 44 | 426 | 1.288e-27 | 3.76e-25 |
3 | EXTRACELLULAR MATRIX COMPONENT | 28 | 125 | 2.464e-27 | 4.797e-25 |
4 | RECEPTOR COMPLEX | 38 | 327 | 9.116e-26 | 1.331e-23 |
5 | PROTEINACEOUS EXTRACELLULAR MATRIX | 39 | 356 | 1.817e-25 | 2.122e-23 |
6 | CELL SURFACE | 53 | 757 | 5.12e-25 | 4.984e-23 |
7 | BASEMENT MEMBRANE | 23 | 93 | 1.048e-23 | 8.741e-22 |
8 | PLASMA MEMBRANE RECEPTOR COMPLEX | 26 | 175 | 1.265e-20 | 9.234e-19 |
9 | CELL SUBSTRATE JUNCTION | 35 | 398 | 9.15e-20 | 5.938e-18 |
10 | SIDE OF MEMBRANE | 36 | 428 | 1.14e-19 | 6.655e-18 |
11 | BASAL LAMINA | 12 | 21 | 2.971e-18 | 1.577e-16 |
12 | COMPLEX OF COLLAGEN TRIMERS | 12 | 23 | 1.337e-17 | 6.506e-16 |
13 | EXTRINSIC COMPONENT OF MEMBRANE | 26 | 252 | 1.328e-16 | 5.925e-15 |
14 | PROTEIN PHOSPHATASE TYPE 2A COMPLEX | 11 | 20 | 1.42e-16 | 5.925e-15 |
15 | PLASMA MEMBRANE PROTEIN COMPLEX | 35 | 510 | 2.293e-16 | 8.926e-15 |
16 | ANCHORING JUNCTION | 34 | 489 | 4.322e-16 | 1.578e-14 |
17 | INTRINSIC COMPONENT OF PLASMA MEMBRANE | 62 | 1649 | 1.763e-15 | 6.056e-14 |
18 | TRANSFERASE COMPLEX TRANSFERRING PHOSPHORUS CONTAINING GROUPS | 24 | 237 | 3.171e-15 | 1.029e-13 |
19 | MEMBRANE PROTEIN COMPLEX | 47 | 1020 | 5.913e-15 | 1.818e-13 |
20 | PHOSPHATIDYLINOSITOL 3 KINASE COMPLEX | 10 | 20 | 1.288e-14 | 3.76e-13 |
21 | COLLAGEN TRIMER | 16 | 88 | 1.427e-14 | 3.968e-13 |
22 | CATALYTIC COMPLEX | 46 | 1038 | 4.988e-14 | 1.324e-12 |
23 | INTRACELLULAR VESICLE | 51 | 1259 | 5.633e-14 | 1.43e-12 |
24 | ENDOPLASMIC RETICULUM LUMEN | 21 | 201 | 9.804e-14 | 2.386e-12 |
25 | CELL JUNCTION | 48 | 1151 | 1.232e-13 | 2.877e-12 |
26 | EXTRACELLULAR SPACE | 52 | 1376 | 4.612e-13 | 1.036e-11 |
27 | MEMBRANE REGION | 46 | 1134 | 1.158e-12 | 2.505e-11 |
28 | VESICLE LUMEN | 15 | 106 | 4.401e-12 | 9.18e-11 |
29 | PLATELET ALPHA GRANULE | 13 | 75 | 8.475e-12 | 1.707e-10 |
30 | PHOSPHATASE COMPLEX | 11 | 48 | 1.404e-11 | 2.733e-10 |
31 | EXTRINSIC COMPONENT OF CYTOPLASMIC SIDE OF PLASMA MEMBRANE | 14 | 98 | 2.028e-11 | 3.821e-10 |
32 | EXTERNAL SIDE OF PLASMA MEMBRANE | 20 | 238 | 2.219e-11 | 4.049e-10 |
33 | PLASMA MEMBRANE REGION | 39 | 929 | 2.812e-11 | 4.976e-10 |
34 | CYTOPLASMIC SIDE OF MEMBRANE | 17 | 170 | 4.783e-11 | 8.216e-10 |
35 | PLATELET ALPHA GRANULE LUMEN | 11 | 55 | 6.883e-11 | 1.148e-09 |
36 | PROTEIN KINASE COMPLEX | 13 | 90 | 9.319e-11 | 1.512e-09 |
37 | EXTRINSIC COMPONENT OF PLASMA MEMBRANE | 15 | 136 | 1.683e-10 | 2.656e-09 |
38 | MEMBRANE MICRODOMAIN | 20 | 288 | 6.688e-10 | 1.028e-08 |
39 | CYCLIN DEPENDENT PROTEIN KINASE HOLOENZYME COMPLEX | 8 | 31 | 3.28e-09 | 4.911e-08 |
40 | HETEROTRIMERIC G PROTEIN COMPLEX | 8 | 32 | 4.326e-09 | 6.316e-08 |
41 | SECRETORY GRANULE LUMEN | 11 | 85 | 8.824e-09 | 1.257e-07 |
42 | VACUOLE | 38 | 1180 | 7.612e-08 | 1.058e-06 |
43 | CYTOPLASMIC VESICLE PART | 25 | 601 | 1.602e-07 | 2.176e-06 |
44 | SECRETORY GRANULE | 18 | 352 | 5.097e-07 | 6.765e-06 |
45 | PERINUCLEAR REGION OF CYTOPLASM | 25 | 642 | 5.474e-07 | 7.105e-06 |
46 | CELL PROJECTION | 47 | 1786 | 7.465e-07 | 9.477e-06 |
47 | TRANSFERASE COMPLEX | 26 | 703 | 8.487e-07 | 1.055e-05 |
48 | ENDOPLASMIC RETICULUM | 44 | 1631 | 9.318e-07 | 1.134e-05 |
49 | PLASMA MEMBRANE RAFT | 9 | 86 | 1.284e-06 | 1.53e-05 |
50 | SECRETORY VESICLE | 19 | 461 | 5.964e-06 | 6.966e-05 |
51 | RUFFLE MEMBRANE | 8 | 80 | 7.11e-06 | 8.142e-05 |
52 | LEADING EDGE MEMBRANE | 10 | 134 | 7.306e-06 | 8.205e-05 |
53 | BANDED COLLAGEN FIBRIL | 4 | 12 | 1.09e-05 | 0.0001201 |
54 | ENDOSOME | 25 | 793 | 2.21e-05 | 0.000239 |
55 | ENDOPLASMIC RETICULUM PART | 32 | 1163 | 2.335e-05 | 0.0002479 |
56 | CELL PROJECTION MEMBRANE | 14 | 298 | 2.493e-05 | 0.00026 |
57 | CELL LEADING EDGE | 15 | 350 | 3.721e-05 | 0.0003812 |
58 | BASAL PART OF CELL | 6 | 51 | 4.04e-05 | 0.0004068 |
59 | NEURON PART | 33 | 1265 | 4.946e-05 | 0.0004896 |
60 | SOMATODENDRITIC COMPARTMENT | 21 | 650 | 7.283e-05 | 0.0007089 |
61 | NEURON PROJECTION | 26 | 942 | 0.0001363 | 0.001305 |
62 | RUFFLE | 9 | 156 | 0.0001561 | 0.00147 |
63 | PIGMENT GRANULE | 7 | 103 | 0.0003134 | 0.002906 |
64 | BASOLATERAL PLASMA MEMBRANE | 10 | 211 | 0.0003369 | 0.003074 |
65 | CELL PROJECTION PART | 25 | 946 | 0.000354 | 0.003181 |
66 | ENDOCYTIC VESICLE | 11 | 256 | 0.0003969 | 0.003512 |
67 | DENDRITE | 15 | 451 | 0.0005862 | 0.005109 |
68 | BASAL PLASMA MEMBRANE | 4 | 33 | 0.0007334 | 0.006298 |
69 | PHOTORECEPTOR INNER SEGMENT | 4 | 36 | 0.001025 | 0.008677 |
70 | CELL CELL JUNCTION | 13 | 383 | 0.001122 | 0.009361 |
Num | Pathway | Pathview | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|---|
1 | PI3K_Akt_signaling_pathway_hsa04151 | 246 | 352 | 0 | 0 | |
2 | Focal_adhesion_hsa04510 | 98 | 199 | 2.031e-138 | 5.281e-137 | |
3 | Ras_signaling_pathway_hsa04014 | 86 | 232 | 6.731e-107 | 1.167e-105 | |
4 | ECM_receptor_interaction_hsa04512 | 55 | 82 | 9.88e-87 | 1.284e-85 | |
5 | Rap1_signaling_pathway_hsa04015 | 69 | 206 | 3.213e-81 | 3.341e-80 | |
6 | MAPK_signaling_pathway_hsa04010 | 73 | 295 | 4.065e-75 | 3.523e-74 | |
7 | Regulation_of_actin_cytoskeleton_hsa04810 | 59 | 208 | 3.664e-64 | 2.722e-63 | |
8 | AMPK_signaling_pathway_hsa04152 | 45 | 121 | 5.908e-55 | 3.84e-54 | |
9 | Jak_STAT_signaling_pathway_hsa04630 | 47 | 162 | 1.912e-51 | 1.105e-50 | |
10 | FoxO_signaling_pathway_hsa04068 | 44 | 132 | 3.19e-51 | 1.659e-50 | |
11 | HIF_1_signaling_pathway_hsa04066 | 37 | 100 | 4.269e-45 | 2.018e-44 | |
12 | Phospholipase_D_signaling_pathway_hsa04072 | 40 | 146 | 1.213e-42 | 5.256e-42 | |
13 | Sphingolipid_signaling_pathway_hsa04071 | 37 | 118 | 6.069e-42 | 2.427e-41 | |
14 | mTOR_signaling_pathway_hsa04150 | 38 | 151 | 5.857e-39 | 2.175e-38 | |
15 | ErbB_signaling_pathway_hsa04012 | 31 | 85 | 1.237e-37 | 4.287e-37 | |
16 | Autophagy_animal_hsa04140 | 33 | 128 | 2.785e-34 | 9.05e-34 | |
17 | Cellular_senescence_hsa04218 | 35 | 160 | 1.354e-33 | 4.142e-33 | |
18 | Apelin_signaling_pathway_hsa04371 | 32 | 137 | 9.359e-32 | 2.704e-31 | |
19 | Cytokine_cytokine_receptor_interaction_hsa04060 | 38 | 270 | 6.976e-29 | 1.909e-28 | |
20 | VEGF_signaling_pathway_hsa04370 | 22 | 59 | 3.161e-27 | 8.218e-27 | |
21 | Signaling_pathways_regulating_pluripotency_of_stem_cells_hsa04550 | 28 | 139 | 5.902e-26 | 1.461e-25 | |
22 | Apoptosis_hsa04210 | 27 | 138 | 1.061e-24 | 2.507e-24 | |
23 | TNF_signaling_pathway_hsa04668 | 22 | 108 | 1.001e-20 | 2.263e-20 | |
24 | Gap_junction_hsa04540 | 19 | 88 | 1.442e-18 | 3.125e-18 | |
25 | Oocyte_meiosis_hsa04114 | 21 | 124 | 4.421e-18 | 9.195e-18 | |
26 | Cell_cycle_hsa04110 | 19 | 124 | 1.245e-15 | 2.489e-15 | |
27 | cAMP_signaling_pathway_hsa04024 | 22 | 198 | 6.802e-15 | 1.31e-14 | |
28 | p53_signaling_pathway_hsa04115 | 13 | 68 | 2.269e-12 | 4.186e-12 | |
29 | cGMP_PKG_signaling_pathway_hsa04022 | 18 | 163 | 2.335e-12 | 4.186e-12 | |
30 | Hippo_signaling_pathway_hsa04390 | 17 | 154 | 9.733e-12 | 1.687e-11 | |
31 | Tight_junction_hsa04530 | 13 | 170 | 2.328e-07 | 3.904e-07 | |
32 | TGF_beta_signaling_pathway_hsa04350 | 9 | 84 | 1.05e-06 | 1.707e-06 | |
33 | Adherens_junction_hsa04520 | 8 | 72 | 3.199e-06 | 5.041e-06 | |
34 | Phagosome_hsa04145 | 11 | 152 | 3.431e-06 | 5.248e-06 | |
35 | Phosphatidylinositol_signaling_system_hsa04070 | 8 | 99 | 3.425e-05 | 5.088e-05 | |
36 | Mitophagy_animal_hsa04137 | 6 | 65 | 0.0001602 | 0.0002313 | |
37 | Necroptosis_hsa04217 | 9 | 164 | 0.0002273 | 0.0003194 | |
38 | Cell_adhesion_molecules_.CAMs._hsa04514 | 8 | 145 | 0.0004872 | 0.0006667 | |
39 | Wnt_signaling_pathway_hsa04310 | 8 | 146 | 0.00051 | 0.00068 | |
40 | Autophagy_other_hsa04136 | 4 | 32 | 0.0006508 | 0.0008461 | |
41 | Apoptosis_multiple_species_hsa04215 | 4 | 33 | 0.0007334 | 0.0009301 | |
42 | Endocytosis_hsa04144 | 10 | 244 | 0.001039 | 0.001286 | |
43 | NF_kappa_B_signaling_pathway_hsa04064 | 6 | 95 | 0.001235 | 0.001493 | |
44 | Hedgehog_signaling_pathway_hsa04340 | 4 | 47 | 0.002789 | 0.003296 | |
45 | Calcium_signaling_pathway_hsa04020 | 7 | 182 | 0.008078 | 0.009335 | |
46 | Neuroactive_ligand_receptor_interaction_hsa04080 | 6 | 278 | 0.1364 | 0.1542 |
Num | lncRNA | miRNAs | miRNAs count | Gene | Sponge regulatory network | lncRNA log2FC | lncRNA pvalue | Gene log2FC | Gene pvalue | lncRNA-gene Pearson correlation |
---|---|---|---|---|---|---|---|---|---|---|
1 | MAGI2-AS3 |
hsa-let-7a-3p;hsa-miR-141-3p;hsa-miR-200a-3p;hsa-miR-26b-5p;hsa-miR-33a-3p;hsa-miR-421;hsa-miR-429;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-7-1-3p | 10 | HGF | Sponge network | -2.588 | 0 | -3.203 | 0 | 0.836 |
2 | TBX5-AS1 |
hsa-miR-141-5p;hsa-miR-186-5p;hsa-miR-200b-3p;hsa-miR-200b-5p;hsa-miR-200c-3p;hsa-miR-335-3p;hsa-miR-421;hsa-miR-576-5p;hsa-miR-590-5p;hsa-miR-7-1-3p | 10 | ITGA1 | Sponge network | -2.901 | 0 | -1.977 | 0 | 0.791 |
3 | MAGI2-AS3 |
hsa-let-7a-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-18a-3p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-33a-3p;hsa-miR-3607-3p;hsa-miR-421;hsa-miR-424-5p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-7-1-3p | 15 | FGF7 | Sponge network | -2.588 | 0 | -2.211 | 0 | 0.785 |
4 | RP11-284N8.3 |
hsa-miR-1271-5p;hsa-miR-141-3p;hsa-miR-182-5p;hsa-miR-18a-3p;hsa-miR-193b-5p;hsa-miR-22-5p;hsa-miR-224-5p;hsa-miR-378a-3p;hsa-miR-590-3p;hsa-miR-939-5p;hsa-miR-940;hsa-miR-96-5p | 12 | GNG7 | Sponge network | -2.956 | 0 | -2.411 | 0 | 0.784 |
5 | TBX5-AS1 |
hsa-miR-141-5p;hsa-miR-200b-3p;hsa-miR-20a-3p;hsa-miR-324-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-421;hsa-miR-452-3p;hsa-miR-576-5p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-877-5p | 12 | ITGA9 | Sponge network | -2.901 | 0 | -2.846 | 0 | 0.775 |
6 | MAGI2-AS3 |
hsa-miR-141-5p;hsa-miR-200b-3p;hsa-miR-20a-3p;hsa-miR-324-5p;hsa-miR-33a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-421;hsa-miR-429;hsa-miR-452-3p;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-616-5p | 14 | ITGA9 | Sponge network | -2.588 | 0 | -2.846 | 0 | 0.769 |
7 | LINC00702 |
hsa-let-7a-3p;hsa-miR-141-3p;hsa-miR-200a-3p;hsa-miR-26b-5p;hsa-miR-335-3p;hsa-miR-33a-3p;hsa-miR-3682-3p;hsa-miR-421;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-7-1-3p | 12 | HGF | Sponge network | -3.658 | 0 | -3.203 | 0 | 0.75 |
8 | MAGI2-AS3 |
hsa-miR-141-5p;hsa-miR-186-5p;hsa-miR-200a-5p;hsa-miR-200b-3p;hsa-miR-200b-5p;hsa-miR-200c-3p;hsa-miR-3607-3p;hsa-miR-421;hsa-miR-429;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-7-1-3p | 12 | ITGA1 | Sponge network | -2.588 | 0 | -1.977 | 0 | 0.746 |
9 | RP11-672A2.4 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-197-3p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-424-5p | 12 | CSF1 | Sponge network | -3.514 | 0 | -1.722 | 0 | 0.738 |
10 | LINC00702 |
hsa-miR-141-5p;hsa-miR-186-5p;hsa-miR-200a-5p;hsa-miR-200b-3p;hsa-miR-200b-5p;hsa-miR-200c-3p;hsa-miR-320b;hsa-miR-335-3p;hsa-miR-421;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-7-1-3p | 13 | ITGA1 | Sponge network | -3.658 | 0 | -1.977 | 0 | 0.738 |
11 | DNM3OS |
hsa-let-7g-5p;hsa-miR-1271-5p;hsa-miR-16-1-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-27b-3p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-96-5p | 10 | FN1 | Sponge network | -1.197 | 0.01767 | -1.199 | 1.0E-5 | 0.734 |
12 | RP11-750H9.5 | hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-423-5p;hsa-miR-532-3p;hsa-miR-629-3p;hsa-miR-939-5p | 10 | CSF1 | Sponge network | -2.941 | 0 | -1.722 | 0 | 0.731 |
13 | MAGI2-AS3 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-186-5p;hsa-miR-19b-1-5p;hsa-miR-20a-3p;hsa-miR-26b-5p;hsa-miR-27a-3p;hsa-miR-28-3p;hsa-miR-301a-3p;hsa-miR-33a-3p;hsa-miR-421;hsa-miR-450b-5p;hsa-miR-454-3p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-940 | 18 | IGF1 | Sponge network | -2.588 | 0 | -1.378 | 1.0E-5 | 0.727 |
14 | LINC00702 |
hsa-let-7a-3p;hsa-let-7d-5p;hsa-miR-151a-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-18a-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-32-5p;hsa-miR-335-3p;hsa-miR-33a-3p;hsa-miR-421;hsa-miR-450b-5p;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-629-3p;hsa-miR-671-5p;hsa-miR-7-1-3p;hsa-miR-92a-3p;hsa-miR-940 | 26 | THBS1 | Sponge network | -3.658 | 0 | -1.792 | 0 | 0.722 |
15 | TBX5-AS1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-200a-3p;hsa-miR-24-3p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-335-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-421;hsa-miR-450b-5p;hsa-miR-550a-5p;hsa-miR-576-5p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-7-1-3p | 22 | PDGFRA | Sponge network | -2.901 | 0 | -1.139 | 0 | 0.721 |
16 | MIR497HG |
hsa-let-7a-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-18a-3p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-33a-3p;hsa-miR-424-5p;hsa-miR-590-5p;hsa-miR-7-1-3p | 11 | FGF7 | Sponge network | -3.004 | 0 | -2.211 | 0 | 0.721 |
17 | LINC00702 |
hsa-let-7d-5p;hsa-let-7g-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-222-3p;hsa-miR-320b;hsa-miR-425-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-3p | 10 | ITGB3 | Sponge network | -3.658 | 0 | -1.502 | 0 | 0.718 |
18 | MAGI2-AS3 |
hsa-let-7d-5p;hsa-let-7g-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-222-3p;hsa-miR-28-5p;hsa-miR-3607-3p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-616-3p;hsa-miR-98-5p | 11 | ITGB3 | Sponge network | -2.588 | 0 | -1.502 | 0 | 0.717 |
19 | TBX5-AS1 |
hsa-let-7d-5p;hsa-miR-151a-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-18a-5p;hsa-miR-200b-5p;hsa-miR-32-5p;hsa-miR-335-3p;hsa-miR-421;hsa-miR-450b-5p;hsa-miR-576-5p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-629-3p;hsa-miR-7-1-3p;hsa-miR-92a-3p | 17 | THBS1 | Sponge network | -2.901 | 0 | -1.792 | 0 | 0.714 |
20 | LINC00968 |
hsa-miR-141-5p;hsa-miR-186-5p;hsa-miR-200a-5p;hsa-miR-200b-3p;hsa-miR-200b-5p;hsa-miR-200c-3p;hsa-miR-320b;hsa-miR-335-5p;hsa-miR-421;hsa-miR-590-3p;hsa-miR-590-5p | 11 | ITGA1 | Sponge network | -4.827 | 0 | -1.977 | 0 | 0.711 |
21 | AC011899.9 |
hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-18a-3p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-424-5p;hsa-miR-455-3p;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-708-3p | 10 | FGF7 | Sponge network | -3.545 | 0 | -2.211 | 0 | 0.705 |
22 | LINC00968 |
hsa-let-7a-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-18a-3p;hsa-miR-27a-3p;hsa-miR-320b;hsa-miR-33a-3p;hsa-miR-421;hsa-miR-424-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p | 13 | FGF7 | Sponge network | -4.827 | 0 | -2.211 | 0 | 0.703 |
23 | MAGI2-AS3 |
hsa-let-7a-3p;hsa-let-7d-5p;hsa-miR-151a-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-33a-3p;hsa-miR-421;hsa-miR-450b-5p;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-629-3p;hsa-miR-671-5p;hsa-miR-7-1-3p;hsa-miR-92a-3p;hsa-miR-940;hsa-miR-98-5p | 21 | THBS1 | Sponge network | -2.588 | 0 | -1.792 | 0 | 0.7 |
24 | MAGI2-AS3 |
hsa-miR-1271-5p;hsa-miR-141-3p;hsa-miR-182-5p;hsa-miR-18a-3p;hsa-miR-193b-5p;hsa-miR-200a-3p;hsa-miR-3127-5p;hsa-miR-378a-3p;hsa-miR-532-3p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-671-5p;hsa-miR-92a-3p;hsa-miR-939-5p;hsa-miR-940 | 15 | GNG7 | Sponge network | -2.588 | 0 | -2.411 | 0 | 0.69 |
25 | LINC00702 |
hsa-let-7a-3p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-196b-5p;hsa-miR-200a-3p;hsa-miR-24-3p;hsa-miR-26b-5p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-320b;hsa-miR-335-3p;hsa-miR-339-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-421;hsa-miR-450b-5p;hsa-miR-454-3p;hsa-miR-550a-5p;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-7-1-3p;hsa-miR-93-5p;hsa-miR-96-5p | 32 | PDGFRA | Sponge network | -3.658 | 0 | -1.139 | 0 | 0.686 |
26 | DNM3OS |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130a-3p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-200a-3p;hsa-miR-24-3p;hsa-miR-27b-3p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-374b-5p;hsa-miR-429;hsa-miR-454-3p;hsa-miR-550a-5p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-7-1-3p;hsa-miR-93-5p;hsa-miR-96-5p | 27 | PDGFRA | Sponge network | -1.197 | 0.01767 | -1.139 | 0 | 0.686 |
27 | MAGI2-AS3 |
hsa-let-7a-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-200a-3p;hsa-miR-24-3p;hsa-miR-26b-5p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-339-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-421;hsa-miR-429;hsa-miR-450b-5p;hsa-miR-454-3p;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-7-1-3p | 27 | PDGFRA | Sponge network | -2.588 | 0 | -1.139 | 0 | 0.684 |
28 | AC109642.1 |
hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-18a-3p;hsa-miR-27a-3p;hsa-miR-320b;hsa-miR-3607-3p;hsa-miR-424-5p;hsa-miR-429;hsa-miR-590-3p | 10 | FGF7 | Sponge network | -3.573 | 0 | -2.211 | 0 | 0.679 |
29 | RP11-166D19.1 |
hsa-let-7a-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-200a-3p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-339-5p;hsa-miR-33a-5p;hsa-miR-429;hsa-miR-450b-5p;hsa-miR-454-3p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-7-1-3p | 19 | PDGFRA | Sponge network | -1.481 | 0.00084 | -1.139 | 0 | 0.675 |
30 | TBX5-AS1 |
hsa-let-7f-1-3p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-186-5p;hsa-miR-19b-1-5p;hsa-miR-20a-3p;hsa-miR-28-3p;hsa-miR-301a-3p;hsa-miR-421;hsa-miR-450b-5p;hsa-miR-576-5p;hsa-miR-629-5p | 12 | IGF1 | Sponge network | -2.901 | 0 | -1.378 | 1.0E-5 | 0.672 |
31 | MIR497HG |
hsa-miR-1271-5p;hsa-miR-141-3p;hsa-miR-182-5p;hsa-miR-18a-3p;hsa-miR-193b-5p;hsa-miR-3127-5p;hsa-miR-378a-3p;hsa-miR-532-3p;hsa-miR-939-5p;hsa-miR-940;hsa-miR-96-5p | 11 | GNG7 | Sponge network | -3.004 | 0 | -2.411 | 0 | 0.672 |
32 | MAGI2-AS3 |
hsa-let-7g-5p;hsa-miR-1271-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-26b-5p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-590-3p | 10 | FN1 | Sponge network | -2.588 | 0 | -1.199 | 1.0E-5 | 0.671 |
33 | LINC00702 |
hsa-let-7a-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-18a-3p;hsa-miR-27b-3p;hsa-miR-320b;hsa-miR-33a-3p;hsa-miR-421;hsa-miR-424-5p;hsa-miR-455-3p;hsa-miR-501-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-7-1-3p | 16 | FGF7 | Sponge network | -3.658 | 0 | -2.211 | 0 | 0.667 |
34 | CTD-2171N6.1 |
hsa-let-7d-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-107;hsa-miR-126-5p;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-218-5p;hsa-miR-29b-3p;hsa-miR-30d-3p;hsa-miR-532-3p | 11 | COL1A1 | Sponge network | 1.382 | 0.09909 | 2.372 | 0 | 0.666 |
35 | DNM3OS |
hsa-let-7d-5p;hsa-let-7g-5p;hsa-miR-185-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-28-5p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-3p | 10 | ITGB3 | Sponge network | -1.197 | 0.01767 | -1.502 | 0 | 0.662 |
36 | RP11-166D19.1 |
hsa-miR-141-5p;hsa-miR-186-5p;hsa-miR-200a-5p;hsa-miR-200b-3p;hsa-miR-200b-5p;hsa-miR-200c-3p;hsa-miR-429;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-7-1-3p | 11 | ITGA1 | Sponge network | -1.481 | 0.00084 | -1.977 | 0 | 0.661 |
37 | LINC00702 |
hsa-miR-103a-2-5p;hsa-miR-141-5p;hsa-miR-200b-3p;hsa-miR-20a-3p;hsa-miR-33a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-421;hsa-miR-452-3p;hsa-miR-501-5p;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-877-5p | 16 | ITGA9 | Sponge network | -3.658 | 0 | -2.846 | 0 | 0.661 |
38 | DNM3OS |
hsa-miR-141-5p;hsa-miR-186-5p;hsa-miR-200a-5p;hsa-miR-200b-3p;hsa-miR-200b-5p;hsa-miR-200c-3p;hsa-miR-374b-5p;hsa-miR-429;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-7-1-3p | 12 | ITGA1 | Sponge network | -1.197 | 0.01767 | -1.977 | 0 | 0.66 |
39 | TBX5-AS1 |
hsa-miR-1271-5p;hsa-miR-141-3p;hsa-miR-182-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-200a-3p;hsa-miR-3127-5p;hsa-miR-378a-3p;hsa-miR-532-3p;hsa-miR-616-5p;hsa-miR-92a-3p;hsa-miR-939-5p | 13 | GNG7 | Sponge network | -2.901 | 0 | -2.411 | 0 | 0.659 |
40 | RP11-314B1.2 |
hsa-miR-106b-5p;hsa-miR-17-5p;hsa-miR-200c-3p;hsa-miR-33a-3p;hsa-miR-3607-3p;hsa-miR-501-3p;hsa-miR-539-5p;hsa-miR-590-3p;hsa-miR-93-3p;hsa-miR-93-5p | 10 | COL4A3 | Sponge network | -3.756 | 0.0001 | -5.064 | 0 | 0.658 |
41 | LINC00702 |
hsa-let-7g-5p;hsa-miR-1271-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-26b-5p;hsa-miR-27b-3p;hsa-miR-320b;hsa-miR-33a-3p;hsa-miR-590-3p;hsa-miR-96-5p | 10 | FN1 | Sponge network | -3.658 | 0 | -1.199 | 1.0E-5 | 0.658 |
42 | LINC00968 |
hsa-miR-141-5p;hsa-miR-200b-3p;hsa-miR-20a-3p;hsa-miR-33a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-421;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p | 10 | ITGA9 | Sponge network | -4.827 | 0 | -2.846 | 0 | 0.657 |
43 | RP11-284N8.3 |
hsa-let-7a-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-18a-3p;hsa-miR-27a-3p;hsa-miR-320b;hsa-miR-33a-3p;hsa-miR-452-5p;hsa-miR-455-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-7-1-3p | 13 | FGF7 | Sponge network | -2.956 | 0 | -2.211 | 0 | 0.652 |
44 | AC011899.9 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-423-5p;hsa-miR-424-5p;hsa-miR-455-3p;hsa-miR-629-3p;hsa-miR-708-5p;hsa-miR-939-5p | 16 | CSF1 | Sponge network | -3.545 | 0 | -1.722 | 0 | 0.652 |
45 | MIR497HG |
hsa-let-7a-3p;hsa-let-7d-5p;hsa-miR-151a-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19b-3p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-33a-3p;hsa-miR-450b-5p;hsa-miR-590-5p;hsa-miR-629-3p;hsa-miR-7-1-3p;hsa-miR-940 | 15 | THBS1 | Sponge network | -3.004 | 0 | -1.792 | 0 | 0.649 |
46 | RP11-1024P17.1 |
hsa-let-7d-5p;hsa-miR-151a-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-629-3p | 11 | THBS1 | Sponge network | -3.322 | 0 | -1.792 | 0 | 0.645 |
47 | DNM3OS |
hsa-let-7d-5p;hsa-miR-151a-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-18a-5p;hsa-miR-19b-3p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-33a-3p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-629-3p;hsa-miR-7-1-3p | 17 | THBS1 | Sponge network | -1.197 | 0.01767 | -1.792 | 0 | 0.642 |
48 | LINC00702 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-103a-2-5p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-1-5p;hsa-miR-19b-3p;hsa-miR-20a-3p;hsa-miR-26b-5p;hsa-miR-28-3p;hsa-miR-301a-3p;hsa-miR-320b;hsa-miR-33a-3p;hsa-miR-362-5p;hsa-miR-421;hsa-miR-450b-5p;hsa-miR-454-3p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-629-5p;hsa-miR-940 | 23 | IGF1 | Sponge network | -3.658 | 0 | -1.378 | 1.0E-5 | 0.642 |
49 | MIR497HG |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-186-5p;hsa-miR-19b-3p;hsa-miR-20a-3p;hsa-miR-26b-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-33a-3p;hsa-miR-450b-5p;hsa-miR-940 | 13 | IGF1 | Sponge network | -3.004 | 0 | -1.378 | 1.0E-5 | 0.64 |
50 | LINC00702 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-197-3p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-424-5p;hsa-miR-454-3p;hsa-miR-455-3p;hsa-miR-505-3p;hsa-miR-532-3p;hsa-miR-629-3p;hsa-miR-708-5p;hsa-miR-93-5p;hsa-miR-939-5p;hsa-miR-940;hsa-miR-96-5p | 22 | CSF1 | Sponge network | -3.658 | 0 | -1.722 | 0 | 0.638 |
51 | LINC00968 |
hsa-miR-1271-5p;hsa-miR-141-3p;hsa-miR-182-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-200a-3p;hsa-miR-532-3p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-671-5p;hsa-miR-96-5p | 12 | GNG7 | Sponge network | -4.827 | 0 | -2.411 | 0 | 0.638 |
52 | AC109642.1 |
hsa-miR-1271-5p;hsa-miR-141-3p;hsa-miR-182-5p;hsa-miR-18a-3p;hsa-miR-193b-5p;hsa-miR-378a-3p;hsa-miR-532-3p;hsa-miR-590-3p;hsa-miR-92a-3p;hsa-miR-940;hsa-miR-96-5p | 11 | GNG7 | Sponge network | -3.573 | 0 | -2.411 | 0 | 0.637 |
53 | RP11-166D19.1 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-1-5p;hsa-miR-19b-3p;hsa-miR-20a-3p;hsa-miR-301a-3p;hsa-miR-450b-5p;hsa-miR-454-3p;hsa-miR-576-5p;hsa-miR-590-3p | 14 | IGF1 | Sponge network | -1.481 | 0.00084 | -1.378 | 1.0E-5 | 0.637 |
54 | TBX5-AS1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-197-3p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-532-3p;hsa-miR-629-3p;hsa-miR-939-5p | 14 | CSF1 | Sponge network | -2.901 | 0 | -1.722 | 0 | 0.636 |
55 | RP11-672A2.4 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-196b-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-339-5p | 11 | PDGFRA | Sponge network | -3.514 | 0 | -1.139 | 0 | 0.636 |
56 | LINC00968 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-186-5p;hsa-miR-19b-1-5p;hsa-miR-19b-3p;hsa-miR-20a-3p;hsa-miR-27a-3p;hsa-miR-28-3p;hsa-miR-301a-3p;hsa-miR-320b;hsa-miR-33a-3p;hsa-miR-421;hsa-miR-450b-5p;hsa-miR-590-3p | 16 | IGF1 | Sponge network | -4.827 | 0 | -1.378 | 1.0E-5 | 0.633 |
57 | RP11-284N8.3 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-19b-1-5p;hsa-miR-20a-3p;hsa-miR-27a-3p;hsa-miR-28-3p;hsa-miR-301a-3p;hsa-miR-320b;hsa-miR-33a-3p;hsa-miR-450b-5p;hsa-miR-452-5p;hsa-miR-590-3p;hsa-miR-940 | 15 | IGF1 | Sponge network | -2.956 | 0 | -1.378 | 1.0E-5 | 0.631 |
58 | MIR497HG |
hsa-let-7a-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-24-3p;hsa-miR-26b-5p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-339-5p;hsa-miR-450b-5p;hsa-miR-590-5p;hsa-miR-7-1-3p;hsa-miR-93-5p;hsa-miR-96-5p | 19 | PDGFRA | Sponge network | -3.004 | 0 | -1.139 | 0 | 0.628 |
59 | RP11-1024P17.1 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-424-5p;hsa-miR-629-3p | 11 | CSF1 | Sponge network | -3.322 | 0 | -1.722 | 0 | 0.627 |
60 | RP11-166D19.1 |
hsa-let-7a-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-27b-3p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-7-1-3p | 10 | FGF7 | Sponge network | -1.481 | 0.00084 | -2.211 | 0 | 0.627 |
61 | LINC00968 |
hsa-let-7a-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-196b-5p;hsa-miR-200a-3p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-320b;hsa-miR-339-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-421;hsa-miR-450b-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-93-5p;hsa-miR-96-5p | 24 | PDGFRA | Sponge network | -4.827 | 0 | -1.139 | 0 | 0.624 |
62 | MAGI2-AS3 |
hsa-miR-128-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-421;hsa-miR-424-5p;hsa-miR-429;hsa-miR-589-3p;hsa-miR-590-3p | 12 | RELN | Sponge network | -2.588 | 0 | -2.872 | 0 | 0.62 |
63 | DNM3OS |
hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-18a-3p;hsa-miR-27b-3p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-501-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-7-1-3p | 14 | FGF7 | Sponge network | -1.197 | 0.01767 | -2.211 | 0 | 0.616 |
64 | RP11-166D19.1 |
hsa-let-7a-3p;hsa-let-7d-5p;hsa-miR-151a-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-32-5p;hsa-miR-450b-5p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-629-3p;hsa-miR-7-1-3p;hsa-miR-92a-3p | 18 | THBS1 | Sponge network | -1.481 | 0.00084 | -1.792 | 0 | 0.613 |
65 | PCED1B-AS1 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-505-3p;hsa-miR-93-5p | 11 | CSF1 | Sponge network | -1.44 | 0.00116 | -1.722 | 0 | 0.613 |
66 | LINC00968 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-197-3p;hsa-miR-23a-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-335-5p;hsa-miR-424-5p;hsa-miR-505-3p;hsa-miR-532-3p;hsa-miR-629-3p;hsa-miR-708-5p;hsa-miR-93-5p;hsa-miR-96-5p | 19 | CSF1 | Sponge network | -4.827 | 0 | -1.722 | 0 | 0.612 |
67 | LINC00968 |
hsa-miR-106b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-33a-3p;hsa-miR-501-3p;hsa-miR-590-3p;hsa-miR-625-5p;hsa-miR-93-3p;hsa-miR-93-5p | 12 | COL4A3 | Sponge network | -4.827 | 0 | -5.064 | 0 | 0.609 |
68 | AP001189.4 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-16-5p;hsa-miR-197-3p;hsa-miR-205-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-940 | 10 | CSF1 | Sponge network | -4.547 | 0 | -1.722 | 0 | 0.601 |
69 | MIR497HG |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-197-3p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-423-5p;hsa-miR-424-5p;hsa-miR-532-3p;hsa-miR-629-3p;hsa-miR-93-5p;hsa-miR-939-5p;hsa-miR-940;hsa-miR-96-5p | 19 | CSF1 | Sponge network | -3.004 | 0 | -1.722 | 0 | 0.6 |
70 | RP11-166D19.1 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-429;hsa-miR-454-3p;hsa-miR-505-3p;hsa-miR-532-3p;hsa-miR-629-3p | 12 | CSF1 | Sponge network | -1.481 | 0.00084 | -1.722 | 0 | 0.6 |
71 | MAGI2-AS3 |
hsa-miR-106b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-33a-3p;hsa-miR-3607-3p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-93-3p | 12 | COL4A3 | Sponge network | -2.588 | 0 | -5.064 | 0 | 0.599 |
72 | TBX5-AS1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-1301-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-188-5p;hsa-miR-200c-3p;hsa-miR-335-3p;hsa-miR-532-3p;hsa-miR-590-5p;hsa-miR-629-3p | 14 | PIK3R1 | Sponge network | -2.901 | 0 | -0.906 | 0 | 0.598 |
73 | LINC00968 |
hsa-let-7a-3p;hsa-let-7d-5p;hsa-miR-151a-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-18a-5p;hsa-miR-19b-3p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-33a-3p;hsa-miR-421;hsa-miR-450b-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-629-3p;hsa-miR-671-5p | 18 | THBS1 | Sponge network | -4.827 | 0 | -1.792 | 0 | 0.598 |
74 | MAGI2-AS3 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-197-3p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-423-5p;hsa-miR-424-5p;hsa-miR-429;hsa-miR-454-3p;hsa-miR-505-3p;hsa-miR-532-3p;hsa-miR-629-3p;hsa-miR-939-5p;hsa-miR-940 | 21 | CSF1 | Sponge network | -2.588 | 0 | -1.722 | 0 | 0.597 |
75 | RP11-401P9.4 |
hsa-miR-103a-2-5p;hsa-miR-141-5p;hsa-miR-200b-3p;hsa-miR-20a-3p;hsa-miR-33a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-421;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-877-5p | 11 | ITGA9 | Sponge network | -3.167 | 0 | -2.846 | 0 | 0.596 |
76 | LINC00702 |
hsa-miR-1271-5p;hsa-miR-141-3p;hsa-miR-182-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-200a-3p;hsa-miR-3127-5p;hsa-miR-378a-3p;hsa-miR-532-3p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-671-5p;hsa-miR-92a-3p;hsa-miR-939-5p;hsa-miR-940;hsa-miR-96-5p | 17 | GNG7 | Sponge network | -3.658 | 0 | -2.411 | 0 | 0.592 |
77 | RP11-284N8.3 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-197-3p;hsa-miR-27a-3p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-455-3p;hsa-miR-629-3p;hsa-miR-93-5p;hsa-miR-939-5p;hsa-miR-940;hsa-miR-96-5p | 16 | CSF1 | Sponge network | -2.956 | 0 | -1.722 | 0 | 0.589 |
78 | DNM3OS |
hsa-let-7f-1-3p;hsa-miR-130a-3p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-16-1-3p;hsa-miR-186-5p;hsa-miR-19b-1-5p;hsa-miR-19b-3p;hsa-miR-20a-3p;hsa-miR-28-3p;hsa-miR-301a-3p;hsa-miR-33a-3p;hsa-miR-362-5p;hsa-miR-454-3p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-629-5p | 17 | IGF1 | Sponge network | -1.197 | 0.01767 | -1.378 | 1.0E-5 | 0.586 |
79 | RP11-284N8.3 |
hsa-miR-128-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-200c-3p;hsa-miR-224-5p;hsa-miR-27a-3p;hsa-miR-331-5p;hsa-miR-452-5p;hsa-miR-455-3p;hsa-miR-590-3p | 10 | RELN | Sponge network | -2.956 | 0 | -2.872 | 0 | 0.585 |
80 | RP11-536K7.3 |
hsa-let-7a-3p;hsa-miR-151a-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19b-3p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-629-3p;hsa-miR-940 | 12 | THBS1 | Sponge network | -2.193 | 0.00149 | -1.792 | 0 | 0.584 |
81 | DLX6-AS1 |
hsa-miR-126-5p;hsa-miR-146b-5p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-181c-5p;hsa-miR-30a-3p;hsa-miR-30a-5p;hsa-miR-30d-5p;hsa-miR-326;hsa-miR-338-3p | 10 | NTRK2 | Sponge network | 6.401 | 0 | 2.257 | 2.0E-5 | 0.582 |
82 | AC109642.1 |
hsa-let-7d-5p;hsa-miR-151a-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-590-3p;hsa-miR-92a-3p;hsa-miR-940;hsa-miR-98-5p | 11 | THBS1 | Sponge network | -3.573 | 0 | -1.792 | 0 | 0.582 |
83 | TBX5-AS1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-335-3p;hsa-miR-7-1-3p;hsa-miR-93-3p | 10 | COL4A3 | Sponge network | -2.901 | 0 | -5.064 | 0 | 0.58 |
84 | MIR205HG |
hsa-miR-107;hsa-miR-126-5p;hsa-miR-139-5p;hsa-miR-15a-5p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-181c-5p;hsa-miR-181d-5p;hsa-miR-30a-5p;hsa-miR-326;hsa-miR-532-5p | 11 | ITGA2 | Sponge network | 9.708 | 0 | 1.327 | 0 | 0.576 |
85 | RP11-701P16.5 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-205-5p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-424-5p;hsa-miR-505-3p;hsa-miR-532-3p;hsa-miR-629-3p;hsa-miR-708-5p;hsa-miR-93-5p;hsa-miR-939-5p | 17 | CSF1 | Sponge network | -5.254 | 0 | -1.722 | 0 | 0.566 |
86 | AC109642.1 |
hsa-let-7f-1-3p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-186-5p;hsa-miR-20a-3p;hsa-miR-27a-3p;hsa-miR-28-3p;hsa-miR-301a-3p;hsa-miR-320b;hsa-miR-590-3p;hsa-miR-629-5p;hsa-miR-940 | 12 | IGF1 | Sponge network | -3.573 | 0 | -1.378 | 1.0E-5 | 0.565 |
87 | AC011899.9 |
hsa-miR-151a-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19b-3p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-590-3p;hsa-miR-629-3p;hsa-miR-7-1-3p | 10 | THBS1 | Sponge network | -3.545 | 0 | -1.792 | 0 | 0.564 |
88 | MAGI2-AS3 |
hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-182-5p;hsa-miR-301a-3p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-454-3p;hsa-miR-532-3p;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-616-3p;hsa-miR-629-3p | 13 | COL4A4 | Sponge network | -2.588 | 0 | -3.737 | 0 | 0.564 |
89 | RP11-284N8.3 |
hsa-miR-106b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-200c-3p;hsa-miR-335-3p;hsa-miR-33a-3p;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-93-3p;hsa-miR-93-5p | 11 | COL4A3 | Sponge network | -2.956 | 0 | -5.064 | 0 | 0.556 |
90 | AC109642.1 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-320b;hsa-miR-429;hsa-miR-550a-5p;hsa-miR-590-3p;hsa-miR-96-5p | 15 | PDGFRA | Sponge network | -3.573 | 0 | -1.139 | 0 | 0.554 |
91 | RP11-284N8.3 |
hsa-let-7a-3p;hsa-let-7d-5p;hsa-miR-151a-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-335-3p;hsa-miR-33a-3p;hsa-miR-450b-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-629-3p;hsa-miR-7-1-3p;hsa-miR-940 | 15 | THBS1 | Sponge network | -2.956 | 0 | -1.792 | 0 | 0.552 |
92 | ZNF582-AS1 |
hsa-let-7a-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-33a-3p;hsa-miR-424-5p;hsa-miR-452-5p;hsa-miR-590-5p;hsa-miR-7-1-3p | 11 | FGF7 | Sponge network | -1.976 | 4.0E-5 | -2.211 | 0 | 0.549 |
93 | MAGI2-AS3 |
hsa-let-7f-1-3p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-193b-3p;hsa-miR-222-3p;hsa-miR-301a-3p;hsa-miR-421;hsa-miR-429;hsa-miR-450b-5p;hsa-miR-454-3p;hsa-miR-590-3p;hsa-miR-671-5p | 12 | KIT | Sponge network | -2.588 | 0 | -2.514 | 0 | 0.543 |
94 | CTB-61M7.2 |
hsa-let-7a-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-182-5p;hsa-miR-24-3p;hsa-miR-27b-3p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-421;hsa-miR-7-1-3p;hsa-miR-96-5p | 14 | PDGFRA | Sponge network | -2.95 | 0.0014 | -1.139 | 0 | 0.541 |
95 | AC011899.9 |
hsa-miR-128-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-424-5p;hsa-miR-455-3p;hsa-miR-590-3p | 10 | RELN | Sponge network | -3.545 | 0 | -2.872 | 0 | 0.54 |
96 | AC005537.2 |
hsa-miR-139-5p;hsa-miR-143-3p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-181c-5p;hsa-miR-1976;hsa-miR-26a-5p;hsa-miR-326;hsa-miR-338-3p;hsa-miR-532-5p | 10 | ITGB8 | Sponge network | 8.008 | 0 | 2.27 | 0 | 0.537 |
97 | DNM3OS |
hsa-miR-16-1-3p;hsa-miR-186-5p;hsa-miR-18a-5p;hsa-miR-26b-3p;hsa-miR-28-5p;hsa-miR-429;hsa-miR-484;hsa-miR-532-3p;hsa-miR-550a-5p;hsa-miR-576-5p;hsa-miR-590-5p;hsa-miR-629-5p | 12 | FGF1 | Sponge network | -1.197 | 0.01767 | -0.804 | 0.00096 | 0.536 |
98 | TBX5-AS1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-24-3p;hsa-miR-28-5p;hsa-miR-335-3p;hsa-miR-378a-3p;hsa-miR-421;hsa-miR-505-5p;hsa-miR-576-5p;hsa-miR-616-5p;hsa-miR-629-3p;hsa-miR-744-3p;hsa-miR-877-5p | 18 | FLT1 | Sponge network | -2.901 | 0 | -1.262 | 0 | 0.536 |
99 | RP11-426C22.4 |
hsa-miR-130a-3p;hsa-miR-141-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-26b-5p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-362-3p;hsa-miR-374a-5p;hsa-miR-374b-5p | 11 | PDGFRA | Sponge network | 0.742 | 0.14065 | -1.139 | 0 | 0.536 |
100 | RP11-286H14.8 | hsa-miR-139-5p;hsa-miR-140-3p;hsa-miR-140-5p;hsa-miR-146b-5p;hsa-miR-16-1-3p;hsa-miR-223-3p;hsa-miR-29a-3p;hsa-miR-29b-2-5p;hsa-miR-29b-3p;hsa-miR-484 | 10 | IGF1R | Sponge network | 6.519 | 0 | 0.983 | 0 | 0.534 |
101 | RP11-401P9.4 |
hsa-miR-103a-2-5p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-16-1-3p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-1-5p;hsa-miR-19b-3p;hsa-miR-20a-3p;hsa-miR-301a-3p;hsa-miR-33a-3p;hsa-miR-421;hsa-miR-454-3p | 13 | IGF1 | Sponge network | -3.167 | 0 | -1.378 | 1.0E-5 | 0.532 |
102 | RP11-1024P17.1 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-3p | 14 | PDGFRA | Sponge network | -3.322 | 0 | -1.139 | 0 | 0.532 |
103 | RP11-325F22.2 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-96-5p | 11 | CSF1 | Sponge network | -1.941 | 0.00827 | -1.722 | 0 | 0.529 |
104 | MAGI2-AS3 |
hsa-miR-16-2-3p;hsa-miR-183-5p;hsa-miR-186-5p;hsa-miR-192-5p;hsa-miR-3607-3p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-7-1-3p;hsa-miR-769-5p | 10 | ITGB1 | Sponge network | -2.588 | 0 | -0.329 | 0.00358 | 0.528 |
105 | FENDRR |
hsa-miR-106b-5p;hsa-miR-149-5p;hsa-miR-186-5p;hsa-miR-200c-3p;hsa-miR-421;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-629-3p;hsa-miR-708-5p;hsa-miR-744-3p | 11 | FLT1 | Sponge network | -4.656 | 0 | -1.262 | 0 | 0.527 |
106 | RP11-536K7.3 |
hsa-let-7a-3p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-339-5p;hsa-miR-33a-5p;hsa-miR-454-3p;hsa-miR-590-3p;hsa-miR-616-5p | 16 | PDGFRA | Sponge network | -2.193 | 0.00149 | -1.139 | 0 | 0.525 |
107 | DNM3OS |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130a-3p;hsa-miR-130b-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-27b-3p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-429;hsa-miR-454-3p;hsa-miR-532-3p;hsa-miR-629-3p;hsa-miR-93-5p;hsa-miR-96-5p | 17 | CSF1 | Sponge network | -1.197 | 0.01767 | -1.722 | 0 | 0.523 |
108 | RP11-536K7.3 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-23a-5p;hsa-miR-27a-3p;hsa-miR-454-3p;hsa-miR-532-3p;hsa-miR-629-3p;hsa-miR-940 | 14 | CSF1 | Sponge network | -2.193 | 0.00149 | -1.722 | 0 | 0.522 |
109 | APCDD1L-AS1 |
hsa-let-7d-5p;hsa-miR-106a-5p;hsa-miR-107;hsa-miR-126-5p;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-218-5p;hsa-miR-29b-3p;hsa-miR-29c-3p;hsa-miR-30b-3p;hsa-miR-338-3p;hsa-miR-532-3p | 12 | COL1A1 | Sponge network | 2.007 | 0.01217 | 2.372 | 0 | 0.522 |
110 | LINC00702 |
hsa-miR-148b-3p;hsa-miR-183-5p;hsa-miR-25-3p;hsa-miR-26b-5p;hsa-miR-27b-3p;hsa-miR-32-5p;hsa-miR-484;hsa-miR-629-3p;hsa-miR-760;hsa-miR-92a-3p;hsa-miR-92b-3p | 11 | ITGA5 | Sponge network | -3.658 | 0 | -0.575 | 0.00104 | 0.522 |
111 | RP11-1024P17.1 |
hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-200c-3p;hsa-miR-20a-3p;hsa-miR-222-3p;hsa-miR-424-5p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-93-3p | 12 | FGF2 | Sponge network | -3.322 | 0 | -1.904 | 0 | 0.521 |
112 | AC109642.1 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-197-3p;hsa-miR-23a-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-424-5p;hsa-miR-429;hsa-miR-532-3p;hsa-miR-940;hsa-miR-96-5p | 16 | CSF1 | Sponge network | -3.573 | 0 | -1.722 | 0 | 0.521 |
113 | RP11-536K7.3 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-130b-3p;hsa-miR-186-5p;hsa-miR-19b-1-5p;hsa-miR-19b-3p;hsa-miR-20a-3p;hsa-miR-27a-3p;hsa-miR-28-3p;hsa-miR-454-3p;hsa-miR-590-3p;hsa-miR-940 | 12 | IGF1 | Sponge network | -2.193 | 0.00149 | -1.378 | 1.0E-5 | 0.52 |
114 | TBX5-AS1 |
hsa-let-7d-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-1271-5p;hsa-miR-128-3p;hsa-miR-141-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-197-3p;hsa-miR-200a-3p;hsa-miR-24-3p;hsa-miR-25-3p;hsa-miR-32-5p;hsa-miR-616-5p;hsa-miR-7-1-3p;hsa-miR-92a-1-5p;hsa-miR-92a-3p;hsa-miR-92b-3p | 21 | CREB3L2 | Sponge network | -2.901 | 0 | -0.289 | 0.01425 | 0.52 |
115 | MAGI2-AS3 |
hsa-let-7g-3p;hsa-miR-106b-5p;hsa-miR-148b-5p;hsa-miR-151a-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-193b-3p;hsa-miR-589-3p;hsa-miR-940;hsa-miR-942-5p | 11 | MCL1 | Sponge network | -2.588 | 0 | -0.943 | 0 | 0.519 |
116 | PCED1B-AS1 |
hsa-let-7a-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-93-5p | 11 | PDGFRA | Sponge network | -1.44 | 0.00116 | -1.139 | 0 | 0.519 |
117 | DNM3OS |
hsa-miR-141-5p;hsa-miR-200b-3p;hsa-miR-20a-3p;hsa-miR-33a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-429;hsa-miR-501-5p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p | 12 | ITGA9 | Sponge network | -1.197 | 0.01767 | -2.846 | 0 | 0.519 |
118 | FENDRR |
hsa-let-7g-3p;hsa-miR-103a-2-5p;hsa-miR-106b-5p;hsa-miR-127-5p;hsa-miR-148b-5p;hsa-miR-151a-3p;hsa-miR-186-5p;hsa-miR-193b-3p;hsa-miR-455-3p;hsa-miR-940 | 10 | MCL1 | Sponge network | -4.656 | 0 | -0.943 | 0 | 0.518 |
119 | RP11-401P9.4 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-149-5p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-200a-3p;hsa-miR-301a-3p;hsa-miR-339-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-421;hsa-miR-454-3p;hsa-miR-550a-5p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-93-5p | 20 | PDGFRA | Sponge network | -3.167 | 0 | -1.139 | 0 | 0.517 |
120 | LINC00968 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-1301-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-188-5p;hsa-miR-200c-3p;hsa-miR-532-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-629-3p;hsa-miR-93-5p;hsa-miR-96-5p | 15 | PIK3R1 | Sponge network | -4.827 | 0 | -0.906 | 0 | 0.516 |
121 | RP11-401P9.4 |
hsa-let-7d-5p;hsa-miR-151a-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-18a-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-33a-3p;hsa-miR-421;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-98-5p | 16 | THBS1 | Sponge network | -3.167 | 0 | -1.792 | 0 | 0.515 |
122 | RP11-815M8.1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-24-3p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-320b | 10 | PDGFRA | Sponge network | -1.16 | 0.16327 | -1.139 | 0 | 0.515 |
123 | LINC00702 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-335-3p;hsa-miR-33a-3p;hsa-miR-501-3p;hsa-miR-590-3p;hsa-miR-625-5p;hsa-miR-7-1-3p;hsa-miR-93-3p;hsa-miR-93-5p | 15 | COL4A3 | Sponge network | -3.658 | 0 | -5.064 | 0 | 0.513 |
124 | MIR497HG |
hsa-miR-106b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-33a-3p;hsa-miR-7-1-3p;hsa-miR-93-3p;hsa-miR-93-5p | 10 | COL4A3 | Sponge network | -3.004 | 0 | -5.064 | 0 | 0.513 |
125 | MAGI2-AS3 |
hsa-let-7a-3p;hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-19b-1-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-3p;hsa-miR-222-3p;hsa-miR-424-5p;hsa-miR-429;hsa-miR-450b-5p;hsa-miR-503-5p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-92a-3p;hsa-miR-93-3p | 19 | FGF2 | Sponge network | -2.588 | 0 | -1.904 | 0 | 0.512 |
126 | RP1-78O14.1 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-197-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-532-3p;hsa-miR-629-3p | 12 | CSF1 | Sponge network | -4.002 | 0 | -1.722 | 0 | 0.511 |
127 | LINC00261 |
hsa-miR-141-5p;hsa-miR-20a-3p;hsa-miR-324-5p;hsa-miR-33a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-452-3p;hsa-miR-452-5p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-877-5p | 11 | ITGA9 | Sponge network | -5.643 | 0 | -2.846 | 0 | 0.51 |
128 | LINC00968 |
hsa-let-7g-3p;hsa-miR-106b-5p;hsa-miR-148b-5p;hsa-miR-151a-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-193b-3p;hsa-miR-320b;hsa-miR-93-5p;hsa-miR-942-5p | 11 | MCL1 | Sponge network | -4.827 | 0 | -0.943 | 0 | 0.51 |
129 | MAGI2-AS3 |
hsa-miR-106b-5p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-24-3p;hsa-miR-28-5p;hsa-miR-339-5p;hsa-miR-378a-3p;hsa-miR-421;hsa-miR-429;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-629-3p | 16 | FLT1 | Sponge network | -2.588 | 0 | -1.262 | 0 | 0.506 |
130 | LINC00702 |
hsa-let-7d-5p;hsa-let-7g-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-25-3p;hsa-miR-26b-5p;hsa-miR-32-5p;hsa-miR-33a-3p;hsa-miR-3934-5p;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-7-5p;hsa-miR-92a-3p | 13 | COL1A2 | Sponge network | -3.658 | 0 | 0.891 | 0.00084 | 0.506 |
131 | RP11-284N8.3 |
hsa-let-7a-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-320b;hsa-miR-335-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-450b-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-7-1-3p;hsa-miR-93-5p;hsa-miR-96-5p | 21 | PDGFRA | Sponge network | -2.956 | 0 | -1.139 | 0 | 0.505 |
132 | AC079630.4 |
hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-18a-3p;hsa-miR-320b;hsa-miR-33a-3p;hsa-miR-421;hsa-miR-424-5p;hsa-miR-616-5p;hsa-miR-7-1-3p | 10 | FGF7 | Sponge network | -4.77 | 0 | -2.211 | 0 | 0.504 |
133 | PWAR6 |
hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-19b-1-5p;hsa-miR-200c-3p;hsa-miR-21-3p;hsa-miR-222-3p;hsa-miR-450b-5p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-93-3p | 11 | FGF2 | Sponge network | -1.994 | 6.0E-5 | -1.904 | 0 | 0.502 |
134 | RP11-284N8.3 |
hsa-miR-141-5p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-200c-3p;hsa-miR-320b;hsa-miR-335-3p;hsa-miR-452-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-7-1-3p | 10 | ITGA1 | Sponge network | -2.956 | 0 | -1.977 | 0 | 0.501 |
135 | AP001189.4 |
hsa-miR-103a-2-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-5p;hsa-miR-182-5p;hsa-miR-193b-3p;hsa-miR-197-3p;hsa-miR-205-5p;hsa-miR-301a-3p;hsa-miR-331-3p;hsa-miR-3928-3p | 11 | IL6R | Sponge network | -4.547 | 0 | -1.861 | 0 | 0.501 |
136 | RP11-284N8.3 |
hsa-let-7a-3p;hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-19b-1-5p;hsa-miR-200c-3p;hsa-miR-20a-3p;hsa-miR-222-3p;hsa-miR-450b-5p;hsa-miR-452-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-93-3p | 14 | FGF2 | Sponge network | -2.956 | 0 | -1.904 | 0 | 0.5 |
137 | RP3-340N1.2 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-23a-5p;hsa-miR-27b-3p;hsa-miR-28-5p;hsa-miR-532-3p;hsa-miR-708-5p;hsa-miR-96-5p | 12 | CSF1 | Sponge network | -0.386 | 0.73912 | -1.722 | 0 | 0.498 |
138 | LINC00702 |
hsa-miR-106b-5p;hsa-miR-182-5p;hsa-miR-25-3p;hsa-miR-421;hsa-miR-501-5p;hsa-miR-590-3p;hsa-miR-629-3p;hsa-miR-92a-3p;hsa-miR-92b-3p;hsa-miR-940 | 10 | PIK3AP1 | Sponge network | -3.658 | 0 | -1.585 | 0 | 0.497 |
139 | DNM3OS |
hsa-miR-1271-5p;hsa-miR-141-3p;hsa-miR-182-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-200a-3p;hsa-miR-378a-3p;hsa-miR-532-3p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-96-5p | 11 | GNG7 | Sponge network | -1.197 | 0.01767 | -2.411 | 0 | 0.495 |
140 | LINC00968 |
hsa-let-7f-1-3p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-193b-3p;hsa-miR-19b-3p;hsa-miR-222-3p;hsa-miR-301a-3p;hsa-miR-421;hsa-miR-450b-5p;hsa-miR-590-3p;hsa-miR-671-5p | 11 | KIT | Sponge network | -4.827 | 0 | -2.514 | 0 | 0.494 |
141 | RP11-284N8.3 |
hsa-let-7g-3p;hsa-miR-106b-5p;hsa-miR-148b-5p;hsa-miR-151a-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-193b-3p;hsa-miR-320b;hsa-miR-335-3p;hsa-miR-455-3p;hsa-miR-93-5p;hsa-miR-940;hsa-miR-942-5p | 13 | MCL1 | Sponge network | -2.956 | 0 | -0.943 | 0 | 0.494 |
142 | AC004540.5 | hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-424-5p;hsa-miR-455-3p;hsa-miR-629-3p | 10 | CSF1 | Sponge network | -2.51 | 0 | -1.722 | 0 | 0.493 |
143 | CTD-2008L17.2 |
hsa-miR-139-5p;hsa-miR-140-3p;hsa-miR-146b-5p;hsa-miR-29a-3p;hsa-miR-29b-3p;hsa-miR-30b-5p;hsa-miR-30d-5p;hsa-miR-34a-5p;hsa-miR-362-3p;hsa-miR-532-5p | 10 | IGF1R | Sponge network | 4.931 | 0.00018 | 0.983 | 0 | 0.49 |
144 | AC109642.1 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-1301-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-188-5p;hsa-miR-200c-3p;hsa-miR-532-3p;hsa-miR-590-3p;hsa-miR-96-5p | 12 | PIK3R1 | Sponge network | -3.573 | 0 | -0.906 | 0 | 0.49 |
145 | TBX5-AS1 |
hsa-let-7g-3p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-148b-5p;hsa-miR-151a-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-193b-3p;hsa-miR-335-3p;hsa-miR-942-5p | 11 | MCL1 | Sponge network | -2.901 | 0 | -0.943 | 0 | 0.49 |
146 | AC109642.1 |
hsa-let-7d-5p;hsa-let-7g-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-222-3p;hsa-miR-320b;hsa-miR-3607-3p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-98-5p | 10 | ITGB3 | Sponge network | -3.573 | 0 | -1.502 | 0 | 0.487 |
147 | LINC00941 |
hsa-miR-107;hsa-miR-126-5p;hsa-miR-130a-3p;hsa-miR-139-5p;hsa-miR-15a-5p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-181c-5p;hsa-miR-26a-5p;hsa-miR-362-3p;hsa-miR-497-5p;hsa-miR-532-5p | 12 | ITGA2 | Sponge network | 2.474 | 0.00018 | 1.327 | 0 | 0.481 |
148 | LINC00968 |
hsa-miR-106b-5p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-24-3p;hsa-miR-3200-3p;hsa-miR-339-5p;hsa-miR-421;hsa-miR-505-5p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-629-3p;hsa-miR-708-5p;hsa-miR-93-5p | 17 | FLT1 | Sponge network | -4.827 | 0 | -1.262 | 0 | 0.481 |
149 | FENDRR |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-301a-3p;hsa-miR-423-5p;hsa-miR-424-5p;hsa-miR-455-3p;hsa-miR-532-3p;hsa-miR-629-3p;hsa-miR-708-5p;hsa-miR-940 | 13 | CSF1 | Sponge network | -4.656 | 0 | -1.722 | 0 | 0.481 |
150 | DNM3OS |
hsa-miR-16-2-3p;hsa-miR-183-5p;hsa-miR-186-5p;hsa-miR-192-5p;hsa-miR-25-3p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-7-1-3p | 10 | ITGB1 | Sponge network | -1.197 | 0.01767 | -0.329 | 0.00358 | 0.48 |
151 | LINC00702 |
hsa-miR-16-2-3p;hsa-miR-183-5p;hsa-miR-186-5p;hsa-miR-192-5p;hsa-miR-25-3p;hsa-miR-374b-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-7-1-3p | 10 | ITGB1 | Sponge network | -3.658 | 0 | -0.329 | 0.00358 | 0.48 |
152 | RP11-389C8.2 | hsa-let-7a-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-24-3p;hsa-miR-27b-3p;hsa-miR-28-5p;hsa-miR-421;hsa-miR-550a-5p;hsa-miR-590-3p;hsa-miR-7-1-3p | 11 | PDGFRA | Sponge network | -2.574 | 0 | -1.139 | 0 | 0.479 |
153 | RP11-527N22.1 |
hsa-let-7a-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-18a-3p;hsa-miR-27a-3p;hsa-miR-3607-3p;hsa-miR-421;hsa-miR-424-5p;hsa-miR-455-3p;hsa-miR-7-1-3p | 11 | FGF7 | Sponge network | -2.999 | 0.02338 | -2.211 | 0 | 0.479 |
154 | AC011899.9 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-196b-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-339-5p;hsa-miR-33a-5p;hsa-miR-550a-5p;hsa-miR-590-3p;hsa-miR-7-1-3p | 17 | PDGFRA | Sponge network | -3.545 | 0 | -1.139 | 0 | 0.478 |
155 | CTD-2171N6.1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130a-3p;hsa-miR-141-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-200a-3p;hsa-miR-20a-5p;hsa-miR-24-3p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-3065-5p;hsa-miR-362-3p;hsa-miR-421;hsa-miR-454-3p;hsa-miR-550a-5p;hsa-miR-576-5p | 18 | PDGFRA | Sponge network | 1.382 | 0.09909 | -1.139 | 0 | 0.477 |
156 | TBX5-AS1 |
hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-19b-1-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-3p;hsa-miR-222-3p;hsa-miR-450b-5p;hsa-miR-590-5p;hsa-miR-92a-3p;hsa-miR-93-3p | 14 | FGF2 | Sponge network | -2.901 | 0 | -1.904 | 0 | 0.476 |
157 | AC011899.9 |
hsa-miR-106b-5p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-24-3p;hsa-miR-339-5p;hsa-miR-378a-3p;hsa-miR-505-5p;hsa-miR-590-3p;hsa-miR-629-3p;hsa-miR-708-5p | 14 | FLT1 | Sponge network | -3.545 | 0 | -1.262 | 0 | 0.476 |
158 | RP11-166D19.1 |
hsa-let-7a-3p;hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-19b-1-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-3p;hsa-miR-222-3p;hsa-miR-429;hsa-miR-450b-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-92a-3p;hsa-miR-93-3p | 17 | FGF2 | Sponge network | -1.481 | 0.00084 | -1.904 | 0 | 0.474 |
159 | RP11-476D10.1 |
hsa-let-7a-3p;hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-200c-3p;hsa-miR-20a-3p;hsa-miR-3682-3p;hsa-miR-539-5p;hsa-miR-589-3p;hsa-miR-590-3p | 10 | FGF2 | Sponge network | -5.75 | 0 | -1.904 | 0 | 0.473 |
160 | RP11-251M1.1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-424-5p;hsa-miR-629-3p | 11 | CSF1 | Sponge network | -4.934 | 0 | -1.722 | 0 | 0.472 |
161 | LINC00702 |
hsa-let-7g-3p;hsa-miR-103a-2-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-148b-5p;hsa-miR-151a-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-193b-3p;hsa-miR-320b;hsa-miR-335-3p;hsa-miR-455-3p;hsa-miR-589-3p;hsa-miR-760;hsa-miR-93-5p;hsa-miR-940;hsa-miR-942-5p | 18 | MCL1 | Sponge network | -3.658 | 0 | -0.943 | 0 | 0.471 |
162 | RP11-401P9.4 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-197-3p;hsa-miR-301a-3p;hsa-miR-454-3p;hsa-miR-532-3p;hsa-miR-708-5p;hsa-miR-93-5p;hsa-miR-939-5p | 15 | CSF1 | Sponge network | -3.167 | 0 | -1.722 | 0 | 0.471 |
163 | LINC00702 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-1301-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-188-5p;hsa-miR-200c-3p;hsa-miR-335-3p;hsa-miR-532-3p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-629-3p;hsa-miR-93-5p;hsa-miR-96-5p | 18 | PIK3R1 | Sponge network | -3.658 | 0 | -0.906 | 0 | 0.47 |
164 | LINC00968 |
hsa-let-7a-3p;hsa-miR-1226-3p;hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-19b-1-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-3p;hsa-miR-222-3p;hsa-miR-3682-3p;hsa-miR-424-5p;hsa-miR-450b-5p;hsa-miR-503-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-93-3p | 19 | FGF2 | Sponge network | -4.827 | 0 | -1.904 | 0 | 0.469 |
165 | MAGI2-AS3 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-1301-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-188-5p;hsa-miR-200c-3p;hsa-miR-532-3p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-629-3p | 13 | PIK3R1 | Sponge network | -2.588 | 0 | -0.906 | 0 | 0.468 |
166 | RP11-284N8.3 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-1301-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-200c-3p;hsa-miR-22-5p;hsa-miR-335-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-629-3p;hsa-miR-93-5p;hsa-miR-96-5p | 15 | PIK3R1 | Sponge network | -2.956 | 0 | -0.906 | 0 | 0.468 |
167 | MIR497HG |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-141-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-192-5p;hsa-miR-197-3p;hsa-miR-301a-3p;hsa-miR-331-3p;hsa-miR-590-5p;hsa-miR-93-5p;hsa-miR-942-5p | 14 | IL6R | Sponge network | -3.004 | 0 | -1.861 | 0 | 0.467 |
168 | GAS6-AS2 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-197-3p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-424-5p;hsa-miR-940 | 10 | CSF1 | Sponge network | -1.656 | 0.00013 | -1.722 | 0 | 0.464 |
169 | LINC00473 |
hsa-let-7a-3p;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-3607-3p;hsa-miR-424-5p;hsa-miR-452-5p;hsa-miR-455-3p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-7-1-3p | 13 | FGF7 | Sponge network | -3.931 | 0.00573 | -2.211 | 0 | 0.462 |
170 | RP11-527N22.1 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-186-5p;hsa-miR-19b-1-5p;hsa-miR-19b-3p;hsa-miR-20a-3p;hsa-miR-26b-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-421;hsa-miR-576-5p | 14 | IGF1 | Sponge network | -2.999 | 0.02338 | -1.378 | 1.0E-5 | 0.461 |
171 | LINC00668 |
hsa-miR-139-5p;hsa-miR-146b-5p;hsa-miR-150-5p;hsa-miR-15a-5p;hsa-miR-16-1-3p;hsa-miR-223-3p;hsa-miR-29a-3p;hsa-miR-29b-2-5p;hsa-miR-29c-3p;hsa-miR-30a-5p;hsa-miR-30d-5p;hsa-miR-34a-5p;hsa-miR-362-3p;hsa-miR-497-5p;hsa-miR-532-5p | 15 | IGF1R | Sponge network | 6.883 | 0 | 0.983 | 0 | 0.461 |
172 | AC011738.4 |
hsa-miR-139-5p;hsa-miR-145-5p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-181c-5p;hsa-miR-1976;hsa-miR-26a-5p;hsa-miR-326;hsa-miR-338-3p;hsa-miR-532-5p | 10 | ITGB8 | Sponge network | 8.148 | 0 | 2.27 | 0 | 0.46 |
173 | RP11-401P9.4 |
hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-19b-1-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-3p;hsa-miR-222-3p;hsa-miR-590-5p;hsa-miR-93-3p | 12 | FGF2 | Sponge network | -3.167 | 0 | -1.904 | 0 | 0.456 |
174 | RP11-1008C21.1 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-197-3p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-629-3p;hsa-miR-940 | 11 | CSF1 | Sponge network | -2.048 | 0.00613 | -1.722 | 0 | 0.456 |
175 | RP11-77A13.1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-301a-3p;hsa-miR-424-5p;hsa-miR-454-3p;hsa-miR-93-5p;hsa-miR-96-5p | 12 | CSF1 | Sponge network | -9.091 | 0 | -1.722 | 0 | 0.454 |
176 | AC011899.9 |
hsa-miR-106b-5p;hsa-miR-1271-5p;hsa-miR-128-3p;hsa-miR-141-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-19b-3p;hsa-miR-24-3p;hsa-miR-25-3p;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-92a-1-5p | 14 | CREB3L2 | Sponge network | -3.545 | 0 | -0.289 | 0.01425 | 0.454 |
177 | RP11-150O12.1 |
hsa-let-7i-5p;hsa-miR-139-5p;hsa-miR-140-3p;hsa-miR-140-5p;hsa-miR-150-5p;hsa-miR-15a-5p;hsa-miR-29b-2-5p;hsa-miR-30a-5p;hsa-miR-30d-5p;hsa-miR-30e-5p;hsa-miR-342-5p;hsa-miR-362-3p;hsa-miR-532-5p | 13 | IGF1R | Sponge network | 4.23 | 1.0E-5 | 0.983 | 0 | 0.453 |
178 | RP11-1008C21.1 |
hsa-let-7d-5p;hsa-miR-106b-5p;hsa-miR-1271-5p;hsa-miR-128-3p;hsa-miR-141-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-197-3p;hsa-miR-19b-3p;hsa-miR-20a-5p;hsa-miR-24-3p;hsa-miR-25-3p | 14 | CREB3L2 | Sponge network | -2.048 | 0.00613 | -0.289 | 0.01425 | 0.453 |
179 | RP11-166D19.1 |
hsa-miR-106b-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-339-5p;hsa-miR-429;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-629-3p | 13 | FLT1 | Sponge network | -1.481 | 0.00084 | -1.262 | 0 | 0.452 |
180 | RP11-77A13.1 |
hsa-let-7g-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-423-3p;hsa-miR-503-5p;hsa-miR-93-5p;hsa-miR-96-5p;hsa-miR-98-5p | 10 | CDKN1A | Sponge network | -9.091 | 0 | -0.663 | 2.0E-5 | 0.45 |
181 | LINC00702 |
hsa-miR-128-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-27b-3p;hsa-miR-421;hsa-miR-424-5p;hsa-miR-455-3p;hsa-miR-589-3p;hsa-miR-590-3p | 11 | RELN | Sponge network | -3.658 | 0 | -2.872 | 0 | 0.449 |
182 | RP11-283G6.4 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-200a-3p;hsa-miR-20b-5p;hsa-miR-224-5p;hsa-miR-301a-3p;hsa-miR-450b-5p;hsa-miR-576-5p;hsa-miR-93-5p;hsa-miR-96-5p | 15 | PDGFRA | Sponge network | -1.912 | 0.08964 | -1.139 | 0 | 0.448 |
183 | SEMA3B |
hsa-miR-182-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-31-5p;hsa-miR-3127-5p;hsa-miR-3615;hsa-miR-532-3p;hsa-miR-590-3p;hsa-miR-939-5p | 10 | GNG7 | Sponge network | -3.358 | 0 | -2.411 | 0 | 0.448 |
184 | FENDRR |
hsa-miR-103a-2-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-141-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-193b-3p;hsa-miR-301a-3p;hsa-miR-331-3p;hsa-miR-33a-5p;hsa-miR-3928-3p;hsa-miR-421;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-98-5p | 16 | IL6R | Sponge network | -4.656 | 0 | -1.861 | 0 | 0.448 |
185 | LINC00702 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-24-3p;hsa-miR-335-3p;hsa-miR-339-5p;hsa-miR-378a-3p;hsa-miR-421;hsa-miR-501-5p;hsa-miR-505-5p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-629-3p;hsa-miR-708-5p;hsa-miR-744-3p;hsa-miR-877-5p;hsa-miR-93-5p | 24 | FLT1 | Sponge network | -3.658 | 0 | -1.262 | 0 | 0.448 |
186 | RP11-1024P17.1 |
hsa-let-7d-5p;hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-141-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-25-3p;hsa-miR-590-3p | 10 | CREB3L2 | Sponge network | -3.322 | 0 | -0.289 | 0.01425 | 0.446 |
187 | RP11-284N8.3 |
hsa-let-7d-5p;hsa-miR-106b-5p;hsa-miR-1271-5p;hsa-miR-128-3p;hsa-miR-141-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-18a-3p;hsa-miR-197-3p;hsa-miR-24-3p;hsa-miR-25-3p;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-92a-1-5p | 15 | CREB3L2 | Sponge network | -2.956 | 0 | -0.289 | 0.01425 | 0.446 |
188 | AC144831.1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-301a-3p;hsa-miR-450b-5p;hsa-miR-550a-5p;hsa-miR-576-5p;hsa-miR-7-1-3p;hsa-miR-93-5p | 13 | PDGFRA | Sponge network | -2 | 0.00032 | -1.139 | 0 | 0.446 |
189 | FENDRR |
hsa-let-7a-3p;hsa-miR-151a-3p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-421;hsa-miR-450b-5p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-629-3p;hsa-miR-671-5p;hsa-miR-7-1-3p;hsa-miR-940;hsa-miR-98-5p | 16 | THBS1 | Sponge network | -4.656 | 0 | -1.792 | 0 | 0.446 |
190 | RP11-150O12.1 |
hsa-miR-107;hsa-miR-126-5p;hsa-miR-139-5p;hsa-miR-142-3p;hsa-miR-15a-5p;hsa-miR-18a-5p;hsa-miR-30a-5p;hsa-miR-30d-5p;hsa-miR-30e-5p;hsa-miR-326;hsa-miR-3607-3p;hsa-miR-362-3p;hsa-miR-532-5p | 13 | ITGA2 | Sponge network | 4.23 | 1.0E-5 | 1.327 | 0 | 0.445 |
191 | CALML3-AS1 | hsa-miR-107;hsa-miR-139-5p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-181c-5p;hsa-miR-195-5p;hsa-miR-26a-5p;hsa-miR-362-3p;hsa-miR-532-5p;hsa-miR-582-5p | 10 | ITGA2 | Sponge network | 4.723 | 3.0E-5 | 1.327 | 0 | 0.444 |
192 | AC144831.1 |
hsa-let-7d-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-1271-5p;hsa-miR-141-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-18a-3p;hsa-miR-19b-3p;hsa-miR-25-3p;hsa-miR-7-1-3p | 12 | CREB3L2 | Sponge network | -2 | 0.00032 | -0.289 | 0.01425 | 0.444 |
193 | RP11-815M8.1 |
hsa-let-7d-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-197-3p;hsa-miR-24-3p;hsa-miR-25-3p | 10 | CREB3L2 | Sponge network | -1.16 | 0.16327 | -0.289 | 0.01425 | 0.444 |
194 | RP11-166D19.1 |
hsa-let-7d-5p;hsa-miR-106b-5p;hsa-miR-1271-5p;hsa-miR-141-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19b-3p;hsa-miR-200a-3p;hsa-miR-32-5p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-7-1-3p;hsa-miR-92a-3p | 16 | CREB3L2 | Sponge network | -1.481 | 0.00084 | -0.289 | 0.01425 | 0.443 |
195 | FENDRR |
hsa-miR-1271-5p;hsa-miR-141-3p;hsa-miR-182-5p;hsa-miR-18a-3p;hsa-miR-193b-5p;hsa-miR-3127-5p;hsa-miR-532-3p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-671-5p;hsa-miR-940 | 11 | GNG7 | Sponge network | -4.656 | 0 | -2.411 | 0 | 0.443 |
196 | RP11-776H12.1 |
hsa-miR-139-5p;hsa-miR-143-3p;hsa-miR-145-5p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-181c-5p;hsa-miR-1976;hsa-miR-26a-5p;hsa-miR-326;hsa-miR-338-3p | 10 | ITGB8 | Sponge network | 7.826 | 0 | 2.27 | 0 | 0.441 |
197 | AC144831.1 |
hsa-let-7d-5p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-450b-5p;hsa-miR-576-5p;hsa-miR-7-1-3p | 11 | THBS1 | Sponge network | -2 | 0.00032 | -1.792 | 0 | 0.44 |
198 | MAGI2-AS3 |
hsa-let-7d-5p;hsa-miR-106b-5p;hsa-miR-1271-5p;hsa-miR-128-3p;hsa-miR-141-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-197-3p;hsa-miR-200a-3p;hsa-miR-24-3p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-7-1-3p;hsa-miR-92a-3p;hsa-miR-92b-3p | 19 | CREB3L2 | Sponge network | -2.588 | 0 | -0.289 | 0.01425 | 0.435 |
199 | CASC2 |
hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-182-5p;hsa-miR-301a-3p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-532-3p;hsa-miR-539-5p;hsa-miR-590-3p;hsa-miR-616-3p;hsa-miR-629-3p;hsa-miR-944 | 12 | COL4A4 | Sponge network | -1.607 | 0 | -3.737 | 0 | 0.432 |
200 | RP11-284N8.3 |
hsa-miR-106b-5p;hsa-miR-17-5p;hsa-miR-200c-3p;hsa-miR-22-5p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-28-5p;hsa-miR-335-3p;hsa-miR-378a-3p;hsa-miR-590-3p;hsa-miR-629-3p;hsa-miR-93-5p | 12 | FLT1 | Sponge network | -2.956 | 0 | -1.262 | 0 | 0.432 |
201 | RP11-1024P17.1 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-141-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-192-5p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-3928-3p;hsa-miR-576-5p;hsa-miR-590-3p | 15 | IL6R | Sponge network | -3.322 | 0 | -1.861 | 0 | 0.431 |
202 | RP11-325F22.2 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-421;hsa-miR-96-5p | 12 | PDGFRA | Sponge network | -1.941 | 0.00827 | -1.139 | 0 | 0.431 |
203 | LINC00702 |
hsa-let-7d-5p;hsa-let-7g-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-345-5p;hsa-miR-423-3p;hsa-miR-503-5p;hsa-miR-505-5p;hsa-miR-616-5p;hsa-miR-708-5p;hsa-miR-93-5p;hsa-miR-942-5p;hsa-miR-96-5p | 15 | CDKN1A | Sponge network | -3.658 | 0 | -0.663 | 2.0E-5 | 0.43 |
204 | RP1-78O14.1 |
hsa-let-7i-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-197-3p;hsa-miR-301a-3p;hsa-miR-331-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-340-5p;hsa-miR-3928-3p;hsa-miR-484;hsa-miR-576-5p | 16 | IL6R | Sponge network | -4.002 | 0 | -1.861 | 0 | 0.427 |
205 | LINC00702 |
hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-182-5p;hsa-miR-301a-3p;hsa-miR-33a-3p;hsa-miR-454-3p;hsa-miR-501-5p;hsa-miR-532-3p;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-616-3p;hsa-miR-629-3p | 13 | COL4A4 | Sponge network | -3.658 | 0 | -3.737 | 0 | 0.427 |
206 | MAGI2-AS3 |
hsa-miR-148b-3p;hsa-miR-183-5p;hsa-miR-26b-5p;hsa-miR-27b-3p;hsa-miR-28-5p;hsa-miR-429;hsa-miR-629-3p;hsa-miR-92a-3p;hsa-miR-92b-3p;hsa-miR-98-5p | 10 | ITGA5 | Sponge network | -2.588 | 0 | -0.575 | 0.00104 | 0.427 |
207 | DNM3OS |
hsa-miR-128-3p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-27b-3p;hsa-miR-331-5p;hsa-miR-429;hsa-miR-590-3p | 10 | RELN | Sponge network | -1.197 | 0.01767 | -2.872 | 0 | 0.425 |
208 | RP11-359E10.1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-301a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-616-5p;hsa-miR-93-5p | 11 | PDGFRA | Sponge network | -1.994 | 0.00061 | -1.139 | 0 | 0.424 |
209 | RP11-1024P17.1 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-1301-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-188-5p;hsa-miR-200c-3p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-629-3p | 12 | PIK3R1 | Sponge network | -3.322 | 0 | -0.906 | 0 | 0.424 |
210 | DNM3OS |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-1301-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-185-5p;hsa-miR-188-5p;hsa-miR-200c-3p;hsa-miR-532-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-629-3p;hsa-miR-93-5p;hsa-miR-96-5p | 17 | PIK3R1 | Sponge network | -1.197 | 0.01767 | -0.906 | 0 | 0.423 |
211 | RP11-221J22.1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-20a-5p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-335-3p;hsa-miR-374a-5p;hsa-miR-374b-5p;hsa-miR-421;hsa-miR-550a-5p;hsa-miR-7-1-3p | 15 | PDGFRA | Sponge network | -0.096 | 0.90015 | -1.139 | 0 | 0.422 |
212 | ZNF582-AS1 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-424-5p;hsa-miR-505-3p;hsa-miR-629-3p | 10 | CSF1 | Sponge network | -1.976 | 4.0E-5 | -1.722 | 0 | 0.422 |
213 | RP11-519G16.3 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-197-3p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-424-5p;hsa-miR-532-3p | 13 | CSF1 | Sponge network | -1.323 | 0.02402 | -1.722 | 0 | 0.422 |
214 | SOX2-OT |
hsa-miR-100-5p;hsa-miR-139-5p;hsa-miR-140-3p;hsa-miR-223-3p;hsa-miR-29a-3p;hsa-miR-29c-3p;hsa-miR-30a-5p;hsa-miR-30d-5p;hsa-miR-34a-5p;hsa-miR-497-5p | 10 | IGF1R | Sponge network | 4.47 | 1.0E-5 | 0.983 | 0 | 0.42 |
215 | RP11-314B1.2 |
hsa-miR-141-5p;hsa-miR-20a-3p;hsa-miR-33a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-452-3p;hsa-miR-452-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p | 10 | ITGA9 | Sponge network | -3.756 | 0.0001 | -2.846 | 0 | 0.416 |
216 | AC144831.1 |
hsa-let-7d-5p;hsa-let-7g-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-345-5p;hsa-miR-423-3p;hsa-miR-505-5p;hsa-miR-93-5p;hsa-miR-942-5p | 11 | CDKN1A | Sponge network | -2 | 0.00032 | -0.663 | 2.0E-5 | 0.416 |
217 | AC011899.9 |
hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-3p;hsa-miR-222-3p;hsa-miR-424-5p;hsa-miR-590-3p;hsa-miR-93-3p | 11 | FGF2 | Sponge network | -3.545 | 0 | -1.904 | 0 | 0.416 |
218 | RP11-720L2.4 |
hsa-let-7d-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-1271-5p;hsa-miR-128-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19b-3p;hsa-miR-24-3p;hsa-miR-25-3p | 11 | CREB3L2 | Sponge network | -3.302 | 0 | -0.289 | 0.01425 | 0.415 |
219 | RP11-283G6.4 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-20b-5p;hsa-miR-23a-5p;hsa-miR-301a-3p;hsa-miR-93-5p;hsa-miR-96-5p | 11 | CSF1 | Sponge network | -1.912 | 0.08964 | -1.722 | 0 | 0.413 |
220 | RP11-221J22.2 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-20a-5p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-335-3p;hsa-miR-374a-5p;hsa-miR-374b-5p;hsa-miR-421;hsa-miR-450b-5p;hsa-miR-550a-5p;hsa-miR-589-3p;hsa-miR-7-1-3p | 17 | PDGFRA | Sponge network | -0.299 | 0.70083 | -1.139 | 0 | 0.413 |
221 | AC109642.1 |
hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-200c-3p;hsa-miR-20a-3p;hsa-miR-21-3p;hsa-miR-222-3p;hsa-miR-3682-3p;hsa-miR-424-5p;hsa-miR-429;hsa-miR-503-5p;hsa-miR-590-3p;hsa-miR-92a-3p;hsa-miR-93-3p | 16 | FGF2 | Sponge network | -3.573 | 0 | -1.904 | 0 | 0.412 |
222 | RP11-401P9.4 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-33a-3p;hsa-miR-501-3p;hsa-miR-93-3p;hsa-miR-93-5p | 11 | COL4A3 | Sponge network | -3.167 | 0 | -5.064 | 0 | 0.41 |
223 | DLX6-AS1 |
hsa-let-7a-5p;hsa-miR-139-5p;hsa-miR-143-3p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-181c-5p;hsa-miR-1976;hsa-miR-26a-5p;hsa-miR-326;hsa-miR-338-3p | 10 | ITGB8 | Sponge network | 6.401 | 0 | 2.27 | 0 | 0.41 |
224 | FENDRR |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-1301-3p;hsa-miR-15b-5p;hsa-miR-182-5p;hsa-miR-188-5p;hsa-miR-200c-3p;hsa-miR-532-3p;hsa-miR-590-3p;hsa-miR-629-3p | 10 | PIK3R1 | Sponge network | -4.656 | 0 | -0.906 | 0 | 0.41 |
225 | MIR497HG |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-1301-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-188-5p;hsa-miR-200c-3p;hsa-miR-532-3p;hsa-miR-590-5p;hsa-miR-629-3p;hsa-miR-93-5p;hsa-miR-96-5p | 14 | PIK3R1 | Sponge network | -3.004 | 0 | -0.906 | 0 | 0.41 |
226 | LINC00968 |
hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-182-5p;hsa-miR-183-5p;hsa-miR-221-5p;hsa-miR-320b;hsa-miR-424-5p;hsa-miR-450b-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-96-5p | 11 | FGF9 | Sponge network | -4.827 | 0 | -2.856 | 0 | 0.408 |
227 | CASC2 |
hsa-miR-106b-5p;hsa-miR-15b-3p;hsa-miR-17-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-539-5p;hsa-miR-590-3p;hsa-miR-625-5p;hsa-miR-7-1-3p;hsa-miR-93-3p;hsa-miR-93-5p;hsa-miR-944 | 14 | COL4A3 | Sponge network | -1.607 | 0 | -5.064 | 0 | 0.408 |
228 | LINC00941 |
hsa-miR-107;hsa-miR-140-3p;hsa-miR-15a-5p;hsa-miR-1976;hsa-miR-218-5p;hsa-miR-26a-5p;hsa-miR-29a-3p;hsa-miR-29b-3p;hsa-miR-29c-3p;hsa-miR-497-5p | 10 | CDK6 | Sponge network | 2.474 | 0.00018 | 1.055 | 0 | 0.407 |
229 | LINC00702 |
hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-182-5p;hsa-miR-183-5p;hsa-miR-320b;hsa-miR-424-5p;hsa-miR-450b-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-744-3p;hsa-miR-96-5p | 11 | FGF9 | Sponge network | -3.658 | 0 | -2.856 | 0 | 0.406 |
230 | CTD-2034I21.2 |
hsa-miR-139-5p;hsa-miR-145-5p;hsa-miR-15a-5p;hsa-miR-16-1-3p;hsa-miR-223-3p;hsa-miR-29a-3p;hsa-miR-29b-2-5p;hsa-miR-29c-3p;hsa-miR-342-5p;hsa-miR-34a-5p;hsa-miR-362-3p;hsa-miR-497-5p | 12 | IGF1R | Sponge network | 7.901 | 0 | 0.983 | 0 | 0.405 |
231 | MEG3 |
hsa-miR-106a-5p;hsa-miR-141-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-301a-3p;hsa-miR-339-5p;hsa-miR-454-3p;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-5p;hsa-miR-616-5p | 12 | PDGFRA | Sponge network | -0.426 | 0.41068 | -1.139 | 0 | 0.402 |
232 | TBX5-AS1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-141-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-192-5p;hsa-miR-193b-3p;hsa-miR-197-3p;hsa-miR-200a-3p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-331-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-3928-3p;hsa-miR-421;hsa-miR-576-5p;hsa-miR-590-5p;hsa-miR-942-5p | 22 | IL6R | Sponge network | -2.901 | 0 | -1.861 | 0 | 0.401 |
233 | LINC00473 |
hsa-let-7a-3p;hsa-let-7d-5p;hsa-miR-16-1-3p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-629-3p;hsa-miR-7-1-3p | 11 | THBS1 | Sponge network | -3.931 | 0.00573 | -1.792 | 0 | 0.4 |
234 | RP11-701P16.5 |
hsa-miR-106b-5p;hsa-miR-129-5p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-196b-5p;hsa-miR-24-3p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-550a-5p;hsa-miR-93-5p | 12 | PDGFRA | Sponge network | -5.254 | 0 | -1.139 | 0 | 0.4 |
235 | FENDRR |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-186-5p;hsa-miR-20a-3p;hsa-miR-28-3p;hsa-miR-301a-3p;hsa-miR-421;hsa-miR-450b-5p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-940 | 13 | IGF1 | Sponge network | -4.656 | 0 | -1.378 | 1.0E-5 | 0.399 |
236 | LINC00261 |
hsa-miR-1271-5p;hsa-miR-18a-3p;hsa-miR-193b-5p;hsa-miR-224-5p;hsa-miR-3127-5p;hsa-miR-3615;hsa-miR-378a-3p;hsa-miR-616-5p;hsa-miR-671-5p;hsa-miR-939-5p;hsa-miR-940 | 11 | GNG7 | Sponge network | -5.643 | 0 | -2.411 | 0 | 0.397 |
237 | DNM3OS |
hsa-let-7d-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-1271-5p;hsa-miR-128-3p;hsa-miR-141-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-19b-3p;hsa-miR-200a-3p;hsa-miR-24-3p;hsa-miR-25-3p;hsa-miR-362-5p;hsa-miR-429;hsa-miR-501-5p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-7-1-3p | 22 | CREB3L2 | Sponge network | -1.197 | 0.01767 | -0.289 | 0.01425 | 0.396 |
238 | RP11-166D19.1 |
hsa-miR-106b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-93-3p | 10 | COL4A3 | Sponge network | -1.481 | 0.00084 | -5.064 | 0 | 0.395 |
239 | ZNF582-AS1 |
hsa-let-7a-3p;hsa-miR-106b-5p;hsa-miR-149-5p;hsa-miR-182-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-33a-5p;hsa-miR-590-5p;hsa-miR-7-1-3p | 10 | PDGFRA | Sponge network | -1.976 | 4.0E-5 | -1.139 | 0 | 0.395 |
240 | LINC00968 |
hsa-let-7d-5p;hsa-miR-106b-5p;hsa-miR-1271-5p;hsa-miR-128-3p;hsa-miR-141-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-197-3p;hsa-miR-19b-3p;hsa-miR-200a-3p;hsa-miR-24-3p;hsa-miR-25-3p;hsa-miR-590-3p;hsa-miR-616-5p | 17 | CREB3L2 | Sponge network | -4.827 | 0 | -0.289 | 0.01425 | 0.395 |
241 | LINC00702 |
hsa-let-7d-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-1271-5p;hsa-miR-128-3p;hsa-miR-141-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-197-3p;hsa-miR-19b-3p;hsa-miR-200a-3p;hsa-miR-24-3p;hsa-miR-25-3p;hsa-miR-32-5p;hsa-miR-362-5p;hsa-miR-501-5p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-7-1-3p;hsa-miR-92a-1-5p;hsa-miR-92a-3p;hsa-miR-92b-3p | 25 | CREB3L2 | Sponge network | -3.658 | 0 | -0.289 | 0.01425 | 0.39 |
242 | HAR1A |
hsa-miR-1271-5p;hsa-miR-141-3p;hsa-miR-182-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-200a-3p;hsa-miR-224-5p;hsa-miR-3127-5p;hsa-miR-671-5p;hsa-miR-939-5p;hsa-miR-940 | 12 | GNG7 | Sponge network | -1.641 | 0 | -2.411 | 0 | 0.39 |
243 | AC109642.1 |
hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-182-5p;hsa-miR-183-5p;hsa-miR-221-5p;hsa-miR-320b;hsa-miR-3607-3p;hsa-miR-424-5p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-744-3p;hsa-miR-96-5p | 12 | FGF9 | Sponge network | -3.573 | 0 | -2.856 | 0 | 0.388 |
244 | RP1-78O14.1 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-339-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-576-5p;hsa-miR-7-1-3p | 14 | PDGFRA | Sponge network | -4.002 | 0 | -1.139 | 0 | 0.388 |
245 | LINC00702 |
hsa-miR-186-5p;hsa-miR-18a-5p;hsa-miR-26b-3p;hsa-miR-320b;hsa-miR-484;hsa-miR-532-3p;hsa-miR-550a-5p;hsa-miR-576-5p;hsa-miR-590-5p;hsa-miR-625-5p;hsa-miR-629-5p;hsa-miR-7-5p;hsa-miR-760 | 13 | FGF1 | Sponge network | -3.658 | 0 | -0.804 | 0.00096 | 0.387 |
246 | RP11-536K7.3 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-188-5p;hsa-miR-200c-3p;hsa-miR-532-3p;hsa-miR-590-3p;hsa-miR-629-3p | 12 | PIK3R1 | Sponge network | -2.193 | 0.00149 | -0.906 | 0 | 0.387 |
247 | RP5-839B4.8 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-205-5p;hsa-miR-23a-5p;hsa-miR-27a-3p;hsa-miR-629-3p | 11 | CSF1 | Sponge network | -6.051 | 0 | -1.722 | 0 | 0.387 |
248 | AC144831.1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-501-3p;hsa-miR-7-1-3p;hsa-miR-93-3p;hsa-miR-93-5p | 11 | COL4A3 | Sponge network | -2 | 0.00032 | -5.064 | 0 | 0.386 |
249 | MIR497HG |
hsa-let-7a-3p;hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-3p;hsa-miR-222-3p;hsa-miR-424-5p;hsa-miR-450b-5p;hsa-miR-590-5p;hsa-miR-93-3p | 14 | FGF2 | Sponge network | -3.004 | 0 | -1.904 | 0 | 0.386 |
250 | LINC00702 |
hsa-let-7f-1-3p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-193b-3p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-222-3p;hsa-miR-301a-3p;hsa-miR-335-3p;hsa-miR-421;hsa-miR-450b-5p;hsa-miR-454-3p;hsa-miR-590-3p;hsa-miR-671-5p | 14 | KIT | Sponge network | -3.658 | 0 | -2.514 | 0 | 0.386 |
251 | DLX6-AS1 |
hsa-miR-100-5p;hsa-miR-139-5p;hsa-miR-140-3p;hsa-miR-146b-5p;hsa-miR-195-5p;hsa-miR-223-3p;hsa-miR-29a-3p;hsa-miR-29c-3p;hsa-miR-30a-5p;hsa-miR-30b-5p;hsa-miR-30d-5p;hsa-miR-375;hsa-miR-497-5p | 13 | IGF1R | Sponge network | 6.401 | 0 | 0.983 | 0 | 0.386 |
252 | AC011899.9 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-135b-5p;hsa-miR-141-3p;hsa-miR-141-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-192-5p;hsa-miR-193b-3p;hsa-miR-301a-3p;hsa-miR-331-3p;hsa-miR-33a-5p;hsa-miR-3928-3p;hsa-miR-590-3p;hsa-miR-708-3p | 16 | IL6R | Sponge network | -3.545 | 0 | -1.861 | 0 | 0.384 |
253 | RP11-1008C21.1 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-186-5p;hsa-miR-19b-1-5p;hsa-miR-19b-3p;hsa-miR-20a-3p;hsa-miR-301a-3p;hsa-miR-320b;hsa-miR-33a-3p;hsa-miR-940 | 12 | IGF1 | Sponge network | -2.048 | 0.00613 | -1.378 | 1.0E-5 | 0.383 |
254 | RP11-314B1.2 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-301a-3p;hsa-miR-424-5p;hsa-miR-532-3p;hsa-miR-629-3p;hsa-miR-93-5p;hsa-miR-96-5p | 10 | CSF1 | Sponge network | -3.756 | 0.0001 | -1.722 | 0 | 0.382 |
255 | LINC00702 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-335-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-7-1-3p;hsa-miR-93-5p;hsa-miR-96-5p | 10 | THBS2 | Sponge network | -3.658 | 0 | 2.009 | 0 | 0.382 |
256 | AC144831.1 |
hsa-miR-103a-2-5p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-16-1-3p;hsa-miR-19a-3p;hsa-miR-19b-1-5p;hsa-miR-19b-3p;hsa-miR-20a-3p;hsa-miR-301a-3p;hsa-miR-450b-5p;hsa-miR-576-5p | 11 | IGF1 | Sponge network | -2 | 0.00032 | -1.378 | 1.0E-5 | 0.382 |
257 | RP11-401P9.4 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-1301-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-188-5p;hsa-miR-200c-3p;hsa-miR-532-3p;hsa-miR-590-5p;hsa-miR-93-5p | 13 | PIK3R1 | Sponge network | -3.167 | 0 | -0.906 | 0 | 0.379 |
258 | DLX6-AS1 |
hsa-miR-139-5p;hsa-miR-140-3p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-181c-5p;hsa-miR-30a-5p;hsa-miR-30b-5p;hsa-miR-30d-5p;hsa-miR-338-5p;hsa-miR-361-3p | 10 | YWHAG | Sponge network | 6.401 | 0 | 0.991 | 0 | 0.377 |
259 | RP11-367G6.3 |
hsa-miR-106b-5p;hsa-miR-130a-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-424-5p | 10 | CSF1 | Sponge network | -1.561 | 0.03245 | -1.722 | 0 | 0.377 |
260 | RP11-426C22.4 |
hsa-miR-107;hsa-miR-148b-3p;hsa-miR-15a-5p;hsa-miR-16-5p;hsa-miR-185-5p;hsa-miR-29b-3p;hsa-miR-338-3p;hsa-miR-374a-5p;hsa-miR-374b-5p;hsa-miR-502-3p | 10 | CDK6 | Sponge network | 0.742 | 0.14065 | 1.055 | 0 | 0.376 |
261 | RP11-91K9.1 |
hsa-let-7a-3p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-320a;hsa-miR-320b;hsa-miR-590-5p;hsa-miR-7-1-3p | 11 | FGF7 | Sponge network | -0.187 | 0.8212 | -2.211 | 0 | 0.376 |
262 | RP1-78O14.1 |
hsa-miR-106b-5p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-22-5p;hsa-miR-24-3p;hsa-miR-339-5p;hsa-miR-576-5p;hsa-miR-629-3p;hsa-miR-744-3p | 10 | FLT1 | Sponge network | -4.002 | 0 | -1.262 | 0 | 0.375 |
263 | PWAR6 |
hsa-miR-103a-2-5p;hsa-miR-16-1-3p;hsa-miR-186-5p;hsa-miR-19b-1-5p;hsa-miR-301a-3p;hsa-miR-362-5p;hsa-miR-450b-5p;hsa-miR-454-3p;hsa-miR-576-5p;hsa-miR-590-3p | 10 | IGF1 | Sponge network | -1.994 | 6.0E-5 | -1.378 | 1.0E-5 | 0.373 |
264 | LINC00473 |
hsa-let-7a-3p;hsa-miR-130a-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-16-1-3p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-196b-5p;hsa-miR-224-5p;hsa-miR-26b-5p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-339-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-374a-5p;hsa-miR-374b-5p;hsa-miR-454-3p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-7-1-3p | 23 | PDGFRA | Sponge network | -3.931 | 0.00573 | -1.139 | 0 | 0.371 |
265 | GCSAML-AS1 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-197-3p;hsa-miR-23a-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-940 | 12 | CSF1 | Sponge network | -2.828 | 0.08354 | -1.722 | 0 | 0.371 |
266 | LINC00511 |
hsa-miR-107;hsa-miR-126-5p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-181c-5p;hsa-miR-181d-5p;hsa-miR-195-5p;hsa-miR-26a-5p;hsa-miR-30b-5p;hsa-miR-30d-5p;hsa-miR-362-3p;hsa-miR-497-5p;hsa-miR-532-5p | 13 | ITGA2 | Sponge network | 4.529 | 0 | 1.327 | 0 | 0.37 |
267 | LINC00327 | hsa-miR-22-5p;hsa-miR-24-2-5p;hsa-miR-27b-5p;hsa-miR-339-5p;hsa-miR-500a-5p;hsa-miR-501-5p;hsa-miR-505-3p;hsa-miR-505-5p;hsa-miR-532-3p;hsa-miR-550a-3p | 10 | PRKCA | Sponge network | -1.436 | 0.00808 | -0.975 | 0 | 0.37 |
268 | RP11-221J22.2 |
hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-1-5p;hsa-miR-19b-3p;hsa-miR-20a-3p;hsa-miR-301a-3p;hsa-miR-421;hsa-miR-450b-5p | 10 | IGF1 | Sponge network | -0.299 | 0.70083 | -1.378 | 1.0E-5 | 0.368 |
269 | AP001189.4 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-182-5p;hsa-miR-196b-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-339-5p;hsa-miR-550a-5p;hsa-miR-589-3p | 10 | PDGFRA | Sponge network | -4.547 | 0 | -1.139 | 0 | 0.368 |
270 | DNM3OS |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-501-3p;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-93-3p;hsa-miR-93-5p | 14 | COL4A3 | Sponge network | -1.197 | 0.01767 | -5.064 | 0 | 0.367 |
271 | RP11-527N22.1 |
hsa-let-7a-3p;hsa-miR-1226-3p;hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-19b-1-5p;hsa-miR-200c-3p;hsa-miR-20a-3p;hsa-miR-222-3p;hsa-miR-3682-3p;hsa-miR-424-5p;hsa-miR-589-3p;hsa-miR-93-3p | 15 | FGF2 | Sponge network | -2.999 | 0.02338 | -1.904 | 0 | 0.367 |
272 | RP11-720L2.4 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-188-5p;hsa-miR-18a-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-25-3p;hsa-miR-93-5p | 13 | PTEN | Sponge network | -3.302 | 0 | -0.689 | 1.0E-5 | 0.366 |
273 | RP11-401P9.4 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-339-5p;hsa-miR-421;hsa-miR-505-5p;hsa-miR-616-5p;hsa-miR-708-5p;hsa-miR-877-5p;hsa-miR-93-5p | 16 | FLT1 | Sponge network | -3.167 | 0 | -1.262 | 0 | 0.364 |
274 | RP11-401P9.4 |
hsa-miR-1271-5p;hsa-miR-141-3p;hsa-miR-182-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-200a-3p;hsa-miR-3127-5p;hsa-miR-532-3p;hsa-miR-616-5p;hsa-miR-939-5p | 11 | GNG7 | Sponge network | -3.167 | 0 | -2.411 | 0 | 0.361 |
275 | MEG3 |
hsa-let-7d-5p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-500a-5p;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-629-3p;hsa-miR-98-5p | 13 | THBS1 | Sponge network | -0.426 | 0.41068 | -1.792 | 0 | 0.361 |
276 | AC109642.1 |
hsa-miR-106b-5p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-200c-3p;hsa-miR-24-3p;hsa-miR-378a-3p;hsa-miR-429;hsa-miR-505-5p;hsa-miR-590-3p;hsa-miR-744-3p | 11 | FLT1 | Sponge network | -3.573 | 0 | -1.262 | 0 | 0.361 |
277 | RP11-191L9.4 |
hsa-miR-139-5p;hsa-miR-140-3p;hsa-miR-140-5p;hsa-miR-145-5p;hsa-miR-146b-5p;hsa-miR-15a-5p;hsa-miR-195-5p;hsa-miR-223-3p;hsa-miR-29a-3p;hsa-miR-29b-2-5p;hsa-miR-29b-3p;hsa-miR-29c-3p;hsa-miR-30a-5p;hsa-miR-497-5p | 14 | IGF1R | Sponge network | 10.302 | 0 | 0.983 | 0 | 0.36 |
278 | RP11-325F22.2 |
hsa-let-7d-5p;hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-141-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-24-3p;hsa-miR-25-3p;hsa-miR-92a-3p;hsa-miR-92b-3p | 10 | CREB3L2 | Sponge network | -1.941 | 0.00827 | -0.289 | 0.01425 | 0.36 |
279 | LINC00968 |
hsa-let-7d-5p;hsa-let-7f-5p;hsa-let-7g-5p;hsa-miR-106b-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-335-5p;hsa-miR-503-5p;hsa-miR-505-5p;hsa-miR-616-5p;hsa-miR-708-5p;hsa-miR-93-5p;hsa-miR-942-5p;hsa-miR-96-5p | 14 | CDKN1A | Sponge network | -4.827 | 0 | -0.663 | 2.0E-5 | 0.359 |
280 | CASC2 |
hsa-miR-141-3p;hsa-miR-200a-3p;hsa-miR-33a-3p;hsa-miR-3682-3p;hsa-miR-421;hsa-miR-429;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-7-1-3p;hsa-miR-944 | 11 | HGF | Sponge network | -1.607 | 0 | -3.203 | 0 | 0.359 |
281 | LINC00640 | hsa-miR-101-3p;hsa-miR-107;hsa-miR-146b-5p;hsa-miR-1976;hsa-miR-218-5p;hsa-miR-29a-3p;hsa-miR-29b-3p;hsa-miR-29c-3p;hsa-miR-32-5p;hsa-miR-34a-5p;hsa-miR-660-5p | 11 | CDK6 | Sponge network | 3.062 | 5.0E-5 | 1.055 | 0 | 0.358 |
282 | RP11-251M1.1 |
hsa-let-7i-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-192-5p;hsa-miR-301a-3p;hsa-miR-320b | 10 | IL6R | Sponge network | -4.934 | 0 | -1.861 | 0 | 0.357 |
283 | RP11-426C22.4 |
hsa-miR-107;hsa-miR-126-5p;hsa-miR-130a-3p;hsa-miR-15a-5p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-26b-5p;hsa-miR-362-3p;hsa-miR-374a-5p;hsa-miR-374b-5p | 10 | ITGA2 | Sponge network | 0.742 | 0.14065 | 1.327 | 0 | 0.356 |
284 | AC011738.4 |
hsa-miR-107;hsa-miR-126-5p;hsa-miR-139-5p;hsa-miR-15a-5p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-181c-5p;hsa-miR-181d-5p;hsa-miR-195-5p;hsa-miR-26a-5p;hsa-miR-326;hsa-miR-497-5p;hsa-miR-532-5p | 13 | ITGA2 | Sponge network | 8.148 | 0 | 1.327 | 0 | 0.356 |
285 | LINC00702 |
hsa-let-7a-3p;hsa-miR-1226-3p;hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-19b-1-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-3p;hsa-miR-21-3p;hsa-miR-222-3p;hsa-miR-3682-3p;hsa-miR-424-5p;hsa-miR-450b-5p;hsa-miR-503-5p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-92a-3p;hsa-miR-93-3p | 22 | FGF2 | Sponge network | -3.658 | 0 | -1.904 | 0 | 0.355 |
286 | LINC00968 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-141-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-192-5p;hsa-miR-193b-3p;hsa-miR-197-3p;hsa-miR-200a-3p;hsa-miR-301a-3p;hsa-miR-320b;hsa-miR-335-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-3928-3p;hsa-miR-421;hsa-miR-484;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-93-5p;hsa-miR-942-5p | 23 | IL6R | Sponge network | -4.827 | 0 | -1.861 | 0 | 0.355 |
287 | RP11-1008C21.1 |
hsa-let-7a-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-20a-5p;hsa-miR-24-3p;hsa-miR-301a-3p;hsa-miR-320b;hsa-miR-33a-5p;hsa-miR-550a-5p | 12 | PDGFRA | Sponge network | -2.048 | 0.00613 | -1.139 | 0 | 0.354 |
288 | FENDRR |
hsa-let-7a-3p;hsa-miR-1226-3p;hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-186-5p;hsa-miR-200c-3p;hsa-miR-20a-3p;hsa-miR-424-5p;hsa-miR-450b-5p;hsa-miR-503-5p;hsa-miR-539-5p;hsa-miR-590-3p;hsa-miR-93-3p | 13 | FGF2 | Sponge network | -4.656 | 0 | -1.904 | 0 | 0.354 |
289 | LINC00702 |
hsa-miR-103a-2-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-141-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-192-5p;hsa-miR-193b-3p;hsa-miR-197-3p;hsa-miR-200a-3p;hsa-miR-301a-3p;hsa-miR-320b;hsa-miR-331-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-3928-3p;hsa-miR-421;hsa-miR-454-3p;hsa-miR-484;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-93-5p;hsa-miR-942-5p | 27 | IL6R | Sponge network | -3.658 | 0 | -1.861 | 0 | 0.353 |
290 | RP11-540A21.2 |
hsa-miR-139-5p;hsa-miR-140-3p;hsa-miR-140-5p;hsa-miR-145-5p;hsa-miR-15a-5p;hsa-miR-195-5p;hsa-miR-29a-3p;hsa-miR-29b-2-5p;hsa-miR-29b-3p;hsa-miR-29c-3p;hsa-miR-30a-5p;hsa-miR-30b-5p;hsa-miR-30d-5p;hsa-miR-342-5p;hsa-miR-497-5p | 15 | IGF1R | Sponge network | 2.421 | 0 | 0.983 | 0 | 0.351 |
291 | PWAR6 |
hsa-let-7d-5p;hsa-miR-1271-5p;hsa-miR-141-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-186-5p;hsa-miR-197-3p;hsa-miR-362-5p;hsa-miR-590-3p;hsa-miR-616-5p | 11 | CREB3L2 | Sponge network | -1.994 | 6.0E-5 | -0.289 | 0.01425 | 0.351 |
292 | RP11-325F22.2 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-188-5p;hsa-miR-18a-5p;hsa-miR-25-3p;hsa-miR-301a-3p;hsa-miR-421;hsa-miR-92a-3p | 11 | PTEN | Sponge network | -1.941 | 0.00827 | -0.689 | 1.0E-5 | 0.35 |
293 | SEMA3B |
hsa-miR-106a-5p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-27b-3p;hsa-miR-28-5p;hsa-miR-423-5p;hsa-miR-424-5p;hsa-miR-455-3p;hsa-miR-532-3p;hsa-miR-708-5p;hsa-miR-939-5p | 12 | CSF1 | Sponge network | -3.358 | 0 | -1.722 | 0 | 0.35 |
294 | RP11-809H16.5 | hsa-miR-139-5p;hsa-miR-140-3p;hsa-miR-140-5p;hsa-miR-145-5p;hsa-miR-223-3p;hsa-miR-29a-3p;hsa-miR-29b-2-5p;hsa-miR-29b-3p;hsa-miR-29c-3p;hsa-miR-497-5p | 10 | IGF1R | Sponge network | 4.886 | 0.0037 | 0.983 | 0 | 0.348 |
295 | LINC00520 |
hsa-miR-107;hsa-miR-126-5p;hsa-miR-15a-5p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-181c-5p;hsa-miR-181d-5p;hsa-miR-186-5p;hsa-miR-374a-5p;hsa-miR-374b-5p;hsa-miR-497-5p | 11 | ITGA2 | Sponge network | 3.143 | 0.0001 | 1.327 | 0 | 0.348 |
296 | LINC00702 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-188-5p;hsa-miR-18a-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200a-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-25-3p;hsa-miR-26b-5p;hsa-miR-301a-3p;hsa-miR-32-5p;hsa-miR-320b;hsa-miR-335-3p;hsa-miR-3613-5p;hsa-miR-421;hsa-miR-425-5p;hsa-miR-454-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-628-3p;hsa-miR-7-1-3p;hsa-miR-92a-3p;hsa-miR-93-5p | 32 | PTEN | Sponge network | -3.658 | 0 | -0.689 | 1.0E-5 | 0.346 |
297 | RP11-79H23.3 | hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-200c-3p;hsa-miR-25-3p;hsa-miR-301a-3p;hsa-miR-421;hsa-miR-92a-3p | 10 | PTEN | Sponge network | -2.935 | 0 | -0.689 | 1.0E-5 | 0.345 |
298 | SLC2A1-AS1 |
hsa-miR-139-5p;hsa-miR-140-3p;hsa-miR-146b-5p;hsa-miR-29a-3p;hsa-miR-29b-2-5p;hsa-miR-29b-3p;hsa-miR-29c-3p;hsa-miR-30a-5p;hsa-miR-34a-5p;hsa-miR-497-5p | 10 | IGF1R | Sponge network | 3.023 | 0 | 0.983 | 0 | 0.344 |
299 | AC109642.1 |
hsa-let-7g-3p;hsa-miR-106b-5p;hsa-miR-148b-5p;hsa-miR-151a-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-193b-3p;hsa-miR-320b;hsa-miR-940;hsa-miR-942-5p | 11 | MCL1 | Sponge network | -3.573 | 0 | -0.943 | 0 | 0.344 |
300 | RP1-78O14.1 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-1301-3p;hsa-miR-15b-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-188-5p;hsa-miR-22-5p;hsa-miR-532-3p;hsa-miR-629-3p | 10 | PIK3R1 | Sponge network | -4.002 | 0 | -0.906 | 0 | 0.343 |
301 | RP11-367G6.3 |
hsa-let-7a-3p;hsa-miR-106b-5p;hsa-miR-130a-3p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-421 | 11 | PDGFRA | Sponge network | -1.561 | 0.03245 | -1.139 | 0 | 0.342 |
302 | AC007879.7 | hsa-miR-101-3p;hsa-miR-107;hsa-miR-140-3p;hsa-miR-15a-5p;hsa-miR-1976;hsa-miR-218-5p;hsa-miR-29b-3p;hsa-miR-29c-3p;hsa-miR-30d-3p;hsa-miR-338-3p | 10 | CDK6 | Sponge network | 2.641 | 2.0E-5 | 1.055 | 0 | 0.342 |
303 | RP11-367F23.2 | hsa-miR-126-5p;hsa-miR-142-3p;hsa-miR-15a-5p;hsa-miR-181c-5p;hsa-miR-18a-5p;hsa-miR-30b-5p;hsa-miR-30d-5p;hsa-miR-30e-5p;hsa-miR-3607-3p;hsa-miR-497-5p | 10 | ITGA2 | Sponge network | 4.926 | 0.00051 | 1.327 | 0 | 0.341 |
304 | LINC00941 |
hsa-miR-139-5p;hsa-miR-140-3p;hsa-miR-140-5p;hsa-miR-145-5p;hsa-miR-15a-5p;hsa-miR-16-1-3p;hsa-miR-29a-3p;hsa-miR-29b-2-5p;hsa-miR-29b-3p;hsa-miR-29c-3p;hsa-miR-342-5p;hsa-miR-362-3p;hsa-miR-497-5p;hsa-miR-532-5p | 14 | IGF1R | Sponge network | 2.474 | 0.00018 | 0.983 | 0 | 0.341 |
305 | AC109642.1 |
hsa-let-7d-5p;hsa-miR-106b-5p;hsa-miR-1271-5p;hsa-miR-128-3p;hsa-miR-141-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-197-3p;hsa-miR-24-3p;hsa-miR-25-3p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-92a-3p;hsa-miR-92b-3p | 17 | CREB3L2 | Sponge network | -3.573 | 0 | -0.289 | 0.01425 | 0.341 |
306 | RP11-536K7.3 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-1271-5p;hsa-miR-128-3p;hsa-miR-141-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-19b-3p;hsa-miR-24-3p;hsa-miR-25-3p;hsa-miR-590-3p;hsa-miR-616-5p | 15 | CREB3L2 | Sponge network | -2.193 | 0.00149 | -0.289 | 0.01425 | 0.34 |
307 | DNM3OS |
hsa-let-7f-1-3p;hsa-miR-16-2-3p;hsa-miR-186-5p;hsa-miR-27b-3p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-501-5p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-7-1-3p;hsa-miR-93-5p;hsa-miR-96-5p | 12 | GNB4 | Sponge network | -1.197 | 0.01767 | -0.48 | 0.00876 | 0.34 |
308 | LINC00511 |
hsa-miR-140-3p;hsa-miR-195-5p;hsa-miR-29a-3p;hsa-miR-29c-3p;hsa-miR-30b-5p;hsa-miR-30d-5p;hsa-miR-34a-5p;hsa-miR-362-3p;hsa-miR-497-5p;hsa-miR-532-5p | 10 | IGF1R | Sponge network | 4.529 | 0 | 0.983 | 0 | 0.34 |
309 | SEMA3B |
hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-18a-3p;hsa-miR-27b-3p;hsa-miR-31-5p;hsa-miR-421;hsa-miR-424-5p;hsa-miR-455-3p;hsa-miR-577;hsa-miR-590-3p;hsa-miR-708-3p | 11 | FGF7 | Sponge network | -3.358 | 0 | -2.211 | 0 | 0.34 |
310 | GCSAML-AS1 |
hsa-let-7d-5p;hsa-miR-106b-5p;hsa-miR-1271-5p;hsa-miR-128-3p;hsa-miR-141-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-197-3p;hsa-miR-200a-3p | 10 | CREB3L2 | Sponge network | -2.828 | 0.08354 | -0.289 | 0.01425 | 0.34 |
311 | RP11-397A16.1 |
hsa-miR-101-3p;hsa-miR-107;hsa-miR-15a-5p;hsa-miR-195-5p;hsa-miR-1976;hsa-miR-218-5p;hsa-miR-26a-5p;hsa-miR-30a-3p;hsa-miR-30d-3p;hsa-miR-34a-5p;hsa-miR-497-5p | 11 | CDK6 | Sponge network | 11.276 | 0 | 1.055 | 0 | 0.339 |
312 | LINC00261 |
hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-205-5p;hsa-miR-424-5p;hsa-miR-455-3p;hsa-miR-629-3p;hsa-miR-708-5p;hsa-miR-939-5p;hsa-miR-940 | 11 | CSF1 | Sponge network | -5.643 | 0 | -1.722 | 0 | 0.338 |
313 | RP11-77A13.1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-192-5p;hsa-miR-193b-3p;hsa-miR-301a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-454-3p;hsa-miR-93-5p;hsa-miR-98-5p | 14 | IL6R | Sponge network | -9.091 | 0 | -1.861 | 0 | 0.337 |
314 | TBX5-AS1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-188-5p;hsa-miR-18a-5p;hsa-miR-200a-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-25-3p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-32-5p;hsa-miR-335-3p;hsa-miR-421;hsa-miR-590-5p;hsa-miR-7-1-3p;hsa-miR-92a-3p | 23 | PTEN | Sponge network | -2.901 | 0 | -0.689 | 1.0E-5 | 0.337 |
315 | ZNF582-AS1 |
hsa-let-7a-3p;hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-20a-3p;hsa-miR-222-3p;hsa-miR-424-5p;hsa-miR-452-5p;hsa-miR-590-5p | 10 | FGF2 | Sponge network | -1.976 | 4.0E-5 | -1.904 | 0 | 0.335 |
316 | MIR497HG |
hsa-miR-130b-5p;hsa-miR-183-5p;hsa-miR-186-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-24-2-5p;hsa-miR-339-5p;hsa-miR-450b-5p;hsa-miR-532-3p;hsa-miR-93-3p | 10 | PRKCA | Sponge network | -3.004 | 0 | -0.975 | 0 | 0.335 |
317 | HOXA11-AS |
hsa-miR-100-5p;hsa-miR-139-5p;hsa-miR-140-3p;hsa-miR-145-3p;hsa-miR-145-5p;hsa-miR-146b-5p;hsa-miR-195-5p;hsa-miR-223-3p;hsa-miR-29a-3p;hsa-miR-29c-3p;hsa-miR-30a-5p;hsa-miR-497-5p | 12 | IGF1R | Sponge network | 7.111 | 0 | 0.983 | 0 | 0.335 |
318 | RP11-77A13.1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-196b-5p;hsa-miR-24-3p;hsa-miR-301a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-454-3p;hsa-miR-93-5p;hsa-miR-96-5p | 15 | PDGFRA | Sponge network | -9.091 | 0 | -1.139 | 0 | 0.335 |
319 | CASC2 |
hsa-miR-1271-5p;hsa-miR-141-3p;hsa-miR-182-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-200a-3p;hsa-miR-22-5p;hsa-miR-224-5p;hsa-miR-3127-5p;hsa-miR-3615;hsa-miR-378a-3p;hsa-miR-532-3p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-671-5p;hsa-miR-9-5p;hsa-miR-92a-3p;hsa-miR-939-5p;hsa-miR-940 | 20 | GNG7 | Sponge network | -1.607 | 0 | -2.411 | 0 | 0.335 |
320 | CTD-2171N6.1 |
hsa-miR-101-3p;hsa-miR-107;hsa-miR-148b-3p;hsa-miR-15a-5p;hsa-miR-16-5p;hsa-miR-185-5p;hsa-miR-1976;hsa-miR-218-5p;hsa-miR-29b-3p;hsa-miR-30b-5p;hsa-miR-30c-5p;hsa-miR-30d-3p;hsa-miR-30d-5p;hsa-miR-30e-5p;hsa-miR-362-5p;hsa-miR-502-3p | 16 | CDK6 | Sponge network | 1.382 | 0.09909 | 1.055 | 0 | 0.333 |
321 | LINC00473 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-16-1-3p;hsa-miR-186-5p;hsa-miR-19b-1-5p;hsa-miR-20a-3p;hsa-miR-26b-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-452-5p;hsa-miR-454-3p;hsa-miR-590-3p | 15 | IGF1 | Sponge network | -3.931 | 0.00573 | -1.378 | 1.0E-5 | 0.333 |
322 | MAGI2-AS3 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-141-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-192-5p;hsa-miR-193b-3p;hsa-miR-197-3p;hsa-miR-200a-3p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-331-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-3928-3p;hsa-miR-421;hsa-miR-454-3p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-942-5p;hsa-miR-98-5p | 23 | IL6R | Sponge network | -2.588 | 0 | -1.861 | 0 | 0.332 |
323 | RP11-397A16.1 |
hsa-miR-107;hsa-miR-126-5p;hsa-miR-139-5p;hsa-miR-15a-5p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-181c-5p;hsa-miR-195-5p;hsa-miR-26a-5p;hsa-miR-326;hsa-miR-497-5p | 11 | ITGA2 | Sponge network | 11.276 | 0 | 1.327 | 0 | 0.331 |
324 | RP11-20D14.6 | hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-103a-2-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-1-5p;hsa-miR-19b-3p;hsa-miR-20a-3p;hsa-miR-26b-5p;hsa-miR-301a-3p | 10 | IGF1 | Sponge network | -2.188 | 0.00518 | -1.378 | 1.0E-5 | 0.33 |
325 | LINC00473 |
hsa-miR-141-5p;hsa-miR-186-5p;hsa-miR-200a-5p;hsa-miR-200b-3p;hsa-miR-200b-5p;hsa-miR-200c-3p;hsa-miR-3607-3p;hsa-miR-374a-5p;hsa-miR-374b-5p;hsa-miR-452-5p;hsa-miR-590-3p;hsa-miR-7-1-3p | 12 | ITGA1 | Sponge network | -3.931 | 0.00573 | -1.977 | 0 | 0.329 |
326 | MAGI2-AS3 |
hsa-miR-130b-5p;hsa-miR-183-5p;hsa-miR-186-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-24-2-5p;hsa-miR-27b-5p;hsa-miR-339-5p;hsa-miR-429;hsa-miR-450b-5p;hsa-miR-505-3p;hsa-miR-532-3p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-92a-3p;hsa-miR-93-3p | 16 | PRKCA | Sponge network | -2.588 | 0 | -0.975 | 0 | 0.329 |
327 | GAS6-AS2 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-186-5p;hsa-miR-200c-3p;hsa-miR-25-3p;hsa-miR-26b-5p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-421;hsa-miR-590-5p;hsa-miR-7-1-3p | 12 | PTEN | Sponge network | -1.656 | 0.00013 | -0.689 | 1.0E-5 | 0.329 |
328 | MIR497HG |
hsa-miR-106b-5p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-24-3p;hsa-miR-339-5p;hsa-miR-378a-3p;hsa-miR-629-3p;hsa-miR-877-5p;hsa-miR-93-5p | 13 | FLT1 | Sponge network | -3.004 | 0 | -1.262 | 0 | 0.329 |
329 | LINC00968 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-188-5p;hsa-miR-18a-5p;hsa-miR-19b-3p;hsa-miR-200a-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-25-3p;hsa-miR-301a-3p;hsa-miR-320b;hsa-miR-421;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-93-5p | 21 | PTEN | Sponge network | -4.827 | 0 | -0.689 | 1.0E-5 | 0.328 |
330 | CTD-2171N6.1 |
hsa-let-7d-5p;hsa-miR-185-5p;hsa-miR-186-5p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-28-5p;hsa-miR-30b-5p;hsa-miR-30c-5p;hsa-miR-3607-3p;hsa-miR-425-5p;hsa-miR-589-5p | 11 | ITGB3 | Sponge network | 1.382 | 0.09909 | -1.502 | 0 | 0.328 |
331 | RP11-325F22.2 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-141-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-193b-3p;hsa-miR-301a-3p;hsa-miR-331-3p;hsa-miR-421 | 10 | IL6R | Sponge network | -1.941 | 0.00827 | -1.861 | 0 | 0.328 |
332 | RP11-815M8.1 |
hsa-miR-103a-2-5p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-16-1-3p;hsa-miR-186-5p;hsa-miR-19b-1-5p;hsa-miR-20a-3p;hsa-miR-28-3p;hsa-miR-301a-3p;hsa-miR-320b | 10 | IGF1 | Sponge network | -1.16 | 0.16327 | -1.378 | 1.0E-5 | 0.328 |
333 | LINC00702 |
hsa-miR-141-3p;hsa-miR-193b-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-210-3p;hsa-miR-301a-3p;hsa-miR-339-5p;hsa-miR-454-3p;hsa-miR-877-5p;hsa-miR-93-5p | 10 | IGF2 | Sponge network | -3.658 | 0 | -0.69 | 0.07937 | 0.328 |
334 | DNM3OS |
hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-19b-1-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-3p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-93-3p | 13 | FGF2 | Sponge network | -1.197 | 0.01767 | -1.904 | 0 | 0.327 |
335 | PRSS51 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-141-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-200a-3p;hsa-miR-20b-5p;hsa-miR-27b-3p;hsa-miR-589-3p;hsa-miR-7-1-3p;hsa-miR-93-5p | 12 | PDGFRA | Sponge network | -1.017 | 0.33759 | -1.139 | 0 | 0.327 |
336 | DNM3OS |
hsa-let-7d-5p;hsa-let-7g-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-28-5p;hsa-miR-345-5p;hsa-miR-429;hsa-miR-616-5p;hsa-miR-93-5p;hsa-miR-96-5p | 12 | CDKN1A | Sponge network | -1.197 | 0.01767 | -0.663 | 2.0E-5 | 0.326 |
337 | CASC2 |
hsa-miR-106b-5p;hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-17-5p;hsa-miR-197-3p;hsa-miR-205-5p;hsa-miR-23a-5p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-424-5p;hsa-miR-429;hsa-miR-455-3p;hsa-miR-532-3p;hsa-miR-629-3p;hsa-miR-708-5p;hsa-miR-93-5p;hsa-miR-939-5p;hsa-miR-940 | 21 | CSF1 | Sponge network | -1.607 | 0 | -1.722 | 0 | 0.326 |
338 | CASC9 |
hsa-miR-107;hsa-miR-140-3p;hsa-miR-15a-5p;hsa-miR-195-5p;hsa-miR-1976;hsa-miR-218-5p;hsa-miR-26a-5p;hsa-miR-29a-3p;hsa-miR-29c-3p;hsa-miR-30a-5p;hsa-miR-30b-5p;hsa-miR-30d-3p;hsa-miR-30d-5p;hsa-miR-497-5p | 14 | CDK6 | Sponge network | 11.098 | 0 | 1.055 | 0 | 0.325 |
339 | XXyac-YM21GA2.4 | hsa-miR-128-3p;hsa-miR-130a-3p;hsa-miR-130b-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-197-3p;hsa-miR-23a-5p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-532-3p | 10 | CSF1 | Sponge network | -2.099 | 0.21362 | -1.722 | 0 | 0.325 |
340 | RP11-218E20.3 |
hsa-miR-107;hsa-miR-139-5p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-181c-5p;hsa-miR-26a-5p;hsa-miR-30a-5p;hsa-miR-30b-5p;hsa-miR-30d-5p;hsa-miR-374b-5p | 10 | ITGA2 | Sponge network | 3.466 | 1.0E-5 | 1.327 | 0 | 0.324 |
341 | GCSAML-AS1 |
hsa-miR-106b-5p;hsa-miR-129-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-196b-5p;hsa-miR-200a-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-421 | 11 | PDGFRA | Sponge network | -2.828 | 0.08354 | -1.139 | 0 | 0.324 |
342 | MIR497HG |
hsa-let-7d-5p;hsa-miR-106b-5p;hsa-miR-1271-5p;hsa-miR-128-3p;hsa-miR-141-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-197-3p;hsa-miR-19b-3p;hsa-miR-24-3p;hsa-miR-25-3p;hsa-miR-7-1-3p;hsa-miR-92a-1-5p | 16 | CREB3L2 | Sponge network | -3.004 | 0 | -0.289 | 0.01425 | 0.324 |
343 | RP4-644L1.2 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-130b-3p;hsa-miR-19a-3p;hsa-miR-19b-1-5p;hsa-miR-19b-3p;hsa-miR-20a-3p;hsa-miR-301a-3p;hsa-miR-454-3p | 10 | IGF1 | Sponge network | -1.329 | 0.23088 | -1.378 | 1.0E-5 | 0.323 |
344 | RP11-77A13.1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-188-5p;hsa-miR-18a-5p;hsa-miR-25-3p;hsa-miR-301a-3p;hsa-miR-454-3p;hsa-miR-93-5p | 13 | PTEN | Sponge network | -9.091 | 0 | -0.689 | 1.0E-5 | 0.322 |
345 | RP1-27K12.2 |
hsa-miR-139-5p;hsa-miR-150-5p;hsa-miR-155-5p;hsa-miR-195-5p;hsa-miR-223-3p;hsa-miR-29a-3p;hsa-miR-29b-2-5p;hsa-miR-29c-3p;hsa-miR-30a-5p;hsa-miR-375;hsa-miR-497-5p | 11 | IGF1R | Sponge network | 8.47 | 0.00163 | 0.983 | 0 | 0.322 |
346 | RP11-536K7.3 |
hsa-miR-1271-5p;hsa-miR-141-3p;hsa-miR-182-5p;hsa-miR-18a-3p;hsa-miR-3127-5p;hsa-miR-3615;hsa-miR-532-3p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-940 | 10 | GNG7 | Sponge network | -2.193 | 0.00149 | -2.411 | 0 | 0.321 |
347 | RP11-401P9.4 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-142-3p;hsa-miR-186-5p;hsa-miR-188-3p;hsa-miR-200a-3p;hsa-miR-200c-3p;hsa-miR-26b-3p;hsa-miR-301a-3p;hsa-miR-454-3p;hsa-miR-532-3p;hsa-miR-590-5p;hsa-miR-616-5p | 14 | CREB5 | Sponge network | -3.167 | 0 | -0.881 | 0.00028 | 0.321 |
348 | APCDD1L-AS1 |
hsa-miR-106a-5p;hsa-miR-130a-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-200a-3p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-3065-5p;hsa-miR-339-5p;hsa-miR-33b-5p;hsa-miR-362-3p;hsa-miR-374b-5p;hsa-miR-589-3p | 13 | PDGFRA | Sponge network | 2.007 | 0.01217 | -1.139 | 0 | 0.321 |
349 | ABCA9-AS1 |
hsa-miR-100-5p;hsa-miR-139-5p;hsa-miR-140-5p;hsa-miR-146b-5p;hsa-miR-15a-5p;hsa-miR-16-1-3p;hsa-miR-195-5p;hsa-miR-223-3p;hsa-miR-29a-3p;hsa-miR-29b-2-5p;hsa-miR-29c-3p;hsa-miR-30a-5p;hsa-miR-497-5p | 13 | IGF1R | Sponge network | 9.918 | 0 | 0.983 | 0 | 0.32 |
350 | TBX5-AS1 |
hsa-miR-130b-5p;hsa-miR-183-5p;hsa-miR-186-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-24-2-5p;hsa-miR-27b-5p;hsa-miR-450b-5p;hsa-miR-505-5p;hsa-miR-532-3p;hsa-miR-550a-3p;hsa-miR-616-5p;hsa-miR-92a-3p;hsa-miR-93-3p | 14 | PRKCA | Sponge network | -2.901 | 0 | -0.975 | 0 | 0.32 |
351 | RP5-839B4.8 |
hsa-let-7a-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-196b-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-320a;hsa-miR-320b;hsa-miR-33a-5p;hsa-miR-7-1-3p | 13 | PDGFRA | Sponge network | -6.051 | 0 | -1.139 | 0 | 0.319 |
352 | RP11-1008C21.1 |
hsa-let-7a-3p;hsa-let-7d-5p;hsa-miR-151a-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-18a-5p;hsa-miR-19b-3p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-20a-5p;hsa-miR-33a-3p;hsa-miR-629-3p;hsa-miR-940 | 13 | THBS1 | Sponge network | -2.048 | 0.00613 | -1.792 | 0 | 0.319 |
353 | AC144831.1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-17-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-505-5p;hsa-miR-576-5p;hsa-miR-93-5p | 10 | FLT1 | Sponge network | -2 | 0.00032 | -1.262 | 0 | 0.319 |
354 | PCED1B-AS1 |
hsa-miR-103a-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-25-3p;hsa-miR-301a-3p;hsa-miR-92a-3p;hsa-miR-93-5p | 14 | PTEN | Sponge network | -1.44 | 0.00116 | -0.689 | 1.0E-5 | 0.318 |
355 | RP11-401P9.4 |
hsa-let-7g-3p;hsa-miR-103a-2-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-148b-5p;hsa-miR-151a-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-193b-3p;hsa-miR-93-5p | 11 | MCL1 | Sponge network | -3.167 | 0 | -0.943 | 0 | 0.318 |
356 | GAS6-AS2 |
hsa-let-7a-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-186-5p;hsa-miR-24-3p;hsa-miR-26b-5p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-421;hsa-miR-550a-5p;hsa-miR-590-5p;hsa-miR-7-1-3p | 12 | PDGFRA | Sponge network | -1.656 | 0.00013 | -1.139 | 0 | 0.317 |
357 | RP11-401P9.4 |
hsa-let-7d-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-345-5p;hsa-miR-505-5p;hsa-miR-616-5p;hsa-miR-708-5p;hsa-miR-93-5p;hsa-miR-98-5p | 11 | CDKN1A | Sponge network | -3.167 | 0 | -0.663 | 2.0E-5 | 0.317 |
358 | RP11-701P16.5 |
hsa-miR-103a-2-5p;hsa-miR-106b-5p;hsa-miR-129-5p;hsa-miR-130b-3p;hsa-miR-135b-5p;hsa-miR-141-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-192-5p;hsa-miR-205-5p;hsa-miR-28-5p;hsa-miR-301a-3p;hsa-miR-3928-3p;hsa-miR-93-5p | 14 | IL6R | Sponge network | -5.254 | 0 | -1.861 | 0 | 0.314 |
359 | CASC2 |
hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-193b-3p;hsa-miR-19a-3p;hsa-miR-205-5p;hsa-miR-222-3p;hsa-miR-301a-3p;hsa-miR-421;hsa-miR-429;hsa-miR-450b-5p;hsa-miR-590-3p;hsa-miR-671-5p | 12 | KIT | Sponge network | -1.607 | 0 | -2.514 | 0 | 0.313 |
360 | RP11-536K7.3 |
hsa-let-7a-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-19b-1-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-3p;hsa-miR-590-3p;hsa-miR-93-3p | 11 | FGF2 | Sponge network | -2.193 | 0.00149 | -1.904 | 0 | 0.313 |
361 | RP11-359E10.1 |
hsa-let-7d-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-1271-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-25-3p;hsa-miR-616-5p | 11 | CREB3L2 | Sponge network | -1.994 | 0.00061 | -0.289 | 0.01425 | 0.313 |
362 | RP11-359M6.1 |
hsa-miR-106a-5p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-205-5p;hsa-miR-301a-3p;hsa-miR-455-3p;hsa-miR-708-5p;hsa-miR-93-5p;hsa-miR-940 | 10 | CSF1 | Sponge network | -5.933 | 0 | -1.722 | 0 | 0.311 |
363 | CTD-2135D7.5 |
hsa-miR-128-3p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-15b-5p;hsa-miR-197-3p;hsa-miR-301a-3p;hsa-miR-423-5p;hsa-miR-532-3p;hsa-miR-629-3p;hsa-miR-940 | 10 | CSF1 | Sponge network | -4.955 | 3.0E-5 | -1.722 | 0 | 0.309 |
364 | LINC00702 |
hsa-let-7f-1-3p;hsa-miR-103a-2-5p;hsa-miR-16-2-3p;hsa-miR-186-5p;hsa-miR-27b-3p;hsa-miR-33a-3p;hsa-miR-501-5p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-7-1-3p;hsa-miR-877-5p;hsa-miR-93-5p;hsa-miR-96-5p | 13 | GNB4 | Sponge network | -3.658 | 0 | -0.48 | 0.00876 | 0.309 |
365 | TBX5-AS1 |
hsa-let-7d-5p;hsa-let-7g-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-28-5p;hsa-miR-505-5p;hsa-miR-616-5p;hsa-miR-942-5p | 10 | CDKN1A | Sponge network | -2.901 | 0 | -0.663 | 2.0E-5 | 0.308 |
366 | RP11-251M1.1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-196b-5p;hsa-miR-24-3p;hsa-miR-27b-3p;hsa-miR-301a-3p;hsa-miR-320b | 11 | PDGFRA | Sponge network | -4.934 | 0 | -1.139 | 0 | 0.308 |
367 | AC011738.4 |
hsa-miR-100-5p;hsa-miR-139-5p;hsa-miR-140-3p;hsa-miR-140-5p;hsa-miR-145-5p;hsa-miR-150-5p;hsa-miR-15a-5p;hsa-miR-16-1-3p;hsa-miR-195-5p;hsa-miR-223-3p;hsa-miR-29a-3p;hsa-miR-29b-2-5p;hsa-miR-29b-3p;hsa-miR-29c-3p;hsa-miR-342-5p;hsa-miR-34a-5p;hsa-miR-497-5p;hsa-miR-532-5p | 18 | IGF1R | Sponge network | 8.148 | 0 | 0.983 | 0 | 0.307 |
368 | MEG3 |
hsa-miR-103a-2-5p;hsa-miR-16-1-3p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-1-5p;hsa-miR-19b-3p;hsa-miR-301a-3p;hsa-miR-362-5p;hsa-miR-454-3p;hsa-miR-576-5p | 10 | IGF1 | Sponge network | -0.426 | 0.41068 | -1.378 | 1.0E-5 | 0.305 |
369 | RP11-742B18.1 |
hsa-miR-139-5p;hsa-miR-140-3p;hsa-miR-146b-5p;hsa-miR-15a-5p;hsa-miR-195-5p;hsa-miR-223-3p;hsa-miR-29a-3p;hsa-miR-29b-2-5p;hsa-miR-29c-3p;hsa-miR-362-3p;hsa-miR-497-5p | 11 | IGF1R | Sponge network | 8.195 | 0 | 0.983 | 0 | 0.305 |
370 | RP11-401P9.4 |
hsa-miR-141-3p;hsa-miR-193b-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-210-3p;hsa-miR-301a-3p;hsa-miR-339-5p;hsa-miR-454-3p;hsa-miR-877-5p;hsa-miR-93-5p | 10 | IGF2 | Sponge network | -3.167 | 0 | -0.69 | 0.07937 | 0.305 |
371 | RP11-532F6.3 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-200c-3p;hsa-miR-25-3p;hsa-miR-28-5p;hsa-miR-590-3p | 10 | PTEN | Sponge network | -2.728 | 0 | -0.689 | 1.0E-5 | 0.304 |
372 | CASC2 |
hsa-miR-15b-5p;hsa-miR-18a-3p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-320b;hsa-miR-33a-3p;hsa-miR-421;hsa-miR-424-5p;hsa-miR-429;hsa-miR-452-5p;hsa-miR-455-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-7-1-3p;hsa-miR-944 | 16 | FGF7 | Sponge network | -1.607 | 0 | -2.211 | 0 | 0.303 |
373 | DNM3OS |
hsa-miR-130a-3p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-182-5p;hsa-miR-301a-3p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-454-3p;hsa-miR-501-5p;hsa-miR-532-3p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-616-3p;hsa-miR-629-3p | 14 | COL4A4 | Sponge network | -1.197 | 0.01767 | -3.737 | 0 | 0.303 |
374 | RP11-401P9.4 |
hsa-miR-103a-2-5p;hsa-miR-130b-5p;hsa-miR-183-5p;hsa-miR-186-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-24-2-5p;hsa-miR-27b-5p;hsa-miR-339-5p;hsa-miR-505-5p;hsa-miR-532-3p;hsa-miR-616-5p;hsa-miR-93-3p | 13 | PRKCA | Sponge network | -3.167 | 0 | -0.975 | 0 | 0.301 |
375 | RP11-401P9.4 |
hsa-let-7d-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-1271-5p;hsa-miR-128-3p;hsa-miR-141-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-18a-3p;hsa-miR-197-3p;hsa-miR-19b-3p;hsa-miR-200a-3p;hsa-miR-616-5p | 15 | CREB3L2 | Sponge network | -3.167 | 0 | -0.289 | 0.01425 | 0.301 |
376 | MEG3 |
hsa-miR-106a-5p;hsa-miR-1301-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-200c-3p;hsa-miR-532-3p;hsa-miR-589-3p;hsa-miR-590-5p;hsa-miR-629-3p | 10 | PIK3R1 | Sponge network | -0.426 | 0.41068 | -0.906 | 0 | 0.3 |
377 | AL035610.1 | hsa-miR-100-5p;hsa-miR-139-5p;hsa-miR-140-3p;hsa-miR-146b-5p;hsa-miR-150-5p;hsa-miR-155-5p;hsa-miR-29a-3p;hsa-miR-29c-3p;hsa-miR-30a-5p;hsa-miR-497-5p | 10 | IGF1R | Sponge network | 5.754 | 0.00079 | 0.983 | 0 | 0.299 |
378 | AC144831.1 |
hsa-miR-103a-2-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-141-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-192-5p;hsa-miR-301a-3p;hsa-miR-3928-3p;hsa-miR-576-5p;hsa-miR-93-5p;hsa-miR-942-5p | 14 | IL6R | Sponge network | -2 | 0.00032 | -1.861 | 0 | 0.299 |
379 | PWAR6 |
hsa-miR-1301-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-200c-3p;hsa-miR-22-5p;hsa-miR-532-3p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-629-3p | 10 | PIK3R1 | Sponge network | -1.994 | 6.0E-5 | -0.906 | 0 | 0.298 |
380 | RP11-166D19.1 |
hsa-miR-130b-5p;hsa-miR-186-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-24-2-5p;hsa-miR-27b-5p;hsa-miR-339-5p;hsa-miR-429;hsa-miR-450b-5p;hsa-miR-505-3p;hsa-miR-532-3p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-92a-3p;hsa-miR-93-3p | 15 | PRKCA | Sponge network | -1.481 | 0.00084 | -0.975 | 0 | 0.297 |
381 | RP11-166D19.1 |
hsa-miR-106b-5p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-188-5p;hsa-miR-200c-3p;hsa-miR-532-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-629-3p | 10 | PIK3R1 | Sponge network | -1.481 | 0.00084 | -0.906 | 0 | 0.296 |
382 | APCDD1L-AS1 |
hsa-miR-101-3p;hsa-miR-107;hsa-miR-148b-3p;hsa-miR-15a-5p;hsa-miR-16-5p;hsa-miR-185-5p;hsa-miR-218-5p;hsa-miR-29b-3p;hsa-miR-29c-3p;hsa-miR-338-3p;hsa-miR-374b-5p;hsa-miR-497-5p | 12 | CDK6 | Sponge network | 2.007 | 0.01217 | 1.055 | 0 | 0.296 |
383 | RP11-536K7.3 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-149-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-24-3p;hsa-miR-339-5p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-629-3p;hsa-miR-744-3p;hsa-miR-877-5p | 15 | FLT1 | Sponge network | -2.193 | 0.00149 | -1.262 | 0 | 0.294 |
384 | CASC2 |
hsa-miR-128-3p;hsa-miR-15b-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-205-5p;hsa-miR-224-5p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-331-5p;hsa-miR-421;hsa-miR-424-5p;hsa-miR-429;hsa-miR-452-5p;hsa-miR-455-3p;hsa-miR-590-3p | 15 | RELN | Sponge network | -1.607 | 0 | -2.872 | 0 | 0.279 |
385 | CASC2 |
hsa-miR-141-5p;hsa-miR-200a-5p;hsa-miR-200b-3p;hsa-miR-200b-5p;hsa-miR-200c-3p;hsa-miR-21-5p;hsa-miR-320b;hsa-miR-421;hsa-miR-429;hsa-miR-452-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-7-1-3p;hsa-miR-944 | 14 | ITGA1 | Sponge network | -1.607 | 0 | -1.977 | 0 | 0.269 |
386 | DNM1P35 |
hsa-let-7a-5p;hsa-miR-139-5p;hsa-miR-142-5p;hsa-miR-143-3p;hsa-miR-145-5p;hsa-miR-1976;hsa-miR-26a-5p;hsa-miR-326;hsa-miR-330-5p;hsa-miR-338-3p | 10 | ITGB8 | Sponge network | 0.956 | 0 | 2.27 | 0 | 0.26 |
387 | DNM1P35 |
hsa-miR-100-5p;hsa-miR-139-5p;hsa-miR-140-5p;hsa-miR-145-3p;hsa-miR-145-5p;hsa-miR-150-5p;hsa-miR-195-5p;hsa-miR-223-3p;hsa-miR-29a-3p;hsa-miR-29c-3p;hsa-miR-497-5p | 11 | IGF1R | Sponge network | 0.956 | 0 | 0.983 | 0 | 0.257 |
388 | HAR1A |
hsa-miR-103a-2-5p;hsa-miR-130b-5p;hsa-miR-183-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-224-5p;hsa-miR-24-2-5p;hsa-miR-27b-5p;hsa-miR-760;hsa-miR-93-3p | 10 | PRKCA | Sponge network | -1.641 | 0 | -0.975 | 0 | 0.253 |
389 | CASC2 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-15b-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-188-5p;hsa-miR-18a-5p;hsa-miR-19a-3p;hsa-miR-200a-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-301a-3p;hsa-miR-320b;hsa-miR-421;hsa-miR-425-5p;hsa-miR-429;hsa-miR-452-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-7-1-3p;hsa-miR-92a-3p;hsa-miR-93-5p | 23 | PTEN | Sponge network | -1.607 | 0 | -0.689 | 1.0E-5 | 0.251 |