This regulatory network was inferred from the input dataset. The miRNAs and mRNAs are
presented as round and rectangle nodes respectively. The numerical value popped up upon mouse over the gene node is the log2 transformed fold-change of the gene expression between the two groups. All of the nodes are clickable, and the detailed information of the miRNAs/mRNAs and related cancer pathway will be displayed in another window. The edges between nodes are supported by both interactions (predicted or experimentally verified) and correlations learnt from cancer dataset. The numerical value popped up upon mouse over the edge is the correlation beat value (effect size) between the two nodes. The experimental evidences of the edges reported in previous cancer studies are highlighted by red/orange color. All of these information can be accessed by the "mouse-over" action. This network shows a full map of the miRNA-mRNA regulation of the input gene list(s), and the hub miRNAs (with the high network degree/betweenness centrality) would be the potential cancer drivers or tumor suppressors. The full result table can be accessed in the "Regulations" tab.
"miRNACancerMAP" is also a network visualization tool for users to draw their regulatory network by personal customization. Users can set the complexity of the network by limiting the number of nodes or edges. And the color of the nodes can be defined by different categories of the mRNAs and miRNAs, such as Gene-Ontology, pathway, and expression status. Users can also select to use network degree or network betweenness centrality to define the node size. And edges can be black or colored by the correlation. Purple edge means negative correlation (mostly found between miRNA and mRNA), and blue edge means positive correlation (found in PPI or miRNA-miRNA sponge effect). We can also add the protein-protein interactions (PPI) into the network. This result will show the cluster of genes regulated by some specific miRNAs. Additionally, miRNA-miRNA edges can be added by the "miRNA sponge" button, presenting some clusters of miRNAs that have the interactions via sponge effect.
Num | microRNA | Gene | miRNA log2FC | miRNA pvalue | Gene log2FC | Gene pvalue | Interaction | Correlation beta | Correlation P-value | PMID | Reported in cancer studies |
---|---|---|---|---|---|---|---|---|---|---|---|
1 | hsa-miR-106b-5p | AKT3 | 2.81 | 0 | -3.33 | 1.0E-5 | miRNATAP | -0.41 | 1.0E-5 | NA | |
2 | hsa-miR-142-3p | AKT3 | 4.35 | 0 | -3.33 | 1.0E-5 | miRanda | -0.16 | 0.00934 | NA | |
3 | hsa-miR-15a-5p | AKT3 | 2.05 | 0 | -3.33 | 1.0E-5 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.37 | 0.00021 | NA | |
4 | hsa-miR-15b-5p | AKT3 | 3.32 | 0 | -3.33 | 1.0E-5 | miRNATAP | -0.25 | 0.00571 | NA | |
5 | hsa-miR-16-5p | AKT3 | 2.94 | 0 | -3.33 | 1.0E-5 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.31 | 0.00086 | NA | |
6 | hsa-miR-29b-3p | AKT3 | 0.67 | 0.23406 | -3.33 | 1.0E-5 | miRNATAP | -0.28 | 0.00031 | 26512921 | MicroRNA 29B mir 29b regulates the Warburg effect in ovarian cancer by targeting AKT2 and AKT3 |
7 | hsa-miR-3065-5p | AKT3 | 2.14 | 0.06094 | -3.33 | 1.0E-5 | mirMAP | -0.22 | 0 | NA | |
8 | hsa-miR-362-3p | AKT3 | 0.68 | 0.22615 | -3.33 | 1.0E-5 | miRanda | -0.25 | 0.00124 | NA | |
9 | hsa-miR-501-3p | AKT3 | 1.72 | 0.00759 | -3.33 | 1.0E-5 | miRNATAP | -0.18 | 0.00733 | NA | |
10 | hsa-miR-93-5p | AKT3 | 2.66 | 0 | -3.33 | 1.0E-5 | miRNATAP | -0.33 | 0.00021 | NA | |
11 | hsa-miR-3065-5p | ANGPT1 | 2.14 | 0.06094 | -3.47 | 0.00041 | mirMAP | -0.19 | 0.00141 | NA | |
12 | hsa-miR-429 | ANGPT1 | 6.4 | 0 | -3.47 | 0.00041 | miRanda | -0.28 | 0.00011 | NA | |
13 | hsa-miR-142-5p | ANGPT2 | 3.96 | 0 | -1.02 | 0.17676 | MirTarget | -0.17 | 0.00375 | NA | |
14 | hsa-miR-34c-5p | ANGPT2 | 2.65 | 0.01574 | -1.02 | 0.17676 | miRanda | -0.1 | 0.00939 | NA | |
15 | hsa-miR-429 | ANGPT2 | 6.4 | 0 | -1.02 | 0.17676 | miRanda | -0.16 | 0.00407 | NA | |
16 | hsa-miR-664a-3p | ANGPT2 | 0.25 | 0.56171 | -1.02 | 0.17676 | mirMAP | -0.29 | 0.00448 | NA | |
17 | hsa-miR-221-3p | ATF2 | 0.94 | 0.17475 | 0.26 | 0.63833 | MirTarget | -0.17 | 0.00016 | NA | |
18 | hsa-miR-222-3p | ATF2 | 1.55 | 0.0223 | 0.26 | 0.63833 | MirTarget | -0.17 | 0.00015 | NA | |
19 | hsa-miR-26a-5p | ATF2 | -0.35 | 0.36204 | 0.26 | 0.63833 | MirTarget; miRNATAP | -0.22 | 0.0074 | NA | |
20 | hsa-miR-29a-5p | ATF2 | 0.07 | 0.88413 | 0.26 | 0.63833 | MirTarget; miRNATAP | -0.21 | 0.00035 | NA | |
21 | hsa-miR-30e-5p | ATF2 | 0.78 | 0.03467 | 0.26 | 0.63833 | mirMAP | -0.26 | 0.00214 | NA | |
22 | hsa-miR-590-3p | ATF2 | 2.35 | 0 | 0.26 | 0.63833 | MirTarget; miRanda; mirMAP; miRNATAP | -0.23 | 0.00018 | NA | |
23 | hsa-miR-320a | ATF6B | -0.91 | 0.05656 | 0.37 | 0.24574 | miRanda | -0.1 | 0.00628 | NA | |
24 | hsa-miR-16-2-3p | BCL2 | 3.8 | 0 | -3.06 | 1.0E-5 | mirMAP | -0.2 | 0.00813 | NA | |
25 | hsa-miR-16-5p | BCL2 | 2.94 | 0 | -3.06 | 1.0E-5 | miRNAWalker2 validate; miRTarBase | -0.27 | 0.00125 | 21336967; 24447552; 18449891; 25435430; 24598659; 18931683; 22966344; 25623762 | P glycoprotein enhances radiation induced apoptotic cell death through the regulation of miR 16 and Bcl 2 expressions in hepatocellular carcinoma cells; RHepG2 cells the multidrug resistant subline of human hepatocellular carcinoma HepG2 cells expressed higher levels of Pgp as well as miR-16 and lower level of Bcl-2 than the parental cells; On the other hand ectopic mdr1 expression enhanced radiation-induced apoptosis in HepG2 cells SK-HEP-1 cells MiHa cells and furthermore induced miR-16 and suppressed its target gene Bcl-2 in HepG2 cells; Moreover the enhancement effects of Pgp and miR-16 on radiation-induced apoptosis were counteracted by overexpression of Bcl-2;To study the expression of miR-16 and bcl-2 in T lymphoblastic lymphoma/leukemia T-LBL/ALL and its relationship to prognosis; The relationship of miR-16 and bcl-2 was significantP = 0.042χ2 = 4.147; The relationship of miR-16 and bcl-2 might suggested that gene regulation may be influenced by them;miR 15b and miR 16 modulate multidrug resistance by targeting BCL2 in human gastric cancer cells; The downregulation of miR-15b and miR-16 in SGC7901/VCR cells was concurrent with the upregulation of Bcl-2 protein; Taken together our findings suggest that miR-15b and miR-16 could play a role in the development of MDR in gastric cancer cells at least in part by modulation of apoptosis via targeting BCL2;We demonstrated that anti-apoptotic protein Bcl-2 was directly targeted miR-16 in paclitaxel resistant lung cancer cells; Combined overexpression of miR-16 and miR-17 greatly reduced Beclin-1 and Bcl-2 expressions respectively; miR-17 overexpression reduced cytoprotective autophagy by targeting Beclin-1 whereas overexpression of miR-16 potentiated paclitaxel induced apoptotic cell death by inhibiting anti-apoptotic protein Bcl-2;The miR-16 expression correlated with BCL-2 protein r = 0.51 P < 0.05;MicroRNAs miRNAs are noncoding small RNAs that repress protein translation by targeting specific messenger RNAs miR-15a and miR-16-1 act as putative tumor suppressors by targeting the oncogene BCL2;The overall objective of our investigation was to assess whether miRNA-16 miR-16 is involved in the regulation of critical genes such as BCL2 that control the sensitivity of pancreatic cancer cells to apoptosis; This study showed that the ectopic overexpression of miR-16 may be therapeutically beneficial as is evidenced by impaired cell survival with concomitant attenuation of anti-apoptotic protein Bcl-2; Moreover the luciferase reporter assay suggested that miR-16 post-transcriptionally regulates Bcl-2 expression in pancreatic cancer cells through the target sites of the 3' untranslated region of this gene;miR 15a and miR 16 modulate drug resistance by targeting bcl 2 in human colon cancer cells; To investigate the reversal effect of targeted modulation of bcl-2 expression by miR-15a and miR-16 on drug resistance of human colon cancer cells |
26 | hsa-miR-192-5p | BCL2 | 1.78 | 0.11349 | -3.06 | 1.0E-5 | miRNAWalker2 validate | -0.13 | 0.00025 | 26550150 | MicroRNA 192 regulates chemo resistance of lung adenocarcinoma for gemcitabine and cisplatin combined therapy by targeting Bcl 2; In this paper we try to test whether miR-192 regulates chemo-resistance in human carcinoma A549 mice model by targeting Bcl-2; MTT assay real-time RT-PCR western blotting assay were used to investigate miR-192 expression levels cell viability ratio and Bcl-2 protein expression levels; Bcl-2 mRNA and protein expression levels up-regulated in miR-192 inhibitor treated tumor; Bcl-2 is a key regulator for miR-192 related chemotherapy resistance; In this study we demonstrate that miR-192 regulates chemoresistance for gemcitabine and cisplatin combined chemotherapy in human adenocarcinoma lung cancer A549 cells and Bcl-2 is the target of miR-192 |
27 | hsa-miR-200a-5p | BCL2 | 6.52 | 0 | -3.06 | 1.0E-5 | mirMAP | -0.2 | 0.00037 | NA | |
28 | hsa-miR-200b-5p | BCL2 | 6.82 | 0 | -3.06 | 1.0E-5 | mirMAP | -0.2 | 0.00019 | NA | |
29 | hsa-miR-200c-3p | BCL2 | 6.47 | 0 | -3.06 | 1.0E-5 | miRNAWalker2 validate; miRTarBase; mirMAP | -0.2 | 0.00073 | NA | |
30 | hsa-miR-21-5p | BCL2 | 2.65 | 0 | -3.06 | 1.0E-5 | miRNAWalker2 validate; miRTarBase | -0.48 | 4.0E-5 | 21468550; 25994220; 25381586; 26555418; 23359184; 22964582; 21376256 | 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;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 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 |
31 | hsa-miR-215-5p | BCL2 | 3.67 | 0.00295 | -3.06 | 1.0E-5 | miRNAWalker2 validate | -0.14 | 1.0E-5 | NA | |
32 | hsa-miR-24-2-5p | BCL2 | 2.07 | 6.0E-5 | -3.06 | 1.0E-5 | miRNAWalker2 validate; miRTarBase | -0.36 | 0 | NA | |
33 | hsa-miR-3065-5p | BCL2 | 2.14 | 0.06094 | -3.06 | 1.0E-5 | mirMAP | -0.17 | 0.00011 | NA | |
34 | hsa-miR-338-5p | BCL2 | -0.11 | 0.89468 | -3.06 | 1.0E-5 | PITA | -0.15 | 0.00173 | NA | |
35 | hsa-miR-33b-5p | BCL2 | 4.78 | 0 | -3.06 | 1.0E-5 | miRTarBase; mirMAP | -0.12 | 0.00899 | NA | |
36 | hsa-miR-365a-3p | BCL2 | 0.26 | 0.65432 | -3.06 | 1.0E-5 | miRNAWalker2 validate; miRTarBase | -0.39 | 0 | NA | |
37 | hsa-miR-429 | BCL2 | 6.4 | 0 | -3.06 | 1.0E-5 | miRNAWalker2 validate; miRTarBase; PITA; mirMAP | -0.16 | 0.00181 | 23999873; 26513239; 26511969 | MiR 429 up regulation induces apoptosis and suppresses invasion by targeting Bcl 2 and SP 1 in esophageal carcinoma; Subsequent Western blotting and luciferase reporter assays showed that miR-429 can bind to putative binding sites within the Bcl-2 and SP1 mRNA 3' untranslated regions UTRs to reduce their expression; Up-regulation of miR-429 inhibits invasion and promotes apoptosis in EC cells by targeting Bcl-2 and SP1; Our findings suggest that Bcl-2 and SP1 may serve as major targets of miR-429;MiR 429 Induces Gastric Carcinoma Cell Apoptosis Through Bcl 2; Here we studied the levels of miR-429 and anti-apoptotic protein Bcl-2 in GC specimens; We performed bioinformatics analyses and used luciferase-reporter assay to analyze the relationship between miR-429 and Bcl-2 in GC cells; MiR-429 levels were significantly decreased and Bcl-2 levels were significantly increased in GC specimens compared to the paired adjacent non-tumor gastric tissue; Moreover the levels of miR-429 and Bcl-2 inversely correlated in GC specimens; Bioinformatics analyses showed that miR-429 targeted the 3'-UTR of Bcl-2 mRNA to inhibit its translation which was confirmed by luciferase-reporter assay;MiR 429 induces apoptosis of glioblastoma cell through Bcl 2; Here we analyzed the levels of miR-429 and anti-apoptotic protein Bcl-2 in GBM specimens; We combined bioinformatics analyses and luciferase reporter assay to determine the relationship between miR-429 and Bcl-2 in GBM cells; We found that miR-429 levels were significantly decreased and Bcl-2 levels were significantly increased in GBM specimens compared to the paired adjacent non-tumor brain tissue; Moreover the levels of miR-429 and Bcl-2 inversely correlated; MiR-429 targeted the 3'-UTR of Bcl-2 mRNA to inhibit its translation |
38 | hsa-miR-582-5p | BCL2 | 0.69 | 0.44776 | -3.06 | 1.0E-5 | PITA | -0.13 | 0.00231 | NA | |
39 | hsa-miR-629-5p | BCL2 | 1.57 | 0.01157 | -3.06 | 1.0E-5 | mirMAP | -0.25 | 7.0E-5 | NA | |
40 | hsa-miR-7-5p | BCL2 | 3.6 | 0.00068 | -3.06 | 1.0E-5 | miRNAWalker2 validate; miRTarBase; mirMAP | -0.12 | 0.00725 | 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 |
41 | hsa-miR-342-3p | BCL2L1 | 1.31 | 0.02072 | 0.39 | 0.37256 | PITA; miRanda; miRNATAP | -0.13 | 0.00344 | NA | |
42 | hsa-miR-30a-5p | BCL2L11 | -0.77 | 0.32049 | 1.51 | 0.0002 | miRNATAP | -0.12 | 4.0E-5 | NA | |
43 | hsa-miR-1-3p | BDNF | -3.85 | 1.0E-5 | 1.93 | 0.15403 | miRTarBase; MirTarget | -0.24 | 0.007 | NA | |
44 | hsa-miR-146b-5p | BDNF | 1.88 | 0.00074 | 1.93 | 0.15403 | miRanda | -0.4 | 0.00389 | NA | |
45 | hsa-let-7a-5p | CCND1 | 0.15 | 0.64531 | 0.15 | 0.87753 | TargetScan; miRNATAP | -0.54 | 0.00245 | NA | |
46 | hsa-miR-106a-5p | CCND1 | 3.99 | 0 | 0.15 | 0.87753 | MirTarget; miRNATAP | -0.43 | 0 | NA | |
47 | hsa-miR-15a-5p | CCND1 | 2.05 | 0 | 0.15 | 0.87753 | miRNAWalker2 validate; miRTarBase; MirTarget; miRNATAP | -0.35 | 0.00776 | 22922827 | CCND1 has been found to be a target of miR-15a and miR-16-1 through analysis of complementary sequences between microRNAs and CCND1 mRNA; Moreover the transcription of CCND1 is suppressed by miR-15a and miR-16-1 via direct binding to the CCND1 3'-untranslated region 3'-UTR |
48 | hsa-miR-15b-5p | CCND1 | 3.32 | 0 | 0.15 | 0.87753 | miRNAWalker2 validate; miRTarBase; MirTarget; miRNATAP | -0.42 | 0.00029 | NA | |
49 | hsa-miR-20b-5p | CCND1 | 4.57 | 5.0E-5 | 0.15 | 0.87753 | MirTarget; miRNATAP | -0.31 | 0 | NA | |
50 | hsa-miR-34a-5p | CCND1 | 0.83 | 0.04775 | 0.15 | 0.87753 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.42 | 0.00174 | 25792709; 21399894 | This inhibition of proliferation was associated with a decrease in cyclin D1 levels orchestrated principally by HNF-4α a target of miR-34a considered to act as a tumour suppressor in the liver;Quantitative PCR and western analysis confirmed decreased expression of two genes BCL-2 and CCND1 in docetaxel-resistant cells which are both targeted by miR-34a |
51 | hsa-miR-497-5p | CCND1 | -1.44 | 0.02251 | 0.15 | 0.87753 | MirTarget; miRNATAP | -0.25 | 0.00498 | 21350001 | Raf-1 and Ccnd1 were identified as novel direct targets of miR-195 and miR-497 miR-195/497 expression levels in clinical specimens were found to be correlated inversely with malignancy of breast cancer |
52 | hsa-miR-106a-5p | CCND2 | 3.99 | 0 | -2.81 | 0.0014 | miRNATAP | -0.44 | 0 | NA | |
53 | hsa-miR-106b-5p | CCND2 | 2.81 | 0 | -2.81 | 0.0014 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.31 | 0.00374 | NA | |
54 | hsa-miR-10a-3p | CCND2 | 0.97 | 0.31667 | -2.81 | 0.0014 | mirMAP | -0.2 | 0.00011 | NA | |
55 | hsa-miR-130b-5p | CCND2 | 3.74 | 0 | -2.81 | 0.0014 | mirMAP | -0.46 | 0 | NA | |
56 | hsa-miR-141-3p | CCND2 | 7.3 | 0 | -2.81 | 0.0014 | MirTarget; TargetScan | -0.24 | 0.00021 | NA | |
57 | hsa-miR-15b-5p | CCND2 | 3.32 | 0 | -2.81 | 0.0014 | miRNATAP | -0.53 | 0 | NA | |
58 | hsa-miR-16-2-3p | CCND2 | 3.8 | 0 | -2.81 | 0.0014 | mirMAP | -0.29 | 0.00207 | NA | |
59 | hsa-miR-182-5p | CCND2 | 5.87 | 0 | -2.81 | 0.0014 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.28 | 2.0E-5 | NA | |
60 | hsa-miR-183-5p | CCND2 | 6.62 | 0 | -2.81 | 0.0014 | miRNATAP | -0.29 | 0 | NA | |
61 | hsa-miR-191-5p | CCND2 | 1.59 | 0.00074 | -2.81 | 0.0014 | MirTarget | -0.32 | 0.00314 | NA | |
62 | hsa-miR-200a-3p | CCND2 | 6.34 | 0 | -2.81 | 0.0014 | MirTarget | -0.41 | 0 | NA | |
63 | hsa-miR-20b-5p | CCND2 | 4.57 | 5.0E-5 | -2.81 | 0.0014 | miRNATAP | -0.3 | 0 | NA | |
64 | hsa-miR-224-3p | CCND2 | 2.85 | 0.00018 | -2.81 | 0.0014 | mirMAP | -0.22 | 0.00101 | NA | |
65 | hsa-miR-28-5p | CCND2 | -0.82 | 0.02212 | -2.81 | 0.0014 | miRanda | -0.43 | 0.00273 | NA | |
66 | hsa-miR-3065-3p | CCND2 | 1.89 | 0.03082 | -2.81 | 0.0014 | MirTarget; miRNATAP | -0.21 | 0.00027 | NA | |
67 | hsa-miR-3065-5p | CCND2 | 2.14 | 0.06094 | -2.81 | 0.0014 | mirMAP | -0.2 | 0.00026 | NA | |
68 | hsa-miR-30d-3p | CCND2 | -0.07 | 0.85742 | -2.81 | 0.0014 | mirMAP | -0.55 | 1.0E-5 | NA | |
69 | hsa-miR-324-3p | CCND2 | 1.51 | 0.00384 | -2.81 | 0.0014 | miRNAWalker2 validate | -0.44 | 0 | NA | |
70 | hsa-miR-33a-3p | CCND2 | 2.06 | 0.00156 | -2.81 | 0.0014 | MirTarget | -0.27 | 0.00041 | NA | |
71 | hsa-miR-378a-3p | CCND2 | 1.47 | 0.04667 | -2.81 | 0.0014 | miRNAWalker2 validate | -0.19 | 0.00601 | NA | |
72 | hsa-miR-429 | CCND2 | 6.4 | 0 | -2.81 | 0.0014 | miRNATAP | -0.46 | 0 | NA | |
73 | hsa-miR-497-5p | CCND2 | -1.44 | 0.02251 | -2.81 | 0.0014 | MirTarget; miRNATAP | -0.27 | 0.00058 | NA | |
74 | hsa-miR-550a-5p | CCND2 | 1.22 | 0.06138 | -2.81 | 0.0014 | MirTarget | -0.22 | 0.00363 | NA | |
75 | hsa-miR-660-5p | CCND2 | -0.07 | 0.88525 | -2.81 | 0.0014 | mirMAP | -0.29 | 0.00793 | NA | |
76 | hsa-miR-9-3p | CCND2 | 1.69 | 0.12517 | -2.81 | 0.0014 | MirTarget; mirMAP; miRNATAP | -0.14 | 0.00185 | NA | |
77 | hsa-miR-93-5p | CCND2 | 2.66 | 0 | -2.81 | 0.0014 | miRNATAP | -0.48 | 0 | NA | |
78 | hsa-miR-96-5p | CCND2 | 5.63 | 0 | -2.81 | 0.0014 | TargetScan; miRNATAP | -0.24 | 0.0003 | NA | |
79 | hsa-miR-27b-3p | CCND3 | -0.09 | 0.85847 | -0.54 | 0.12437 | miRNAWalker2 validate | -0.14 | 0.00019 | NA | |
80 | hsa-miR-429 | CCND3 | 6.4 | 0 | -0.54 | 0.12437 | miRNATAP | -0.11 | 1.0E-5 | NA | |
81 | hsa-miR-96-5p | CCND3 | 5.63 | 0 | -0.54 | 0.12437 | TargetScan | -0.12 | 1.0E-5 | NA | |
82 | hsa-miR-125b-5p | CCNE1 | -2.01 | 0.00516 | 3.91 | 0 | miRNAWalker2 validate | -0.13 | 0.00065 | NA | |
83 | hsa-miR-195-5p | CCNE1 | -1.59 | 0.01691 | 3.91 | 0 | miRNAWalker2 validate; MirTarget; miRNATAP | -0.12 | 0.0047 | 24402230 | Furthermore through qPCR and western blot assays we showed that overexpression of miR-195-5p reduced CCNE1 mRNA and protein levels respectively |
84 | hsa-miR-26a-5p | CCNE1 | -0.35 | 0.36204 | 3.91 | 0 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.18 | 0.00988 | 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 |
85 | hsa-miR-497-5p | CCNE1 | -1.44 | 0.02251 | 3.91 | 0 | MirTarget; miRNATAP | -0.13 | 0.00315 | 24909281; 24112607; 25909221 | 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;Western blot assays confirmed that overexpression of miR-497 reduced cyclin E1 protein levels; Inhibited cellular growth suppressed cellular migration and invasion and G1 cell cycle arrest were observed upon overexpression of miR-497 in cells possibly by targeting cyclin E1;The effect of simultaneous overexpression of miR-497 and miR-34a on the inhibition of cell proliferation colony formation and tumor growth and the downregulation of cyclin E1 was stronger than the effect of each miRNA alone; The synergistic actions of miR-497 and miR-34a partly correlated with cyclin E1 levels; These results indicate cyclin E1 is downregulated by both miR-497 and miR-34a which synergistically retard the growth of human lung cancer cells |
86 | hsa-miR-28-3p | CCNE2 | -0.99 | 0.01882 | 4.78 | 0 | PITA; miRNATAP | -0.21 | 0.00739 | NA | |
87 | hsa-miR-30a-5p | CCNE2 | -0.77 | 0.32049 | 4.78 | 0 | miRNATAP | -0.23 | 0 | NA | |
88 | hsa-miR-140-5p | CDK2 | -0.63 | 0.12667 | 1.42 | 2.0E-5 | miRanda | -0.12 | 0.00814 | NA | |
89 | hsa-let-7a-5p | CDK6 | 0.15 | 0.64531 | 0.5 | 0.55124 | miRNAWalker2 validate; miRTarBase; TargetScan | -0.65 | 2.0E-5 | NA | |
90 | hsa-let-7b-5p | CDK6 | -0.19 | 0.65188 | 0.5 | 0.55124 | miRNAWalker2 validate; miRTarBase | -0.47 | 5.0E-5 | NA | |
91 | hsa-miR-101-3p | CDK6 | -1.12 | 0.02009 | 0.5 | 0.55124 | mirMAP | -0.42 | 2.0E-5 | NA | |
92 | hsa-miR-106a-5p | CDK6 | 3.99 | 0 | 0.5 | 0.55124 | mirMAP | -0.39 | 0 | NA | |
93 | hsa-miR-141-3p | CDK6 | 7.3 | 0 | 0.5 | 0.55124 | TargetScan; miRNATAP | -0.2 | 0.0009 | NA | |
94 | hsa-miR-148b-3p | CDK6 | 1.76 | 0 | 0.5 | 0.55124 | mirMAP | -0.47 | 0.00118 | NA | |
95 | hsa-miR-200a-3p | CDK6 | 6.34 | 0 | 0.5 | 0.55124 | miRNATAP | -0.35 | 0 | 24009066 | microRNA 200a is an independent prognostic factor of hepatocellular carcinoma and induces cell cycle arrest by targeting CDK6 |
96 | hsa-miR-200b-3p | CDK6 | 5.56 | 0 | 0.5 | 0.55124 | mirMAP | -0.39 | 0 | NA | |
97 | hsa-miR-20b-5p | CDK6 | 4.57 | 5.0E-5 | 0.5 | 0.55124 | mirMAP | -0.28 | 0 | 26166554 | The transfection of miR-20b into EJ cells induced G1 phase cell cycle arrest via the decreased expression of cyclin D1 CDK2 and CDK6 without affecting another G1 phase cell cycle regulator cyclin E |
98 | hsa-miR-30a-5p | CDK6 | -0.77 | 0.32049 | 0.5 | 0.55124 | mirMAP | -0.17 | 0.00517 | NA | |
99 | hsa-miR-30d-5p | CDK6 | 0.3 | 0.38019 | 0.5 | 0.55124 | mirMAP | -0.5 | 0.00043 | NA | |
100 | hsa-miR-30e-5p | CDK6 | 0.78 | 0.03467 | 0.5 | 0.55124 | mirMAP | -0.54 | 4.0E-5 | NA | |
101 | hsa-miR-34a-5p | CDK6 | 0.83 | 0.04775 | 0.5 | 0.55124 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.36 | 0.00175 | 21702042; 26104764 | Molecular analyses identified Cdk6 and sirtuin SIRT-1 as being targeted by miR-34a in MI-TCC cells however inhibition of Cdk6 and SIRT-1 was not as effective as pre-miR-34a in mediating chemosensitization;The expression of microRNA 34a is inversely correlated with c MET and CDK6 and has a prognostic significance in lung adenocarcinoma patients; We found significant inverse correlations between miR-34a and c-MET R = -0.316 P = 0.028 and CDK6 expression R = -0.4582 P = 0.004 |
102 | hsa-miR-362-5p | CDK6 | -1.22 | 0.04527 | 0.5 | 0.55124 | mirMAP | -0.29 | 0.00026 | NA | |
103 | hsa-miR-429 | CDK6 | 6.4 | 0 | 0.5 | 0.55124 | mirMAP; miRNATAP | -0.25 | 4.0E-5 | NA | |
104 | hsa-miR-497-5p | CDK6 | -1.44 | 0.02251 | 0.5 | 0.55124 | miRNATAP | -0.31 | 3.0E-5 | NA | |
105 | hsa-miR-502-3p | CDK6 | -0.1 | 0.80889 | 0.5 | 0.55124 | PITA; miRNATAP | -0.42 | 0.00027 | NA | |
106 | hsa-miR-592 | CDK6 | 2.8 | 0.02935 | 0.5 | 0.55124 | mirMAP | -0.23 | 0 | NA | |
107 | hsa-miR-660-5p | CDK6 | -0.07 | 0.88525 | 0.5 | 0.55124 | mirMAP | -0.37 | 0.00036 | NA | |
108 | hsa-let-7e-5p | CDKN1A | -0.11 | 0.81474 | 0.58 | 0.35758 | MirTarget | -0.27 | 0.00026 | NA | |
109 | hsa-let-7g-5p | CDKN1A | 0.86 | 0.00648 | 0.58 | 0.35758 | MirTarget | -0.32 | 0.00586 | NA | |
110 | hsa-miR-125a-5p | CDKN1A | -1.32 | 0.00714 | 0.58 | 0.35758 | miRNAWalker2 validate; miRTarBase | -0.35 | 0 | NA | |
111 | hsa-miR-28-5p | CDKN1A | -0.82 | 0.02212 | 0.58 | 0.35758 | miRNAWalker2 validate; miRTarBase; MirTarget; miRanda; miRNATAP | -0.55 | 0 | NA | |
112 | hsa-miR-30b-3p | CDKN1A | 0.17 | 0.76608 | 0.58 | 0.35758 | MirTarget | -0.16 | 0.00864 | NA | |
113 | hsa-miR-335-5p | CDKN1A | 0.17 | 0.8039 | 0.58 | 0.35758 | miRNAWalker2 validate | -0.25 | 0 | NA | |
114 | hsa-miR-345-5p | CDKN1A | 2.77 | 4.0E-5 | 0.58 | 0.35758 | miRNAWalker2 validate; miRTarBase; MirTarget | -0.23 | 1.0E-5 | NA | |
115 | hsa-miR-423-3p | CDKN1A | 1.71 | 2.0E-5 | 0.58 | 0.35758 | miRNAWalker2 validate; miRTarBase | -0.27 | 0.00253 | NA | |
116 | hsa-miR-505-5p | CDKN1A | -0.55 | 0.33141 | 0.58 | 0.35758 | miRNAWalker2 validate; MirTarget | -0.18 | 0.00519 | NA | |
117 | hsa-miR-616-5p | CDKN1A | 2.48 | 0.00318 | 0.58 | 0.35758 | mirMAP | -0.14 | 0.0061 | NA | |
118 | hsa-miR-96-5p | CDKN1A | 5.63 | 0 | 0.58 | 0.35758 | miRNAWalker2 validate; miRTarBase | -0.17 | 0.00034 | 26582573 | Upregulation of microRNA 96 and its oncogenic functions by targeting CDKN1A in bladder cancer; Bioinformatics prediction combined with luciferase reporter assay were used to verify whether the cyclin-dependent kinase inhibitor CDKN1A was a potential target gene of miR-96; According to the data of miRTarBase CDKN1A might be a candidate target gene of miR-96; In addition luciferase reporter and Western blot assays respectively demonstrated that miR-96 could bind to the putative seed region in CDKN1A mRNA 3'UTR and significantly reduce the expression level of CDKN1A protein; Moreover we found that the inhibition of miR-96 expression remarkably decreased cell proliferation and promoted cell apoptosis of BC cell lines which was consistent with the findings observed following the introduction of CDKN1A cDNA without 3'UTR restored miR-96; Upregulation of miR-96 may contribute to aggressive malignancy partly through suppressing CDKN1A protein expression in BC cells |
119 | hsa-miR-221-3p | CDKN1B | 0.94 | 0.17475 | -0.76 | 0.02874 | miRNAWalker2 validate; miRTarBase; MirTarget; miRNATAP | -0.2 | 0 | 23637992; 19953484; 23939688; 19126397; 20146005; 23967190; 17569667; 22992757; 17721077; 20461750 | miR-221 knockdown not only blocked cell cycle progression induced cell apoptosis and inhibited cell proliferation in-vitro but it also inhibited in-vivo tumor growth by targeting p27kip1;Based on bioinformatic analysis we found that the seed sequences of miR-221 and miR-222 coincide with each other and p27kip1 is a target for miRNA-221/222;A Slug/miR-221 network has been suggested linking miR-221 activity with the downregulation of a Slug repressor leading to Slug/miR-221 upregulation and p27Kip1 downregulation; Interference with this process can be achieved using antisense miRNA antagomiR molecules targeting miR-221 inducing the downregulation of Slug and the upregulation of p27Kip1;Moreover a series of functional assays demonstrated that mir-221 could directly inhibit cKit p27Kip1 and possibly other pivotal proteins in melanoma;Matched HCC and adjacent non-cancerous samples were assayed for the expression of miR-221 and three G1/S transition inhibitors: p27Kip1 p21WAF1/Cip1and TGF-β1 by in situ hybridization and immunohistochemistry respectively; Real time qRT-PCR was used to investigate miR-221 and p27Kip1 transcripts in different clinical stages; In result miR-221 and TGF-β1 are frequently up-regulated in HCC while p27Kip1 and p21WAF1/Cip1 proteins are frequently down-regulated; In conclusion miR-221 is important in tumorigenesis of HCC possibly by specifically down-regulating p27Kip1 a cell-cycle inhibitor;Additionally the PDGF-dependent increase in cell proliferation appears to be mediated by inhibition of a specific target of miR-221 and down-regulation of p27Kip1;miR 221 and miR 222 expression affects the proliferation potential of human prostate carcinoma cell lines by targeting p27Kip1; In all cell lines tested we show an inverse relationship between the expression of miR-221 and miR-222 and the cell cycle inhibitor p27Kip1; Consistently miR-221 and miR-222 knock-down through antisense LNA oligonucleotides increases p27Kip1 in PC3 cells and strongly reduces their clonogenicity in vitro;Peptide nucleic acids targeting miR 221 modulate p27Kip1 expression in breast cancer MDA MB 231 cells; Targeting miR-221 by PNA resulted in i lowering of the hybridization levels of miR-221 measured by RT-qPCR ii upregulation of p27Kip1 gene expression measured by RT-qPCR and western blot analysis;Antagonism of either microRNA 221 or 222 in glioblastoma cells also caused an increase in p27Kip1 levels and enhanced expression of the luciferase reporter gene fused to the p27Kip1 3'UTR;MiR 221 and MiR 222 alterations in sporadic ovarian carcinoma: Relationship to CDKN1B CDKNIC and overall survival; miR-221 and miR-222 negatively regulate expression of CDKN1B p27 and CDKN1C p57 two cell cycle regulators expressed in ovarian surface epithelium and down-regulated in ovarian carcinomas; In contrast CDKN1B expression was not associated with miR-221 or miR-222 expression |
120 | hsa-miR-222-3p | CDKN1B | 1.55 | 0.0223 | -0.76 | 0.02874 | miRNAWalker2 validate; miRTarBase; MirTarget; miRNATAP | -0.2 | 0 | 24895988; 19953484; 26912358; 24137356; 17569667; 27282281; 20461750 | MiR-222 plays an important role in the tumorigenesis of CC possibly by specifically down-regulating p27Kip1 and PTEN;Based on bioinformatic analysis we found that the seed sequences of miR-221 and miR-222 coincide with each other and p27kip1 is a target for miRNA-221/222;Besides microvesicle marker characterization we evidenced that miR-222 exosomal expression mostly reflected its abundance in the cells of origin correctly paralleled by repression of its target genes such as p27Kip1 and induction of the PI3K/AKT pathway thus confirming its functional implication in cancer;miR 222 is upregulated in epithelial ovarian cancer and promotes cell proliferation by downregulating P27kip1; miR-222 upregulation induced an enhancement of ovarian cancer cell proliferation potential possibly by downregulating its target P27Kip1; A bioinformatic analysis showed that the 3'-UTR of the P27Kip1 mRNA contained a highly-conserved putative miR-222 binding site; Luciferase reporter assays demonstrated that P27Kip1 was a direct target of miR-222; Consistently there was an inverse correlation between the P27Kip1 and miR-222 expression levels in the ovarian cancer cell lines and tissues;miR 221 and miR 222 expression affects the proliferation potential of human prostate carcinoma cell lines by targeting p27Kip1; In all cell lines tested we show an inverse relationship between the expression of miR-221 and miR-222 and the cell cycle inhibitor p27Kip1; Consistently miR-221 and miR-222 knock-down through antisense LNA oligonucleotides increases p27Kip1 in PC3 cells and strongly reduces their clonogenicity in vitro;miR 222 confers the resistance of breast cancer cells to Adriamycin through suppression of p27kip1 expression; Immunofluorescence showed that miR-222 altered the subcellular location of p27kip1 in nucleus; The results showed that downregulation of miR-222 in MCF-7/Adr increased sensitivity to Adr and Adr-induced apoptosis and arrested the cells in G1 phase accompanied by more expressions of p27kip1 especially in nucleus; Taken together the results found that miR-222 induced Adr-resistance at least in part via suppressing p27kip1 expression and altering its subcellular localization and miR-222 inhibitors could reverse Adr-resistance of breast cancer cells;MiR 221 and MiR 222 alterations in sporadic ovarian carcinoma: Relationship to CDKN1B CDKNIC and overall survival; miR-221 and miR-222 negatively regulate expression of CDKN1B p27 and CDKN1C p57 two cell cycle regulators expressed in ovarian surface epithelium and down-regulated in ovarian carcinomas; In contrast CDKN1B expression was not associated with miR-221 or miR-222 expression |
121 | hsa-miR-24-3p | CDKN1B | 1.56 | 0.00052 | -0.76 | 0.02874 | miRNAWalker2 validate; miRNATAP | -0.23 | 0 | 26847530; 26044523 | The biological significance of miR-24 expression in prostate cancer cells was assessed by a series of in vitro bioassays and the effect on proposed targets p27 CDKN1B and p16 CDK2NA was investigated;With the bioinformatic method we further identified that p27Kip1 is a direct target of miR-24-3p and its protein level was negatively regulated by miR-24-3p |
122 | hsa-miR-421 | CDKN1B | 1.98 | 0.00092 | -0.76 | 0.02874 | miRanda | -0.11 | 0.0006 | NA | |
123 | hsa-miR-455-5p | CDKN1B | -0.32 | 0.6163 | -0.76 | 0.02874 | miRanda; miRNATAP | -0.11 | 0.00022 | NA | |
124 | hsa-miR-221-5p | CHAD | 2.07 | 0.07573 | -0.72 | 0.5484 | MirTarget | -0.29 | 0 | NA | |
125 | hsa-miR-222-5p | CHAD | 2.52 | 0.00142 | -0.72 | 0.5484 | MirTarget | -0.35 | 5.0E-5 | NA | |
126 | hsa-miR-27a-3p | CHRM1 | 1.76 | 0.00022 | -0.18 | 0.90095 | miRNATAP | -0.83 | 0 | NA | |
127 | hsa-miR-342-3p | CHRM1 | 1.31 | 0.02072 | -0.18 | 0.90095 | miRanda | -0.43 | 0.00215 | NA | |
128 | hsa-let-7d-5p | COL1A1 | 0.83 | 0.0127 | -1.84 | 0.04283 | miRNATAP | -0.74 | 0 | NA | |
129 | hsa-let-7f-5p | COL1A1 | 0.97 | 0.02403 | -1.84 | 0.04283 | miRNATAP | -0.33 | 0.0062 | NA | |
130 | hsa-let-7g-5p | COL1A1 | 0.86 | 0.00648 | -1.84 | 0.04283 | miRNATAP | -0.78 | 0 | NA | |
131 | hsa-miR-106a-5p | COL1A1 | 3.99 | 0 | -1.84 | 0.04283 | mirMAP | -0.27 | 1.0E-5 | NA | |
132 | hsa-miR-106b-5p | COL1A1 | 2.81 | 0 | -1.84 | 0.04283 | mirMAP | -0.53 | 0 | NA | |
133 | hsa-miR-107 | COL1A1 | 1.49 | 0.00013 | -1.84 | 0.04283 | PITA; miRanda | -0.36 | 0.00642 | NA | |
134 | hsa-miR-17-5p | COL1A1 | 2.33 | 2.0E-5 | -1.84 | 0.04283 | mirMAP | -0.33 | 0.00039 | NA | |
135 | hsa-miR-196a-5p | COL1A1 | 2.72 | 0.02338 | -1.84 | 0.04283 | miRNATAP | -0.14 | 0.00102 | NA | |
136 | hsa-miR-20a-5p | COL1A1 | 2.14 | 0.00018 | -1.84 | 0.04283 | mirMAP | -0.31 | 0.00051 | NA | |
137 | hsa-miR-20b-5p | COL1A1 | 4.57 | 5.0E-5 | -1.84 | 0.04283 | mirMAP | -0.14 | 0.00174 | NA | |
138 | hsa-miR-23a-5p | COL1A1 | 2.87 | 0.00029 | -1.84 | 0.04283 | mirMAP | -0.17 | 0.00705 | NA | |
139 | hsa-miR-29c-3p | COL1A1 | -0.41 | 0.52934 | -1.84 | 0.04283 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.25 | 0.00176 | NA | |
140 | hsa-miR-30d-3p | COL1A1 | -0.07 | 0.85742 | -1.84 | 0.04283 | mirMAP | -0.51 | 6.0E-5 | NA | |
141 | hsa-miR-30e-3p | COL1A1 | -0.04 | 0.93258 | -1.84 | 0.04283 | mirMAP | -0.48 | 8.0E-5 | NA | |
142 | hsa-miR-330-3p | COL1A1 | 2.49 | 0.00013 | -1.84 | 0.04283 | mirMAP | -0.27 | 0.00063 | NA | |
143 | hsa-miR-361-3p | COL1A1 | 0.81 | 0.04185 | -1.84 | 0.04283 | PITA | -0.55 | 2.0E-5 | NA | |
144 | hsa-miR-532-3p | COL1A1 | 0.64 | 0.21484 | -1.84 | 0.04283 | PITA; miRNATAP | -0.26 | 0.00868 | NA | |
145 | hsa-miR-590-3p | COL1A1 | 2.35 | 0 | -1.84 | 0.04283 | miRanda | -0.37 | 0.00025 | NA | |
146 | hsa-miR-616-5p | COL1A1 | 2.48 | 0.00318 | -1.84 | 0.04283 | mirMAP; miRNATAP | -0.2 | 0.00773 | NA | |
147 | hsa-miR-625-5p | COL1A1 | 2.03 | 0.00094 | -1.84 | 0.04283 | MirTarget | -0.26 | 0.00211 | NA | |
148 | hsa-miR-92a-1-5p | COL1A1 | 2.15 | 0.00155 | -1.84 | 0.04283 | MirTarget | -0.43 | 0 | NA | |
149 | hsa-miR-93-5p | COL1A1 | 2.66 | 0 | -1.84 | 0.04283 | mirMAP | -0.4 | 0.00014 | NA | |
150 | hsa-let-7d-5p | COL1A2 | 0.83 | 0.0127 | -2.41 | 0.0132 | MirTarget; miRNATAP | -0.81 | 0 | NA |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | REGULATION OF PHOSPHORUS METABOLIC PROCESS | 107 | 1618 | 2.077e-61 | 9.665e-58 |
2 | TRANSMEMBRANE RECEPTOR PROTEIN TYROSINE KINASE SIGNALING PATHWAY | 67 | 498 | 4.294e-56 | 9.99e-53 |
3 | REGULATION OF PROTEIN MODIFICATION PROCESS | 103 | 1710 | 1.064e-54 | 1.65e-51 |
4 | POSITIVE REGULATION OF PHOSPHATE METABOLIC PROCESS | 83 | 1036 | 3.736e-52 | 3.476e-49 |
5 | POSITIVE REGULATION OF PHOSPHORUS METABOLIC PROCESS | 83 | 1036 | 3.736e-52 | 3.476e-49 |
6 | REGULATION OF KINASE ACTIVITY | 74 | 776 | 2.473e-51 | 1.918e-48 |
7 | ENZYME LINKED RECEPTOR PROTEIN SIGNALING PATHWAY | 70 | 689 | 3.231e-50 | 2.148e-47 |
8 | CELLULAR RESPONSE TO ORGANIC SUBSTANCE | 100 | 1848 | 1.812e-48 | 1.054e-45 |
9 | POSITIVE REGULATION OF CELL PROLIFERATION | 72 | 814 | 1.543e-47 | 7.975e-45 |
10 | POSITIVE REGULATION OF KINASE ACTIVITY | 59 | 482 | 1.328e-46 | 6.078e-44 |
11 | REGULATION OF CELL PROLIFERATION | 90 | 1496 | 1.437e-46 | 6.078e-44 |
12 | LOCOMOTION | 80 | 1114 | 1.972e-46 | 7.646e-44 |
13 | REGULATION OF TRANSFERASE ACTIVITY | 75 | 946 | 2.833e-46 | 1.014e-43 |
14 | POSITIVE REGULATION OF RESPONSE TO STIMULUS | 99 | 1929 | 8.424e-46 | 2.613e-43 |
15 | POSITIVE REGULATION OF PROTEIN MODIFICATION PROCESS | 80 | 1135 | 8.072e-46 | 2.613e-43 |
16 | POSITIVE REGULATION OF PROTEIN METABOLIC PROCESS | 89 | 1492 | 1.151e-45 | 3.349e-43 |
17 | PROTEIN PHOSPHORYLATION | 74 | 944 | 2.992e-45 | 8.188e-43 |
18 | REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 92 | 1656 | 7.664e-45 | 1.952e-42 |
19 | POSITIVE REGULATION OF MOLECULAR FUNCTION | 95 | 1791 | 7.969e-45 | 1.952e-42 |
20 | REGULATION OF CELLULAR COMPONENT MOVEMENT | 67 | 771 | 1.746e-43 | 4.063e-41 |
21 | POSITIVE REGULATION OF LOCOMOTION | 53 | 420 | 2.187e-42 | 4.845e-40 |
22 | POSITIVE REGULATION OF CATALYTIC ACTIVITY | 86 | 1518 | 3.999e-42 | 8.457e-40 |
23 | POSITIVE REGULATION OF CELL COMMUNICATION | 86 | 1532 | 8.229e-42 | 1.665e-39 |
24 | EXTRACELLULAR STRUCTURE ORGANIZATION | 47 | 304 | 1.08e-41 | 2.094e-39 |
25 | POSITIVE REGULATION OF TRANSFERASE ACTIVITY | 60 | 616 | 1.539e-41 | 2.864e-39 |
26 | CELL MOTILITY | 67 | 835 | 2.907e-41 | 5.01e-39 |
27 | LOCALIZATION OF CELL | 67 | 835 | 2.907e-41 | 5.01e-39 |
28 | POSITIVE REGULATION OF MAPK CASCADE | 54 | 470 | 5.158e-41 | 8.571e-39 |
29 | POSITIVE REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 68 | 876 | 5.355e-41 | 8.592e-39 |
30 | REGULATION OF MAPK CASCADE | 61 | 660 | 6.41e-41 | 9.941e-39 |
31 | REGULATION OF MULTICELLULAR ORGANISMAL DEVELOPMENT | 88 | 1672 | 1.074e-40 | 1.613e-38 |
32 | REGULATION OF PHOSPHATIDYLINOSITOL 3 KINASE SIGNALING | 36 | 138 | 1.153e-40 | 1.677e-38 |
33 | PHOSPHORYLATION | 77 | 1228 | 2.905e-40 | 4.096e-38 |
34 | MOVEMENT OF CELL OR SUBCELLULAR COMPONENT | 78 | 1275 | 4.455e-40 | 6.097e-38 |
35 | INTRACELLULAR SIGNAL TRANSDUCTION | 85 | 1572 | 5.398e-40 | 7.176e-38 |
36 | REGULATION OF PROTEIN SERINE THREONINE KINASE ACTIVITY | 51 | 470 | 2.064e-37 | 2.668e-35 |
37 | REGULATION OF CELL DEATH | 79 | 1472 | 1.458e-36 | 1.834e-34 |
38 | RESPONSE TO ENDOGENOUS STIMULUS | 77 | 1450 | 3.322e-35 | 4.068e-33 |
39 | POSITIVE REGULATION OF PROTEIN SERINE THREONINE KINASE ACTIVITY | 41 | 289 | 9.563e-35 | 1.141e-32 |
40 | POSITIVE REGULATION OF MULTICELLULAR ORGANISMAL PROCESS | 75 | 1395 | 1.52e-34 | 1.768e-32 |
41 | BIOLOGICAL ADHESION | 66 | 1032 | 1.606e-34 | 1.823e-32 |
42 | CELLULAR RESPONSE TO ENDOGENOUS STIMULUS | 64 | 1008 | 3.263e-33 | 3.615e-31 |
43 | NEGATIVE REGULATION OF CELL DEATH | 60 | 872 | 6.237e-33 | 6.749e-31 |
44 | POSITIVE REGULATION OF DEVELOPMENTAL PROCESS | 67 | 1142 | 8.505e-33 | 8.994e-31 |
45 | TISSUE DEVELOPMENT | 75 | 1518 | 4.278e-32 | 4.424e-30 |
46 | CELL SUBSTRATE ADHESION | 32 | 164 | 8.883e-32 | 8.986e-30 |
47 | RESPONSE TO EXTERNAL STIMULUS | 81 | 1821 | 9.215e-32 | 9.123e-30 |
48 | REGULATION OF MAP KINASE ACTIVITY | 40 | 319 | 9.882e-32 | 9.579e-30 |
49 | PHOSPHATE CONTAINING COMPOUND METABOLIC PROCESS | 84 | 1977 | 1.137e-31 | 1.08e-29 |
50 | RESPONSE TO GROWTH FACTOR | 46 | 475 | 1.891e-31 | 1.759e-29 |
51 | PEPTIDYL TYROSINE MODIFICATION | 33 | 186 | 2.577e-31 | 2.306e-29 |
52 | INOSITOL LIPID MEDIATED SIGNALING | 29 | 124 | 2.558e-31 | 2.306e-29 |
53 | POSITIVE REGULATION OF MAP KINASE ACTIVITY | 34 | 207 | 4.605e-31 | 4.043e-29 |
54 | VASCULATURE DEVELOPMENT | 45 | 469 | 1.396e-30 | 1.203e-28 |
55 | REGULATION OF CELL DIFFERENTIATION | 70 | 1492 | 2.322e-28 | 1.964e-26 |
56 | ANATOMICAL STRUCTURE FORMATION INVOLVED IN MORPHOGENESIS | 57 | 957 | 6.103e-28 | 5.071e-26 |
57 | ACTIVATION OF PROTEIN KINASE ACTIVITY | 35 | 279 | 8.528e-28 | 6.961e-26 |
58 | TAXIS | 42 | 464 | 1.661e-27 | 1.332e-25 |
59 | REGULATION OF ANATOMICAL STRUCTURE MORPHOGENESIS | 58 | 1021 | 2.187e-27 | 1.725e-25 |
60 | CELL MATRIX ADHESION | 26 | 119 | 2.55e-27 | 1.978e-25 |
61 | REGULATION OF CELL ADHESION | 47 | 629 | 4.027e-27 | 3.071e-25 |
62 | ANGIOGENESIS | 35 | 293 | 4.694e-27 | 3.523e-25 |
63 | RESPONSE TO HORMONE | 54 | 893 | 9.996e-27 | 7.382e-25 |
64 | SIGNAL TRANSDUCTION BY PROTEIN PHOSPHORYLATION | 39 | 404 | 1.371e-26 | 9.97e-25 |
65 | CARDIOVASCULAR SYSTEM DEVELOPMENT | 51 | 788 | 1.489e-26 | 1.049e-24 |
66 | CIRCULATORY SYSTEM DEVELOPMENT | 51 | 788 | 1.489e-26 | 1.049e-24 |
67 | RESPONSE TO OXYGEN CONTAINING COMPOUND | 65 | 1381 | 3.078e-26 | 2.137e-24 |
68 | BLOOD VESSEL MORPHOGENESIS | 37 | 364 | 4.88e-26 | 3.339e-24 |
69 | REGULATION OF HYDROLASE ACTIVITY | 63 | 1327 | 1.42e-25 | 9.573e-24 |
70 | REGULATION OF PEPTIDYL TYROSINE PHOSPHORYLATION | 30 | 213 | 2.032e-25 | 1.351e-23 |
71 | LEUKOCYTE MIGRATION | 32 | 259 | 3.045e-25 | 1.995e-23 |
72 | POSITIVE REGULATION OF PEPTIDYL TYROSINE PHOSPHORYLATION | 27 | 162 | 5.636e-25 | 3.642e-23 |
73 | LIPID PHOSPHORYLATION | 23 | 99 | 6.124e-25 | 3.904e-23 |
74 | ORGAN MORPHOGENESIS | 50 | 841 | 2.35e-24 | 1.478e-22 |
75 | CELL DEVELOPMENT | 63 | 1426 | 6.91e-24 | 4.287e-22 |
76 | INTEGRIN MEDIATED SIGNALING PATHWAY | 21 | 82 | 7.743e-24 | 4.741e-22 |
77 | PEPTIDYL AMINO ACID MODIFICATION | 49 | 841 | 1.792e-23 | 1.083e-21 |
78 | RESPONSE TO NITROGEN COMPOUND | 49 | 859 | 4.507e-23 | 2.689e-21 |
79 | CELLULAR RESPONSE TO OXYGEN CONTAINING COMPOUND | 47 | 799 | 1.133e-22 | 6.672e-21 |
80 | REGULATION OF IMMUNE SYSTEM PROCESS | 60 | 1403 | 5.832e-22 | 3.392e-20 |
81 | IMMUNE SYSTEM PROCESS | 71 | 1984 | 8.761e-22 | 5.033e-20 |
82 | POSITIVE REGULATION OF PHOSPHATIDYLINOSITOL 3 KINASE SIGNALING | 18 | 62 | 1.088e-21 | 6.174e-20 |
83 | REGULATION OF EPITHELIAL CELL PROLIFERATION | 30 | 285 | 1.186e-21 | 6.65e-20 |
84 | PHOSPHATIDYLINOSITOL METABOLIC PROCESS | 26 | 193 | 1.257e-21 | 6.962e-20 |
85 | POSITIVE REGULATION OF CELL DIFFERENTIATION | 46 | 823 | 2.798e-21 | 1.532e-19 |
86 | CELLULAR RESPONSE TO NITROGEN COMPOUND | 37 | 505 | 4.638e-21 | 2.509e-19 |
87 | CELL DEATH | 50 | 1001 | 4.982e-21 | 2.664e-19 |
88 | POSITIVE REGULATION OF CELLULAR COMPONENT ORGANIZATION | 53 | 1152 | 1.052e-20 | 5.562e-19 |
89 | REGULATION OF VASCULATURE DEVELOPMENT | 27 | 233 | 1.144e-20 | 5.978e-19 |
90 | REGULATION OF LIPID KINASE ACTIVITY | 16 | 48 | 1.625e-20 | 8.401e-19 |
91 | PHOSPHATIDYLINOSITOL 3 PHOSPHATE BIOSYNTHETIC PROCESS | 16 | 49 | 2.391e-20 | 1.223e-18 |
92 | CELL ACTIVATION | 38 | 568 | 3.008e-20 | 1.521e-18 |
93 | POSITIVE REGULATION OF CELL ADHESION | 32 | 376 | 3.186e-20 | 1.594e-18 |
94 | EMBRYO DEVELOPMENT | 46 | 894 | 7.785e-20 | 3.854e-18 |
95 | CELLULAR RESPONSE TO HORMONE STIMULUS | 37 | 552 | 9.416e-20 | 4.612e-18 |
96 | POSITIVE REGULATION OF HYDROLASE ACTIVITY | 46 | 905 | 1.266e-19 | 6.138e-18 |
97 | LIPID MODIFICATION | 25 | 210 | 1.713e-19 | 8.216e-18 |
98 | RESPONSE TO WOUNDING | 37 | 563 | 1.824e-19 | 8.659e-18 |
99 | RESPONSE TO PEPTIDE | 32 | 404 | 2.743e-19 | 1.289e-17 |
100 | POSITIVE REGULATION OF EPITHELIAL CELL PROLIFERATION | 22 | 154 | 5.139e-19 | 2.391e-17 |
101 | POSITIVE REGULATION OF CHEMOTAXIS | 20 | 120 | 9.355e-19 | 4.31e-17 |
102 | REGULATION OF CHEMOTAXIS | 23 | 180 | 1.031e-18 | 4.702e-17 |
103 | CELL PROLIFERATION | 39 | 672 | 1.289e-18 | 5.825e-17 |
104 | REGULATION OF PHOSPHATIDYLINOSITOL 3 KINASE ACTIVITY | 14 | 40 | 1.902e-18 | 8.511e-17 |
105 | NEUROGENESIS | 55 | 1402 | 2.425e-18 | 1.074e-16 |
106 | REGULATION OF EPITHELIAL CELL MIGRATION | 22 | 166 | 2.711e-18 | 1.19e-16 |
107 | WOUND HEALING | 33 | 470 | 2.807e-18 | 1.22e-16 |
108 | CELLULAR COMPONENT MORPHOGENESIS | 44 | 900 | 3.946e-18 | 1.7e-16 |
109 | CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 34 | 513 | 4.855e-18 | 2.073e-16 |
110 | POSITIVE REGULATION OF IMMUNE SYSTEM PROCESS | 43 | 867 | 5.982e-18 | 2.531e-16 |
111 | POSITIVE REGULATION OF CELL DIVISION | 20 | 132 | 6.637e-18 | 2.782e-16 |
112 | REGULATION OF CELL SUBSTRATE ADHESION | 22 | 173 | 6.719e-18 | 2.791e-16 |
113 | REGULATION OF ENDOTHELIAL CELL MIGRATION | 19 | 114 | 7.129e-18 | 2.935e-16 |
114 | SINGLE ORGANISM CELL ADHESION | 32 | 459 | 1.18e-17 | 4.818e-16 |
115 | REGULATION OF NEURON DEATH | 25 | 252 | 1.456e-17 | 5.889e-16 |
116 | PHOSPHATIDYLINOSITOL BIOSYNTHETIC PROCESS | 19 | 120 | 1.947e-17 | 7.808e-16 |
117 | PLATELET ACTIVATION | 20 | 142 | 2.924e-17 | 1.163e-15 |
118 | REGULATION OF ERK1 AND ERK2 CASCADE | 24 | 238 | 4.596e-17 | 1.812e-15 |
119 | POSITIVE REGULATION OF RESPONSE TO EXTERNAL STIMULUS | 26 | 296 | 6.426e-17 | 2.513e-15 |
120 | GLYCEROPHOSPHOLIPID METABOLIC PROCESS | 26 | 297 | 6.98e-17 | 2.707e-15 |
121 | NEGATIVE REGULATION OF RESPONSE TO STIMULUS | 52 | 1360 | 7.656e-17 | 2.944e-15 |
122 | RESPONSE TO LIPID | 42 | 888 | 8.459e-17 | 3.226e-15 |
123 | POSITIVE REGULATION OF ERK1 AND ERK2 CASCADE | 21 | 172 | 9.138e-17 | 3.457e-15 |
124 | CELLULAR RESPONSE TO PEPTIDE | 25 | 274 | 1.075e-16 | 4.033e-15 |
125 | REGULATION OF BODY FLUID LEVELS | 32 | 506 | 1.973e-16 | 7.343e-15 |
126 | NEURON PROJECTION DEVELOPMENT | 33 | 545 | 2.281e-16 | 8.424e-15 |
127 | ACTIVATION OF MAPK ACTIVITY | 19 | 137 | 2.519e-16 | 9.228e-15 |
128 | TUBE DEVELOPMENT | 33 | 552 | 3.313e-16 | 1.204e-14 |
129 | POSITIVE REGULATION OF GENE EXPRESSION | 58 | 1733 | 3.428e-16 | 1.237e-14 |
130 | REGULATION OF DEVELOPMENTAL GROWTH | 25 | 289 | 3.788e-16 | 1.356e-14 |
131 | REGULATION OF RESPONSE TO STRESS | 53 | 1468 | 4.06e-16 | 1.442e-14 |
132 | RESPONSE TO ABIOTIC STIMULUS | 44 | 1024 | 4.673e-16 | 1.647e-14 |
133 | GLYCEROLIPID METABOLIC PROCESS | 27 | 356 | 6.299e-16 | 2.204e-14 |
134 | PROTEIN AUTOPHOSPHORYLATION | 21 | 192 | 8.831e-16 | 3.066e-14 |
135 | POSITIVE REGULATION OF CELL CYCLE | 26 | 332 | 1.048e-15 | 3.611e-14 |
136 | FORMATION OF PRIMARY GERM LAYER | 17 | 110 | 1.533e-15 | 5.208e-14 |
137 | REGULATION OF PHOSPHOLIPID METABOLIC PROCESS | 14 | 61 | 1.526e-15 | 5.208e-14 |
138 | NEURON PROJECTION MORPHOGENESIS | 28 | 402 | 1.55e-15 | 5.227e-14 |
139 | REGULATION OF RESPONSE TO EXTERNAL STIMULUS | 41 | 926 | 2.024e-15 | 6.775e-14 |
140 | REGULATION OF TRANSPORT | 58 | 1804 | 2.071e-15 | 6.883e-14 |
141 | POSITIVE REGULATION OF BIOSYNTHETIC PROCESS | 58 | 1805 | 2.123e-15 | 7.005e-14 |
142 | POSITIVE REGULATION OF VASCULATURE DEVELOPMENT | 18 | 133 | 2.464e-15 | 8.073e-14 |
143 | NEGATIVE REGULATION OF DEVELOPMENTAL PROCESS | 38 | 801 | 2.83e-15 | 9.208e-14 |
144 | NEGATIVE REGULATION OF MULTICELLULAR ORGANISMAL PROCESS | 42 | 983 | 2.986e-15 | 9.649e-14 |
145 | CELL PROJECTION ORGANIZATION | 40 | 902 | 4.478e-15 | 1.437e-13 |
146 | REGULATION OF CELL CYCLE | 41 | 949 | 4.655e-15 | 1.484e-13 |
147 | POSITIVE REGULATION OF CELL DEATH | 33 | 605 | 4.7e-15 | 1.488e-13 |
148 | RESPONSE TO STEROID HORMONE | 30 | 497 | 6.522e-15 | 2.05e-13 |
149 | UROGENITAL SYSTEM DEVELOPMENT | 24 | 299 | 8.204e-15 | 2.562e-13 |
150 | PHOSPHOLIPID METABOLIC PROCESS | 26 | 364 | 9.449e-15 | 2.931e-13 |
151 | POSITIVE REGULATION OF EPITHELIAL CELL MIGRATION | 16 | 103 | 9.841e-15 | 3.032e-13 |
152 | POSITIVE REGULATION OF TRANSPORT | 40 | 936 | 1.521e-14 | 4.656e-13 |
153 | REGULATION OF GROWTH | 33 | 633 | 1.707e-14 | 5.19e-13 |
154 | REGULATION OF NEURON DIFFERENTIATION | 31 | 554 | 1.739e-14 | 5.255e-13 |
155 | HEMOSTASIS | 24 | 311 | 1.968e-14 | 5.908e-13 |
156 | REGULATION OF CELL MATRIX ADHESION | 15 | 90 | 2.327e-14 | 6.94e-13 |
157 | REGULATION OF IMMUNE RESPONSE | 38 | 858 | 2.513e-14 | 7.448e-13 |
158 | VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 14 | 74 | 2.747e-14 | 8.091e-13 |
159 | NEURON DEVELOPMENT | 34 | 687 | 2.951e-14 | 8.637e-13 |
160 | REGULATION OF PHOSPHOPROTEIN PHOSPHATASE ACTIVITY | 13 | 60 | 3.608e-14 | 1.049e-12 |
161 | APOPTOTIC SIGNALING PATHWAY | 23 | 289 | 3.691e-14 | 1.067e-12 |
162 | NEURON DIFFERENTIATION | 38 | 874 | 4.49e-14 | 1.29e-12 |
163 | EMBRYONIC MORPHOGENESIS | 30 | 539 | 5.521e-14 | 1.576e-12 |
164 | REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 35 | 750 | 6.66e-14 | 1.89e-12 |
165 | CELL CHEMOTAXIS | 18 | 162 | 8.264e-14 | 2.33e-12 |
166 | RESPONSE TO CYTOKINE | 34 | 714 | 8.938e-14 | 2.505e-12 |
167 | REGULATION OF GTPASE ACTIVITY | 33 | 673 | 9.578e-14 | 2.669e-12 |
168 | EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 15 | 99 | 1.009e-13 | 2.778e-12 |
169 | POSITIVE REGULATION OF CELL PROJECTION ORGANIZATION | 23 | 303 | 1.009e-13 | 2.778e-12 |
170 | EPITHELIUM DEVELOPMENT | 39 | 945 | 1.042e-13 | 2.851e-12 |
171 | REGULATION OF CELL PROJECTION ORGANIZATION | 30 | 558 | 1.359e-13 | 3.698e-12 |
172 | REGULATION OF NEURON APOPTOTIC PROCESS | 19 | 192 | 1.379e-13 | 3.729e-12 |
173 | POSITIVE REGULATION OF SMALL GTPASE MEDIATED SIGNAL TRANSDUCTION | 11 | 39 | 1.454e-13 | 3.912e-12 |
174 | POSITIVE REGULATION OF ENDOTHELIAL CELL MIGRATION | 13 | 67 | 1.663e-13 | 4.447e-12 |
175 | CELL SUBSTRATE JUNCTION ASSEMBLY | 11 | 41 | 2.692e-13 | 7.159e-12 |
176 | REGULATION OF CELL DEVELOPMENT | 36 | 836 | 3.066e-13 | 8.106e-12 |
177 | GASTRULATION | 17 | 155 | 5.148e-13 | 1.353e-11 |
178 | POSITIVE REGULATION OF DEVELOPMENTAL GROWTH | 17 | 156 | 5.726e-13 | 1.497e-11 |
179 | REGULATION OF APOPTOTIC SIGNALING PATHWAY | 24 | 363 | 5.781e-13 | 1.503e-11 |
180 | POSITIVE REGULATION OF CELL DEVELOPMENT | 27 | 472 | 5.899e-13 | 1.525e-11 |
181 | POSITIVE REGULATION OF LIPID KINASE ACTIVITY | 10 | 32 | 6e-13 | 1.543e-11 |
182 | POSITIVE REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 26 | 437 | 6.691e-13 | 1.711e-11 |
183 | GLYCEROLIPID BIOSYNTHETIC PROCESS | 19 | 211 | 7.599e-13 | 1.932e-11 |
184 | REGULATION OF CELL DIVISION | 21 | 272 | 9.109e-13 | 2.304e-11 |
185 | RESPONSE TO ORGANIC CYCLIC COMPOUND | 37 | 917 | 9.692e-13 | 2.438e-11 |
186 | REGULATION OF NEURON PROJECTION DEVELOPMENT | 25 | 408 | 1.002e-12 | 2.507e-11 |
187 | GROWTH | 25 | 410 | 1.117e-12 | 2.778e-11 |
188 | RESPONSE TO ESTROGEN | 19 | 218 | 1.364e-12 | 3.375e-11 |
189 | TISSUE MORPHOGENESIS | 28 | 533 | 1.669e-12 | 4.11e-11 |
190 | REGULATION OF LIPID METABOLIC PROCESS | 21 | 282 | 1.829e-12 | 4.479e-11 |
191 | REGULATION OF PROTEIN KINASE B SIGNALING | 15 | 121 | 2.072e-12 | 5.048e-11 |
192 | NEGATIVE REGULATION OF ANOIKIS | 8 | 17 | 2.581e-12 | 6.222e-11 |
193 | REGULATION OF ENDOTHELIAL CELL CHEMOTAXIS | 8 | 17 | 2.581e-12 | 6.222e-11 |
194 | PEPTIDYL SERINE MODIFICATION | 16 | 148 | 3.187e-12 | 7.643e-11 |
195 | RESPONSE TO ALCOHOL | 23 | 362 | 4.107e-12 | 9.787e-11 |
196 | POSITIVE REGULATION OF NEURON PROJECTION DEVELOPMENT | 19 | 232 | 4.123e-12 | 9.787e-11 |
197 | SUBSTRATE ADHESION DEPENDENT CELL SPREADING | 10 | 38 | 4.166e-12 | 9.84e-11 |
198 | RESPONSE TO INSULIN | 18 | 205 | 4.795e-12 | 1.127e-10 |
199 | PHOSPHOLIPID BIOSYNTHETIC PROCESS | 19 | 235 | 5.173e-12 | 1.21e-10 |
200 | REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 16 | 153 | 5.332e-12 | 1.241e-10 |
201 | CELL MORPHOGENESIS INVOLVED IN NEURON DIFFERENTIATION | 23 | 368 | 5.748e-12 | 1.331e-10 |
202 | POSITIVE REGULATION OF PHOSPHOLIPASE ACTIVITY | 11 | 53 | 5.829e-12 | 1.343e-10 |
203 | POSITIVE REGULATION OF GROWTH | 19 | 238 | 6.47e-12 | 1.483e-10 |
204 | REPRODUCTIVE SYSTEM DEVELOPMENT | 24 | 408 | 6.973e-12 | 1.59e-10 |
205 | NEGATIVE REGULATION OF CELL COMMUNICATION | 41 | 1192 | 8.048e-12 | 1.827e-10 |
206 | POSITIVE REGULATION OF NEURON DIFFERENTIATION | 21 | 306 | 8.711e-12 | 1.967e-10 |
207 | HEAD DEVELOPMENT | 31 | 709 | 1.13e-11 | 2.54e-10 |
208 | POSITIVE REGULATION OF PHOSPHOLIPID METABOLIC PROCESS | 10 | 42 | 1.251e-11 | 2.798e-10 |
209 | IMMUNE SYSTEM DEVELOPMENT | 28 | 582 | 1.35e-11 | 2.991e-10 |
210 | MULTICELLULAR ORGANISM METABOLIC PROCESS | 13 | 93 | 1.345e-11 | 2.991e-10 |
211 | CELL PART MORPHOGENESIS | 29 | 633 | 1.835e-11 | 4.047e-10 |
212 | RESPONSE TO ACID CHEMICAL | 21 | 319 | 1.912e-11 | 4.196e-10 |
213 | REGULATION OF CELL MORPHOGENESIS | 27 | 552 | 2.222e-11 | 4.854e-10 |
214 | REGULATION OF AXONOGENESIS | 16 | 168 | 2.24e-11 | 4.871e-10 |
215 | CENTRAL NERVOUS SYSTEM DEVELOPMENT | 34 | 872 | 2.336e-11 | 5.056e-10 |
216 | POSITIVE REGULATION OF SMOOTH MUSCLE CELL PROLIFERATION | 11 | 60 | 2.46e-11 | 5.3e-10 |
217 | POSITIVE REGULATION OF CELLULAR PROTEIN LOCALIZATION | 22 | 360 | 2.644e-11 | 5.67e-10 |
218 | NEGATIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 13 | 98 | 2.66e-11 | 5.679e-10 |
219 | DEVELOPMENTAL PROCESS INVOLVED IN REPRODUCTION | 28 | 602 | 2.977e-11 | 6.325e-10 |
220 | MYELOID LEUKOCYTE MIGRATION | 13 | 99 | 3.035e-11 | 6.39e-10 |
221 | POSITIVE REGULATION OF CELL SUBSTRATE ADHESION | 13 | 99 | 3.035e-11 | 6.39e-10 |
222 | MULTICELLULAR ORGANISMAL MACROMOLECULE METABOLIC PROCESS | 12 | 79 | 3.061e-11 | 6.415e-10 |
223 | RESPONSE TO ESTRADIOL | 15 | 146 | 3.245e-11 | 6.772e-10 |
224 | POSITIVE REGULATION OF MITOTIC CELL CYCLE | 14 | 123 | 3.73e-11 | 7.749e-10 |
225 | CELL CELL ADHESION | 28 | 608 | 3.75e-11 | 7.755e-10 |
226 | REGULATION OF CELL ACTIVATION | 25 | 484 | 4.103e-11 | 8.447e-10 |
227 | REGULATION OF PHOSPHOLIPASE ACTIVITY | 11 | 64 | 5.149e-11 | 1.056e-09 |
228 | REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 21 | 337 | 5.341e-11 | 1.09e-09 |
229 | REGULATION OF PROTEIN LOCALIZATION | 35 | 950 | 5.442e-11 | 1.106e-09 |
230 | REGULATION OF REACTIVE OXYGEN SPECIES METABOLIC PROCESS | 15 | 152 | 5.797e-11 | 1.173e-09 |
231 | REGULATION OF PHOSPHATASE ACTIVITY | 14 | 128 | 6.425e-11 | 1.294e-09 |
232 | FIBROBLAST GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 12 | 84 | 6.455e-11 | 1.295e-09 |
233 | CELL JUNCTION ASSEMBLY | 14 | 129 | 7.142e-11 | 1.426e-09 |
234 | REGULATION OF ANOIKIS | 8 | 24 | 7.337e-11 | 1.44e-09 |
235 | POSITIVE REGULATION OF LIPASE ACTIVITY | 11 | 66 | 7.305e-11 | 1.44e-09 |
236 | CELLULAR RESPONSE TO STRESS | 46 | 1565 | 7.248e-11 | 1.44e-09 |
237 | REGULATION OF PROTEIN PHOSPHATASE TYPE 2A ACTIVITY | 8 | 24 | 7.337e-11 | 1.44e-09 |
238 | HOMEOSTATIC PROCESS | 42 | 1337 | 7.565e-11 | 1.479e-09 |
239 | POSITIVE CHEMOTAXIS | 9 | 36 | 8.463e-11 | 1.648e-09 |
240 | POSITIVE REGULATION OF DNA REPLICATION | 12 | 86 | 8.578e-11 | 1.663e-09 |
241 | RESPONSE TO OXYGEN LEVELS | 20 | 311 | 8.983e-11 | 1.727e-09 |
242 | POSITIVE REGULATION OF CELL ACTIVATION | 20 | 311 | 8.983e-11 | 1.727e-09 |
243 | POSITIVE REGULATION OF DNA METABOLIC PROCESS | 16 | 185 | 9.629e-11 | 1.836e-09 |
244 | CELL JUNCTION ORGANIZATION | 16 | 185 | 9.629e-11 | 1.836e-09 |
245 | REGULATION OF BLOOD VESSEL ENDOTHELIAL CELL MIGRATION | 10 | 51 | 1.002e-10 | 1.903e-09 |
246 | REGULATION OF DEPHOSPHORYLATION | 15 | 158 | 1.009e-10 | 1.909e-09 |
247 | REGULATION OF HEMOPOIESIS | 20 | 314 | 1.066e-10 | 2.006e-09 |
248 | PHOSPHATIDYLINOSITOL 3 KINASE SIGNALING | 8 | 25 | 1.069e-10 | 2.006e-09 |
249 | POSITIVE REGULATION OF AXONOGENESIS | 11 | 69 | 1.207e-10 | 2.256e-09 |
250 | REGULATION OF CELLULAR PROTEIN LOCALIZATION | 26 | 552 | 1.225e-10 | 2.281e-09 |
251 | RESPONSE TO DRUG | 23 | 431 | 1.374e-10 | 2.547e-09 |
252 | POSITIVE REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 15 | 162 | 1.441e-10 | 2.661e-09 |
253 | POSITIVE REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION | 25 | 514 | 1.465e-10 | 2.694e-09 |
254 | POSITIVE REGULATION OF FIBROBLAST PROLIFERATION | 10 | 53 | 1.502e-10 | 2.751e-09 |
255 | GLAND DEVELOPMENT | 22 | 395 | 1.577e-10 | 2.878e-09 |
256 | CELLULAR RESPONSE TO CYTOKINE STIMULUS | 27 | 606 | 1.811e-10 | 3.291e-09 |
257 | CONNECTIVE TISSUE DEVELOPMENT | 16 | 194 | 1.959e-10 | 3.547e-09 |
258 | NEGATIVE REGULATION OF CELL DIFFERENTIATION | 27 | 609 | 2.02e-10 | 3.643e-09 |
259 | NEPHRON DEVELOPMENT | 13 | 115 | 2.074e-10 | 3.726e-09 |
260 | LEUKOCYTE DIFFERENTIATION | 19 | 292 | 2.223e-10 | 3.964e-09 |
261 | MORPHOGENESIS OF A BRANCHING STRUCTURE | 15 | 167 | 2.218e-10 | 3.964e-09 |
262 | POSITIVE REGULATION OF STAT CASCADE | 11 | 73 | 2.272e-10 | 4.02e-09 |
263 | POSITIVE REGULATION OF JAK STAT CASCADE | 11 | 73 | 2.272e-10 | 4.02e-09 |
264 | RESPONSE TO FIBROBLAST GROWTH FACTOR | 13 | 116 | 2.315e-10 | 4.079e-09 |
265 | ENDODERMAL CELL DIFFERENTIATION | 9 | 40 | 2.372e-10 | 4.164e-09 |
266 | REGULATION OF CELLULAR LOCALIZATION | 40 | 1277 | 2.549e-10 | 4.459e-09 |
267 | LEUKOCYTE CHEMOTAXIS | 13 | 117 | 2.58e-10 | 4.497e-09 |
268 | NEGATIVE REGULATION OF NEURON DEATH | 15 | 171 | 3.099e-10 | 5.381e-09 |
269 | REGULATION OF LEUKOCYTE DIFFERENTIATION | 17 | 232 | 3.321e-10 | 5.744e-09 |
270 | CELL CELL SIGNALING | 30 | 767 | 3.736e-10 | 6.438e-09 |
271 | REGULATION OF ENDOTHELIAL CELL PROLIFERATION | 12 | 98 | 4.089e-10 | 7.021e-09 |
272 | HOMEOSTASIS OF NUMBER OF CELLS | 15 | 175 | 4.291e-10 | 7.341e-09 |
273 | NEURON PROJECTION GUIDANCE | 16 | 205 | 4.439e-10 | 7.565e-09 |
274 | REGULATION OF CELL CELL ADHESION | 21 | 380 | 4.858e-10 | 8.251e-09 |
275 | POSITIVE REGULATION OF ENDOTHELIAL CELL CHEMOTAXIS | 6 | 11 | 5.059e-10 | 8.56e-09 |
276 | REGULATION OF SMOOTH MUSCLE CELL PROLIFERATION | 12 | 100 | 5.193e-10 | 8.754e-09 |
277 | POSITIVE REGULATION OF SMOOTH MUSCLE CELL MIGRATION | 8 | 30 | 5.536e-10 | 9.299e-09 |
278 | SINGLE ORGANISM BEHAVIOR | 21 | 384 | 5.874e-10 | 9.832e-09 |
279 | REGULATION OF MITOTIC CELL CYCLE | 23 | 468 | 6.875e-10 | 1.147e-08 |
280 | REGULATION OF LIPASE ACTIVITY | 11 | 83 | 9.418e-10 | 1.565e-08 |
281 | POSITIVE REGULATION OF LEUKOCYTE DIFFERENTIATION | 13 | 131 | 1.067e-09 | 1.766e-08 |
282 | OSSIFICATION | 17 | 251 | 1.117e-09 | 1.842e-08 |
283 | IMMUNE RESPONSE REGULATING CELL SURFACE RECEPTOR SIGNALING PATHWAY | 19 | 323 | 1.212e-09 | 1.992e-08 |
284 | MORPHOGENESIS OF AN EPITHELIUM | 21 | 400 | 1.226e-09 | 2.009e-08 |
285 | SIGNAL TRANSDUCTION IN ABSENCE OF LIGAND | 8 | 33 | 1.279e-09 | 2.08e-08 |
286 | EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 8 | 33 | 1.279e-09 | 2.08e-08 |
287 | CELLULAR LIPID METABOLIC PROCESS | 32 | 913 | 1.393e-09 | 2.259e-08 |
288 | LEUKOCYTE CELL CELL ADHESION | 17 | 255 | 1.422e-09 | 2.297e-08 |
289 | POSITIVE REGULATION OF LEUKOCYTE MIGRATION | 12 | 109 | 1.428e-09 | 2.299e-08 |
290 | POSITIVE REGULATION OF HEMOPOIESIS | 14 | 163 | 1.624e-09 | 2.606e-08 |
291 | PLATELET DERIVED GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 8 | 34 | 1.657e-09 | 2.65e-08 |
292 | POSITIVE REGULATION OF NEURON DEATH | 10 | 67 | 1.684e-09 | 2.684e-08 |
293 | POSITIVE REGULATION OF INTRACELLULAR TRANSPORT | 20 | 370 | 1.884e-09 | 2.992e-08 |
294 | RESPONSE TO AMINO ACID | 12 | 112 | 1.959e-09 | 3.101e-08 |
295 | ENDODERM FORMATION | 9 | 50 | 1.987e-09 | 3.135e-08 |
296 | TELENCEPHALON DEVELOPMENT | 16 | 228 | 2.102e-09 | 3.304e-08 |
297 | REGULATION OF CELLULAR RESPONSE TO GROWTH FACTOR STIMULUS | 16 | 229 | 2.239e-09 | 3.509e-08 |
298 | REGULATION OF DNA METABOLIC PROCESS | 19 | 340 | 2.83e-09 | 4.419e-08 |
299 | ENDODERM DEVELOPMENT | 10 | 71 | 3.025e-09 | 4.707e-08 |
300 | POSITIVE REGULATION OF APOPTOTIC SIGNALING PATHWAY | 14 | 171 | 3.037e-09 | 4.711e-08 |
301 | LYMPHOCYTE ACTIVATION | 19 | 342 | 3.117e-09 | 4.818e-08 |
302 | REGULATION OF CELLULAR RESPONSE TO STRESS | 27 | 691 | 3.159e-09 | 4.867e-08 |
303 | VASCULAR ENDOTHELIAL GROWTH FACTOR SIGNALING PATHWAY | 6 | 14 | 3.204e-09 | 4.92e-08 |
304 | REGULATION OF JAK STAT CASCADE | 13 | 144 | 3.435e-09 | 5.223e-08 |
305 | POSITIVE REGULATION OF TYROSINE PHOSPHORYLATION OF STAT3 PROTEIN | 8 | 37 | 3.432e-09 | 5.223e-08 |
306 | REGULATION OF STAT CASCADE | 13 | 144 | 3.435e-09 | 5.223e-08 |
307 | CELLULAR RESPONSE TO INSULIN STIMULUS | 13 | 146 | 4.068e-09 | 6.165e-08 |
308 | FC RECEPTOR SIGNALING PATHWAY | 15 | 206 | 4.115e-09 | 6.217e-08 |
309 | POSITIVE REGULATION OF BLOOD VESSEL ENDOTHELIAL CELL MIGRATION | 7 | 25 | 4.718e-09 | 7.104e-08 |
310 | POSITIVE REGULATION OF CELL CELL ADHESION | 16 | 243 | 5.262e-09 | 7.897e-08 |
311 | REGULATION OF PHOSPHOLIPASE C ACTIVITY | 8 | 39 | 5.373e-09 | 8.038e-08 |
312 | MEMORY | 11 | 98 | 5.711e-09 | 8.517e-08 |
313 | NEGATIVE REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 21 | 437 | 5.893e-09 | 8.761e-08 |
314 | MESODERMAL CELL DIFFERENTIATION | 7 | 26 | 6.399e-09 | 9.483e-08 |
315 | POSITIVE REGULATION OF CELL MATRIX ADHESION | 8 | 40 | 6.656e-09 | 9.832e-08 |
316 | REGULATION OF INTRACELLULAR TRANSPORT | 25 | 621 | 7.045e-09 | 1.037e-07 |
317 | PALLIUM DEVELOPMENT | 13 | 153 | 7.203e-09 | 1.057e-07 |
318 | AMEBOIDAL TYPE CELL MIGRATION | 13 | 154 | 7.796e-09 | 1.141e-07 |
319 | COGNITION | 16 | 251 | 8.353e-09 | 1.218e-07 |
320 | POSITIVE REGULATION OF VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 6 | 16 | 8.398e-09 | 1.221e-07 |
321 | REGULATION OF VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 7 | 27 | 8.563e-09 | 1.237e-07 |
322 | HETEROTYPIC CELL CELL ADHESION | 7 | 27 | 8.563e-09 | 1.237e-07 |
323 | ERBB SIGNALING PATHWAY | 10 | 79 | 8.784e-09 | 1.265e-07 |
324 | POSITIVE REGULATION OF LIPID METABOLIC PROCESS | 12 | 128 | 9.107e-09 | 1.308e-07 |
325 | LIPID BIOSYNTHETIC PROCESS | 23 | 539 | 1.006e-08 | 1.441e-07 |
326 | CYTOKINE MEDIATED SIGNALING PATHWAY | 21 | 452 | 1.063e-08 | 1.517e-07 |
327 | REGULATION OF FIBROBLAST PROLIFERATION | 10 | 81 | 1.125e-08 | 1.596e-07 |
328 | POSITIVE REGULATION OF PROTEIN KINASE B SIGNALING | 10 | 81 | 1.125e-08 | 1.596e-07 |
329 | INFLAMMATORY RESPONSE | 21 | 454 | 1.148e-08 | 1.623e-07 |
330 | BRANCHING MORPHOGENESIS OF AN EPITHELIAL TUBE | 12 | 131 | 1.185e-08 | 1.671e-07 |
331 | REGULATION OF RESPONSE TO WOUNDING | 20 | 413 | 1.217e-08 | 1.711e-07 |
332 | LEUKOCYTE ACTIVATION | 20 | 414 | 1.267e-08 | 1.776e-07 |
333 | PLATELET DEGRANULATION | 11 | 107 | 1.456e-08 | 2.035e-07 |
334 | REGULATION OF TYROSINE PHOSPHORYLATION OF STAT3 PROTEIN | 8 | 44 | 1.481e-08 | 2.063e-07 |
335 | TISSUE MIGRATION | 10 | 84 | 1.609e-08 | 2.235e-07 |
336 | REPRODUCTION | 37 | 1297 | 1.64e-08 | 2.272e-07 |
337 | NEGATIVE REGULATION OF NEURON APOPTOTIC PROCESS | 12 | 135 | 1.666e-08 | 2.301e-07 |
338 | SPROUTING ANGIOGENESIS | 8 | 45 | 1.785e-08 | 2.457e-07 |
339 | POSITIVE REGULATION OF LEUKOCYTE PROLIFERATION | 12 | 136 | 1.811e-08 | 2.486e-07 |
340 | RESPIRATORY SYSTEM DEVELOPMENT | 14 | 197 | 1.875e-08 | 2.565e-07 |
341 | CELLULAR RESPONSE TO VASCULAR ENDOTHELIAL GROWTH FACTOR STIMULUS | 7 | 30 | 1.912e-08 | 2.609e-07 |
342 | POSITIVE REGULATION OF REACTIVE OXYGEN SPECIES METABOLIC PROCESS | 10 | 86 | 2.027e-08 | 2.758e-07 |
343 | CELL CYCLE G1 S PHASE TRANSITION | 11 | 111 | 2.145e-08 | 2.902e-07 |
344 | G1 S TRANSITION OF MITOTIC CELL CYCLE | 11 | 111 | 2.145e-08 | 2.902e-07 |
345 | NEGATIVE REGULATION OF APOPTOTIC SIGNALING PATHWAY | 14 | 200 | 2.271e-08 | 3.062e-07 |
346 | HOMEOSTASIS OF NUMBER OF CELLS WITHIN A TISSUE | 7 | 31 | 2.448e-08 | 3.292e-07 |
347 | OVULATION CYCLE PROCESS | 10 | 88 | 2.538e-08 | 3.404e-07 |
348 | TISSUE HOMEOSTASIS | 13 | 171 | 2.75e-08 | 3.677e-07 |
349 | FC EPSILON RECEPTOR SIGNALING PATHWAY | 12 | 142 | 2.943e-08 | 3.919e-07 |
350 | REGULATION OF CELL SIZE | 13 | 172 | 2.948e-08 | 3.919e-07 |
351 | REGULATION OF TYROSINE PHOSPHORYLATION OF STAT PROTEIN | 9 | 68 | 3.328e-08 | 4.387e-07 |
352 | REGULATION OF CELL JUNCTION ASSEMBLY | 9 | 68 | 3.328e-08 | 4.387e-07 |
353 | POSITIVE REGULATION OF ENDOTHELIAL CELL PROLIFERATION | 9 | 68 | 3.328e-08 | 4.387e-07 |
354 | RESPONSE TO TOXIC SUBSTANCE | 15 | 241 | 3.408e-08 | 4.48e-07 |
355 | LIPID METABOLIC PROCESS | 34 | 1158 | 3.432e-08 | 4.498e-07 |
356 | CELLULAR RESPONSE TO ACID CHEMICAL | 13 | 175 | 3.622e-08 | 4.694e-07 |
357 | GLIOGENESIS | 13 | 175 | 3.622e-08 | 4.694e-07 |
358 | GLOMERULUS DEVELOPMENT | 8 | 49 | 3.604e-08 | 4.694e-07 |
359 | REGULATION OF SMOOTH MUSCLE CELL MIGRATION | 8 | 49 | 3.604e-08 | 4.694e-07 |
360 | FOREBRAIN DEVELOPMENT | 18 | 357 | 3.67e-08 | 4.743e-07 |
361 | MAMMARY GLAND DEVELOPMENT | 11 | 117 | 3.726e-08 | 4.803e-07 |
362 | MITOCHONDRIAL MEMBRANE ORGANIZATION | 10 | 92 | 3.912e-08 | 5.028e-07 |
363 | CELLULAR RESPONSE TO GROWTH HORMONE STIMULUS | 6 | 20 | 3.927e-08 | 5.033e-07 |
364 | LYMPHOCYTE DIFFERENTIATION | 14 | 209 | 3.956e-08 | 5.057e-07 |
365 | REGULATION OF PEPTIDYL SERINE PHOSPHORYLATION | 11 | 118 | 4.073e-08 | 5.177e-07 |
366 | MESODERM DEVELOPMENT | 11 | 118 | 4.073e-08 | 5.177e-07 |
367 | REGULATION OF ADHERENS JUNCTION ORGANIZATION | 8 | 50 | 4.253e-08 | 5.392e-07 |
368 | REGULATION OF MEMBRANE PERMEABILITY | 9 | 70 | 4.315e-08 | 5.455e-07 |
369 | REGULATION OF HOMEOSTATIC PROCESS | 20 | 447 | 4.516e-08 | 5.694e-07 |
370 | POSITIVE REGULATION OF CELL CYCLE PROCESS | 15 | 247 | 4.72e-08 | 5.933e-07 |
371 | SENSORY ORGAN DEVELOPMENT | 21 | 493 | 4.73e-08 | 5.933e-07 |
372 | TUBE MORPHOGENESIS | 17 | 323 | 4.8e-08 | 6.004e-07 |
373 | INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO DNA DAMAGE | 9 | 71 | 4.897e-08 | 6.109e-07 |
374 | REGULATION OF LEUKOCYTE MIGRATION | 12 | 149 | 5.037e-08 | 6.224e-07 |
375 | NEGATIVE REGULATION OF PHOSPHORUS METABOLIC PROCESS | 22 | 541 | 5.043e-08 | 6.224e-07 |
376 | REGULATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY | 14 | 213 | 5.018e-08 | 6.224e-07 |
377 | NEGATIVE REGULATION OF PHOSPHATE METABOLIC PROCESS | 22 | 541 | 5.043e-08 | 6.224e-07 |
378 | REGULATION OF ORGANELLE ORGANIZATION | 34 | 1178 | 5.191e-08 | 6.389e-07 |
379 | RESPONSE TO KETONE | 13 | 182 | 5.763e-08 | 7.075e-07 |
380 | DEVELOPMENT OF PRIMARY SEXUAL CHARACTERISTICS | 14 | 216 | 5.977e-08 | 7.318e-07 |
381 | SKELETAL SYSTEM DEVELOPMENT | 20 | 455 | 6.035e-08 | 7.371e-07 |
382 | INTRINSIC APOPTOTIC SIGNALING PATHWAY | 12 | 152 | 6.285e-08 | 7.655e-07 |
383 | MAMMARY GLAND EPITHELIUM DEVELOPMENT | 8 | 53 | 6.836e-08 | 8.284e-07 |
384 | CELLULAR RESPONSE TO AMINO ACID STIMULUS | 8 | 53 | 6.836e-08 | 8.284e-07 |
385 | POSITIVE REGULATION OF MITOCHONDRIAL OUTER MEMBRANE PERMEABILIZATION INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 7 | 36 | 7.439e-08 | 8.967e-07 |
386 | POSITIVE REGULATION OF CYCLIN DEPENDENT PROTEIN KINASE ACTIVITY | 7 | 36 | 7.439e-08 | 8.967e-07 |
387 | DEVELOPMENTAL GROWTH | 17 | 333 | 7.46e-08 | 8.969e-07 |
388 | HEMIDESMOSOME ASSEMBLY | 5 | 12 | 8.449e-08 | 1.011e-06 |
389 | CELL ADHESION MEDIATED BY INTEGRIN | 5 | 12 | 8.449e-08 | 1.011e-06 |
390 | NEGATIVE REGULATION OF PROTEIN METABOLIC PROCESS | 32 | 1087 | 8.658e-08 | 1.033e-06 |
391 | RHYTHMIC PROCESS | 16 | 298 | 9.196e-08 | 1.094e-06 |
392 | EPIDERMAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 8 | 55 | 9.227e-08 | 1.095e-06 |
393 | REGULATED EXOCYTOSIS | 14 | 224 | 9.396e-08 | 1.112e-06 |
394 | POSITIVE REGULATION OF IMMUNE RESPONSE | 22 | 563 | 1.011e-07 | 1.194e-06 |
395 | RESPONSE TO REACTIVE OXYGEN SPECIES | 13 | 191 | 1.016e-07 | 1.197e-06 |
396 | BEHAVIOR | 21 | 516 | 1.021e-07 | 1.2e-06 |
397 | ACTIVATION OF IMMUNE RESPONSE | 19 | 427 | 1.087e-07 | 1.274e-06 |
398 | CHEMICAL HOMEOSTASIS | 28 | 874 | 1.101e-07 | 1.287e-06 |
399 | CELLULAR RESPONSE TO EXTERNAL STIMULUS | 15 | 264 | 1.13e-07 | 1.317e-06 |
400 | REGULATION OF DNA REPLICATION | 12 | 161 | 1.185e-07 | 1.379e-06 |
401 | ENDOTHELIAL CELL MIGRATION | 8 | 57 | 1.23e-07 | 1.427e-06 |
402 | REGULATION OF POSITIVE CHEMOTAXIS | 6 | 24 | 1.317e-07 | 1.525e-06 |
403 | ERBB2 SIGNALING PATHWAY | 7 | 39 | 1.335e-07 | 1.538e-06 |
404 | PEPTIDYL TYROSINE AUTOPHOSPHORYLATION | 7 | 39 | 1.335e-07 | 1.538e-06 |
405 | NEGATIVE REGULATION OF CELL CYCLE | 19 | 433 | 1.349e-07 | 1.55e-06 |
406 | POSITIVE REGULATION OF ORGANELLE ORGANIZATION | 22 | 573 | 1.371e-07 | 1.571e-06 |
407 | REGULATION OF HOMOTYPIC CELL CELL ADHESION | 16 | 307 | 1.381e-07 | 1.579e-06 |
408 | CEREBRAL CORTEX DEVELOPMENT | 10 | 105 | 1.393e-07 | 1.585e-06 |
409 | ODONTOGENESIS | 10 | 105 | 1.393e-07 | 1.585e-06 |
410 | POSITIVE REGULATION OF LYMPHOCYTE DIFFERENTIATION | 9 | 80 | 1.407e-07 | 1.593e-06 |
411 | INSULIN RECEPTOR SIGNALING PATHWAY | 9 | 80 | 1.407e-07 | 1.593e-06 |
412 | REGULATION OF CELL GROWTH | 18 | 391 | 1.441e-07 | 1.628e-06 |
413 | REGULATION OF SYNAPSE STRUCTURE OR ACTIVITY | 14 | 232 | 1.449e-07 | 1.633e-06 |
414 | INTERACTION WITH HOST | 11 | 134 | 1.515e-07 | 1.702e-06 |
415 | REGULATION OF CELLULAR RESPONSE TO INSULIN STIMULUS | 8 | 59 | 1.622e-07 | 1.818e-06 |
416 | CELL GROWTH | 11 | 135 | 1.634e-07 | 1.828e-06 |
417 | RESPONSE TO OXIDATIVE STRESS | 17 | 352 | 1.65e-07 | 1.841e-06 |
418 | CELLULAR EXTRAVASATION | 6 | 25 | 1.718e-07 | 1.913e-06 |
419 | GLIAL CELL DIFFERENTIATION | 11 | 136 | 1.762e-07 | 1.957e-06 |
420 | RESPONSE TO EXTRACELLULAR STIMULUS | 19 | 441 | 1.79e-07 | 1.983e-06 |
421 | REGULATION OF GLUCOSE IMPORT | 8 | 60 | 1.855e-07 | 2.05e-06 |
422 | INSULIN LIKE GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 5 | 14 | 2.1e-07 | 2.316e-06 |
423 | OVARIAN FOLLICLE DEVELOPMENT | 8 | 61 | 2.116e-07 | 2.328e-06 |
424 | SECRETION | 22 | 588 | 2.136e-07 | 2.344e-06 |
425 | CELL CYCLE | 35 | 1316 | 2.338e-07 | 2.559e-06 |
426 | RESPONSE TO LIGHT STIMULUS | 15 | 280 | 2.419e-07 | 2.642e-06 |
427 | REGULATION OF LEUKOCYTE PROLIFERATION | 13 | 206 | 2.446e-07 | 2.659e-06 |
428 | ORGANOPHOSPHATE BIOSYNTHETIC PROCESS | 19 | 450 | 2.442e-07 | 2.659e-06 |
429 | NEGATIVE REGULATION OF CELL PROLIFERATION | 23 | 643 | 2.466e-07 | 2.674e-06 |
430 | EMBRYONIC ORGAN DEVELOPMENT | 18 | 406 | 2.515e-07 | 2.715e-06 |
431 | CELL CYCLE PROCESS | 31 | 1081 | 2.515e-07 | 2.715e-06 |
432 | REGULATION OF MITOCHONDRIAL OUTER MEMBRANE PERMEABILIZATION INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 7 | 43 | 2.701e-07 | 2.909e-06 |
433 | OVULATION CYCLE | 10 | 113 | 2.79e-07 | 2.998e-06 |
434 | TISSUE REMODELING | 9 | 87 | 2.924e-07 | 3.135e-06 |
435 | REGULATION OF METAL ION TRANSPORT | 16 | 325 | 2.986e-07 | 3.194e-06 |
436 | RESPONSE TO MECHANICAL STIMULUS | 13 | 210 | 3.052e-07 | 3.257e-06 |
437 | CELLULAR RESPONSE TO LIPID | 19 | 457 | 3.091e-07 | 3.291e-06 |
438 | RESPONSE TO CORTICOSTEROID | 12 | 176 | 3.128e-07 | 3.322e-06 |
439 | NEGATIVE REGULATION OF CELL PROJECTION ORGANIZATION | 11 | 144 | 3.149e-07 | 3.337e-06 |
440 | SKIN DEVELOPMENT | 13 | 211 | 3.223e-07 | 3.408e-06 |
441 | RESPONSE TO RADIATION | 18 | 413 | 3.232e-07 | 3.41e-06 |
442 | REGULATION OF SYSTEM PROCESS | 20 | 507 | 3.431e-07 | 3.612e-06 |
443 | REGULATION OF GENERATION OF PRECURSOR METABOLITES AND ENERGY | 9 | 89 | 3.559e-07 | 3.739e-06 |
444 | FEMALE SEX DIFFERENTIATION | 10 | 116 | 3.568e-07 | 3.74e-06 |
445 | CARTILAGE DEVELOPMENT | 11 | 147 | 3.877e-07 | 4.054e-06 |
446 | MESODERM MORPHOGENESIS | 8 | 66 | 3.948e-07 | 4.119e-06 |
447 | REGULATION OF CELLULAR COMPONENT BIOGENESIS | 25 | 767 | 4.088e-07 | 4.256e-06 |
448 | DIGESTIVE SYSTEM DEVELOPMENT | 11 | 148 | 4.15e-07 | 4.309e-06 |
449 | HEART DEVELOPMENT | 19 | 466 | 4.158e-07 | 4.309e-06 |
450 | REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 7 | 46 | 4.37e-07 | 4.518e-06 |
451 | REGULATION OF PROTEIN INSERTION INTO MITOCHONDRIAL MEMBRANE INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 6 | 29 | 4.453e-07 | 4.584e-06 |
452 | POSITIVE REGULATION OF PROTEIN INSERTION INTO MITOCHONDRIAL MEMBRANE INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 6 | 29 | 4.453e-07 | 4.584e-06 |
453 | DEFENSE RESPONSE | 33 | 1231 | 4.563e-07 | 4.687e-06 |
454 | CELL CYCLE PHASE TRANSITION | 14 | 255 | 4.586e-07 | 4.7e-06 |
455 | REGULATION OF RAS PROTEIN SIGNAL TRANSDUCTION | 12 | 184 | 5.046e-07 | 5.148e-06 |
456 | CELLULAR RESPONSE TO OXIDATIVE STRESS | 12 | 184 | 5.046e-07 | 5.148e-06 |
457 | RESPONSE TO ANTIBIOTIC | 7 | 47 | 5.089e-07 | 5.171e-06 |
458 | POSITIVE REGULATION OF NEURON APOPTOTIC PROCESS | 7 | 47 | 5.089e-07 | 5.171e-06 |
459 | RESPONSE TO GROWTH HORMONE | 6 | 30 | 5.518e-07 | 5.594e-06 |
460 | RESPONSE TO ACTIVITY | 8 | 69 | 5.598e-07 | 5.662e-06 |
461 | RESPONSE TO GLUCAGON | 7 | 48 | 5.906e-07 | 5.949e-06 |
462 | REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION TO PLASMA MEMBRANE | 7 | 48 | 5.906e-07 | 5.949e-06 |
463 | T CELL DIFFERENTIATION | 10 | 123 | 6.163e-07 | 6.194e-06 |
464 | REGULATION OF GLUCOSE IMPORT IN RESPONSE TO INSULIN STIMULUS | 5 | 17 | 6.329e-07 | 6.347e-06 |
465 | CELLULAR RESPONSE TO ABIOTIC STIMULUS | 14 | 263 | 6.648e-07 | 6.652e-06 |
466 | REGULATION OF PLATELET ACTIVATION | 6 | 31 | 6.784e-07 | 6.773e-06 |
467 | GLAND MORPHOGENESIS | 9 | 97 | 7.452e-07 | 7.409e-06 |
468 | REGULATION OF CYCLIN DEPENDENT PROTEIN KINASE ACTIVITY | 9 | 97 | 7.452e-07 | 7.409e-06 |
469 | SEX DIFFERENTIATION | 14 | 266 | 7.614e-07 | 7.554e-06 |
470 | SECRETION BY CELL | 19 | 486 | 7.828e-07 | 7.75e-06 |
471 | STAT CASCADE | 7 | 50 | 7.874e-07 | 7.762e-06 |
472 | JAK STAT CASCADE | 7 | 50 | 7.874e-07 | 7.762e-06 |
473 | NEGATIVE REGULATION OF CELL CYCLE G1 S PHASE TRANSITION | 9 | 98 | 8.133e-07 | 8e-06 |
474 | REGULATION OF COLLATERAL SPROUTING | 5 | 18 | 8.689e-07 | 8.512e-06 |
475 | REGULATION OF ORGAN GROWTH | 8 | 73 | 8.686e-07 | 8.512e-06 |
476 | POSITIVE REGULATION OF MITOTIC NUCLEAR DIVISION | 7 | 51 | 9.047e-07 | 8.843e-06 |
477 | ANTIGEN RECEPTOR MEDIATED SIGNALING PATHWAY | 12 | 195 | 9.366e-07 | 9.137e-06 |
478 | LIMBIC SYSTEM DEVELOPMENT | 9 | 100 | 9.657e-07 | 9.401e-06 |
479 | MULTICELLULAR ORGANISMAL HOMEOSTASIS | 14 | 272 | 9.932e-07 | 9.647e-06 |
480 | KIDNEY VASCULATURE DEVELOPMENT | 5 | 19 | 1.169e-06 | 1.131e-05 |
481 | RENAL SYSTEM VASCULATURE DEVELOPMENT | 5 | 19 | 1.169e-06 | 1.131e-05 |
482 | REGULATION OF LYMPHOCYTE DIFFERENTIATION | 10 | 132 | 1.183e-06 | 1.142e-05 |
483 | PROTEIN KINASE B SIGNALING | 6 | 34 | 1.207e-06 | 1.163e-05 |
484 | REGULATION OF SEQUENCE SPECIFIC DNA BINDING TRANSCRIPTION FACTOR ACTIVITY | 16 | 365 | 1.388e-06 | 1.334e-05 |
485 | EMBRYONIC HEMOPOIESIS | 5 | 20 | 1.546e-06 | 1.483e-05 |
486 | INTERSPECIES INTERACTION BETWEEN ORGANISMS | 22 | 662 | 1.553e-06 | 1.484e-05 |
487 | SYMBIOSIS ENCOMPASSING MUTUALISM THROUGH PARASITISM | 22 | 662 | 1.553e-06 | 1.484e-05 |
488 | GLUCOSE HOMEOSTASIS | 11 | 170 | 1.645e-06 | 1.565e-05 |
489 | CARBOHYDRATE HOMEOSTASIS | 11 | 170 | 1.645e-06 | 1.565e-05 |
490 | ORGANOPHOSPHATE METABOLIC PROCESS | 26 | 885 | 1.661e-06 | 1.578e-05 |
491 | RESPONSE TO BIOTIC STIMULUS | 26 | 886 | 1.696e-06 | 1.607e-05 |
492 | REGULATION OF T CELL DIFFERENTIATION | 9 | 107 | 1.71e-06 | 1.617e-05 |
493 | ANATOMICAL STRUCTURE HOMEOSTASIS | 14 | 285 | 1.724e-06 | 1.627e-05 |
494 | POSITIVE REGULATION OF MUSCLE TISSUE DEVELOPMENT | 7 | 56 | 1.735e-06 | 1.634e-05 |
495 | NEGATIVE REGULATION OF VASCULATURE DEVELOPMENT | 8 | 80 | 1.761e-06 | 1.655e-05 |
496 | POSITIVE REGULATION OF LEUKOCYTE CHEMOTAXIS | 8 | 81 | 1.936e-06 | 1.817e-05 |
497 | RESPONSE TO HYDROGEN PEROXIDE | 9 | 109 | 1.998e-06 | 1.87e-05 |
498 | REGULATION OF PROTEIN IMPORT INTO NUCLEUS TRANSLOCATION | 5 | 21 | 2.012e-06 | 1.88e-05 |
499 | REGULATION OF SYNAPTIC PLASTICITY | 10 | 140 | 2.024e-06 | 1.887e-05 |
500 | NEGATIVE REGULATION OF PHOSPHORYLATION | 17 | 422 | 2.04e-06 | 1.899e-05 |
501 | REGULATION OF CATABOLIC PROCESS | 23 | 731 | 2.234e-06 | 2.075e-05 |
502 | NEGATIVE REGULATION OF MOLECULAR FUNCTION | 29 | 1079 | 2.354e-06 | 2.182e-05 |
503 | SYSTEM PROCESS | 40 | 1785 | 2.364e-06 | 2.186e-05 |
504 | CELLULAR RESPONSE TO GLUCAGON STIMULUS | 6 | 38 | 2.395e-06 | 2.206e-05 |
505 | REGULATION OF MULTICELLULAR ORGANISMAL METABOLIC PROCESS | 6 | 38 | 2.395e-06 | 2.206e-05 |
506 | MITOCHONDRIAL TRANSPORT | 11 | 177 | 2.439e-06 | 2.243e-05 |
507 | POSITIVE REGULATION OF PROTEIN AUTOPHOSPHORYLATION | 5 | 22 | 2.582e-06 | 2.37e-05 |
508 | RESPONSE TO INORGANIC SUBSTANCE | 18 | 479 | 2.7e-06 | 2.473e-05 |
509 | CHONDROCYTE DIFFERENTIATION | 7 | 60 | 2.789e-06 | 2.55e-05 |
510 | MUSCLE STRUCTURE DEVELOPMENT | 17 | 432 | 2.796e-06 | 2.551e-05 |
511 | T CELL RECEPTOR SIGNALING PATHWAY | 10 | 146 | 2.959e-06 | 2.694e-05 |
512 | POSITIVE REGULATION OF STEM CELL PROLIFERATION | 7 | 61 | 3.123e-06 | 2.839e-05 |
513 | REGULATION OF CELL CYCLE G1 S PHASE TRANSITION | 10 | 147 | 3.146e-06 | 2.854e-05 |
514 | NEUROTROPHIN SIGNALING PATHWAY | 5 | 23 | 3.272e-06 | 2.962e-05 |
515 | MOVEMENT IN ENVIRONMENT OF OTHER ORGANISM INVOLVED IN SYMBIOTIC INTERACTION | 8 | 87 | 3.336e-06 | 2.974e-05 |
516 | ENTRY INTO CELL OF OTHER ORGANISM INVOLVED IN SYMBIOTIC INTERACTION | 8 | 87 | 3.336e-06 | 2.974e-05 |
517 | VIRAL ENTRY INTO HOST CELL | 8 | 87 | 3.336e-06 | 2.974e-05 |
518 | ENTRY INTO OTHER ORGANISM INVOLVED IN SYMBIOTIC INTERACTION | 8 | 87 | 3.336e-06 | 2.974e-05 |
519 | MOVEMENT IN HOST ENVIRONMENT | 8 | 87 | 3.336e-06 | 2.974e-05 |
520 | ENTRY INTO HOST | 8 | 87 | 3.336e-06 | 2.974e-05 |
521 | ENTRY INTO HOST CELL | 8 | 87 | 3.336e-06 | 2.974e-05 |
522 | IMMUNE EFFECTOR PROCESS | 18 | 486 | 3.306e-06 | 2.974e-05 |
523 | POSITIVE REGULATION OF CELL GROWTH | 10 | 148 | 3.344e-06 | 2.975e-05 |
524 | REGULATION OF PEPTIDASE ACTIVITY | 16 | 392 | 3.483e-06 | 3.093e-05 |
525 | POSITIVE REGULATION OF NUCLEAR DIVISION | 7 | 62 | 3.49e-06 | 3.093e-05 |
526 | NEGATIVE REGULATION OF CELL DEVELOPMENT | 14 | 303 | 3.522e-06 | 3.115e-05 |
527 | NEGATIVE REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 9 | 117 | 3.604e-06 | 3.182e-05 |
528 | REGULATION OF COAGULATION | 8 | 88 | 3.638e-06 | 3.2e-05 |
529 | POSITIVE REGULATION OF PEPTIDYL SERINE PHOSPHORYLATION | 8 | 88 | 3.638e-06 | 3.2e-05 |
530 | REGULATION OF ION TRANSPORT | 20 | 592 | 3.727e-06 | 3.272e-05 |
531 | RESPONSE TO HEAT | 8 | 89 | 3.962e-06 | 3.465e-05 |
532 | EPITHELIAL CELL PROLIFERATION | 8 | 89 | 3.962e-06 | 3.465e-05 |
533 | REGULATION OF DENDRITE DEVELOPMENT | 9 | 120 | 4.442e-06 | 3.878e-05 |
534 | EXOCYTOSIS | 14 | 310 | 4.583e-06 | 3.993e-05 |
535 | CELL CYCLE ARREST | 10 | 154 | 4.775e-06 | 4.132e-05 |
536 | POSITIVE REGULATION OF PEPTIDASE ACTIVITY | 10 | 154 | 4.775e-06 | 4.132e-05 |
537 | POSITIVE REGULATION OF SEQUENCE SPECIFIC DNA BINDING TRANSCRIPTION FACTOR ACTIVITY | 12 | 228 | 4.778e-06 | 4.132e-05 |
538 | POSITIVE REGULATION OF NUCLEOCYTOPLASMIC TRANSPORT | 9 | 121 | 4.757e-06 | 4.132e-05 |
539 | MESENCHYME DEVELOPMENT | 11 | 190 | 4.839e-06 | 4.177e-05 |
540 | NEGATIVE REGULATION OF NEURON DIFFERENTIATION | 11 | 191 | 5.088e-06 | 4.352e-05 |
541 | REGULATION OF POLYSACCHARIDE METABOLIC PROCESS | 6 | 43 | 5.065e-06 | 4.352e-05 |
542 | CEREBRAL CORTEX CELL MIGRATION | 6 | 43 | 5.065e-06 | 4.352e-05 |
543 | RESPONSE TO NUTRIENT | 11 | 191 | 5.088e-06 | 4.352e-05 |
544 | HISTONE PHOSPHORYLATION | 5 | 25 | 5.08e-06 | 4.352e-05 |
545 | ACTIVATION OF TRANSMEMBRANE RECEPTOR PROTEIN TYROSINE KINASE ACTIVITY | 4 | 12 | 5.171e-06 | 4.414e-05 |
546 | EMBRYO DEVELOPMENT ENDING IN BIRTH OR EGG HATCHING | 19 | 554 | 5.319e-06 | 4.533e-05 |
547 | BONE DEVELOPMENT | 10 | 156 | 5.357e-06 | 4.557e-05 |
548 | POSITIVE REGULATION OF CELLULAR COMPONENT BIOGENESIS | 16 | 406 | 5.437e-06 | 4.617e-05 |
549 | NEGATIVE REGULATION OF TRANSPORT | 17 | 458 | 6.076e-06 | 5.15e-05 |
550 | EAR DEVELOPMENT | 11 | 195 | 6.204e-06 | 5.239e-05 |
551 | REGULATION OF MUSCLE SYSTEM PROCESS | 11 | 195 | 6.204e-06 | 5.239e-05 |
552 | DEVELOPMENTAL PROGRAMMED CELL DEATH | 5 | 26 | 6.236e-06 | 5.257e-05 |
553 | FC GAMMA RECEPTOR SIGNALING PATHWAY | 8 | 95 | 6.466e-06 | 5.431e-05 |
554 | ACTIVATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY | 8 | 95 | 6.466e-06 | 5.431e-05 |
555 | MULTICELLULAR ORGANISMAL RESPONSE TO STRESS | 7 | 68 | 6.529e-06 | 5.454e-05 |
556 | ORGAN GROWTH | 7 | 68 | 6.529e-06 | 5.454e-05 |
557 | REGULATION OF NEUROLOGICAL SYSTEM PROCESS | 7 | 68 | 6.529e-06 | 5.454e-05 |
558 | REGULATION OF WOUND HEALING | 9 | 126 | 6.632e-06 | 5.52e-05 |
559 | RESPONSE TO UV | 9 | 126 | 6.632e-06 | 5.52e-05 |
560 | EXOCRINE SYSTEM DEVELOPMENT | 6 | 45 | 6.652e-06 | 5.527e-05 |
561 | POSITIVE REGULATION OF ION TRANSPORT | 12 | 236 | 6.792e-06 | 5.634e-05 |
562 | REGULATION OF STRESS ACTIVATED PROTEIN KINASE SIGNALING CASCADE | 11 | 197 | 6.837e-06 | 5.661e-05 |
563 | REGULATION OF SMALL GTPASE MEDIATED SIGNAL TRANSDUCTION | 13 | 278 | 6.954e-06 | 5.747e-05 |
564 | REGULATION OF LEUKOCYTE CHEMOTAXIS | 8 | 96 | 6.992e-06 | 5.769e-05 |
565 | SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR | 9 | 127 | 7.075e-06 | 5.826e-05 |
566 | REGENERATION | 10 | 161 | 7.088e-06 | 5.827e-05 |
567 | CELLULAR RESPONSE TO ORGANIC CYCLIC COMPOUND | 17 | 465 | 7.413e-06 | 6.073e-05 |
568 | POSITIVE REGULATION OF PROTEIN IMPORT INTO NUCLEUS TRANSLOCATION | 4 | 13 | 7.408e-06 | 6.073e-05 |
569 | NEGATIVE REGULATION OF MITOTIC CELL CYCLE | 11 | 199 | 7.526e-06 | 6.155e-05 |
570 | POSITIVE REGULATION OF MESENCHYMAL CELL PROLIFERATION | 5 | 27 | 7.59e-06 | 6.195e-05 |
571 | CELLULAR HOMEOSTASIS | 21 | 676 | 7.696e-06 | 6.271e-05 |
572 | SENSORY ORGAN MORPHOGENESIS | 12 | 239 | 7.721e-06 | 6.281e-05 |
573 | RESPONSE TO VITAMIN | 8 | 98 | 8.153e-06 | 6.621e-05 |
574 | REGULATION OF ANATOMICAL STRUCTURE SIZE | 17 | 472 | 9.009e-06 | 7.303e-05 |
575 | REGULATION OF SPROUTING ANGIOGENESIS | 5 | 28 | 9.162e-06 | 7.414e-05 |
576 | NEGATIVE REGULATION OF CELLULAR COMPONENT ORGANIZATION | 21 | 684 | 9.198e-06 | 7.43e-05 |
577 | MITOTIC DNA INTEGRITY CHECKPOINT | 8 | 100 | 9.472e-06 | 7.625e-05 |
578 | REGULATION OF GLUCOSE TRANSPORT | 8 | 100 | 9.472e-06 | 7.625e-05 |
579 | POSITIVE REGULATION OF REACTIVE OXYGEN SPECIES BIOSYNTHETIC PROCESS | 6 | 48 | 9.766e-06 | 7.848e-05 |
580 | REGULATION OF EXTENT OF CELL GROWTH | 8 | 101 | 1.02e-05 | 8.18e-05 |
581 | POSITIVE REGULATION OF RHO PROTEIN SIGNAL TRANSDUCTION | 4 | 14 | 1.029e-05 | 8.224e-05 |
582 | POSITIVE REGULATION OF SPROUTING ANGIOGENESIS | 4 | 14 | 1.029e-05 | 8.224e-05 |
583 | HIPPOCAMPUS DEVELOPMENT | 7 | 73 | 1.05e-05 | 8.355e-05 |
584 | G1 DNA DAMAGE CHECKPOINT | 7 | 73 | 1.05e-05 | 8.355e-05 |
585 | REGULATION OF PLASMA MEMBRANE ORGANIZATION | 7 | 73 | 1.05e-05 | 8.355e-05 |
586 | REGULATION OF DENDRITE MORPHOGENESIS | 7 | 74 | 1.15e-05 | 9.124e-05 |
587 | REGULATION OF CYTOPLASMIC TRANSPORT | 17 | 481 | 1.151e-05 | 9.124e-05 |
588 | REGULATION OF MUSCLE ORGAN DEVELOPMENT | 8 | 103 | 1.179e-05 | 9.327e-05 |
589 | REGULATION OF CALCIUM ION TRANSPORT | 11 | 209 | 1.196e-05 | 9.449e-05 |
590 | RESPONSE TO ETHANOL | 9 | 136 | 1.233e-05 | 9.726e-05 |
591 | POSITIVE REGULATION OF CARBOHYDRATE METABOLIC PROCESS | 7 | 75 | 1.257e-05 | 9.883e-05 |
592 | GRANULOCYTE MIGRATION | 7 | 75 | 1.257e-05 | 9.883e-05 |
593 | REGULATION OF CARBOHYDRATE METABOLIC PROCESS | 10 | 172 | 1.267e-05 | 9.928e-05 |
594 | CELLULAR RESPONSE TO REACTIVE OXYGEN SPECIES | 8 | 104 | 1.266e-05 | 9.928e-05 |
595 | NEGATIVE REGULATION OF TOR SIGNALING | 5 | 30 | 1.306e-05 | 0.0001022 |
596 | REGULATION OF DEFENSE RESPONSE | 22 | 759 | 1.368e-05 | 0.0001067 |
597 | EPIDERMIS DEVELOPMENT | 12 | 253 | 1.369e-05 | 0.0001067 |
598 | CELL MIGRATION INVOLVED IN SPROUTING ANGIOGENESIS | 4 | 15 | 1.391e-05 | 0.0001077 |
599 | NEGATIVE REGULATION OF DENDRITE MORPHOGENESIS | 4 | 15 | 1.391e-05 | 0.0001077 |
600 | JAK STAT CASCADE INVOLVED IN GROWTH HORMONE SIGNALING PATHWAY | 4 | 15 | 1.391e-05 | 0.0001077 |
601 | NEUROTROPHIN TRK RECEPTOR SIGNALING PATHWAY | 4 | 15 | 1.391e-05 | 0.0001077 |
602 | MITOTIC CELL CYCLE CHECKPOINT | 9 | 139 | 1.47e-05 | 0.0001134 |
603 | REGULATION OF CELL SHAPE | 9 | 139 | 1.47e-05 | 0.0001134 |
604 | MITOTIC CELL CYCLE | 22 | 766 | 1.576e-05 | 0.0001214 |
605 | MODULATION OF SYNAPTIC TRANSMISSION | 13 | 301 | 1.623e-05 | 0.0001248 |
606 | REGULATION OF OSSIFICATION | 10 | 178 | 1.708e-05 | 0.0001311 |
607 | NEGATIVE REGULATION OF CATALYTIC ACTIVITY | 23 | 829 | 1.733e-05 | 0.0001328 |
608 | REGULATION OF MORPHOGENESIS OF A BRANCHING STRUCTURE | 6 | 53 | 1.75e-05 | 0.0001335 |
609 | REGULATION OF NITRIC OXIDE BIOSYNTHETIC PROCESS | 6 | 53 | 1.75e-05 | 0.0001335 |
610 | NEGATIVE REGULATION OF CELL SUBSTRATE ADHESION | 6 | 53 | 1.75e-05 | 0.0001335 |
611 | PROTEIN COMPLEX SUBUNIT ORGANIZATION | 34 | 1527 | 1.762e-05 | 0.0001342 |
612 | REGULATION OF MITOCHONDRION ORGANIZATION | 11 | 218 | 1.774e-05 | 0.0001347 |
613 | REGULATION OF PROTEIN LOCALIZATION TO NUCLEUS | 11 | 218 | 1.774e-05 | 0.0001347 |
614 | REGULATION OF RHO PROTEIN SIGNAL TRANSDUCTION | 8 | 109 | 1.786e-05 | 0.0001354 |
615 | SALIVARY GLAND DEVELOPMENT | 5 | 32 | 1.815e-05 | 0.0001369 |
616 | NEGATIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 5 | 32 | 1.815e-05 | 0.0001369 |
617 | NEGATIVE REGULATION OF SIGNAL TRANSDUCTION IN ABSENCE OF LIGAND | 5 | 32 | 1.815e-05 | 0.0001369 |
618 | POSITIVE REGULATION OF TYROSINE PHOSPHORYLATION OF STAT5 PROTEIN | 4 | 16 | 1.84e-05 | 0.0001381 |
619 | BRANCHING INVOLVED IN SALIVARY GLAND MORPHOGENESIS | 4 | 16 | 1.84e-05 | 0.0001381 |
620 | REGULATION OF DEVELOPMENTAL PIGMENTATION | 4 | 16 | 1.84e-05 | 0.0001381 |
621 | NEURON MIGRATION | 8 | 110 | 1.909e-05 | 0.0001431 |
622 | CELLULAR RESPONSE TO MECHANICAL STIMULUS | 7 | 80 | 1.927e-05 | 0.0001441 |
623 | REGULATION OF NUCLEOCYTOPLASMIC TRANSPORT | 11 | 220 | 1.931e-05 | 0.0001442 |
624 | RESPONSE TO TRANSFORMING GROWTH FACTOR BETA | 9 | 144 | 1.951e-05 | 0.0001455 |
625 | CELLULAR RESPONSE TO DNA DAMAGE STIMULUS | 21 | 720 | 1.98e-05 | 0.0001474 |
626 | COLUMNAR CUBOIDAL EPITHELIAL CELL DIFFERENTIATION | 8 | 111 | 2.04e-05 | 0.0001516 |
627 | REGULATION OF MYELOID CELL DIFFERENTIATION | 10 | 183 | 2.17e-05 | 0.0001606 |
628 | REGULATION OF PROTEIN IMPORT | 10 | 183 | 2.17e-05 | 0.0001606 |
629 | REGULATION OF OSTEOBLAST DIFFERENTIATION | 8 | 112 | 2.177e-05 | 0.0001606 |
630 | NEGATIVE REGULATION OF CELL CYCLE PHASE TRANSITION | 9 | 146 | 2.178e-05 | 0.0001606 |
631 | ZYMOGEN ACTIVATION | 8 | 112 | 2.177e-05 | 0.0001606 |
632 | NEGATIVE REGULATION OF CELL ADHESION | 11 | 223 | 2.189e-05 | 0.0001612 |
633 | NEGATIVE REGULATION OF PROTEIN MODIFICATION PROCESS | 19 | 616 | 2.348e-05 | 0.0001726 |
634 | POSITIVE REGULATION OF GLYCOGEN METABOLIC PROCESS | 4 | 17 | 2.387e-05 | 0.0001749 |
635 | POSITIVE REGULATION OF NUCLEOTIDE CATABOLIC PROCESS | 4 | 17 | 2.387e-05 | 0.0001749 |
636 | RESPONSE TO TEMPERATURE STIMULUS | 9 | 148 | 2.426e-05 | 0.0001775 |
637 | ORGAN REGENERATION | 7 | 83 | 2.453e-05 | 0.0001792 |
638 | REGULATION OF MESENCHYMAL CELL PROLIFERATION | 5 | 34 | 2.466e-05 | 0.0001799 |
639 | APOPTOTIC MITOCHONDRIAL CHANGES | 6 | 57 | 2.673e-05 | 0.0001946 |
640 | REGULATION OF VESICLE MEDIATED TRANSPORT | 16 | 462 | 2.684e-05 | 0.0001951 |
641 | POSITIVE REGULATION OF PROTEOLYSIS | 14 | 363 | 2.702e-05 | 0.0001961 |
642 | CELLULAR RESPONSE TO EXTRACELLULAR STIMULUS | 10 | 188 | 2.736e-05 | 0.0001983 |
643 | BONE REMODELING | 5 | 35 | 2.853e-05 | 0.0002058 |
644 | REGULATION OF GLYCOGEN METABOLIC PROCESS | 5 | 35 | 2.853e-05 | 0.0002058 |
645 | CELLULAR CHEMICAL HOMEOSTASIS | 18 | 570 | 2.853e-05 | 0.0002058 |
646 | EPHRIN RECEPTOR SIGNALING PATHWAY | 7 | 85 | 2.866e-05 | 0.0002064 |
647 | CIRCULATORY SYSTEM PROCESS | 14 | 366 | 2.957e-05 | 0.0002127 |
648 | STEM CELL DIFFERENTIATION | 10 | 190 | 2.995e-05 | 0.0002148 |
649 | PHAGOCYTOSIS | 10 | 190 | 2.995e-05 | 0.0002148 |
650 | CELLULAR RESPONSE TO PROSTAGLANDIN E STIMULUS | 4 | 18 | 3.044e-05 | 0.0002179 |
651 | RESPONSE TO MOLECULE OF BACTERIAL ORIGIN | 13 | 321 | 3.18e-05 | 0.0002273 |
652 | REGULATION OF EPITHELIAL CELL APOPTOTIC PROCESS | 6 | 59 | 3.262e-05 | 0.0002321 |
653 | POSITIVE REGULATION OF DNA BIOSYNTHETIC PROCESS | 6 | 59 | 3.262e-05 | 0.0002321 |
654 | VASCULOGENESIS | 6 | 59 | 3.262e-05 | 0.0002321 |
655 | RESPONSE TO ENDOPLASMIC RETICULUM STRESS | 11 | 233 | 3.278e-05 | 0.0002329 |
656 | REGULATION OF NUCLEOTIDE CATABOLIC PROCESS | 5 | 36 | 3.286e-05 | 0.0002331 |
657 | REGULATION OF CARBOHYDRATE BIOSYNTHETIC PROCESS | 7 | 87 | 3.334e-05 | 0.0002361 |
658 | LEUKOCYTE PROLIFERATION | 7 | 88 | 3.591e-05 | 0.0002528 |
659 | NEGATIVE REGULATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY | 7 | 88 | 3.591e-05 | 0.0002528 |
660 | REGULATION OF STEM CELL PROLIFERATION | 7 | 88 | 3.591e-05 | 0.0002528 |
661 | CELL CYCLE CHECKPOINT | 10 | 194 | 3.578e-05 | 0.0002528 |
662 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO CELL PERIPHERY | 5 | 37 | 3.767e-05 | 0.000264 |
663 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO PLASMA MEMBRANE | 5 | 37 | 3.767e-05 | 0.000264 |
664 | REGULATION OF PROTEIN AUTOPHOSPHORYLATION | 5 | 37 | 3.767e-05 | 0.000264 |
665 | POSITIVE REGULATION OF CARDIAC MUSCLE CELL PROLIFERATION | 4 | 19 | 3.825e-05 | 0.0002676 |
666 | MESONEPHROS DEVELOPMENT | 7 | 90 | 4.153e-05 | 0.0002901 |
667 | REGULATION OF TRANSPORTER ACTIVITY | 10 | 198 | 4.254e-05 | 0.0002968 |
668 | POSITIVE REGULATION OF ORGAN GROWTH | 5 | 38 | 4.302e-05 | 0.0002997 |
669 | FOREBRAIN CELL MIGRATION | 6 | 62 | 4.338e-05 | 0.0003013 |
670 | REGULATION OF TISSUE REMODELING | 6 | 62 | 4.338e-05 | 0.0003013 |
671 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 25 | 1004 | 4.432e-05 | 0.0003073 |
672 | REGULATION OF ENDOCYTOSIS | 10 | 199 | 4.44e-05 | 0.0003074 |
673 | PROTEIN COMPLEX BIOGENESIS | 27 | 1132 | 4.509e-05 | 0.0003113 |
674 | PROTEIN COMPLEX ASSEMBLY | 27 | 1132 | 4.509e-05 | 0.0003113 |
675 | REGULATION OF ORGAN MORPHOGENESIS | 11 | 242 | 4.63e-05 | 0.0003192 |
676 | AMELOGENESIS | 4 | 20 | 4.742e-05 | 0.0003255 |
677 | REGULATION OF NEURON PROJECTION REGENERATION | 4 | 20 | 4.742e-05 | 0.0003255 |
678 | REGULATION OF TYROSINE PHOSPHORYLATION OF STAT5 PROTEIN | 4 | 20 | 4.742e-05 | 0.0003255 |
679 | REGULATION OF CELL ADHESION MEDIATED BY INTEGRIN | 5 | 39 | 4.893e-05 | 0.0003348 |
680 | ASTROCYTE DIFFERENTIATION | 5 | 39 | 4.893e-05 | 0.0003348 |
681 | REGULATION OF CELLULAR COMPONENT SIZE | 13 | 337 | 5.241e-05 | 0.0003581 |
682 | REGULATION OF DNA BIOSYNTHETIC PROCESS | 7 | 94 | 5.495e-05 | 0.0003749 |
683 | REGULATION OF REACTIVE OXYGEN SPECIES BIOSYNTHETIC PROCESS | 6 | 65 | 5.68e-05 | 0.000387 |
684 | REGULATION OF PROTEIN SECRETION | 14 | 389 | 5.723e-05 | 0.0003893 |
685 | POSITIVE REGULATION OF ADHERENS JUNCTION ORGANIZATION | 4 | 21 | 5.811e-05 | 0.0003947 |
686 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO NUCLEUS | 8 | 129 | 6.009e-05 | 0.0004076 |
687 | MEMBRANE ORGANIZATION | 23 | 899 | 6.075e-05 | 0.0004114 |
688 | EPITHELIAL CELL DIFFERENTIATION | 16 | 495 | 6.109e-05 | 0.0004132 |
689 | REGULATION OF MULTICELLULAR ORGANISM GROWTH | 6 | 66 | 6.195e-05 | 0.0004184 |
690 | POSITIVE REGULATION OF KIDNEY DEVELOPMENT | 5 | 41 | 6.263e-05 | 0.0004224 |
691 | MYELOID LEUKOCYTE DIFFERENTIATION | 7 | 96 | 6.288e-05 | 0.0004228 |
692 | SIGNAL TRANSDUCTION IN RESPONSE TO DNA DAMAGE | 7 | 96 | 6.288e-05 | 0.0004228 |
693 | RESPONSE TO CARBOHYDRATE | 9 | 168 | 6.551e-05 | 0.0004399 |
694 | POSITIVE REGULATION OF CATABOLIC PROCESS | 14 | 395 | 6.741e-05 | 0.000452 |
695 | REGULATION OF CELLULAR CARBOHYDRATE CATABOLIC PROCESS | 5 | 42 | 7.05e-05 | 0.0004686 |
696 | POSITIVE REGULATION OF GLUCOSE TRANSPORT | 5 | 42 | 7.05e-05 | 0.0004686 |
697 | SOMATIC STEM CELL DIVISION | 4 | 22 | 7.045e-05 | 0.0004686 |
698 | ACTIVATION OF PROTEIN KINASE B ACTIVITY | 4 | 22 | 7.045e-05 | 0.0004686 |
699 | REGULATION OF CARBOHYDRATE CATABOLIC PROCESS | 5 | 42 | 7.05e-05 | 0.0004686 |
700 | ERK1 AND ERK2 CASCADE | 4 | 22 | 7.045e-05 | 0.0004686 |
701 | B CELL ACTIVATION | 8 | 132 | 7.07e-05 | 0.0004693 |
702 | REGULATION OF NUCLEOTIDE METABOLIC PROCESS | 10 | 211 | 7.259e-05 | 0.0004811 |
703 | REGULATION OF TOR SIGNALING | 6 | 68 | 7.336e-05 | 0.0004855 |
704 | REGULATION OF CELL CYCLE PROCESS | 17 | 558 | 7.439e-05 | 0.0004916 |
705 | CELLULAR MACROMOLECULE LOCALIZATION | 28 | 1234 | 7.683e-05 | 0.0005071 |
706 | MESENCHYMAL CELL DIFFERENTIATION | 8 | 134 | 7.86e-05 | 0.0005173 |
707 | MULTI MULTICELLULAR ORGANISM PROCESS | 10 | 213 | 7.852e-05 | 0.0005173 |
708 | MYELOID LEUKOCYTE MEDIATED IMMUNITY | 5 | 43 | 7.911e-05 | 0.0005199 |
709 | VESICLE MEDIATED TRANSPORT | 28 | 1239 | 8.234e-05 | 0.0005404 |
710 | POSITIVE REGULATION OF CELLULAR RESPONSE TO INSULIN STIMULUS | 4 | 23 | 8.459e-05 | 0.0005528 |
711 | POSITIVE REGULATION OF NEUROLOGICAL SYSTEM PROCESS | 4 | 23 | 8.459e-05 | 0.0005528 |
712 | LEUKOCYTE APOPTOTIC PROCESS | 4 | 23 | 8.459e-05 | 0.0005528 |
713 | CENTRAL NERVOUS SYSTEM NEURON DEVELOPMENT | 6 | 70 | 8.638e-05 | 0.0005637 |
714 | BRANCHING INVOLVED IN URETERIC BUD MORPHOGENESIS | 5 | 44 | 8.851e-05 | 0.0005768 |
715 | RESPONSE TO ALKALOID | 8 | 137 | 9.183e-05 | 0.0005976 |
716 | REGULATION OF INNATE IMMUNE RESPONSE | 13 | 357 | 9.384e-05 | 0.0006098 |
717 | NEGATIVE REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 11 | 262 | 9.436e-05 | 0.0006124 |
718 | PLACENTA DEVELOPMENT | 8 | 138 | 9.662e-05 | 0.0006262 |
719 | REGULATION OF MUSCLE TISSUE DEVELOPMENT | 7 | 103 | 9.834e-05 | 0.0006364 |
720 | ENDOCHONDRAL BONE MORPHOGENESIS | 5 | 45 | 9.874e-05 | 0.0006381 |
721 | CELLULAR RESPONSE TO PROSTAGLANDIN STIMULUS | 4 | 24 | 0.0001007 | 0.0006453 |
722 | POSITIVE REGULATION OF NUCLEOSIDE METABOLIC PROCESS | 4 | 24 | 0.0001007 | 0.0006453 |
723 | BLOOD VESSEL ENDOTHELIAL CELL MIGRATION | 4 | 24 | 0.0001007 | 0.0006453 |
724 | POSITIVE REGULATION OF CELL JUNCTION ASSEMBLY | 4 | 24 | 0.0001007 | 0.0006453 |
725 | POSITIVE REGULATION OF RECEPTOR INTERNALIZATION | 4 | 24 | 0.0001007 | 0.0006453 |
726 | POSITIVE REGULATION OF ATP METABOLIC PROCESS | 4 | 24 | 0.0001007 | 0.0006453 |
727 | IN UTERO EMBRYONIC DEVELOPMENT | 12 | 311 | 0.0001017 | 0.0006506 |
728 | POSITIVE REGULATION OF PROTEIN IMPORT | 7 | 104 | 0.0001045 | 0.0006672 |
729 | DEVELOPMENTAL GROWTH INVOLVED IN MORPHOGENESIS | 7 | 104 | 0.0001045 | 0.0006672 |
730 | REGULATION OF PROTEIN STABILITY | 10 | 221 | 0.0001065 | 0.0006791 |
731 | ION HOMEOSTASIS | 17 | 576 | 0.0001092 | 0.0006953 |
732 | PEPTIDYL THREONINE MODIFICATION | 5 | 46 | 0.0001099 | 0.0006983 |
733 | POSITIVE REGULATION OF DEFENSE RESPONSE | 13 | 364 | 0.0001139 | 0.0007229 |
734 | RESPONSE TO PROSTAGLANDIN E | 4 | 25 | 0.0001189 | 0.0007537 |
735 | POSITIVE REGULATION OF DEPHOSPHORYLATION | 5 | 47 | 0.0001219 | 0.0007718 |
736 | CELLULAR RESPONSE TO OXYGEN LEVELS | 8 | 143 | 0.0001238 | 0.0007818 |
737 | RAS PROTEIN SIGNAL TRANSDUCTION | 8 | 143 | 0.0001238 | 0.0007818 |
738 | BIOMINERAL TISSUE DEVELOPMENT | 6 | 75 | 0.0001271 | 0.0008013 |
739 | REGULATION OF RESPONSE TO CYTOKINE STIMULUS | 8 | 144 | 0.00013 | 0.0008183 |
740 | REGULATION OF CELL CYCLE ARREST | 7 | 108 | 0.0001325 | 0.0008321 |
741 | REGULATION OF MYELOID LEUKOCYTE DIFFERENTIATION | 7 | 108 | 0.0001325 | 0.0008321 |
742 | POSITIVE REGULATION OF CYTOKINE PRODUCTION | 13 | 370 | 0.0001339 | 0.0008398 |
743 | COLUMNAR CUBOIDAL EPITHELIAL CELL DEVELOPMENT | 5 | 48 | 0.0001349 | 0.0008451 |
744 | RESPONSE TO IONIZING RADIATION | 8 | 145 | 0.0001364 | 0.0008516 |
745 | SYNAPSE ORGANIZATION | 8 | 145 | 0.0001364 | 0.0008516 |
746 | GLIAL CELL DEVELOPMENT | 6 | 76 | 0.0001368 | 0.0008533 |
747 | REPLACEMENT OSSIFICATION | 4 | 26 | 0.0001394 | 0.000867 |
748 | ENDOCHONDRAL OSSIFICATION | 4 | 26 | 0.0001394 | 0.000867 |
749 | NEGATIVE REGULATION OF RESPONSE TO EXTERNAL STIMULUS | 11 | 274 | 0.00014 | 0.0008698 |
750 | NEGATIVE REGULATION OF IMMUNE SYSTEM PROCESS | 13 | 372 | 0.0001412 | 0.0008762 |
751 | REGULATION OF IMMUNE EFFECTOR PROCESS | 14 | 424 | 0.0001421 | 0.0008806 |
752 | DNA INTEGRITY CHECKPOINT | 8 | 146 | 0.000143 | 0.0008848 |
753 | REGULATION OF SODIUM ION TRANSPORT | 6 | 77 | 0.0001471 | 0.000909 |
754 | REGULATION OF NITRIC OXIDE SYNTHASE ACTIVITY | 5 | 49 | 0.000149 | 0.0009136 |
755 | REGULATION OF NUCLEOSIDE METABOLIC PROCESS | 5 | 49 | 0.000149 | 0.0009136 |
756 | POSITIVE REGULATION OF CHEMOKINE PRODUCTION | 5 | 49 | 0.000149 | 0.0009136 |
757 | POSITIVE REGULATION OF SYNAPTIC TRANSMISSION | 7 | 110 | 0.0001486 | 0.0009136 |
758 | REGULATION OF ATP METABOLIC PROCESS | 5 | 49 | 0.000149 | 0.0009136 |
759 | MULTICELLULAR ORGANISM REPRODUCTION | 20 | 768 | 0.0001484 | 0.0009136 |
760 | RESPONSE TO TRANSITION METAL NANOPARTICLE | 8 | 148 | 0.0001571 | 0.0009596 |
761 | REGULATION OF PROTEOLYSIS | 19 | 711 | 0.0001571 | 0.0009596 |
762 | MALE SEX DIFFERENTIATION | 8 | 148 | 0.0001571 | 0.0009596 |
763 | REGULATION OF RECEPTOR MEDIATED ENDOCYTOSIS | 6 | 78 | 0.000158 | 0.0009611 |
764 | RENAL TUBULE DEVELOPMENT | 6 | 78 | 0.000158 | 0.0009611 |
765 | EYE DEVELOPMENT | 12 | 326 | 0.0001579 | 0.0009611 |
766 | POSITIVE REGULATION OF HEART GROWTH | 4 | 27 | 0.0001623 | 0.0009846 |
767 | SUBSTRATE DEPENDENT CELL MIGRATION | 4 | 27 | 0.0001623 | 0.0009846 |
768 | REGULATION OF COENZYME METABOLIC PROCESS | 5 | 50 | 0.0001642 | 0.0009936 |
769 | REGULATION OF COFACTOR METABOLIC PROCESS | 5 | 50 | 0.0001642 | 0.0009936 |
770 | REGULATION OF CYTOKINE SECRETION | 8 | 149 | 0.0001645 | 0.0009943 |
771 | EAR MORPHOGENESIS | 7 | 112 | 0.0001663 | 0.001003 |
772 | PROSTATE GLAND GROWTH | 3 | 11 | 0.0001696 | 0.001021 |
773 | BONE MORPHOGENESIS | 6 | 79 | 0.0001695 | 0.001021 |
774 | REGULATION OF SYNAPSE ORGANIZATION | 7 | 113 | 0.0001757 | 0.001056 |
775 | POSITIVE REGULATION OF CYTOPLASMIC TRANSPORT | 11 | 282 | 0.0001799 | 0.00108 |
776 | NEGATIVE REGULATION OF GROWTH | 10 | 236 | 0.0001822 | 0.001092 |
777 | POSITIVE REGULATION OF ENDOCYTOSIS | 7 | 114 | 0.0001856 | 0.001111 |
778 | NEGATIVE REGULATION OF DENDRITE DEVELOPMENT | 4 | 28 | 0.0001878 | 0.001118 |
779 | LONG TERM MEMORY | 4 | 28 | 0.0001878 | 0.001118 |
780 | IMMUNE RESPONSE | 25 | 1100 | 0.000187 | 0.001118 |
781 | MAMMARY GLAND DUCT MORPHOGENESIS | 4 | 28 | 0.0001878 | 0.001118 |
782 | POSITIVE REGULATION OF PHOSPHATASE ACTIVITY | 4 | 28 | 0.0001878 | 0.001118 |
783 | NEGATIVE REGULATION OF EPITHELIAL CELL PROLIFERATION | 7 | 115 | 0.0001959 | 0.001164 |
784 | ACTIVATION OF MAPKK ACTIVITY | 5 | 52 | 0.0001981 | 0.001176 |
785 | KIDNEY MORPHOGENESIS | 6 | 82 | 0.0002082 | 0.001234 |
786 | SENSORY PERCEPTION OF MECHANICAL STIMULUS | 8 | 155 | 0.0002157 | 0.001275 |
787 | REGULATION OF CARDIAC MUSCLE CELL PROLIFERATION | 4 | 29 | 0.0002161 | 0.001275 |
788 | STEM CELL DIVISION | 4 | 29 | 0.0002161 | 0.001275 |
789 | POSITIVE REGULATION OF CARDIAC MUSCLE TISSUE DEVELOPMENT | 4 | 29 | 0.0002161 | 0.001275 |
790 | NEGATIVE REGULATION OF AUTOPHAGY | 5 | 53 | 0.0002169 | 0.001276 |
791 | MESONEPHRIC TUBULE MORPHOGENESIS | 5 | 53 | 0.0002169 | 0.001276 |
792 | PRODUCTION OF MOLECULAR MEDIATOR INVOLVED IN INFLAMMATORY RESPONSE | 3 | 12 | 0.0002244 | 0.001315 |
793 | MAMMARY GLAND EPITHELIAL CELL PROLIFERATION | 3 | 12 | 0.0002244 | 0.001315 |
794 | POSITIVE REGULATION OF GLUCOSE IMPORT IN RESPONSE TO INSULIN STIMULUS | 3 | 12 | 0.0002244 | 0.001315 |
795 | PROTEIN LOCALIZATION TO NUCLEUS | 8 | 156 | 0.0002254 | 0.001319 |
796 | REGULATION OF MITOCHONDRIAL MEMBRANE POTENTIAL | 5 | 54 | 0.000237 | 0.001386 |
797 | RESPONSE TO PURINE CONTAINING COMPOUND | 8 | 158 | 0.0002458 | 0.001435 |
798 | RESPONSE TO EPIDERMAL GROWTH FACTOR | 4 | 30 | 0.0002474 | 0.001439 |
799 | NEGATIVE REGULATION OF MUSCLE CELL APOPTOTIC PROCESS | 4 | 30 | 0.0002474 | 0.001439 |
800 | OSTEOCLAST DIFFERENTIATION | 4 | 30 | 0.0002474 | 0.001439 |
801 | POSTTRANSCRIPTIONAL REGULATION OF GENE EXPRESSION | 14 | 448 | 0.0002503 | 0.001454 |
802 | POSITIVE REGULATION OF CELL CYCLE ARREST | 6 | 85 | 0.0002534 | 0.00147 |
803 | REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY VIA DEATH DOMAIN RECEPTORS | 5 | 55 | 0.0002586 | 0.001496 |
804 | REGULATION OF KIDNEY DEVELOPMENT | 5 | 55 | 0.0002586 | 0.001496 |
805 | ACTIN FILAMENT BASED PROCESS | 14 | 450 | 0.0002619 | 0.001514 |
806 | REGULATION OF CYTOKINE PRODUCTION | 16 | 563 | 0.0002666 | 0.001539 |
807 | POSITIVE REGULATION OF B CELL ACTIVATION | 6 | 86 | 0.0002701 | 0.001557 |
808 | NEGATIVE REGULATION OF CATABOLIC PROCESS | 9 | 203 | 0.0002741 | 0.001578 |
809 | REGULATION OF AUTOPHAGY | 10 | 249 | 0.0002802 | 0.001612 |
810 | NEGATIVE REGULATION OF CELLULAR RESPONSE TO INSULIN STIMULUS | 4 | 31 | 0.0002817 | 0.001618 |
811 | ENDOCYTOSIS | 15 | 509 | 0.000283 | 0.001624 |
812 | NEURONAL STEM CELL DIVISION | 3 | 13 | 0.0002895 | 0.001643 |
813 | NEGATIVE REGULATION OF KINASE ACTIVITY | 10 | 250 | 0.0002893 | 0.001643 |
814 | INDUCTION OF POSITIVE CHEMOTAXIS | 3 | 13 | 0.0002895 | 0.001643 |
815 | REGULATION OF CELL PROLIFERATION INVOLVED IN KIDNEY DEVELOPMENT | 3 | 13 | 0.0002895 | 0.001643 |
816 | LEUKOCYTE TETHERING OR ROLLING | 3 | 13 | 0.0002895 | 0.001643 |
817 | CELLULAR RESPONSE TO HEPATOCYTE GROWTH FACTOR STIMULUS | 3 | 13 | 0.0002895 | 0.001643 |
818 | RESPONSE TO HEPATOCYTE GROWTH FACTOR | 3 | 13 | 0.0002895 | 0.001643 |
819 | LEUKOCYTE ADHESION TO VASCULAR ENDOTHELIAL CELL | 3 | 13 | 0.0002895 | 0.001643 |
820 | NEUROBLAST DIVISION | 3 | 13 | 0.0002895 | 0.001643 |
821 | POSITIVE REGULATION OF RESPONSE TO WOUNDING | 8 | 162 | 0.0002911 | 0.00165 |
822 | ENDOCRINE SYSTEM DEVELOPMENT | 7 | 123 | 0.0002963 | 0.001677 |
823 | CELLULAR PROCESS INVOLVED IN REPRODUCTION IN MULTICELLULAR ORGANISM | 10 | 252 | 0.0003082 | 0.001743 |
824 | CELL DIVISION | 14 | 460 | 0.0003269 | 0.001844 |
825 | KIDNEY EPITHELIUM DEVELOPMENT | 7 | 125 | 0.0003269 | 0.001844 |
826 | REGULATION OF CELLULAR AMIDE METABOLIC PROCESS | 12 | 354 | 0.0003355 | 0.00189 |
827 | OSTEOBLAST DIFFERENTIATION | 7 | 126 | 0.0003432 | 0.001931 |
828 | MIDBRAIN DEVELOPMENT | 6 | 90 | 0.0003457 | 0.001942 |
829 | POSITIVE REGULATION OF MITOCHONDRION ORGANIZATION | 8 | 167 | 0.0003573 | 0.002005 |
830 | REGULATION OF BONE RESORPTION | 4 | 33 | 0.0003605 | 0.002021 |
831 | POSITIVE REGULATION OF METANEPHROS DEVELOPMENT | 3 | 14 | 0.0003656 | 0.002031 |
832 | POSITIVE REGULATION OF NITRIC OXIDE SYNTHASE BIOSYNTHETIC PROCESS | 3 | 14 | 0.0003656 | 0.002031 |
833 | EPITHELIAL CELL CELL ADHESION | 3 | 14 | 0.0003656 | 0.002031 |
834 | REGULATION OF FIBROBLAST APOPTOTIC PROCESS | 3 | 14 | 0.0003656 | 0.002031 |
835 | T CELL MIGRATION | 3 | 14 | 0.0003656 | 0.002031 |
836 | BONE MATURATION | 3 | 14 | 0.0003656 | 0.002031 |
837 | POSITIVE REGULATION OF CYTOSOLIC CALCIUM ION CONCENTRATION INVOLVED IN PHOSPHOLIPASE C ACTIVATING G PROTEIN COUPLED SIGNALING PATHWAY | 3 | 14 | 0.0003656 | 0.002031 |
838 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 34 | 1784 | 0.0003658 | 0.002031 |
839 | POSITIVE REGULATION OF INTRACELLULAR PROTEIN TRANSPORT | 10 | 258 | 0.0003713 | 0.002059 |
840 | HEART MORPHOGENESIS | 9 | 212 | 0.0003769 | 0.002088 |
841 | REGULATION OF MONOOXYGENASE ACTIVITY | 5 | 60 | 0.0003893 | 0.002149 |
842 | LEUKOCYTE HOMEOSTASIS | 5 | 60 | 0.0003893 | 0.002149 |
843 | INNER EAR MORPHOGENESIS | 6 | 92 | 0.0003892 | 0.002149 |
844 | NEGATIVE REGULATION OF CELL CYCLE PROCESS | 9 | 214 | 0.0004036 | 0.002225 |
845 | POSITIVE REGULATION OF SODIUM ION TRANSPORT | 4 | 34 | 0.0004053 | 0.002229 |
846 | RESPONSE TO PROSTAGLANDIN | 4 | 34 | 0.0004053 | 0.002229 |
847 | RESPONSE TO BACTERIUM | 15 | 528 | 0.0004161 | 0.002286 |
848 | CELLULAR RESPONSE TO HYDROGEN PEROXIDE | 5 | 61 | 0.0004205 | 0.002308 |
849 | LEARNING | 7 | 131 | 0.0004343 | 0.00238 |
850 | STRIATED MUSCLE CELL DIFFERENTIATION | 8 | 173 | 0.0004523 | 0.00247 |
851 | RESPONSE TO VITAMIN E | 3 | 15 | 0.0004536 | 0.00247 |
852 | T CELL LINEAGE COMMITMENT | 3 | 15 | 0.0004536 | 0.00247 |
853 | RESPONSE TO MINERALOCORTICOID | 4 | 35 | 0.0004539 | 0.00247 |
854 | T CELL APOPTOTIC PROCESS | 3 | 15 | 0.0004536 | 0.00247 |
855 | RESPONSE TO IRON ION | 4 | 35 | 0.0004539 | 0.00247 |
856 | CELLULAR RESPONSE TO STEROID HORMONE STIMULUS | 9 | 218 | 0.0004617 | 0.00251 |
857 | MITOCHONDRION ORGANIZATION | 16 | 594 | 0.0004801 | 0.002607 |
858 | CARDIOCYTE DIFFERENTIATION | 6 | 96 | 0.000489 | 0.002646 |
859 | REGULATION OF MUSCLE ADAPTATION | 5 | 63 | 0.0004886 | 0.002646 |
860 | RESPONSE TO OSMOTIC STRESS | 5 | 63 | 0.0004886 | 0.002646 |
861 | NEUROMUSCULAR JUNCTION DEVELOPMENT | 4 | 36 | 0.0005065 | 0.002728 |
862 | OLFACTORY LOBE DEVELOPMENT | 4 | 36 | 0.0005065 | 0.002728 |
863 | T CELL SELECTION | 4 | 36 | 0.0005065 | 0.002728 |
864 | POSITIVE REGULATION OF GLUCOSE METABOLIC PROCESS | 4 | 36 | 0.0005065 | 0.002728 |
865 | MYELOID LEUKOCYTE ACTIVATION | 6 | 98 | 0.0005458 | 0.002936 |
866 | POSITIVE REGULATION OF PHOSPHOPROTEIN PHOSPHATASE ACTIVITY | 3 | 16 | 0.000554 | 0.00297 |
867 | RETINA VASCULATURE DEVELOPMENT IN CAMERA TYPE EYE | 3 | 16 | 0.000554 | 0.00297 |
868 | RESPONSE TO UV B | 3 | 16 | 0.000554 | 0.00297 |
869 | POSITIVE REGULATION OF B CELL PROLIFERATION | 4 | 37 | 0.0005633 | 0.003006 |
870 | POSITIVE REGULATION OF PROTEIN TYROSINE KINASE ACTIVITY | 4 | 37 | 0.0005633 | 0.003006 |
871 | REGULATION OF RECEPTOR INTERNALIZATION | 4 | 37 | 0.0005633 | 0.003006 |
872 | POSITIVE REGULATION OF ALPHA BETA T CELL DIFFERENTIATION | 4 | 37 | 0.0005633 | 0.003006 |
873 | REGULATION OF CHEMOKINE PRODUCTION | 5 | 65 | 0.0005647 | 0.003006 |
874 | NEGATIVE REGULATION OF AXONOGENESIS | 5 | 65 | 0.0005647 | 0.003006 |
875 | CELLULAR RESPONSE TO RADIATION | 7 | 137 | 0.0005683 | 0.003022 |
876 | CELLULAR RESPONSE TO UV | 5 | 66 | 0.0006059 | 0.003218 |
877 | MUSCLE TISSUE DEVELOPMENT | 10 | 275 | 0.0006109 | 0.003241 |
878 | CELL ACTIVATION INVOLVED IN IMMUNE RESPONSE | 7 | 139 | 0.0006195 | 0.003283 |
879 | COLLAGEN FIBRIL ORGANIZATION | 4 | 38 | 0.0006246 | 0.003302 |
880 | BONE MINERALIZATION | 4 | 38 | 0.0006246 | 0.003302 |
881 | REGULATION OF INTRACELLULAR PROTEIN TRANSPORT | 12 | 381 | 0.0006448 | 0.003405 |
882 | CARDIAC MUSCLE TISSUE DEVELOPMENT | 7 | 140 | 0.0006465 | 0.003411 |
883 | NEGATIVE REGULATION OF PLATELET ACTIVATION | 3 | 17 | 0.0006676 | 0.003502 |
884 | NEGATIVE REGULATION OF RELEASE OF CYTOCHROME C FROM MITOCHONDRIA | 3 | 17 | 0.0006676 | 0.003502 |
885 | NEGATIVE REGULATION OF LIPID STORAGE | 3 | 17 | 0.0006676 | 0.003502 |
886 | MAMMARY GLAND ALVEOLUS DEVELOPMENT | 3 | 17 | 0.0006676 | 0.003502 |
887 | MAMMARY GLAND LOBULE DEVELOPMENT | 3 | 17 | 0.0006676 | 0.003502 |
888 | EMBRYONIC ORGAN MORPHOGENESIS | 10 | 279 | 0.0006828 | 0.003578 |
889 | REGULATION OF GRANULOCYTE CHEMOTAXIS | 4 | 39 | 0.0006903 | 0.003597 |
890 | EXTRINSIC APOPTOTIC SIGNALING PATHWAY VIA DEATH DOMAIN RECEPTORS | 4 | 39 | 0.0006903 | 0.003597 |
891 | CELLULAR RESPONSE TO NUTRIENT | 4 | 39 | 0.0006903 | 0.003597 |
892 | LONG TERM SYNAPTIC POTENTIATION | 4 | 39 | 0.0006903 | 0.003597 |
893 | PLATELET AGGREGATION | 4 | 39 | 0.0006903 | 0.003597 |
894 | EPITHELIAL CELL DEVELOPMENT | 8 | 186 | 0.000729 | 0.003794 |
895 | RESPONSE TO METAL ION | 11 | 333 | 0.0007319 | 0.003805 |
896 | RESPONSE TO TUMOR NECROSIS FACTOR | 9 | 233 | 0.0007441 | 0.003864 |
897 | MAMMARY GLAND MORPHOGENESIS | 4 | 40 | 0.0007609 | 0.003943 |
898 | ENDOCRINE PANCREAS DEVELOPMENT | 4 | 40 | 0.0007609 | 0.003943 |
899 | REGULATION OF CYTOSKELETON ORGANIZATION | 14 | 502 | 0.0007736 | 0.004004 |
900 | REGULATION OF MITOCHONDRIAL DEPOLARIZATION | 3 | 18 | 0.000795 | 0.004061 |
901 | POSITIVE REGULATION OF SYNAPTIC TRANSMISSION GLUTAMATERGIC | 3 | 18 | 0.000795 | 0.004061 |
902 | REGULATION OF CELL MATURATION | 3 | 18 | 0.000795 | 0.004061 |
903 | ORGAN MATURATION | 3 | 18 | 0.000795 | 0.004061 |
904 | OVULATION | 3 | 18 | 0.000795 | 0.004061 |
905 | RESPONSE TO PLATELET DERIVED GROWTH FACTOR | 3 | 18 | 0.000795 | 0.004061 |
906 | RESPONSE TO CAFFEINE | 3 | 18 | 0.000795 | 0.004061 |
907 | POSITIVE REGULATION OF T HELPER CELL DIFFERENTIATION | 3 | 18 | 0.000795 | 0.004061 |
908 | MAST CELL MEDIATED IMMUNITY | 3 | 18 | 0.000795 | 0.004061 |
909 | NOTOCHORD DEVELOPMENT | 3 | 18 | 0.000795 | 0.004061 |
910 | LYMPHOCYTE APOPTOTIC PROCESS | 3 | 18 | 0.000795 | 0.004061 |
911 | MUSCLE CELL MIGRATION | 3 | 18 | 0.000795 | 0.004061 |
912 | MYELOID CELL DIFFERENTIATION | 8 | 189 | 0.000809 | 0.004128 |
913 | POSITIVE REGULATION OF CALCIUM ION TRANSPORT | 6 | 106 | 0.0008262 | 0.004197 |
914 | INNATE IMMUNE RESPONSE ACTIVATING CELL SURFACE RECEPTOR SIGNALING PATHWAY | 6 | 106 | 0.0008262 | 0.004197 |
915 | REGULATION OF GLUCOSE METABOLIC PROCESS | 6 | 106 | 0.0008262 | 0.004197 |
916 | FAT CELL DIFFERENTIATION | 6 | 106 | 0.0008262 | 0.004197 |
917 | REGULATION OF MEMBRANE DEPOLARIZATION | 4 | 41 | 0.0008364 | 0.00423 |
918 | CELLULAR RESPONSE TO ESTROGEN STIMULUS | 4 | 41 | 0.0008364 | 0.00423 |
919 | MYELOID CELL ACTIVATION INVOLVED IN IMMUNE RESPONSE | 4 | 41 | 0.0008364 | 0.00423 |
920 | MONOCYTE CHEMOTAXIS | 4 | 41 | 0.0008364 | 0.00423 |
921 | MUSCLE CELL DIFFERENTIATION | 9 | 237 | 0.0008395 | 0.004241 |
922 | SKIN EPIDERMIS DEVELOPMENT | 5 | 71 | 0.0008467 | 0.004273 |
923 | REGULATION OF ENDOTHELIAL CELL APOPTOTIC PROCESS | 4 | 42 | 0.000917 | 0.004613 |
924 | REGULATION OF BONE REMODELING | 4 | 42 | 0.000917 | 0.004613 |
925 | REGULATION OF HEART GROWTH | 4 | 42 | 0.000917 | 0.004613 |
926 | DEVELOPMENTAL MATURATION | 8 | 193 | 0.0009266 | 0.004656 |
927 | REGULATION OF NITRIC OXIDE SYNTHASE BIOSYNTHETIC PROCESS | 3 | 19 | 0.0009369 | 0.004683 |
928 | CELLULAR SODIUM ION HOMEOSTASIS | 3 | 19 | 0.0009369 | 0.004683 |
929 | CARTILAGE DEVELOPMENT INVOLVED IN ENDOCHONDRAL BONE MORPHOGENESIS | 3 | 19 | 0.0009369 | 0.004683 |
930 | MACROPHAGE DIFFERENTIATION | 3 | 19 | 0.0009369 | 0.004683 |
931 | ASTROCYTE DEVELOPMENT | 3 | 19 | 0.0009369 | 0.004683 |
932 | ASSOCIATIVE LEARNING | 5 | 73 | 0.0009606 | 0.004786 |
933 | PANCREAS DEVELOPMENT | 5 | 73 | 0.0009606 | 0.004786 |
934 | CELLULAR RESPONSE TO KETONE | 5 | 73 | 0.0009606 | 0.004786 |
935 | MULTI ORGANISM REPRODUCTIVE PROCESS | 20 | 891 | 0.0009815 | 0.004885 |
936 | RESPONSE TO ELECTRICAL STIMULUS | 4 | 43 | 0.001003 | 0.004973 |
937 | REGULATION OF SECRETION | 17 | 699 | 0.001004 | 0.004973 |
938 | REGULATION OF MUSCLE CELL APOPTOTIC PROCESS | 4 | 43 | 0.001003 | 0.004973 |
939 | REGULATION OF INSULIN RECEPTOR SIGNALING PATHWAY | 4 | 43 | 0.001003 | 0.004973 |
940 | CARDIAC MUSCLE CELL DIFFERENTIATION | 5 | 74 | 0.001022 | 0.005057 |
941 | POSITIVE REGULATION OF CELLULAR AMIDE METABOLIC PROCESS | 6 | 111 | 0.001051 | 0.005197 |
942 | NEGATIVE REGULATION OF PEPTIDASE ACTIVITY | 9 | 245 | 0.00106 | 0.005236 |
943 | SINGLE ORGANISM CELLULAR LOCALIZATION | 20 | 898 | 0.001079 | 0.005324 |
944 | ODONTOGENESIS OF DENTIN CONTAINING TOOTH | 5 | 75 | 0.001086 | 0.005345 |
945 | POSITIVE REGULATION OF AUTOPHAGY | 5 | 75 | 0.001086 | 0.005345 |
946 | REGULATION OF SMOOTH MUSCLE CELL DIFFERENTIATION | 3 | 20 | 0.001094 | 0.005366 |
947 | NEGATIVE REGULATION OF CELL JUNCTION ASSEMBLY | 3 | 20 | 0.001094 | 0.005366 |
948 | REGULATION OF RELEASE OF CYTOCHROME C FROM MITOCHONDRIA | 4 | 44 | 0.001094 | 0.005366 |
949 | LYMPH VESSEL DEVELOPMENT | 3 | 20 | 0.001094 | 0.005366 |
950 | NEUROLOGICAL SYSTEM PROCESS | 25 | 1242 | 0.001107 | 0.005421 |
951 | ESTABLISHMENT OF LOCALIZATION IN CELL | 31 | 1676 | 0.001115 | 0.005456 |
952 | WNT SIGNALING PATHWAY | 11 | 351 | 0.001122 | 0.005472 |
953 | NEGATIVE REGULATION OF TRANSFERASE ACTIVITY | 11 | 351 | 0.001122 | 0.005472 |
954 | RESPONSE TO VIRUS | 9 | 247 | 0.001122 | 0.005472 |
955 | POSITIVE REGULATION OF TRANSPORTER ACTIVITY | 5 | 76 | 0.001152 | 0.0056 |
956 | EXTRACELLULAR MATRIX DISASSEMBLY | 5 | 76 | 0.001152 | 0.0056 |
957 | POSITIVE REGULATION OF INFLAMMATORY RESPONSE | 6 | 113 | 0.001153 | 0.0056 |
958 | PROTEIN HETEROOLIGOMERIZATION | 6 | 113 | 0.001153 | 0.0056 |
959 | PROTEIN IMPORT | 7 | 155 | 0.001175 | 0.005703 |
960 | LUNG MORPHOGENESIS | 4 | 45 | 0.001192 | 0.005769 |
961 | MODIFICATION BY SYMBIONT OF HOST MORPHOLOGY OR PHYSIOLOGY | 4 | 45 | 0.001192 | 0.005769 |
962 | SKELETAL SYSTEM MORPHOGENESIS | 8 | 201 | 0.001203 | 0.005818 |
963 | REGULATION OF EMBRYONIC DEVELOPMENT | 6 | 114 | 0.001207 | 0.00583 |
964 | NEGATIVE REGULATION OF CELLULAR CATABOLIC PROCESS | 7 | 156 | 0.00122 | 0.005876 |
965 | REGULATION OF LEUKOCYTE MEDIATED IMMUNITY | 7 | 156 | 0.00122 | 0.005876 |
966 | NEGATIVE REGULATION OF RESPONSE TO WOUNDING | 7 | 156 | 0.00122 | 0.005876 |
967 | B CELL HOMEOSTASIS | 3 | 21 | 0.001267 | 0.006069 |
968 | MAST CELL ACTIVATION | 3 | 21 | 0.001267 | 0.006069 |
969 | POSITIVE T CELL SELECTION | 3 | 21 | 0.001267 | 0.006069 |
970 | POSITIVE REGULATION OF EXCITATORY POSTSYNAPTIC POTENTIAL | 3 | 21 | 0.001267 | 0.006069 |
971 | CELLULAR RESPONSE TO ALCOHOL | 6 | 115 | 0.001262 | 0.006069 |
972 | MACROMOLECULAR COMPLEX ASSEMBLY | 27 | 1398 | 0.001283 | 0.006141 |
973 | REGULATION OF ALPHA BETA T CELL DIFFERENTIATION | 4 | 46 | 0.001295 | 0.006191 |
974 | ACTIVATION OF INNATE IMMUNE RESPONSE | 8 | 204 | 0.001322 | 0.006315 |
975 | REGULATION OF SYNAPSE ASSEMBLY | 5 | 79 | 0.001371 | 0.006544 |
976 | THYMUS DEVELOPMENT | 4 | 47 | 0.001404 | 0.006685 |
977 | POSITIVE REGULATION OF RECEPTOR MEDIATED ENDOCYTOSIS | 4 | 47 | 0.001404 | 0.006685 |
978 | REGULATION OF PROTEIN TARGETING | 10 | 307 | 0.001407 | 0.006693 |
979 | NEGATIVE REGULATION OF LIPID METABOLIC PROCESS | 5 | 80 | 0.00145 | 0.006894 |
980 | SINGLE ORGANISM BIOSYNTHETIC PROCESS | 26 | 1340 | 0.001483 | 0.007043 |
981 | REGULATION OF CARDIAC MUSCLE TISSUE DEVELOPMENT | 4 | 48 | 0.001519 | 0.007197 |
982 | DIGESTIVE TRACT MORPHOGENESIS | 4 | 48 | 0.001519 | 0.007197 |
983 | METANEPHROS DEVELOPMENT | 5 | 81 | 0.001533 | 0.007249 |
984 | POSITIVE REGULATION OF MYELOID CELL DIFFERENTIATION | 5 | 81 | 0.001533 | 0.007249 |
985 | NEGATIVE REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION | 8 | 209 | 0.001541 | 0.00728 |
986 | REGULATION OF NUCLEAR DIVISION | 7 | 163 | 0.001571 | 0.007398 |
987 | CELLULAR RESPONSE TO BIOTIC STIMULUS | 7 | 163 | 0.001571 | 0.007398 |
988 | RESPONSE TO TOPOLOGICALLY INCORRECT PROTEIN | 7 | 163 | 0.001571 | 0.007398 |
989 | POSITIVE REGULATION OF PROTEIN SECRETION | 8 | 211 | 0.001636 | 0.007691 |
990 | NEGATIVE REGULATION OF CYTOKINE PRODUCTION | 8 | 211 | 0.001636 | 0.007691 |
991 | REGULATION OF B CELL ACTIVATION | 6 | 121 | 0.001638 | 0.007693 |
992 | POSITIVE REGULATION OF MULTICELLULAR ORGANISMAL METABOLIC PROCESS | 3 | 23 | 0.001661 | 0.007729 |
993 | RESPONSE TO MAGNESIUM ION | 3 | 23 | 0.001661 | 0.007729 |
994 | RESPONSE TO INCREASED OXYGEN LEVELS | 3 | 23 | 0.001661 | 0.007729 |
995 | LYSOSOME LOCALIZATION | 3 | 23 | 0.001661 | 0.007729 |
996 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER IN RESPONSE TO STRESS | 3 | 23 | 0.001661 | 0.007729 |
997 | REGULATION OF OSTEOBLAST PROLIFERATION | 3 | 23 | 0.001661 | 0.007729 |
998 | REGULATION OF METANEPHROS DEVELOPMENT | 3 | 23 | 0.001661 | 0.007729 |
999 | RESPONSE TO HYPEROXIA | 3 | 23 | 0.001661 | 0.007729 |
1000 | POSITIVE REGULATION OF COLLAGEN METABOLIC PROCESS | 3 | 23 | 0.001661 | 0.007729 |
1001 | REGULATION OF TRANSMEMBRANE TRANSPORT | 12 | 426 | 0.001676 | 0.00779 |
1002 | REGULATION OF ERBB SIGNALING PATHWAY | 5 | 83 | 0.001709 | 0.007887 |
1003 | HAIR CYCLE | 5 | 83 | 0.001709 | 0.007887 |
1004 | REGULATION OF EPITHELIAL CELL DIFFERENTIATION | 6 | 122 | 0.001709 | 0.007887 |
1005 | EMBRYONIC PLACENTA DEVELOPMENT | 5 | 83 | 0.001709 | 0.007887 |
1006 | MOLTING CYCLE | 5 | 83 | 0.001709 | 0.007887 |
1007 | RESPONSE TO FATTY ACID | 5 | 83 | 0.001709 | 0.007887 |
1008 | LOCALIZATION WITHIN MEMBRANE | 6 | 122 | 0.001709 | 0.007887 |
1009 | CENTRAL NERVOUS SYSTEM NEURON DIFFERENTIATION | 7 | 166 | 0.001743 | 0.008039 |
1010 | LYMPHOCYTE HOMEOSTASIS | 4 | 50 | 0.001769 | 0.008126 |
1011 | RESPONSE TO GAMMA RADIATION | 4 | 50 | 0.001769 | 0.008126 |
1012 | VISUAL BEHAVIOR | 4 | 50 | 0.001769 | 0.008126 |
1013 | POSITIVE REGULATION OF MYELOID LEUKOCYTE DIFFERENTIATION | 4 | 50 | 0.001769 | 0.008126 |
1014 | AGING | 9 | 264 | 0.001775 | 0.008146 |
1015 | NEGATIVE REGULATION OF DEVELOPMENTAL GROWTH | 5 | 84 | 0.001802 | 0.00826 |
1016 | PROTEIN LOCALIZATION | 32 | 1805 | 0.001836 | 0.008408 |
1017 | FOCAL ADHESION ASSEMBLY | 3 | 24 | 0.001884 | 0.008569 |
1018 | NEGATIVE REGULATION OF BLOOD VESSEL ENDOTHELIAL CELL MIGRATION | 3 | 24 | 0.001884 | 0.008569 |
1019 | REGULATION OF MYELOID CELL APOPTOTIC PROCESS | 3 | 24 | 0.001884 | 0.008569 |
1020 | POSITIVE REGULATION OF CELLULAR RESPONSE TO TRANSFORMING GROWTH FACTOR BETA STIMULUS | 3 | 24 | 0.001884 | 0.008569 |
1021 | POSITIVE REGULATION OF EPITHELIAL CELL APOPTOTIC PROCESS | 3 | 24 | 0.001884 | 0.008569 |
1022 | POSITIVE REGULATION OF TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 3 | 24 | 0.001884 | 0.008569 |
1023 | CELL SUBSTRATE ADHERENS JUNCTION ASSEMBLY | 3 | 24 | 0.001884 | 0.008569 |
1024 | CELLULAR RESPONSE TO FATTY ACID | 4 | 51 | 0.001904 | 0.008636 |
1025 | HOMOTYPIC CELL CELL ADHESION | 4 | 51 | 0.001904 | 0.008636 |
1026 | POSITIVE REGULATION OF ALPHA BETA T CELL ACTIVATION | 4 | 51 | 0.001904 | 0.008636 |
1027 | REGULATION OF BLOOD PRESSURE | 7 | 169 | 0.00193 | 0.008727 |
1028 | APPENDAGE DEVELOPMENT | 7 | 169 | 0.00193 | 0.008727 |
1029 | LIMB DEVELOPMENT | 7 | 169 | 0.00193 | 0.008727 |
1030 | REGULATION OF CELL CYCLE PHASE TRANSITION | 10 | 321 | 0.001953 | 0.008825 |
1031 | NEGATIVE REGULATION OF CELL GROWTH | 7 | 170 | 0.001996 | 0.009006 |
1032 | POSITIVE REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY | 4 | 52 | 0.002046 | 0.009227 |
1033 | CELLULAR RESPONSE TO EPIDERMAL GROWTH FACTOR STIMULUS | 3 | 25 | 0.002125 | 0.009542 |
1034 | DETECTION OF MECHANICAL STIMULUS INVOLVED IN SENSORY PERCEPTION | 3 | 25 | 0.002125 | 0.009542 |
1035 | POSITIVE REGULATION OF COAGULATION | 3 | 25 | 0.002125 | 0.009542 |
1036 | EPITHELIAL CELL APOPTOTIC PROCESS | 3 | 25 | 0.002125 | 0.009542 |
1037 | REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION TO MITOCHONDRION | 6 | 128 | 0.002179 | 0.009775 |
1038 | INTRINSIC APOPTOTIC SIGNALING PATHWAY BY P53 CLASS MEDIATOR | 4 | 53 | 0.002196 | 0.009843 |
1039 | MYELOID CELL HOMEOSTASIS | 5 | 88 | 0.002212 | 0.009905 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | RECEPTOR BINDING | 81 | 1476 | 2.542e-38 | 2.362e-35 |
2 | KINASE ACTIVITY | 62 | 842 | 8.468e-36 | 3.933e-33 |
3 | PROTEIN KINASE ACTIVITY | 52 | 640 | 7.371e-32 | 2.283e-29 |
4 | TRANSFERASE ACTIVITY TRANSFERRING PHOSPHORUS CONTAINING GROUPS | 62 | 992 | 1.021e-31 | 2.371e-29 |
5 | PHOSPHATIDYLINOSITOL 3 KINASE ACTIVITY | 24 | 70 | 1.351e-30 | 2.511e-28 |
6 | MOLECULAR FUNCTION REGULATOR | 65 | 1353 | 9.711e-27 | 1.504e-24 |
7 | PROTEIN TYROSINE KINASE ACTIVITY | 29 | 176 | 1.279e-26 | 1.697e-24 |
8 | GROWTH FACTOR ACTIVITY | 28 | 160 | 1.726e-26 | 2.005e-24 |
9 | GROWTH FACTOR BINDING | 25 | 123 | 1.856e-25 | 1.915e-23 |
10 | GROWTH FACTOR RECEPTOR BINDING | 23 | 129 | 4.112e-22 | 3.82e-20 |
11 | X1 PHOSPHATIDYLINOSITOL 3 KINASE ACTIVITY | 16 | 43 | 2e-21 | 1.689e-19 |
12 | PHOSPHATIDYLINOSITOL KINASE ACTIVITY | 16 | 51 | 5.032e-20 | 3.896e-18 |
13 | PROTEIN COMPLEX BINDING | 47 | 935 | 7.375e-20 | 5.27e-18 |
14 | TRANSMEMBRANE RECEPTOR PROTEIN TYROSINE KINASE ACTIVITY | 17 | 64 | 8.302e-20 | 5.509e-18 |
15 | ENZYME BINDING | 63 | 1737 | 2.035e-19 | 1.26e-17 |
16 | TRANSMEMBRANE RECEPTOR PROTEIN KINASE ACTIVITY | 17 | 81 | 6.631e-18 | 3.85e-16 |
17 | KINASE BINDING | 36 | 606 | 1.542e-17 | 8.424e-16 |
18 | RAS GUANYL NUCLEOTIDE EXCHANGE FACTOR ACTIVITY | 24 | 228 | 1.698e-17 | 8.764e-16 |
19 | SIGNAL TRANSDUCER ACTIVITY | 59 | 1731 | 7.533e-17 | 3.683e-15 |
20 | MACROMOLECULAR COMPLEX BINDING | 52 | 1399 | 2.492e-16 | 1.158e-14 |
21 | CELL ADHESION MOLECULE BINDING | 21 | 186 | 4.606e-16 | 2.037e-14 |
22 | INTEGRIN BINDING | 17 | 105 | 6.812e-16 | 2.877e-14 |
23 | PLATELET DERIVED GROWTH FACTOR RECEPTOR BINDING | 9 | 15 | 5.429e-15 | 2.193e-13 |
24 | GUANYL NUCLEOTIDE EXCHANGE FACTOR ACTIVITY | 24 | 303 | 1.103e-14 | 4.27e-13 |
25 | COLLAGEN BINDING | 13 | 65 | 1.096e-13 | 4.073e-12 |
26 | HEPARIN BINDING | 17 | 157 | 6.363e-13 | 2.274e-11 |
27 | EXTRACELLULAR MATRIX STRUCTURAL CONSTITUENT | 13 | 76 | 9.227e-13 | 3.175e-11 |
28 | ENZYME REGULATOR ACTIVITY | 37 | 959 | 3.651e-12 | 1.173e-10 |
29 | PLATELET DERIVED GROWTH FACTOR BINDING | 7 | 11 | 3.662e-12 | 1.173e-10 |
30 | KINASE REGULATOR ACTIVITY | 17 | 186 | 1.009e-11 | 3.125e-10 |
31 | PROTEIN PHOSPHATASE TYPE 2A REGULATOR ACTIVITY | 8 | 21 | 2.085e-11 | 6.247e-10 |
32 | PROTEIN PHOSPHATASE BINDING | 14 | 120 | 2.659e-11 | 7.72e-10 |
33 | SULFUR COMPOUND BINDING | 18 | 234 | 4.403e-11 | 1.24e-09 |
34 | GLYCOSAMINOGLYCAN BINDING | 17 | 205 | 4.771e-11 | 1.304e-09 |
35 | INSULIN LIKE GROWTH FACTOR RECEPTOR BINDING | 7 | 15 | 6.895e-11 | 1.83e-09 |
36 | EXTRACELLULAR MATRIX BINDING | 10 | 51 | 1.002e-10 | 2.585e-09 |
37 | PHOSPHATASE BINDING | 15 | 162 | 1.441e-10 | 3.618e-09 |
38 | PROTEIN SERINE THREONINE KINASE ACTIVITY | 23 | 445 | 2.577e-10 | 6.299e-09 |
39 | FIBROBLAST GROWTH FACTOR RECEPTOR BINDING | 8 | 28 | 2.992e-10 | 6.95e-09 |
40 | FIBRONECTIN BINDING | 8 | 28 | 2.992e-10 | 6.95e-09 |
41 | RECEPTOR ACTIVITY | 46 | 1649 | 4.066e-10 | 9.212e-09 |
42 | CYTOKINE RECEPTOR BINDING | 18 | 271 | 4.861e-10 | 1.075e-08 |
43 | INSULIN RECEPTOR SUBSTRATE BINDING | 6 | 11 | 5.059e-10 | 1.093e-08 |
44 | IDENTICAL PROTEIN BINDING | 38 | 1209 | 7.054e-10 | 1.489e-08 |
45 | ADENYL NUCLEOTIDE BINDING | 43 | 1514 | 1.002e-09 | 2.069e-08 |
46 | CYTOKINE BINDING | 11 | 92 | 2.892e-09 | 5.84e-08 |
47 | SIGNALING RECEPTOR ACTIVITY | 40 | 1393 | 3.182e-09 | 6.201e-08 |
48 | NEUROTROPHIN RECEPTOR BINDING | 6 | 14 | 3.204e-09 | 6.201e-08 |
49 | RIBONUCLEOTIDE BINDING | 47 | 1860 | 6.217e-09 | 1.179e-07 |
50 | CHEMOATTRACTANT ACTIVITY | 7 | 27 | 8.563e-09 | 1.591e-07 |
51 | PHOSPHATIDYLINOSITOL 3 KINASE BINDING | 7 | 30 | 1.912e-08 | 3.483e-07 |
52 | CYTOKINE RECEPTOR ACTIVITY | 10 | 89 | 2.834e-08 | 5.063e-07 |
53 | PROTEIN DIMERIZATION ACTIVITY | 33 | 1149 | 9.421e-08 | 1.651e-06 |
54 | LAMININ BINDING | 6 | 30 | 5.518e-07 | 9.493e-06 |
55 | PROTEIN DOMAIN SPECIFIC BINDING | 22 | 624 | 5.837e-07 | 9.859e-06 |
56 | PROTEIN BINDING INVOLVED IN CELL ADHESION | 5 | 17 | 6.329e-07 | 1.031e-05 |
57 | VIRUS RECEPTOR ACTIVITY | 8 | 70 | 6.264e-07 | 1.031e-05 |
58 | INSULIN RECEPTOR BINDING | 6 | 32 | 8.277e-07 | 1.303e-05 |
59 | SODIUM CHANNEL REGULATOR ACTIVITY | 6 | 32 | 8.277e-07 | 1.303e-05 |
60 | HISTONE KINASE ACTIVITY | 5 | 19 | 1.169e-06 | 1.811e-05 |
61 | PROTEIN TYROSINE KINASE BINDING | 7 | 54 | 1.348e-06 | 2.053e-05 |
62 | PROTEIN HETERODIMERIZATION ACTIVITY | 18 | 468 | 1.949e-06 | 2.92e-05 |
63 | PHOSPHATASE REGULATOR ACTIVITY | 8 | 87 | 3.336e-06 | 4.92e-05 |
64 | KINASE ACTIVATOR ACTIVITY | 7 | 62 | 3.49e-06 | 5.066e-05 |
65 | EPHRIN RECEPTOR BINDING | 5 | 24 | 4.098e-06 | 5.857e-05 |
66 | PROTEIN HOMODIMERIZATION ACTIVITY | 22 | 722 | 6.27e-06 | 8.825e-05 |
67 | CAMP RESPONSE ELEMENT BINDING | 4 | 13 | 7.408e-06 | 0.0001027 |
68 | CYCLIN DEPENDENT PROTEIN SERINE THREONINE KINASE REGULATOR ACTIVITY | 5 | 28 | 9.162e-06 | 0.0001252 |
69 | PROTEASE BINDING | 8 | 104 | 1.266e-05 | 0.0001682 |
70 | RECEPTOR SIGNALING PROTEIN ACTIVITY | 10 | 172 | 1.267e-05 | 0.0001682 |
71 | PHOSPHATIDYLINOSITOL PHOSPHATE KINASE ACTIVITY | 4 | 16 | 1.84e-05 | 0.0002408 |
72 | PEPTIDE HORMONE BINDING | 5 | 36 | 3.286e-05 | 0.000424 |
73 | PROTEIN SERINE THREONINE TYROSINE KINASE ACTIVITY | 5 | 39 | 4.893e-05 | 0.0006227 |
74 | CHEMOKINE BINDING | 4 | 21 | 5.811e-05 | 0.0007295 |
75 | FIBROBLAST GROWTH FACTOR BINDING | 4 | 23 | 8.459e-05 | 0.001048 |
76 | PROTEIN PHOSPHATASE 2A BINDING | 4 | 28 | 0.0001878 | 0.002296 |
77 | TAU PROTEIN BINDING | 3 | 12 | 0.0002244 | 0.002707 |
78 | ENZYME ACTIVATOR ACTIVITY | 14 | 471 | 0.0004141 | 0.004932 |
79 | CHANNEL REGULATOR ACTIVITY | 7 | 131 | 0.0004343 | 0.005108 |
80 | CYTOKINE ACTIVITY | 9 | 219 | 0.0004773 | 0.005542 |
81 | CHLORIDE CHANNEL REGULATOR ACTIVITY | 3 | 16 | 0.000554 | 0.006354 |
82 | HORMONE BINDING | 5 | 65 | 0.0005647 | 0.006398 |
83 | CORECEPTOR ACTIVITY | 4 | 38 | 0.0006246 | 0.006991 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | PROTEIN COMPLEX INVOLVED IN CELL ADHESION | 19 | 30 | 4.094e-31 | 2.391e-28 |
2 | RECEPTOR COMPLEX | 35 | 327 | 2.06e-25 | 6.015e-23 |
3 | CELL SURFACE | 47 | 757 | 1.166e-23 | 2.27e-21 |
4 | PLASMA MEMBRANE RECEPTOR COMPLEX | 26 | 175 | 9.542e-23 | 1.393e-20 |
5 | EXTRACELLULAR MATRIX | 36 | 426 | 1.396e-22 | 1.631e-20 |
6 | EXTRACELLULAR MATRIX COMPONENT | 23 | 125 | 1.923e-22 | 1.872e-20 |
7 | PROTEINACEOUS EXTRACELLULAR MATRIX | 32 | 356 | 6.091e-21 | 5.081e-19 |
8 | BASEMENT MEMBRANE | 19 | 93 | 1.223e-19 | 8.928e-18 |
9 | SIDE OF MEMBRANE | 31 | 428 | 1.355e-17 | 8.794e-16 |
10 | COMPLEX OF COLLAGEN TRIMERS | 11 | 23 | 1.355e-16 | 7.461e-15 |
11 | CELL SUBSTRATE JUNCTION | 29 | 398 | 1.405e-16 | 7.461e-15 |
12 | PLASMA MEMBRANE PROTEIN COMPLEX | 32 | 510 | 2.471e-16 | 1.202e-14 |
13 | INTRINSIC COMPONENT OF PLASMA MEMBRANE | 55 | 1649 | 2.928e-15 | 1.315e-13 |
14 | MEMBRANE PROTEIN COMPLEX | 42 | 1020 | 1.065e-14 | 4.442e-13 |
15 | TRANSFERASE COMPLEX TRANSFERRING PHOSPHORUS CONTAINING GROUPS | 21 | 237 | 6.13e-14 | 2.387e-12 |
16 | EXTRACELLULAR SPACE | 47 | 1376 | 2.146e-13 | 7.371e-12 |
17 | ANCHORING JUNCTION | 28 | 489 | 2.066e-13 | 7.371e-12 |
18 | BASAL LAMINA | 9 | 21 | 3.022e-13 | 9.804e-12 |
19 | MEMBRANE REGION | 41 | 1134 | 1.65e-12 | 5.073e-11 |
20 | EXTRINSIC COMPONENT OF MEMBRANE | 20 | 252 | 1.959e-12 | 5.719e-11 |
21 | INTRACELLULAR VESICLE | 43 | 1259 | 2.826e-12 | 7.859e-11 |
22 | EXTERNAL SIDE OF PLASMA MEMBRANE | 19 | 238 | 6.47e-12 | 1.652e-10 |
23 | COLLAGEN TRIMER | 13 | 88 | 6.507e-12 | 1.652e-10 |
24 | PROTEIN KINASE COMPLEX | 13 | 90 | 8.747e-12 | 2.128e-10 |
25 | PHOSPHATIDYLINOSITOL 3 KINASE COMPLEX | 8 | 20 | 1.302e-11 | 2.925e-10 |
26 | PROTEIN PHOSPHATASE TYPE 2A COMPLEX | 8 | 20 | 1.302e-11 | 2.925e-10 |
27 | CELL JUNCTION | 39 | 1151 | 4.471e-11 | 9.671e-10 |
28 | PLASMA MEMBRANE REGION | 34 | 929 | 1.272e-10 | 2.652e-09 |
29 | CATALYTIC COMPLEX | 36 | 1038 | 1.491e-10 | 3.002e-09 |
30 | PLATELET ALPHA GRANULE | 11 | 75 | 3.072e-10 | 5.98e-09 |
31 | VESICLE LUMEN | 12 | 106 | 1.031e-09 | 1.941e-08 |
32 | MEMBRANE MICRODOMAIN | 18 | 288 | 1.29e-09 | 2.355e-08 |
33 | ENDOPLASMIC RETICULUM LUMEN | 15 | 201 | 2.939e-09 | 5.201e-08 |
34 | PLATELET ALPHA GRANULE LUMEN | 9 | 55 | 4.823e-09 | 8.284e-08 |
35 | CYCLIN DEPENDENT PROTEIN KINASE HOLOENZYME COMPLEX | 7 | 31 | 2.448e-08 | 4.085e-07 |
36 | CYTOPLASMIC SIDE OF MEMBRANE | 13 | 170 | 2.564e-08 | 4.159e-07 |
37 | PHOSPHATASE COMPLEX | 8 | 48 | 3.042e-08 | 4.802e-07 |
38 | PERINUCLEAR REGION OF CYTOPLASM | 24 | 642 | 5.851e-08 | 8.992e-07 |
39 | EXTRINSIC COMPONENT OF CYTOPLASMIC SIDE OF PLASMA MEMBRANE | 10 | 98 | 7.2e-08 | 1.078e-06 |
40 | EXTRINSIC COMPONENT OF PLASMA MEMBRANE | 11 | 136 | 1.762e-07 | 2.573e-06 |
41 | SECRETORY GRANULE LUMEN | 9 | 85 | 2.389e-07 | 3.403e-06 |
42 | CYTOPLASMIC VESICLE PART | 21 | 601 | 1.234e-06 | 1.717e-05 |
43 | PLASMA MEMBRANE RAFT | 8 | 86 | 3.056e-06 | 4.151e-05 |
44 | CELL LEADING EDGE | 15 | 350 | 3.939e-06 | 5.228e-05 |
45 | TRANSFERASE COMPLEX | 22 | 703 | 4.105e-06 | 5.327e-05 |
46 | SECRETORY GRANULE | 15 | 352 | 4.221e-06 | 5.359e-05 |
47 | BANDED COLLAGEN FIBRIL | 4 | 12 | 5.171e-06 | 6.425e-05 |
48 | LEADING EDGE MEMBRANE | 9 | 134 | 1.094e-05 | 0.0001331 |
49 | HETEROTRIMERIC G PROTEIN COMPLEX | 5 | 32 | 1.815e-05 | 0.0002163 |
50 | RUFFLE MEMBRANE | 7 | 80 | 1.927e-05 | 0.000225 |
51 | SECRETORY VESICLE | 16 | 461 | 2.614e-05 | 0.0002994 |
52 | ENDOPLASMIC RETICULUM | 35 | 1631 | 2.827e-05 | 0.0003175 |
53 | SYNAPSE | 21 | 754 | 3.884e-05 | 0.000428 |
54 | LAMELLIPODIUM | 9 | 172 | 7.855e-05 | 0.0008364 |
55 | CELL PROJECTION | 36 | 1786 | 7.877e-05 | 0.0008364 |
56 | NEURON PART | 28 | 1265 | 0.0001172 | 0.001222 |
57 | SOMATODENDRITIC COMPARTMENT | 18 | 650 | 0.0001519 | 0.001556 |
58 | BASAL PART OF CELL | 5 | 51 | 0.0001805 | 0.001818 |
59 | VACUOLE | 26 | 1180 | 0.0002247 | 0.002194 |
60 | RUFFLE | 8 | 156 | 0.0002254 | 0.002194 |
61 | NEUROMUSCULAR JUNCTION | 5 | 54 | 0.000237 | 0.002269 |
62 | CELL PROJECTION MEMBRANE | 11 | 298 | 0.0002892 | 0.002724 |
63 | CELL PROJECTION PART | 22 | 946 | 0.0003391 | 0.003144 |
64 | BASOLATERAL PLASMA MEMBRANE | 9 | 211 | 0.0003641 | 0.003322 |
65 | ENDOSOME | 19 | 793 | 0.0006092 | 0.005474 |
66 | PIGMENT GRANULE | 6 | 103 | 0.0007105 | 0.006286 |
67 | FILOPODIUM MEMBRANE | 3 | 18 | 0.000795 | 0.006869 |
68 | NEURON PROJECTION | 21 | 942 | 0.0007999 | 0.006869 |
69 | PERIKARYON | 6 | 108 | 0.0009111 | 0.007712 |
70 | LAMELLIPODIUM MEMBRANE | 3 | 19 | 0.0009369 | 0.007817 |
71 | ENDOPLASMIC RETICULUM PART | 24 | 1163 | 0.000996 | 0.008192 |
72 | EXCITATORY SYNAPSE | 8 | 197 | 0.001058 | 0.008578 |
73 | VACUOLAR LUMEN | 6 | 115 | 0.001262 | 0.009995 |
74 | MAST CELL GRANULE | 3 | 21 | 0.001267 | 0.009995 |
Num | Pathway | Pathview | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|---|
1 | hsa04151_PI3K_AKT_signaling_pathway | 207 | 351 | 0 | 0 | |
2 | hsa04510_Focal_adhesion | 85 | 200 | 1.724e-120 | 1.551e-118 | |
3 | hsa04014_Ras_signaling_pathway | 75 | 236 | 7.292e-94 | 4.375e-92 | |
4 | hsa04512_ECM.receptor_interaction | 47 | 85 | 2.846e-72 | 1.281e-70 | |
5 | hsa04810_Regulation_of_actin_cytoskeleton | 57 | 214 | 2.15e-65 | 7.74e-64 | |
6 | hsa04722_Neurotrophin_signaling_pathway | 30 | 127 | 1.61e-32 | 4.406e-31 | |
7 | hsa04150_mTOR_signaling_pathway | 23 | 52 | 1.713e-32 | 4.406e-31 | |
8 | hsa04010_MAPK_signaling_pathway | 36 | 268 | 1.182e-29 | 2.65e-28 | |
9 | hsa04012_ErbB_signaling_pathway | 25 | 87 | 1.325e-29 | 2.65e-28 | |
10 | hsa04630_Jak.STAT_signaling_pathway | 29 | 155 | 2.705e-28 | 4.869e-27 | |
11 | hsa04062_Chemokine_signaling_pathway | 29 | 189 | 1.077e-25 | 1.763e-24 | |
12 | hsa04910_Insulin_signaling_pathway | 26 | 138 | 1.569e-25 | 2.353e-24 | |
13 | hsa04662_B_cell_receptor_signaling_pathway | 20 | 75 | 3.819e-23 | 5.288e-22 | |
14 | hsa04640_Hematopoietic_cell_lineage | 19 | 88 | 3.965e-20 | 5.098e-19 | |
15 | hsa04370_VEGF_signaling_pathway | 18 | 76 | 6.499e-20 | 7.799e-19 | |
16 | hsa04960_Aldosterone.regulated_sodium_reabsorption | 15 | 42 | 7.742e-20 | 8.71e-19 | |
17 | hsa04664_Fc_epsilon_RI_signaling_pathway | 17 | 79 | 4.201e-18 | 4.448e-17 | |
18 | hsa04380_Osteoclast_differentiation | 19 | 128 | 6.817e-17 | 6.817e-16 | |
19 | hsa04620_Toll.like_receptor_signaling_pathway | 17 | 102 | 4.097e-16 | 3.882e-15 | |
20 | hsa04660_T_cell_receptor_signaling_pathway | 17 | 108 | 1.114e-15 | 1.003e-14 | |
21 | hsa04650_Natural_killer_cell_mediated_cytotoxicity | 18 | 136 | 3.684e-15 | 3.158e-14 | |
22 | hsa04914_Progesterone.mediated_oocyte_maturation | 15 | 87 | 1.374e-14 | 1.124e-13 | |
23 | hsa04110_Cell_cycle | 17 | 128 | 2.076e-14 | 1.625e-13 | |
24 | hsa04114_Oocyte_meiosis | 16 | 114 | 5.116e-14 | 3.837e-13 | |
25 | hsa04666_Fc_gamma_R.mediated_phagocytosis | 15 | 95 | 5.36e-14 | 3.859e-13 | |
26 | hsa04210_Apoptosis | 14 | 89 | 4.015e-13 | 2.779e-12 | |
27 | hsa04540_Gap_junction | 14 | 90 | 4.711e-13 | 3.141e-12 | |
28 | hsa04115_p53_signaling_pathway | 12 | 69 | 5.767e-12 | 3.707e-11 | |
29 | hsa04390_Hippo_signaling_pathway | 15 | 154 | 6.993e-11 | 4.341e-10 | |
30 | hsa04974_Protein_digestion_and_absorption | 11 | 81 | 7.203e-10 | 4.322e-09 | |
31 | hsa04360_Axon_guidance | 13 | 130 | 9.694e-10 | 5.629e-09 | |
32 | hsa04350_TGF.beta_signaling_pathway | 11 | 85 | 1.223e-09 | 6.877e-09 | |
33 | hsa04670_Leukocyte_transendothelial_migration | 12 | 117 | 3.249e-09 | 1.772e-08 | |
34 | hsa04973_Carbohydrate_digestion_and_absorption | 8 | 44 | 1.481e-08 | 7.838e-08 | |
35 | hsa04144_Endocytosis | 14 | 203 | 2.741e-08 | 1.41e-07 | |
36 | hsa04730_Long.term_depression | 9 | 70 | 4.315e-08 | 2.157e-07 | |
37 | hsa04310_Wnt_signaling_pathway | 12 | 151 | 5.841e-08 | 2.842e-07 | |
38 | hsa04145_Phagosome | 12 | 156 | 8.376e-08 | 3.968e-07 | |
39 | hsa04916_Melanogenesis | 10 | 101 | 9.615e-08 | 4.438e-07 | |
40 | hsa04070_Phosphatidylinositol_signaling_system | 9 | 78 | 1.126e-07 | 5.069e-07 | |
41 | hsa04320_Dorso.ventral_axis_formation | 6 | 25 | 1.718e-07 | 7.544e-07 | |
42 | hsa03015_mRNA_surveillance_pathway | 9 | 83 | 1.942e-07 | 8.322e-07 | |
43 | hsa04920_Adipocytokine_signaling_pathway | 8 | 68 | 4.993e-07 | 2.09e-06 | |
44 | hsa04530_Tight_junction | 10 | 133 | 1.267e-06 | 5.185e-06 | |
45 | hsa04912_GnRH_signaling_pathway | 8 | 101 | 1.02e-05 | 4.079e-05 | |
46 | hsa04520_Adherens_junction | 7 | 73 | 1.05e-05 | 4.11e-05 | |
47 | hsa04514_Cell_adhesion_molecules_.CAMs. | 8 | 136 | 8.723e-05 | 0.0003341 | |
48 | hsa00562_Inositol_phosphate_metabolism | 5 | 57 | 0.000306 | 0.001148 | |
49 | hsa04621_NOD.like_receptor_signaling_pathway | 5 | 59 | 0.0003599 | 0.001322 | |
50 | hsa04720_Long.term_potentiation | 5 | 70 | 0.0007936 | 0.002857 | |
51 | hsa04020_Calcium_signaling_pathway | 7 | 177 | 0.002504 | 0.008839 | |
52 | hsa04962_Vasopressin.regulated_water_reabsorption | 3 | 44 | 0.0106 | 0.03668 | |
53 | hsa04672_Intestinal_immune_network_for_IgA_production | 3 | 49 | 0.0142 | 0.04822 | |
54 | hsa04623_Cytosolic_DNA.sensing_pathway | 3 | 56 | 0.02027 | 0.06756 | |
55 | hsa04140_Regulation_of_autophagy | 2 | 34 | 0.04816 | 0.1576 | |
56 | hsa04270_Vascular_smooth_muscle_contraction | 3 | 116 | 0.1192 | 0.3832 | |
57 | hsa04610_Complement_and_coagulation_cascades | 2 | 69 | 0.16 | 0.5054 | |
58 | hsa04622_RIG.I.like_receptor_signaling_pathway | 2 | 71 | 0.1673 | 0.5193 | |
59 | hsa04141_Protein_processing_in_endoplasmic_reticulum | 3 | 168 | 0.2524 | 0.77 | |
60 | hsa04972_Pancreatic_secretion | 2 | 101 | 0.281 | 0.8431 | |
61 | hsa03013_RNA_transport | 2 | 152 | 0.468 | 1 |
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-7f-1-3p;hsa-miR-107;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-20a-5p;hsa-miR-27a-3p;hsa-miR-30d-3p;hsa-miR-31-5p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-501-5p;hsa-miR-590-3p;hsa-miR-616-5p | 17 | FGF7 | Sponge network | -4.563 | 0 | -5.509 | 0 | 0.773 |
2 | MAGI2-AS3 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-let-7g-3p;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-193a-3p;hsa-miR-200a-3p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-2110;hsa-miR-219a-5p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-330-5p;hsa-miR-335-3p;hsa-miR-339-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-429;hsa-miR-454-3p;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-93-5p | 32 | PDGFRA | Sponge network | -4.563 | 0 | -4.316 | 1.0E-5 | 0.763 |
3 | MEG3 |
hsa-let-7d-5p;hsa-let-7f-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-107;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-330-3p;hsa-miR-92a-1-5p;hsa-miR-93-5p | 11 | COL1A1 | Sponge network | -3.613 | 0.00075 | -1.841 | 0.04283 | 0.709 |
4 | MAGI2-AS3 |
hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-let-7g-5p;hsa-miR-193a-3p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-25-3p;hsa-miR-30d-3p;hsa-miR-32-3p;hsa-miR-32-5p;hsa-miR-330-5p;hsa-miR-33a-3p;hsa-miR-363-3p;hsa-miR-590-3p;hsa-miR-7-5p;hsa-miR-92a-3p;hsa-miR-92b-3p | 17 | COL1A2 | Sponge network | -4.563 | 0 | -2.407 | 0.0132 | 0.707 |
5 | RP11-166D19.1 |
hsa-let-7f-1-3p;hsa-let-7g-3p;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-193a-3p;hsa-miR-200a-3p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-219a-5p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-339-5p;hsa-miR-33a-5p;hsa-miR-33b-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-944;hsa-miR-96-5p | 29 | PDGFRA | Sponge network | -4.209 | 2.0E-5 | -4.316 | 1.0E-5 | 0.697 |
6 | MAGI2-AS3 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-142-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-32-3p;hsa-miR-335-3p;hsa-miR-3614-5p;hsa-miR-590-3p;hsa-miR-93-5p | 13 | THBS2 | Sponge network | -4.563 | 0 | -2.628 | 0.00636 | 0.694 |
7 | MAGI2-AS3 |
hsa-let-7d-5p;hsa-let-7g-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-107;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-23a-5p;hsa-miR-30d-3p;hsa-miR-532-3p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-92a-1-5p;hsa-miR-93-5p | 15 | COL1A1 | Sponge network | -4.563 | 0 | -1.841 | 0.04283 | 0.694 |
8 | MIR143HG |
hsa-let-7f-1-3p;hsa-let-7g-3p;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-193a-3p;hsa-miR-196a-5p;hsa-miR-200a-3p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-2110;hsa-miR-219a-5p;hsa-miR-224-5p;hsa-miR-301a-3p;hsa-miR-330-5p;hsa-miR-339-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-429;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-93-5p | 30 | PDGFRA | Sponge network | -6.51 | 0 | -4.316 | 1.0E-5 | 0.692 |
9 | MAGI2-AS3 |
hsa-miR-130b-3p;hsa-miR-16-1-3p;hsa-miR-183-5p;hsa-miR-19b-1-5p;hsa-miR-301a-3p;hsa-miR-30b-5p;hsa-miR-30c-5p;hsa-miR-32-3p;hsa-miR-335-3p;hsa-miR-33a-5p;hsa-miR-454-3p | 11 | ITGA8 | Sponge network | -4.563 | 0 | -4.419 | 0.00157 | 0.691 |
10 | MEG3 |
hsa-let-7f-1-3p;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-193a-3p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-2110;hsa-miR-219a-5p;hsa-miR-224-5p;hsa-miR-330-5p;hsa-miR-429;hsa-miR-550a-5p;hsa-miR-576-5p;hsa-miR-93-5p;hsa-miR-944;hsa-miR-96-5p | 21 | PDGFRA | Sponge network | -3.613 | 0.00075 | -4.316 | 1.0E-5 | 0.69 |
11 | HAND2-AS1 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-let-7g-3p;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-193a-3p;hsa-miR-200a-3p;hsa-miR-20a-5p;hsa-miR-2110;hsa-miR-219a-5p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-330-5p;hsa-miR-335-3p;hsa-miR-339-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-421;hsa-miR-429;hsa-miR-550a-5p;hsa-miR-590-3p;hsa-miR-93-5p;hsa-miR-944 | 29 | PDGFRA | Sponge network | -7.871 | 0 | -4.316 | 1.0E-5 | 0.672 |
12 | DNM3OS |
hsa-let-7f-1-3p;hsa-let-7g-3p;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-193a-3p;hsa-miR-196a-5p;hsa-miR-200a-3p;hsa-miR-20a-5p;hsa-miR-2110;hsa-miR-219a-5p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-33a-5p;hsa-miR-33b-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-93-5p;hsa-miR-96-5p | 30 | PDGFRA | Sponge network | -3.933 | 0.00059 | -4.316 | 1.0E-5 | 0.671 |
13 | DNM3OS |
hsa-let-7f-1-3p;hsa-miR-107;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-20a-5p;hsa-miR-27a-3p;hsa-miR-30d-3p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-484;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p | 17 | FGF7 | Sponge network | -3.933 | 0.00059 | -5.509 | 0 | 0.667 |
14 | MAGI2-AS3 |
hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19b-3p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-20a-5p;hsa-miR-3065-5p;hsa-miR-33a-3p;hsa-miR-500a-5p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-616-5p | 13 | THBS1 | Sponge network | -4.563 | 0 | -3.751 | 0.0001 | 0.664 |
15 | MIR143HG |
hsa-let-7f-1-3p;hsa-miR-107;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-20a-5p;hsa-miR-30d-3p;hsa-miR-31-5p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-484;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p | 17 | FGF7 | Sponge network | -6.51 | 0 | -5.509 | 0 | 0.658 |
16 | MAGI2-AS3 |
hsa-miR-130a-5p;hsa-miR-149-5p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-19b-1-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-429;hsa-miR-590-3p | 10 | KDR | Sponge network | -4.563 | 0 | -3.788 | 0 | 0.657 |
17 | MIR143HG |
hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-let-7g-5p;hsa-miR-193a-3p;hsa-miR-196a-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-25-3p;hsa-miR-30d-3p;hsa-miR-32-5p;hsa-miR-330-5p;hsa-miR-33a-3p;hsa-miR-363-3p;hsa-miR-590-3p;hsa-miR-7-5p;hsa-miR-92a-3p;hsa-miR-92b-3p | 17 | COL1A2 | Sponge network | -6.51 | 0 | -2.407 | 0.0132 | 0.654 |
18 | HAND2-AS1 |
hsa-let-7f-1-3p;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-27a-3p;hsa-miR-32-3p;hsa-miR-33a-3p;hsa-miR-486-5p;hsa-miR-629-5p;hsa-miR-940 | 15 | IGF1 | Sponge network | -7.871 | 0 | -4.485 | 0.00149 | 0.653 |
19 | DNM3OS |
hsa-let-7d-5p;hsa-let-7g-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-107;hsa-miR-17-5p;hsa-miR-196a-5p;hsa-miR-20a-5p;hsa-miR-23a-5p;hsa-miR-30d-3p;hsa-miR-330-3p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-93-5p | 14 | COL1A1 | Sponge network | -3.933 | 0.00059 | -1.841 | 0.04283 | 0.646 |
20 | RP11-166D19.1 |
hsa-let-7f-1-3p;hsa-miR-107;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-20a-5p;hsa-miR-27a-3p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-452-5p;hsa-miR-484;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-616-5p | 17 | FGF7 | Sponge network | -4.209 | 2.0E-5 | -5.509 | 0 | 0.645 |
21 | HAND2-AS1 |
hsa-let-7f-1-3p;hsa-miR-107;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-20a-5p;hsa-miR-27a-3p;hsa-miR-31-5p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-486-5p;hsa-miR-590-3p | 15 | FGF7 | Sponge network | -7.871 | 0 | -5.509 | 0 | 0.642 |
22 | RP11-166D19.1 |
hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19b-3p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-20a-5p;hsa-miR-33a-3p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-616-5p | 11 | THBS1 | Sponge network | -4.209 | 2.0E-5 | -3.751 | 0.0001 | 0.639 |
23 | RP11-554A11.4 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-193a-3p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-2110;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-339-5p;hsa-miR-421 | 14 | PDGFRA | Sponge network | -5.361 | 2.0E-5 | -4.316 | 1.0E-5 | 0.638 |
24 | DNM3OS |
hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-let-7g-5p;hsa-miR-193a-3p;hsa-miR-196a-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-25-3p;hsa-miR-30d-3p;hsa-miR-33a-3p;hsa-miR-590-3p;hsa-miR-7-5p | 12 | COL1A2 | Sponge network | -3.933 | 0.00059 | -2.407 | 0.0132 | 0.638 |
25 | MAGI2-AS3 |
hsa-let-7f-2-3p;hsa-miR-141-5p;hsa-miR-200b-3p;hsa-miR-20a-3p;hsa-miR-3065-5p;hsa-miR-33a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-429;hsa-miR-452-3p;hsa-miR-590-3p | 11 | ITGA9 | Sponge network | -4.563 | 0 | -4.473 | 0 | 0.634 |
26 | RP11-389C8.2 |
hsa-miR-130a-5p;hsa-miR-149-5p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-19b-1-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-3065-3p;hsa-miR-429 | 10 | KDR | Sponge network | -3.089 | 2.0E-5 | -3.788 | 0 | 0.633 |
27 | MIR143HG |
hsa-let-7d-5p;hsa-let-7g-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-107;hsa-miR-17-5p;hsa-miR-196a-5p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-23a-5p;hsa-miR-30d-3p;hsa-miR-330-3p;hsa-miR-361-3p;hsa-miR-590-3p;hsa-miR-616-5p;hsa-miR-625-5p;hsa-miR-92a-1-5p;hsa-miR-93-5p | 18 | COL1A1 | Sponge network | -6.51 | 0 | -1.841 | 0.04283 | 0.631 |
28 | EMX2OS |
hsa-let-7f-1-3p;hsa-miR-103a-2-5p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-16-1-3p;hsa-miR-19b-1-5p;hsa-miR-19b-3p;hsa-miR-20a-3p;hsa-miR-27a-3p;hsa-miR-32-3p;hsa-miR-452-5p;hsa-miR-486-5p;hsa-miR-629-5p;hsa-miR-940 | 14 | IGF1 | Sponge network | -6.205 | 0.00015 | -4.485 | 0.00149 | 0.631 |
29 | MIR143HG |
hsa-miR-141-5p;hsa-miR-200b-3p;hsa-miR-20a-3p;hsa-miR-3065-5p;hsa-miR-330-3p;hsa-miR-33a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-429;hsa-miR-590-3p | 10 | ITGA9 | Sponge network | -6.51 | 0 | -4.473 | 0 | 0.624 |
30 | DNM3OS |
hsa-miR-141-5p;hsa-miR-200b-3p;hsa-miR-20a-3p;hsa-miR-3065-5p;hsa-miR-330-3p;hsa-miR-33a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-429;hsa-miR-590-3p | 10 | ITGA9 | Sponge network | -3.933 | 0.00059 | -4.473 | 0 | 0.608 |
31 | MIR143HG |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-142-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-3614-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-93-5p | 12 | THBS2 | Sponge network | -6.51 | 0 | -2.628 | 0.00636 | 0.606 |
32 | RP11-161M6.2 |
hsa-miR-1271-5p;hsa-miR-17-3p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-224-5p;hsa-miR-23a-3p;hsa-miR-330-5p;hsa-miR-3615;hsa-miR-940 | 10 | GNG7 | Sponge network | -2.608 | 0.00296 | -4.495 | 0 | 0.605 |
33 | ADAMTS9-AS1 |
hsa-let-7f-1-3p;hsa-miR-107;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-20a-5p;hsa-miR-27a-3p;hsa-miR-31-5p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-7-1-3p | 15 | FGF7 | Sponge network | -8.573 | 0.00012 | -5.509 | 0 | 0.603 |
34 | MIR143HG |
hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19b-3p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-20a-5p;hsa-miR-3065-5p;hsa-miR-33a-3p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-616-5p | 12 | THBS1 | Sponge network | -6.51 | 0 | -3.751 | 0.0001 | 0.603 |
35 | DNM3OS |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-93-5p;hsa-miR-96-5p | 10 | THBS2 | Sponge network | -3.933 | 0.00059 | -2.628 | 0.00636 | 0.597 |
36 | EMX2OS |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-193a-3p;hsa-miR-20a-5p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-330-5p;hsa-miR-339-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-421;hsa-miR-590-3p;hsa-miR-93-5p;hsa-miR-944 | 19 | PDGFRA | Sponge network | -6.205 | 0.00015 | -4.316 | 1.0E-5 | 0.593 |
37 | MEG3 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-3614-5p;hsa-miR-93-5p;hsa-miR-96-5p | 10 | THBS2 | Sponge network | -3.613 | 0.00075 | -2.628 | 0.00636 | 0.586 |
38 | DNM3OS |
hsa-miR-149-5p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-19b-1-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-3065-3p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-590-5p | 11 | KDR | Sponge network | -3.933 | 0.00059 | -3.788 | 0 | 0.586 |
39 | RP11-166D19.1 |
hsa-let-7d-5p;hsa-let-7g-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-107;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-23a-5p;hsa-miR-532-3p;hsa-miR-590-3p;hsa-miR-616-5p | 12 | COL1A1 | Sponge network | -4.209 | 2.0E-5 | -1.841 | 0.04283 | 0.586 |
40 | RP11-166D19.1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-142-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-3614-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-96-5p | 12 | THBS2 | Sponge network | -4.209 | 2.0E-5 | -2.628 | 0.00636 | 0.584 |
41 | DNM3OS |
hsa-miR-16-1-3p;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-20a-5p;hsa-miR-3065-5p;hsa-miR-33a-3p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-616-5p | 13 | THBS1 | Sponge network | -3.933 | 0.00059 | -3.751 | 0.0001 | 0.584 |
42 | RP11-389C8.2 |
hsa-miR-1271-5p;hsa-miR-130a-5p;hsa-miR-141-3p;hsa-miR-17-3p;hsa-miR-182-5p;hsa-miR-185-3p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-1976;hsa-miR-200a-3p;hsa-miR-23a-3p;hsa-miR-31-5p | 13 | GNG7 | Sponge network | -3.089 | 2.0E-5 | -4.495 | 0 | 0.582 |
43 | MAGI2-AS3 |
hsa-miR-130a-5p;hsa-miR-141-3p;hsa-miR-17-3p;hsa-miR-182-5p;hsa-miR-185-3p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-1976;hsa-miR-200a-3p;hsa-miR-224-5p;hsa-miR-23a-3p;hsa-miR-31-5p;hsa-miR-330-5p;hsa-miR-3615;hsa-miR-616-5p;hsa-miR-92a-3p;hsa-miR-940 | 17 | GNG7 | Sponge network | -4.563 | 0 | -4.495 | 0 | 0.578 |
44 | RP11-389C8.2 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-let-7g-3p;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-193a-3p;hsa-miR-200a-3p;hsa-miR-20a-5p;hsa-miR-2110;hsa-miR-219a-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-421;hsa-miR-429;hsa-miR-550a-5p;hsa-miR-589-3p;hsa-miR-93-5p | 23 | PDGFRA | Sponge network | -3.089 | 2.0E-5 | -4.316 | 1.0E-5 | 0.578 |
45 | RP11-389C8.2 |
hsa-let-7f-1-3p;hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-16-1-3p;hsa-miR-19b-1-5p;hsa-miR-19b-3p;hsa-miR-20a-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-33a-3p | 10 | IGF1 | Sponge network | -3.089 | 2.0E-5 | -4.485 | 0.00149 | 0.575 |
46 | RP11-166D19.1 |
hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-let-7g-5p;hsa-miR-193a-3p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-25-3p;hsa-miR-32-5p;hsa-miR-33a-3p;hsa-miR-363-3p;hsa-miR-590-3p;hsa-miR-92a-3p | 12 | COL1A2 | Sponge network | -4.209 | 2.0E-5 | -2.407 | 0.0132 | 0.573 |
47 | RP11-166D19.1 |
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-452-3p;hsa-miR-452-5p;hsa-miR-590-3p | 10 | ITGA9 | Sponge network | -4.209 | 2.0E-5 | -4.473 | 0 | 0.572 |
48 | MAGI2-AS3 |
hsa-let-7f-1-3p;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-27a-3p;hsa-miR-301a-3p;hsa-miR-32-3p;hsa-miR-33a-3p;hsa-miR-576-5p;hsa-miR-629-5p;hsa-miR-940 | 16 | IGF1 | Sponge network | -4.563 | 0 | -4.485 | 0.00149 | 0.572 |
49 | MEG3 |
hsa-let-7f-1-3p;hsa-miR-107;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-20a-5p;hsa-miR-31-5p;hsa-miR-33a-3p;hsa-miR-429 | 12 | FGF7 | Sponge network | -3.613 | 0.00075 | -5.509 | 0 | 0.571 |
50 | HAND2-AS1 |
hsa-let-7f-2-3p;hsa-miR-141-5p;hsa-miR-200b-3p;hsa-miR-20a-3p;hsa-miR-330-3p;hsa-miR-33a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-429;hsa-miR-452-3p;hsa-miR-590-3p | 11 | ITGA9 | Sponge network | -7.871 | 0 | -4.473 | 0 | 0.568 |
51 | RP11-887P2.5 |
hsa-let-7f-1-3p;hsa-miR-103a-2-5p;hsa-miR-130b-3p;hsa-miR-16-1-3p;hsa-miR-19a-3p;hsa-miR-19b-1-5p;hsa-miR-19b-3p;hsa-miR-27a-3p;hsa-miR-486-5p;hsa-miR-576-5p;hsa-miR-940 | 11 | IGF1 | Sponge network | -9.865 | 1.0E-5 | -4.485 | 0.00149 | 0.567 |
52 | MIR143HG |
hsa-miR-130a-5p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-19b-1-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-3065-3p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-590-5p | 11 | KDR | Sponge network | -6.51 | 0 | -3.788 | 0 | 0.565 |
53 | RP11-389C8.2 |
hsa-let-7f-1-3p;hsa-miR-107;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-20a-5p;hsa-miR-27a-3p;hsa-miR-31-5p;hsa-miR-33a-3p;hsa-miR-429 | 13 | FGF7 | Sponge network | -3.089 | 2.0E-5 | -5.509 | 0 | 0.564 |
54 | AC003090.1 |
hsa-let-7f-1-3p;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-27a-3p;hsa-miR-576-5p | 11 | IGF1 | Sponge network | -7.817 | 0.00161 | -4.485 | 0.00149 | 0.561 |
55 | AC003090.1 |
hsa-let-7f-1-3p;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-20a-5p;hsa-miR-27a-3p;hsa-miR-31-5p;hsa-miR-590-5p;hsa-miR-7-1-3p | 12 | FGF7 | Sponge network | -7.817 | 0.00161 | -5.509 | 0 | 0.547 |
56 | WT1-AS |
hsa-let-7f-1-3p;hsa-let-7g-3p;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-193a-3p;hsa-miR-20a-5p;hsa-miR-2110;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-330-5p;hsa-miR-335-3p;hsa-miR-339-5p;hsa-miR-421;hsa-miR-429;hsa-miR-550a-5p;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-93-5p;hsa-miR-944;hsa-miR-96-5p | 26 | PDGFRA | Sponge network | -6.875 | 2.0E-5 | -4.316 | 1.0E-5 | 0.546 |
57 | MEG3 |
hsa-let-7a-5p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19b-3p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-20a-5p;hsa-miR-33a-3p;hsa-miR-576-5p | 10 | THBS1 | Sponge network | -3.613 | 0.00075 | -3.751 | 0.0001 | 0.544 |
58 | TPTEP1 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-2110;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-330-5p;hsa-miR-33b-5p;hsa-miR-590-3p | 15 | PDGFRA | Sponge network | -4.398 | 5.0E-5 | -4.316 | 1.0E-5 | 0.542 |
59 | AC003090.1 |
hsa-let-7f-1-3p;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-193a-3p;hsa-miR-20a-5p;hsa-miR-219a-5p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-576-5p;hsa-miR-590-5p;hsa-miR-7-1-3p;hsa-miR-93-5p;hsa-miR-96-5p | 20 | PDGFRA | Sponge network | -7.817 | 0.00161 | -4.316 | 1.0E-5 | 0.529 |
60 | RP11-887P2.5 |
hsa-let-7f-1-3p;hsa-miR-107;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-20a-5p;hsa-miR-27a-3p;hsa-miR-486-5p;hsa-miR-590-5p;hsa-miR-7-1-3p | 12 | FGF7 | Sponge network | -9.865 | 1.0E-5 | -5.509 | 0 | 0.528 |
61 | MAGI2-AS3 |
hsa-miR-141-5p;hsa-miR-200a-5p;hsa-miR-200b-3p;hsa-miR-200b-5p;hsa-miR-200c-3p;hsa-miR-3065-5p;hsa-miR-3607-3p;hsa-miR-362-3p;hsa-miR-429;hsa-miR-590-3p | 10 | ITGA1 | Sponge network | -4.563 | 0 | -1.265 | 0.08839 | 0.521 |
62 | MIR497HG |
hsa-let-7f-1-3p;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-27a-3p;hsa-miR-301a-3p;hsa-miR-33a-3p;hsa-miR-940 | 13 | IGF1 | Sponge network | -6.146 | 0.00024 | -4.485 | 0.00149 | 0.518 |
63 | MIR143HG |
hsa-miR-130a-5p;hsa-miR-141-3p;hsa-miR-17-3p;hsa-miR-182-5p;hsa-miR-185-3p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-1976;hsa-miR-200a-3p;hsa-miR-224-5p;hsa-miR-31-3p;hsa-miR-31-5p;hsa-miR-3127-5p;hsa-miR-330-5p;hsa-miR-3615;hsa-miR-616-5p;hsa-miR-92a-3p;hsa-miR-940 | 18 | GNG7 | Sponge network | -6.51 | 0 | -4.495 | 0 | 0.514 |
64 | EMX2OS |
hsa-miR-142-5p;hsa-miR-155-5p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-205-5p;hsa-miR-221-5p;hsa-miR-330-5p;hsa-miR-590-3p;hsa-miR-944 | 10 | FGF9 | Sponge network | -6.205 | 0.00015 | -4.087 | 0.01073 | 0.507 |
65 | RP11-401P9.4 | hsa-let-7g-3p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-16-1-3p;hsa-miR-182-5p;hsa-miR-193a-3p;hsa-miR-20b-5p;hsa-miR-2110;hsa-miR-224-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-454-3p;hsa-miR-550a-5p | 15 | PDGFRA | Sponge network | -3.793 | 0.00144 | -4.316 | 1.0E-5 | 0.506 |
66 | RP11-344E13.3 |
hsa-miR-107;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-20a-5p;hsa-miR-27a-3p;hsa-miR-31-5p;hsa-miR-486-5p;hsa-miR-590-3p;hsa-miR-590-5p | 12 | FGF7 | Sponge network | -4.307 | 3.0E-5 | -5.509 | 0 | 0.506 |
67 | CTD-2554C21.2 |
hsa-let-7g-3p;hsa-miR-106b-5p;hsa-miR-141-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-193a-3p;hsa-miR-20a-5p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-339-5p;hsa-miR-93-5p;hsa-miR-944 | 14 | PDGFRA | Sponge network | -6.968 | 0.00817 | -4.316 | 1.0E-5 | 0.502 |
68 | RP11-822E23.8 | hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-141-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-193a-3p;hsa-miR-196a-5p;hsa-miR-200a-3p;hsa-miR-20a-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-589-3p;hsa-miR-93-5p | 16 | PDGFRA | Sponge network | -8.351 | 0.00374 | -4.316 | 1.0E-5 | 0.501 |
69 | ADAMTS9-AS1 |
hsa-let-7f-1-3p;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-27a-3p;hsa-miR-301a-3p;hsa-miR-576-5p;hsa-miR-629-5p;hsa-miR-940 | 14 | IGF1 | Sponge network | -8.573 | 0.00012 | -4.485 | 0.00149 | 0.499 |
70 | ACTA2-AS1 |
hsa-let-7f-1-3p;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-20a-5p;hsa-miR-27a-3p;hsa-miR-33a-3p;hsa-miR-484;hsa-miR-590-3p | 12 | FGF7 | Sponge network | -6.142 | 0.00223 | -5.509 | 0 | 0.495 |
71 | NR2F2-AS1 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-142-5p;hsa-miR-15a-5p;hsa-miR-15b-3p;hsa-miR-16-5p;hsa-miR-205-5p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-590-3p | 10 | INSR | Sponge network | -3.785 | 0.00281 | -1.824 | 0.00037 | 0.493 |
72 | NR2F2-AS1 |
hsa-miR-1271-5p;hsa-miR-16-2-3p;hsa-miR-18a-3p;hsa-miR-1976;hsa-miR-24-3p;hsa-miR-25-3p;hsa-miR-9-3p;hsa-miR-92a-1-5p;hsa-miR-92a-3p;hsa-miR-944 | 10 | CREB3L2 | Sponge network | -3.785 | 0.00281 | -2.05 | 0.00075 | 0.493 |
73 | WT1-AS |
hsa-let-7f-1-3p;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-27a-3p;hsa-miR-301a-3p;hsa-miR-32-3p;hsa-miR-33a-3p;hsa-miR-576-5p;hsa-miR-629-5p;hsa-miR-940 | 16 | IGF1 | Sponge network | -6.875 | 2.0E-5 | -4.485 | 0.00149 | 0.493 |
74 | MIR143HG |
hsa-let-7f-1-3p;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-33a-3p;hsa-miR-576-5p;hsa-miR-629-5p;hsa-miR-940 | 14 | IGF1 | Sponge network | -6.51 | 0 | -4.485 | 0.00149 | 0.49 |
75 | WT1-AS |
hsa-let-7f-1-3p;hsa-miR-107;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-20a-5p;hsa-miR-27a-3p;hsa-miR-31-5p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-501-5p;hsa-miR-590-3p | 15 | FGF7 | Sponge network | -6.875 | 2.0E-5 | -5.509 | 0 | 0.49 |
76 | RP11-999E24.3 | hsa-let-7f-1-3p;hsa-let-7g-3p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-193a-3p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-2110;hsa-miR-27a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p | 13 | PDGFRA | Sponge network | -4.893 | 2.0E-5 | -4.316 | 1.0E-5 | 0.487 |
77 | MIR497HG |
hsa-let-7f-1-3p;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-20a-5p;hsa-miR-27a-3p;hsa-miR-31-5p;hsa-miR-33a-3p;hsa-miR-501-5p;hsa-miR-590-5p;hsa-miR-7-1-3p | 14 | FGF7 | Sponge network | -6.146 | 0.00024 | -5.509 | 0 | 0.487 |
78 | RP11-344E13.3 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-142-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-3614-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-93-5p | 11 | THBS2 | Sponge network | -4.307 | 3.0E-5 | -2.628 | 0.00636 | 0.485 |
79 | RP11-384L8.1 | hsa-let-7a-3p;hsa-let-7b-3p;hsa-let-7f-1-3p;hsa-miR-142-5p;hsa-miR-205-5p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-330-3p;hsa-miR-330-5p;hsa-miR-590-3p | 10 | INSR | Sponge network | -1.784 | 0.21615 | -1.824 | 0.00037 | 0.485 |
80 | RP11-130L8.1 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-2110;hsa-miR-219a-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-93-5p;hsa-miR-944 | 16 | PDGFRA | Sponge network | -4.329 | 1.0E-5 | -4.316 | 1.0E-5 | 0.484 |
81 | RP11-13K12.1 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-141-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-193a-3p;hsa-miR-20a-5p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-944 | 11 | PDGFRA | Sponge network | -5.093 | 0.01151 | -4.316 | 1.0E-5 | 0.484 |
82 | DNM3OS |
hsa-let-7f-1-3p;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-27a-3p;hsa-miR-301a-3p;hsa-miR-33a-3p;hsa-miR-576-5p;hsa-miR-940 | 14 | IGF1 | Sponge network | -3.933 | 0.00059 | -4.485 | 0.00149 | 0.483 |
83 | NR2F1-AS1 |
hsa-let-7f-1-3p;hsa-let-7g-3p;hsa-miR-141-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-193a-3p;hsa-miR-20a-5p;hsa-miR-224-5p;hsa-miR-27a-3p;hsa-miR-330-5p;hsa-miR-454-3p;hsa-miR-590-3p | 12 | PDGFRA | Sponge network | -2.961 | 0.00154 | -4.316 | 1.0E-5 | 0.481 |
84 | EMX2OS |
hsa-let-7a-3p;hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-miR-103a-2-5p;hsa-miR-15b-3p;hsa-miR-19b-1-5p;hsa-miR-20a-3p;hsa-miR-22-5p;hsa-miR-32-3p;hsa-miR-330-3p;hsa-miR-3614-5p;hsa-miR-421;hsa-miR-944 | 13 | PRLR | Sponge network | -6.205 | 0.00015 | -5.28 | 0.00088 | 0.479 |
85 | HAND2-AS1 |
hsa-let-7a-3p;hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-miR-103a-2-5p;hsa-miR-15b-3p;hsa-miR-19b-1-5p;hsa-miR-20a-3p;hsa-miR-22-5p;hsa-miR-32-3p;hsa-miR-330-3p;hsa-miR-33a-3p;hsa-miR-3614-5p;hsa-miR-421;hsa-miR-944 | 14 | PRLR | Sponge network | -7.871 | 0 | -5.28 | 0.00088 | 0.478 |
86 | RP11-166D19.1 |
hsa-let-7f-1-3p;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-27a-3p;hsa-miR-33a-3p;hsa-miR-452-5p;hsa-miR-576-5p | 12 | IGF1 | Sponge network | -4.209 | 2.0E-5 | -4.485 | 0.00149 | 0.477 |
87 | MEG3 |
hsa-miR-141-3p;hsa-miR-17-3p;hsa-miR-182-5p;hsa-miR-185-3p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-1976;hsa-miR-224-5p;hsa-miR-31-3p;hsa-miR-31-5p;hsa-miR-330-5p;hsa-miR-3615;hsa-miR-96-5p | 13 | GNG7 | Sponge network | -3.613 | 0.00075 | -4.495 | 0 | 0.476 |
88 | CTD-2334D19.1 | hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-219a-5p;hsa-miR-224-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-590-3p;hsa-miR-93-5p | 11 | PDGFRA | Sponge network | -4.489 | 0.03789 | -4.316 | 1.0E-5 | 0.472 |
89 | AC003090.1 |
hsa-miR-130a-5p;hsa-miR-141-3p;hsa-miR-17-3p;hsa-miR-182-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-1976;hsa-miR-22-5p;hsa-miR-224-5p;hsa-miR-31-5p;hsa-miR-96-5p | 12 | GNG7 | Sponge network | -7.817 | 0.00161 | -4.495 | 0 | 0.472 |
90 | HAND2-AS1 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-130b-3p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-205-5p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-421;hsa-miR-590-3p;hsa-miR-671-5p | 11 | KIT | Sponge network | -7.871 | 0 | -2.927 | 0.01211 | 0.47 |
91 | ADAMTS9-AS1 |
hsa-let-7f-1-3p;hsa-let-7g-3p;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-193a-3p;hsa-miR-200a-3p;hsa-miR-20a-5p;hsa-miR-2110;hsa-miR-219a-5p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-330-5p;hsa-miR-335-3p;hsa-miR-339-5p;hsa-miR-421;hsa-miR-429;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-7-1-3p;hsa-miR-93-5p;hsa-miR-96-5p | 32 | PDGFRA | Sponge network | -8.573 | 0.00012 | -4.316 | 1.0E-5 | 0.469 |
92 | EMX2OS |
hsa-let-7f-1-3p;hsa-miR-107;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-20a-5p;hsa-miR-27a-3p;hsa-miR-31-5p;hsa-miR-452-5p;hsa-miR-484;hsa-miR-486-5p;hsa-miR-590-3p | 15 | FGF7 | Sponge network | -6.205 | 0.00015 | -5.509 | 0 | 0.468 |
93 | HAND2-AS1 |
hsa-miR-130a-5p;hsa-miR-141-3p;hsa-miR-17-3p;hsa-miR-182-5p;hsa-miR-185-3p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-1976;hsa-miR-200a-3p;hsa-miR-22-5p;hsa-miR-224-5p;hsa-miR-23a-3p;hsa-miR-31-3p;hsa-miR-31-5p;hsa-miR-330-5p;hsa-miR-92a-3p;hsa-miR-940 | 18 | GNG7 | Sponge network | -7.871 | 0 | -4.495 | 0 | 0.468 |
94 | RP11-887P2.5 |
hsa-let-7f-1-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-193a-3p;hsa-miR-196a-5p;hsa-miR-20a-5p;hsa-miR-2110;hsa-miR-219a-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-330-5p;hsa-miR-339-5p;hsa-miR-454-3p;hsa-miR-550a-5p;hsa-miR-576-5p;hsa-miR-590-5p;hsa-miR-7-1-3p;hsa-miR-93-5p | 21 | PDGFRA | Sponge network | -9.865 | 1.0E-5 | -4.316 | 1.0E-5 | 0.464 |
95 | RP11-344E13.3 |
hsa-let-7g-3p;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-200a-3p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-2110;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-330-5p;hsa-miR-339-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-454-3p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-93-5p | 22 | PDGFRA | Sponge network | -4.307 | 3.0E-5 | -4.316 | 1.0E-5 | 0.461 |
96 | CTD-2554C21.3 |
hsa-let-7f-1-3p;hsa-miR-106b-5p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-193a-3p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-330-5p;hsa-miR-339-5p;hsa-miR-7-1-3p | 11 | PDGFRA | Sponge network | -6.258 | 0.00703 | -4.316 | 1.0E-5 | 0.459 |
97 | RP11-166D19.1 |
hsa-miR-141-5p;hsa-miR-200a-5p;hsa-miR-200b-3p;hsa-miR-200b-5p;hsa-miR-200c-3p;hsa-miR-3607-3p;hsa-miR-429;hsa-miR-452-5p;hsa-miR-590-3p;hsa-miR-944 | 10 | ITGA1 | Sponge network | -4.209 | 2.0E-5 | -1.265 | 0.08839 | 0.458 |
98 | ZNF667-AS1 |
hsa-let-7f-1-3p;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-20a-5p;hsa-miR-27a-3p;hsa-miR-31-5p;hsa-miR-452-5p;hsa-miR-484 | 12 | FGF7 | Sponge network | -4.019 | 0.00137 | -5.509 | 0 | 0.458 |
99 | RP11-344E13.3 |
hsa-let-7d-5p;hsa-let-7g-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-107;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-532-3p;hsa-miR-590-3p;hsa-miR-625-5p;hsa-miR-93-5p | 12 | COL1A1 | Sponge network | -4.307 | 3.0E-5 | -1.841 | 0.04283 | 0.458 |
100 | USP3-AS1 |
hsa-let-7f-1-3p;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-20a-5p;hsa-miR-27a-3p;hsa-miR-452-5p;hsa-miR-486-5p | 11 | FGF7 | Sponge network | -4.151 | 0 | -5.509 | 0 | 0.456 |
101 | MAGI2-AS3 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-130b-3p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-205-5p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-590-3p;hsa-miR-671-5p | 10 | KIT | Sponge network | -4.563 | 0 | -2.927 | 0.01211 | 0.45 |
102 | RP11-760H22.2 | hsa-let-7a-3p;hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-miR-142-3p;hsa-miR-15b-3p;hsa-miR-20a-3p;hsa-miR-22-5p;hsa-miR-320b;hsa-miR-9-3p;hsa-miR-944 | 10 | PRLR | Sponge network | -3.418 | 0.00912 | -5.28 | 0.00088 | 0.447 |
103 | HAND2-AS1 |
hsa-miR-130a-5p;hsa-miR-149-5p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-19b-1-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-429;hsa-miR-590-3p | 10 | KDR | Sponge network | -7.871 | 0 | -3.788 | 0 | 0.447 |
104 | CTC-559E9.5 | hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-576-5p | 10 | PDGFRA | Sponge network | -2.253 | 0.00403 | -4.316 | 1.0E-5 | 0.447 |
105 | TRHDE-AS1 |
hsa-let-7f-1-3p;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-27a-3p;hsa-miR-31-5p;hsa-miR-484;hsa-miR-590-3p;hsa-miR-590-5p | 12 | FGF7 | Sponge network | -6.205 | 0.01165 | -5.509 | 0 | 0.439 |
106 | ACTA2-AS1 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-let-7g-3p;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-193a-3p;hsa-miR-200a-3p;hsa-miR-20a-5p;hsa-miR-2110;hsa-miR-219a-5p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-454-3p;hsa-miR-550a-5p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-944;hsa-miR-96-5p | 26 | PDGFRA | Sponge network | -6.142 | 0.00223 | -4.316 | 1.0E-5 | 0.439 |
107 | HOXA11-AS | hsa-let-7g-3p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-141-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-193a-3p;hsa-miR-200a-3p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-2110;hsa-miR-224-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-454-3p | 16 | PDGFRA | Sponge network | -3.349 | 0.00194 | -4.316 | 1.0E-5 | 0.438 |
108 | RP11-166D19.1 |
hsa-miR-141-3p;hsa-miR-17-3p;hsa-miR-182-5p;hsa-miR-185-3p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-1976;hsa-miR-200a-3p;hsa-miR-224-5p;hsa-miR-23a-3p;hsa-miR-3615;hsa-miR-616-5p;hsa-miR-9-5p;hsa-miR-92a-3p;hsa-miR-96-5p | 15 | GNG7 | Sponge network | -4.209 | 2.0E-5 | -4.495 | 0 | 0.435 |
109 | WT1-AS |
hsa-miR-141-3p;hsa-miR-17-3p;hsa-miR-182-5p;hsa-miR-185-3p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-1976;hsa-miR-22-5p;hsa-miR-23a-3p;hsa-miR-31-5p;hsa-miR-330-5p;hsa-miR-3615;hsa-miR-9-5p;hsa-miR-92a-3p;hsa-miR-940;hsa-miR-96-5p | 17 | GNG7 | Sponge network | -6.875 | 2.0E-5 | -4.495 | 0 | 0.435 |
110 | HAND2-AS1 |
hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-miR-193a-3p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-25-3p;hsa-miR-32-3p;hsa-miR-32-5p;hsa-miR-330-5p;hsa-miR-33a-3p;hsa-miR-590-3p;hsa-miR-7-5p;hsa-miR-92a-3p;hsa-miR-92b-3p | 14 | COL1A2 | Sponge network | -7.871 | 0 | -2.407 | 0.0132 | 0.435 |
111 | CTD-2554C21.3 |
hsa-let-7f-1-3p;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-27a-3p;hsa-miR-484;hsa-miR-7-1-3p | 10 | FGF7 | Sponge network | -6.258 | 0.00703 | -5.509 | 0 | 0.435 |
112 | MIR497HG |
hsa-miR-130a-5p;hsa-miR-141-3p;hsa-miR-17-3p;hsa-miR-185-3p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-1976;hsa-miR-200a-3p;hsa-miR-22-5p;hsa-miR-224-5p;hsa-miR-23a-3p;hsa-miR-31-5p;hsa-miR-3127-5p;hsa-miR-330-5p;hsa-miR-3615;hsa-miR-940 | 17 | GNG7 | Sponge network | -6.146 | 0.00024 | -4.495 | 0 | 0.434 |
113 | CTC-296K1.3 | hsa-let-7f-1-3p;hsa-let-7g-3p;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-193a-3p;hsa-miR-200a-3p;hsa-miR-20a-5p;hsa-miR-2110;hsa-miR-301a-3p;hsa-miR-330-5p;hsa-miR-454-3p;hsa-miR-616-5p | 17 | PDGFRA | Sponge network | -6.944 | 0.00011 | -4.316 | 1.0E-5 | 0.43 |
114 | PGM5-AS1 |
hsa-let-7f-1-3p;hsa-miR-107;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-18a-3p;hsa-miR-20a-5p;hsa-miR-27a-3p;hsa-miR-33a-3p;hsa-miR-484;hsa-miR-7-1-3p | 10 | FGF7 | Sponge network | -14.107 | 0 | -5.509 | 0 | 0.427 |
115 | ADAMTS9-AS1 |
hsa-miR-130a-5p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-19b-1-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-590-5p | 10 | KDR | Sponge network | -8.573 | 0.00012 | -3.788 | 0 | 0.425 |
116 | TRHDE-AS1 |
hsa-let-7f-1-3p;hsa-let-7g-3p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-141-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-193a-3p;hsa-miR-200a-3p;hsa-miR-2110;hsa-miR-224-5p;hsa-miR-27a-3p;hsa-miR-330-5p;hsa-miR-339-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-550a-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-93-5p | 20 | PDGFRA | Sponge network | -6.205 | 0.01165 | -4.316 | 1.0E-5 | 0.425 |
117 | RP11-130L8.1 |
hsa-let-7f-1-3p;hsa-miR-107;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-1-3p;hsa-miR-16-5p;hsa-miR-20a-5p;hsa-miR-27a-3p;hsa-miR-590-3p;hsa-miR-590-5p | 10 | FGF7 | Sponge network | -4.329 | 1.0E-5 | -5.509 | 0 | 0.424 |
118 | ZNF582-AS1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-193a-3p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-224-5p;hsa-miR-33a-5p;hsa-miR-576-5p;hsa-miR-93-5p;hsa-miR-944 | 14 | PDGFRA | Sponge network | -4.925 | 0.00112 | -4.316 | 1.0E-5 | 0.424 |
119 | MIR497HG |
hsa-let-7f-1-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-193a-3p;hsa-miR-196a-5p;hsa-miR-200a-3p;hsa-miR-20a-5p;hsa-miR-2110;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-330-5p;hsa-miR-339-5p;hsa-miR-589-3p;hsa-miR-590-5p;hsa-miR-7-1-3p | 20 | PDGFRA | Sponge network | -6.146 | 0.00024 | -4.316 | 1.0E-5 | 0.424 |
120 | NR2F2-AS1 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-106b-5p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-193a-3p;hsa-miR-20a-5p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-339-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-590-3p;hsa-miR-93-5p;hsa-miR-944 | 16 | PDGFRA | Sponge network | -3.785 | 0.00281 | -4.316 | 1.0E-5 | 0.422 |
121 | EMX2OS |
hsa-miR-1271-5p;hsa-miR-17-3p;hsa-miR-185-3p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-1976;hsa-miR-22-5p;hsa-miR-224-5p;hsa-miR-23a-3p;hsa-miR-31-5p;hsa-miR-330-5p;hsa-miR-92a-3p;hsa-miR-940 | 14 | GNG7 | Sponge network | -6.205 | 0.00015 | -4.495 | 0 | 0.42 |
122 | MAGI2-AS3 |
hsa-let-7d-5p;hsa-miR-16-2-3p;hsa-miR-18a-3p;hsa-miR-1976;hsa-miR-24-3p;hsa-miR-25-3p;hsa-miR-33a-3p;hsa-miR-9-3p;hsa-miR-92a-1-5p;hsa-miR-92a-3p | 10 | CREB3L2 | Sponge network | -4.563 | 0 | -2.05 | 0.00075 | 0.417 |
123 | PGM5-AS1 |
hsa-miR-130a-5p;hsa-miR-141-3p;hsa-miR-17-3p;hsa-miR-182-5p;hsa-miR-185-3p;hsa-miR-18a-3p;hsa-miR-193b-5p;hsa-miR-1976;hsa-miR-200a-3p;hsa-miR-22-5p;hsa-miR-23a-3p | 11 | GNG7 | Sponge network | -14.107 | 0 | -4.495 | 0 | 0.417 |
124 | PGM5-AS1 |
hsa-let-7a-3p;hsa-let-7f-1-3p;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-193a-3p;hsa-miR-200a-3p;hsa-miR-20a-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-7-1-3p | 15 | PDGFRA | Sponge network | -14.107 | 0 | -4.316 | 1.0E-5 | 0.412 |
125 | ADAMTS9-AS1 |
hsa-miR-130a-5p;hsa-miR-141-3p;hsa-miR-17-3p;hsa-miR-182-5p;hsa-miR-185-3p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-1976;hsa-miR-200a-3p;hsa-miR-224-5p;hsa-miR-23a-3p;hsa-miR-31-3p;hsa-miR-31-5p;hsa-miR-330-5p;hsa-miR-92a-3p;hsa-miR-940;hsa-miR-96-5p | 18 | GNG7 | Sponge network | -8.573 | 0.00012 | -4.495 | 0 | 0.412 |
126 | RP11-597D13.9 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-200a-3p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-219a-5p;hsa-miR-301a-3p;hsa-miR-421;hsa-miR-429;hsa-miR-454-3p;hsa-miR-93-5p;hsa-miR-96-5p | 16 | PDGFRA | Sponge network | -2.494 | 0.07597 | -4.316 | 1.0E-5 | 0.41 |
127 | RP11-284N8.3 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-200a-3p;hsa-miR-219a-5p;hsa-miR-24-3p;hsa-miR-335-3p;hsa-miR-33a-5p;hsa-miR-590-5p;hsa-miR-93-5p;hsa-miR-96-5p | 13 | PDGFRA | Sponge network | -0.845 | 0.52848 | -4.316 | 1.0E-5 | 0.409 |
128 | EMX2OS |
hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-let-7f-5p;hsa-miR-193a-3p;hsa-miR-19b-3p;hsa-miR-32-3p;hsa-miR-32-5p;hsa-miR-330-5p;hsa-miR-590-3p;hsa-miR-7-5p;hsa-miR-92a-3p | 11 | COL1A2 | Sponge network | -6.205 | 0.00015 | -2.407 | 0.0132 | 0.408 |
129 | RP11-116O18.1 | hsa-let-7f-1-3p;hsa-let-7g-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-193a-3p;hsa-miR-219a-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-330-5p;hsa-miR-339-5p;hsa-miR-590-3p;hsa-miR-590-5p | 14 | PDGFRA | Sponge network | -5.007 | 0.06008 | -4.316 | 1.0E-5 | 0.406 |
130 | HAND2-AS1 |
hsa-let-7d-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-107;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-23a-5p;hsa-miR-330-3p;hsa-miR-590-3p;hsa-miR-93-5p | 10 | COL1A1 | Sponge network | -7.871 | 0 | -1.841 | 0.04283 | 0.405 |
131 | HAND2-AS1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-32-3p;hsa-miR-335-3p;hsa-miR-3614-5p;hsa-miR-590-3p;hsa-miR-93-5p | 11 | THBS2 | Sponge network | -7.871 | 0 | -2.628 | 0.00636 | 0.398 |
132 | NR2F1-AS1 |
hsa-let-7f-1-3p;hsa-miR-15a-5p;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-18a-3p;hsa-miR-20a-5p;hsa-miR-27a-3p;hsa-miR-31-5p;hsa-miR-452-5p;hsa-miR-484;hsa-miR-590-3p | 12 | FGF7 | Sponge network | -2.961 | 0.00154 | -5.509 | 0 | 0.395 |
133 | AC005682.5 | hsa-miR-106a-5p;hsa-miR-10a-3p;hsa-miR-130b-5p;hsa-miR-141-3p;hsa-miR-182-5p;hsa-miR-191-5p;hsa-miR-200a-3p;hsa-miR-20b-5p;hsa-miR-28-5p;hsa-miR-3065-3p;hsa-miR-3065-5p | 11 | CCND2 | Sponge network | -2.193 | 0.07184 | -2.811 | 0.0014 | 0.394 |
134 | RP11-150O12.3 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-193a-3p;hsa-miR-20a-5p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-330-5p;hsa-miR-339-5p;hsa-miR-33a-5p;hsa-miR-33b-5p | 13 | PDGFRA | Sponge network | -4.03 | 0.14448 | -4.316 | 1.0E-5 | 0.393 |
135 | RP11-887P2.5 |
hsa-miR-17-3p;hsa-miR-182-5p;hsa-miR-185-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-1976;hsa-miR-22-5p;hsa-miR-23a-3p;hsa-miR-330-5p;hsa-miR-3615;hsa-miR-940 | 11 | GNG7 | Sponge network | -9.865 | 1.0E-5 | -4.495 | 0 | 0.393 |
136 | EMX2OS |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-142-5p;hsa-miR-15a-5p;hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-205-5p;hsa-miR-27a-3p;hsa-miR-330-3p;hsa-miR-330-5p;hsa-miR-590-3p | 12 | INSR | Sponge network | -6.205 | 0.00015 | -1.824 | 0.00037 | 0.392 |
137 | FAM66C |
hsa-let-7a-3p;hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-miR-103a-2-5p;hsa-miR-142-3p;hsa-miR-15b-3p;hsa-miR-19b-1-5p;hsa-miR-20a-3p;hsa-miR-22-5p;hsa-miR-3614-5p | 10 | PRLR | Sponge network | -2.927 | 0.00012 | -5.28 | 0.00088 | 0.392 |
138 | MAGI2-AS3 |
hsa-let-7a-3p;hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-miR-103a-2-5p;hsa-miR-142-3p;hsa-miR-15b-3p;hsa-miR-19b-1-5p;hsa-miR-20a-3p;hsa-miR-32-3p;hsa-miR-320b;hsa-miR-33a-3p;hsa-miR-3614-5p;hsa-miR-9-3p | 13 | PRLR | Sponge network | -4.563 | 0 | -5.28 | 0.00088 | 0.391 |
139 | TPTEP1 |
hsa-miR-141-3p;hsa-miR-17-3p;hsa-miR-182-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-1976;hsa-miR-224-5p;hsa-miR-31-3p;hsa-miR-31-5p;hsa-miR-330-5p;hsa-miR-92a-3p | 11 | GNG7 | Sponge network | -4.398 | 5.0E-5 | -4.495 | 0 | 0.39 |
140 | RASSF8-AS1 |
hsa-let-7a-3p;hsa-miR-106b-5p;hsa-miR-16-1-3p;hsa-miR-193a-3p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-590-3p;hsa-miR-944 | 11 | PDGFRA | Sponge network | -2.562 | 0.00163 | -4.316 | 1.0E-5 | 0.388 |
141 | RP11-54O7.3 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-16-1-3p;hsa-miR-193a-3p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-330-5p;hsa-miR-33a-5p;hsa-miR-33b-5p | 10 | PDGFRA | Sponge network | -2.864 | 0.01902 | -4.316 | 1.0E-5 | 0.386 |
142 | ADAMTS9-AS1 |
hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-miR-193a-3p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-25-3p;hsa-miR-32-5p;hsa-miR-330-5p;hsa-miR-363-3p;hsa-miR-590-3p;hsa-miR-7-5p;hsa-miR-92a-3p;hsa-miR-92b-3p | 13 | COL1A2 | Sponge network | -8.573 | 0.00012 | -2.407 | 0.0132 | 0.385 |
143 | ZNF667-AS1 |
hsa-let-7f-1-3p;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-27a-3p;hsa-miR-452-5p;hsa-miR-629-5p | 10 | IGF1 | Sponge network | -4.019 | 0.00137 | -4.485 | 0.00149 | 0.383 |
144 | DIO3OS |
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-200a-3p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-219a-5p;hsa-miR-33a-5p;hsa-miR-33b-5p | 13 | PDGFRA | Sponge network | -4.295 | 0.00689 | -4.316 | 1.0E-5 | 0.383 |
145 | RP11-244O19.1 | hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-141-3p;hsa-miR-15b-5p;hsa-miR-182-5p;hsa-miR-183-5p;hsa-miR-191-5p;hsa-miR-200a-3p;hsa-miR-3065-3p;hsa-miR-3065-5p;hsa-miR-30d-3p;hsa-miR-93-5p | 12 | CCND2 | Sponge network | -1.318 | 0.0924 | -2.811 | 0.0014 | 0.383 |
146 | FAM66C |
hsa-let-7f-1-3p;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-20a-3p;hsa-miR-27a-3p;hsa-miR-940 | 10 | IGF1 | Sponge network | -2.927 | 0.00012 | -4.485 | 0.00149 | 0.38 |
147 | ADAMTS9-AS1 |
hsa-let-7f-1-3p;hsa-miR-130b-3p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-205-5p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-421;hsa-miR-590-3p;hsa-miR-671-5p | 10 | KIT | Sponge network | -8.573 | 0.00012 | -2.927 | 0.01211 | 0.379 |
148 | ADAMTS9-AS1 |
hsa-let-7d-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-107;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-23a-5p;hsa-miR-590-3p;hsa-miR-625-5p;hsa-miR-92a-1-5p;hsa-miR-93-5p | 11 | COL1A1 | Sponge network | -8.573 | 0.00012 | -1.841 | 0.04283 | 0.378 |
149 | LINC00284 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-17-5p;hsa-miR-193a-3p;hsa-miR-20a-5p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-330-5p;hsa-miR-339-5p;hsa-miR-33a-5p;hsa-miR-590-3p;hsa-miR-944 | 13 | PDGFRA | Sponge network | -5.478 | 0.02716 | -4.316 | 1.0E-5 | 0.375 |
150 | DIO3OS |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-5p;hsa-miR-141-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-182-5p;hsa-miR-183-5p;hsa-miR-191-5p;hsa-miR-200a-3p;hsa-miR-20b-5p;hsa-miR-324-3p;hsa-miR-378a-3p | 13 | CCND2 | Sponge network | -4.295 | 0.00689 | -2.811 | 0.0014 | 0.374 |
151 | ACTA2-AS1 |
hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19b-3p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-20a-5p;hsa-miR-33a-3p;hsa-miR-576-5p;hsa-miR-590-3p | 10 | THBS1 | Sponge network | -6.142 | 0.00223 | -3.751 | 0.0001 | 0.37 |
152 | ZNF667-AS1 |
hsa-let-7f-1-3p;hsa-miR-106b-5p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-193a-3p;hsa-miR-20a-5p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-330-5p;hsa-miR-339-5p | 11 | PDGFRA | Sponge network | -4.019 | 0.00137 | -4.316 | 1.0E-5 | 0.369 |
153 | EMX2OS |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-130b-3p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-205-5p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-421;hsa-miR-590-3p;hsa-miR-671-5p | 11 | KIT | Sponge network | -6.205 | 0.00015 | -2.927 | 0.01211 | 0.363 |
154 | WT1-AS |
hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-miR-193a-3p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-25-3p;hsa-miR-32-3p;hsa-miR-32-5p;hsa-miR-330-5p;hsa-miR-33a-3p;hsa-miR-590-3p;hsa-miR-92a-3p | 12 | COL1A2 | Sponge network | -6.875 | 2.0E-5 | -2.407 | 0.0132 | 0.36 |
155 | CTB-92J24.3 | hsa-let-7f-1-3p;hsa-let-7g-3p;hsa-miR-106b-5p;hsa-miR-141-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-33a-5p;hsa-miR-93-5p;hsa-miR-944 | 12 | PDGFRA | Sponge network | -7.226 | 0.0046 | -4.316 | 1.0E-5 | 0.36 |
156 | RP11-130L8.1 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-142-5p;hsa-miR-15a-5p;hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-205-5p;hsa-miR-27a-3p;hsa-miR-590-3p;hsa-miR-590-5p | 11 | INSR | Sponge network | -4.329 | 1.0E-5 | -1.824 | 0.00037 | 0.36 |
157 | RP11-774O3.3 |
hsa-let-7f-1-3p;hsa-miR-107;hsa-miR-15b-5p;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-18a-3p;hsa-miR-27a-3p;hsa-miR-31-5p;hsa-miR-7-1-3p | 10 | FGF7 | Sponge network | -1.989 | 0.00136 | -5.509 | 0 | 0.358 |
158 | RP11-161M6.2 |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-193a-3p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-330-5p;hsa-miR-339-5p;hsa-miR-550a-5p;hsa-miR-93-5p | 12 | PDGFRA | Sponge network | -2.608 | 0.00296 | -4.316 | 1.0E-5 | 0.357 |
159 | ADAMTS9-AS1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-335-3p;hsa-miR-3614-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-93-5p;hsa-miR-96-5p | 12 | THBS2 | Sponge network | -8.573 | 0.00012 | -2.628 | 0.00636 | 0.355 |
160 | DNM3OS |
hsa-miR-141-3p;hsa-miR-17-3p;hsa-miR-182-5p;hsa-miR-185-3p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-1976;hsa-miR-200a-3p;hsa-miR-224-5p;hsa-miR-31-3p;hsa-miR-616-5p;hsa-miR-940;hsa-miR-96-5p | 13 | GNG7 | Sponge network | -3.933 | 0.00059 | -4.495 | 0 | 0.355 |
161 | RP11-54O7.3 |
hsa-let-7a-3p;hsa-let-7b-3p;hsa-let-7b-5p;hsa-let-7f-1-3p;hsa-miR-142-5p;hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-205-5p;hsa-miR-27a-3p;hsa-miR-330-5p | 11 | INSR | Sponge network | -2.864 | 0.01902 | -1.824 | 0.00037 | 0.351 |
162 | ACTA2-AS1 |
hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-let-7g-5p;hsa-miR-193a-3p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-25-3p;hsa-miR-33a-3p;hsa-miR-590-3p;hsa-miR-7-5p | 10 | COL1A2 | Sponge network | -6.142 | 0.00223 | -2.407 | 0.0132 | 0.351 |
163 | WT1-AS |
hsa-miR-106b-5p;hsa-miR-142-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-32-3p;hsa-miR-335-3p;hsa-miR-590-3p;hsa-miR-93-5p;hsa-miR-96-5p | 11 | THBS2 | Sponge network | -6.875 | 2.0E-5 | -2.628 | 0.00636 | 0.351 |
164 | HAND2-AS1 |
hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-200c-3p;hsa-miR-21-5p;hsa-miR-24-2-5p;hsa-miR-33b-5p;hsa-miR-365a-3p;hsa-miR-429;hsa-miR-629-5p;hsa-miR-7-5p | 12 | BCL2 | Sponge network | -7.871 | 0 | -3.063 | 1.0E-5 | 0.35 |
165 | HAND2-AS1 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-15a-5p;hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-205-5p;hsa-miR-27a-3p;hsa-miR-330-3p;hsa-miR-330-5p;hsa-miR-590-3p | 11 | INSR | Sponge network | -7.871 | 0 | -1.824 | 0.00037 | 0.348 |
166 | LINC00284 |
hsa-miR-142-3p;hsa-miR-142-5p;hsa-miR-155-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-205-5p;hsa-miR-221-5p;hsa-miR-330-5p;hsa-miR-590-3p;hsa-miR-944 | 10 | FGF9 | Sponge network | -5.478 | 0.02716 | -4.087 | 0.01073 | 0.346 |
167 | ADAMTS9-AS1 |
hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-200c-3p;hsa-miR-21-5p;hsa-miR-24-2-5p;hsa-miR-365a-3p;hsa-miR-429;hsa-miR-629-5p;hsa-miR-7-5p | 11 | BCL2 | Sponge network | -8.573 | 0.00012 | -3.063 | 1.0E-5 | 0.346 |
168 | FAM66C |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-let-7g-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-193a-3p;hsa-miR-20a-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-330-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-7-1-3p | 18 | PDGFRA | Sponge network | -2.927 | 0.00012 | -4.316 | 1.0E-5 | 0.346 |
169 | EMX2OS |
hsa-let-7d-5p;hsa-let-7f-5p;hsa-miR-106b-5p;hsa-miR-107;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-23a-5p;hsa-miR-330-3p;hsa-miR-590-3p;hsa-miR-93-5p | 10 | COL1A1 | Sponge network | -6.205 | 0.00015 | -1.841 | 0.04283 | 0.346 |
170 | FAM66C |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-142-5p;hsa-miR-15a-5p;hsa-miR-15b-3p;hsa-miR-16-5p;hsa-miR-27a-3p;hsa-miR-330-5p;hsa-miR-590-3p;hsa-miR-590-5p | 10 | INSR | Sponge network | -2.927 | 0.00012 | -1.824 | 0.00037 | 0.341 |
171 | RP11-166D19.1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-5p;hsa-miR-141-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-182-5p;hsa-miR-183-5p;hsa-miR-191-5p;hsa-miR-200a-3p;hsa-miR-20b-5p;hsa-miR-224-3p;hsa-miR-324-3p;hsa-miR-33a-3p;hsa-miR-378a-3p;hsa-miR-429;hsa-miR-550a-5p;hsa-miR-96-5p | 18 | CCND2 | Sponge network | -4.209 | 2.0E-5 | -2.811 | 0.0014 | 0.339 |
172 | RP11-344E13.3 |
hsa-miR-1271-5p;hsa-miR-141-3p;hsa-miR-17-3p;hsa-miR-185-3p;hsa-miR-18a-5p;hsa-miR-1976;hsa-miR-200a-3p;hsa-miR-31-3p;hsa-miR-31-5p;hsa-miR-330-5p;hsa-miR-3615 | 11 | GNG7 | Sponge network | -4.307 | 3.0E-5 | -4.495 | 0 | 0.339 |
173 | RP11-890B15.3 | hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-20b-5p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-330-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-576-5p;hsa-miR-93-5p | 13 | PDGFRA | Sponge network | -2.059 | 0.00641 | -4.316 | 1.0E-5 | 0.337 |
174 | RP11-439M11.1 | hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-5p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-182-5p;hsa-miR-183-5p;hsa-miR-191-5p;hsa-miR-20b-5p;hsa-miR-324-3p | 10 | CCND2 | Sponge network | -2.662 | 0.21003 | -2.811 | 0.0014 | 0.337 |
175 | LINC00861 | hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-219a-5p;hsa-miR-24-3p;hsa-miR-301a-3p;hsa-miR-335-3p;hsa-miR-33a-5p;hsa-miR-429;hsa-miR-589-3p;hsa-miR-590-5p;hsa-miR-96-5p | 14 | PDGFRA | Sponge network | 0.999 | 0.45301 | -4.316 | 1.0E-5 | 0.334 |
176 | RP11-166D19.1 |
hsa-let-7d-5p;hsa-miR-16-2-3p;hsa-miR-18a-3p;hsa-miR-1976;hsa-miR-24-3p;hsa-miR-25-3p;hsa-miR-33a-3p;hsa-miR-9-5p;hsa-miR-92a-3p;hsa-miR-944 | 10 | CREB3L2 | Sponge network | -4.209 | 2.0E-5 | -2.05 | 0.00075 | 0.333 |
177 | ACTA2-AS1 |
hsa-let-7f-1-3p;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-27a-3p;hsa-miR-33a-3p;hsa-miR-576-5p | 12 | IGF1 | Sponge network | -6.142 | 0.00223 | -4.485 | 0.00149 | 0.332 |
178 | WT1-AS |
hsa-let-7f-1-3p;hsa-miR-142-5p;hsa-miR-15a-5p;hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-205-5p;hsa-miR-27a-3p;hsa-miR-330-5p;hsa-miR-590-3p | 10 | INSR | Sponge network | -6.875 | 2.0E-5 | -1.824 | 0.00037 | 0.332 |
179 | NR2F2-AS1 |
hsa-let-7f-1-3p;hsa-miR-15a-5p;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-18a-3p;hsa-miR-20a-5p;hsa-miR-27a-3p;hsa-miR-31-5p;hsa-miR-452-5p;hsa-miR-590-3p | 11 | FGF7 | Sponge network | -3.785 | 0.00281 | -5.509 | 0 | 0.329 |
180 | MAGI2-AS3 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-142-5p;hsa-miR-15a-5p;hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-205-5p;hsa-miR-27a-3p;hsa-miR-330-5p;hsa-miR-590-3p | 11 | INSR | Sponge network | -4.563 | 0 | -1.824 | 0.00037 | 0.327 |
181 | RASSF8-AS1 |
hsa-let-7a-3p;hsa-let-7b-3p;hsa-miR-142-5p;hsa-miR-15a-5p;hsa-miR-15b-3p;hsa-miR-16-5p;hsa-miR-205-5p;hsa-miR-27a-3p;hsa-miR-342-3p;hsa-miR-590-3p | 10 | INSR | Sponge network | -2.562 | 0.00163 | -1.824 | 0.00037 | 0.327 |
182 | LINC00865 |
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-200a-3p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-219a-5p;hsa-miR-301a-3p;hsa-miR-339-5p;hsa-miR-429;hsa-miR-616-5p | 15 | PDGFRA | Sponge network | -1.585 | 0.19508 | -4.316 | 1.0E-5 | 0.321 |
183 | RP11-13K12.1 |
hsa-miR-130a-5p;hsa-miR-141-3p;hsa-miR-17-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-1976;hsa-miR-22-5p;hsa-miR-224-5p;hsa-miR-23a-3p;hsa-miR-31-5p | 10 | GNG7 | Sponge network | -5.093 | 0.01151 | -4.495 | 0 | 0.319 |
184 | MAGI2-AS3 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-5p;hsa-miR-141-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-182-5p;hsa-miR-183-5p;hsa-miR-191-5p;hsa-miR-200a-3p;hsa-miR-20b-5p;hsa-miR-224-3p;hsa-miR-3065-5p;hsa-miR-30d-3p;hsa-miR-33a-3p;hsa-miR-378a-3p;hsa-miR-429;hsa-miR-9-3p;hsa-miR-93-5p | 19 | CCND2 | Sponge network | -4.563 | 0 | -2.811 | 0.0014 | 0.315 |
185 | ACTA2-AS1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-142-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-3614-5p;hsa-miR-590-3p;hsa-miR-96-5p | 10 | THBS2 | Sponge network | -6.142 | 0.00223 | -2.628 | 0.00636 | 0.313 |
186 | RP11-284N8.3 |
hsa-miR-106b-5p;hsa-miR-130b-5p;hsa-miR-141-3p;hsa-miR-182-5p;hsa-miR-183-5p;hsa-miR-200a-3p;hsa-miR-3065-5p;hsa-miR-324-3p;hsa-miR-93-5p;hsa-miR-96-5p | 10 | CCND2 | Sponge network | -0.845 | 0.52848 | -2.811 | 0.0014 | 0.313 |
187 | TRHDE-AS1 |
hsa-miR-130a-5p;hsa-miR-141-3p;hsa-miR-17-3p;hsa-miR-185-3p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-1976;hsa-miR-200a-3p;hsa-miR-22-5p;hsa-miR-224-5p;hsa-miR-23a-3p;hsa-miR-31-3p;hsa-miR-31-5p;hsa-miR-330-5p;hsa-miR-92a-3p | 15 | GNG7 | Sponge network | -6.205 | 0.01165 | -4.495 | 0 | 0.312 |
188 | RP11-567M16.1 | hsa-let-7g-3p;hsa-miR-141-3p;hsa-miR-17-5p;hsa-miR-200a-3p;hsa-miR-2110;hsa-miR-219a-5p;hsa-miR-330-5p;hsa-miR-339-5p;hsa-miR-590-5p;hsa-miR-616-5p;hsa-miR-93-5p | 11 | PDGFRA | Sponge network | -2.638 | 0.21408 | -4.316 | 1.0E-5 | 0.309 |
189 | RP11-166D19.1 |
hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-miR-142-3p;hsa-miR-15b-3p;hsa-miR-19b-1-5p;hsa-miR-20a-3p;hsa-miR-33a-3p;hsa-miR-3614-5p;hsa-miR-9-5p;hsa-miR-944 | 10 | PRLR | Sponge network | -4.209 | 2.0E-5 | -5.28 | 0.00088 | 0.309 |
190 | NR2F2-AS1 |
hsa-miR-1271-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-1976;hsa-miR-22-5p;hsa-miR-224-5p;hsa-miR-23a-3p;hsa-miR-31-5p;hsa-miR-3615;hsa-miR-92a-3p | 11 | GNG7 | Sponge network | -3.785 | 0.00281 | -4.495 | 0 | 0.308 |
191 | KTN1-AS1 | hsa-let-7c-5p;hsa-miR-125b-5p;hsa-miR-192-5p;hsa-miR-194-3p;hsa-miR-194-5p;hsa-miR-215-5p;hsa-miR-29b-2-5p;hsa-miR-378c;hsa-miR-592;hsa-miR-99a-5p | 10 | IGF1R | Sponge network | 0.218 | 0.748 | -0.352 | 0.58959 | 0.306 |
192 | ADAMTS9-AS1 |
hsa-let-7f-1-3p;hsa-miR-15a-5p;hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-205-5p;hsa-miR-27a-3p;hsa-miR-330-5p;hsa-miR-590-3p;hsa-miR-590-5p | 10 | INSR | Sponge network | -8.573 | 0.00012 | -1.824 | 0.00037 | 0.305 |
193 | MIR143HG |
hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-200c-3p;hsa-miR-21-5p;hsa-miR-215-5p;hsa-miR-24-2-5p;hsa-miR-3065-5p;hsa-miR-33b-5p;hsa-miR-429;hsa-miR-629-5p;hsa-miR-7-5p | 13 | BCL2 | Sponge network | -6.51 | 0 | -3.063 | 1.0E-5 | 0.304 |
194 | TPTEP1 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-142-5p;hsa-miR-15a-5p;hsa-miR-15b-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-27a-3p;hsa-miR-330-5p;hsa-miR-590-3p | 10 | INSR | Sponge network | -4.398 | 5.0E-5 | -1.824 | 0.00037 | 0.302 |
195 | GAS6-AS2 | hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-5p;hsa-miR-141-3p;hsa-miR-15b-5p;hsa-miR-182-5p;hsa-miR-183-5p;hsa-miR-191-5p;hsa-miR-200a-3p;hsa-miR-20b-5p;hsa-miR-28-5p;hsa-miR-3065-5p;hsa-miR-324-3p;hsa-miR-429 | 14 | CCND2 | Sponge network | -1.941 | 0.0681 | -2.811 | 0.0014 | 0.301 |
196 | FAM66C |
hsa-miR-17-3p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-1976;hsa-miR-22-5p;hsa-miR-23a-3p;hsa-miR-330-5p;hsa-miR-92a-3p;hsa-miR-940 | 10 | GNG7 | Sponge network | -2.927 | 0.00012 | -4.495 | 0 | 0.301 |
197 | TRHDE-AS1 |
hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-miR-103a-2-5p;hsa-miR-15b-3p;hsa-miR-19b-1-5p;hsa-miR-22-5p;hsa-miR-32-3p;hsa-miR-330-3p;hsa-miR-3614-5p;hsa-miR-582-5p | 10 | PRLR | Sponge network | -6.205 | 0.01165 | -5.28 | 0.00088 | 0.297 |
198 | RP11-389C8.2 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-5p;hsa-miR-141-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-182-5p;hsa-miR-183-5p;hsa-miR-191-5p;hsa-miR-200a-3p;hsa-miR-224-3p;hsa-miR-3065-3p;hsa-miR-3065-5p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-550a-5p;hsa-miR-93-5p | 17 | CCND2 | Sponge network | -3.089 | 2.0E-5 | -2.811 | 0.0014 | 0.293 |
199 | BZRAP1-AS1 | hsa-let-7a-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-17-5p;hsa-miR-193a-3p;hsa-miR-219a-5p;hsa-miR-224-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-339-5p;hsa-miR-33a-5p;hsa-miR-93-5p | 12 | PDGFRA | Sponge network | -1.931 | 0.08861 | -4.316 | 1.0E-5 | 0.292 |
200 | ACTA2-AS1 |
hsa-let-7a-3p;hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-142-3p;hsa-miR-15b-3p;hsa-miR-19b-1-5p;hsa-miR-20a-3p;hsa-miR-22-5p;hsa-miR-33a-3p;hsa-miR-3614-5p;hsa-miR-944 | 13 | PRLR | Sponge network | -6.142 | 0.00223 | -5.28 | 0.00088 | 0.291 |
201 | RP11-554A11.4 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-5p;hsa-miR-15b-5p;hsa-miR-182-5p;hsa-miR-183-5p;hsa-miR-191-5p;hsa-miR-20b-5p;hsa-miR-324-3p;hsa-miR-33a-3p | 10 | CCND2 | Sponge network | -5.361 | 2.0E-5 | -2.811 | 0.0014 | 0.29 |
202 | FAM66C |
hsa-let-7f-1-3p;hsa-miR-15a-5p;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-18a-3p;hsa-miR-20a-5p;hsa-miR-27a-3p;hsa-miR-429;hsa-miR-484;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-7-1-3p | 13 | FGF7 | Sponge network | -2.927 | 0.00012 | -5.509 | 0 | 0.29 |
203 | SOCS2-AS1 |
hsa-let-7g-3p;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-200a-3p;hsa-miR-20b-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-616-5p;hsa-miR-93-5p | 14 | PDGFRA | Sponge network | -4.167 | 1.0E-5 | -4.316 | 1.0E-5 | 0.288 |
204 | LINC00865 |
hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-20a-5p;hsa-miR-30d-3p;hsa-miR-429;hsa-miR-501-5p;hsa-miR-616-5p | 10 | FGF7 | Sponge network | -1.585 | 0.19508 | -5.509 | 0 | 0.287 |
205 | WT1-AS |
hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-miR-103a-2-5p;hsa-miR-15b-3p;hsa-miR-19b-1-5p;hsa-miR-20a-3p;hsa-miR-22-5p;hsa-miR-32-3p;hsa-miR-33a-3p;hsa-miR-421;hsa-miR-9-3p;hsa-miR-9-5p;hsa-miR-944 | 13 | PRLR | Sponge network | -6.875 | 2.0E-5 | -5.28 | 0.00088 | 0.286 |
206 | MIR143HG |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-5p;hsa-miR-141-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-182-5p;hsa-miR-183-5p;hsa-miR-191-5p;hsa-miR-200a-3p;hsa-miR-20b-5p;hsa-miR-224-3p;hsa-miR-3065-3p;hsa-miR-3065-5p;hsa-miR-30d-3p;hsa-miR-324-3p;hsa-miR-33a-3p;hsa-miR-378a-3p;hsa-miR-429;hsa-miR-550a-5p;hsa-miR-93-5p | 21 | CCND2 | Sponge network | -6.51 | 0 | -2.811 | 0.0014 | 0.285 |
207 | TRHDE-AS1 |
hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-miR-193a-3p;hsa-miR-25-3p;hsa-miR-32-3p;hsa-miR-32-5p;hsa-miR-330-5p;hsa-miR-590-3p;hsa-miR-92a-3p;hsa-miR-92b-3p | 10 | COL1A2 | Sponge network | -6.205 | 0.01165 | -2.407 | 0.0132 | 0.282 |
208 | DNM3OS |
hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-miR-103a-2-5p;hsa-miR-142-3p;hsa-miR-15b-3p;hsa-miR-19b-1-5p;hsa-miR-20a-3p;hsa-miR-320b;hsa-miR-330-3p;hsa-miR-33a-3p | 10 | PRLR | Sponge network | -3.933 | 0.00059 | -5.28 | 0.00088 | 0.279 |
209 | MAGI2-AS3 |
hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-200a-5p;hsa-miR-200b-5p;hsa-miR-200c-3p;hsa-miR-21-5p;hsa-miR-24-2-5p;hsa-miR-3065-5p;hsa-miR-33b-5p;hsa-miR-429;hsa-miR-629-5p;hsa-miR-7-5p | 12 | BCL2 | Sponge network | -4.563 | 0 | -3.063 | 1.0E-5 | 0.277 |
210 | LINC00284 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-142-5p;hsa-miR-15b-3p;hsa-miR-16-5p;hsa-miR-205-5p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-330-5p;hsa-miR-590-3p | 10 | INSR | Sponge network | -5.478 | 0.02716 | -1.824 | 0.00037 | 0.276 |
211 | HAND2-AS1 |
hsa-let-7d-5p;hsa-miR-16-2-3p;hsa-miR-18a-3p;hsa-miR-1976;hsa-miR-24-3p;hsa-miR-25-3p;hsa-miR-330-3p;hsa-miR-33a-3p;hsa-miR-92a-3p;hsa-miR-944 | 10 | CREB3L2 | Sponge network | -7.871 | 0 | -2.05 | 0.00075 | 0.274 |
212 | RP11-774O3.3 |
hsa-let-7f-1-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-193a-3p;hsa-miR-2110;hsa-miR-219a-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-330-5p;hsa-miR-335-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-421;hsa-miR-7-1-3p | 16 | PDGFRA | Sponge network | -1.989 | 0.00136 | -4.316 | 1.0E-5 | 0.269 |
213 | ACTA2-AS1 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-130b-3p;hsa-miR-193a-3p;hsa-miR-193b-3p;hsa-miR-205-5p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-590-3p;hsa-miR-671-5p | 10 | KIT | Sponge network | -6.142 | 0.00223 | -2.927 | 0.01211 | 0.267 |
214 | MIR143HG |
hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-miR-103a-2-5p;hsa-miR-142-3p;hsa-miR-15b-3p;hsa-miR-19b-1-5p;hsa-miR-20a-3p;hsa-miR-330-3p;hsa-miR-33a-3p;hsa-miR-3614-5p | 10 | PRLR | Sponge network | -6.51 | 0 | -5.28 | 0.00088 | 0.267 |
215 | RP11-819C21.1 | hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-106b-5p;hsa-miR-16-1-3p;hsa-miR-219a-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-550a-5p;hsa-miR-590-3p;hsa-miR-93-5p | 12 | PDGFRA | Sponge network | -1.571 | 0.00379 | -4.316 | 1.0E-5 | 0.264 |
216 | CTD-2554C21.2 |
hsa-miR-130a-5p;hsa-miR-141-3p;hsa-miR-17-3p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-1976;hsa-miR-22-5p;hsa-miR-224-5p;hsa-miR-23a-3p | 10 | GNG7 | Sponge network | -6.968 | 0.00817 | -4.495 | 0 | 0.26 |
217 | PCED1B-AS1 | hsa-miR-130b-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-219a-5p;hsa-miR-24-3p;hsa-miR-335-3p;hsa-miR-429;hsa-miR-93-5p;hsa-miR-96-5p | 10 | PDGFRA | Sponge network | 0.764 | 0.37397 | -4.316 | 1.0E-5 | 0.26 |
218 | SOCS2-AS1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-5p;hsa-miR-141-3p;hsa-miR-15b-5p;hsa-miR-182-5p;hsa-miR-183-5p;hsa-miR-200a-3p;hsa-miR-20b-5p;hsa-miR-324-3p;hsa-miR-33a-3p;hsa-miR-93-5p | 12 | CCND2 | Sponge network | -4.167 | 1.0E-5 | -2.811 | 0.0014 | 0.258 |
219 | RP11-597D13.9 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-5p;hsa-miR-141-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-182-5p;hsa-miR-183-5p;hsa-miR-200a-3p;hsa-miR-20b-5p;hsa-miR-30d-3p;hsa-miR-429;hsa-miR-93-5p;hsa-miR-96-5p | 14 | CCND2 | Sponge network | -2.494 | 0.07597 | -2.811 | 0.0014 | 0.252 |
220 | LINC00672 |
hsa-let-7a-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-24-3p;hsa-miR-27a-3p;hsa-miR-339-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-550a-5p;hsa-miR-590-3p;hsa-miR-93-5p | 15 | PDGFRA | Sponge network | -2.547 | 4.0E-5 | -4.316 | 1.0E-5 | 0.252 |
221 | RP11-597D13.9 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-32-3p;hsa-miR-93-5p;hsa-miR-96-5p | 10 | THBS2 | Sponge network | -2.494 | 0.07597 | -2.628 | 0.00636 | 0.252 |
222 | RP11-150O12.3 |
hsa-miR-1271-5p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-22-5p;hsa-miR-224-5p;hsa-miR-23a-3p;hsa-miR-330-5p;hsa-miR-3615;hsa-miR-92a-3p | 10 | GNG7 | Sponge network | -4.03 | 0.14448 | -4.495 | 0 | 0.251 |
223 | LINC00839 | hsa-let-7g-3p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-196a-5p;hsa-miR-20b-5p;hsa-miR-301a-3p;hsa-miR-330-5p;hsa-miR-550a-5p;hsa-miR-93-5p | 13 | PDGFRA | Sponge network | -2.505 | 0.08591 | -4.316 | 1.0E-5 | 0.251 |
224 | RP11-774O3.3 |
hsa-miR-17-3p;hsa-miR-185-3p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-1976;hsa-miR-22-5p;hsa-miR-23a-3p;hsa-miR-31-5p;hsa-miR-330-5p | 10 | GNG7 | Sponge network | -1.989 | 0.00136 | -4.495 | 0 | 0.25 |
225 | DNM3OS |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-5p;hsa-miR-141-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-182-5p;hsa-miR-183-5p;hsa-miR-191-5p;hsa-miR-200a-3p;hsa-miR-3065-3p;hsa-miR-3065-5p;hsa-miR-30d-3p;hsa-miR-33a-3p;hsa-miR-378a-3p;hsa-miR-429;hsa-miR-550a-5p;hsa-miR-93-5p;hsa-miR-96-5p | 19 | CCND2 | Sponge network | -3.933 | 0.00059 | -2.811 | 0.0014 | 0.25 |
226 | NR2F1-AS1 |
hsa-miR-130a-5p;hsa-miR-141-3p;hsa-miR-18a-3p;hsa-miR-18a-5p;hsa-miR-193b-5p;hsa-miR-1976;hsa-miR-22-5p;hsa-miR-224-5p;hsa-miR-31-5p;hsa-miR-330-5p;hsa-miR-3615 | 11 | GNG7 | Sponge network | -2.961 | 0.00154 | -4.495 | 0 | 0.25 |