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-let-7c-5p | ACTB | -2.08 | 0 | 0.19 | 0.03017 | miRNAWalker2 validate | -0.11 | 0 | NA | |
2 | hsa-miR-378a-3p | ACTB | -1.5 | 0 | 0.19 | 0.03017 | miRNAWalker2 validate | -0.13 | 0 | NA | |
3 | hsa-miR-107 | ACTG1 | -0.04 | 0.67162 | -0.14 | 0.09417 | miRanda; miRNATAP | -0.14 | 5.0E-5 | NA | |
4 | hsa-miR-652-3p | ACTG1 | 0.36 | 0.00317 | -0.14 | 0.09417 | miRNAWalker2 validate | -0.1 | 0.00079 | NA | |
5 | hsa-let-7a-3p | AMOT | 0.1 | 0.42376 | -3.27 | 0 | mirMAP | -0.64 | 0 | NA | |
6 | hsa-let-7f-1-3p | AMOT | 0.7 | 0 | -3.27 | 0 | mirMAP | -0.48 | 6.0E-5 | NA | |
7 | hsa-miR-16-1-3p | AMOT | 0.96 | 0 | -3.27 | 0 | mirMAP | -0.57 | 0 | NA | |
8 | hsa-miR-203a-3p | AMOT | 0.04 | 0.88046 | -3.27 | 0 | MirTarget | -0.35 | 0 | NA | |
9 | hsa-miR-205-5p | AMOT | 1.51 | 0 | -3.27 | 0 | MirTarget; miRNATAP | -0.77 | 0 | 26239614 | MicroRNA 205 inhibits the proliferation and invasion of breast cancer by regulating AMOT expression; In the present study miR-205 was significantly downregulated in breast cancer samples and it was identified to directly target the 3'-untranslated region 3'-UTR of AMOT in breast cancer MCF-7 cells by luciferase assay; miR-205 and small interfering RNA siRNA-mediated AMOT-knockdown experiments revealed that miR-205 significantly inhibited the proliferation and the invasion of MCF-7 cells through a decrease in the expression of AMOT yet had no effect on apoptosis; Furthermore we observed that the overexpression of AMOT partially reversed the inhibitory effect of miR-205 on the growth and the invasion of MCF-7 cells; The data indicated that miR-205 regulated the proliferation and the invasion of breast cancer cells through suppression of AMOT expression at least partly; Therefore the disordered decreased expression of miR-205 and the resulting AMOT upregulation contributes to breast carcinogenesis and miR-205-AMOT represents a new potential therapeutic target for the treatment of breast carcinoma |
10 | hsa-miR-21-3p | AMOT | 1.25 | 0 | -3.27 | 0 | mirMAP | -1 | 0 | NA | |
11 | hsa-miR-221-3p | AMOT | 0.41 | 0.00074 | -3.27 | 0 | miRNAWalker2 validate | -0.74 | 0 | NA | |
12 | hsa-miR-2355-3p | AMOT | 1.58 | 0 | -3.27 | 0 | MirTarget; miRNATAP | -0.86 | 0 | NA | |
13 | hsa-miR-330-5p | AMOT | 0.94 | 0 | -3.27 | 0 | miRanda | -0.55 | 0 | NA | |
14 | hsa-miR-342-3p | AMOT | 1 | 0 | -3.27 | 0 | miRanda | -0.27 | 0.00462 | NA | |
15 | hsa-miR-450b-5p | AMOT | 1.26 | 0 | -3.27 | 0 | mirMAP | -0.39 | 7.0E-5 | NA | |
16 | hsa-miR-576-5p | AMOT | 0.94 | 0 | -3.27 | 0 | mirMAP | -0.89 | 0 | NA | |
17 | hsa-miR-627-5p | AMOT | 0.35 | 0.04712 | -3.27 | 0 | MirTarget | -0.24 | 0.00922 | NA | |
18 | hsa-miR-629-3p | AMOT | 1.43 | 0 | -3.27 | 0 | MirTarget | -0.49 | 0 | NA | |
19 | hsa-miR-7-1-3p | AMOT | 1.14 | 0 | -3.27 | 0 | MirTarget; mirMAP | -0.51 | 0 | NA | |
20 | hsa-miR-766-3p | AMOT | 1.07 | 0 | -3.27 | 0 | MirTarget | -0.35 | 0.00315 | NA | |
21 | hsa-miR-944 | AMOT | 1.47 | 0 | -3.27 | 0 | mirMAP; miRNATAP | -0.57 | 0 | NA | |
22 | hsa-let-7a-3p | APC | 0.1 | 0.42376 | -0.55 | 0 | mirMAP | -0.18 | 2.0E-5 | NA | |
23 | hsa-miR-125a-5p | APC | 0.22 | 0.11955 | -0.55 | 0 | miRanda | -0.24 | 0 | NA | |
24 | hsa-miR-135b-5p | APC | 1.56 | 0 | -0.55 | 0 | miRTarBase; MirTarget | -0.1 | 1.0E-5 | 24735923; 18632633; 23328512 | We show that miR-135b overexpression is triggered in mice and humans by APC loss PTEN/PI3K pathway deregulation and SRC overexpression and promotes tumor transformation and progression;Regulation of the adenomatous polyposis coli gene by the miR 135 family in colorectal cancer;Real-time quantitative PCR and Western blot were used to explore the relationship between miR-135b and adenomatous polyposis coli APC; MiR-135b promoted gastric cancer cell proliferation inhibited its apoptosis and directly regulated the expression of APC in gastric cancer cell |
25 | hsa-miR-182-5p | APC | 1.15 | 0 | -0.55 | 0 | MirTarget | -0.11 | 0.00011 | NA | |
26 | hsa-miR-186-5p | APC | 0.35 | 0.00015 | -0.55 | 0 | miRNAWalker2 validate | -0.29 | 0 | NA | |
27 | hsa-miR-193a-3p | APC | 0.22 | 0.11183 | -0.55 | 0 | miRanda | -0.16 | 2.0E-5 | NA | |
28 | hsa-miR-21-5p | APC | 1.62 | 0 | -0.55 | 0 | miRNAWalker2 validate | -0.28 | 0 | 23773491; 24832083 | The prognostic significance of APC gene mutation and miR 21 expression in advanced stage colorectal cancer; The aim of this study was to analyse the association of APC gene mutation and miR-21 expression with clinical outcome in CRC patients; APC gene mutation and expression of APC and miR-21 were analysed by direct DNA sequencing and real-time reverse transcription polymerase chain reaction; APC gene expression was low in CRC and negatively correlated with miR-21 expression and gene mutation; In Taiwan downregulation of the APC gene in CRC correlated with gene mutation and miR-21 upregulation; APC mutation and miR-21 expression could be used to predict the clinical outcome of CRC especially in patients with advanced disease;MicroRNA 21 promotes tumour malignancy via increased nuclear translocation of β catenin and predicts poor outcome in APC mutated but not in APC wild type colorectal cancer; However in our preliminary data the prognostic value of miR-21 levels was observed only in adenomatous polyposis coli APC-mutated tumours not in APC-wild-type tumours; We enrolled 165 colorectal tumour to determine APC mutation miR-21 levels and nuclear β-catenin expression by direct sequencing real-time PCR and immunohistochemistry |
29 | hsa-miR-320a | APC | 0.8 | 0 | -0.55 | 0 | miRanda | -0.17 | 1.0E-5 | NA | |
30 | hsa-miR-338-3p | APC | -0.95 | 0 | -0.55 | 0 | miRanda | -0.16 | 0 | NA | |
31 | hsa-miR-374b-5p | APC | -0.29 | 0.00415 | -0.55 | 0 | mirMAP | -0.26 | 0 | NA | |
32 | hsa-miR-450b-5p | APC | 1.26 | 0 | -0.55 | 0 | miRNATAP | -0.18 | 0 | NA | |
33 | hsa-miR-501-3p | APC | 0.82 | 0 | -0.55 | 0 | TargetScan | -0.24 | 0 | NA | |
34 | hsa-miR-589-3p | APC | 1.6 | 0 | -0.55 | 0 | MirTarget | -0.15 | 0 | NA | |
35 | hsa-miR-655-3p | APC | -1.15 | 0 | -0.55 | 0 | MirTarget | -0.11 | 1.0E-5 | NA | |
36 | hsa-let-7a-5p | APC2 | -0.44 | 3.0E-5 | 1.4 | 0 | TargetScan | -0.38 | 0.00058 | NA | |
37 | hsa-miR-107 | AREG | -0.04 | 0.67162 | 0.42 | 0.22179 | miRanda | -0.61 | 2.0E-5 | NA | |
38 | hsa-miR-129-5p | AREG | -0.25 | 0.43645 | 0.42 | 0.22179 | miRanda | -0.13 | 0.00495 | NA | |
39 | hsa-miR-217 | AREG | -1.35 | 0 | 0.42 | 0.22179 | miRanda | -0.23 | 0.00031 | NA | |
40 | hsa-miR-326 | AREG | -0.43 | 0.0415 | 0.42 | 0.22179 | miRanda | -0.26 | 0.00028 | NA | |
41 | hsa-miR-335-5p | AREG | -1.17 | 0 | 0.42 | 0.22179 | miRNAWalker2 validate | -0.41 | 0 | NA | |
42 | hsa-let-7a-3p | AXIN2 | 0.1 | 0.42376 | -0.65 | 0.00118 | miRNATAP | -0.35 | 0 | NA | |
43 | hsa-miR-103a-3p | AXIN2 | 0.56 | 0 | -0.65 | 0.00118 | miRNAWalker2 validate; MirTarget; miRNATAP | -0.33 | 0.00063 | NA | |
44 | hsa-miR-15a-5p | AXIN2 | 0.78 | 0 | -0.65 | 0.00118 | MirTarget; miRNATAP | -0.57 | 0 | 26252081 | The combination of miR-15a and AXIN2 significantly improved the diagnostic accuracy |
45 | hsa-miR-15b-5p | AXIN2 | 0.85 | 0 | -0.65 | 0.00118 | miRTarBase; MirTarget; miRNATAP | -0.35 | 0 | NA | |
46 | hsa-miR-16-2-3p | AXIN2 | 1.16 | 0 | -0.65 | 0.00118 | mirMAP | -0.49 | 0 | NA | |
47 | hsa-miR-16-5p | AXIN2 | 0.52 | 0 | -0.65 | 0.00118 | miRNAWalker2 validate; miRTarBase; MirTarget; miRNATAP | -0.52 | 0 | NA | |
48 | hsa-miR-205-5p | AXIN2 | 1.51 | 0 | -0.65 | 0.00118 | miRNATAP | -0.4 | 0 | NA | |
49 | hsa-miR-221-3p | AXIN2 | 0.41 | 0.00074 | -0.65 | 0.00118 | miRNATAP | -0.38 | 0 | NA | |
50 | hsa-miR-222-3p | AXIN2 | 1.08 | 0 | -0.65 | 0.00118 | miRNATAP | -0.45 | 0 | NA | |
51 | hsa-miR-26b-3p | AXIN2 | 0.42 | 0.00223 | -0.65 | 0.00118 | MirTarget | -0.2 | 0.00225 | NA | |
52 | hsa-miR-29a-5p | AXIN2 | 0.32 | 0.03704 | -0.65 | 0.00118 | MirTarget | -0.26 | 1.0E-5 | NA | |
53 | hsa-miR-34a-5p | AXIN2 | -0.12 | 0.364 | -0.65 | 0.00118 | miRNAWalker2 validate; miRTarBase | -0.18 | 0.00764 | 23624843 | p53 regulates nuclear GSK 3 levels through miR 34 mediated Axin2 suppression in colorectal cancer cells; Exogenous miR-34a decreases Axin2 UTR-reporter activity through multiple binding sites within the 5' and 3' UTR of Axin2; Further RNA transcripts of miR-34 target were correlated with Axin2 in clinical data set of colorectal cancer patients |
54 | hsa-miR-3614-5p | AXIN2 | 0.96 | 3.0E-5 | -0.65 | 0.00118 | MirTarget; miRNATAP | -0.19 | 0 | NA | |
55 | hsa-miR-429 | AXIN2 | 0.56 | 0.00564 | -0.65 | 0.00118 | miRanda | -0.16 | 0.00016 | NA | |
56 | hsa-miR-582-5p | AXIN2 | -0.04 | 0.82183 | -0.65 | 0.00118 | miRNATAP | -0.27 | 0 | NA | |
57 | hsa-miR-590-3p | AXIN2 | 0.22 | 0.09659 | -0.65 | 0.00118 | MirTarget; PITA; miRanda; miRNATAP | -0.27 | 4.0E-5 | NA | |
58 | hsa-miR-944 | AXIN2 | 1.47 | 0 | -0.65 | 0.00118 | MirTarget; PITA; miRNATAP | -0.18 | 2.0E-5 | NA | |
59 | hsa-miR-139-5p | BBC3 | -1.46 | 0 | 0.91 | 0 | miRNATAP | -0.22 | 0 | NA | |
60 | hsa-miR-144-3p | BBC3 | -1.65 | 0 | 0.91 | 0 | miRNATAP | -0.11 | 0 | NA | |
61 | hsa-miR-24-3p | BBC3 | 0.13 | 0.20389 | 0.91 | 0 | miRNATAP | -0.23 | 0.00021 | NA | |
62 | hsa-let-7b-5p | BIRC5 | -0.25 | 0.02114 | 2.16 | 0 | miRNAWalker2 validate | -0.31 | 1.0E-5 | NA | |
63 | hsa-miR-101-3p | BIRC5 | -1.91 | 0 | 2.16 | 0 | miRNAWalker2 validate | -0.43 | 0 | NA | |
64 | hsa-miR-218-5p | BIRC5 | -1.07 | 0 | 2.16 | 0 | miRTarBase; MirTarget | -0.11 | 0.0072 | 25473903; 25900794; 26442524 | Survivin BIRC5 was subsequently identified as an important cervical cancer target of miR-218 using in silico prediction mRNA profiling and quantitative real-time PCR qRT-PCR;miR-218 binds survivin BIRC5 mRNA 3'-UTR and down-regulated reporter luciferase activity;MiR-218 promoted apoptosis inhibited cell proliferation and caused cell cycle arrest in CRC cells by suppressing BIRC5 expression; In conclusion we demonstrated that high miR-218 expression had a positive prognostic value in 5-FU-based treatments for CRC patients and discovered a novel mechanism mediated by miR-218 to promote apoptosis and to function synergistically with 5-FU to promote chemosensitivity by suppressing BIRC5 and TS in CRC |
65 | hsa-miR-335-5p | BIRC5 | -1.17 | 0 | 2.16 | 0 | miRNAWalker2 validate; MirTarget | -0.13 | 0.00122 | 23232114 | Genetic variation in a miR 335 binding site in BIRC5 alters susceptibility to lung cancer in Chinese Han populations; In support of the postulation that the 3' UTR SNP may directly affect miRNA-binding site reporter gene assays indicated BIRC5 was a direct target of miR-335 and the rs2239680 T>C change resulted in altered regulation of BIRC5 expression; Our findings defined a 3' UTR SNP in human BIRC5 oncogene that may increase individual susceptibility to lung cancer probably by attenuating the interaction between miR-335 and BIRC5 |
66 | hsa-miR-375 | BIRC5 | -4.24 | 0 | 2.16 | 0 | miRanda | -0.13 | 0 | NA | |
67 | hsa-miR-106b-5p | BMP2 | 0.5 | 1.0E-5 | 0.81 | 0.0004 | miRNATAP | -0.34 | 7.0E-5 | NA | |
68 | hsa-miR-335-3p | BMP2 | 0.34 | 0.05424 | 0.81 | 0.0004 | mirMAP | -0.31 | 0 | NA | |
69 | hsa-miR-335-5p | BMP2 | -1.17 | 0 | 0.81 | 0.0004 | miRNAWalker2 validate | -0.36 | 0 | NA | |
70 | hsa-miR-374b-5p | BMP2 | -0.29 | 0.00415 | 0.81 | 0.0004 | miRNATAP | -0.42 | 3.0E-5 | NA | |
71 | hsa-miR-378c | BMP2 | -1.83 | 0 | 0.81 | 0.0004 | miRNATAP | -0.21 | 2.0E-5 | NA | |
72 | hsa-miR-429 | BMP2 | 0.56 | 0.00564 | 0.81 | 0.0004 | miRNATAP | -0.29 | 0 | NA | |
73 | hsa-miR-142-3p | BMP4 | 1.13 | 0 | -1.05 | 0 | PITA; miRanda | -0.16 | 0.00028 | NA | |
74 | hsa-miR-130a-3p | BMP6 | 0.67 | 0 | -0.25 | 0.21347 | MirTarget | -0.3 | 0 | NA | |
75 | hsa-miR-301a-3p | BMP6 | 2.14 | 0 | -0.25 | 0.21347 | MirTarget | -0.19 | 0 | NA | |
76 | hsa-miR-320a | BMP6 | 0.8 | 0 | -0.25 | 0.21347 | PITA; miRanda | -0.22 | 0.0004 | NA | |
77 | hsa-miR-320b | BMP6 | 1.23 | 0 | -0.25 | 0.21347 | PITA; miRanda | -0.19 | 0.00019 | NA | |
78 | hsa-miR-454-3p | BMP6 | 1.54 | 0 | -0.25 | 0.21347 | MirTarget | -0.24 | 0 | NA | |
79 | hsa-miR-590-5p | BMP6 | 0.76 | 0 | -0.25 | 0.21347 | miRanda | -0.23 | 0.0005 | NA | |
80 | hsa-miR-125a-3p | BMP7 | 0.12 | 0.44483 | -0.21 | 0.49209 | miRanda | -0.41 | 0 | NA | |
81 | hsa-miR-338-3p | BMP7 | -0.95 | 0 | -0.21 | 0.49209 | miRanda | -0.21 | 0.00394 | NA | |
82 | hsa-miR-455-5p | BMP7 | 1.41 | 0 | -0.21 | 0.49209 | miRanda | -0.34 | 9.0E-5 | NA | |
83 | hsa-miR-495-3p | BMP7 | -1.48 | 0 | -0.21 | 0.49209 | MirTarget | -0.17 | 0.0081 | NA | |
84 | hsa-miR-542-3p | BMP7 | 0.64 | 0 | -0.21 | 0.49209 | miRanda; miRNATAP | -0.31 | 0.00166 | NA | |
85 | hsa-miR-30a-3p | BMP8A | -2.26 | 0 | 2.59 | 0 | MirTarget | -0.16 | 0.00064 | NA | |
86 | hsa-miR-30b-3p | BMP8A | -0.34 | 0.02234 | 2.59 | 0 | MirTarget | -0.21 | 0.00171 | NA | |
87 | hsa-miR-30d-3p | BMP8A | -0.58 | 0 | 2.59 | 0 | MirTarget | -0.4 | 0 | NA | |
88 | hsa-miR-30e-3p | BMP8A | -0.89 | 0 | 2.59 | 0 | MirTarget | -0.44 | 0 | NA | |
89 | hsa-miR-125a-5p | BMP8B | 0.22 | 0.11955 | 0.91 | 4.0E-5 | miRanda | -0.24 | 0.00074 | NA | |
90 | hsa-miR-17-5p | BMP8B | 1.42 | 0 | 0.91 | 4.0E-5 | MirTarget | -0.16 | 0.00478 | NA | |
91 | hsa-miR-20a-5p | BMP8B | 1.15 | 0 | 0.91 | 4.0E-5 | MirTarget | -0.22 | 0.0001 | NA | |
92 | hsa-miR-2355-5p | BMP8B | 1.47 | 0 | 0.91 | 4.0E-5 | mirMAP | -0.2 | 0.00034 | NA | |
93 | hsa-miR-26b-5p | BMP8B | -0.25 | 0.02852 | 0.91 | 4.0E-5 | miRNAWalker2 validate | -0.33 | 8.0E-5 | NA | |
94 | hsa-miR-362-5p | BMP8B | 0.41 | 0.04043 | 0.91 | 4.0E-5 | mirMAP | -0.25 | 0 | NA | |
95 | hsa-miR-455-5p | BMP8B | 1.41 | 0 | 0.91 | 4.0E-5 | miRanda | -0.3 | 0 | NA | |
96 | hsa-miR-186-5p | BMPR1A | 0.35 | 0.00015 | -0.41 | 4.0E-5 | MirTarget | -0.14 | 0.0031 | NA | |
97 | hsa-miR-320a | BMPR1A | 0.8 | 0 | -0.41 | 4.0E-5 | MirTarget; PITA; miRanda | -0.11 | 0.00035 | NA | |
98 | hsa-miR-101-3p | BMPR1B | -1.91 | 0 | 1.01 | 0.00106 | miRNATAP | -0.44 | 0 | NA | |
99 | hsa-miR-125b-5p | BMPR1B | -0.99 | 0 | 1.01 | 0.00106 | miRNAWalker2 validate; miRTarBase; MirTarget | -0.33 | 0.00036 | 19738052; 21556765 | A risk variant in an miR 125b binding site in BMPR1B is associated with breast cancer pathogenesis; Furthermore luciferase reporter assays and overexpression of miR-125b-mimics combined with quantitative reverse transcription-PCR showed that BMPR1B transcript is a direct target of miR-125b and that miR-125b differentially regulates the C and T alleles of rs1434536; These results suggest that allele-specific regulation of BMPR1B by miR-125b explains the observed disease risk;Our findings show that rs1434536 in the 3'UTR of BMPR1B gene affects the binding ability of miR-125b to BMPR1B mRNA and contributes to the genetic predisposition to localized prostate cancer and patients aged>70 years |
100 | hsa-miR-142-5p | BMPR1B | 0.29 | 0.09 | 1.01 | 0.00106 | mirMAP | -0.22 | 0.00535 | NA | |
101 | hsa-miR-150-5p | BMPR1B | -0.24 | 0.33155 | 1.01 | 0.00106 | MirTarget | -0.21 | 0.00011 | NA | |
102 | hsa-miR-16-2-3p | BMPR1B | 1.16 | 0 | 1.01 | 0.00106 | mirMAP | -0.39 | 1.0E-5 | NA | |
103 | hsa-miR-23b-3p | BMPR1B | -0.5 | 3.0E-5 | 1.01 | 0.00106 | mirMAP | -0.38 | 0.00089 | NA | |
104 | hsa-miR-26a-5p | BMPR1B | -1.09 | 0 | 1.01 | 0.00106 | mirMAP | -0.34 | 0.00395 | NA | |
105 | hsa-miR-374a-5p | BMPR1B | -0.62 | 0 | 1.01 | 0.00106 | MirTarget | -0.52 | 0.00048 | NA | |
106 | hsa-miR-374b-5p | BMPR1B | -0.29 | 0.00415 | 1.01 | 0.00106 | MirTarget | -0.43 | 0.00158 | NA | |
107 | hsa-miR-429 | BMPR1B | 0.56 | 0.00564 | 1.01 | 0.00106 | miRNATAP | -0.28 | 3.0E-5 | NA | |
108 | hsa-miR-629-3p | BMPR1B | 1.43 | 0 | 1.01 | 0.00106 | MirTarget | -0.23 | 0.00537 | NA | |
109 | hsa-let-7a-3p | BMPR2 | 0.1 | 0.42376 | -0.14 | 0.18459 | MirTarget; miRNATAP | -0.21 | 0 | NA | |
110 | hsa-miR-103a-2-5p | BMPR2 | 1.38 | 0 | -0.14 | 0.18459 | MirTarget | -0.17 | 0 | NA | |
111 | hsa-miR-106a-5p | BMPR2 | 0.68 | 0.00222 | -0.14 | 0.18459 | MirTarget; miRNATAP | -0.12 | 0 | NA | |
112 | hsa-miR-106b-5p | BMPR2 | 0.5 | 1.0E-5 | -0.14 | 0.18459 | MirTarget; miRNATAP | -0.16 | 4.0E-5 | NA | |
113 | hsa-miR-125a-5p | BMPR2 | 0.22 | 0.11955 | -0.14 | 0.18459 | PITA | -0.13 | 8.0E-5 | NA | |
114 | hsa-miR-130a-3p | BMPR2 | 0.67 | 0 | -0.14 | 0.18459 | miRNAWalker2 validate; MirTarget; miRNATAP | -0.21 | 0 | NA | |
115 | hsa-miR-16-2-3p | BMPR2 | 1.16 | 0 | -0.14 | 0.18459 | mirMAP | -0.27 | 0 | NA | |
116 | hsa-miR-17-5p | BMPR2 | 1.42 | 0 | -0.14 | 0.18459 | miRNAWalker2 validate; MirTarget; TargetScan; miRNATAP | -0.25 | 0 | NA | |
117 | hsa-miR-182-5p | BMPR2 | 1.15 | 0 | -0.14 | 0.18459 | mirMAP | -0.13 | 0 | NA | |
118 | hsa-miR-186-5p | BMPR2 | 0.35 | 0.00015 | -0.14 | 0.18459 | mirMAP | -0.31 | 0 | NA | |
119 | hsa-miR-19a-3p | BMPR2 | 1.36 | 0 | -0.14 | 0.18459 | miRNAWalker2 validate; MirTarget; miRNATAP | -0.25 | 0 | NA | |
120 | hsa-miR-19b-3p | BMPR2 | 0.54 | 0.00062 | -0.14 | 0.18459 | miRNAWalker2 validate; MirTarget; miRNATAP | -0.32 | 0 | NA | |
121 | hsa-miR-200b-3p | BMPR2 | 0.07 | 0.68286 | -0.14 | 0.18459 | mirMAP | -0.17 | 0 | NA | |
122 | hsa-miR-200c-3p | BMPR2 | 0.63 | 0.00013 | -0.14 | 0.18459 | mirMAP | -0.11 | 8.0E-5 | NA | |
123 | hsa-miR-205-3p | BMPR2 | 1.3 | 0 | -0.14 | 0.18459 | mirMAP | -0.11 | 0 | NA | |
124 | hsa-miR-205-5p | BMPR2 | 1.51 | 0 | -0.14 | 0.18459 | mirMAP | -0.15 | 0 | NA | |
125 | hsa-miR-20a-5p | BMPR2 | 1.15 | 0 | -0.14 | 0.18459 | miRNAWalker2 validate; miRTarBase; MirTarget; miRNATAP | -0.27 | 0 | NA | |
126 | hsa-miR-20b-5p | BMPR2 | 0.35 | 0.23201 | -0.14 | 0.18459 | MirTarget; miRNATAP | -0.1 | 0 | NA | |
127 | hsa-miR-25-3p | BMPR2 | 0.77 | 0 | -0.14 | 0.18459 | miRNATAP | -0.3 | 0 | NA | |
128 | hsa-miR-26a-2-3p | BMPR2 | -0.44 | 0.00326 | -0.14 | 0.18459 | mirMAP | -0.17 | 0 | NA | |
129 | hsa-miR-26b-5p | BMPR2 | -0.25 | 0.02852 | -0.14 | 0.18459 | miRNAWalker2 validate | -0.24 | 0 | NA | |
130 | hsa-miR-28-3p | BMPR2 | 0.46 | 0 | -0.14 | 0.18459 | mirMAP | -0.16 | 0.00155 | NA | |
131 | hsa-miR-29a-5p | BMPR2 | 0.32 | 0.03704 | -0.14 | 0.18459 | mirMAP | -0.18 | 0 | NA | |
132 | hsa-miR-301a-3p | BMPR2 | 2.14 | 0 | -0.14 | 0.18459 | MirTarget; miRNATAP | -0.17 | 0 | NA | |
133 | hsa-miR-30b-5p | BMPR2 | -0.4 | 0.00347 | -0.14 | 0.18459 | mirMAP | -0.28 | 0 | NA | |
134 | hsa-miR-30c-5p | BMPR2 | 0.02 | 0.88637 | -0.14 | 0.18459 | mirMAP | -0.28 | 0 | NA | |
135 | hsa-miR-30e-5p | BMPR2 | -1.02 | 0 | -0.14 | 0.18459 | mirMAP | -0.1 | 0.00475 | NA | |
136 | hsa-miR-32-5p | BMPR2 | -0.32 | 0.01025 | -0.14 | 0.18459 | miRNATAP | -0.17 | 1.0E-5 | NA | |
137 | hsa-miR-320a | BMPR2 | 0.8 | 0 | -0.14 | 0.18459 | mirMAP | -0.2 | 0 | NA | |
138 | hsa-miR-335-3p | BMPR2 | 0.34 | 0.05424 | -0.14 | 0.18459 | mirMAP | -0.11 | 1.0E-5 | NA | |
139 | hsa-miR-33a-5p | BMPR2 | 1.13 | 0 | -0.14 | 0.18459 | mirMAP | -0.13 | 0 | NA | |
140 | hsa-miR-342-3p | BMPR2 | 1 | 0 | -0.14 | 0.18459 | PITA; miRanda; miRNATAP | -0.19 | 0 | NA | |
141 | hsa-miR-3607-3p | BMPR2 | 1.01 | 9.0E-5 | -0.14 | 0.18459 | mirMAP; miRNATAP | -0.12 | 0 | NA | |
142 | hsa-miR-362-3p | BMPR2 | -0.7 | 0 | -0.14 | 0.18459 | MirTarget; PITA; miRanda; miRNATAP | -0.12 | 6.0E-5 | NA | |
143 | hsa-miR-374a-3p | BMPR2 | -0.3 | 0.00683 | -0.14 | 0.18459 | MirTarget; miRNATAP | -0.2 | 0 | NA | |
144 | hsa-miR-374b-5p | BMPR2 | -0.29 | 0.00415 | -0.14 | 0.18459 | mirMAP | -0.24 | 0 | NA | |
145 | hsa-miR-429 | BMPR2 | 0.56 | 0.00564 | -0.14 | 0.18459 | mirMAP; miRNATAP | -0.19 | 0 | NA | |
146 | hsa-miR-454-3p | BMPR2 | 1.54 | 0 | -0.14 | 0.18459 | MirTarget; miRNATAP | -0.25 | 0 | NA | |
147 | hsa-miR-532-5p | BMPR2 | -0.02 | 0.83099 | -0.14 | 0.18459 | PITA | -0.17 | 0.00023 | NA | |
148 | hsa-miR-582-3p | BMPR2 | -0.25 | 0.1438 | -0.14 | 0.18459 | PITA; miRNATAP | -0.17 | 0 | NA | |
149 | hsa-miR-582-5p | BMPR2 | -0.04 | 0.82183 | -0.14 | 0.18459 | mirMAP | -0.21 | 0 | NA | |
150 | hsa-miR-590-3p | BMPR2 | 0.22 | 0.09659 | -0.14 | 0.18459 | MirTarget; miRanda; mirMAP; miRNATAP | -0.2 | 0 | NA |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | REGULATION OF MULTICELLULAR ORGANISMAL DEVELOPMENT | 69 | 1672 | 9.111e-44 | 4.239e-40 |
2 | TISSUE DEVELOPMENT | 66 | 1518 | 7.33e-43 | 1.705e-39 |
3 | EPITHELIUM DEVELOPMENT | 55 | 945 | 2.956e-41 | 3.438e-38 |
4 | ORGAN MORPHOGENESIS | 53 | 841 | 2.336e-41 | 3.438e-38 |
5 | REGULATION OF PROTEIN MODIFICATION PROCESS | 66 | 1710 | 1.311e-39 | 1.22e-36 |
6 | CANONICAL WNT SIGNALING PATHWAY | 27 | 95 | 7.446e-39 | 5.708e-36 |
7 | REGULATION OF PHOSPHORUS METABOLIC PROCESS | 64 | 1618 | 8.587e-39 | 5.708e-36 |
8 | POSITIVE REGULATION OF RESPONSE TO STIMULUS | 68 | 1929 | 1.441e-38 | 8.383e-36 |
9 | WNT SIGNALING PATHWAY | 38 | 351 | 9.056e-38 | 4.682e-35 |
10 | TISSUE MORPHOGENESIS | 43 | 533 | 1.867e-37 | 8.688e-35 |
11 | REGULATION OF CELL DIFFERENTIATION | 60 | 1492 | 2.589e-36 | 1.095e-33 |
12 | REGULATION OF ANATOMICAL STRUCTURE MORPHOGENESIS | 52 | 1021 | 7.904e-36 | 3.065e-33 |
13 | POSITIVE REGULATION OF DEVELOPMENTAL PROCESS | 54 | 1142 | 1.021e-35 | 3.655e-33 |
14 | POSITIVE REGULATION OF CELL COMMUNICATION | 60 | 1532 | 1.156e-35 | 3.841e-33 |
15 | NEUROGENESIS | 58 | 1402 | 1.445e-35 | 4.483e-33 |
16 | RESPONSE TO GROWTH FACTOR | 40 | 475 | 1.931e-35 | 5.614e-33 |
17 | REGULATION OF WNT SIGNALING PATHWAY | 35 | 310 | 2.409e-35 | 6.593e-33 |
18 | REGULATION OF CANONICAL WNT SIGNALING PATHWAY | 32 | 236 | 7.053e-35 | 1.823e-32 |
19 | POSITIVE REGULATION OF PROTEIN METABOLIC PROCESS | 57 | 1492 | 5.287e-33 | 1.295e-30 |
20 | TUBE DEVELOPMENT | 40 | 552 | 7.41e-33 | 1.724e-30 |
21 | EMBRYONIC MORPHOGENESIS | 39 | 539 | 5.703e-32 | 1.264e-29 |
22 | POSITIVE REGULATION OF CELL DIFFERENTIATION | 45 | 823 | 6.989e-32 | 1.478e-29 |
23 | POSITIVE REGULATION OF GENE EXPRESSION | 59 | 1733 | 1.286e-31 | 2.602e-29 |
24 | NEGATIVE REGULATION OF DEVELOPMENTAL PROCESS | 44 | 801 | 3.335e-31 | 6.466e-29 |
25 | REGULATION OF CELL DEATH | 55 | 1472 | 3.599e-31 | 6.698e-29 |
26 | CELLULAR RESPONSE TO ORGANIC SUBSTANCE | 60 | 1848 | 4.077e-31 | 7.296e-29 |
27 | CELL FATE COMMITMENT | 29 | 227 | 8.43e-31 | 1.453e-28 |
28 | REGULATION OF CELLULAR PROTEIN LOCALIZATION | 38 | 552 | 2.614e-30 | 4.243e-28 |
29 | NEGATIVE REGULATION OF CELL COMMUNICATION | 50 | 1192 | 2.644e-30 | 4.243e-28 |
30 | POSITIVE REGULATION OF PROTEIN MODIFICATION PROCESS | 49 | 1135 | 3.33e-30 | 5.164e-28 |
31 | MORPHOGENESIS OF AN EPITHELIUM | 34 | 400 | 4.406e-30 | 6.614e-28 |
32 | REGULATION OF CARTILAGE DEVELOPMENT | 20 | 63 | 5.276e-30 | 7.671e-28 |
33 | CELL DEVELOPMENT | 53 | 1426 | 9.249e-30 | 1.304e-27 |
34 | CELLULAR RESPONSE TO ENDOGENOUS STIMULUS | 46 | 1008 | 3.25e-29 | 4.447e-27 |
35 | POSITIVE REGULATION OF PHOSPHATE METABOLIC PROCESS | 46 | 1036 | 1.063e-28 | 1.374e-26 |
36 | POSITIVE REGULATION OF PHOSPHORUS METABOLIC PROCESS | 46 | 1036 | 1.063e-28 | 1.374e-26 |
37 | REGULATION OF ORGAN MORPHOGENESIS | 28 | 242 | 1.691e-28 | 2.126e-26 |
38 | TRANSMEMBRANE RECEPTOR PROTEIN SERINE THREONINE KINASE SIGNALING PATHWAY | 26 | 190 | 2.004e-28 | 2.454e-26 |
39 | REGULATION OF CELL DEVELOPMENT | 42 | 836 | 3.903e-28 | 4.656e-26 |
40 | EMBRYO DEVELOPMENT | 43 | 894 | 4.407e-28 | 5.127e-26 |
41 | REGULATION OF CELL PROLIFERATION | 52 | 1496 | 9.938e-28 | 1.128e-25 |
42 | NEGATIVE REGULATION OF RESPONSE TO STIMULUS | 50 | 1360 | 1.21e-27 | 1.34e-25 |
43 | NEURON DIFFERENTIATION | 42 | 874 | 2.282e-27 | 2.469e-25 |
44 | SENSORY ORGAN DEVELOPMENT | 34 | 493 | 4.823e-27 | 5.101e-25 |
45 | CARDIOVASCULAR SYSTEM DEVELOPMENT | 40 | 788 | 6.944e-27 | 7.024e-25 |
46 | CIRCULATORY SYSTEM DEVELOPMENT | 40 | 788 | 6.944e-27 | 7.024e-25 |
47 | POSITIVE REGULATION OF BIOSYNTHETIC PROCESS | 55 | 1805 | 1.056e-26 | 1.046e-24 |
48 | CARTILAGE DEVELOPMENT | 23 | 147 | 1.376e-26 | 1.334e-24 |
49 | NEGATIVE REGULATION OF WNT SIGNALING PATHWAY | 25 | 197 | 1.707e-26 | 1.621e-24 |
50 | RESPONSE TO ENDOGENOUS STIMULUS | 50 | 1450 | 2.286e-26 | 2.127e-24 |
51 | POSITIVE REGULATION OF MULTICELLULAR ORGANISMAL PROCESS | 49 | 1395 | 3.899e-26 | 3.557e-24 |
52 | REGULATION OF STEM CELL DIFFERENTIATION | 21 | 113 | 5.37e-26 | 4.805e-24 |
53 | REGULATION OF PROTEIN LOCALIZATION | 42 | 950 | 6.114e-26 | 5.368e-24 |
54 | GROWTH | 31 | 410 | 7.925e-26 | 6.828e-24 |
55 | ANATOMICAL STRUCTURE FORMATION INVOLVED IN MORPHOGENESIS | 42 | 957 | 8.154e-26 | 6.898e-24 |
56 | NEGATIVE REGULATION OF CANONICAL WNT SIGNALING PATHWAY | 23 | 162 | 1.433e-25 | 1.191e-23 |
57 | NEGATIVE REGULATION OF MULTICELLULAR ORGANISMAL PROCESS | 42 | 983 | 2.328e-25 | 1.9e-23 |
58 | CONNECTIVE TISSUE DEVELOPMENT | 24 | 194 | 3.55e-25 | 2.848e-23 |
59 | TUBE MORPHOGENESIS | 28 | 323 | 5.836e-25 | 4.602e-23 |
60 | POSITIVE REGULATION OF CELLULAR COMPONENT ORGANIZATION | 44 | 1152 | 1.12e-24 | 8.688e-23 |
61 | REGULATION OF OSSIFICATION | 23 | 178 | 1.355e-24 | 1.034e-22 |
62 | SKELETAL SYSTEM DEVELOPMENT | 31 | 455 | 1.854e-24 | 1.391e-22 |
63 | POSITIVE REGULATION OF STEM CELL DIFFERENTIATION | 16 | 50 | 3.126e-24 | 2.309e-22 |
64 | POSITIVE REGULATION OF CELL DEATH | 34 | 605 | 3.96e-24 | 2.879e-22 |
65 | NEGATIVE REGULATION OF CELL DIFFERENTIATION | 34 | 609 | 4.903e-24 | 3.51e-22 |
66 | POSITIVE REGULATION OF CELL DEVELOPMENT | 31 | 472 | 5.582e-24 | 3.935e-22 |
67 | REGULATION OF EPITHELIAL TO MESENCHYMAL TRANSITION | 17 | 67 | 1.013e-23 | 7.035e-22 |
68 | RESPONSE TO TRANSFORMING GROWTH FACTOR BETA | 21 | 144 | 1.184e-23 | 8.1e-22 |
69 | EMBRYONIC ORGAN DEVELOPMENT | 29 | 406 | 1.884e-23 | 1.271e-21 |
70 | POSITIVE REGULATION OF EPITHELIAL TO MESENCHYMAL TRANSITION | 14 | 34 | 3.522e-23 | 2.341e-21 |
71 | REGULATION OF TRANSMEMBRANE RECEPTOR PROTEIN SERINE THREONINE KINASE SIGNALING PATHWAY | 23 | 207 | 4.739e-23 | 3.106e-21 |
72 | REGULATION OF MAPK CASCADE | 34 | 660 | 6.559e-23 | 4.238e-21 |
73 | CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 31 | 513 | 6.714e-23 | 4.28e-21 |
74 | REGULATION OF CELLULAR LOCALIZATION | 44 | 1277 | 6.997e-23 | 4.4e-21 |
75 | REGULATION OF OSTEOBLAST DIFFERENTIATION | 19 | 112 | 8.731e-23 | 5.417e-21 |
76 | REGULATION OF PATHWAY RESTRICTED SMAD PROTEIN PHOSPHORYLATION | 16 | 60 | 9.052e-23 | 5.542e-21 |
77 | POSITIVE REGULATION OF PATHWAY RESTRICTED SMAD PROTEIN PHOSPHORYLATION | 15 | 48 | 1.352e-22 | 8.171e-21 |
78 | MESENCHYME DEVELOPMENT | 22 | 190 | 1.787e-22 | 1.052e-20 |
79 | STEM CELL DIFFERENTIATION | 22 | 190 | 1.787e-22 | 1.052e-20 |
80 | EMBRYO DEVELOPMENT ENDING IN BIRTH OR EGG HATCHING | 31 | 554 | 6.538e-22 | 3.803e-20 |
81 | CELL PROLIFERATION | 33 | 672 | 1.413e-21 | 8.118e-20 |
82 | SMAD PROTEIN SIGNAL TRANSDUCTION | 15 | 56 | 1.934e-21 | 1.084e-19 |
83 | EPITHELIAL TO MESENCHYMAL TRANSITION | 15 | 56 | 1.934e-21 | 1.084e-19 |
84 | GLAND DEVELOPMENT | 27 | 395 | 2.435e-21 | 1.349e-19 |
85 | CELL JUNCTION ORGANIZATION | 21 | 185 | 2.683e-21 | 1.469e-19 |
86 | MESENCHYMAL CELL DIFFERENTIATION | 19 | 134 | 3.14e-21 | 1.699e-19 |
87 | REGULATION OF EPITHELIAL CELL PROLIFERATION | 24 | 285 | 3.895e-21 | 2.083e-19 |
88 | NEGATIVE REGULATION OF CELL PROLIFERATION | 32 | 643 | 4.367e-21 | 2.309e-19 |
89 | EYE DEVELOPMENT | 25 | 326 | 5.342e-21 | 2.793e-19 |
90 | ESTABLISHMENT OR MAINTENANCE OF CELL POLARITY | 19 | 141 | 8.57e-21 | 4.431e-19 |
91 | UROGENITAL SYSTEM DEVELOPMENT | 24 | 299 | 1.212e-20 | 6.195e-19 |
92 | CELLULAR COMPONENT MORPHOGENESIS | 36 | 900 | 1.292e-20 | 6.536e-19 |
93 | HIPPO SIGNALING | 12 | 27 | 1.617e-20 | 8.089e-19 |
94 | POSITIVE REGULATION OF TRANSMEMBRANE RECEPTOR PROTEIN SERINE THREONINE KINASE SIGNALING PATHWAY | 17 | 100 | 1.706e-20 | 8.443e-19 |
95 | POSITIVE REGULATION OF OSSIFICATION | 16 | 84 | 3.442e-20 | 1.686e-18 |
96 | GASTRULATION | 19 | 155 | 5.461e-20 | 2.647e-18 |
97 | BRANCHING MORPHOGENESIS OF AN EPITHELIAL TUBE | 18 | 131 | 6.681e-20 | 3.205e-18 |
98 | HEAD DEVELOPMENT | 32 | 709 | 8.07e-20 | 3.832e-18 |
99 | REGULATION OF CELL MORPHOGENESIS | 29 | 552 | 9.653e-20 | 4.537e-18 |
100 | HEART DEVELOPMENT | 27 | 466 | 1.77e-19 | 8.237e-18 |
101 | REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 24 | 337 | 2.006e-19 | 9.241e-18 |
102 | REGULATION OF INTRACELLULAR TRANSPORT | 30 | 621 | 2.136e-19 | 9.742e-18 |
103 | NON CANONICAL WNT SIGNALING PATHWAY | 18 | 140 | 2.298e-19 | 1.037e-17 |
104 | MORPHOGENESIS OF A BRANCHING STRUCTURE | 19 | 167 | 2.318e-19 | 1.037e-17 |
105 | RESPIRATORY SYSTEM DEVELOPMENT | 20 | 197 | 2.446e-19 | 1.084e-17 |
106 | TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 16 | 95 | 2.82e-19 | 1.238e-17 |
107 | ENZYME LINKED RECEPTOR PROTEIN SIGNALING PATHWAY | 31 | 689 | 3.722e-19 | 1.618e-17 |
108 | REGULATION OF CHONDROCYTE DIFFERENTIATION | 13 | 46 | 4.597e-19 | 1.981e-17 |
109 | EMBRYONIC ORGAN MORPHOGENESIS | 22 | 279 | 8.379e-19 | 3.544e-17 |
110 | EPITHELIAL CELL DIFFERENTIATION | 27 | 495 | 8.305e-19 | 3.544e-17 |
111 | POSITIVE REGULATION OF CELLULAR PROTEIN LOCALIZATION | 24 | 360 | 9.299e-19 | 3.898e-17 |
112 | REGULATION OF APOPTOTIC SIGNALING PATHWAY | 24 | 363 | 1.127e-18 | 4.681e-17 |
113 | OSSIFICATION | 21 | 251 | 1.643e-18 | 6.764e-17 |
114 | REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 44 | 1656 | 1.761e-18 | 7.187e-17 |
115 | PATTERN SPECIFICATION PROCESS | 25 | 418 | 2.172e-18 | 8.789e-17 |
116 | DEVELOPMENTAL GROWTH | 23 | 333 | 2.43e-18 | 9.749e-17 |
117 | REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 31 | 750 | 4.186e-18 | 1.665e-16 |
118 | MESONEPHROS DEVELOPMENT | 15 | 90 | 4.62e-18 | 1.806e-16 |
119 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 45 | 1784 | 4.596e-18 | 1.806e-16 |
120 | POSITIVE REGULATION OF CELL PROLIFERATION | 32 | 814 | 4.669e-18 | 1.811e-16 |
121 | REGULATION OF TRANSFERASE ACTIVITY | 34 | 946 | 5.256e-18 | 2.021e-16 |
122 | REGULATION OF EMBRYONIC DEVELOPMENT | 16 | 114 | 6.013e-18 | 2.293e-16 |
123 | POSITIVE REGULATION OF APOPTOTIC SIGNALING PATHWAY | 18 | 171 | 8.992e-18 | 3.402e-16 |
124 | RESPONSE TO BMP | 15 | 94 | 9.196e-18 | 3.423e-16 |
125 | CELLULAR RESPONSE TO BMP STIMULUS | 15 | 94 | 9.196e-18 | 3.423e-16 |
126 | REGULATION OF KINASE ACTIVITY | 31 | 776 | 1.098e-17 | 4.054e-16 |
127 | CHONDROCYTE DIFFERENTIATION | 13 | 60 | 2.179e-17 | 7.985e-16 |
128 | HEART MORPHOGENESIS | 19 | 212 | 2.199e-17 | 7.995e-16 |
129 | POSITIVE REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION | 26 | 514 | 2.538e-17 | 9.155e-16 |
130 | KIDNEY EPITHELIUM DEVELOPMENT | 16 | 125 | 2.755e-17 | 9.862e-16 |
131 | REGULATION OF PROTEIN IMPORT | 18 | 183 | 3.065e-17 | 1.089e-15 |
132 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 34 | 1004 | 3.212e-17 | 1.132e-15 |
133 | NEGATIVE REGULATION OF CELL DEATH | 32 | 872 | 3.424e-17 | 1.198e-15 |
134 | REGULATION OF PROTEIN LOCALIZATION TO NUCLEUS | 19 | 218 | 3.719e-17 | 1.291e-15 |
135 | REGULATION OF NUCLEOCYTOPLASMIC TRANSPORT | 19 | 220 | 4.415e-17 | 1.522e-15 |
136 | NEGATIVE REGULATION OF PROTEIN METABOLIC PROCESS | 35 | 1087 | 4.668e-17 | 1.591e-15 |
137 | CELLULAR MACROMOLECULE LOCALIZATION | 37 | 1234 | 4.684e-17 | 1.591e-15 |
138 | POSITIVE REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 17 | 162 | 8.181e-17 | 2.758e-15 |
139 | NEGATIVE REGULATION OF GENE EXPRESSION | 40 | 1493 | 8.296e-17 | 2.777e-15 |
140 | LENS DEVELOPMENT IN CAMERA TYPE EYE | 13 | 66 | 8.376e-17 | 2.784e-15 |
141 | FORMATION OF PRIMARY GERM LAYER | 15 | 110 | 1.076e-16 | 3.552e-15 |
142 | NEGATIVE REGULATION OF NITROGEN COMPOUND METABOLIC PROCESS | 40 | 1517 | 1.435e-16 | 4.702e-15 |
143 | SKELETAL SYSTEM MORPHOGENESIS | 18 | 201 | 1.649e-16 | 5.365e-15 |
144 | POSITIVE REGULATION OF BIOMINERAL TISSUE DEVELOPMENT | 11 | 38 | 1.97e-16 | 6.323e-15 |
145 | MESENCHYME MORPHOGENESIS | 11 | 38 | 1.97e-16 | 6.323e-15 |
146 | MAMMARY GLAND DEVELOPMENT | 15 | 117 | 2.794e-16 | 8.905e-15 |
147 | MESODERM DEVELOPMENT | 15 | 118 | 3.185e-16 | 1.008e-14 |
148 | CELL CYCLE | 37 | 1316 | 3.715e-16 | 1.168e-14 |
149 | POSITIVE REGULATION OF MAPK CASCADE | 24 | 470 | 4.063e-16 | 1.26e-14 |
150 | REGULATION OF PROTEIN SERINE THREONINE KINASE ACTIVITY | 24 | 470 | 4.063e-16 | 1.26e-14 |
151 | RESPONSE TO LIPID | 31 | 888 | 4.743e-16 | 1.462e-14 |
152 | POSITIVE REGULATION OF CARTILAGE DEVELOPMENT | 10 | 29 | 6.314e-16 | 1.933e-14 |
153 | POSITIVE REGULATION OF EPITHELIAL CELL PROLIFERATION | 16 | 154 | 8.204e-16 | 2.495e-14 |
154 | CELL JUNCTION ASSEMBLY | 15 | 129 | 1.248e-15 | 3.772e-14 |
155 | REGULATION OF CELLULAR RESPONSE TO GROWTH FACTOR STIMULUS | 18 | 229 | 1.664e-15 | 4.996e-14 |
156 | RESPONSE TO OXYGEN CONTAINING COMPOUND | 37 | 1381 | 1.723e-15 | 5.14e-14 |
157 | REGIONALIZATION | 20 | 311 | 1.918e-15 | 5.686e-14 |
158 | REGULATION OF STRESS ACTIVATED PROTEIN KINASE SIGNALING CASCADE | 17 | 197 | 2.254e-15 | 6.638e-14 |
159 | CENTRAL NERVOUS SYSTEM DEVELOPMENT | 30 | 872 | 2.299e-15 | 6.727e-14 |
160 | PALATE DEVELOPMENT | 13 | 85 | 2.757e-15 | 8.019e-14 |
161 | REGULATION OF CELL CYCLE | 31 | 949 | 2.944e-15 | 8.508e-14 |
162 | REGULATION OF GROWTH | 26 | 633 | 3.751e-15 | 1.077e-13 |
163 | MESODERM MORPHOGENESIS | 12 | 66 | 3.78e-15 | 1.079e-13 |
164 | POSITIVE REGULATION OF INTRACELLULAR TRANSPORT | 21 | 370 | 4.31e-15 | 1.223e-13 |
165 | REGULATION OF STEM CELL PROLIFERATION | 13 | 88 | 4.416e-15 | 1.245e-13 |
166 | REGULATION OF BINDING | 19 | 283 | 4.697e-15 | 1.317e-13 |
167 | POSITIVE REGULATION OF KINASE ACTIVITY | 23 | 482 | 7.682e-15 | 2.14e-13 |
168 | POSITIVE REGULATION OF MITOCHONDRIAL OUTER MEMBRANE PERMEABILIZATION INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 10 | 36 | 7.741e-15 | 2.144e-13 |
169 | NEGATIVE REGULATION OF PHOSPHORUS METABOLIC PROCESS | 24 | 541 | 9.277e-15 | 2.539e-13 |
170 | NEGATIVE REGULATION OF PHOSPHATE METABOLIC PROCESS | 24 | 541 | 9.277e-15 | 2.539e-13 |
171 | MAMMARY GLAND EPITHELIUM DEVELOPMENT | 11 | 53 | 1.159e-14 | 3.155e-13 |
172 | REGULATION OF SMAD PROTEIN IMPORT INTO NUCLEUS | 8 | 16 | 1.428e-14 | 3.862e-13 |
173 | POSITIVE REGULATION OF TRANSFERASE ACTIVITY | 25 | 616 | 1.807e-14 | 4.831e-13 |
174 | NEGATIVE REGULATION OF PROTEIN MODIFICATION PROCESS | 25 | 616 | 1.807e-14 | 4.831e-13 |
175 | NEGATIVE REGULATION OF CARTILAGE DEVELOPMENT | 9 | 26 | 1.824e-14 | 4.851e-13 |
176 | REGULATION OF PROTEIN TARGETING | 19 | 307 | 2.067e-14 | 5.464e-13 |
177 | OSTEOBLAST DIFFERENTIATION | 14 | 126 | 2.226e-14 | 5.852e-13 |
178 | REGULATION OF ORGANELLE ORGANIZATION | 33 | 1178 | 2.498e-14 | 6.531e-13 |
179 | APICAL JUNCTION ASSEMBLY | 10 | 40 | 2.531e-14 | 6.58e-13 |
180 | DEVELOPMENTAL INDUCTION | 9 | 27 | 2.723e-14 | 7.039e-13 |
181 | REPRODUCTIVE SYSTEM DEVELOPMENT | 21 | 408 | 2.966e-14 | 7.624e-13 |
182 | ANTERIOR POSTERIOR PATTERN SPECIFICATION | 16 | 194 | 3.227e-14 | 8.249e-13 |
183 | POSITIVE REGULATION OF ORGANELLE ORGANIZATION | 24 | 573 | 3.272e-14 | 8.32e-13 |
184 | POSITIVE REGULATION OF MOLECULAR FUNCTION | 40 | 1791 | 3.845e-14 | 9.723e-13 |
185 | VASCULATURE DEVELOPMENT | 22 | 469 | 4.49e-14 | 1.129e-12 |
186 | NEGATIVE REGULATION OF GROWTH | 17 | 236 | 4.542e-14 | 1.136e-12 |
187 | PROTEIN LOCALIZATION | 40 | 1805 | 4.97e-14 | 1.237e-12 |
188 | POSITIVE REGULATION OF OSTEOBLAST DIFFERENTIATION | 11 | 60 | 5.036e-14 | 1.246e-12 |
189 | REGULATION OF MITOCHONDRIAL OUTER MEMBRANE PERMEABILIZATION INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 10 | 43 | 5.641e-14 | 1.389e-12 |
190 | REGULATION OF PROTEIN INSERTION INTO MITOCHONDRIAL MEMBRANE INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 9 | 29 | 5.762e-14 | 1.404e-12 |
191 | POSITIVE REGULATION OF PROTEIN INSERTION INTO MITOCHONDRIAL MEMBRANE INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 9 | 29 | 5.762e-14 | 1.404e-12 |
192 | POSITIVE REGULATION OF STRESS ACTIVATED PROTEIN KINASE SIGNALING CASCADE | 14 | 135 | 5.895e-14 | 1.428e-12 |
193 | RESPONSE TO RETINOIC ACID | 13 | 107 | 6.07e-14 | 1.463e-12 |
194 | RESPONSE TO ORGANIC CYCLIC COMPOUND | 29 | 917 | 6.341e-14 | 1.521e-12 |
195 | APPENDAGE DEVELOPMENT | 15 | 169 | 7.261e-14 | 1.724e-12 |
196 | LIMB DEVELOPMENT | 15 | 169 | 7.261e-14 | 1.724e-12 |
197 | REGULATION OF INTRACELLULAR PROTEIN TRANSPORT | 20 | 381 | 8.972e-14 | 2.119e-12 |
198 | NEGATIVE REGULATION OF MOLECULAR FUNCTION | 31 | 1079 | 9.419e-14 | 2.213e-12 |
199 | NEGATIVE REGULATION OF CELL CYCLE | 21 | 433 | 9.477e-14 | 2.216e-12 |
200 | DEVELOPMENTAL PROCESS INVOLVED IN REPRODUCTION | 24 | 602 | 9.582e-14 | 2.229e-12 |
201 | CELLULAR RESPONSE TO RETINOIC ACID | 11 | 65 | 1.283e-13 | 2.971e-12 |
202 | PROTEIN PHOSPHORYLATION | 29 | 944 | 1.32e-13 | 3.041e-12 |
203 | BICELLULAR TIGHT JUNCTION ASSEMBLY | 9 | 32 | 1.59e-13 | 3.645e-12 |
204 | POSITIVE REGULATION OF SMAD PROTEIN IMPORT INTO NUCLEUS | 7 | 12 | 1.606e-13 | 3.664e-12 |
205 | NEGATIVE REGULATION OF CELL DEVELOPMENT | 18 | 303 | 2.14e-13 | 4.857e-12 |
206 | LOCOMOTION | 31 | 1114 | 2.2e-13 | 4.968e-12 |
207 | REGULATION OF CELL ADHESION | 24 | 629 | 2.473e-13 | 5.558e-12 |
208 | REGULATION OF TRANSPORT | 39 | 1804 | 2.559e-13 | 5.724e-12 |
209 | CELL DIVISION | 21 | 460 | 3.06e-13 | 6.813e-12 |
210 | IN UTERO EMBRYONIC DEVELOPMENT | 18 | 311 | 3.336e-13 | 7.393e-12 |
211 | BETA CATENIN DESTRUCTION COMPLEX DISASSEMBLY | 8 | 22 | 3.445e-13 | 7.596e-12 |
212 | PATHWAY RESTRICTED SMAD PROTEIN PHOSPHORYLATION | 7 | 13 | 3.463e-13 | 7.601e-12 |
213 | BLOOD VESSEL MORPHOGENESIS | 19 | 364 | 4.384e-13 | 9.576e-12 |
214 | CELL CELL JUNCTION ASSEMBLY | 11 | 74 | 5.733e-13 | 1.247e-11 |
215 | REGULATION OF BIOMINERAL TISSUE DEVELOPMENT | 11 | 75 | 6.685e-13 | 1.447e-11 |
216 | SENSORY ORGAN MORPHOGENESIS | 16 | 239 | 8.256e-13 | 1.778e-11 |
217 | POSITIVE REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 27 | 876 | 1.003e-12 | 2.15e-11 |
218 | POSITIVE REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 20 | 437 | 1.141e-12 | 2.435e-11 |
219 | WNT SIGNALING PATHWAY CALCIUM MODULATING PATHWAY | 9 | 39 | 1.161e-12 | 2.455e-11 |
220 | MORPHOGENESIS OF EMBRYONIC EPITHELIUM | 13 | 134 | 1.161e-12 | 2.455e-11 |
221 | ODONTOGENESIS | 12 | 105 | 1.237e-12 | 2.605e-11 |
222 | REGULATION OF CELLULAR RESPONSE TO STRESS | 24 | 691 | 1.843e-12 | 3.853e-11 |
223 | KIDNEY MORPHOGENESIS | 11 | 82 | 1.846e-12 | 3.853e-11 |
224 | RHYTHMIC PROCESS | 17 | 298 | 2.013e-12 | 4.182e-11 |
225 | REGULATION OF ESTABLISHMENT OF PLANAR POLARITY | 12 | 110 | 2.176e-12 | 4.5e-11 |
226 | PARAXIAL MESODERM DEVELOPMENT | 7 | 16 | 2.275e-12 | 4.685e-11 |
227 | REGULATION OF CELLULAR COMPONENT MOVEMENT | 25 | 771 | 2.672e-12 | 5.477e-11 |
228 | INTRACELLULAR SIGNAL TRANSDUCTION | 35 | 1572 | 2.792e-12 | 5.697e-11 |
229 | NEPHRON DEVELOPMENT | 12 | 115 | 3.722e-12 | 7.563e-11 |
230 | CELL CYCLE PROCESS | 29 | 1081 | 3.831e-12 | 7.751e-11 |
231 | DIGESTIVE SYSTEM DEVELOPMENT | 13 | 148 | 4.182e-12 | 8.424e-11 |
232 | POSITIVE REGULATION OF TRANSPORT | 27 | 936 | 4.68e-12 | 9.387e-11 |
233 | REGULATION OF SEQUENCE SPECIFIC DNA BINDING TRANSCRIPTION FACTOR ACTIVITY | 18 | 365 | 4.954e-12 | 9.894e-11 |
234 | MIDBRAIN DEVELOPMENT | 11 | 90 | 5.274e-12 | 1.049e-10 |
235 | POSITIVE REGULATION OF CATALYTIC ACTIVITY | 34 | 1518 | 5.341e-12 | 1.058e-10 |
236 | NEGATIVE REGULATION OF PHOSPHORYLATION | 19 | 422 | 5.894e-12 | 1.157e-10 |
237 | POSITIVE REGULATION OF WNT SIGNALING PATHWAY | 13 | 152 | 5.886e-12 | 1.157e-10 |
238 | REGULATION OF CYTOPLASMIC TRANSPORT | 20 | 481 | 6.566e-12 | 1.284e-10 |
239 | MOVEMENT OF CELL OR SUBCELLULAR COMPONENT | 31 | 1275 | 7.439e-12 | 1.448e-10 |
240 | EMBRYONIC SKELETAL SYSTEM DEVELOPMENT | 12 | 122 | 7.57e-12 | 1.468e-10 |
241 | ENDOCRINE SYSTEM DEVELOPMENT | 12 | 123 | 8.347e-12 | 1.612e-10 |
242 | REGULATION OF MEMBRANE PERMEABILITY | 10 | 70 | 1.022e-11 | 1.965e-10 |
243 | REGULATION OF ORGAN FORMATION | 8 | 32 | 1.079e-11 | 2.066e-10 |
244 | REPRODUCTION | 31 | 1297 | 1.153e-11 | 2.199e-10 |
245 | GLAND MORPHOGENESIS | 11 | 97 | 1.218e-11 | 2.314e-10 |
246 | REGULATION OF DEVELOPMENTAL GROWTH | 16 | 289 | 1.482e-11 | 2.791e-10 |
247 | POSITIVE REGULATION OF PROTEIN SERINE THREONINE KINASE ACTIVITY | 16 | 289 | 1.482e-11 | 2.791e-10 |
248 | NEGATIVE REGULATION OF CHONDROCYTE DIFFERENTIATION | 7 | 20 | 1.512e-11 | 2.837e-10 |
249 | PHOSPHORYLATION | 30 | 1228 | 1.566e-11 | 2.926e-10 |
250 | REGULATION OF MESENCHYMAL CELL PROLIFERATION | 8 | 34 | 1.844e-11 | 3.432e-10 |
251 | PHOSPHATE CONTAINING COMPOUND METABOLIC PROCESS | 38 | 1977 | 2.072e-11 | 3.841e-10 |
252 | MESONEPHRIC TUBULE MORPHOGENESIS | 9 | 53 | 2.266e-11 | 4.184e-10 |
253 | CELLULAR RESPONSE TO LIPID | 19 | 457 | 2.339e-11 | 4.301e-10 |
254 | DEVELOPMENTAL GROWTH INVOLVED IN MORPHOGENESIS | 11 | 104 | 2.639e-11 | 4.835e-10 |
255 | RENAL TUBULE DEVELOPMENT | 10 | 78 | 3.116e-11 | 5.686e-10 |
256 | REGULATION OF KIDNEY DEVELOPMENT | 9 | 55 | 3.219e-11 | 5.851e-10 |
257 | RESPONSE TO ABIOTIC STIMULUS | 27 | 1024 | 3.656e-11 | 6.619e-10 |
258 | NEGATIVE REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 15 | 262 | 4.179e-11 | 7.537e-10 |
259 | RESPONSE TO ALCOHOL | 17 | 362 | 4.387e-11 | 7.882e-10 |
260 | POSITIVE REGULATION OF LOCOMOTION | 18 | 420 | 5.033e-11 | 9.007e-10 |
261 | EMBRYONIC PATTERN SPECIFICATION | 9 | 58 | 5.312e-11 | 9.439e-10 |
262 | NEGATIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 23 | 740 | 5.315e-11 | 9.439e-10 |
263 | REGULATION OF RESPONSE TO STRESS | 32 | 1468 | 5.435e-11 | 9.615e-10 |
264 | REGULATION OF MAP KINASE ACTIVITY | 16 | 319 | 6.476e-11 | 1.141e-09 |
265 | CARDIAC EPITHELIAL TO MESENCHYMAL TRANSITION | 7 | 24 | 6.621e-11 | 1.163e-09 |
266 | STEM CELL PROLIFERATION | 9 | 60 | 7.303e-11 | 1.277e-09 |
267 | MAMMARY GLAND MORPHOGENESIS | 8 | 40 | 7.585e-11 | 1.322e-09 |
268 | NEGATIVE REGULATION OF CATALYTIC ACTIVITY | 24 | 829 | 8.19e-11 | 1.422e-09 |
269 | REGULATION OF NEURON DIFFERENTIATION | 20 | 554 | 8.254e-11 | 1.428e-09 |
270 | REGULATION OF HYDROLASE ACTIVITY | 30 | 1327 | 1.053e-10 | 1.815e-09 |
271 | ESTABLISHMENT OF CELL POLARITY | 10 | 88 | 1.064e-10 | 1.827e-09 |
272 | PITUITARY GLAND DEVELOPMENT | 8 | 42 | 1.153e-10 | 1.972e-09 |
273 | CELL DEATH | 26 | 1001 | 1.254e-10 | 2.138e-09 |
274 | CELL ACTIVATION | 20 | 568 | 1.283e-10 | 2.179e-09 |
275 | AXIS SPECIFICATION | 10 | 90 | 1.335e-10 | 2.259e-09 |
276 | POSITIVE REGULATION OF NUCLEOCYTOPLASMIC TRANSPORT | 11 | 121 | 1.389e-10 | 2.342e-09 |
277 | DORSAL VENTRAL PATTERN FORMATION | 10 | 91 | 1.493e-10 | 2.508e-09 |
278 | REGULATION OF DEPHOSPHORYLATION | 12 | 158 | 1.609e-10 | 2.693e-09 |
279 | MITOCHONDRIAL MEMBRANE ORGANIZATION | 10 | 92 | 1.667e-10 | 2.772e-09 |
280 | REGULATION OF CATENIN IMPORT INTO NUCLEUS | 7 | 27 | 1.674e-10 | 2.772e-09 |
281 | AXIS ELONGATION | 7 | 27 | 1.674e-10 | 2.772e-09 |
282 | BRANCHING INVOLVED IN URETERIC BUD MORPHOGENESIS | 8 | 44 | 1.714e-10 | 2.828e-09 |
283 | REGULATION OF JNK CASCADE | 12 | 159 | 1.732e-10 | 2.847e-09 |
284 | EMBRYONIC SKELETAL SYSTEM MORPHOGENESIS | 10 | 93 | 1.858e-10 | 3.034e-09 |
285 | NEPHRON EPITHELIUM DEVELOPMENT | 10 | 93 | 1.858e-10 | 3.034e-09 |
286 | SINGLE ORGANISM CELL ADHESION | 18 | 459 | 2.129e-10 | 3.464e-09 |
287 | CELLULAR RESPONSE TO ORGANIC CYCLIC COMPOUND | 18 | 465 | 2.625e-10 | 4.255e-09 |
288 | ORGAN INDUCTION | 6 | 16 | 2.831e-10 | 4.574e-09 |
289 | REGULATION OF HEART MORPHOGENESIS | 7 | 29 | 2.914e-10 | 4.692e-09 |
290 | REGULATION OF PROTEIN BINDING | 12 | 168 | 3.283e-10 | 5.268e-09 |
291 | FOREBRAIN DEVELOPMENT | 16 | 357 | 3.397e-10 | 5.431e-09 |
292 | DIGESTIVE TRACT MORPHOGENESIS | 8 | 48 | 3.579e-10 | 5.703e-09 |
293 | SKIN DEVELOPMENT | 13 | 211 | 3.641e-10 | 5.782e-09 |
294 | ESTABLISHMENT OR MAINTENANCE OF EPITHELIAL CELL APICAL BASAL POLARITY | 7 | 30 | 3.783e-10 | 5.986e-09 |
295 | MEMBRANE ORGANIZATION | 24 | 899 | 4.24e-10 | 6.687e-09 |
296 | BRANCH ELONGATION OF AN EPITHELIUM | 6 | 17 | 4.355e-10 | 6.822e-09 |
297 | NEGATIVE REGULATION OF STEM CELL PROLIFERATION | 6 | 17 | 4.355e-10 | 6.822e-09 |
298 | REGULATION OF ORGAN GROWTH | 9 | 73 | 4.499e-10 | 7.024e-09 |
299 | EYE MORPHOGENESIS | 11 | 136 | 4.921e-10 | 7.659e-09 |
300 | REGULATION OF MUSCLE TISSUE DEVELOPMENT | 10 | 103 | 5.165e-10 | 7.985e-09 |
301 | REGULATION OF MUSCLE ORGAN DEVELOPMENT | 10 | 103 | 5.165e-10 | 7.985e-09 |
302 | RESPONSE TO ESTROGEN | 13 | 218 | 5.444e-10 | 8.388e-09 |
303 | SEX DIFFERENTIATION | 14 | 266 | 5.858e-10 | 8.996e-09 |
304 | RESPONSE TO ACID CHEMICAL | 15 | 319 | 6.529e-10 | 9.993e-09 |
305 | CELL CELL SIGNALING | 22 | 767 | 6.717e-10 | 1.025e-08 |
306 | REGULATION OF FAT CELL DIFFERENTIATION | 10 | 106 | 6.872e-10 | 1.045e-08 |
307 | DIENCEPHALON DEVELOPMENT | 9 | 77 | 7.33e-10 | 1.107e-08 |
308 | REGULATION OF BMP SIGNALING PATHWAY | 9 | 77 | 7.33e-10 | 1.107e-08 |
309 | REGULATION OF MORPHOGENESIS OF A BRANCHING STRUCTURE | 8 | 53 | 8.202e-10 | 1.235e-08 |
310 | REGULATION OF CELL CELL ADHESION | 16 | 380 | 8.422e-10 | 1.264e-08 |
311 | CRANIAL SKELETAL SYSTEM DEVELOPMENT | 8 | 55 | 1.116e-09 | 1.669e-08 |
312 | DORSAL VENTRAL AXIS SPECIFICATION | 6 | 20 | 1.344e-09 | 2.005e-08 |
313 | CELLULAR RESPONSE TO OXYGEN CONTAINING COMPOUND | 22 | 799 | 1.436e-09 | 2.135e-08 |
314 | NEGATIVE REGULATION OF MUSCLE ORGAN DEVELOPMENT | 7 | 36 | 1.506e-09 | 2.225e-08 |
315 | NEGATIVE REGULATION OF MUSCLE TISSUE DEVELOPMENT | 7 | 36 | 1.506e-09 | 2.225e-08 |
316 | NEGATIVE REGULATION OF EPITHELIAL CELL PROLIFERATION | 10 | 115 | 1.538e-09 | 2.265e-08 |
317 | NEGATIVE REGULATION OF DEVELOPMENTAL GROWTH | 9 | 84 | 1.616e-09 | 2.372e-08 |
318 | REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 11 | 153 | 1.733e-09 | 2.536e-08 |
319 | CARDIAC SEPTUM DEVELOPMENT | 9 | 85 | 1.799e-09 | 2.623e-08 |
320 | ESTABLISHMENT OR MAINTENANCE OF APICAL BASAL CELL POLARITY | 7 | 37 | 1.849e-09 | 2.68e-08 |
321 | ESTABLISHMENT OR MAINTENANCE OF BIPOLAR CELL POLARITY | 7 | 37 | 1.849e-09 | 2.68e-08 |
322 | RESPONSE TO HORMONE | 23 | 893 | 2.068e-09 | 2.989e-08 |
323 | POSITIVE REGULATION OF CELLULAR COMPONENT BIOGENESIS | 16 | 406 | 2.185e-09 | 3.147e-08 |
324 | NEGATIVE REGULATION OF CELLULAR RESPONSE TO GROWTH FACTOR STIMULUS | 10 | 121 | 2.535e-09 | 3.641e-08 |
325 | EMBRYONIC DIGIT MORPHOGENESIS | 8 | 61 | 2.62e-09 | 3.74e-08 |
326 | POSITIVE REGULATION OF STEM CELL PROLIFERATION | 8 | 61 | 2.62e-09 | 3.74e-08 |
327 | SEGMENTATION | 9 | 89 | 2.723e-09 | 3.862e-08 |
328 | EPITHELIAL CELL PROLIFERATION | 9 | 89 | 2.723e-09 | 3.862e-08 |
329 | PROTEIN COMPLEX SUBUNIT ORGANIZATION | 30 | 1527 | 2.99e-09 | 4.229e-08 |
330 | CELL MOTILITY | 22 | 835 | 3.232e-09 | 4.544e-08 |
331 | LOCALIZATION OF CELL | 22 | 835 | 3.232e-09 | 4.544e-08 |
332 | NEURON PROJECTION DEVELOPMENT | 18 | 545 | 3.264e-09 | 4.575e-08 |
333 | EPIDERMIS DEVELOPMENT | 13 | 253 | 3.343e-09 | 4.672e-08 |
334 | NEURON DEVELOPMENT | 20 | 687 | 3.458e-09 | 4.817e-08 |
335 | CELL CYCLE PHASE TRANSITION | 13 | 255 | 3.677e-09 | 5.107e-08 |
336 | REGULATION OF CELLULAR COMPONENT BIOGENESIS | 21 | 767 | 3.951e-09 | 5.472e-08 |
337 | POSITIVE REGULATION OF MITOCHONDRION ORGANIZATION | 11 | 167 | 4.375e-09 | 6.04e-08 |
338 | REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION TO MITOCHONDRION | 10 | 128 | 4.391e-09 | 6.045e-08 |
339 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO NUCLEUS | 10 | 129 | 4.737e-09 | 6.483e-08 |
340 | TUBE FORMATION | 10 | 129 | 4.737e-09 | 6.483e-08 |
341 | MAMMARY GLAND EPITHELIAL CELL PROLIFERATION | 5 | 12 | 5.03e-09 | 6.864e-08 |
342 | RESPONSE TO WOUNDING | 18 | 563 | 5.419e-09 | 7.373e-08 |
343 | RESPONSE TO STEROID HORMONE | 17 | 497 | 5.541e-09 | 7.517e-08 |
344 | CELLULAR RESPONSE TO ACID CHEMICAL | 11 | 175 | 7.148e-09 | 9.668e-08 |
345 | NEGATIVE REGULATION OF EMBRYONIC DEVELOPMENT | 6 | 26 | 7.758e-09 | 1.046e-07 |
346 | CAMERA TYPE EYE MORPHOGENESIS | 9 | 101 | 8.432e-09 | 1.134e-07 |
347 | NEGATIVE REGULATION OF NUCLEOCYTOPLASMIC TRANSPORT | 8 | 71 | 9.015e-09 | 1.205e-07 |
348 | ENDODERM DEVELOPMENT | 8 | 71 | 9.015e-09 | 1.205e-07 |
349 | NEGATIVE REGULATION OF TRANSMEMBRANE RECEPTOR PROTEIN SERINE THREONINE KINASE SIGNALING PATHWAY | 9 | 102 | 9.203e-09 | 1.223e-07 |
350 | EMBRYONIC CRANIAL SKELETON MORPHOGENESIS | 7 | 46 | 9.2e-09 | 1.223e-07 |
351 | POSITIVE REGULATION OF MESENCHYMAL CELL PROLIFERATION | 6 | 27 | 9.926e-09 | 1.316e-07 |
352 | POSITIVE REGULATION OF PROTEIN IMPORT | 9 | 104 | 1.093e-08 | 1.445e-07 |
353 | VENTRICULAR SEPTUM MORPHOGENESIS | 6 | 28 | 1.257e-08 | 1.648e-07 |
354 | REGULATION OF CARDIAC MUSCLE TISSUE DEVELOPMENT | 7 | 48 | 1.253e-08 | 1.648e-07 |
355 | MAMMARY GLAND DUCT MORPHOGENESIS | 6 | 28 | 1.257e-08 | 1.648e-07 |
356 | EPITHELIAL CELL DEVELOPMENT | 11 | 186 | 1.35e-08 | 1.764e-07 |
357 | CARDIAC CHAMBER DEVELOPMENT | 10 | 144 | 1.373e-08 | 1.79e-07 |
358 | ODONTOGENESIS OF DENTIN CONTAINING TOOTH | 8 | 75 | 1.402e-08 | 1.822e-07 |
359 | CARDIAC SEPTUM MORPHOGENESIS | 7 | 49 | 1.455e-08 | 1.886e-07 |
360 | RESPONSE TO ESTRADIOL | 10 | 146 | 1.568e-08 | 2.026e-07 |
361 | STEM CELL DIVISION | 6 | 29 | 1.578e-08 | 2.034e-07 |
362 | SIGNAL TRANSDUCTION BY PROTEIN PHOSPHORYLATION | 15 | 404 | 1.6e-08 | 2.057e-07 |
363 | WOUND HEALING | 16 | 470 | 1.734e-08 | 2.222e-07 |
364 | MALE SEX DIFFERENTIATION | 10 | 148 | 1.786e-08 | 2.284e-07 |
365 | SOMITE DEVELOPMENT | 8 | 78 | 1.92e-08 | 2.447e-07 |
366 | ANGIOGENESIS | 13 | 293 | 1.934e-08 | 2.458e-07 |
367 | BONE MORPHOGENESIS | 8 | 79 | 2.126e-08 | 2.695e-07 |
368 | EAR DEVELOPMENT | 11 | 195 | 2.202e-08 | 2.785e-07 |
369 | CELL CYCLE ARREST | 10 | 154 | 2.613e-08 | 3.295e-07 |
370 | NEGATIVE REGULATION OF MITOTIC CELL CYCLE | 11 | 199 | 2.716e-08 | 3.415e-07 |
371 | ENDOCARDIAL CUSHION DEVELOPMENT | 6 | 32 | 2.967e-08 | 3.701e-07 |
372 | POSITIVE REGULATION OF BMP SIGNALING PATHWAY | 6 | 32 | 2.967e-08 | 3.701e-07 |
373 | BONE DEVELOPMENT | 10 | 156 | 2.955e-08 | 3.701e-07 |
374 | NEGATIVE REGULATION OF CYTOPLASMIC TRANSPORT | 9 | 117 | 3.083e-08 | 3.825e-07 |
375 | NEGATIVE REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 9 | 117 | 3.083e-08 | 3.825e-07 |
376 | POSITIVE REGULATION OF NEURON DIFFERENTIATION | 13 | 306 | 3.227e-08 | 3.993e-07 |
377 | POSITIVE REGULATION OF CANONICAL WNT SIGNALING PATHWAY | 9 | 119 | 3.575e-08 | 4.412e-07 |
378 | EMBRYONIC AXIS SPECIFICATION | 6 | 33 | 3.609e-08 | 4.442e-07 |
379 | LEUKOCYTE CELL CELL ADHESION | 12 | 255 | 3.678e-08 | 4.513e-07 |
380 | CELL MORPHOGENESIS INVOLVED IN NEURON DIFFERENTIATION | 14 | 368 | 3.686e-08 | 4.513e-07 |
381 | POSITIVE REGULATION OF MAP KINASE ACTIVITY | 11 | 207 | 4.073e-08 | 4.974e-07 |
382 | POSITIVE REGULATION OF INTRACELLULAR PROTEIN TRANSPORT | 12 | 258 | 4.183e-08 | 5.095e-07 |
383 | ORGAN FORMATION | 6 | 34 | 4.361e-08 | 5.298e-07 |
384 | RESPONSE TO EXTERNAL STIMULUS | 31 | 1821 | 4.42e-08 | 5.355e-07 |
385 | NOTOCHORD DEVELOPMENT | 5 | 18 | 5.29e-08 | 6.393e-07 |
386 | VASCULOGENESIS | 7 | 59 | 5.505e-08 | 6.636e-07 |
387 | NEGATIVE REGULATION OF PROTEIN SERINE THREONINE KINASE ACTIVITY | 9 | 126 | 5.88e-08 | 7.07e-07 |
388 | ENDOTHELIUM DEVELOPMENT | 8 | 90 | 5.985e-08 | 7.177e-07 |
389 | REGULATION OF PHOSPHATASE ACTIVITY | 9 | 128 | 6.741e-08 | 8.063e-07 |
390 | REGULATION OF MITOCHONDRION ORGANIZATION | 11 | 218 | 6.913e-08 | 8.248e-07 |
391 | POSITIVE REGULATION OF CHONDROCYTE DIFFERENTIATION | 5 | 19 | 7.145e-08 | 8.503e-07 |
392 | HINDLIMB MORPHOGENESIS | 6 | 37 | 7.43e-08 | 8.797e-07 |
393 | REGULATION OF PEPTIDYL THREONINE PHOSPHORYLATION | 6 | 37 | 7.43e-08 | 8.797e-07 |
394 | SOMITOGENESIS | 7 | 62 | 7.821e-08 | 9.236e-07 |
395 | REGULATION OF PROTEIN STABILITY | 11 | 221 | 7.945e-08 | 9.359e-07 |
396 | POSITIVE REGULATION OF CELL CYCLE | 13 | 332 | 8.367e-08 | 9.831e-07 |
397 | NEURAL TUBE FORMATION | 8 | 94 | 8.427e-08 | 9.877e-07 |
398 | NEGATIVE REGULATION OF INTRACELLULAR PROTEIN TRANSPORT | 8 | 95 | 9.157e-08 | 1.071e-06 |
399 | TRACHEA DEVELOPMENT | 5 | 20 | 9.482e-08 | 1.103e-06 |
400 | BRANCHING INVOLVED IN MAMMARY GLAND DUCT MORPHOGENESIS | 5 | 20 | 9.482e-08 | 1.103e-06 |
401 | MITOCHONDRIAL TRANSPORT | 10 | 177 | 9.763e-08 | 1.133e-06 |
402 | CELL CELL ADHESION | 17 | 608 | 1.046e-07 | 1.211e-06 |
403 | NEGATIVE REGULATION OF CELLULAR PROTEIN LOCALIZATION | 9 | 135 | 1.068e-07 | 1.233e-06 |
404 | POSITIVE REGULATION OF SEQUENCE SPECIFIC DNA BINDING TRANSCRIPTION FACTOR ACTIVITY | 11 | 228 | 1.09e-07 | 1.256e-06 |
405 | NEURON PROJECTION MORPHOGENESIS | 14 | 402 | 1.098e-07 | 1.262e-06 |
406 | POSITIVE REGULATION OF CYTOPLASMIC TRANSPORT | 12 | 282 | 1.105e-07 | 1.267e-06 |
407 | MITOTIC CELL CYCLE | 19 | 766 | 1.127e-07 | 1.288e-06 |
408 | NEGATIVE REGULATION OF CELLULAR RESPONSE TO TRANSFORMING GROWTH FACTOR BETA STIMULUS | 7 | 66 | 1.215e-07 | 1.378e-06 |
409 | NEGATIVE REGULATION OF TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 7 | 66 | 1.215e-07 | 1.378e-06 |
410 | NEGATIVE REGULATION OF OSTEOBLAST DIFFERENTIATION | 6 | 40 | 1.209e-07 | 1.378e-06 |
411 | NEGATIVE REGULATION OF ORGAN GROWTH | 5 | 21 | 1.239e-07 | 1.402e-06 |
412 | REGULATION OF TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 8 | 99 | 1.265e-07 | 1.425e-06 |
413 | REGULATION OF CELLULAR RESPONSE TO TRANSFORMING GROWTH FACTOR BETA STIMULUS | 8 | 99 | 1.265e-07 | 1.425e-06 |
414 | CELL CYCLE G2 M PHASE TRANSITION | 9 | 138 | 1.29e-07 | 1.45e-06 |
415 | REGULATION OF VASCULATURE DEVELOPMENT | 11 | 233 | 1.358e-07 | 1.522e-06 |
416 | POSITIVE REGULATION OF ENDOTHELIAL CELL PROLIFERATION | 7 | 68 | 1.497e-07 | 1.675e-06 |
417 | ENDOCARDIAL CUSHION MORPHOGENESIS | 5 | 22 | 1.595e-07 | 1.772e-06 |
418 | ACTIVIN RECEPTOR SIGNALING PATHWAY | 5 | 22 | 1.595e-07 | 1.772e-06 |
419 | SOMATIC STEM CELL DIVISION | 5 | 22 | 1.595e-07 | 1.772e-06 |
420 | NEGATIVE REGULATION OF OSSIFICATION | 7 | 69 | 1.658e-07 | 1.837e-06 |
421 | POSITIVE REGULATION OF EPITHELIAL CELL MIGRATION | 8 | 103 | 1.722e-07 | 1.904e-06 |
422 | NEGATIVE REGULATION OF INTRACELLULAR TRANSPORT | 9 | 143 | 1.751e-07 | 1.93e-06 |
423 | REGULATION OF CELL CYCLE PROCESS | 16 | 558 | 1.831e-07 | 2.015e-06 |
424 | CARDIAC CHAMBER MORPHOGENESIS | 8 | 104 | 1.857e-07 | 2.038e-06 |
425 | REGULATION OF PROTEOLYSIS | 18 | 711 | 1.87e-07 | 2.048e-06 |
426 | POSITIVE REGULATION OF MULTICELLULAR ORGANISMAL METABOLIC PROCESS | 5 | 23 | 2.029e-07 | 2.206e-06 |
427 | REGULATION OF METANEPHROS DEVELOPMENT | 5 | 23 | 2.029e-07 | 2.206e-06 |
428 | POSITIVE REGULATION OF COLLAGEN METABOLIC PROCESS | 5 | 23 | 2.029e-07 | 2.206e-06 |
429 | PANCREAS DEVELOPMENT | 7 | 73 | 2.456e-07 | 2.658e-06 |
430 | REGULATION OF NEURAL PRECURSOR CELL PROLIFERATION | 7 | 73 | 2.456e-07 | 2.658e-06 |
431 | NEURAL TUBE DEVELOPMENT | 9 | 149 | 2.487e-07 | 2.685e-06 |
432 | LUNG MORPHOGENESIS | 6 | 45 | 2.505e-07 | 2.692e-06 |
433 | ENDOCHONDRAL BONE MORPHOGENESIS | 6 | 45 | 2.505e-07 | 2.692e-06 |
434 | REGULATION OF CYTOSKELETON ORGANIZATION | 15 | 502 | 2.711e-07 | 2.907e-06 |
435 | NEGATIVE REGULATION OF KINASE ACTIVITY | 11 | 250 | 2.754e-07 | 2.946e-06 |
436 | SINGLE ORGANISM CELLULAR LOCALIZATION | 20 | 898 | 2.838e-07 | 3.029e-06 |
437 | COLUMNAR CUBOIDAL EPITHELIAL CELL DIFFERENTIATION | 8 | 111 | 3.076e-07 | 3.275e-06 |
438 | LENS FIBER CELL DIFFERENTIATION | 5 | 25 | 3.174e-07 | 3.364e-06 |
439 | RESPONSE TO OXYGEN LEVELS | 12 | 311 | 3.172e-07 | 3.364e-06 |
440 | IMMUNE SYSTEM DEVELOPMENT | 16 | 582 | 3.224e-07 | 3.409e-06 |
441 | REGULATION OF ACTIN FILAMENT BASED PROCESS | 12 | 312 | 3.282e-07 | 3.463e-06 |
442 | POSITIVE REGULATION OF CELL ADHESION | 13 | 376 | 3.495e-07 | 3.679e-06 |
443 | OVULATION CYCLE | 8 | 113 | 3.53e-07 | 3.708e-06 |
444 | ANTERIOR POSTERIOR AXIS SPECIFICATION | 6 | 48 | 3.72e-07 | 3.89e-06 |
445 | POSITIVE REGULATION OF ACTIN FILAMENT BUNDLE ASSEMBLY | 6 | 48 | 3.72e-07 | 3.89e-06 |
446 | AGING | 11 | 264 | 4.737e-07 | 4.942e-06 |
447 | RESPONSE TO LITHIUM ION | 5 | 27 | 4.777e-07 | 4.973e-06 |
448 | METANEPHROS DEVELOPMENT | 7 | 81 | 5.042e-07 | 5.225e-06 |
449 | REGULATION OF JUN KINASE ACTIVITY | 7 | 81 | 5.042e-07 | 5.225e-06 |
450 | POSITIVE REGULATION OF FAT CELL DIFFERENTIATION | 6 | 51 | 5.382e-07 | 5.565e-06 |
451 | REGULATION OF CELL GROWTH | 13 | 391 | 5.442e-07 | 5.614e-06 |
452 | ANATOMICAL STRUCTURE REGRESSION | 4 | 12 | 5.495e-07 | 5.619e-06 |
453 | REGULATION OF MACROPHAGE CYTOKINE PRODUCTION | 4 | 12 | 5.495e-07 | 5.619e-06 |
454 | TRACHEA MORPHOGENESIS | 4 | 12 | 5.495e-07 | 5.619e-06 |
455 | NEGATIVE REGULATION OF CELLULAR COMPONENT ORGANIZATION | 17 | 684 | 5.486e-07 | 5.619e-06 |
456 | DOPAMINERGIC NEURON DIFFERENTIATION | 5 | 28 | 5.788e-07 | 5.906e-06 |
457 | BIOLOGICAL ADHESION | 21 | 1032 | 6.058e-07 | 6.168e-06 |
458 | DEVELOPMENT OF PRIMARY SEXUAL CHARACTERISTICS | 10 | 216 | 6.189e-07 | 6.287e-06 |
459 | REGULATION OF EPITHELIAL CELL MIGRATION | 9 | 166 | 6.206e-07 | 6.291e-06 |
460 | TAXIS | 14 | 464 | 6.221e-07 | 6.293e-06 |
461 | REGULATION OF EPITHELIAL CELL DIFFERENTIATION | 8 | 122 | 6.356e-07 | 6.41e-06 |
462 | REGULATION OF CELL DIVISION | 11 | 272 | 6.364e-07 | 6.41e-06 |
463 | RESPONSE TO NITROGEN COMPOUND | 19 | 859 | 6.492e-07 | 6.524e-06 |
464 | POSITIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 6 | 53 | 6.795e-07 | 6.814e-06 |
465 | REGULATION OF MITOTIC CELL CYCLE | 14 | 468 | 6.891e-07 | 6.895e-06 |
466 | NEGATIVE REGULATION OF CELL GROWTH | 9 | 170 | 7.579e-07 | 7.568e-06 |
467 | VENTRICULAR SEPTUM DEVELOPMENT | 6 | 54 | 7.607e-07 | 7.58e-06 |
468 | MESENCHYMAL CELL PROLIFERATION | 4 | 13 | 7.901e-07 | 7.855e-06 |
469 | REGULATION OF DNA METABOLIC PROCESS | 12 | 340 | 8.163e-07 | 8.092e-06 |
470 | ACTIVATION OF PROTEIN KINASE ACTIVITY | 11 | 279 | 8.174e-07 | 8.092e-06 |
471 | NEGATIVE REGULATION OF CELL ADHESION | 10 | 223 | 8.28e-07 | 8.18e-06 |
472 | POSITIVE REGULATION OF BINDING | 8 | 127 | 8.634e-07 | 8.512e-06 |
473 | LYMPHOCYTE ACTIVATION | 12 | 342 | 8.683e-07 | 8.542e-06 |
474 | OVULATION CYCLE PROCESS | 7 | 88 | 8.897e-07 | 8.734e-06 |
475 | GLIOGENESIS | 9 | 175 | 9.66e-07 | 9.462e-06 |
476 | LEUKOCYTE ACTIVATION | 13 | 414 | 1.033e-06 | 1.01e-05 |
477 | REGULATION OF CYTOKINE PRODUCTION INVOLVED IN IMMUNE RESPONSE | 6 | 57 | 1.054e-06 | 1.028e-05 |
478 | REGULATION OF ESTABLISHMENT OF PLANAR POLARITY INVOLVED IN NEURAL TUBE CLOSURE | 4 | 14 | 1.101e-06 | 1.067e-05 |
479 | POSITIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 4 | 14 | 1.101e-06 | 1.067e-05 |
480 | EMBRYONIC SKELETAL JOINT DEVELOPMENT | 4 | 14 | 1.101e-06 | 1.067e-05 |
481 | NEGATIVE REGULATION OF TRANSFERASE ACTIVITY | 12 | 351 | 1.14e-06 | 1.103e-05 |
482 | MAINTENANCE OF CELL NUMBER | 8 | 132 | 1.158e-06 | 1.117e-05 |
483 | CELL PROJECTION ORGANIZATION | 19 | 902 | 1.346e-06 | 1.296e-05 |
484 | POSITIVE REGULATION OF EMBRYONIC DEVELOPMENT | 5 | 33 | 1.365e-06 | 1.313e-05 |
485 | POSITIVE REGULATION OF DNA METABOLIC PROCESS | 9 | 185 | 1.534e-06 | 1.472e-05 |
486 | MUSCLE STRUCTURE DEVELOPMENT | 13 | 432 | 1.657e-06 | 1.587e-05 |
487 | POSITIVE REGULATION OF CELL PROJECTION ORGANIZATION | 11 | 303 | 1.829e-06 | 1.747e-05 |
488 | REGULATION OF ENDOTHELIAL CELL PROLIFERATION | 7 | 98 | 1.847e-06 | 1.761e-05 |
489 | NEGATIVE REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 13 | 437 | 1.882e-06 | 1.791e-05 |
490 | POSITIVE REGULATION OF JUN KINASE ACTIVITY | 6 | 63 | 1.917e-06 | 1.82e-05 |
491 | NEGATIVE REGULATION OF NEURON DIFFERENTIATION | 9 | 191 | 1.998e-06 | 1.893e-05 |
492 | EPIDERMAL CELL DIFFERENTIATION | 8 | 142 | 2.008e-06 | 1.899e-05 |
493 | HEAD MORPHOGENESIS | 5 | 36 | 2.138e-06 | 2.018e-05 |
494 | PROTEIN LOCALIZATION TO MEMBRANE | 12 | 376 | 2.331e-06 | 2.196e-05 |
495 | SYNAPSE ORGANIZATION | 8 | 145 | 2.349e-06 | 2.208e-05 |
496 | NEGATIVE REGULATION OF EPITHELIAL CELL DIFFERENTIATION | 5 | 37 | 2.461e-06 | 2.308e-05 |
497 | CELLULAR RESPONSE TO LITHIUM ION | 4 | 17 | 2.582e-06 | 2.408e-05 |
498 | ESTABLISHMENT OF TISSUE POLARITY | 4 | 17 | 2.582e-06 | 2.408e-05 |
499 | NEGATIVE REGULATION OF CARDIAC MUSCLE TISSUE DEVELOPMENT | 4 | 17 | 2.582e-06 | 2.408e-05 |
500 | PROTEIN COMPLEX BIOGENESIS | 21 | 1132 | 2.656e-06 | 2.467e-05 |
501 | PROTEIN COMPLEX ASSEMBLY | 21 | 1132 | 2.656e-06 | 2.467e-05 |
502 | POSITIVE REGULATION OF ENDOTHELIAL CELL MIGRATION | 6 | 67 | 2.762e-06 | 2.555e-05 |
503 | NEURON FATE COMMITMENT | 6 | 67 | 2.762e-06 | 2.555e-05 |
504 | REGULATION OF MULTICELLULAR ORGANISMAL METABOLIC PROCESS | 5 | 38 | 2.82e-06 | 2.604e-05 |
505 | GLANDULAR EPITHELIAL CELL DIFFERENTIATION | 5 | 39 | 3.22e-06 | 2.967e-05 |
506 | SYNAPSE ASSEMBLY | 6 | 69 | 3.286e-06 | 3.022e-05 |
507 | PERICARDIUM DEVELOPMENT | 4 | 18 | 3.305e-06 | 3.027e-05 |
508 | KIDNEY MESENCHYME DEVELOPMENT | 4 | 18 | 3.305e-06 | 3.027e-05 |
509 | NEURAL PRECURSOR CELL PROLIFERATION | 6 | 70 | 3.577e-06 | 3.263e-05 |
510 | NEURON PROJECTION GUIDANCE | 9 | 205 | 3.572e-06 | 3.263e-05 |
511 | FORELIMB MORPHOGENESIS | 5 | 40 | 3.663e-06 | 3.335e-05 |
512 | SKIN EPIDERMIS DEVELOPMENT | 6 | 71 | 3.888e-06 | 3.534e-05 |
513 | PROTEIN LOCALIZATION TO NUCLEUS | 8 | 156 | 4.052e-06 | 3.675e-05 |
514 | NEGATIVE REGULATION OF HYDROLASE ACTIVITY | 12 | 397 | 4.073e-06 | 3.687e-05 |
515 | POSITIVE REGULATION OF KIDNEY DEVELOPMENT | 5 | 41 | 4.152e-06 | 3.737e-05 |
516 | LUNG ALVEOLUS DEVELOPMENT | 5 | 41 | 4.152e-06 | 3.737e-05 |
517 | RECEPTOR CLUSTERING | 5 | 41 | 4.152e-06 | 3.737e-05 |
518 | NEGATIVE REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION | 9 | 209 | 4.182e-06 | 3.757e-05 |
519 | ENDOTHELIAL CELL DIFFERENTIATION | 6 | 72 | 4.221e-06 | 3.785e-05 |
520 | POSITIVE REGULATION OF PROTEIN BINDING | 6 | 73 | 4.577e-06 | 4.096e-05 |
521 | POSTTRANSCRIPTIONAL GENE SILENCING | 5 | 42 | 4.691e-06 | 4.181e-05 |
522 | EPITHELIAL CELL MORPHOGENESIS | 5 | 42 | 4.691e-06 | 4.181e-05 |
523 | CELL PART MORPHOGENESIS | 15 | 633 | 4.825e-06 | 4.293e-05 |
524 | REGULATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY | 9 | 213 | 4.88e-06 | 4.333e-05 |
525 | REGULATION OF ENDOTHELIAL CELL MIGRATION | 7 | 114 | 5.083e-06 | 4.505e-05 |
526 | PROTEIN TARGETING | 12 | 406 | 5.118e-06 | 4.511e-05 |
527 | REGENERATION | 8 | 161 | 5.119e-06 | 4.511e-05 |
528 | REGULATION OF DNA REPLICATION | 8 | 161 | 5.119e-06 | 4.511e-05 |
529 | TONGUE DEVELOPMENT | 4 | 20 | 5.186e-06 | 4.561e-05 |
530 | NEGATIVE REGULATION OF STEM CELL DIFFERENTIATION | 5 | 43 | 5.283e-06 | 4.629e-05 |
531 | BETA CATENIN TCF COMPLEX ASSEMBLY | 5 | 43 | 5.283e-06 | 4.629e-05 |
532 | REGULATION OF CELL PROJECTION ORGANIZATION | 14 | 558 | 5.361e-06 | 4.689e-05 |
533 | FEMALE SEX DIFFERENTIATION | 7 | 116 | 5.705e-06 | 4.98e-05 |
534 | BODY MORPHOGENESIS | 5 | 44 | 5.932e-06 | 5.169e-05 |
535 | REGULATION OF ACTIN FILAMENT BUNDLE ASSEMBLY | 6 | 77 | 6.254e-06 | 5.439e-05 |
536 | CELL AGGREGATION | 4 | 21 | 6.377e-06 | 5.505e-05 |
537 | COCHLEA MORPHOGENESIS | 4 | 21 | 6.377e-06 | 5.505e-05 |
538 | NEGATIVE REGULATION OF NEURAL PRECURSOR CELL PROLIFERATION | 4 | 21 | 6.377e-06 | 5.505e-05 |
539 | CARTILAGE CONDENSATION | 4 | 21 | 6.377e-06 | 5.505e-05 |
540 | THYMOCYTE AGGREGATION | 5 | 45 | 6.642e-06 | 5.702e-05 |
541 | T CELL DIFFERENTIATION IN THYMUS | 5 | 45 | 6.642e-06 | 5.702e-05 |
542 | REGULATION OF ALCOHOL BIOSYNTHETIC PROCESS | 5 | 45 | 6.642e-06 | 5.702e-05 |
543 | NEGATIVE REGULATION OF PROTEIN BINDING | 6 | 79 | 7.262e-06 | 6.223e-05 |
544 | REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 5 | 46 | 7.418e-06 | 6.344e-05 |
545 | T CELL DIFFERENTIATION | 7 | 123 | 8.4e-06 | 7.171e-05 |
546 | LEUKOCYTE DIFFERENTIATION | 10 | 292 | 9.173e-06 | 7.818e-05 |
547 | RESPONSE TO DRUG | 12 | 431 | 9.358e-06 | 7.96e-05 |
548 | HAIR CYCLE | 6 | 83 | 9.674e-06 | 8.199e-05 |
549 | MOLTING CYCLE | 6 | 83 | 9.674e-06 | 8.199e-05 |
550 | REGULATION OF LEUKOCYTE DIFFERENTIATION | 9 | 232 | 9.729e-06 | 8.23e-05 |
551 | REGULATION OF STEROID BIOSYNTHETIC PROCESS | 5 | 49 | 1.017e-05 | 8.592e-05 |
552 | EMBRYONIC CAMERA TYPE EYE MORPHOGENESIS | 4 | 24 | 1.117e-05 | 9.363e-05 |
553 | RESPONSE TO STEROL | 4 | 24 | 1.117e-05 | 9.363e-05 |
554 | REGULATION OF ODONTOGENESIS | 4 | 24 | 1.117e-05 | 9.363e-05 |
555 | REGULATION OF PROTEIN PHOSPHATASE TYPE 2A ACTIVITY | 4 | 24 | 1.117e-05 | 9.363e-05 |
556 | FACE DEVELOPMENT | 5 | 50 | 1.125e-05 | 9.416e-05 |
557 | POSITIVE REGULATION OF DNA REPLICATION | 6 | 86 | 1.188e-05 | 9.923e-05 |
558 | POSITIVE REGULATION OF GROWTH | 9 | 238 | 1.193e-05 | 9.952e-05 |
559 | CELLULAR RESPONSE TO STRESS | 24 | 1565 | 1.229e-05 | 0.0001023 |
560 | MACROMOLECULAR COMPLEX DISASSEMBLY | 8 | 182 | 1.258e-05 | 0.0001045 |
561 | PROTEIN STABILIZATION | 7 | 131 | 1.27e-05 | 0.0001049 |
562 | NEGATIVE REGULATION OF BINDING | 7 | 131 | 1.27e-05 | 0.0001049 |
563 | TISSUE REMODELING | 6 | 87 | 1.27e-05 | 0.0001049 |
564 | FOREBRAIN REGIONALIZATION | 4 | 25 | 1.323e-05 | 0.0001088 |
565 | REGULATION OF TRANSFORMING GROWTH FACTOR BETA PRODUCTION | 4 | 25 | 1.323e-05 | 0.0001088 |
566 | POSITIVE REGULATION OF PEPTIDYL THREONINE PHOSPHORYLATION | 4 | 25 | 1.323e-05 | 0.0001088 |
567 | POSITIVE REGULATION OF CELL DIVISION | 7 | 132 | 1.334e-05 | 0.0001095 |
568 | POSITIVE REGULATION OF CELL CELL ADHESION | 9 | 243 | 1.409e-05 | 0.0001154 |
569 | REGULATION OF GLIOGENESIS | 6 | 90 | 1.543e-05 | 0.0001262 |
570 | REGULATION OF HORMONE METABOLIC PROCESS | 4 | 26 | 1.557e-05 | 0.0001271 |
571 | POSITIVE REGULATION OF CELL CYCLE PROCESS | 9 | 247 | 1.604e-05 | 0.0001307 |
572 | NEGATIVE REGULATION OF SEQUENCE SPECIFIC DNA BINDING TRANSCRIPTION FACTOR ACTIVITY | 7 | 136 | 1.621e-05 | 0.0001316 |
573 | GLIAL CELL DIFFERENTIATION | 7 | 136 | 1.621e-05 | 0.0001316 |
574 | CIRCADIAN RHYTHM | 7 | 137 | 1.7e-05 | 0.0001378 |
575 | PROTEIN DEPHOSPHORYLATION | 8 | 190 | 1.718e-05 | 0.000139 |
576 | INNER EAR MORPHOGENESIS | 6 | 92 | 1.751e-05 | 0.0001414 |
577 | NEGATIVE REGULATION OF CELL CELL ADHESION | 7 | 138 | 1.782e-05 | 0.0001437 |
578 | REGULATION OF ENDOTHELIAL CELL DIFFERENTIATION | 4 | 27 | 1.819e-05 | 0.0001465 |
579 | REGULATION OF NEURON APOPTOTIC PROCESS | 8 | 192 | 1.853e-05 | 0.0001489 |
580 | REGULATION OF NEURON DEATH | 9 | 252 | 1.88e-05 | 0.0001508 |
581 | CARDIAC MUSCLE TISSUE DEVELOPMENT | 7 | 140 | 1.956e-05 | 0.0001566 |
582 | MACROMOLECULAR COMPLEX ASSEMBLY | 22 | 1398 | 2.039e-05 | 0.000163 |
583 | REGULATION OF PEPTIDASE ACTIVITY | 11 | 392 | 2.09e-05 | 0.0001668 |
584 | GASTRULATION WITH MOUTH FORMING SECOND | 4 | 28 | 2.113e-05 | 0.0001672 |
585 | CELL FATE COMMITMENT INVOLVED IN FORMATION OF PRIMARY GERM LAYER | 4 | 28 | 2.113e-05 | 0.0001672 |
586 | REGULATION OF NEUROBLAST PROLIFERATION | 4 | 28 | 2.113e-05 | 0.0001672 |
587 | MORPHOGENESIS OF A POLARIZED EPITHELIUM | 4 | 28 | 2.113e-05 | 0.0001672 |
588 | METANEPHROS MORPHOGENESIS | 4 | 28 | 2.113e-05 | 0.0001672 |
589 | REGULATION OF PROTEIN CATABOLIC PROCESS | 11 | 393 | 2.14e-05 | 0.0001691 |
590 | TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 15 | 724 | 2.362e-05 | 0.0001863 |
591 | REGULATION OF CYCLIN DEPENDENT PROTEIN KINASE ACTIVITY | 6 | 97 | 2.369e-05 | 0.0001865 |
592 | REGULATION OF CARDIAC MUSCLE CELL PROLIFERATION | 4 | 29 | 2.44e-05 | 0.0001911 |
593 | EMBRYONIC HINDLIMB MORPHOGENESIS | 4 | 29 | 2.44e-05 | 0.0001911 |
594 | REGULATION OF OLIGODENDROCYTE DIFFERENTIATION | 4 | 29 | 2.44e-05 | 0.0001911 |
595 | NEGATIVE REGULATION OF MAPK CASCADE | 7 | 145 | 2.454e-05 | 0.0001919 |
596 | NEGATIVE REGULATION OF APOPTOTIC SIGNALING PATHWAY | 8 | 200 | 2.484e-05 | 0.000194 |
597 | NEGATIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 6 | 98 | 2.511e-05 | 0.0001957 |
598 | REGULATION OF GLIAL CELL DIFFERENTIATION | 5 | 59 | 2.549e-05 | 0.0001983 |
599 | POSITIVE REGULATION OF PROTEIN CATABOLIC PROCESS | 9 | 263 | 2.632e-05 | 0.0002041 |
600 | NEGATIVE REGULATION OF LOCOMOTION | 9 | 263 | 2.632e-05 | 0.0002041 |
601 | PEPTIDYL SERINE MODIFICATION | 7 | 148 | 2.8e-05 | 0.0002167 |
602 | REGULATION OF SMOOTH MUSCLE CELL PROLIFERATION | 6 | 100 | 2.817e-05 | 0.0002177 |
603 | REGULATION OF CYTOKINE PRODUCTION | 13 | 563 | 2.837e-05 | 0.0002189 |
604 | KERATINOCYTE DIFFERENTIATION | 6 | 101 | 2.98e-05 | 0.0002292 |
605 | REGULATION OF PRODUCTION OF MOLECULAR MEDIATOR OF IMMUNE RESPONSE | 6 | 101 | 2.98e-05 | 0.0002292 |
606 | REGULATION OF NEURON PROJECTION DEVELOPMENT | 11 | 408 | 3.017e-05 | 0.0002316 |
607 | POSITIVE REGULATION OF NON CANONICAL WNT SIGNALING PATHWAY | 3 | 11 | 3.191e-05 | 0.0002442 |
608 | REGULATION OF ODONTOGENESIS OF DENTIN CONTAINING TOOTH | 3 | 11 | 3.191e-05 | 0.0002442 |
609 | REGULATION OF CIRCADIAN RHYTHM | 6 | 103 | 3.33e-05 | 0.0002544 |
610 | LYMPHOCYTE DIFFERENTIATION | 8 | 209 | 3.402e-05 | 0.0002595 |
611 | AMEBOIDAL TYPE CELL MIGRATION | 7 | 154 | 3.612e-05 | 0.0002751 |
612 | SALIVARY GLAND DEVELOPMENT | 4 | 32 | 3.644e-05 | 0.0002766 |
613 | EMBRYONIC FORELIMB MORPHOGENESIS | 4 | 32 | 3.644e-05 | 0.0002766 |
614 | MUSCLE TISSUE DEVELOPMENT | 9 | 275 | 3.731e-05 | 0.0002827 |
615 | ESTABLISHMENT OF LOCALIZATION IN CELL | 24 | 1676 | 3.775e-05 | 0.0002856 |
616 | CARDIAC VENTRICLE DEVELOPMENT | 6 | 106 | 3.917e-05 | 0.0002954 |
617 | FAT CELL DIFFERENTIATION | 6 | 106 | 3.917e-05 | 0.0002954 |
618 | REGULATION OF T CELL APOPTOTIC PROCESS | 4 | 33 | 4.128e-05 | 0.0003103 |
619 | EMBRYONIC EYE MORPHOGENESIS | 4 | 33 | 4.128e-05 | 0.0003103 |
620 | NEGATIVE REGULATION OF CARDIAC MUSCLE TISSUE GROWTH | 3 | 12 | 4.237e-05 | 0.0003159 |
621 | REGULATION OF THYMOCYTE APOPTOTIC PROCESS | 3 | 12 | 4.237e-05 | 0.0003159 |
622 | HEART FORMATION | 3 | 12 | 4.237e-05 | 0.0003159 |
623 | NEGATIVE REGULATION OF HEART GROWTH | 3 | 12 | 4.237e-05 | 0.0003159 |
624 | LENS FIBER CELL DEVELOPMENT | 3 | 12 | 4.237e-05 | 0.0003159 |
625 | HORMONE MEDIATED SIGNALING PATHWAY | 7 | 158 | 4.255e-05 | 0.0003167 |
626 | SOMATIC STEM CELL POPULATION MAINTENANCE | 5 | 66 | 4.402e-05 | 0.0003272 |
627 | CELLULAR RESPONSE TO NITROGEN COMPOUND | 12 | 505 | 4.449e-05 | 0.0003302 |
628 | LUNG EPITHELIUM DEVELOPMENT | 4 | 34 | 4.657e-05 | 0.0003439 |
629 | PROTEIN DESTABILIZATION | 4 | 34 | 4.657e-05 | 0.0003439 |
630 | MULTICELLULAR ORGANISM REPRODUCTION | 15 | 768 | 4.647e-05 | 0.0003439 |
631 | POSITIVE REGULATION OF NEURON DEATH | 5 | 67 | 4.735e-05 | 0.0003492 |
632 | REGULATION OF NUCLEAR DIVISION | 7 | 163 | 5.186e-05 | 0.0003818 |
633 | BONE REMODELING | 4 | 35 | 5.234e-05 | 0.0003841 |
634 | EMBRYONIC CAMERA TYPE EYE DEVELOPMENT | 4 | 35 | 5.234e-05 | 0.0003841 |
635 | EAR MORPHOGENESIS | 6 | 112 | 5.337e-05 | 0.0003911 |
636 | NEGATIVE REGULATION OF OLIGODENDROCYTE DIFFERENTIATION | 3 | 13 | 5.484e-05 | 0.0003987 |
637 | TYPE B PANCREATIC CELL DEVELOPMENT | 3 | 13 | 5.484e-05 | 0.0003987 |
638 | POSITIVE REGULATION OF STEROID BIOSYNTHETIC PROCESS | 3 | 13 | 5.484e-05 | 0.0003987 |
639 | REGULATION OF CELL PROLIFERATION INVOLVED IN KIDNEY DEVELOPMENT | 3 | 13 | 5.484e-05 | 0.0003987 |
640 | GDP METABOLIC PROCESS | 3 | 13 | 5.484e-05 | 0.0003987 |
641 | MUSCLE ORGAN MORPHOGENESIS | 5 | 70 | 5.851e-05 | 0.0004247 |
642 | POSITIVE REGULATION OF PROTEOLYSIS | 10 | 363 | 5.88e-05 | 0.0004262 |
643 | CELL FATE SPECIFICATION | 5 | 71 | 6.265e-05 | 0.0004534 |
644 | TELENCEPHALON DEVELOPMENT | 8 | 228 | 6.292e-05 | 0.0004546 |
645 | REGULATION OF GENE EXPRESSION EPIGENETIC | 8 | 229 | 6.488e-05 | 0.000468 |
646 | REGULATION OF IMMUNE SYSTEM PROCESS | 21 | 1403 | 6.702e-05 | 0.0004827 |
647 | RENAL VESICLE DEVELOPMENT | 3 | 14 | 6.95e-05 | 0.0004952 |
648 | CELL MIGRATION INVOLVED IN GASTRULATION | 3 | 14 | 6.95e-05 | 0.0004952 |
649 | METANEPHRIC MESENCHYME DEVELOPMENT | 3 | 14 | 6.95e-05 | 0.0004952 |
650 | CONVERGENT EXTENSION | 3 | 14 | 6.95e-05 | 0.0004952 |
651 | CRANIOFACIAL SUTURE MORPHOGENESIS | 3 | 14 | 6.95e-05 | 0.0004952 |
652 | ADENOHYPOPHYSIS DEVELOPMENT | 3 | 14 | 6.95e-05 | 0.0004952 |
653 | RESPONSE TO LAMINAR FLUID SHEAR STRESS | 3 | 14 | 6.95e-05 | 0.0004952 |
654 | POSITIVE REGULATION OF NEURON PROJECTION DEVELOPMENT | 8 | 232 | 7.107e-05 | 0.0005056 |
655 | NEGATIVE REGULATION OF MAP KINASE ACTIVITY | 5 | 73 | 7.16e-05 | 0.0005079 |
656 | EMBRYONIC HEART TUBE DEVELOPMENT | 5 | 73 | 7.16e-05 | 0.0005079 |
657 | REGULATION OF CELL SUBSTRATE ADHESION | 7 | 173 | 7.554e-05 | 0.000535 |
658 | REGULATION OF STEROID METABOLIC PROCESS | 5 | 74 | 7.643e-05 | 0.0005405 |
659 | COCHLEA DEVELOPMENT | 4 | 39 | 8.074e-05 | 0.0005701 |
660 | POSITIVE REGULATION OF CYTOSKELETON ORGANIZATION | 7 | 175 | 8.12e-05 | 0.0005724 |
661 | ARTERY DEVELOPMENT | 5 | 75 | 8.151e-05 | 0.0005729 |
662 | NEURAL CREST CELL DIFFERENTIATION | 5 | 75 | 8.151e-05 | 0.0005729 |
663 | MUSCLE CELL DIFFERENTIATION | 8 | 237 | 8.247e-05 | 0.0005788 |
664 | RESPONSE TO CORTICOSTEROID | 7 | 176 | 8.415e-05 | 0.0005897 |
665 | NEGATIVE REGULATION OF TRANSPORT | 11 | 458 | 8.535e-05 | 0.0005972 |
666 | POSITIVE REGULATION OF ENDOTHELIAL CELL DIFFERENTIATION | 3 | 15 | 8.65e-05 | 0.000598 |
667 | MESENCHYMAL TO EPITHELIAL TRANSITION | 3 | 15 | 8.65e-05 | 0.000598 |
668 | NEGATIVE REGULATION OF DENDRITE MORPHOGENESIS | 3 | 15 | 8.65e-05 | 0.000598 |
669 | REGULATION OF EPITHELIAL CELL DIFFERENTIATION INVOLVED IN KIDNEY DEVELOPMENT | 3 | 15 | 8.65e-05 | 0.000598 |
670 | ENDOCARDIAL CUSHION FORMATION | 3 | 15 | 8.65e-05 | 0.000598 |
671 | REGULATION OF CELL PROLIFERATION INVOLVED IN HEART MORPHOGENESIS | 3 | 15 | 8.65e-05 | 0.000598 |
672 | POSITIVE REGULATION OF T CELL APOPTOTIC PROCESS | 3 | 15 | 8.65e-05 | 0.000598 |
673 | LOCALIZATION WITHIN MEMBRANE | 6 | 122 | 8.597e-05 | 0.000598 |
674 | POSITIVE REGULATION OF CELL MATRIX ADHESION | 4 | 40 | 8.93e-05 | 0.0006165 |
675 | NEGATIVE REGULATION OF DEPHOSPHORYLATION | 5 | 77 | 9.243e-05 | 0.0006372 |
676 | REGULATION OF CHEMOTAXIS | 7 | 180 | 9.687e-05 | 0.0006667 |
677 | NEGATIVE REGULATION OF FAT CELL DIFFERENTIATION | 4 | 41 | 9.851e-05 | 0.000676 |
678 | PROSTATE GLAND DEVELOPMENT | 4 | 41 | 9.851e-05 | 0.000676 |
679 | REGULATION OF HEMOPOIESIS | 9 | 314 | 0.0001034 | 0.0007082 |
680 | CELLULAR RESPONSE TO HORMONE STIMULUS | 12 | 552 | 0.0001038 | 0.0007104 |
681 | REGULATION OF CATABOLIC PROCESS | 14 | 731 | 0.0001042 | 0.000712 |
682 | PROTEIN LOCALIZATION TO SYNAPSE | 3 | 16 | 0.000106 | 0.0007222 |
683 | APOPTOTIC PROCESS INVOLVED IN MORPHOGENESIS | 3 | 16 | 0.000106 | 0.0007222 |
684 | REGULATION OF HEART GROWTH | 4 | 42 | 0.0001084 | 0.0007373 |
685 | NEGATIVE REGULATION OF VASCULATURE DEVELOPMENT | 5 | 80 | 0.0001109 | 0.0007533 |
686 | REGULATION OF REPRODUCTIVE PROCESS | 6 | 129 | 0.000117 | 0.0007936 |
687 | REGULATION OF FIBROBLAST PROLIFERATION | 5 | 81 | 0.0001176 | 0.0007968 |
688 | MORPHOGENESIS OF AN EPITHELIAL SHEET | 4 | 43 | 0.000119 | 0.0008033 |
689 | REGULATION OF POLYSACCHARIDE METABOLIC PROCESS | 4 | 43 | 0.000119 | 0.0008033 |
690 | RESPONSE TO INORGANIC SUBSTANCE | 11 | 479 | 0.0001267 | 0.0008544 |
691 | NEGATIVE REGULATION OF KIDNEY DEVELOPMENT | 3 | 17 | 0.0001282 | 0.0008556 |
692 | NEGATIVE REGULATION OF ALCOHOL BIOSYNTHETIC PROCESS | 3 | 17 | 0.0001282 | 0.0008556 |
693 | POSITIVE REGULATION OF LEUKOCYTE DIFFERENTIATION | 6 | 131 | 0.0001273 | 0.0008556 |
694 | POSITIVE REGULATION OF EXTRACELLULAR MATRIX ORGANIZATION | 3 | 17 | 0.0001282 | 0.0008556 |
695 | REGULATION OF STEM CELL POPULATION MAINTENANCE | 3 | 17 | 0.0001282 | 0.0008556 |
696 | MAMMARY GLAND ALVEOLUS DEVELOPMENT | 3 | 17 | 0.0001282 | 0.0008556 |
697 | MAMMARY GLAND LOBULE DEVELOPMENT | 3 | 17 | 0.0001282 | 0.0008556 |
698 | LABYRINTHINE LAYER DEVELOPMENT | 4 | 44 | 0.0001303 | 0.0008683 |
699 | EMBRYONIC PLACENTA DEVELOPMENT | 5 | 83 | 0.0001321 | 0.0008791 |
700 | REGULATION OF LYMPHOCYTE DIFFERENTIATION | 6 | 132 | 0.0001328 | 0.0008824 |
701 | ENDOTHELIAL CELL DEVELOPMENT | 4 | 45 | 0.0001423 | 0.0009406 |
702 | RESPONSE TO PEPTIDE | 10 | 404 | 0.0001419 | 0.0009406 |
703 | SUBSTANTIA NIGRA DEVELOPMENT | 4 | 45 | 0.0001423 | 0.0009406 |
704 | EXOCRINE SYSTEM DEVELOPMENT | 4 | 45 | 0.0001423 | 0.0009406 |
705 | CELL GROWTH | 6 | 135 | 0.0001501 | 0.000991 |
706 | GLANDULAR EPITHELIAL CELL DEVELOPMENT | 3 | 18 | 0.0001531 | 0.001005 |
707 | REGULATION OF HORMONE BIOSYNTHETIC PROCESS | 3 | 18 | 0.0001531 | 0.001005 |
708 | OSTEOBLAST DEVELOPMENT | 3 | 18 | 0.0001531 | 0.001005 |
709 | UTERUS DEVELOPMENT | 3 | 18 | 0.0001531 | 0.001005 |
710 | CELL CYCLE CHECKPOINT | 7 | 194 | 0.0001543 | 0.001011 |
711 | HINDBRAIN DEVELOPMENT | 6 | 137 | 0.0001627 | 0.001065 |
712 | PLACENTA DEVELOPMENT | 6 | 138 | 0.0001693 | 0.001102 |
713 | POSITIVE REGULATION OF NEURON APOPTOTIC PROCESS | 4 | 47 | 0.0001688 | 0.001102 |
714 | CELLULAR RESPONSE TO ABIOTIC STIMULUS | 8 | 263 | 0.0001691 | 0.001102 |
715 | POSITIVE REGULATION OF GLIOGENESIS | 4 | 47 | 0.0001688 | 0.001102 |
716 | CELLULAR RESPONSE TO EXTERNAL STIMULUS | 8 | 264 | 0.0001735 | 0.001128 |
717 | MITOTIC CELL CYCLE CHECKPOINT | 6 | 139 | 0.0001761 | 0.001143 |
718 | POSITIVE REGULATION OF IMMUNE SYSTEM PROCESS | 15 | 867 | 0.0001786 | 0.001157 |
719 | REGULATION OF NON CANONICAL WNT SIGNALING PATHWAY | 3 | 19 | 0.0001811 | 0.001167 |
720 | ENTRAINMENT OF CIRCADIAN CLOCK BY PHOTOPERIOD | 3 | 19 | 0.0001811 | 0.001167 |
721 | REGULATION OF CARDIAC MUSCLE CELL DIFFERENTIATION | 3 | 19 | 0.0001811 | 0.001167 |
722 | ENTEROENDOCRINE CELL DIFFERENTIATION | 3 | 19 | 0.0001811 | 0.001167 |
723 | SECRETION | 12 | 588 | 0.0001869 | 0.001203 |
724 | REGULATION OF CELL MATRIX ADHESION | 5 | 90 | 0.0001935 | 0.001243 |
725 | IMMUNE SYSTEM PROCESS | 25 | 1984 | 0.000199 | 0.001277 |
726 | MITOCHONDRION ORGANIZATION | 12 | 594 | 0.0002052 | 0.001315 |
727 | INTRACELLULAR PROTEIN TRANSPORT | 14 | 781 | 0.0002072 | 0.001326 |
728 | POSITIVE REGULATION OF LYMPHOCYTE APOPTOTIC PROCESS | 3 | 20 | 0.0002121 | 0.001354 |
729 | GMP METABOLIC PROCESS | 3 | 20 | 0.0002121 | 0.001354 |
730 | ENDODERM FORMATION | 4 | 50 | 0.000215 | 0.001371 |
731 | REGULATION OF DNA BINDING | 5 | 93 | 0.0002256 | 0.001436 |
732 | ARTERY MORPHOGENESIS | 4 | 51 | 0.0002323 | 0.001477 |
733 | CELLULAR COMPONENT DISASSEMBLY | 11 | 515 | 0.0002374 | 0.001507 |
734 | REGULATION OF GENE SILENCING BY RNA | 3 | 21 | 0.0002464 | 0.001554 |
735 | CHONDROCYTE DEVELOPMENT | 3 | 21 | 0.0002464 | 0.001554 |
736 | POSITIVE REGULATION OF EXCITATORY POSTSYNAPTIC POTENTIAL | 3 | 21 | 0.0002464 | 0.001554 |
737 | APOPTOTIC PROCESS INVOLVED IN DEVELOPMENT | 3 | 21 | 0.0002464 | 0.001554 |
738 | REGULATION OF POSTTRANSCRIPTIONAL GENE SILENCING | 3 | 21 | 0.0002464 | 0.001554 |
739 | POSITIVE REGULATION OF CELL GROWTH | 6 | 148 | 0.0002475 | 0.001558 |
740 | REGULATION OF TRANSCRIPTION FACTOR IMPORT INTO NUCLEUS | 5 | 95 | 0.0002492 | 0.001567 |
741 | POSITIVE REGULATION OF PROTEIN SECRETION | 7 | 211 | 0.0002581 | 0.001621 |
742 | MYELOID LEUKOCYTE DIFFERENTIATION | 5 | 96 | 0.0002616 | 0.001641 |
743 | POSITIVE REGULATION OF FIBROBLAST PROLIFERATION | 4 | 53 | 0.0002697 | 0.001689 |
744 | NEGATIVE REGULATION OF CYTOKINE PRODUCTION INVOLVED IN IMMUNE RESPONSE | 3 | 22 | 0.0002841 | 0.001767 |
745 | POSITIVE REGULATION OF HYDROLASE ACTIVITY | 15 | 905 | 0.0002832 | 0.001767 |
746 | DSRNA FRAGMENTATION | 3 | 22 | 0.0002841 | 0.001767 |
747 | EMBRYONIC PLACENTA MORPHOGENESIS | 3 | 22 | 0.0002841 | 0.001767 |
748 | PRODUCTION OF SMALL RNA INVOLVED IN GENE SILENCING BY RNA | 3 | 22 | 0.0002841 | 0.001767 |
749 | RESPONSE TO EXTRACELLULAR STIMULUS | 10 | 441 | 0.0002869 | 0.001783 |
750 | NEGATIVE REGULATION OF REPRODUCTIVE PROCESS | 4 | 54 | 0.00029 | 0.001794 |
751 | REGULATION OF LYMPHOCYTE APOPTOTIC PROCESS | 4 | 54 | 0.00029 | 0.001794 |
752 | CARDIAC MUSCLE TISSUE MORPHOGENESIS | 4 | 54 | 0.00029 | 0.001794 |
753 | DEPHOSPHORYLATION | 8 | 286 | 0.0002982 | 0.001843 |
754 | ESTABLISHMENT OF EPITHELIAL CELL POLARITY | 3 | 23 | 0.0003253 | 0.001994 |
755 | NEGATIVE REGULATION OF EPITHELIAL TO MESENCHYMAL TRANSITION | 3 | 23 | 0.0003253 | 0.001994 |
756 | POSITIVE REGULATION OF ALCOHOL BIOSYNTHETIC PROCESS | 3 | 23 | 0.0003253 | 0.001994 |
757 | POSTTRANSCRIPTIONAL REGULATION OF GENE EXPRESSION | 10 | 448 | 0.000325 | 0.001994 |
758 | SCF DEPENDENT PROTEASOMAL UBIQUITIN DEPENDENT PROTEIN CATABOLIC PROCESS | 3 | 23 | 0.0003253 | 0.001994 |
759 | POSITIVE REGULATION OF STEROID METABOLIC PROCESS | 3 | 23 | 0.0003253 | 0.001994 |
760 | POSITIVE REGULATION OF DEVELOPMENTAL GROWTH | 6 | 156 | 0.0003284 | 0.002008 |
761 | CELLULAR RESPONSE TO INORGANIC SUBSTANCE | 6 | 156 | 0.0003284 | 0.002008 |
762 | POSITIVE REGULATION OF MUSCLE TISSUE DEVELOPMENT | 4 | 56 | 0.0003337 | 0.002035 |
763 | OUTFLOW TRACT MORPHOGENESIS | 4 | 56 | 0.0003337 | 0.002035 |
764 | CIRCADIAN REGULATION OF GENE EXPRESSION | 4 | 57 | 0.0003573 | 0.002173 |
765 | ENDOTHELIAL CELL MIGRATION | 4 | 57 | 0.0003573 | 0.002173 |
766 | PHOTOPERIODISM | 3 | 24 | 0.0003702 | 0.002243 |
767 | NEGATIVE REGULATION OF STEROID METABOLIC PROCESS | 3 | 24 | 0.0003702 | 0.002243 |
768 | ENDOTHELIAL CELL PROLIFERATION | 3 | 24 | 0.0003702 | 0.002243 |
769 | REGULATION OF EPITHELIAL CELL APOPTOTIC PROCESS | 4 | 59 | 0.000408 | 0.002469 |
770 | POSITIVE REGULATION OF HEMOPOIESIS | 6 | 163 | 0.0004151 | 0.002508 |
771 | EPITHELIAL TUBE BRANCHING INVOLVED IN LUNG MORPHOGENESIS | 3 | 25 | 0.0004188 | 0.002518 |
772 | LUNG CELL DIFFERENTIATION | 3 | 25 | 0.0004188 | 0.002518 |
773 | REGULATION OF FIBROBLAST GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 3 | 25 | 0.0004188 | 0.002518 |
774 | EPITHELIAL CELL APOPTOTIC PROCESS | 3 | 25 | 0.0004188 | 0.002518 |
775 | CELL SUBSTRATE ADHESION | 6 | 164 | 0.0004288 | 0.002575 |
776 | REGULATION OF T CELL DIFFERENTIATION | 5 | 107 | 0.0004322 | 0.002592 |
777 | NEGATIVE REGULATION OF CELL DIVISION | 4 | 60 | 0.0004351 | 0.002599 |
778 | POSITIVE REGULATION OF SMOOTH MUSCLE CELL PROLIFERATION | 4 | 60 | 0.0004351 | 0.002599 |
779 | REGULATION OF PHOSPHOPROTEIN PHOSPHATASE ACTIVITY | 4 | 60 | 0.0004351 | 0.002599 |
780 | REGULATION OF CELL CYCLE ARREST | 5 | 108 | 0.0004511 | 0.002691 |
781 | CENTRAL NERVOUS SYSTEM NEURON DIFFERENTIATION | 6 | 166 | 0.0004573 | 0.002725 |
782 | OVARIAN FOLLICLE DEVELOPMENT | 4 | 61 | 0.0004636 | 0.002758 |
783 | DEVELOPMENTAL PROGRAMMED CELL DEATH | 3 | 26 | 0.0004714 | 0.002784 |
784 | NEGATIVE REGULATION OF GLIAL CELL DIFFERENTIATION | 3 | 26 | 0.0004714 | 0.002784 |
785 | REGULATION OF MESONEPHROS DEVELOPMENT | 3 | 26 | 0.0004714 | 0.002784 |
786 | ENTRAINMENT OF CIRCADIAN CLOCK | 3 | 26 | 0.0004714 | 0.002784 |
787 | REGULATION OF P38MAPK CASCADE | 3 | 26 | 0.0004714 | 0.002784 |
788 | REGULATION OF CELL FATE COMMITMENT | 3 | 26 | 0.0004714 | 0.002784 |
789 | REGULATION OF SMOOTHENED SIGNALING PATHWAY | 4 | 62 | 0.0004933 | 0.002905 |
790 | POSITIVE REGULATION OF NUCLEAR DIVISION | 4 | 62 | 0.0004933 | 0.002905 |
791 | REGULATION OF PROTEIN SECRETION | 9 | 389 | 0.0005032 | 0.00296 |
792 | NEUROEPITHELIAL CELL DIFFERENTIATION | 4 | 63 | 0.0005244 | 0.003081 |
793 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER INVOLVED IN CELLULAR RESPONSE TO CHEMICAL STIMULUS | 3 | 27 | 0.0005281 | 0.003099 |
794 | POSITIVE REGULATION OF PRODUCTION OF MOLECULAR MEDIATOR OF IMMUNE RESPONSE | 4 | 64 | 0.0005568 | 0.003263 |
795 | POSITIVE REGULATION OF CATABOLIC PROCESS | 9 | 395 | 0.0005616 | 0.003287 |
796 | NOTCH SIGNALING PATHWAY | 5 | 114 | 0.0005776 | 0.003377 |
797 | POSITIVE REGULATION OF LEUKOCYTE APOPTOTIC PROCESS | 3 | 28 | 0.0005889 | 0.003434 |
798 | NEGATIVE REGULATION OF DENDRITE DEVELOPMENT | 3 | 28 | 0.0005889 | 0.003434 |
799 | REGULATION OF CELL ACTIVATION | 10 | 484 | 0.0005944 | 0.003462 |
800 | CELLULAR RESPONSE TO ALCOHOL | 5 | 115 | 0.0006011 | 0.003496 |
801 | SECRETION BY CELL | 10 | 486 | 0.0006136 | 0.003564 |
802 | NEURAL NUCLEUS DEVELOPMENT | 4 | 66 | 0.0006259 | 0.003631 |
803 | EPIDERMIS MORPHOGENESIS | 3 | 29 | 0.0006541 | 0.003771 |
804 | NEGATIVE REGULATION OF PRODUCTION OF MOLECULAR MEDIATOR OF IMMUNE RESPONSE | 3 | 29 | 0.0006541 | 0.003771 |
805 | ESTABLISHMENT OF PROTEIN LOCALIZATION | 19 | 1423 | 0.0006526 | 0.003771 |
806 | REGULATION OF EXTRACELLULAR MATRIX ORGANIZATION | 3 | 29 | 0.0006541 | 0.003771 |
807 | POSITIVE REGULATION OF CARDIAC MUSCLE TISSUE DEVELOPMENT | 3 | 29 | 0.0006541 | 0.003771 |
808 | REGULATION OF PEPTIDYL SERINE PHOSPHORYLATION | 5 | 118 | 0.0006757 | 0.003891 |
809 | REGULATION OF CELL JUNCTION ASSEMBLY | 4 | 68 | 0.0007008 | 0.004026 |
810 | ORGAN GROWTH | 4 | 68 | 0.0007008 | 0.004026 |
811 | SMOOTH MUSCLE CELL DIFFERENTIATION | 3 | 30 | 0.0007236 | 0.004131 |
812 | POSITIVE REGULATION OF CYTOKINE PRODUCTION INVOLVED IN IMMUNE RESPONSE | 3 | 30 | 0.0007236 | 0.004131 |
813 | MODULATION OF EXCITATORY POSTSYNAPTIC POTENTIAL | 3 | 30 | 0.0007236 | 0.004131 |
814 | REGULATION OF PROTEASOMAL PROTEIN CATABOLIC PROCESS | 6 | 181 | 0.000721 | 0.004131 |
815 | ESTABLISHMENT OF ENDOTHELIAL BARRIER | 3 | 30 | 0.0007236 | 0.004131 |
816 | POSITIVE REGULATION OF CHEMOTAXIS | 5 | 120 | 0.0007292 | 0.004158 |
817 | RESPONSE TO KETONE | 6 | 182 | 0.0007421 | 0.004226 |
818 | CELLULAR PROCESS INVOLVED IN REPRODUCTION IN MULTICELLULAR ORGANISM | 7 | 252 | 0.0007463 | 0.004245 |
819 | REGULATION OF PROTEIN KINASE B SIGNALING | 5 | 121 | 0.0007571 | 0.004301 |
820 | RESPONSE TO RADIATION | 9 | 413 | 0.0007712 | 0.004376 |
821 | RESPONSE TO METAL ION | 8 | 333 | 0.0008128 | 0.004606 |
822 | CELL SURFACE RECEPTOR SIGNALING PATHWAY INVOLVED IN CELL CELL SIGNALING | 4 | 71 | 0.0008249 | 0.004664 |
823 | ADHERENS JUNCTION ORGANIZATION | 4 | 71 | 0.0008249 | 0.004664 |
824 | ENERGY RESERVE METABOLIC PROCESS | 4 | 72 | 0.0008695 | 0.00491 |
825 | NEGATIVE REGULATION OF CYCLIN DEPENDENT PROTEIN KINASE ACTIVITY | 3 | 32 | 0.0008765 | 0.004926 |
826 | POSITIVE REGULATION OF GLIAL CELL DIFFERENTIATION | 3 | 32 | 0.0008765 | 0.004926 |
827 | PATTERNING OF BLOOD VESSELS | 3 | 32 | 0.0008765 | 0.004926 |
828 | STEROID HORMONE MEDIATED SIGNALING PATHWAY | 5 | 125 | 0.0008766 | 0.004926 |
829 | REGULATION OF CELLULAR COMPONENT SIZE | 8 | 337 | 0.0008779 | 0.004928 |
830 | MYELOID CELL DIFFERENTIATION | 6 | 189 | 0.000903 | 0.005062 |
831 | REGULATION OF PLASMA MEMBRANE ORGANIZATION | 4 | 73 | 0.0009157 | 0.005127 |
832 | REGULATION OF MYELINATION | 3 | 33 | 0.00096 | 0.005356 |
833 | EMBRYONIC DIGESTIVE TRACT DEVELOPMENT | 3 | 33 | 0.00096 | 0.005356 |
834 | RESPONSE TO VITAMIN D | 3 | 33 | 0.00096 | 0.005356 |
835 | REGULATION OF LIPID BIOSYNTHETIC PROCESS | 5 | 128 | 0.0009752 | 0.005434 |
836 | NUCLEAR IMPORT | 5 | 129 | 0.00101 | 0.00562 |
837 | RESPONSE TO FLUID SHEAR STRESS | 3 | 34 | 0.001048 | 0.005807 |
838 | HEART VALVE DEVELOPMENT | 3 | 34 | 0.001048 | 0.005807 |
839 | NEGATIVE REGULATION OF MITOTIC NUCLEAR DIVISION | 3 | 34 | 0.001048 | 0.005807 |
840 | BRAIN MORPHOGENESIS | 3 | 34 | 0.001048 | 0.005807 |
841 | GLIAL CELL DEVELOPMENT | 4 | 76 | 0.001065 | 0.005892 |
842 | NEGATIVE REGULATION OF CELLULAR AMIDE METABOLIC PROCESS | 5 | 131 | 0.001082 | 0.005978 |
843 | POSITIVE REGULATION OF NF KAPPAB TRANSCRIPTION FACTOR ACTIVITY | 5 | 132 | 0.001119 | 0.006177 |
844 | REGULATION OF GLYCOGEN METABOLIC PROCESS | 3 | 35 | 0.001142 | 0.00628 |
845 | PROTEASOMAL PROTEIN CATABOLIC PROCESS | 7 | 271 | 0.00114 | 0.00628 |
846 | RESPONSE TO IRON ION | 3 | 35 | 0.001142 | 0.00628 |
847 | POSITIVE REGULATION OF VASCULATURE DEVELOPMENT | 5 | 133 | 0.001157 | 0.006358 |
848 | NEGATIVE REGULATION OF RESPONSE TO EXTERNAL STIMULUS | 7 | 274 | 0.001214 | 0.006663 |
849 | REGULATION OF LEUKOCYTE APOPTOTIC PROCESS | 4 | 79 | 0.00123 | 0.006743 |
850 | POSITIVE REGULATION OF PROTEIN ACETYLATION | 3 | 36 | 0.00124 | 0.006773 |
851 | REGULATION OF TRANSCRIPTION REGULATORY REGION DNA BINDING | 3 | 36 | 0.00124 | 0.006773 |
852 | POSITIVE REGULATION OF CYCLIN DEPENDENT PROTEIN KINASE ACTIVITY | 3 | 36 | 0.00124 | 0.006773 |
853 | POSITIVE REGULATION OF LYMPHOCYTE DIFFERENTIATION | 4 | 80 | 0.001289 | 0.007024 |
854 | CELLULAR RESPONSE TO MECHANICAL STIMULUS | 4 | 80 | 0.001289 | 0.007024 |
855 | REGULATION OF CHROMOSOME ORGANIZATION | 7 | 278 | 0.00132 | 0.007182 |
856 | REGULATION OF HOMEOSTATIC PROCESS | 9 | 447 | 0.00134 | 0.007284 |
857 | NEGATIVE REGULATION OF GLIOGENESIS | 3 | 37 | 0.001344 | 0.007297 |
858 | POSITIVE REGULATION OF PROTEIN KINASE B SIGNALING | 4 | 81 | 0.00135 | 0.007321 |
859 | GENE SILENCING BY RNA | 5 | 139 | 0.001408 | 0.007627 |
860 | NEGATIVE REGULATION OF LEUKOCYTE DIFFERENTIATION | 4 | 82 | 0.001413 | 0.007644 |
861 | REGULATION OF LIPID METABOLIC PROCESS | 7 | 282 | 0.001432 | 0.007741 |
862 | BONE MINERALIZATION | 3 | 38 | 0.001453 | 0.007833 |
863 | CELLULAR RESPONSE TO DSRNA | 3 | 38 | 0.001453 | 0.007833 |
864 | ORGAN REGENERATION | 4 | 83 | 0.001478 | 0.007958 |
865 | POSITIVE REGULATION OF MUSCLE CELL DIFFERENTIATION | 4 | 84 | 0.001545 | 0.008299 |
866 | TISSUE MIGRATION | 4 | 84 | 0.001545 | 0.008299 |
867 | RESPONSE TO MECHANICAL STIMULUS | 6 | 210 | 0.00155 | 0.00832 |
868 | NEGATIVE REGULATION OF TRANSCRIPTION FACTOR IMPORT INTO NUCLEUS | 3 | 39 | 0.001567 | 0.008382 |
869 | REGULATION OF AXON GUIDANCE | 3 | 39 | 0.001567 | 0.008382 |
870 | REGULATION OF CELL ADHESION MEDIATED BY INTEGRIN | 3 | 39 | 0.001567 | 0.008382 |
871 | POSITIVE REGULATION OF CYTOKINE PRODUCTION | 8 | 370 | 0.001591 | 0.00849 |
872 | POSITIVE REGULATION OF SECRETION | 8 | 370 | 0.001591 | 0.00849 |
873 | POSITIVE REGULATION OF CHROMATIN MODIFICATION | 4 | 85 | 0.001614 | 0.0086 |
874 | APOPTOTIC SIGNALING PATHWAY | 7 | 289 | 0.001647 | 0.00875 |
875 | NEGATIVE REGULATION OF CELL PROJECTION ORGANIZATION | 5 | 144 | 0.001646 | 0.00875 |
876 | NEGATIVE REGULATION OF IMMUNE SYSTEM PROCESS | 8 | 372 | 0.001646 | 0.00875 |
877 | MULTI MULTICELLULAR ORGANISM PROCESS | 6 | 213 | 0.001666 | 0.008839 |
878 | ENDOCRINE PANCREAS DEVELOPMENT | 3 | 40 | 0.001687 | 0.00893 |
879 | ENDODERMAL CELL DIFFERENTIATION | 3 | 40 | 0.001687 | 0.00893 |
880 | PROTEIN LOCALIZATION TO ORGANELLE | 10 | 556 | 0.001691 | 0.008942 |
881 | RESPONSE TO IONIZING RADIATION | 5 | 145 | 0.001697 | 0.00896 |
882 | NEGATIVE REGULATION OF CELL CYCLE PROCESS | 6 | 214 | 0.001706 | 0.008999 |
883 | REGULATION OF CARBOHYDRATE BIOSYNTHETIC PROCESS | 4 | 87 | 0.001758 | 0.009264 |
884 | NEGATIVE REGULATION OF STRESS ACTIVATED MAPK CASCADE | 3 | 41 | 0.001812 | 0.009529 |
885 | NEGATIVE REGULATION OF STRESS ACTIVATED PROTEIN KINASE SIGNALING CASCADE | 3 | 41 | 0.001812 | 0.009529 |
886 | POSITIVE REGULATION OF HORMONE METABOLIC PROCESS | 2 | 11 | 0.001833 | 0.009532 |
887 | ENDOCARDIUM DEVELOPMENT | 2 | 11 | 0.001833 | 0.009532 |
888 | REGULATION OF EXTRACELLULAR MATRIX ASSEMBLY | 2 | 11 | 0.001833 | 0.009532 |
889 | NEGATIVE REGULATION OF FIBROBLAST GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 2 | 11 | 0.001833 | 0.009532 |
890 | LATERAL MESODERM DEVELOPMENT | 2 | 11 | 0.001833 | 0.009532 |
891 | LEUKOCYTE PROLIFERATION | 4 | 88 | 0.001833 | 0.009532 |
892 | NEGATIVE REGULATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY | 4 | 88 | 0.001833 | 0.009532 |
893 | EPITHELIAL TO MESENCHYMAL TRANSITION INVOLVED IN ENDOCARDIAL CUSHION FORMATION | 2 | 11 | 0.001833 | 0.009532 |
894 | POSITIVE REGULATION OF PEPTIDYL SERINE PHOSPHORYLATION | 4 | 88 | 0.001833 | 0.009532 |
895 | ENDOTHELIAL TUBE MORPHOGENESIS | 2 | 11 | 0.001833 | 0.009532 |
896 | POSITIVE REGULATION OF IMMUNE RESPONSE | 10 | 563 | 0.001854 | 0.009627 |
897 | REGULATION OF PROTEASOMAL UBIQUITIN DEPENDENT PROTEIN CATABOLIC PROCESS | 5 | 148 | 0.001856 | 0.009628 |
898 | CELLULAR RESPONSE TO STEROID HORMONE STIMULUS | 6 | 218 | 0.001873 | 0.009705 |
899 | POST EMBRYONIC DEVELOPMENT | 4 | 89 | 0.001911 | 0.009891 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | FRIZZLED BINDING | 16 | 36 | 4.964e-27 | 4.611e-24 |
2 | TRANSFORMING GROWTH FACTOR BETA RECEPTOR BINDING | 16 | 50 | 3.126e-24 | 1.452e-21 |
3 | RECEPTOR BINDING | 47 | 1476 | 3.855e-23 | 1.194e-20 |
4 | ENZYME BINDING | 46 | 1737 | 2.399e-19 | 5.573e-17 |
5 | BETA CATENIN BINDING | 13 | 84 | 2.347e-15 | 4.361e-13 |
6 | SMAD BINDING | 12 | 72 | 1.146e-14 | 1.654e-12 |
7 | KINASE BINDING | 25 | 606 | 1.246e-14 | 1.654e-12 |
8 | I SMAD BINDING | 7 | 11 | 6.726e-14 | 7.81e-12 |
9 | PROTEIN DOMAIN SPECIFIC BINDING | 24 | 624 | 2.082e-13 | 2.149e-11 |
10 | WNT ACTIVATED RECEPTOR ACTIVITY | 8 | 22 | 3.445e-13 | 3.2e-11 |
11 | GROWTH FACTOR ACTIVITY | 14 | 160 | 6.298e-13 | 5.319e-11 |
12 | G PROTEIN COUPLED RECEPTOR BINDING | 16 | 259 | 2.823e-12 | 2.185e-10 |
13 | CYTOKINE ACTIVITY | 15 | 219 | 3.226e-12 | 2.305e-10 |
14 | CYTOKINE RECEPTOR BINDING | 16 | 271 | 5.615e-12 | 3.726e-10 |
15 | WNT PROTEIN BINDING | 8 | 31 | 8.131e-12 | 5.036e-10 |
16 | GAMMA CATENIN BINDING | 6 | 12 | 3.33e-11 | 1.934e-09 |
17 | RECEPTOR SERINE THREONINE KINASE BINDING | 6 | 15 | 1.778e-10 | 9.717e-09 |
18 | RECEPTOR SIGNALING PROTEIN ACTIVITY | 12 | 172 | 4.311e-10 | 2.225e-08 |
19 | UBIQUITIN LIKE PROTEIN LIGASE BINDING | 13 | 264 | 5.582e-09 | 2.729e-07 |
20 | PROTEIN DIMERIZATION ACTIVITY | 25 | 1149 | 1.122e-08 | 5.21e-07 |
21 | MOLECULAR FUNCTION REGULATOR | 27 | 1353 | 1.607e-08 | 7.107e-07 |
22 | RECEPTOR AGONIST ACTIVITY | 5 | 16 | 2.722e-08 | 1.15e-06 |
23 | TRANSMEMBRANE RECEPTOR PROTEIN SERINE THREONINE KINASE ACTIVITY | 5 | 17 | 3.838e-08 | 1.55e-06 |
24 | PDZ DOMAIN BINDING | 8 | 90 | 5.985e-08 | 2.317e-06 |
25 | TRANSCRIPTION FACTOR BINDING | 16 | 524 | 7.797e-08 | 2.897e-06 |
26 | PROTEIN HETERODIMERIZATION ACTIVITY | 15 | 468 | 1.101e-07 | 3.935e-06 |
27 | IONOTROPIC GLUTAMATE RECEPTOR BINDING | 5 | 23 | 2.029e-07 | 6.981e-06 |
28 | PROTEIN SERINE THREONINE KINASE ACTIVITY | 14 | 445 | 3.772e-07 | 1.251e-05 |
29 | KINASE ACTIVITY | 19 | 842 | 4.803e-07 | 1.536e-05 |
30 | MACROMOLECULAR COMPLEX BINDING | 25 | 1399 | 4.96e-07 | 1.536e-05 |
31 | SIGNAL TRANSDUCER ACTIVITY | 28 | 1731 | 6.689e-07 | 2.004e-05 |
32 | PROTEIN KINASE ACTIVITY | 16 | 640 | 1.131e-06 | 3.277e-05 |
33 | RECEPTOR ACTIVATOR ACTIVITY | 5 | 32 | 1.164e-06 | 3.277e-05 |
34 | RECEPTOR SIGNALING PROTEIN SERINE THREONINE KINASE ACTIVITY | 7 | 92 | 1.204e-06 | 3.29e-05 |
35 | PROTEIN C TERMINUS BINDING | 9 | 186 | 1.604e-06 | 4.258e-05 |
36 | IDENTICAL PROTEIN BINDING | 22 | 1209 | 2.026e-06 | 5.229e-05 |
37 | PROTEIN COMPLEX BINDING | 19 | 935 | 2.284e-06 | 5.735e-05 |
38 | GLUTAMATE RECEPTOR BINDING | 5 | 37 | 2.461e-06 | 6.016e-05 |
39 | PHOSPHATASE BINDING | 8 | 162 | 5.359e-06 | 0.0001251 |
40 | TRANSFERASE ACTIVITY TRANSFERRING PHOSPHORUS CONTAINING GROUPS | 19 | 992 | 5.385e-06 | 0.0001251 |
41 | REGULATORY REGION NUCLEIC ACID BINDING | 17 | 818 | 6.166e-06 | 0.0001397 |
42 | PROTEIN PHOSPHATASE TYPE 2A REGULATOR ACTIVITY | 4 | 21 | 6.377e-06 | 0.000141 |
43 | RECEPTOR REGULATOR ACTIVITY | 5 | 45 | 6.642e-06 | 0.0001435 |
44 | R SMAD BINDING | 4 | 23 | 9.349e-06 | 0.0001974 |
45 | CORE PROMOTER PROXIMAL REGION DNA BINDING | 11 | 371 | 1.255e-05 | 0.0002591 |
46 | CYTOKINE BINDING | 6 | 92 | 1.751e-05 | 0.0003535 |
47 | TRANSCRIPTION FACTOR ACTIVITY RNA POLYMERASE II CORE PROMOTER PROXIMAL REGION SEQUENCE SPECIFIC BINDING | 10 | 328 | 2.5e-05 | 0.0004942 |
48 | GLYCOPROTEIN BINDING | 6 | 101 | 2.98e-05 | 0.0005768 |
49 | RNA POLYMERASE II TRANSCRIPTION FACTOR BINDING | 6 | 104 | 3.517e-05 | 0.0006668 |
50 | GUANYLATE KINASE ACTIVITY | 3 | 12 | 4.237e-05 | 0.0007718 |
51 | CO SMAD BINDING | 3 | 12 | 4.237e-05 | 0.0007718 |
52 | ENZYME REGULATOR ACTIVITY | 17 | 959 | 4.727e-05 | 0.0008444 |
53 | ION CHANNEL BINDING | 6 | 111 | 5.076e-05 | 0.0008897 |
54 | ARMADILLO REPEAT DOMAIN BINDING | 3 | 13 | 5.484e-05 | 0.0009435 |
55 | TRANSCRIPTIONAL ACTIVATOR ACTIVITY RNA POLYMERASE II CORE PROMOTER PROXIMAL REGION SEQUENCE SPECIFIC BINDING | 8 | 226 | 5.915e-05 | 0.000999 |
56 | TRANSFORMING GROWTH FACTOR BETA BINDING | 3 | 16 | 0.000106 | 0.001759 |
57 | TRANSMEMBRANE RECEPTOR PROTEIN KINASE ACTIVITY | 5 | 81 | 0.0001176 | 0.001903 |
58 | CELL ADHESION MOLECULE BINDING | 7 | 186 | 0.0001188 | 0.001903 |
59 | PHOSPHATASE REGULATOR ACTIVITY | 5 | 87 | 0.000165 | 0.002597 |
60 | NUCLEIC ACID BINDING TRANSCRIPTION FACTOR ACTIVITY | 18 | 1199 | 0.0002287 | 0.003541 |
61 | CHROMATIN BINDING | 10 | 435 | 0.0002573 | 0.003919 |
62 | PROTEIN HOMODIMERIZATION ACTIVITY | 13 | 722 | 0.0003387 | 0.005013 |
63 | RNA POLYMERASE II TRANSCRIPTION FACTOR ACTIVITY SEQUENCE SPECIFIC DNA BINDING | 12 | 629 | 0.0003453 | 0.005013 |
64 | TRANSCRIPTION COREPRESSOR ACTIVITY | 7 | 221 | 0.0003417 | 0.005013 |
65 | PROTEIN PHOSPHORYLATED AMINO ACID BINDING | 3 | 24 | 0.0003702 | 0.00521 |
66 | NUCLEOTIDE KINASE ACTIVITY | 3 | 24 | 0.0003702 | 0.00521 |
67 | PROTEIN SERINE THREONINE PHOSPHATASE ACTIVITY | 4 | 64 | 0.0005568 | 0.00772 |
68 | TRANSCRIPTIONAL ACTIVATOR ACTIVITY RNA POLYMERASE II TRANSCRIPTION REGULATORY REGION SEQUENCE SPECIFIC BINDING | 8 | 315 | 0.000566 | 0.007732 |
69 | DOUBLE STRANDED DNA BINDING | 13 | 764 | 0.0005775 | 0.007775 |
70 | CADHERIN BINDING | 3 | 28 | 0.0005889 | 0.007816 |
71 | PHOSPHOPROTEIN PHOSPHATASE ACTIVITY | 6 | 178 | 0.0006607 | 0.008645 |
72 | PROTEIN PHOSPHATASE BINDING | 5 | 120 | 0.0007292 | 0.009279 |
73 | TRANSCRIPTION FACTOR ACTIVITY PROTEIN BINDING | 11 | 588 | 0.0007217 | 0.009279 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | APICAL JUNCTION COMPLEX | 18 | 128 | 4.334e-20 | 2.531e-17 |
2 | CELL JUNCTION | 35 | 1151 | 2.716e-16 | 5.286e-14 |
3 | WNT SIGNALOSOME | 8 | 11 | 1.876e-16 | 5.286e-14 |
4 | CELL CELL JUNCTION | 21 | 383 | 8.541e-15 | 1.247e-12 |
5 | EXTRACELLULAR MATRIX | 21 | 426 | 6.899e-14 | 8.058e-12 |
6 | EXTRACELLULAR SPACE | 32 | 1376 | 1.009e-11 | 9.819e-10 |
7 | PROTEINACEOUS EXTRACELLULAR MATRIX | 17 | 356 | 3.377e-11 | 2.818e-09 |
8 | PHOSPHATASE COMPLEX | 8 | 48 | 3.579e-10 | 2.322e-08 |
9 | CYTOPLASMIC VESICLE PART | 20 | 601 | 3.455e-10 | 2.322e-08 |
10 | ANCHORING JUNCTION | 18 | 489 | 5.88e-10 | 3.434e-08 |
11 | PROTEIN PHOSPHATASE TYPE 2A COMPLEX | 6 | 20 | 1.344e-09 | 7.137e-08 |
12 | BETA CATENIN DESTRUCTION COMPLEX | 5 | 14 | 1.26e-08 | 6.13e-07 |
13 | CELL SURFACE | 20 | 757 | 1.766e-08 | 7.933e-07 |
14 | VESICLE MEMBRANE | 16 | 512 | 5.675e-08 | 2.21e-06 |
15 | PLASMA MEMBRANE PROTEIN COMPLEX | 16 | 510 | 5.378e-08 | 2.21e-06 |
16 | INTRACELLULAR VESICLE | 25 | 1259 | 6.726e-08 | 2.455e-06 |
17 | CELL SUBSTRATE JUNCTION | 14 | 398 | 9.714e-08 | 3.337e-06 |
18 | MEMBRANE MICRODOMAIN | 12 | 288 | 1.388e-07 | 4.505e-06 |
19 | CELL CORTEX | 11 | 238 | 1.682e-07 | 5.169e-06 |
20 | TRANSCRIPTION FACTOR COMPLEX | 12 | 298 | 2.006e-07 | 5.859e-06 |
21 | CELL BODY | 15 | 494 | 2.208e-07 | 6.141e-06 |
22 | LATERAL PLASMA MEMBRANE | 6 | 50 | 4.771e-07 | 1.267e-05 |
23 | CYTOSKELETON | 30 | 1967 | 8.358e-07 | 2.122e-05 |
24 | PLASMA MEMBRANE RECEPTOR COMPLEX | 9 | 175 | 9.66e-07 | 2.351e-05 |
25 | CYTOPLASMIC REGION | 11 | 287 | 1.078e-06 | 2.519e-05 |
26 | SOMATODENDRITIC COMPARTMENT | 16 | 650 | 1.384e-06 | 3.014e-05 |
27 | GOLGI LUMEN | 7 | 94 | 1.393e-06 | 3.014e-05 |
28 | NEURON PROJECTION | 19 | 942 | 2.548e-06 | 5.313e-05 |
29 | ENDOCYTIC VESICLE MEMBRANE | 8 | 152 | 3.34e-06 | 6.727e-05 |
30 | MICROTUBULE CYTOSKELETON | 20 | 1068 | 4.134e-06 | 8.047e-05 |
31 | AXON | 12 | 418 | 6.875e-06 | 0.0001295 |
32 | CYTOSKELETAL PART | 23 | 1436 | 9.602e-06 | 0.0001752 |
33 | MEMBRANE REGION | 20 | 1134 | 1.006e-05 | 0.000178 |
34 | PLASMA MEMBRANE RAFT | 6 | 86 | 1.188e-05 | 0.000204 |
35 | NEURON PART | 21 | 1265 | 1.466e-05 | 0.0002446 |
36 | CELL CELL ADHERENS JUNCTION | 5 | 54 | 1.648e-05 | 0.0002674 |
37 | ENDOCYTIC VESICLE | 9 | 256 | 2.129e-05 | 0.000336 |
38 | RECEPTOR COMPLEX | 10 | 327 | 2.436e-05 | 0.0003744 |
39 | CELL PROJECTION | 25 | 1786 | 3.672e-05 | 0.0005498 |
40 | CELL LEADING EDGE | 10 | 350 | 4.332e-05 | 0.0006325 |
41 | CHROMOSOME | 16 | 880 | 5.985e-05 | 0.0008524 |
42 | MICROTUBULE ORGANIZING CENTER | 13 | 623 | 7.978e-05 | 0.001109 |
43 | SPINDLE POLE | 6 | 126 | 0.0001028 | 0.001396 |
44 | PLASMA MEMBRANE REGION | 16 | 929 | 0.0001127 | 0.001496 |
45 | CELL PROJECTION PART | 16 | 946 | 0.0001389 | 0.001802 |
46 | EXTRINSIC COMPONENT OF PLASMA MEMBRANE | 6 | 136 | 0.0001563 | 0.001985 |
47 | PROTEIN KINASE COMPLEX | 5 | 90 | 0.0001935 | 0.002404 |
48 | AXONAL GROWTH CONE | 3 | 20 | 0.0002121 | 0.002581 |
49 | INTERCALATED DISC | 4 | 51 | 0.0002323 | 0.002768 |
50 | SITE OF POLARIZED GROWTH | 6 | 149 | 0.0002566 | 0.002997 |
51 | NUCLEAR CHROMOSOME | 11 | 523 | 0.0002708 | 0.003101 |
52 | CHROMATIN | 10 | 441 | 0.0002869 | 0.003223 |
53 | PLATELET ALPHA GRANULE LUMEN | 4 | 55 | 0.0003113 | 0.00343 |
54 | RNA POLYMERASE II TRANSCRIPTION FACTOR COMPLEX | 5 | 101 | 0.0003312 | 0.003493 |
55 | NUCLEAR CHROMATIN | 8 | 291 | 0.0003349 | 0.003493 |
56 | MEMBRANE PROTEIN COMPLEX | 16 | 1020 | 0.0003247 | 0.003493 |
57 | DENDRITE | 10 | 451 | 0.0003426 | 0.00351 |
58 | CYTOPLASMIC MICROTUBULE | 4 | 57 | 0.0003573 | 0.003598 |
59 | CATALYTIC COMPLEX | 16 | 1038 | 0.0003939 | 0.003899 |
60 | MYELIN SHEATH | 6 | 168 | 0.0004873 | 0.004743 |
61 | CELL CELL CONTACT ZONE | 4 | 64 | 0.0005568 | 0.005245 |
62 | LAMELLIPODIUM | 6 | 172 | 0.0005517 | 0.005245 |
63 | GOLGI APPARATUS | 19 | 1445 | 0.0007852 | 0.007165 |
64 | ACTIN FILAMENT | 4 | 70 | 0.000782 | 0.007165 |
65 | CYCLIN DEPENDENT PROTEIN KINASE HOLOENZYME COMPLEX | 3 | 31 | 0.0007977 | 0.007167 |
66 | NUCLEAR TRANSCRIPTION FACTOR COMPLEX | 5 | 127 | 0.0009415 | 0.008331 |
67 | PLATELET ALPHA GRANULE | 4 | 75 | 0.001013 | 0.008833 |
68 | EXCITATORY SYNAPSE | 6 | 197 | 0.001118 | 0.009606 |
Num | Pathway | Pathview | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|---|
1 | hsa04390_Hippo_signaling_pathway | 118 | 154 | 3.532e-278 | 6.358e-276 | |
2 | hsa04310_Wnt_signaling_pathway | 43 | 151 | 1.626e-62 | 1.463e-60 | |
3 | hsa04350_TGF.beta_signaling_pathway | 27 | 85 | 2.239e-40 | 1.344e-38 | |
4 | hsa04340_Hedgehog_signaling_pathway | 23 | 56 | 1.491e-37 | 6.711e-36 | |
5 | hsa04916_Melanogenesis | 26 | 101 | 3.848e-36 | 1.385e-34 | |
6 | hsa04530_Tight_junction | 18 | 133 | 8.862e-20 | 2.659e-18 | |
7 | hsa04110_Cell_cycle | 17 | 128 | 1.379e-18 | 3.546e-17 | |
8 | hsa04520_Adherens_junction | 14 | 73 | 7.735e-18 | 1.74e-16 | |
9 | hsa04114_Oocyte_meiosis | 13 | 114 | 1.403e-13 | 2.806e-12 | |
10 | hsa04151_PI3K_AKT_signaling_pathway | 18 | 351 | 2.576e-12 | 4.637e-11 | |
11 | hsa04144_Endocytosis | 14 | 203 | 1.623e-11 | 2.656e-10 | |
12 | hsa04722_Neurotrophin_signaling_pathway | 8 | 127 | 8.634e-07 | 1.295e-05 | |
13 | hsa04510_Focal_adhesion | 9 | 200 | 2.918e-06 | 4.04e-05 | |
14 | hsa04115_p53_signaling_pathway | 6 | 69 | 3.286e-06 | 4.225e-05 | |
15 | hsa03015_mRNA_surveillance_pathway | 6 | 83 | 9.674e-06 | 0.0001161 | |
16 | hsa04810_Regulation_of_actin_cytoskeleton | 8 | 214 | 4.024e-05 | 0.0004528 | |
17 | hsa04010_MAPK_signaling_pathway | 8 | 268 | 0.0001922 | 0.002035 | |
18 | hsa04710_Circadian_rhythm_._mammal | 3 | 23 | 0.0003253 | 0.003253 | |
19 | hsa04670_Leukocyte_transendothelial_migration | 5 | 117 | 0.0006501 | 0.006159 | |
20 | hsa04910_Insulin_signaling_pathway | 5 | 138 | 0.001364 | 0.01227 | |
21 | hsa04380_Osteoclast_differentiation | 4 | 128 | 0.007007 | 0.06006 | |
22 | hsa04730_Long.term_depression | 3 | 70 | 0.008224 | 0.06729 | |
23 | hsa04630_Jak.STAT_signaling_pathway | 4 | 155 | 0.01347 | 0.1054 | |
24 | hsa04012_ErbB_signaling_pathway | 3 | 87 | 0.01482 | 0.1111 | |
25 | hsa04330_Notch_signaling_pathway | 2 | 47 | 0.0314 | 0.2261 | |
26 | hsa04720_Long.term_potentiation | 2 | 70 | 0.06431 | 0.4333 | |
27 | hsa04145_Phagosome | 3 | 156 | 0.065 | 0.4333 | |
28 | hsa04062_Chemokine_signaling_pathway | 3 | 189 | 0.1012 | 0.6509 | |
29 | hsa04660_T_cell_receptor_signaling_pathway | 2 | 108 | 0.1336 | 0.8292 | |
30 | hsa04270_Vascular_smooth_muscle_contraction | 2 | 116 | 0.1498 | 0.8985 | |
31 | hsa04514_Cell_adhesion_molecules_.CAMs. | 2 | 136 | 0.1916 | 1 | |
32 | hsa04120_Ubiquitin_mediated_proteolysis | 2 | 139 | 0.198 | 1 | |
33 | hsa04014_Ras_signaling_pathway | 2 | 236 | 0.4067 | 1 |
Num | lncRNA | miRNAs | miRNAs count | Gene | Sponge regulatory network | lncRNA log2FC | lncRNA pvalue | Gene log2FC | Gene pvalue | lncRNA-gene Pearson correlation |
---|---|---|---|---|---|---|---|---|---|---|
1 | RP11-815I9.4 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-103a-3p;hsa-miR-10b-5p;hsa-miR-15a-5p;hsa-miR-181b-5p;hsa-miR-193a-3p;hsa-miR-19b-1-5p;hsa-miR-29a-5p;hsa-miR-320a;hsa-miR-590-5p | 11 | LATS1 | Sponge network | 0.004 | 0.98116 | -0.188 | 0.29287 | 0.818 |
2 | MAGI2-AS3 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-let-7g-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-224-3p;hsa-miR-25-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-33a-3p;hsa-miR-3934-5p;hsa-miR-429;hsa-miR-452-5p;hsa-miR-454-3p;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-629-3p;hsa-miR-7-1-3p;hsa-miR-708-5p;hsa-miR-92a-3p;hsa-miR-940 | 33 | FZD4 | Sponge network | -0.939 | 4.0E-5 | -0.816 | 0 | 0.755 |
3 | MAGI2-AS3 |
hsa-let-7a-3p;hsa-miR-103a-3p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-205-5p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-26b-3p;hsa-miR-29a-5p;hsa-miR-429;hsa-miR-582-5p;hsa-miR-590-3p;hsa-miR-944 | 15 | AXIN2 | Sponge network | -0.939 | 4.0E-5 | -0.655 | 0.00118 | 0.682 |
4 | MAGI2-AS3 |
hsa-miR-149-5p;hsa-miR-16-2-3p;hsa-miR-18a-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-26b-3p;hsa-miR-26b-5p;hsa-miR-590-3p;hsa-miR-7-1-3p | 10 | CTGF | Sponge network | -0.939 | 4.0E-5 | -0.7 | 0.00294 | 0.659 |
5 | RP11-815I9.4 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-26a-2-3p;hsa-miR-26b-5p;hsa-miR-29a-5p;hsa-miR-301a-3p;hsa-miR-30c-5p;hsa-miR-320a;hsa-miR-590-5p;hsa-miR-671-5p | 17 | BMPR2 | Sponge network | 0.004 | 0.98116 | -0.139 | 0.18459 | 0.606 |
6 | RP11-166D19.1 |
hsa-let-7a-3p;hsa-let-7g-3p;hsa-miR-141-3p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-224-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-324-3p;hsa-miR-33a-3p;hsa-miR-3934-5p;hsa-miR-429;hsa-miR-452-5p;hsa-miR-454-3p;hsa-miR-455-3p;hsa-miR-484;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-5p;hsa-miR-629-3p;hsa-miR-7-1-3p;hsa-miR-92a-3p;hsa-miR-940 | 30 | FZD4 | Sponge network | -0.882 | 5.0E-5 | -0.816 | 0 | 0.603 |
7 | LINC00702 |
hsa-let-7g-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-3p;hsa-miR-17-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-224-3p;hsa-miR-25-3p;hsa-miR-301a-3p;hsa-miR-3065-3p;hsa-miR-324-3p;hsa-miR-33a-3p;hsa-miR-3934-5p;hsa-miR-454-3p;hsa-miR-484;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-629-3p;hsa-miR-7-1-3p;hsa-miR-92a-3p;hsa-miR-92b-3p;hsa-miR-940 | 30 | FZD4 | Sponge network | -0.573 | 0.0699 | -0.816 | 0 | 0.568 |
8 | RP11-815I9.4 |
hsa-let-7a-3p;hsa-miR-103a-3p;hsa-miR-130a-3p;hsa-miR-146b-5p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-29b-3p;hsa-miR-301a-3p;hsa-miR-320a;hsa-miR-576-5p;hsa-miR-664a-3p | 16 | TEAD1 | Sponge network | 0.004 | 0.98116 | -0.582 | 1.0E-5 | 0.567 |
9 | MAGI2-AS3 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-16-1-3p;hsa-miR-205-5p;hsa-miR-21-3p;hsa-miR-221-3p;hsa-miR-2355-3p;hsa-miR-330-5p;hsa-miR-342-3p;hsa-miR-576-5p;hsa-miR-629-3p;hsa-miR-7-1-3p;hsa-miR-766-3p;hsa-miR-944 | 14 | AMOT | Sponge network | -0.939 | 4.0E-5 | -3.271 | 0 | 0.562 |
10 | RP11-774O3.3 |
hsa-miR-1301-3p;hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-23a-3p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-320b;hsa-miR-33a-5p;hsa-miR-421;hsa-miR-576-5p;hsa-miR-7-1-3p;hsa-miR-93-3p;hsa-miR-944 | 24 | DLG2 | Sponge network | -1.712 | 0 | -4.457 | 0 | 0.558 |
11 | RP11-389C8.2 |
hsa-let-7a-3p;hsa-miR-141-3p;hsa-miR-17-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-224-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-3065-3p;hsa-miR-429;hsa-miR-589-3p | 12 | FZD4 | Sponge network | 0.187 | 0.31051 | -0.816 | 0 | 0.54 |
12 | EMX2OS |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-let-7g-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-224-3p;hsa-miR-25-3p;hsa-miR-301a-3p;hsa-miR-3065-3p;hsa-miR-324-3p;hsa-miR-33a-3p;hsa-miR-3934-5p;hsa-miR-454-3p;hsa-miR-484;hsa-miR-505-5p;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-3p;hsa-miR-629-3p;hsa-miR-7-1-3p;hsa-miR-708-5p;hsa-miR-92a-3p;hsa-miR-92b-3p;hsa-miR-940 | 35 | FZD4 | Sponge network | -1.459 | 1.0E-5 | -0.816 | 0 | 0.538 |
13 | TPTEP1 |
hsa-let-7a-3p;hsa-miR-16-1-3p;hsa-miR-205-5p;hsa-miR-21-3p;hsa-miR-221-3p;hsa-miR-2355-3p;hsa-miR-342-3p;hsa-miR-576-5p;hsa-miR-627-5p;hsa-miR-629-3p;hsa-miR-944 | 11 | AMOT | Sponge network | -2.193 | 0 | -3.271 | 0 | 0.526 |
14 | LINC00330 |
hsa-miR-1301-3p;hsa-miR-130a-3p;hsa-miR-130b-5p;hsa-miR-146b-5p;hsa-miR-148b-5p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-205-5p;hsa-miR-22-5p;hsa-miR-29b-1-5p;hsa-miR-320a;hsa-miR-320b;hsa-miR-374b-3p;hsa-miR-576-5p;hsa-miR-708-3p;hsa-miR-93-3p | 16 | DLG2 | Sponge network | -6.523 | 0 | -4.457 | 0 | 0.525 |
15 | RP11-517P14.2 |
hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-93-5p | 12 | BMPR2 | Sponge network | -0.402 | 0.1503 | -0.139 | 0.18459 | 0.52 |
16 | RP11-193H5.1 |
hsa-miR-103a-3p;hsa-miR-130a-3p;hsa-miR-141-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-20a-5p;hsa-miR-25-3p;hsa-miR-29b-2-5p;hsa-miR-29b-3p;hsa-miR-301a-3p;hsa-miR-320a;hsa-miR-576-5p;hsa-miR-7-1-3p | 17 | TEAD1 | Sponge network | -0.426 | 0.01062 | -0.582 | 1.0E-5 | 0.513 |
17 | MEG3 |
hsa-let-7f-1-3p;hsa-miR-106b-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-224-3p;hsa-miR-27a-3p;hsa-miR-324-3p;hsa-miR-33a-3p;hsa-miR-3934-5p;hsa-miR-429;hsa-miR-452-5p;hsa-miR-455-3p;hsa-miR-629-3p;hsa-miR-7-1-3p | 17 | FZD4 | Sponge network | -0.286 | 0.30726 | -0.816 | 0 | 0.51 |
18 | RP11-594N15.3 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-141-3p;hsa-miR-15a-5p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-484;hsa-miR-940 | 14 | FZD4 | Sponge network | -2.86 | 0 | -0.816 | 0 | 0.499 |
19 | AC007743.1 |
hsa-let-7a-3p;hsa-miR-16-1-3p;hsa-miR-205-5p;hsa-miR-221-3p;hsa-miR-2355-3p;hsa-miR-342-3p;hsa-miR-627-5p;hsa-miR-629-3p;hsa-miR-7-1-3p;hsa-miR-766-3p | 10 | AMOT | Sponge network | -1.053 | 0.00923 | -3.271 | 0 | 0.498 |
20 | DNM3OS |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-141-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-3p;hsa-miR-17-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-224-3p;hsa-miR-27a-3p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-590-5p;hsa-miR-7-1-3p | 16 | FZD4 | Sponge network | 0.932 | 0.00442 | -0.816 | 0 | 0.495 |
21 | SH3RF3-AS1 |
hsa-let-7a-3p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-205-5p;hsa-miR-222-3p;hsa-miR-26b-3p;hsa-miR-29a-5p;hsa-miR-582-5p | 10 | AXIN2 | Sponge network | -0.175 | 0.58985 | -0.655 | 0.00118 | 0.494 |
22 | LINC00900 |
hsa-miR-1301-3p;hsa-miR-130a-3p;hsa-miR-130b-5p;hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-23a-3p;hsa-miR-25-3p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-3127-5p;hsa-miR-320a;hsa-miR-320b;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-505-5p;hsa-miR-576-5p;hsa-miR-590-5p;hsa-miR-7-1-3p;hsa-miR-708-3p;hsa-miR-769-3p;hsa-miR-92a-3p;hsa-miR-92b-3p | 30 | DLG2 | Sponge network | -1.803 | 0 | -4.457 | 0 | 0.489 |
23 | RP5-1198O20.4 | hsa-miR-125a-5p;hsa-miR-140-3p;hsa-miR-217;hsa-miR-28-5p;hsa-miR-30a-5p;hsa-miR-328-3p;hsa-miR-335-3p;hsa-miR-374a-3p;hsa-miR-582-3p;hsa-miR-664a-3p | 10 | YWHAZ | Sponge network | 0.114 | 0.54508 | 0.345 | 0.0016 | 0.481 |
24 | SH3RF3-AS1 |
hsa-let-7a-3p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-505-5p;hsa-miR-576-5p;hsa-miR-590-5p;hsa-miR-7-1-3p | 10 | FZD4 | Sponge network | -0.175 | 0.58985 | -0.816 | 0 | 0.475 |
25 | RP11-760H22.2 | hsa-miR-1301-3p;hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-15b-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-708-3p;hsa-miR-944 | 14 | DLG2 | Sponge network | -2.79 | 0 | -4.457 | 0 | 0.471 |
26 | ZNF667-AS1 |
hsa-miR-141-3p;hsa-miR-15a-5p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-224-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-452-5p;hsa-miR-484;hsa-miR-589-3p;hsa-miR-590-5p;hsa-miR-629-3p | 14 | FZD4 | Sponge network | -1.395 | 0 | -0.816 | 0 | 0.471 |
27 | SNHG14 |
hsa-miR-141-3p;hsa-miR-15a-5p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-3934-5p;hsa-miR-452-5p;hsa-miR-454-3p;hsa-miR-455-3p;hsa-miR-484;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-629-3p;hsa-miR-92a-3p | 17 | FZD4 | Sponge network | -1.125 | 0.0001 | -0.816 | 0 | 0.469 |
28 | AC006116.24 |
hsa-miR-103a-3p;hsa-miR-130a-3p;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-224-5p;hsa-miR-301a-3p;hsa-miR-454-3p;hsa-miR-93-5p | 15 | TEAD1 | Sponge network | -1.832 | 1.0E-5 | -0.582 | 1.0E-5 | 0.468 |
29 | AC006116.24 |
hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-342-3p;hsa-miR-454-3p;hsa-miR-93-5p | 15 | BMPR2 | Sponge network | -1.832 | 1.0E-5 | -0.139 | 0.18459 | 0.468 |
30 | AC007743.1 |
hsa-let-7a-3p;hsa-miR-15a-5p;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-589-3p;hsa-miR-590-5p;hsa-miR-629-3p;hsa-miR-7-1-3p;hsa-miR-92a-3p | 12 | FZD4 | Sponge network | -1.053 | 0.00923 | -0.816 | 0 | 0.465 |
31 | RP11-193H5.1 |
hsa-miR-103a-2-5p;hsa-miR-125a-5p;hsa-miR-130a-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-20a-5p;hsa-miR-25-3p;hsa-miR-26a-2-3p;hsa-miR-26b-5p;hsa-miR-29a-5p;hsa-miR-301a-3p;hsa-miR-320a;hsa-miR-374a-3p;hsa-miR-671-5p;hsa-miR-7-1-3p;hsa-miR-93-3p | 20 | BMPR2 | Sponge network | -0.426 | 0.01062 | -0.139 | 0.18459 | 0.465 |
32 | HCG22 | hsa-miR-1301-3p;hsa-miR-130b-5p;hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-22-5p;hsa-miR-25-3p;hsa-miR-7-1-3p;hsa-miR-93-3p | 10 | DLG2 | Sponge network | -4.567 | 0 | -4.457 | 0 | 0.462 |
33 | RP1-193H18.2 |
hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-205-5p;hsa-miR-22-5p;hsa-miR-23a-3p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-421;hsa-miR-511-5p;hsa-miR-576-5p;hsa-miR-708-3p;hsa-miR-944 | 16 | DLG2 | Sponge network | -1.539 | 0 | -4.457 | 0 | 0.461 |
34 | MAGI2-AS3 |
hsa-miR-103a-3p;hsa-miR-130b-5p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-188-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-25-3p;hsa-miR-30c-5p;hsa-miR-33a-3p;hsa-miR-342-3p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-92a-3p;hsa-miR-93-5p | 16 | LATS2 | Sponge network | -0.939 | 4.0E-5 | -0.377 | 0.00275 | 0.459 |
35 | RP11-166D19.1 |
hsa-let-7a-3p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-205-5p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-26b-3p;hsa-miR-429;hsa-miR-944 | 11 | AXIN2 | Sponge network | -0.882 | 5.0E-5 | -0.655 | 0.00118 | 0.459 |
36 | AC003090.1 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-141-3p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-452-5p;hsa-miR-576-5p;hsa-miR-590-5p;hsa-miR-629-3p;hsa-miR-7-1-3p;hsa-miR-708-5p;hsa-miR-940 | 20 | FZD4 | Sponge network | -4.323 | 0 | -0.816 | 0 | 0.457 |
37 | EMX2OS |
hsa-let-7a-3p;hsa-miR-103a-3p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-205-5p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-26b-3p;hsa-miR-29a-5p;hsa-miR-34a-5p;hsa-miR-590-3p;hsa-miR-944 | 14 | AXIN2 | Sponge network | -1.459 | 1.0E-5 | -0.655 | 0.00118 | 0.456 |
38 | FGF14-AS2 | hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-23a-3p;hsa-miR-27a-5p;hsa-miR-29b-1-5p | 11 | DLG2 | Sponge network | -1.914 | 0 | -4.457 | 0 | 0.455 |
39 | RP11-150O12.1 | hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-140-3p;hsa-miR-140-5p;hsa-miR-20b-5p;hsa-miR-217;hsa-miR-29b-2-5p;hsa-miR-30a-5p;hsa-miR-30d-5p;hsa-miR-30e-5p | 10 | FRMD6 | Sponge network | 1.523 | 0 | 0.249 | 0.05024 | 0.454 |
40 | APCDD1L-AS1 |
hsa-miR-107;hsa-miR-126-5p;hsa-miR-140-5p;hsa-miR-148b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-330-3p;hsa-miR-335-3p;hsa-miR-375;hsa-miR-532-5p;hsa-miR-9-5p | 11 | SNAI2 | Sponge network | 2.077 | 0 | 1.574 | 0 | 0.453 |
41 | CTC-429P9.5 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-29a-5p;hsa-miR-301a-3p;hsa-miR-454-3p | 12 | BMPR2 | Sponge network | -0.72 | 0.01036 | -0.139 | 0.18459 | 0.453 |
42 | MAGI2-AS3 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130a-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-205-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-25-3p;hsa-miR-26b-5p;hsa-miR-29a-5p;hsa-miR-301a-3p;hsa-miR-30c-5p;hsa-miR-320a;hsa-miR-33a-5p;hsa-miR-342-3p;hsa-miR-3607-3p;hsa-miR-429;hsa-miR-454-3p;hsa-miR-582-3p;hsa-miR-582-5p;hsa-miR-590-3p;hsa-miR-651-5p;hsa-miR-671-5p;hsa-miR-7-1-3p;hsa-miR-92a-3p;hsa-miR-93-3p;hsa-miR-93-5p | 36 | BMPR2 | Sponge network | -0.939 | 4.0E-5 | -0.139 | 0.18459 | 0.452 |
43 | MIR497HG |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-141-3p;hsa-miR-17-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-224-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-3065-3p;hsa-miR-33a-3p;hsa-miR-455-3p;hsa-miR-589-3p;hsa-miR-590-5p;hsa-miR-7-1-3p | 16 | FZD4 | Sponge network | -1.263 | 0.00248 | -0.816 | 0 | 0.451 |
44 | PWAR6 |
hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-23a-3p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-576-5p;hsa-miR-944 | 15 | DLG2 | Sponge network | -1.629 | 0 | -4.457 | 0 | 0.448 |
45 | CTC-429P9.5 |
hsa-let-7a-3p;hsa-miR-103a-3p;hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-425-5p;hsa-miR-454-3p | 12 | TEAD1 | Sponge network | -0.72 | 0.01036 | -0.582 | 1.0E-5 | 0.443 |
46 | RP1-193H18.2 |
hsa-let-7a-3p;hsa-miR-130a-3p;hsa-miR-18a-5p;hsa-miR-19a-3p;hsa-miR-21-3p;hsa-miR-224-5p;hsa-miR-2355-5p;hsa-miR-27a-3p;hsa-miR-450b-5p;hsa-miR-576-5p | 10 | SMAD4 | Sponge network | -1.539 | 0 | -0.43 | 0 | 0.443 |
47 | LINC00702 |
hsa-miR-103a-3p;hsa-miR-130b-5p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-25-3p;hsa-miR-27b-3p;hsa-miR-30d-5p;hsa-miR-33a-3p;hsa-miR-590-3p;hsa-miR-92a-3p;hsa-miR-93-5p;hsa-miR-96-5p | 15 | LATS2 | Sponge network | -0.573 | 0.0699 | -0.377 | 0.00275 | 0.44 |
48 | RP11-282O18.3 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-26b-5p;hsa-miR-301a-3p;hsa-miR-590-5p | 12 | BMPR2 | Sponge network | -0.266 | 0.05794 | -0.139 | 0.18459 | 0.439 |
49 | PWAR6 |
hsa-miR-141-3p;hsa-miR-15a-5p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-224-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-452-5p;hsa-miR-454-3p;hsa-miR-455-3p;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-629-3p | 15 | FZD4 | Sponge network | -1.629 | 0 | -0.816 | 0 | 0.438 |
50 | LINC00707 |
hsa-miR-195-3p;hsa-miR-217;hsa-miR-28-5p;hsa-miR-30a-5p;hsa-miR-30b-5p;hsa-miR-30c-5p;hsa-miR-30d-5p;hsa-miR-30e-5p;hsa-miR-328-3p;hsa-miR-335-3p;hsa-miR-374a-3p;hsa-miR-378a-3p;hsa-miR-664a-3p | 13 | YWHAZ | Sponge network | 2.018 | 1.0E-5 | 0.345 | 0.0016 | 0.436 |
51 | ZNF667-AS1 |
hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-484;hsa-miR-590-5p;hsa-miR-877-5p | 16 | DLG2 | Sponge network | -1.395 | 0 | -4.457 | 0 | 0.434 |
52 | RP11-517P14.2 |
hsa-miR-103a-3p;hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-93-5p | 11 | TEAD1 | Sponge network | -0.402 | 0.1503 | -0.582 | 1.0E-5 | 0.432 |
53 | TPTEP1 |
hsa-let-7a-3p;hsa-miR-15a-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-205-5p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-29a-5p;hsa-miR-3614-5p;hsa-miR-944 | 10 | AXIN2 | Sponge network | -2.193 | 0 | -0.655 | 0.00118 | 0.432 |
54 | EMX2OS |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-16-1-3p;hsa-miR-205-5p;hsa-miR-21-3p;hsa-miR-221-3p;hsa-miR-2355-3p;hsa-miR-330-5p;hsa-miR-342-3p;hsa-miR-576-5p;hsa-miR-627-5p;hsa-miR-629-3p;hsa-miR-7-1-3p;hsa-miR-766-3p;hsa-miR-944 | 15 | AMOT | Sponge network | -1.459 | 1.0E-5 | -3.271 | 0 | 0.432 |
55 | MAGI2-AS3 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130a-3p;hsa-miR-130b-3p;hsa-miR-17-5p;hsa-miR-18a-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-320a;hsa-miR-320b;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-454-3p;hsa-miR-590-3p;hsa-miR-92a-3p;hsa-miR-93-5p | 18 | TGFBR2 | Sponge network | -0.939 | 4.0E-5 | -0.434 | 0.01351 | 0.431 |
56 | MAGI2-AS3 |
hsa-miR-141-3p;hsa-miR-142-3p;hsa-miR-149-5p;hsa-miR-200a-3p;hsa-miR-29b-3p;hsa-miR-33a-3p;hsa-miR-362-5p;hsa-miR-429;hsa-miR-454-3p;hsa-miR-500a-5p;hsa-miR-500b-5p;hsa-miR-589-3p;hsa-miR-944 | 13 | TGFB2 | Sponge network | -0.939 | 4.0E-5 | 0.078 | 0.72302 | 0.43 |
57 | AL035610.1 |
hsa-miR-1301-3p;hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-146b-5p;hsa-miR-148b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-205-5p;hsa-miR-22-5p;hsa-miR-29b-1-5p;hsa-miR-3613-5p;hsa-miR-93-3p | 15 | DLG2 | Sponge network | -5.893 | 0 | -4.457 | 0 | 0.425 |
58 | RP11-594N15.3 |
hsa-miR-1301-3p;hsa-miR-130a-3p;hsa-miR-130b-5p;hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-185-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-320b;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-374b-3p;hsa-miR-484;hsa-miR-769-3p;hsa-miR-877-5p;hsa-miR-940 | 25 | DLG2 | Sponge network | -2.86 | 0 | -4.457 | 0 | 0.425 |
59 | PART1 | hsa-miR-1301-3p;hsa-miR-130a-3p;hsa-miR-146b-5p;hsa-miR-185-5p;hsa-miR-22-5p;hsa-miR-29b-1-5p;hsa-miR-374b-3p;hsa-miR-505-5p;hsa-miR-576-5p;hsa-miR-877-5p | 10 | DLG2 | Sponge network | -3.265 | 0 | -4.457 | 0 | 0.422 |
60 | RP11-166D19.1 |
hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-188-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-92a-3p;hsa-miR-96-5p | 10 | LATS2 | Sponge network | -0.882 | 5.0E-5 | -0.377 | 0.00275 | 0.419 |
61 | RP11-282O18.3 |
hsa-let-7a-3p;hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-224-5p;hsa-miR-301a-3p | 10 | TEAD1 | Sponge network | -0.266 | 0.05794 | -0.582 | 1.0E-5 | 0.417 |
62 | RP11-344B5.2 | hsa-miR-130b-5p;hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-15b-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-185-5p;hsa-miR-205-5p;hsa-miR-22-5p;hsa-miR-23a-3p;hsa-miR-29b-1-5p | 11 | DLG2 | Sponge network | -2.517 | 0 | -4.457 | 0 | 0.417 |
63 | SNHG14 |
hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-146b-5p;hsa-miR-148b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-484;hsa-miR-576-5p;hsa-miR-877-5p;hsa-miR-92a-3p;hsa-miR-944 | 18 | DLG2 | Sponge network | -1.125 | 0.0001 | -4.457 | 0 | 0.416 |
64 | LINC00702 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-17-5p;hsa-miR-18a-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-29b-2-5p;hsa-miR-301a-3p;hsa-miR-320a;hsa-miR-320b;hsa-miR-335-3p;hsa-miR-33a-3p;hsa-miR-454-3p;hsa-miR-501-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-92a-3p;hsa-miR-93-5p | 22 | TGFBR2 | Sponge network | -0.573 | 0.0699 | -0.434 | 0.01351 | 0.416 |
65 | BHLHE40-AS1 |
hsa-miR-1301-3p;hsa-miR-130a-3p;hsa-miR-148b-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-23a-3p;hsa-miR-29b-1-5p;hsa-miR-3127-5p;hsa-miR-374b-3p;hsa-miR-421;hsa-miR-505-5p;hsa-miR-576-5p;hsa-miR-590-5p;hsa-miR-92a-3p;hsa-miR-93-3p;hsa-miR-940 | 21 | DLG2 | Sponge network | -0.932 | 0 | -4.457 | 0 | 0.416 |
66 | FZD10-AS1 |
hsa-let-7a-3p;hsa-miR-15a-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-205-5p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-26b-3p;hsa-miR-29a-5p;hsa-miR-3614-5p;hsa-miR-590-3p | 11 | AXIN2 | Sponge network | -0.218 | 0.34607 | -0.655 | 0.00118 | 0.414 |
67 | AC006116.24 |
hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p | 10 | DLG2 | Sponge network | -1.832 | 1.0E-5 | -4.457 | 0 | 0.413 |
68 | MAGI2-AS3 |
hsa-miR-1301-3p;hsa-miR-130a-3p;hsa-miR-130b-5p;hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-185-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-23a-3p;hsa-miR-25-3p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-3127-5p;hsa-miR-320a;hsa-miR-320b;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-3613-5p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-708-3p;hsa-miR-769-3p;hsa-miR-877-5p;hsa-miR-92a-3p;hsa-miR-93-3p;hsa-miR-940;hsa-miR-944 | 35 | DLG2 | Sponge network | -0.939 | 4.0E-5 | -4.457 | 0 | 0.41 |
69 | RP11-876N24.4 | hsa-miR-103a-2-5p;hsa-miR-125a-5p;hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-301a-3p | 10 | BMPR2 | Sponge network | 0.037 | 0.92383 | -0.139 | 0.18459 | 0.41 |
70 | FGD5-AS1 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-454-3p;hsa-miR-671-5p | 10 | BMPR2 | Sponge network | -0.292 | 0.01482 | -0.139 | 0.18459 | 0.407 |
71 | TP73-AS1 |
hsa-miR-141-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-452-5p;hsa-miR-455-3p;hsa-miR-589-3p;hsa-miR-92a-3p | 11 | FZD4 | Sponge network | -0.533 | 0.00643 | -0.816 | 0 | 0.402 |
72 | RP11-35G9.5 |
hsa-let-7a-3p;hsa-miR-141-3p;hsa-miR-17-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-224-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-454-3p;hsa-miR-589-3p | 11 | FZD4 | Sponge network | -0.33 | 0.08136 | -0.816 | 0 | 0.401 |
73 | SH3RF3-AS1 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-16-2-3p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-205-3p;hsa-miR-205-5p;hsa-miR-26b-5p;hsa-miR-29a-5p;hsa-miR-30b-5p;hsa-miR-30c-5p;hsa-miR-320a;hsa-miR-582-5p;hsa-miR-590-5p;hsa-miR-7-1-3p | 20 | BMPR2 | Sponge network | -0.175 | 0.58985 | -0.139 | 0.18459 | 0.4 |
74 | RP11-166D19.1 |
hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-18a-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-454-3p;hsa-miR-590-5p;hsa-miR-92a-3p | 12 | TGFBR2 | Sponge network | -0.882 | 5.0E-5 | -0.434 | 0.01351 | 0.398 |
75 | LINC00639 |
hsa-miR-141-3p;hsa-miR-15a-5p;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-452-5p;hsa-miR-455-3p;hsa-miR-484;hsa-miR-589-3p;hsa-miR-629-3p | 11 | FZD4 | Sponge network | -0.91 | 0.00848 | -0.816 | 0 | 0.398 |
76 | C10orf71-AS1 |
hsa-let-7g-3p;hsa-miR-130b-3p;hsa-miR-185-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-224-3p;hsa-miR-25-3p;hsa-miR-301a-3p;hsa-miR-3065-3p;hsa-miR-324-3p;hsa-miR-33a-3p;hsa-miR-3934-5p;hsa-miR-576-5p;hsa-miR-7-1-3p | 14 | FZD4 | Sponge network | -3.382 | 0.00013 | -0.816 | 0 | 0.397 |
77 | LINC00702 |
hsa-miR-141-3p;hsa-miR-142-3p;hsa-miR-149-5p;hsa-miR-200a-3p;hsa-miR-33a-3p;hsa-miR-454-3p;hsa-miR-500a-5p;hsa-miR-500b-5p;hsa-miR-589-3p;hsa-miR-590-5p | 10 | TGFB2 | Sponge network | -0.573 | 0.0699 | 0.078 | 0.72302 | 0.396 |
78 | BDNF-AS | hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-484;hsa-miR-511-5p;hsa-miR-944 | 12 | DLG2 | Sponge network | -1.18 | 0 | -4.457 | 0 | 0.395 |
79 | RP11-400K9.4 |
hsa-miR-106a-5p;hsa-miR-130a-3p;hsa-miR-130b-3p;hsa-miR-17-5p;hsa-miR-18a-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-501-3p;hsa-miR-93-5p | 11 | TGFBR2 | Sponge network | -0.304 | 0.38627 | -0.434 | 0.01351 | 0.394 |
80 | RP11-193H5.1 |
hsa-miR-130b-5p;hsa-miR-141-3p;hsa-miR-18a-5p;hsa-miR-29a-5p;hsa-miR-29b-3p;hsa-miR-320a;hsa-miR-501-5p;hsa-miR-576-5p;hsa-miR-7-1-3p;hsa-miR-93-3p | 10 | WWTR1 | Sponge network | -0.426 | 0.01062 | -0.275 | 0.0614 | 0.394 |
81 | FGD5-AS1 |
hsa-let-7a-3p;hsa-miR-103a-3p;hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-454-3p;hsa-miR-576-5p | 10 | TEAD1 | Sponge network | -0.292 | 0.01482 | -0.582 | 1.0E-5 | 0.392 |
82 | TPTEP1 |
hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-23a-3p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-3613-5p;hsa-miR-484;hsa-miR-576-5p;hsa-miR-590-5p;hsa-miR-92a-3p;hsa-miR-944 | 19 | DLG2 | Sponge network | -2.193 | 0 | -4.457 | 0 | 0.39 |
83 | DLGAP1-AS5 |
hsa-miR-130a-3p;hsa-miR-130b-5p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-29b-1-5p;hsa-miR-484;hsa-miR-576-5p;hsa-miR-93-3p;hsa-miR-940;hsa-miR-944 | 14 | DLG2 | Sponge network | -6.207 | 0 | -4.457 | 0 | 0.387 |
84 | SH3RF3-AS1 |
hsa-let-7a-3p;hsa-miR-130a-3p;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200a-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-205-5p;hsa-miR-224-5p;hsa-miR-29b-3p;hsa-miR-320a;hsa-miR-576-5p;hsa-miR-7-1-3p | 17 | TEAD1 | Sponge network | -0.175 | 0.58985 | -0.582 | 1.0E-5 | 0.385 |
85 | CASC15 |
hsa-miR-141-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-3p;hsa-miR-200b-3p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-452-5p;hsa-miR-590-3p;hsa-miR-7-1-3p | 10 | FZD4 | Sponge network | 1.485 | 0 | -0.816 | 0 | 0.384 |
86 | AC006116.24 |
hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-454-3p;hsa-miR-93-5p | 10 | FBXW11 | Sponge network | -1.832 | 1.0E-5 | -0.523 | 0 | 0.384 |
87 | AL161668.5 | hsa-miR-1301-3p;hsa-miR-130b-5p;hsa-miR-135b-5p;hsa-miR-146b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-421;hsa-miR-484;hsa-miR-7-1-3p;hsa-miR-769-3p | 15 | DLG2 | Sponge network | -5.841 | 0 | -4.457 | 0 | 0.383 |
88 | CASC15 |
hsa-miR-142-3p;hsa-miR-155-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-205-3p;hsa-miR-26b-5p;hsa-miR-30b-5p;hsa-miR-30d-3p;hsa-miR-30e-3p;hsa-miR-30e-5p;hsa-miR-582-5p;hsa-miR-590-3p;hsa-miR-7-1-3p | 14 | WNT5A | Sponge network | 1.485 | 0 | 0.23 | 0.27604 | 0.383 |
89 | FZD10-AS1 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-16-1-3p;hsa-miR-205-5p;hsa-miR-21-3p;hsa-miR-221-3p;hsa-miR-2355-3p;hsa-miR-330-5p;hsa-miR-576-5p;hsa-miR-627-5p;hsa-miR-7-1-3p | 11 | AMOT | Sponge network | -0.218 | 0.34607 | -3.271 | 0 | 0.383 |
90 | CTA-221G9.11 |
hsa-miR-130a-3p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-20a-5p;hsa-miR-224-3p;hsa-miR-224-5p;hsa-miR-301a-3p;hsa-miR-576-5p;hsa-miR-93-5p | 11 | TEAD1 | Sponge network | -2.198 | 0 | -0.582 | 1.0E-5 | 0.381 |
91 | RP11-999E24.3 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-let-7g-3p;hsa-miR-16-5p;hsa-miR-17-3p;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-33a-3p | 10 | FZD4 | Sponge network | -1.447 | 0.0004 | -0.816 | 0 | 0.379 |
92 | MAGI2-AS3 |
hsa-let-7a-3p;hsa-miR-130a-3p;hsa-miR-18a-5p;hsa-miR-19a-3p;hsa-miR-21-3p;hsa-miR-224-5p;hsa-miR-2355-5p;hsa-miR-27a-3p;hsa-miR-454-3p;hsa-miR-576-5p | 10 | SMAD4 | Sponge network | -0.939 | 4.0E-5 | -0.43 | 0 | 0.379 |
93 | CTD-3099C6.9 | hsa-miR-130a-3p;hsa-miR-141-3p;hsa-miR-17-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-20a-5p;hsa-miR-224-5p;hsa-miR-301a-3p;hsa-miR-425-5p;hsa-miR-576-5p | 10 | TEAD1 | Sponge network | -0.515 | 0.15915 | -0.582 | 1.0E-5 | 0.376 |
94 | RP11-166D19.1 |
hsa-let-7a-3p;hsa-miR-16-1-3p;hsa-miR-205-5p;hsa-miR-221-3p;hsa-miR-2355-3p;hsa-miR-576-5p;hsa-miR-627-5p;hsa-miR-629-3p;hsa-miR-7-1-3p;hsa-miR-944 | 10 | AMOT | Sponge network | -0.882 | 5.0E-5 | -3.271 | 0 | 0.375 |
95 | HHIP-AS1 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-15a-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-455-3p;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-92a-3p | 11 | FZD4 | Sponge network | -1.293 | 0.01561 | -0.816 | 0 | 0.374 |
96 | AC093627.10 |
hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-877-5p | 11 | DLG2 | Sponge network | -0.893 | 0.00123 | -4.457 | 0 | 0.372 |
97 | RP11-284N8.3 |
hsa-let-7a-3p;hsa-miR-141-3p;hsa-miR-17-5p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-224-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-3065-3p;hsa-miR-452-5p;hsa-miR-455-3p;hsa-miR-576-5p;hsa-miR-590-5p | 13 | FZD4 | Sponge network | 0.003 | 0.99478 | -0.816 | 0 | 0.371 |
98 | CTD-2269F5.1 |
hsa-miR-142-3p;hsa-miR-155-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-205-3p;hsa-miR-29a-5p;hsa-miR-576-5p;hsa-miR-7-1-3p;hsa-miR-92a-3p | 11 | WNT5A | Sponge network | -0.168 | 0.67173 | 0.23 | 0.27604 | 0.371 |
99 | CTD-2620I22.1 | hsa-miR-103a-3p;hsa-miR-141-3p;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-200a-3p;hsa-miR-20a-5p;hsa-miR-224-5p;hsa-miR-505-3p | 10 | TEAD1 | Sponge network | -1.967 | 0.00106 | -0.582 | 1.0E-5 | 0.366 |
100 | CTC-297N7.7 |
hsa-miR-141-3p;hsa-miR-15b-5p;hsa-miR-17-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-224-3p;hsa-miR-3065-3p;hsa-miR-33a-3p;hsa-miR-589-3p;hsa-miR-629-3p | 11 | FZD4 | Sponge network | -1.666 | 0.01558 | -0.816 | 0 | 0.366 |
101 | RP11-166D19.1 |
hsa-let-7a-3p;hsa-miR-130a-3p;hsa-miR-141-3p;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200a-3p;hsa-miR-200a-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-224-3p;hsa-miR-224-5p;hsa-miR-301a-3p;hsa-miR-425-5p;hsa-miR-429;hsa-miR-454-3p;hsa-miR-576-5p;hsa-miR-7-1-3p;hsa-miR-92a-3p;hsa-miR-96-5p | 25 | TEAD1 | Sponge network | -0.882 | 5.0E-5 | -0.582 | 1.0E-5 | 0.365 |
102 | SLC8A1-AS1 | hsa-miR-1301-3p;hsa-miR-135b-5p;hsa-miR-146b-5p;hsa-miR-148b-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-205-5p;hsa-miR-22-5p;hsa-miR-29b-1-5p;hsa-miR-576-5p;hsa-miR-93-3p | 11 | DLG2 | Sponge network | -3.641 | 0 | -4.457 | 0 | 0.363 |
103 | AC007743.1 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-15a-5p;hsa-miR-16-2-3p;hsa-miR-193a-3p;hsa-miR-19b-1-5p;hsa-miR-21-5p;hsa-miR-29a-5p;hsa-miR-590-5p;hsa-miR-92a-3p | 10 | LATS1 | Sponge network | -1.053 | 0.00923 | -0.188 | 0.29287 | 0.363 |
104 | AF127936.7 |
hsa-miR-106a-5p;hsa-miR-16-2-3p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20b-5p;hsa-miR-25-3p;hsa-miR-26a-2-3p;hsa-miR-26b-5p;hsa-miR-320a;hsa-miR-362-3p;hsa-miR-532-5p;hsa-miR-7-1-3p | 13 | BMPR2 | Sponge network | 0.453 | 0.00811 | -0.139 | 0.18459 | 0.363 |
105 | RP11-10H3.1 |
hsa-miR-1301-3p;hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-23a-3p;hsa-miR-29b-1-5p;hsa-miR-92a-3p | 15 | DLG2 | Sponge network | -5.781 | 0 | -4.457 | 0 | 0.362 |
106 | RP11-166D19.1 |
hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-205-5p;hsa-miR-2355-5p;hsa-miR-484;hsa-miR-532-3p;hsa-miR-576-5p;hsa-miR-590-5p;hsa-miR-629-5p;hsa-miR-944 | 10 | FGF1 | Sponge network | -0.882 | 5.0E-5 | -0.258 | 0.2676 | 0.361 |
107 | CTD-2015G9.2 |
hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-25-3p;hsa-miR-301a-3p;hsa-miR-342-3p;hsa-miR-454-3p;hsa-miR-671-5p;hsa-miR-7-1-3p;hsa-miR-93-5p | 17 | BMPR2 | Sponge network | -3.112 | 5.0E-5 | -0.139 | 0.18459 | 0.358 |
108 | SH3RF3-AS1 |
hsa-let-7a-3p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-205-3p;hsa-miR-26b-5p;hsa-miR-29a-5p;hsa-miR-30b-5p;hsa-miR-30c-5p;hsa-miR-576-5p;hsa-miR-582-5p;hsa-miR-7-1-3p | 13 | WNT5A | Sponge network | -0.175 | 0.58985 | 0.23 | 0.27604 | 0.358 |
109 | PSMG3-AS1 |
hsa-let-7a-3p;hsa-miR-141-3p;hsa-miR-17-5p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-324-3p;hsa-miR-3934-5p;hsa-miR-455-3p;hsa-miR-484;hsa-miR-708-5p;hsa-miR-92a-3p;hsa-miR-940 | 14 | FZD4 | Sponge network | -0.793 | 0 | -0.816 | 0 | 0.356 |
110 | RP11-757G1.6 |
hsa-miR-15a-5p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-452-5p;hsa-miR-454-3p;hsa-miR-576-5p;hsa-miR-589-3p | 11 | FZD4 | Sponge network | -1.346 | 0.00088 | -0.816 | 0 | 0.356 |
111 | RP11-557H15.3 | hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-140-3p;hsa-miR-140-5p;hsa-miR-20b-5p;hsa-miR-217;hsa-miR-29b-2-5p;hsa-miR-30a-5p;hsa-miR-340-5p;hsa-miR-374b-5p | 10 | FRMD6 | Sponge network | 1.673 | 8.0E-5 | 0.249 | 0.05024 | 0.355 |
112 | FZD10-AS1 |
hsa-let-7a-3p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-205-3p;hsa-miR-26b-5p;hsa-miR-29a-5p;hsa-miR-330-5p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-92a-3p | 13 | WNT5A | Sponge network | -0.218 | 0.34607 | 0.23 | 0.27604 | 0.354 |
113 | RP11-477H21.2 | hsa-miR-130a-3p;hsa-miR-146b-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-205-5p;hsa-miR-23a-3p;hsa-miR-29b-1-5p;hsa-miR-374b-3p;hsa-miR-576-5p;hsa-miR-944 | 10 | DLG2 | Sponge network | -2.192 | 0.00014 | -4.457 | 0 | 0.354 |
114 | RAMP2-AS1 |
hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-146b-5p;hsa-miR-148b-5p;hsa-miR-17-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-23a-3p;hsa-miR-29b-1-5p;hsa-miR-484;hsa-miR-511-5p;hsa-miR-877-5p | 15 | DLG2 | Sponge network | -1.258 | 0.00026 | -4.457 | 0 | 0.353 |
115 | RP11-30P6.6 |
hsa-miR-140-3p;hsa-miR-148a-3p;hsa-miR-181c-5p;hsa-miR-200a-3p;hsa-miR-200b-3p;hsa-miR-30a-5p;hsa-miR-30b-5p;hsa-miR-30c-5p;hsa-miR-30d-5p;hsa-miR-30e-5p | 10 | YWHAG | Sponge network | 2.847 | 0 | 0.33 | 0.00014 | 0.353 |
116 | BHLHE40-AS1 |
hsa-let-7a-3p;hsa-miR-130a-3p;hsa-miR-18a-5p;hsa-miR-19a-3p;hsa-miR-224-5p;hsa-miR-2355-5p;hsa-miR-27a-3p;hsa-miR-450b-5p;hsa-miR-576-5p;hsa-miR-590-5p | 10 | SMAD4 | Sponge network | -0.932 | 0 | -0.43 | 0 | 0.353 |
117 | EMX2OS |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130a-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-205-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-25-3p;hsa-miR-28-3p;hsa-miR-29a-5p;hsa-miR-301a-3p;hsa-miR-335-3p;hsa-miR-33a-5p;hsa-miR-342-3p;hsa-miR-3607-3p;hsa-miR-454-3p;hsa-miR-582-3p;hsa-miR-590-3p;hsa-miR-651-5p;hsa-miR-671-5p;hsa-miR-7-1-3p;hsa-miR-92a-3p;hsa-miR-93-3p;hsa-miR-93-5p | 34 | BMPR2 | Sponge network | -1.459 | 1.0E-5 | -0.139 | 0.18459 | 0.352 |
118 | RP13-379O24.2 |
hsa-miR-106b-5p;hsa-miR-141-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-324-3p;hsa-miR-940 | 10 | FZD4 | Sponge network | -2.013 | 0.02568 | -0.816 | 0 | 0.351 |
119 | AC011738.4 |
hsa-miR-101-3p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-140-3p;hsa-miR-140-5p;hsa-miR-146a-5p;hsa-miR-20b-5p;hsa-miR-29b-2-5p;hsa-miR-320a;hsa-miR-7-1-3p | 10 | FRMD6 | Sponge network | 3.153 | 0 | 0.249 | 0.05024 | 0.351 |
120 | LINC00702 |
hsa-miR-103a-3p;hsa-miR-141-3p;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200a-3p;hsa-miR-200a-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-224-3p;hsa-miR-224-5p;hsa-miR-25-3p;hsa-miR-29b-2-5p;hsa-miR-301a-3p;hsa-miR-320a;hsa-miR-425-5p;hsa-miR-454-3p;hsa-miR-505-3p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-92a-3p;hsa-miR-93-5p;hsa-miR-96-5p | 29 | TEAD1 | Sponge network | -0.573 | 0.0699 | -0.582 | 1.0E-5 | 0.35 |
121 | LINC00957 |
hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-484;hsa-miR-576-5p | 13 | DLG2 | Sponge network | -0.677 | 2.0E-5 | -4.457 | 0 | 0.349 |
122 | RP11-218E20.3 | hsa-miR-101-3p;hsa-miR-140-3p;hsa-miR-140-5p;hsa-miR-146a-5p;hsa-miR-195-3p;hsa-miR-20b-5p;hsa-miR-217;hsa-miR-29b-2-5p;hsa-miR-30a-5p;hsa-miR-30b-5p;hsa-miR-30d-5p;hsa-miR-30e-5p;hsa-miR-374a-5p;hsa-miR-374b-5p | 14 | FRMD6 | Sponge network | 4.613 | 0 | 0.249 | 0.05024 | 0.348 |
123 | CTD-2015G9.2 |
hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-450b-5p;hsa-miR-454-3p;hsa-miR-93-5p | 11 | FBXW11 | Sponge network | -3.112 | 5.0E-5 | -0.523 | 0 | 0.348 |
124 | EMX2OS |
hsa-miR-103a-3p;hsa-miR-130b-5p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-188-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-25-3p;hsa-miR-33a-3p;hsa-miR-342-3p;hsa-miR-590-3p;hsa-miR-92a-3p;hsa-miR-93-5p | 14 | LATS2 | Sponge network | -1.459 | 1.0E-5 | -0.377 | 0.00275 | 0.348 |
125 | LINC00900 |
hsa-let-7a-3p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-25-3p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-3934-5p;hsa-miR-454-3p;hsa-miR-455-3p;hsa-miR-505-5p;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-5p;hsa-miR-7-1-3p;hsa-miR-708-5p;hsa-miR-92a-3p;hsa-miR-92b-3p | 26 | FZD4 | Sponge network | -1.803 | 0 | -0.816 | 0 | 0.347 |
126 | BHLHE40-AS1 |
hsa-miR-130a-3p;hsa-miR-130b-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-450b-5p;hsa-miR-96-5p | 10 | FBXW11 | Sponge network | -0.932 | 0 | -0.523 | 0 | 0.347 |
127 | BZRAP1-AS1 |
hsa-let-7a-3p;hsa-miR-141-3p;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-3065-3p;hsa-miR-452-5p;hsa-miR-454-3p;hsa-miR-455-3p | 10 | FZD4 | Sponge network | -0.233 | 0.50729 | -0.816 | 0 | 0.347 |
128 | AC007879.7 | hsa-miR-101-3p;hsa-miR-140-3p;hsa-miR-140-5p;hsa-miR-146a-5p;hsa-miR-195-3p;hsa-miR-20b-5p;hsa-miR-217;hsa-miR-29b-2-5p;hsa-miR-30a-5p;hsa-miR-340-5p | 10 | FRMD6 | Sponge network | 2.7 | 0 | 0.249 | 0.05024 | 0.347 |
129 | RP11-384L8.1 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-16-1-3p;hsa-miR-205-5p;hsa-miR-21-3p;hsa-miR-221-3p;hsa-miR-2355-3p;hsa-miR-330-5p;hsa-miR-576-5p;hsa-miR-766-3p | 10 | AMOT | Sponge network | -1.152 | 0.00016 | -3.271 | 0 | 0.346 |
130 | RP11-693J15.4 |
hsa-let-7a-3p;hsa-miR-141-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-455-3p;hsa-miR-590-5p;hsa-miR-940 | 11 | FZD4 | Sponge network | -0.732 | 0.18487 | -0.816 | 0 | 0.346 |
131 | MAGI2-AS3 |
hsa-let-7a-3p;hsa-miR-103a-3p;hsa-miR-130a-3p;hsa-miR-141-3p;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200a-3p;hsa-miR-200a-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-224-3p;hsa-miR-224-5p;hsa-miR-25-3p;hsa-miR-29b-3p;hsa-miR-301a-3p;hsa-miR-320a;hsa-miR-3607-3p;hsa-miR-425-5p;hsa-miR-429;hsa-miR-454-3p;hsa-miR-505-3p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-708-3p;hsa-miR-92a-3p;hsa-miR-93-5p | 34 | TEAD1 | Sponge network | -0.939 | 4.0E-5 | -0.582 | 1.0E-5 | 0.346 |
132 | DHRS4-AS1 |
hsa-miR-130a-3p;hsa-miR-146b-5p;hsa-miR-16-1-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-454-3p | 10 | TEAD1 | Sponge network | -0.068 | 0.72321 | -0.582 | 1.0E-5 | 0.344 |
133 | AC144831.1 |
hsa-miR-1301-3p;hsa-miR-130a-3p;hsa-miR-130b-5p;hsa-miR-135b-5p;hsa-miR-146b-5p;hsa-miR-148b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-25-3p;hsa-miR-29b-1-5p;hsa-miR-3127-5p;hsa-miR-320a;hsa-miR-320b;hsa-miR-374b-3p;hsa-miR-505-5p;hsa-miR-576-5p;hsa-miR-7-1-3p;hsa-miR-769-3p;hsa-miR-877-5p;hsa-miR-93-3p;hsa-miR-940 | 25 | DLG2 | Sponge network | -1.546 | 0 | -4.457 | 0 | 0.344 |
134 | FAM225B |
hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-205-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-26b-5p;hsa-miR-30b-5p;hsa-miR-30c-5p;hsa-miR-30e-5p;hsa-miR-33a-5p;hsa-miR-362-3p;hsa-miR-651-5p;hsa-miR-92a-3p | 15 | BMPR2 | Sponge network | 2.186 | 0 | -0.139 | 0.18459 | 0.343 |
135 | BZRAP1-AS1 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-454-3p;hsa-miR-671-5p | 12 | BMPR2 | Sponge network | -0.233 | 0.50729 | -0.139 | 0.18459 | 0.343 |
136 | EMX2OS |
hsa-miR-1301-3p;hsa-miR-130a-3p;hsa-miR-130b-5p;hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-185-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-25-3p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-3127-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-484;hsa-miR-505-5p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-769-3p;hsa-miR-877-5p;hsa-miR-92a-3p;hsa-miR-92b-3p;hsa-miR-93-3p;hsa-miR-940;hsa-miR-944 | 33 | DLG2 | Sponge network | -1.459 | 1.0E-5 | -4.457 | 0 | 0.343 |
137 | RP11-999E24.3 |
hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-23a-3p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-33a-5p;hsa-miR-33b-5p | 14 | DLG2 | Sponge network | -1.447 | 0.0004 | -4.457 | 0 | 0.341 |
138 | AC003090.1 |
hsa-miR-1301-3p;hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-23a-3p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-320a;hsa-miR-320b;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-576-5p;hsa-miR-590-5p;hsa-miR-7-1-3p;hsa-miR-940 | 24 | DLG2 | Sponge network | -4.323 | 0 | -4.457 | 0 | 0.337 |
139 | TPTEP1 |
hsa-let-7a-3p;hsa-miR-15a-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-3934-5p;hsa-miR-454-3p;hsa-miR-455-3p;hsa-miR-484;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-5p;hsa-miR-629-3p;hsa-miR-92a-3p | 17 | FZD4 | Sponge network | -2.193 | 0 | -0.816 | 0 | 0.337 |
140 | CTA-221G9.11 |
hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-224-3p;hsa-miR-301a-3p;hsa-miR-3934-5p;hsa-miR-484;hsa-miR-576-5p;hsa-miR-629-3p | 10 | FZD4 | Sponge network | -2.198 | 0 | -0.816 | 0 | 0.336 |
141 | RP1-193H18.2 |
hsa-let-7a-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-452-5p;hsa-miR-455-3p;hsa-miR-576-5p;hsa-miR-589-3p | 10 | FZD4 | Sponge network | -1.539 | 0 | -0.816 | 0 | 0.336 |
142 | RP11-693J15.4 |
hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-23a-3p;hsa-miR-29b-1-5p;hsa-miR-590-5p;hsa-miR-769-3p;hsa-miR-940 | 15 | DLG2 | Sponge network | -0.732 | 0.18487 | -4.457 | 0 | 0.335 |
143 | RP4-798P15.3 |
hsa-let-7a-3p;hsa-miR-103a-3p;hsa-miR-130a-3p;hsa-miR-146b-5p;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-576-5p;hsa-miR-7-1-3p;hsa-miR-96-5p | 17 | TEAD1 | Sponge network | -1.213 | 0.00098 | -0.582 | 1.0E-5 | 0.335 |
144 | RP11-389C8.2 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-205-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-429;hsa-miR-671-5p;hsa-miR-93-5p | 16 | BMPR2 | Sponge network | 0.187 | 0.31051 | -0.139 | 0.18459 | 0.335 |
145 | RP11-400K9.4 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-106a-5p;hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-25-3p;hsa-miR-26b-5p;hsa-miR-301a-3p;hsa-miR-30b-5p;hsa-miR-30c-5p;hsa-miR-33a-5p;hsa-miR-671-5p;hsa-miR-93-3p;hsa-miR-93-5p | 21 | BMPR2 | Sponge network | -0.304 | 0.38627 | -0.139 | 0.18459 | 0.334 |
146 | LINC00284 |
hsa-miR-1301-3p;hsa-miR-148b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-421;hsa-miR-576-5p;hsa-miR-590-5p;hsa-miR-877-5p;hsa-miR-93-3p;hsa-miR-944 | 18 | DLG2 | Sponge network | -4.159 | 0 | -4.457 | 0 | 0.333 |
147 | LINC00702 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-205-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-25-3p;hsa-miR-301a-3p;hsa-miR-30e-5p;hsa-miR-320a;hsa-miR-335-3p;hsa-miR-33a-5p;hsa-miR-454-3p;hsa-miR-532-5p;hsa-miR-582-3p;hsa-miR-582-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-651-5p;hsa-miR-7-1-3p;hsa-miR-92a-3p;hsa-miR-93-3p;hsa-miR-93-5p;hsa-miR-96-5p | 31 | BMPR2 | Sponge network | -0.573 | 0.0699 | -0.139 | 0.18459 | 0.331 |
148 | RP11-166D19.1 |
hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-29b-1-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-3613-5p;hsa-miR-484;hsa-miR-576-5p;hsa-miR-590-5p;hsa-miR-7-1-3p;hsa-miR-769-3p;hsa-miR-877-5p;hsa-miR-92a-3p;hsa-miR-93-3p;hsa-miR-940;hsa-miR-944 | 26 | DLG2 | Sponge network | -0.882 | 5.0E-5 | -4.457 | 0 | 0.331 |
149 | CTA-221G9.11 |
hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-3p;hsa-miR-20a-5p;hsa-miR-29a-5p;hsa-miR-301a-3p;hsa-miR-671-5p;hsa-miR-93-5p | 11 | BMPR2 | Sponge network | -2.198 | 0 | -0.139 | 0.18459 | 0.331 |
150 | CLDN10-AS1 |
hsa-miR-1301-3p;hsa-miR-130b-5p;hsa-miR-146b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-374b-3p;hsa-miR-484;hsa-miR-708-3p;hsa-miR-92a-3p;hsa-miR-944 | 17 | DLG2 | Sponge network | -5.599 | 0 | -4.457 | 0 | 0.329 |
151 | RP4-794H19.1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-20b-5p;hsa-miR-23b-3p;hsa-miR-29b-2-5p;hsa-miR-320a;hsa-miR-320b;hsa-miR-335-3p;hsa-miR-9-5p;hsa-miR-92a-3p | 11 | TGFBR2 | Sponge network | 1.019 | 8.0E-5 | -0.434 | 0.01351 | 0.329 |
152 | LINC00702 |
hsa-miR-106b-5p;hsa-miR-15b-5p;hsa-miR-200b-3p;hsa-miR-20a-5p;hsa-miR-25-3p;hsa-miR-324-3p;hsa-miR-34a-5p;hsa-miR-590-5p;hsa-miR-92a-3p;hsa-miR-93-5p | 10 | SMAD7 | Sponge network | -0.573 | 0.0699 | 0.47 | 8.0E-5 | 0.328 |
153 | CTC-297N7.7 |
hsa-miR-103a-3p;hsa-miR-141-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200a-3p;hsa-miR-200a-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-224-3p;hsa-miR-96-5p | 14 | TEAD1 | Sponge network | -1.666 | 0.01558 | -0.582 | 1.0E-5 | 0.328 |
154 | TP73-AS1 |
hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-23a-3p;hsa-miR-29b-1-5p;hsa-miR-708-3p;hsa-miR-92a-3p | 13 | DLG2 | Sponge network | -0.533 | 0.00643 | -4.457 | 0 | 0.328 |
155 | AC007743.1 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-29a-5p;hsa-miR-301a-3p;hsa-miR-33a-5p;hsa-miR-342-3p;hsa-miR-590-5p;hsa-miR-671-5p;hsa-miR-7-1-3p;hsa-miR-92a-3p | 19 | BMPR2 | Sponge network | -1.053 | 0.00923 | -0.139 | 0.18459 | 0.326 |
156 | AF127936.7 |
hsa-miR-106a-5p;hsa-miR-140-3p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-200a-3p;hsa-miR-20b-5p;hsa-miR-29b-2-5p;hsa-miR-320a;hsa-miR-362-3p;hsa-miR-374a-5p;hsa-miR-7-1-3p | 11 | FRMD6 | Sponge network | 0.453 | 0.00811 | 0.249 | 0.05024 | 0.325 |
157 | CTA-221G9.11 |
hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-29b-1-5p;hsa-miR-484;hsa-miR-576-5p | 12 | DLG2 | Sponge network | -2.198 | 0 | -4.457 | 0 | 0.325 |
158 | RP11-35G9.5 |
hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-20a-5p;hsa-miR-23a-3p;hsa-miR-29b-1-5p;hsa-miR-769-3p | 10 | DLG2 | Sponge network | -0.33 | 0.08136 | -4.457 | 0 | 0.324 |
159 | SOX21-AS1 | hsa-miR-130a-3p;hsa-miR-146b-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-22-5p;hsa-miR-29b-1-5p;hsa-miR-374b-3p;hsa-miR-505-5p;hsa-miR-511-5p;hsa-miR-576-5p | 10 | DLG2 | Sponge network | -1.061 | 0.01562 | -4.457 | 0 | 0.324 |
160 | AC007743.1 |
hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-33a-5p;hsa-miR-590-5p;hsa-miR-7-1-3p;hsa-miR-92a-3p | 17 | DLG2 | Sponge network | -1.053 | 0.00923 | -4.457 | 0 | 0.324 |
161 | RP4-798P15.3 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-26b-5p;hsa-miR-29a-5p;hsa-miR-301a-3p;hsa-miR-590-5p;hsa-miR-671-5p;hsa-miR-7-1-3p;hsa-miR-96-5p | 19 | BMPR2 | Sponge network | -1.213 | 0.00098 | -0.139 | 0.18459 | 0.323 |
162 | RP11-30P6.6 |
hsa-miR-101-3p;hsa-miR-106a-5p;hsa-miR-140-3p;hsa-miR-200a-3p;hsa-miR-20b-5p;hsa-miR-217;hsa-miR-29b-2-5p;hsa-miR-30a-5p;hsa-miR-30b-5p;hsa-miR-30c-5p;hsa-miR-30d-5p;hsa-miR-30e-5p;hsa-miR-374a-5p | 13 | FRMD6 | Sponge network | 2.847 | 0 | 0.249 | 0.05024 | 0.323 |
163 | HHIP-AS1 |
hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-23a-3p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-33a-5p;hsa-miR-33b-5p;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-92a-3p;hsa-miR-944 | 19 | DLG2 | Sponge network | -1.293 | 0.01561 | -4.457 | 0 | 0.322 |
164 | CTD-2015G9.2 |
hsa-miR-103a-3p;hsa-miR-130a-3p;hsa-miR-141-3p;hsa-miR-146b-5p;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-224-5p;hsa-miR-25-3p;hsa-miR-301a-3p;hsa-miR-425-5p;hsa-miR-454-3p;hsa-miR-576-5p;hsa-miR-7-1-3p;hsa-miR-708-3p;hsa-miR-93-5p | 22 | TEAD1 | Sponge network | -3.112 | 5.0E-5 | -0.582 | 1.0E-5 | 0.322 |
165 | NOP14-AS1 |
hsa-miR-140-3p;hsa-miR-195-3p;hsa-miR-217;hsa-miR-28-5p;hsa-miR-30a-5p;hsa-miR-30b-5p;hsa-miR-30d-5p;hsa-miR-30e-5p;hsa-miR-374a-3p;hsa-miR-378a-3p | 10 | YWHAZ | Sponge network | 0.939 | 0 | 0.345 | 0.0016 | 0.321 |
166 | MAGI2-AS3 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-103a-3p;hsa-miR-142-3p;hsa-miR-15a-5p;hsa-miR-16-2-3p;hsa-miR-188-5p;hsa-miR-193a-3p;hsa-miR-19b-1-5p;hsa-miR-21-5p;hsa-miR-25-3p;hsa-miR-29a-5p;hsa-miR-320a;hsa-miR-3607-3p;hsa-miR-429;hsa-miR-532-3p;hsa-miR-590-3p;hsa-miR-92a-3p | 18 | LATS1 | Sponge network | -0.939 | 4.0E-5 | -0.188 | 0.29287 | 0.32 |
167 | SH3RF3-AS1 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-15a-5p;hsa-miR-16-2-3p;hsa-miR-188-5p;hsa-miR-193a-3p;hsa-miR-19b-1-5p;hsa-miR-29a-5p;hsa-miR-320a;hsa-miR-590-5p | 10 | LATS1 | Sponge network | -0.175 | 0.58985 | -0.188 | 0.29287 | 0.319 |
168 | LINC01088 |
hsa-miR-1301-3p;hsa-miR-130a-3p;hsa-miR-146b-5p;hsa-miR-148b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-185-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-22-5p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-3613-5p;hsa-miR-576-5p;hsa-miR-590-3p | 15 | DLG2 | Sponge network | -1.372 | 0.00022 | -4.457 | 0 | 0.318 |
169 | EMX2OS |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130a-3p;hsa-miR-130b-3p;hsa-miR-17-5p;hsa-miR-18a-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-29b-2-5p;hsa-miR-301a-3p;hsa-miR-335-3p;hsa-miR-33a-3p;hsa-miR-454-3p;hsa-miR-501-3p;hsa-miR-590-3p;hsa-miR-9-5p;hsa-miR-92a-3p;hsa-miR-93-5p | 20 | TGFBR2 | Sponge network | -1.459 | 1.0E-5 | -0.434 | 0.01351 | 0.318 |
170 | LINC00957 |
hsa-miR-141-3p;hsa-miR-15a-5p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-301a-3p;hsa-miR-3934-5p;hsa-miR-455-3p;hsa-miR-484;hsa-miR-576-5p | 11 | FZD4 | Sponge network | -0.677 | 2.0E-5 | -0.816 | 0 | 0.318 |
171 | HHIP-AS1 |
hsa-let-7a-3p;hsa-miR-142-3p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-205-3p;hsa-miR-29a-5p;hsa-miR-330-5p;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-92a-3p | 12 | WNT5A | Sponge network | -1.293 | 0.01561 | 0.23 | 0.27604 | 0.315 |
172 | RP11-594N15.3 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-205-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-33a-5p;hsa-miR-3607-3p;hsa-miR-651-5p;hsa-miR-671-5p;hsa-miR-93-5p | 20 | BMPR2 | Sponge network | -2.86 | 0 | -0.139 | 0.18459 | 0.313 |
173 | FZD10-AS1 |
hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-23a-3p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-320b;hsa-miR-33a-5p;hsa-miR-484;hsa-miR-505-5p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-877-5p;hsa-miR-92a-3p;hsa-miR-92b-3p;hsa-miR-940 | 26 | DLG2 | Sponge network | -0.218 | 0.34607 | -4.457 | 0 | 0.313 |
174 | LINC00605 |
hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-19a-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-23a-3p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-7-1-3p;hsa-miR-944 | 13 | DLG2 | Sponge network | -2.602 | 0.00047 | -4.457 | 0 | 0.311 |
175 | LINC00941 | hsa-miR-106a-5p;hsa-miR-140-3p;hsa-miR-140-5p;hsa-miR-146a-5p;hsa-miR-195-3p;hsa-miR-200a-3p;hsa-miR-20b-5p;hsa-miR-217;hsa-miR-29b-2-5p;hsa-miR-340-5p | 10 | FRMD6 | Sponge network | 4.292 | 0 | 0.249 | 0.05024 | 0.311 |
176 | XXyac-YX65C7_A.2 | hsa-miR-103a-2-5p;hsa-miR-106a-5p;hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-205-3p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-26b-5p;hsa-miR-362-3p;hsa-miR-651-5p | 10 | BMPR2 | Sponge network | 0.549 | 0.00949 | -0.139 | 0.18459 | 0.311 |
177 | CTD-2135D7.5 | hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-185-5p;hsa-miR-21-5p;hsa-miR-224-3p;hsa-miR-301a-3p;hsa-miR-452-5p;hsa-miR-589-3p;hsa-miR-590-5p;hsa-miR-629-3p | 10 | FZD4 | Sponge network | -2.579 | 0.0001 | -0.816 | 0 | 0.31 |
178 | CTD-2008P7.9 |
hsa-miR-103a-2-5p;hsa-miR-103a-3p;hsa-miR-15a-5p;hsa-miR-16-2-3p;hsa-miR-181a-5p;hsa-miR-181b-5p;hsa-miR-19b-1-5p;hsa-miR-21-5p;hsa-miR-25-3p;hsa-miR-29a-5p | 10 | LATS1 | Sponge network | -1.202 | 0.00093 | -0.188 | 0.29287 | 0.309 |
179 | AC005532.5 | hsa-miR-1301-3p;hsa-miR-130b-5p;hsa-miR-146b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-205-5p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-320a;hsa-miR-576-5p;hsa-miR-93-3p | 11 | DLG2 | Sponge network | -3.114 | 0 | -4.457 | 0 | 0.306 |
180 | AC011738.4 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-20b-5p;hsa-miR-25-3p;hsa-miR-26b-5p;hsa-miR-320a;hsa-miR-3607-3p;hsa-miR-374a-3p;hsa-miR-532-5p;hsa-miR-582-3p;hsa-miR-7-1-3p | 11 | BMPR2 | Sponge network | 3.153 | 0 | -0.139 | 0.18459 | 0.306 |
181 | CASC15 |
hsa-miR-16-2-3p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-205-3p;hsa-miR-205-5p;hsa-miR-26b-5p;hsa-miR-30b-5p;hsa-miR-30e-5p;hsa-miR-32-5p;hsa-miR-33a-5p;hsa-miR-429;hsa-miR-582-5p;hsa-miR-590-3p;hsa-miR-7-1-3p | 14 | BMPR2 | Sponge network | 1.485 | 0 | -0.139 | 0.18459 | 0.304 |
182 | PSMG3-AS1 |
hsa-miR-130a-3p;hsa-miR-148b-5p;hsa-miR-17-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-23a-3p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-484;hsa-miR-877-5p;hsa-miR-92a-3p;hsa-miR-940 | 15 | DLG2 | Sponge network | -0.793 | 0 | -4.457 | 0 | 0.302 |
183 | FAM66C |
hsa-miR-135b-5p;hsa-miR-17-5p;hsa-miR-19a-3p;hsa-miR-205-5p;hsa-miR-22-5p;hsa-miR-23a-3p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-3613-5p;hsa-miR-484;hsa-miR-576-5p;hsa-miR-944 | 12 | DLG2 | Sponge network | -0.798 | 0.00038 | -4.457 | 0 | 0.301 |
184 | AC093627.10 |
hsa-let-7a-3p;hsa-miR-130a-3p;hsa-miR-18a-5p;hsa-miR-19a-3p;hsa-miR-21-3p;hsa-miR-224-5p;hsa-miR-2355-5p;hsa-miR-27a-3p;hsa-miR-450b-5p;hsa-miR-454-3p | 10 | SMAD4 | Sponge network | -0.893 | 0.00123 | -0.43 | 0 | 0.301 |
185 | RP11-536O18.1 | hsa-miR-130a-3p;hsa-miR-15b-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-23a-3p;hsa-miR-27a-5p;hsa-miR-29b-1-5p | 10 | DLG2 | Sponge network | -2.284 | 0.00025 | -4.457 | 0 | 0.301 |
186 | RP11-401P9.4 |
hsa-miR-106a-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-3p;hsa-miR-20a-5p;hsa-miR-20b-5p;hsa-miR-25-3p;hsa-miR-454-3p | 10 | BMPR2 | Sponge network | 0.517 | 0.04893 | -0.139 | 0.18459 | 0.299 |
187 | RP11-384L8.1 |
hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-15b-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-23a-3p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-484;hsa-miR-576-5p | 13 | DLG2 | Sponge network | -1.152 | 0.00016 | -4.457 | 0 | 0.297 |
188 | RP4-798P15.3 |
hsa-let-7a-3p;hsa-miR-15a-5p;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-301a-3p;hsa-miR-3934-5p;hsa-miR-455-3p;hsa-miR-484;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-5p;hsa-miR-7-1-3p;hsa-miR-708-5p | 14 | FZD4 | Sponge network | -1.213 | 0.00098 | -0.816 | 0 | 0.295 |
189 | FAM66C |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-15a-5p;hsa-miR-17-5p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-3934-5p;hsa-miR-452-5p;hsa-miR-455-3p;hsa-miR-484;hsa-miR-576-5p | 11 | FZD4 | Sponge network | -0.798 | 0.00038 | -0.816 | 0 | 0.295 |
190 | DIO3OS |
hsa-miR-106b-5p;hsa-miR-107;hsa-miR-141-3p;hsa-miR-183-5p;hsa-miR-200a-3p;hsa-miR-205-3p;hsa-miR-27b-3p;hsa-miR-324-3p;hsa-miR-331-3p;hsa-miR-33b-5p;hsa-miR-3615 | 11 | WTIP | Sponge network | -0.462 | 0.26057 | 0.095 | 0.55367 | 0.295 |
191 | LINC00284 |
hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-301a-3p;hsa-miR-455-3p;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-590-5p;hsa-miR-629-3p | 13 | FZD4 | Sponge network | -4.159 | 0 | -0.816 | 0 | 0.295 |
192 | AC097499.1 | hsa-miR-130b-5p;hsa-miR-146b-5p;hsa-miR-148b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-19a-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-29b-1-5p;hsa-miR-92a-3p | 12 | DLG2 | Sponge network | -4.904 | 0 | -4.457 | 0 | 0.294 |
193 | RP4-798P15.3 |
hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-146b-5p;hsa-miR-148b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-29b-1-5p;hsa-miR-484;hsa-miR-576-5p;hsa-miR-590-5p;hsa-miR-7-1-3p;hsa-miR-944 | 19 | DLG2 | Sponge network | -1.213 | 0.00098 | -4.457 | 0 | 0.294 |
194 | AF131215.2 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-454-3p;hsa-miR-671-5p | 11 | BMPR2 | Sponge network | -1.136 | 0.00092 | -0.139 | 0.18459 | 0.292 |
195 | MAGI2-AS3 |
hsa-let-7a-3p;hsa-miR-142-3p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-186-5p;hsa-miR-205-3p;hsa-miR-26b-5p;hsa-miR-29a-5p;hsa-miR-30c-5p;hsa-miR-330-5p;hsa-miR-576-5p;hsa-miR-582-5p;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-92a-3p | 16 | WNT5A | Sponge network | -0.939 | 4.0E-5 | 0.23 | 0.27604 | 0.291 |
196 | BZRAP1-AS1 |
hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-29b-1-5p;hsa-miR-877-5p;hsa-miR-944 | 11 | DLG2 | Sponge network | -0.233 | 0.50729 | -4.457 | 0 | 0.291 |
197 | XXyac-YX65C7_A.3 | hsa-miR-101-3p;hsa-miR-106a-5p;hsa-miR-140-3p;hsa-miR-140-5p;hsa-miR-146a-5p;hsa-miR-195-3p;hsa-miR-20b-5p;hsa-miR-217;hsa-miR-29b-2-5p;hsa-miR-30a-5p;hsa-miR-30b-5p;hsa-miR-30d-5p;hsa-miR-30e-5p | 13 | FRMD6 | Sponge network | 6.112 | 0 | 0.249 | 0.05024 | 0.288 |
198 | RP1-122P22.2 | hsa-miR-1301-3p;hsa-miR-135b-5p;hsa-miR-146b-5p;hsa-miR-148b-5p;hsa-miR-16-2-3p;hsa-miR-182-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-22-5p;hsa-miR-29b-1-5p;hsa-miR-3127-5p | 12 | DLG2 | Sponge network | -1.073 | 6.0E-5 | -4.457 | 0 | 0.287 |
199 | RP4-794H19.1 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-107;hsa-miR-141-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-183-5p;hsa-miR-200a-3p;hsa-miR-20b-5p;hsa-miR-25-3p;hsa-miR-27b-3p;hsa-miR-32-5p;hsa-miR-363-3p | 13 | WTIP | Sponge network | 1.019 | 8.0E-5 | 0.095 | 0.55367 | 0.287 |
200 | DNM3OS |
hsa-let-7a-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-205-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-26b-5p;hsa-miR-33a-5p;hsa-miR-429;hsa-miR-590-5p;hsa-miR-651-5p;hsa-miR-7-1-3p;hsa-miR-96-5p | 18 | BMPR2 | Sponge network | 0.932 | 0.00442 | -0.139 | 0.18459 | 0.287 |
201 | RP11-62F24.2 |
hsa-miR-135b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-185-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-7-1-3p | 13 | DLG2 | Sponge network | -3.195 | 1.0E-5 | -4.457 | 0 | 0.286 |
202 | MIR133A1 |
hsa-miR-148b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-29b-1-5p;hsa-miR-33a-5p;hsa-miR-7-1-3p;hsa-miR-944 | 10 | DLG2 | Sponge network | -3.563 | 0 | -4.457 | 0 | 0.286 |
203 | AC090587.5 | hsa-miR-130a-3p;hsa-miR-130b-5p;hsa-miR-135b-5p;hsa-miR-146b-5p;hsa-miR-148b-5p;hsa-miR-182-5p;hsa-miR-205-5p;hsa-miR-22-5p;hsa-miR-29b-1-5p;hsa-miR-3127-5p;hsa-miR-93-3p | 11 | DLG2 | Sponge network | -0.612 | 0.00023 | -4.457 | 0 | 0.284 |
204 | LINC00702 |
hsa-miR-103a-3p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-205-5p;hsa-miR-222-3p;hsa-miR-26b-3p;hsa-miR-34a-5p;hsa-miR-582-5p;hsa-miR-590-3p | 11 | AXIN2 | Sponge network | -0.573 | 0.0699 | -0.655 | 0.00118 | 0.284 |
205 | MEG3 |
hsa-miR-106b-5p;hsa-miR-107;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-205-3p;hsa-miR-224-3p;hsa-miR-27a-3p;hsa-miR-27b-3p;hsa-miR-324-3p;hsa-miR-331-3p;hsa-miR-3615 | 11 | WTIP | Sponge network | -0.286 | 0.30726 | 0.095 | 0.55367 | 0.282 |
206 | DIO3OS |
hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-17-3p;hsa-miR-17-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-3065-3p;hsa-miR-324-3p;hsa-miR-3934-5p;hsa-miR-629-3p;hsa-miR-940 | 12 | FZD4 | Sponge network | -0.462 | 0.26057 | -0.816 | 0 | 0.28 |
207 | RP11-594N15.3 |
hsa-let-7a-3p;hsa-miR-130a-3p;hsa-miR-141-3p;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200a-3p;hsa-miR-200a-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-224-5p;hsa-miR-301a-3p;hsa-miR-3607-3p;hsa-miR-93-5p | 20 | TEAD1 | Sponge network | -2.86 | 0 | -0.582 | 1.0E-5 | 0.28 |
208 | RP11-284N8.3 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200c-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-590-5p;hsa-miR-93-5p;hsa-miR-96-5p | 14 | BMPR2 | Sponge network | 0.003 | 0.99478 | -0.139 | 0.18459 | 0.28 |
209 | MIR133A1 |
hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200a-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-205-5p;hsa-miR-224-5p;hsa-miR-429;hsa-miR-7-1-3p | 11 | TEAD1 | Sponge network | -3.563 | 0 | -0.582 | 1.0E-5 | 0.277 |
210 | CTD-2554C21.3 |
hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-301a-3p;hsa-miR-3934-5p;hsa-miR-455-3p;hsa-miR-629-3p | 11 | FZD4 | Sponge network | -2.118 | 6.0E-5 | -0.816 | 0 | 0.277 |
211 | KB-1732A1.1 | hsa-miR-101-3p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-140-3p;hsa-miR-140-5p;hsa-miR-146a-5p;hsa-miR-195-3p;hsa-miR-200a-3p;hsa-miR-20b-5p;hsa-miR-217;hsa-miR-29b-2-5p | 11 | FRMD6 | Sponge network | 1.697 | 0 | 0.249 | 0.05024 | 0.277 |
212 | LINC00702 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-141-3p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-183-5p;hsa-miR-200a-3p;hsa-miR-205-3p;hsa-miR-20b-5p;hsa-miR-224-3p;hsa-miR-25-3p;hsa-miR-27b-3p;hsa-miR-324-3p;hsa-miR-331-3p;hsa-miR-33b-5p;hsa-miR-3615;hsa-miR-363-3p;hsa-miR-92b-3p | 18 | WTIP | Sponge network | -0.573 | 0.0699 | 0.095 | 0.55367 | 0.276 |
213 | RP11-166D19.1 |
hsa-let-7a-3p;hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-205-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-33a-5p;hsa-miR-429;hsa-miR-454-3p;hsa-miR-590-5p;hsa-miR-651-5p;hsa-miR-671-5p;hsa-miR-7-1-3p;hsa-miR-92a-3p;hsa-miR-93-3p;hsa-miR-96-5p | 24 | BMPR2 | Sponge network | -0.882 | 5.0E-5 | -0.139 | 0.18459 | 0.275 |
214 | SNHG14 |
hsa-miR-103a-2-5p;hsa-miR-130a-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-342-3p;hsa-miR-454-3p;hsa-miR-671-5p;hsa-miR-92a-3p | 14 | BMPR2 | Sponge network | -1.125 | 0.0001 | -0.139 | 0.18459 | 0.272 |
215 | CTD-2015G9.2 |
hsa-miR-1301-3p;hsa-miR-130a-3p;hsa-miR-130b-5p;hsa-miR-146b-5p;hsa-miR-148b-5p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-185-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-25-3p;hsa-miR-29b-1-5p;hsa-miR-505-5p;hsa-miR-576-5p;hsa-miR-7-1-3p;hsa-miR-708-3p;hsa-miR-769-3p | 22 | DLG2 | Sponge network | -3.112 | 5.0E-5 | -4.457 | 0 | 0.272 |
216 | AC108142.1 |
hsa-miR-106b-5p;hsa-miR-141-3p;hsa-miR-15b-5p;hsa-miR-200a-3p;hsa-miR-20b-5p;hsa-miR-224-3p;hsa-miR-25-3p;hsa-miR-27b-3p;hsa-miR-29c-3p;hsa-miR-33b-5p | 10 | WTIP | Sponge network | 2.31 | 0 | 0.095 | 0.55367 | 0.271 |
217 | MAGI2-AS3 |
hsa-miR-130b-5p;hsa-miR-141-3p;hsa-miR-149-5p;hsa-miR-17-3p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-1976;hsa-miR-200a-3p;hsa-miR-205-5p;hsa-miR-29a-5p;hsa-miR-29b-3p;hsa-miR-30c-5p;hsa-miR-320a;hsa-miR-320b;hsa-miR-3607-3p;hsa-miR-501-5p;hsa-miR-576-5p;hsa-miR-582-3p;hsa-miR-582-5p;hsa-miR-590-3p;hsa-miR-651-5p;hsa-miR-7-1-3p;hsa-miR-93-3p | 23 | WWTR1 | Sponge network | -0.939 | 4.0E-5 | -0.275 | 0.0614 | 0.269 |
218 | RP11-456K23.1 |
hsa-miR-103a-3p;hsa-miR-130b-5p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-188-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-25-3p;hsa-miR-27b-3p;hsa-miR-32-5p;hsa-miR-362-3p;hsa-miR-429;hsa-miR-590-3p;hsa-miR-92a-3p;hsa-miR-93-5p | 16 | LATS2 | Sponge network | -0.223 | 0.27461 | -0.377 | 0.00275 | 0.268 |
219 | RP11-389C8.2 |
hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-148b-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-27a-5p;hsa-miR-944 | 11 | DLG2 | Sponge network | 0.187 | 0.31051 | -4.457 | 0 | 0.268 |
220 | RP11-282O18.3 |
hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-29b-1-5p;hsa-miR-505-5p;hsa-miR-590-5p | 11 | DLG2 | Sponge network | -0.266 | 0.05794 | -4.457 | 0 | 0.267 |
221 | RP11-400K9.4 |
hsa-miR-130a-3p;hsa-miR-130b-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-20a-5p;hsa-miR-301a-3p;hsa-miR-93-5p | 10 | FBXW11 | Sponge network | -0.304 | 0.38627 | -0.523 | 0 | 0.267 |
222 | LINC00865 |
hsa-miR-135b-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-23a-3p;hsa-miR-27a-5p;hsa-miR-29b-1-5p | 10 | DLG2 | Sponge network | -0.336 | 0.22355 | -4.457 | 0 | 0.266 |
223 | RP11-774O3.3 |
hsa-let-7a-3p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-15a-5p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-27a-3p;hsa-miR-301a-3p;hsa-miR-324-3p;hsa-miR-576-5p;hsa-miR-589-3p;hsa-miR-7-1-3p;hsa-miR-708-5p | 15 | FZD4 | Sponge network | -1.712 | 0 | -0.816 | 0 | 0.264 |
224 | MIR22HG |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-130b-3p;hsa-miR-17-5p;hsa-miR-18a-5p;hsa-miR-20a-5p;hsa-miR-320b;hsa-miR-335-3p;hsa-miR-590-5p;hsa-miR-92a-3p;hsa-miR-93-5p | 11 | TGFBR2 | Sponge network | -0.601 | 4.0E-5 | -0.434 | 0.01351 | 0.262 |
225 | CTC-205M6.5 | hsa-miR-141-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19b-3p;hsa-miR-200a-3p;hsa-miR-200a-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-29b-2-5p;hsa-miR-425-5p;hsa-miR-7-1-3p;hsa-miR-96-5p | 13 | TEAD1 | Sponge network | 0.381 | 0.01756 | -0.582 | 1.0E-5 | 0.26 |
226 | AC007743.1 |
hsa-let-7a-3p;hsa-miR-130a-3p;hsa-miR-16-1-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-224-5p;hsa-miR-301a-3p;hsa-miR-425-5p;hsa-miR-7-1-3p;hsa-miR-92a-3p | 15 | TEAD1 | Sponge network | -1.053 | 0.00923 | -0.582 | 1.0E-5 | 0.26 |
227 | RP11-166D19.1 |
hsa-let-7a-3p;hsa-miR-130a-3p;hsa-miR-18a-5p;hsa-miR-19a-3p;hsa-miR-224-5p;hsa-miR-2355-5p;hsa-miR-27a-3p;hsa-miR-454-3p;hsa-miR-576-5p;hsa-miR-590-5p | 10 | SMAD4 | Sponge network | -0.882 | 5.0E-5 | -0.43 | 0 | 0.259 |
228 | RP11-284N8.3 |
hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-23a-3p;hsa-miR-576-5p;hsa-miR-590-5p;hsa-miR-944 | 12 | DLG2 | Sponge network | 0.003 | 0.99478 | -4.457 | 0 | 0.257 |
229 | TPTEP1 |
hsa-let-7a-3p;hsa-miR-130a-3p;hsa-miR-18a-5p;hsa-miR-19a-3p;hsa-miR-21-3p;hsa-miR-224-5p;hsa-miR-2355-5p;hsa-miR-27a-3p;hsa-miR-454-3p;hsa-miR-576-5p;hsa-miR-590-5p | 11 | SMAD4 | Sponge network | -2.193 | 0 | -0.43 | 0 | 0.257 |
230 | AC108142.1 |
hsa-miR-141-3p;hsa-miR-182-5p;hsa-miR-200a-3p;hsa-miR-200a-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-224-3p;hsa-miR-25-3p;hsa-miR-29b-2-5p;hsa-miR-429;hsa-miR-7-1-3p;hsa-miR-96-5p | 12 | TEAD1 | Sponge network | 2.31 | 0 | -0.582 | 1.0E-5 | 0.256 |
231 | LINC00707 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-146a-5p;hsa-miR-195-3p;hsa-miR-200a-3p;hsa-miR-20b-5p;hsa-miR-217;hsa-miR-29b-2-5p;hsa-miR-30a-5p;hsa-miR-30b-5p;hsa-miR-30c-5p;hsa-miR-30d-5p;hsa-miR-30e-5p;hsa-miR-340-5p | 14 | FRMD6 | Sponge network | 2.018 | 1.0E-5 | 0.249 | 0.05024 | 0.256 |
232 | MIR497HG |
hsa-miR-130a-3p;hsa-miR-135b-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-23a-3p;hsa-miR-27a-5p;hsa-miR-29b-1-5p;hsa-miR-590-5p;hsa-miR-7-1-3p;hsa-miR-877-5p | 16 | DLG2 | Sponge network | -1.263 | 0.00248 | -4.457 | 0 | 0.254 |
233 | RP11-321G12.1 |
hsa-miR-130a-3p;hsa-miR-146b-5p;hsa-miR-148b-5p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-20a-5p;hsa-miR-22-5p;hsa-miR-29b-1-5p;hsa-miR-484;hsa-miR-576-5p | 10 | DLG2 | Sponge network | -3.552 | 0 | -4.457 | 0 | 0.252 |
234 | SH3RF3-AS1 |
hsa-miR-149-5p;hsa-miR-18a-5p;hsa-miR-193a-3p;hsa-miR-1976;hsa-miR-205-5p;hsa-miR-29a-5p;hsa-miR-29b-3p;hsa-miR-30b-5p;hsa-miR-30c-5p;hsa-miR-320a;hsa-miR-320b;hsa-miR-576-5p;hsa-miR-582-5p;hsa-miR-7-1-3p | 14 | WWTR1 | Sponge network | -0.175 | 0.58985 | -0.275 | 0.0614 | 0.251 |
235 | BZRAP1-AS1 |
hsa-let-7a-3p;hsa-miR-130a-3p;hsa-miR-141-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200a-3p;hsa-miR-205-5p;hsa-miR-20a-5p;hsa-miR-224-5p;hsa-miR-301a-3p;hsa-miR-454-3p | 13 | TEAD1 | Sponge network | -0.233 | 0.50729 | -0.582 | 1.0E-5 | 0.25 |
236 | LINC01006 | hsa-miR-130a-3p;hsa-miR-17-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-205-5p;hsa-miR-22-5p;hsa-miR-23a-3p;hsa-miR-29b-1-5p;hsa-miR-33b-5p;hsa-miR-484;hsa-miR-511-5p;hsa-miR-576-5p | 12 | DLG2 | Sponge network | -0.754 | 0.09126 | -4.457 | 0 | 0.25 |