This regulatory network was inferred from the input dataset. The miRNAs and mRNAs are
presented as round and rectangle nodes respectively. The numerical value popped up upon mouse over the gene node is the log2 transformed fold-change of the gene expression between the two groups. All of the nodes are clickable, and the detailed information of the miRNAs/mRNAs and related cancer pathway will be displayed in another window. The edges between nodes are supported by both interactions (predicted or experimentally verified) and correlations learnt from cancer dataset. The numerical value popped up upon mouse over the edge is the correlation beat value (effect size) between the two nodes. The experimental evidences of the edges reported in previous cancer studies are highlighted by red/orange color. All of these information can be accessed by the "mouse-over" action. This network shows a full map of the miRNA-mRNA regulation of the input gene list(s), and the hub miRNAs (with the high network degree/betweenness centrality) would be the potential cancer drivers or tumor suppressors. The full result table can be accessed in the "Regulations" tab.
"miRNACancerMAP" is also a network visualization tool for users to draw their regulatory network by personal customization. Users can set the complexity of the network by limiting the number of nodes or edges. And the color of the nodes can be defined by different categories of the mRNAs and miRNAs, such as Gene-Ontology, pathway, and expression status. Users can also select to use network degree or network betweenness centrality to define the node size. And edges can be black or colored by the correlation. Purple edge means negative correlation (mostly found between miRNA and mRNA), and blue edge means positive correlation (found in PPI or miRNA-miRNA sponge effect). We can also add the protein-protein interactions (PPI) into the network. This result will show the cluster of genes regulated by some specific miRNAs. Additionally, miRNA-miRNA edges can be added by the "miRNA sponge" button, presenting some clusters of miRNAs that have the interactions via sponge effect.
Num | microRNA | Gene | miRNA log2FC | miRNA pvalue | Gene log2FC | Gene pvalue | Interaction | Correlation beta | Correlation P-value | PMID | Reported in cancer studies |
---|---|---|---|---|---|---|---|---|---|---|---|
1 | hsa-miR-30c-5p | ABCD2 | -0.43 | 0.00403 | -1.62 | 0 | MirTarget | -0.19 | 0.04591 | NA | |
2 | hsa-miR-30c-5p | ABCE1 | -0.43 | 0.00403 | 0.66 | 0 | miRNAWalker2 validate | -0.15 | 0 | NA | |
3 | hsa-miR-30c-5p | ABL1 | -0.43 | 0.00403 | -0.12 | 0.14608 | MirTarget; miRNATAP | -0.1 | 0.00032 | NA | |
4 | hsa-miR-30c-5p | ABL2 | -0.43 | 0.00403 | -0.01 | 0.94193 | mirMAP; miRNATAP | -0.14 | 7.0E-5 | NA | |
5 | hsa-miR-30c-5p | ACAP2 | -0.43 | 0.00403 | 0.87 | 0 | MirTarget; miRNATAP | -0.14 | 0.00513 | NA | |
6 | hsa-miR-30d-5p | ACAP2 | -2.07 | 0 | 0.87 | 0 | MirTarget; miRNATAP | -0.18 | 4.0E-5 | NA | |
7 | hsa-miR-30c-5p | ACTN1 | -0.43 | 0.00403 | 0.44 | 0.00456 | miRNATAP | -0.29 | 0 | NA | |
8 | hsa-miR-30d-5p | ACTN1 | -2.07 | 0 | 0.44 | 0.00456 | miRNATAP | -0.28 | 0 | NA | |
9 | hsa-miR-30c-5p | ACVR1 | -0.43 | 0.00403 | 0.36 | 0.00091 | MirTarget; miRNATAP | -0.2 | 0 | NA | |
10 | hsa-miR-30d-5p | ACVR1 | -2.07 | 0 | 0.36 | 0.00091 | MirTarget; miRNATAP | -0.17 | 0 | NA | |
11 | hsa-miR-30d-5p | ADAM11 | -2.07 | 0 | 1.92 | 0 | miRNATAP | -0.18 | 0.04426 | NA | |
12 | hsa-miR-30c-5p | ADAM19 | -0.43 | 0.00403 | 0.34 | 0.11219 | MirTarget; miRNATAP | -0.34 | 0 | 25799050 | Furthermore bioinformatics algorithm and luciferase reporter assay indicated ADAM19 as a direct target of miR-30c; Of interest further experiments demonstrated that inhibition of ADAM19 by miR-30c partially mediated the anti-tumor effect of miR-30c; Overall our study provides the new insight that miR-30c inhibited colon cancer cells via targeting ADAM19 |
13 | hsa-miR-30d-5p | ADAM19 | -2.07 | 0 | 0.34 | 0.11219 | MirTarget; miRNATAP | -0.32 | 0 | NA | |
14 | hsa-miR-30c-5p | ADRA2A | -0.43 | 0.00403 | -1.31 | 1.0E-5 | MirTarget; miRNATAP | -0.21 | 0.03795 | NA | |
15 | hsa-miR-30d-5p | AFAP1L2 | -2.07 | 0 | 0.42 | 0.09414 | MirTarget; miRNATAP | -0.39 | 0 | NA | |
16 | hsa-miR-30c-5p | AKR1C1 | -0.43 | 0.00403 | 2.49 | 0 | mirMAP | -0.54 | 0.00274 | NA | |
17 | hsa-miR-30d-5p | AKR1C1 | -2.07 | 0 | 2.49 | 0 | mirMAP | -0.56 | 0.00058 | NA | |
18 | hsa-miR-30c-5p | ALG10 | -0.43 | 0.00403 | 1.21 | 0 | MirTarget | -0.16 | 0.0003 | NA | |
19 | hsa-miR-30d-5p | ALG10 | -2.07 | 0 | 1.21 | 0 | MirTarget | -0.3 | 0 | NA | |
20 | hsa-miR-30d-5p | ALG6 | -2.07 | 0 | 0.84 | 0 | MirTarget | -0.18 | 0 | NA | |
21 | hsa-miR-30d-5p | AMMECR1 | -2.07 | 0 | 1.35 | 0 | miRNATAP | -0.29 | 0 | NA | |
22 | hsa-miR-30d-5p | ANKRD52 | -2.07 | 0 | 0.72 | 0 | miRNATAP | -0.12 | 9.0E-5 | NA | |
23 | hsa-miR-30c-5p | ANTXR1 | -0.43 | 0.00403 | -0.56 | 0.00196 | mirMAP | -0.41 | 0 | NA | |
24 | hsa-miR-30c-5p | ANTXR2 | -0.43 | 0.00403 | -1.4 | 0 | mirMAP | -0.15 | 0.01982 | NA | |
25 | hsa-miR-30d-5p | AP2A1 | -2.07 | 0 | 0.52 | 0 | miRNATAP | -0.18 | 0 | NA | |
26 | hsa-miR-30d-5p | ARHGAP32 | -2.07 | 0 | 0.78 | 0 | MirTarget; mirMAP | -0.17 | 3.0E-5 | NA | |
27 | hsa-miR-30c-5p | ARID3A | -0.43 | 0.00403 | 0.86 | 0 | mirMAP | -0.19 | 6.0E-5 | NA | |
28 | hsa-miR-30d-5p | ARID3A | -2.07 | 0 | 0.86 | 0 | mirMAP | -0.12 | 0.00621 | NA | |
29 | hsa-miR-30d-5p | ARL4C | -2.07 | 0 | 1.08 | 0 | miRNATAP | -0.24 | 0 | NA | |
30 | hsa-miR-30c-5p | ARL5B | -0.43 | 0.00403 | 0.2 | 0.10264 | mirMAP | -0.17 | 4.0E-5 | NA | |
31 | hsa-miR-30d-5p | ARL6IP6 | -2.07 | 0 | 0.85 | 0 | miRNATAP | -0.22 | 0 | NA | |
32 | hsa-miR-30c-5p | ASAP2 | -0.43 | 0.00403 | 0.55 | 0 | mirMAP | -0.15 | 0.00047 | NA | |
33 | hsa-miR-30d-5p | ASAP2 | -2.07 | 0 | 0.55 | 0 | mirMAP | -0.15 | 0.0001 | NA | |
34 | hsa-miR-30c-5p | ASCC3 | -0.43 | 0.00403 | 0.57 | 0 | MirTarget | -0.11 | 0.00119 | NA | |
35 | hsa-miR-30d-5p | ASCC3 | -2.07 | 0 | 0.57 | 0 | MirTarget | -0.19 | 0 | NA | |
36 | hsa-miR-30d-5p | ATAD2B | -2.07 | 0 | 0.78 | 0 | MirTarget; miRNATAP | -0.1 | 0.0004 | NA | |
37 | hsa-miR-30c-5p | ATF2 | -0.43 | 0.00403 | 0.03 | 0.68356 | mirMAP | -0.1 | 0.00026 | NA | |
38 | hsa-miR-30d-5p | ATG5 | -2.07 | 0 | 0.32 | 0.00015 | MirTarget; miRNATAP | -0.11 | 2.0E-5 | NA | |
39 | hsa-miR-30d-5p | ATL2 | -2.07 | 0 | 0.79 | 0 | miRNATAP | -0.21 | 0 | NA | |
40 | hsa-miR-30c-5p | ATL3 | -0.43 | 0.00403 | -0 | 0.98093 | mirMAP | -0.17 | 0.00264 | NA | |
41 | hsa-miR-30d-5p | ATL3 | -2.07 | 0 | -0 | 0.98093 | mirMAP | -0.11 | 0.0335 | NA | |
42 | hsa-miR-30c-5p | ATP2A2 | -0.43 | 0.00403 | 1.05 | 0 | mirMAP | -0.19 | 0 | NA | |
43 | hsa-miR-30d-5p | ATP2A2 | -2.07 | 0 | 1.05 | 0 | mirMAP | -0.27 | 0 | NA | |
44 | hsa-miR-30c-5p | ATP2B1 | -0.43 | 0.00403 | 0.37 | 0.04291 | MirTarget; mirMAP; miRNATAP | -0.17 | 0.00764 | NA | |
45 | hsa-miR-30c-5p | ATP8B1 | -0.43 | 0.00403 | 0.69 | 0 | miRNATAP | -0.13 | 0.00835 | NA | |
46 | hsa-miR-30d-5p | ATP8B1 | -2.07 | 0 | 0.69 | 0 | miRNATAP | -0.1 | 0.02713 | NA | |
47 | hsa-miR-30c-5p | ATP8B2 | -0.43 | 0.00403 | -0.6 | 0.00035 | miRNATAP | -0.13 | 0.02867 | NA | |
48 | hsa-miR-30d-5p | ATR | -2.07 | 0 | 0.96 | 0 | mirMAP | -0.22 | 0 | NA | |
49 | hsa-miR-30c-5p | AVL9 | -0.43 | 0.00403 | 0.9 | 0 | MirTarget; mirMAP; miRNATAP | -0.18 | 0 | NA | |
50 | hsa-miR-30d-5p | AVL9 | -2.07 | 0 | 0.9 | 0 | MirTarget; mirMAP; miRNATAP | -0.27 | 0 | NA | |
51 | hsa-miR-30c-5p | AZIN1 | -0.43 | 0.00403 | 0.54 | 0 | mirMAP; miRNATAP | -0.13 | 3.0E-5 | NA | |
52 | hsa-miR-30d-5p | AZIN1 | -2.07 | 0 | 0.54 | 0 | miRNATAP | -0.15 | 0 | NA | |
53 | hsa-miR-30c-5p | B3GNT5 | -0.43 | 0.00403 | 1.19 | 0 | miRNAWalker2 validate; MirTarget; miRNATAP | -0.28 | 1.0E-5 | NA | |
54 | hsa-miR-30d-5p | B3GNT5 | -2.07 | 0 | 1.19 | 0 | MirTarget; miRNATAP | -0.3 | 0 | NA | |
55 | hsa-miR-30c-5p | B4GALT1 | -0.43 | 0.00403 | 0.12 | 0.31404 | mirMAP | -0.12 | 0.00514 | NA | |
56 | hsa-miR-30d-5p | B4GALT6 | -2.07 | 0 | 0.87 | 1.0E-5 | MirTarget | -0.16 | 0.0082 | NA | |
57 | hsa-miR-30c-5p | BACH1 | -0.43 | 0.00403 | -0.34 | 0.00185 | miRNATAP | -0.12 | 0.00118 | NA | |
58 | hsa-miR-30c-5p | BAG4 | -0.43 | 0.00403 | 0.72 | 2.0E-5 | mirMAP | -0.17 | 0.00325 | NA | |
59 | hsa-miR-30d-5p | BAG4 | -2.07 | 0 | 0.72 | 2.0E-5 | mirMAP | -0.16 | 0.00236 | NA | |
60 | hsa-miR-30c-5p | BCL11B | -0.43 | 0.00403 | 1.57 | 0 | miRNATAP | -0.2 | 0.01879 | NA | |
61 | hsa-miR-30d-5p | BCL11B | -2.07 | 0 | 1.57 | 0 | miRNATAP | -0.36 | 0 | NA | |
62 | hsa-miR-30d-5p | BCL2L11 | -2.07 | 0 | 0.77 | 0 | miRNATAP | -0.19 | 0 | NA | |
63 | hsa-miR-30d-5p | BCL9 | -2.07 | 0 | 0.8 | 0 | miRNATAP | -0.18 | 0 | NA | |
64 | hsa-miR-30d-5p | BEND3 | -2.07 | 0 | 1.04 | 0 | mirMAP; miRNATAP | -0.21 | 0 | NA | |
65 | hsa-miR-30c-5p | BICD1 | -0.43 | 0.00403 | 0.8 | 0 | mirMAP | -0.22 | 3.0E-5 | NA | |
66 | hsa-miR-30d-5p | BICD1 | -2.07 | 0 | 0.8 | 0 | mirMAP | -0.27 | 0 | NA | |
67 | hsa-miR-30c-5p | BIRC5 | -0.43 | 0.00403 | 5.23 | 0 | miRNAWalker2 validate | -0.4 | 0.00025 | NA | |
68 | hsa-miR-30c-5p | BLMH | -0.43 | 0.00403 | 0.93 | 0 | miRNAWalker2 validate | -0.14 | 0.01515 | NA | |
69 | hsa-miR-30c-5p | BMP7 | -0.43 | 0.00403 | 3.61 | 0 | mirMAP; miRNATAP | -0.28 | 0.04166 | NA | |
70 | hsa-miR-30d-5p | BMP7 | -2.07 | 0 | 3.61 | 0 | mirMAP; miRNATAP | -0.84 | 0 | NA | |
71 | hsa-miR-30c-5p | BNC1 | -0.43 | 0.00403 | 5.3 | 0 | MirTarget; miRNATAP | -0.48 | 0.00638 | NA | |
72 | hsa-miR-30d-5p | BNC1 | -2.07 | 0 | 5.3 | 0 | MirTarget; miRNATAP | -1.42 | 0 | NA | |
73 | hsa-miR-30c-5p | BNC2 | -0.43 | 0.00403 | -1.29 | 0 | mirMAP; miRNATAP | -0.32 | 0.00022 | NA | |
74 | hsa-miR-30c-5p | BRD4 | -0.43 | 0.00403 | 0.62 | 0 | mirMAP | -0.16 | 1.0E-5 | NA | |
75 | hsa-miR-30d-5p | BRD4 | -2.07 | 0 | 0.62 | 0 | mirMAP | -0.13 | 9.0E-5 | NA | |
76 | hsa-miR-30d-5p | BRWD3 | -2.07 | 0 | 0.69 | 0 | MirTarget; miRNATAP | -0.11 | 0.01992 | NA | |
77 | hsa-miR-30c-5p | BTBD10 | -0.43 | 0.00403 | 0.7 | 0 | MirTarget; miRNATAP | -0.1 | 0.00693 | NA | |
78 | hsa-miR-30d-5p | BTBD10 | -2.07 | 0 | 0.7 | 0 | MirTarget; miRNATAP | -0.22 | 0 | NA | |
79 | hsa-miR-30d-5p | C16orf87 | -2.07 | 0 | 0.78 | 0 | miRNATAP | -0.21 | 0 | NA | |
80 | hsa-miR-30c-5p | C1QBP | -0.43 | 0.00403 | 0.97 | 0 | miRNAWalker2 validate | -0.16 | 0.00036 | NA | |
81 | hsa-miR-30c-5p | C21orf91 | -0.43 | 0.00403 | 0.57 | 0.0004 | mirMAP | -0.12 | 0.03733 | NA | |
82 | hsa-miR-30d-5p | C21orf91 | -2.07 | 0 | 0.57 | 0.0004 | mirMAP | -0.15 | 0.00428 | NA | |
83 | hsa-miR-30c-5p | C4orf46 | -0.43 | 0.00403 | 0.91 | 0 | mirMAP | -0.13 | 0.00135 | NA | |
84 | hsa-miR-30d-5p | C4orf46 | -2.07 | 0 | 0.91 | 0 | mirMAP | -0.23 | 0 | NA | |
85 | hsa-miR-30c-5p | C6orf132 | -0.43 | 0.00403 | 0.58 | 0.00071 | mirMAP | -0.17 | 0.00417 | NA | |
86 | hsa-miR-30d-5p | C6orf132 | -2.07 | 0 | 0.58 | 0.00071 | mirMAP | -0.16 | 0.00221 | NA | |
87 | hsa-miR-30d-5p | C7orf43 | -2.07 | 0 | 0.79 | 0 | miRNATAP | -0.16 | 0 | NA | |
88 | hsa-miR-30c-5p | CALU | -0.43 | 0.00403 | 0.75 | 0 | MirTarget | -0.25 | 0 | NA | |
89 | hsa-miR-30d-5p | CALU | -2.07 | 0 | 0.75 | 0 | MirTarget | -0.25 | 0 | NA | |
90 | hsa-miR-30c-5p | CAND1 | -0.43 | 0.00403 | 0.85 | 0 | mirMAP | -0.13 | 0.00015 | NA | |
91 | hsa-miR-30d-5p | CAND1 | -2.07 | 0 | 0.85 | 0 | mirMAP | -0.21 | 0 | NA | |
92 | hsa-miR-30d-5p | CAPZA1 | -2.07 | 0 | 0.28 | 0.00102 | MirTarget; miRNATAP | -0.12 | 1.0E-5 | NA | |
93 | hsa-miR-30d-5p | CARS | -2.07 | 0 | 0.58 | 0 | MirTarget; miRNATAP | -0.19 | 0 | NA | |
94 | hsa-miR-30c-5p | CASP3 | -0.43 | 0.00403 | 0.86 | 0 | miRNATAP | -0.14 | 5.0E-5 | NA | |
95 | hsa-miR-30d-5p | CASP3 | -2.07 | 0 | 0.86 | 0 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.24 | 0 | NA | |
96 | hsa-miR-30c-5p | CBFB | -0.43 | 0.00403 | 0.45 | 0 | MirTarget; mirMAP; miRNATAP | -0.14 | 0 | NA | |
97 | hsa-miR-30d-5p | CBFB | -2.07 | 0 | 0.45 | 0 | MirTarget; mirMAP; miRNATAP | -0.21 | 0 | NA | |
98 | hsa-miR-30d-5p | CBLB | -2.07 | 0 | 0.65 | 0 | MirTarget; mirMAP | -0.17 | 1.0E-5 | NA | |
99 | hsa-miR-30c-5p | CBX2 | -0.43 | 0.00403 | 3.27 | 0 | miRNATAP | -0.38 | 0.00011 | NA | |
100 | hsa-miR-30d-5p | CBX2 | -2.07 | 0 | 3.27 | 0 | miRNATAP | -0.8 | 0 | NA | |
101 | hsa-miR-30d-5p | CBX3 | -2.07 | 0 | 1.09 | 0 | MirTarget | -0.29 | 0 | NA | |
102 | hsa-miR-30c-5p | CCDC117 | -0.43 | 0.00403 | 0.53 | 0 | miRNAWalker2 validate; MirTarget; miRNATAP | -0.13 | 0.00014 | NA | |
103 | hsa-miR-30d-5p | CCDC117 | -2.07 | 0 | 0.53 | 0 | MirTarget; miRNATAP | -0.12 | 0.00016 | NA | |
104 | hsa-miR-30d-5p | CCDC43 | -2.07 | 0 | 0.56 | 0 | MirTarget | -0.15 | 0 | NA | |
105 | hsa-miR-30d-5p | CCNA1 | -2.07 | 0 | 0.88 | 0.09811 | MirTarget | -0.37 | 0.02913 | NA | |
106 | hsa-miR-30c-5p | CCNE2 | -0.43 | 0.00403 | 2.53 | 0 | miRNATAP | -0.21 | 0.00294 | NA | |
107 | hsa-miR-30d-5p | CCNE2 | -2.07 | 0 | 2.53 | 0 | miRNATAP | -0.54 | 0 | 25843294 | MicroRNA 30d 5p inhibits tumour cell proliferation and motility by directly targeting CCNE2 in non small cell lung cancer; In addition the re-introduction of CCNE2 expression antagonised the inhibitory effects of miR-30d-5p on the capacity of NSCLC cells for proliferation and motility |
108 | hsa-let-7a-5p | CCNF | -0.64 | 0 | 2.78 | 0 | MirTarget; TargetScan | -0.68 | 0 | NA | |
109 | hsa-let-7b-5p | CCNF | -0.76 | 0 | 2.78 | 0 | miRNAWalker2 validate; MirTarget | -0.4 | 0 | NA | |
110 | hsa-let-7c-5p | CCNF | -1.1 | 0 | 2.78 | 0 | miRNAWalker2 validate; MirTarget | -0.19 | 7.0E-5 | NA | |
111 | hsa-miR-139-5p | CCNF | -2.26 | 0 | 2.78 | 0 | miRanda | -0.43 | 0 | NA | |
112 | hsa-miR-140-5p | CCNF | -0.62 | 0 | 2.78 | 0 | miRanda | -0.44 | 0 | NA | |
113 | hsa-miR-34c-3p | CCNF | -1.49 | 4.0E-5 | 2.78 | 0 | mirMAP | -0.11 | 1.0E-5 | NA | |
114 | hsa-miR-30c-5p | CCPG1 | -0.43 | 0.00403 | -1.19 | 0 | miRNATAP | -0.1 | 0.02981 | NA | |
115 | hsa-miR-30d-5p | CDCA7 | -2.07 | 0 | 3.7 | 0 | MirTarget | -0.86 | 0 | NA | |
116 | hsa-miR-30c-5p | CDH1 | -0.43 | 0.00403 | 1.16 | 0 | miRNAWalker2 validate | -0.16 | 0.00213 | 24112779 | Repression of miR-30c through its inhibitor resulted in reduction of E-cadherin production and promotion of epithelial-mesenchymal transition EMT while overexpression of miR-30c inhibited EMT in RCC cells; Our findings propose a model that hypoxia induces EMT in RCC cells through downregulation of miR-30c which leads to subsequent increase of Slug expression and repression of E-cadherin production and suggest a potential application of miR-30c in RCC treatment |
117 | hsa-miR-30c-5p | CDH13 | -0.43 | 0.00403 | -1.14 | 0.00013 | miRNATAP | -0.38 | 0.00022 | NA | |
118 | hsa-miR-30d-5p | CDH8 | -2.07 | 0 | 2.35 | 0 | mirMAP | -0.59 | 1.0E-5 | NA | |
119 | hsa-miR-30c-5p | CDK12 | -0.43 | 0.00403 | 0.51 | 0 | MirTarget; miRNATAP | -0.12 | 7.0E-5 | NA | |
120 | hsa-miR-30d-5p | CDK12 | -2.07 | 0 | 0.51 | 0 | MirTarget; miRNATAP | -0.11 | 5.0E-5 | NA | |
121 | hsa-miR-30c-5p | CDK6 | -0.43 | 0.00403 | 1.06 | 0 | mirMAP | -0.15 | 0.01225 | NA | |
122 | hsa-miR-30d-5p | CDK6 | -2.07 | 0 | 1.06 | 0 | mirMAP | -0.3 | 0 | NA | |
123 | hsa-miR-30d-5p | CELSR3 | -2.07 | 0 | 2.2 | 0 | MirTarget; miRNATAP | -0.4 | 0 | NA | |
124 | hsa-miR-30c-5p | CEP76 | -0.43 | 0.00403 | 1.09 | 0 | MirTarget | -0.19 | 1.0E-5 | NA | |
125 | hsa-miR-30d-5p | CEP76 | -2.07 | 0 | 1.09 | 0 | MirTarget | -0.21 | 0 | NA | |
126 | hsa-miR-30c-5p | CHRM3 | -0.43 | 0.00403 | 1.64 | 0 | mirMAP | -0.26 | 0.01782 | NA | |
127 | hsa-miR-30d-5p | CHST1 | -2.07 | 0 | 0.3 | 0.25431 | MirTarget | -0.17 | 0.04171 | NA | |
128 | hsa-miR-30d-5p | CHST2 | -2.07 | 0 | 1.23 | 1.0E-5 | MirTarget; miRNATAP | -0.33 | 0.00018 | NA | |
129 | hsa-miR-30c-5p | CIT | -0.43 | 0.00403 | 0.96 | 0 | miRNATAP | -0.1 | 0.0373 | NA | |
130 | hsa-miR-30d-5p | CIT | -2.07 | 0 | 0.96 | 0 | miRNATAP | -0.16 | 0.0003 | NA | |
131 | hsa-miR-30c-5p | CKAP4 | -0.43 | 0.00403 | 1.53 | 0 | miRNAWalker2 validate | -0.21 | 1.0E-5 | NA | |
132 | hsa-miR-30d-5p | CLDN12 | -2.07 | 0 | 0.43 | 7.0E-5 | mirMAP | -0.15 | 1.0E-5 | NA | |
133 | hsa-miR-30d-5p | CLDND1 | -2.07 | 0 | 0.87 | 0 | MirTarget; miRNATAP | -0.19 | 0 | NA | |
134 | hsa-miR-30c-5p | CLOCK | -0.43 | 0.00403 | -0.07 | 0.61101 | MirTarget | -0.2 | 2.0E-5 | NA | |
135 | hsa-miR-30c-5p | CLTC | -0.43 | 0.00403 | 0.2 | 0.0074 | mirMAP | -0.17 | 0 | NA | |
136 | hsa-miR-30d-5p | CLTC | -2.07 | 0 | 0.2 | 0.0074 | mirMAP | -0.1 | 1.0E-5 | NA | |
137 | hsa-miR-30d-5p | COG2 | -2.07 | 0 | 0.32 | 3.0E-5 | miRNATAP | -0.1 | 1.0E-5 | NA | |
138 | hsa-miR-30c-5p | COL12A1 | -0.43 | 0.00403 | 0.1 | 0.74262 | mirMAP | -0.65 | 0 | NA | |
139 | hsa-miR-30d-5p | COL12A1 | -2.07 | 0 | 0.1 | 0.74262 | mirMAP | -0.44 | 0 | NA | |
140 | hsa-miR-30c-5p | COL8A1 | -0.43 | 0.00403 | -1.62 | 0 | MirTarget | -0.49 | 0 | NA | |
141 | hsa-miR-30d-5p | COL9A3 | -2.07 | 0 | 2.72 | 0 | MirTarget | -0.58 | 1.0E-5 | NA | |
142 | hsa-miR-30d-5p | COPS2 | -2.07 | 0 | 0.35 | 1.0E-5 | mirMAP | -0.12 | 0 | NA | |
143 | hsa-miR-30d-5p | COPS7A | -2.07 | 0 | 0.56 | 0 | miRNAWalker2 validate | -0.19 | 0 | NA | |
144 | hsa-miR-30d-5p | COPS7B | -2.07 | 0 | 0.7 | 0 | mirMAP | -0.14 | 0 | NA | |
145 | hsa-miR-30c-5p | CPD | -0.43 | 0.00403 | 0.23 | 0.05807 | mirMAP | -0.16 | 0.00011 | NA | |
146 | hsa-miR-30c-5p | CPSF2 | -0.43 | 0.00403 | 0.47 | 0 | mirMAP | -0.13 | 2.0E-5 | NA | |
147 | hsa-miR-30d-5p | CPSF6 | -2.07 | 0 | 0.87 | 0 | MirTarget; miRNATAP | -0.15 | 0 | NA | |
148 | hsa-miR-30c-5p | CRK | -0.43 | 0.00403 | -0.63 | 0 | miRNATAP | -0.17 | 0 | NA | |
149 | hsa-miR-30c-5p | CRKL | -0.43 | 0.00403 | 0.92 | 0 | MirTarget; mirMAP; miRNATAP | -0.11 | 0.0086 | NA | |
150 | hsa-miR-30d-5p | CRKL | -2.07 | 0 | 0.92 | 0 | MirTarget; mirMAP; miRNATAP | -0.23 | 0 | NA |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 128 | 1784 | 1.085e-17 | 5.048e-14 |
2 | CELL DEVELOPMENT | 108 | 1426 | 1.573e-16 | 3.66e-13 |
3 | TISSUE DEVELOPMENT | 110 | 1518 | 1.748e-15 | 2.712e-12 |
4 | POSITIVE REGULATION OF GENE EXPRESSION | 118 | 1733 | 1.225e-14 | 1.425e-11 |
5 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 81 | 1004 | 5.629e-14 | 5.238e-11 |
6 | POSITIVE REGULATION OF BIOSYNTHETIC PROCESS | 119 | 1805 | 9.031e-14 | 7.003e-11 |
7 | TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 64 | 724 | 5.77e-13 | 3.835e-10 |
8 | EPITHELIUM DEVELOPMENT | 73 | 945 | 8.987e-12 | 5.042e-09 |
9 | NEUROGENESIS | 95 | 1402 | 9.752e-12 | 5.042e-09 |
10 | NEURON DIFFERENTIATION | 68 | 874 | 3.611e-11 | 1.68e-08 |
11 | EMBRYO DEVELOPMENT | 68 | 894 | 9.708e-11 | 4.107e-08 |
12 | ANATOMICAL STRUCTURE FORMATION INVOLVED IN MORPHOGENESIS | 71 | 957 | 1.105e-10 | 4.284e-08 |
13 | EMBRYONIC MORPHOGENESIS | 49 | 539 | 1.314e-10 | 4.702e-08 |
14 | HEAD DEVELOPMENT | 58 | 709 | 1.633e-10 | 5.426e-08 |
15 | TISSUE MORPHOGENESIS | 48 | 533 | 2.813e-10 | 8.726e-08 |
16 | MORPHOGENESIS OF AN EPITHELIUM | 40 | 400 | 4.326e-10 | 1.258e-07 |
17 | CENTRAL NERVOUS SYSTEM DEVELOPMENT | 65 | 872 | 5.97e-10 | 1.634e-07 |
18 | NEGATIVE REGULATION OF NITROGEN COMPOUND METABOLIC PROCESS | 94 | 1517 | 1.502e-09 | 3.882e-07 |
19 | TUBE DEVELOPMENT | 47 | 552 | 2.7e-09 | 6.613e-07 |
20 | NEGATIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 56 | 740 | 5.85e-09 | 1.361e-06 |
21 | NEGATIVE REGULATION OF GENE EXPRESSION | 91 | 1493 | 6.403e-09 | 1.419e-06 |
22 | EMBRYO DEVELOPMENT ENDING IN BIRTH OR EGG HATCHING | 46 | 554 | 8.756e-09 | 1.852e-06 |
23 | ORGAN MORPHOGENESIS | 60 | 841 | 1.448e-08 | 2.93e-06 |
24 | NEURON DEVELOPMENT | 52 | 687 | 2.085e-08 | 3.824e-06 |
25 | CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 43 | 513 | 2.062e-08 | 3.824e-06 |
26 | EPITHELIAL CELL DIFFERENTIATION | 42 | 495 | 2.137e-08 | 3.824e-06 |
27 | MORPHOGENESIS OF A BRANCHING STRUCTURE | 22 | 167 | 3.116e-08 | 5e-06 |
28 | TUBE MORPHOGENESIS | 32 | 323 | 3.079e-08 | 5e-06 |
29 | CELLULAR RESPONSE TO STRESS | 92 | 1565 | 2.975e-08 | 5e-06 |
30 | MITOTIC CELL CYCLE | 55 | 766 | 4.835e-08 | 7.5e-06 |
31 | CELL PROLIFERATION | 50 | 672 | 6.749e-08 | 1.013e-05 |
32 | REGULATION OF CELLULAR RESPONSE TO STRESS | 50 | 691 | 1.595e-07 | 2.319e-05 |
33 | APPENDAGE DEVELOPMENT | 21 | 169 | 1.764e-07 | 2.414e-05 |
34 | LIMB DEVELOPMENT | 21 | 169 | 1.764e-07 | 2.414e-05 |
35 | REGULATION OF PROTEIN INSERTION INTO MITOCHONDRIAL MEMBRANE INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 9 | 29 | 2.343e-07 | 3.029e-05 |
36 | POSITIVE REGULATION OF PROTEIN INSERTION INTO MITOCHONDRIAL MEMBRANE INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 9 | 29 | 2.343e-07 | 3.029e-05 |
37 | CELL CYCLE | 78 | 1316 | 2.757e-07 | 3.467e-05 |
38 | MORPHOGENESIS OF EMBRYONIC EPITHELIUM | 18 | 134 | 4.132e-07 | 5.06e-05 |
39 | CELL CYCLE PROCESS | 67 | 1081 | 4.294e-07 | 5.123e-05 |
40 | REGULATION OF ANATOMICAL STRUCTURE MORPHOGENESIS | 64 | 1021 | 5.376e-07 | 6.254e-05 |
41 | FORMATION OF PRIMARY GERM LAYER | 16 | 110 | 6.082e-07 | 6.738e-05 |
42 | REGULATION OF MULTICELLULAR ORGANISMAL DEVELOPMENT | 92 | 1672 | 5.976e-07 | 6.738e-05 |
43 | PROTEIN MODIFICATION BY SMALL PROTEIN CONJUGATION OR REMOVAL | 57 | 873 | 6.47e-07 | 7.001e-05 |
44 | UROGENITAL SYSTEM DEVELOPMENT | 28 | 299 | 7.084e-07 | 7.491e-05 |
45 | REGULATION OF CELL DIFFERENTIATION | 84 | 1492 | 7.852e-07 | 8.119e-05 |
46 | REGULATION OF CELL DEATH | 83 | 1472 | 8.662e-07 | 8.762e-05 |
47 | PROTEASOMAL PROTEIN CATABOLIC PROCESS | 26 | 271 | 1.116e-06 | 0.0001105 |
48 | STEM CELL DIFFERENTIATION | 21 | 190 | 1.257e-06 | 0.0001219 |
49 | BRANCHING MORPHOGENESIS OF AN EPITHELIAL TUBE | 17 | 131 | 1.411e-06 | 0.000134 |
50 | REGULATION OF ORGAN MORPHOGENESIS | 24 | 242 | 1.6e-06 | 0.0001489 |
51 | MITOCHONDRIAL MEMBRANE ORGANIZATION | 14 | 92 | 1.757e-06 | 0.0001574 |
52 | REGULATION OF CELLULAR COMPONENT MOVEMENT | 51 | 771 | 1.769e-06 | 0.0001574 |
53 | POSITIVE REGULATION OF MITOCHONDRIAL OUTER MEMBRANE PERMEABILIZATION INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 9 | 36 | 1.793e-06 | 0.0001574 |
54 | EMBRYONIC ORGAN DEVELOPMENT | 33 | 406 | 1.828e-06 | 0.0001575 |
55 | NEURON PROJECTION DEVELOPMENT | 40 | 545 | 2.005e-06 | 0.0001696 |
56 | GROWTH | 33 | 410 | 2.263e-06 | 0.0001847 |
57 | MORPHOGENESIS OF A POLARIZED EPITHELIUM | 8 | 28 | 2.256e-06 | 0.0001847 |
58 | PROTEIN LOCALIZATION | 95 | 1805 | 2.653e-06 | 0.0002096 |
59 | REGULATION OF MEMBRANE PERMEABILITY | 12 | 70 | 2.658e-06 | 0.0002096 |
60 | SENSORY ORGAN DEVELOPMENT | 37 | 493 | 2.907e-06 | 0.0002254 |
61 | SYMPATHETIC NERVOUS SYSTEM DEVELOPMENT | 7 | 21 | 3.11e-06 | 0.0002334 |
62 | REGULATION OF CELL PROLIFERATION | 82 | 1496 | 3.07e-06 | 0.0002334 |
63 | CARDIOVASCULAR SYSTEM DEVELOPMENT | 51 | 788 | 3.302e-06 | 0.00024 |
64 | CIRCULATORY SYSTEM DEVELOPMENT | 51 | 788 | 3.302e-06 | 0.00024 |
65 | EPITHELIAL CELL DEVELOPMENT | 20 | 186 | 3.435e-06 | 0.0002422 |
66 | INTRACELLULAR SIGNAL TRANSDUCTION | 85 | 1572 | 3.393e-06 | 0.0002422 |
67 | REGULATION OF CELL DEVELOPMENT | 53 | 836 | 3.851e-06 | 0.0002675 |
68 | MESENCHYME DEVELOPMENT | 20 | 190 | 4.76e-06 | 0.0003257 |
69 | TUBE FORMATION | 16 | 129 | 5.211e-06 | 0.0003514 |
70 | HEART DEVELOPMENT | 35 | 466 | 5.296e-06 | 0.000352 |
71 | DEVELOPMENTAL GROWTH | 28 | 333 | 5.809e-06 | 0.0003807 |
72 | CELL FATE COMMITMENT | 22 | 227 | 6.276e-06 | 0.0004056 |
73 | MEMBRANE ORGANIZATION | 55 | 899 | 7.176e-06 | 0.0004574 |
74 | CELLULAR COMPONENT MORPHOGENESIS | 55 | 900 | 7.411e-06 | 0.000466 |
75 | REGULATION OF CELL CYCLE | 57 | 949 | 8.402e-06 | 0.0005213 |
76 | MESENCHYMAL CELL DIFFERENTIATION | 16 | 134 | 8.544e-06 | 0.0005231 |
77 | MOVEMENT OF CELL OR SUBCELLULAR COMPONENT | 71 | 1275 | 8.842e-06 | 0.0005275 |
78 | REGULATION OF MITOCHONDRIAL OUTER MEMBRANE PERMEABILIZATION INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 9 | 43 | 8.745e-06 | 0.0005275 |
79 | MESODERM MORPHOGENESIS | 11 | 66 | 9.181e-06 | 0.0005407 |
80 | PEPTIDYL AMINO ACID MODIFICATION | 52 | 841 | 9.597e-06 | 0.0005582 |
81 | CELLULAR MACROMOLECULE LOCALIZATION | 69 | 1234 | 1.043e-05 | 0.0005993 |
82 | REGULATION OF APOPTOTIC SIGNALING PATHWAY | 29 | 363 | 1.066e-05 | 0.0006048 |
83 | NEURON PROJECTION MORPHOGENESIS | 31 | 402 | 1.082e-05 | 0.0006066 |
84 | ESTABLISHMENT OF TISSUE POLARITY | 6 | 17 | 1.115e-05 | 0.0006177 |
85 | PROTEIN UBIQUITINATION | 42 | 629 | 1.174e-05 | 0.0006428 |
86 | NEGATIVE REGULATION OF CELL DEATH | 53 | 872 | 1.269e-05 | 0.0006867 |
87 | LUNG MORPHOGENESIS | 9 | 45 | 1.296e-05 | 0.0006931 |
88 | CELL MORPHOGENESIS INVOLVED IN NEURON DIFFERENTIATION | 29 | 368 | 1.381e-05 | 0.00073 |
89 | GASTRULATION | 17 | 155 | 1.413e-05 | 0.0007387 |
90 | MESODERMAL CELL DIFFERENTIATION | 7 | 26 | 1.525e-05 | 0.0007883 |
91 | WNT SIGNALING PATHWAY | 28 | 351 | 1.549e-05 | 0.0007921 |
92 | CELL CYCLE G1 S PHASE TRANSITION | 14 | 111 | 1.652e-05 | 0.0008093 |
93 | SMALL GTPASE MEDIATED SIGNAL TRANSDUCTION | 28 | 352 | 1.632e-05 | 0.0008093 |
94 | G1 S TRANSITION OF MITOTIC CELL CYCLE | 14 | 111 | 1.652e-05 | 0.0008093 |
95 | CELL PROJECTION ORGANIZATION | 54 | 902 | 1.602e-05 | 0.0008093 |
96 | REGULATION OF NEURON DIFFERENTIATION | 38 | 554 | 1.694e-05 | 0.000821 |
97 | PROTEIN POLYUBIQUITINATION | 22 | 243 | 1.847e-05 | 0.0008726 |
98 | EMBRYONIC ORGAN MORPHOGENESIS | 24 | 279 | 1.833e-05 | 0.0008726 |
99 | GOLGI ORGANIZATION | 12 | 84 | 1.857e-05 | 0.0008726 |
100 | PROTEIN CATABOLIC PROCESS | 39 | 579 | 1.981e-05 | 0.0009052 |
101 | SKELETAL SYSTEM DEVELOPMENT | 33 | 455 | 2.004e-05 | 0.0009052 |
102 | GLAND DEVELOPMENT | 30 | 395 | 2.001e-05 | 0.0009052 |
103 | REGULATION OF CELL CYCLE PROCESS | 38 | 558 | 1.986e-05 | 0.0009052 |
104 | PHOSPHATE CONTAINING COMPOUND METABOLIC PROCESS | 98 | 1977 | 2.205e-05 | 0.0009864 |
105 | CONNECTIVE TISSUE DEVELOPMENT | 19 | 194 | 2.29e-05 | 0.001015 |
106 | POSITIVE REGULATION OF CELL COMMUNICATION | 80 | 1532 | 2.372e-05 | 0.001041 |
107 | BIOLOGICAL ADHESION | 59 | 1032 | 2.506e-05 | 0.00109 |
108 | POSITIVE REGULATION OF CELLULAR COMPONENT ORGANIZATION | 64 | 1152 | 2.705e-05 | 0.001165 |
109 | CARTILAGE DEVELOPMENT | 16 | 147 | 2.761e-05 | 0.001179 |
110 | ENDOMEMBRANE SYSTEM ORGANIZATION | 33 | 465 | 3.095e-05 | 0.001309 |
111 | NEURAL TUBE DEVELOPMENT | 16 | 149 | 3.264e-05 | 0.001356 |
112 | ASTROCYTE DIFFERENTIATION | 8 | 39 | 3.245e-05 | 0.001356 |
113 | EPITHELIAL CELL PROLIFERATION | 12 | 89 | 3.36e-05 | 0.001383 |
114 | REPRODUCTIVE SYSTEM DEVELOPMENT | 30 | 408 | 3.674e-05 | 0.001487 |
115 | VASCULATURE DEVELOPMENT | 33 | 469 | 3.667e-05 | 0.001487 |
116 | IN UTERO EMBRYONIC DEVELOPMENT | 25 | 311 | 3.856e-05 | 0.001547 |
117 | ODONTOGENESIS | 13 | 105 | 4.012e-05 | 0.001596 |
118 | CELL JUNCTION ORGANIZATION | 18 | 185 | 4.074e-05 | 0.001606 |
119 | MUSCLE TISSUE DEVELOPMENT | 23 | 275 | 4.233e-05 | 0.001655 |
120 | POSITIVE REGULATION OF CELL DIFFERENTIATION | 49 | 823 | 4.575e-05 | 0.001774 |
121 | DEVELOPMENTAL PROCESS INVOLVED IN REPRODUCTION | 39 | 602 | 4.677e-05 | 0.001799 |
122 | NEURON PROJECTION GUIDANCE | 19 | 205 | 4.912e-05 | 0.001873 |
123 | POSITIVE REGULATION OF CELL DEATH | 39 | 605 | 5.208e-05 | 0.00197 |
124 | REGULATION OF ORGANELLE ORGANIZATION | 64 | 1178 | 5.26e-05 | 0.001974 |
125 | PROTEIN PHOSPHORYLATION | 54 | 944 | 5.492e-05 | 0.002045 |
126 | AUTONOMIC NERVOUS SYSTEM DEVELOPMENT | 8 | 42 | 5.708e-05 | 0.002108 |
127 | NEURAL TUBE FORMATION | 12 | 94 | 5.822e-05 | 0.002133 |
128 | POSITIVE REGULATION OF NEURON DEATH | 10 | 67 | 6.257e-05 | 0.002275 |
129 | LOCOMOTION | 61 | 1114 | 6.357e-05 | 0.002293 |
130 | REGULATION OF CELL AGING | 7 | 33 | 8.107e-05 | 0.002902 |
131 | REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION TO MITOCHONDRION | 14 | 128 | 8.195e-05 | 0.002911 |
132 | EYE DEVELOPMENT | 25 | 326 | 8.276e-05 | 0.002917 |
133 | POSITIVE REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 16 | 162 | 9.001e-05 | 0.003149 |
134 | NEGATIVE REGULATION OF CELL PROLIFERATION | 40 | 643 | 9.075e-05 | 0.003151 |
135 | RESPIRATORY SYSTEM DEVELOPMENT | 18 | 197 | 9.251e-05 | 0.003189 |
136 | REGULATION OF NEURON DEATH | 21 | 252 | 9.483e-05 | 0.003245 |
137 | POSITIVE REGULATION OF CELL DEVELOPMENT | 32 | 472 | 9.653e-05 | 0.003279 |
138 | NEGATIVE REGULATION OF MITOTIC CELL CYCLE | 18 | 199 | 0.0001053 | 0.00355 |
139 | CELL CYCLE PHASE TRANSITION | 21 | 255 | 0.0001121 | 0.003736 |
140 | PEPTIDYL THREONINE MODIFICATION | 8 | 46 | 0.0001124 | 0.003736 |
141 | REGULATION OF PROTEIN MODIFICATION PROCESS | 84 | 1710 | 0.000124 | 0.004093 |
142 | DNA TEMPLATED TRANSCRIPTION INITIATION | 18 | 202 | 0.0001274 | 0.004174 |
143 | THYMUS DEVELOPMENT | 8 | 47 | 0.0001316 | 0.004282 |
144 | POSITIVE REGULATION OF CELL PROLIFERATION | 47 | 814 | 0.0001349 | 0.004347 |
145 | MESODERM DEVELOPMENT | 13 | 118 | 0.0001355 | 0.004347 |
146 | FOREBRAIN DEVELOPMENT | 26 | 357 | 0.0001393 | 0.004414 |
147 | POSITIVE REGULATION OF OSTEOBLAST DIFFERENTIATION | 9 | 60 | 0.0001394 | 0.004414 |
148 | REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 44 | 750 | 0.0001551 | 0.004853 |
149 | DEVELOPMENTAL GROWTH INVOLVED IN MORPHOGENESIS | 12 | 104 | 0.0001565 | 0.004853 |
150 | REPRODUCTION | 67 | 1297 | 0.0001559 | 0.004853 |
151 | REGULATION OF CELLULAR SENESCENCE | 6 | 26 | 0.0001612 | 0.004901 |
152 | REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 15 | 153 | 0.0001607 | 0.004901 |
153 | TRANSCRIPTION INITIATION FROM RNA POLYMERASE II PROMOTER | 15 | 153 | 0.0001607 | 0.004901 |
154 | POSITIVE REGULATION OF RESPONSE TO STIMULUS | 92 | 1929 | 0.0001639 | 0.004952 |
155 | ODONTOGENESIS OF DENTIN CONTAINING TOOTH | 10 | 75 | 0.0001653 | 0.004962 |
156 | POSITIVE REGULATION OF APOPTOTIC SIGNALING PATHWAY | 16 | 171 | 0.0001698 | 0.005065 |
157 | REGULATION OF TRANSMEMBRANE RECEPTOR PROTEIN SERINE THREONINE KINASE SIGNALING PATHWAY | 18 | 207 | 0.0001733 | 0.005071 |
158 | PHOSPHORYLATION | 64 | 1228 | 0.0001723 | 0.005071 |
159 | REGULATION OF CELL MORPHOGENESIS | 35 | 552 | 0.0001719 | 0.005071 |
160 | TELENCEPHALON DEVELOPMENT | 19 | 228 | 0.0002011 | 0.005849 |
161 | REGULATION OF CARTILAGE DEVELOPMENT | 9 | 63 | 0.0002046 | 0.005912 |
162 | ENDOCRINE SYSTEM DEVELOPMENT | 13 | 123 | 0.000206 | 0.005916 |
163 | MACROMOLECULE CATABOLIC PROCESS | 51 | 926 | 0.0002229 | 0.006364 |
164 | POST ANAL TAIL MORPHOGENESIS | 5 | 18 | 0.0002261 | 0.006415 |
165 | EMBRYONIC SKELETAL SYSTEM MORPHOGENESIS | 11 | 93 | 0.000234 | 0.006598 |
166 | HOMOTYPIC CELL CELL ADHESION | 8 | 51 | 0.0002375 | 0.006616 |
167 | CELL CYCLE CHECKPOINT | 17 | 194 | 0.0002373 | 0.006616 |
168 | REGULATION OF RESPONSE TO STRESS | 73 | 1468 | 0.0002482 | 0.006796 |
169 | COCHLEA DEVELOPMENT | 7 | 39 | 0.000246 | 0.006796 |
170 | NEGATIVE REGULATION OF CELL CYCLE | 29 | 433 | 0.0002483 | 0.006796 |
171 | POSITIVE REGULATION OF MULTICELLULAR ORGANISMAL PROCESS | 70 | 1395 | 0.0002586 | 0.007037 |
172 | OSTEOBLAST DIFFERENTIATION | 13 | 126 | 0.0002618 | 0.007063 |
173 | NEGATIVE REGULATION OF CELL DIFFERENTIATION | 37 | 609 | 0.0002626 | 0.007063 |
174 | REGULATION OF ESTABLISHMENT OF PLANAR POLARITY | 12 | 110 | 0.0002664 | 0.007123 |
175 | EPIDERMIS DEVELOPMENT | 20 | 253 | 0.0002786 | 0.007408 |
176 | PROTEIN COMPLEX SUBUNIT ORGANIZATION | 75 | 1527 | 0.0002947 | 0.00779 |
177 | METANEPHROS DEVELOPMENT | 10 | 81 | 0.0003141 | 0.008229 |
178 | PATTERN SPECIFICATION PROCESS | 28 | 418 | 0.0003148 | 0.008229 |
179 | NEGATIVE REGULATION OF CELL CYCLE PHASE TRANSITION | 14 | 146 | 0.000331 | 0.008508 |
180 | CELL AGING | 9 | 67 | 0.0003289 | 0.008508 |
181 | CELL JUNCTION ASSEMBLY | 13 | 129 | 0.0003301 | 0.008508 |
182 | PROSTATE GLAND DEVELOPMENT | 7 | 41 | 0.0003397 | 0.008686 |
183 | CARBOHYDRATE DERIVATIVE BIOSYNTHETIC PROCESS | 36 | 595 | 0.0003424 | 0.008706 |
184 | REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 24 | 337 | 0.0003449 | 0.008721 |
185 | REGULATION OF CELL CYCLE G1 S PHASE TRANSITION | 14 | 147 | 0.000355 | 0.008929 |
186 | SENSORY ORGAN MORPHOGENESIS | 19 | 239 | 0.0003656 | 0.009145 |
187 | EMBRYONIC PLACENTA DEVELOPMENT | 10 | 83 | 0.0003835 | 0.009478 |
188 | CENTRAL NERVOUS SYSTEM NEURON DIFFERENTIATION | 15 | 166 | 0.0003911 | 0.009478 |
189 | TRACHEA DEVELOPMENT | 5 | 20 | 0.0003875 | 0.009478 |
190 | POSITIVE REGULATION OF DEVELOPMENTAL PROCESS | 59 | 1142 | 0.0003875 | 0.009478 |
191 | REGULATION OF INTRACELLULAR TRANSPORT | 37 | 621 | 0.0003815 | 0.009478 |
192 | REGULATION OF PHOSPHORUS METABOLIC PROCESS | 78 | 1618 | 0.0003907 | 0.009478 |
193 | REGULATION OF KIDNEY DEVELOPMENT | 8 | 55 | 0.0004047 | 0.009756 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | MACROMOLECULAR COMPLEX BINDING | 99 | 1399 | 2.478e-13 | 2.302e-10 |
2 | RNA POLYMERASE II TRANSCRIPTION FACTOR ACTIVITY SEQUENCE SPECIFIC DNA BINDING | 58 | 629 | 1.336e-12 | 6.204e-10 |
3 | TRANSCRIPTIONAL ACTIVATOR ACTIVITY RNA POLYMERASE II TRANSCRIPTION REGULATORY REGION SEQUENCE SPECIFIC BINDING | 38 | 315 | 4.714e-12 | 1.46e-09 |
4 | REGULATORY REGION NUCLEIC ACID BINDING | 64 | 818 | 1.131e-10 | 2.101e-08 |
5 | SEQUENCE SPECIFIC DNA BINDING | 75 | 1037 | 1.026e-10 | 2.101e-08 |
6 | DOUBLE STRANDED DNA BINDING | 60 | 764 | 3.883e-10 | 6.012e-08 |
7 | NUCLEIC ACID BINDING TRANSCRIPTION FACTOR ACTIVITY | 79 | 1199 | 2.449e-09 | 3.251e-07 |
8 | TRANSCRIPTION FACTOR ACTIVITY RNA POLYMERASE II CORE PROMOTER PROXIMAL REGION SEQUENCE SPECIFIC BINDING | 32 | 328 | 4.422e-08 | 5.135e-06 |
9 | PROTEIN COMPLEX BINDING | 62 | 935 | 1.18e-07 | 1.137e-05 |
10 | TRANSCRIPTIONAL ACTIVATOR ACTIVITY RNA POLYMERASE II CORE PROMOTER PROXIMAL REGION SEQUENCE SPECIFIC BINDING | 25 | 226 | 1.223e-07 | 1.137e-05 |
11 | ENZYME BINDING | 96 | 1737 | 2.67e-07 | 2.255e-05 |
12 | CHROMATIN BINDING | 36 | 435 | 4.044e-07 | 3.131e-05 |
13 | CORE PROMOTER BINDING | 19 | 152 | 6.163e-07 | 4.404e-05 |
14 | PROTEIN DOMAIN SPECIFIC BINDING | 44 | 624 | 1.79e-06 | 0.0001188 |
15 | TRANSCRIPTION FACTOR ACTIVITY PROTEIN BINDING | 41 | 588 | 5.312e-06 | 0.000329 |
16 | RIBONUCLEOTIDE BINDING | 95 | 1860 | 9.197e-06 | 0.000534 |
17 | KINASE BINDING | 40 | 606 | 2.463e-05 | 0.001346 |
18 | ADENYL NUCLEOTIDE BINDING | 79 | 1514 | 2.751e-05 | 0.00142 |
19 | CORE PROMOTER PROXIMAL REGION DNA BINDING | 28 | 371 | 4.198e-05 | 0.002053 |
20 | CYTOSKELETAL PROTEIN BINDING | 48 | 819 | 8.02e-05 | 0.003725 |
21 | IDENTICAL PROTEIN BINDING | 64 | 1209 | 0.0001113 | 0.004924 |
22 | ACTIN MONOMER BINDING | 6 | 25 | 0.0001275 | 0.005231 |
23 | TRANSCRIPTION COACTIVATOR ACTIVITY | 23 | 296 | 0.0001295 | 0.005231 |
24 | POLY A RNA BINDING | 62 | 1170 | 0.0001389 | 0.005375 |
25 | KINASE ACTIVITY | 48 | 842 | 0.0001547 | 0.005748 |
26 | TRANSFERASE ACTIVITY TRANSFERRING PHOSPHORUS CONTAINING GROUPS | 54 | 992 | 0.0001954 | 0.006982 |
27 | PROTEIN KINASE C BINDING | 8 | 50 | 0.0002061 | 0.00709 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | ANCHORING JUNCTION | 43 | 489 | 5.032e-09 | 2.939e-06 |
2 | CELL JUNCTION | 73 | 1151 | 5.007e-08 | 9.746e-06 |
3 | CELL SUBSTRATE JUNCTION | 36 | 398 | 4.485e-08 | 9.746e-06 |
4 | TRANSCRIPTION FACTOR COMPLEX | 27 | 298 | 2.108e-06 | 0.0003077 |
5 | CATALYTIC COMPLEX | 62 | 1038 | 3.963e-06 | 0.0004628 |
6 | TRANSFERASE COMPLEX | 44 | 703 | 3.524e-05 | 0.00343 |
7 | GOLGI APPARATUS | 75 | 1445 | 5.31e-05 | 0.00443 |
Num | Pathway | Pathview | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|---|
1 | Cellular_senescence_hsa04218 | 20 | 160 | 3.133e-07 | 1.629e-05 | |
2 | ErbB_signaling_pathway_hsa04012 | 11 | 85 | 0.0001038 | 0.00265 | |
3 | Signaling_pathways_regulating_pluripotency_of_stem_cells_hsa04550 | 14 | 139 | 0.0001984 | 0.00265 | |
4 | Cell_cycle_hsa04110 | 13 | 124 | 0.0002233 | 0.00265 | |
5 | PI3K_Akt_signaling_pathway_hsa04151 | 25 | 352 | 0.0002727 | 0.00265 | |
6 | Autophagy_animal_hsa04140 | 13 | 128 | 0.0003058 | 0.00265 | |
7 | mTOR_signaling_pathway_hsa04150 | 14 | 151 | 0.0004667 | 0.002959 | |
8 | Sphingolipid_signaling_pathway_hsa04071 | 12 | 118 | 0.0005095 | 0.002959 | |
9 | Regulation_of_actin_cytoskeleton_hsa04810 | 17 | 208 | 0.0005342 | 0.002959 | |
10 | Hippo_signaling_pathway_hsa04390 | 14 | 154 | 0.000569 | 0.002959 | |
11 | MAPK_signaling_pathway_hsa04010 | 21 | 295 | 0.0007947 | 0.003757 | |
12 | cGMP_PKG_signaling_pathway_hsa04022 | 14 | 163 | 0.000997 | 0.004289 | |
13 | Wnt_signaling_pathway_hsa04310 | 13 | 146 | 0.001072 | 0.004289 | |
14 | FoxO_signaling_pathway_hsa04068 | 12 | 132 | 0.001377 | 0.005115 | |
15 | p53_signaling_pathway_hsa04115 | 8 | 68 | 0.001692 | 0.005866 | |
16 | Adherens_junction_hsa04520 | 8 | 72 | 0.002444 | 0.007943 | |
17 | Endocytosis_hsa04144 | 17 | 244 | 0.003017 | 0.009228 | |
18 | Focal_adhesion_hsa04510 | 14 | 199 | 0.006213 | 0.01795 | |
19 | AMPK_signaling_pathway_hsa04152 | 10 | 121 | 0.006596 | 0.01805 | |
20 | Rap1_signaling_pathway_hsa04015 | 14 | 206 | 0.008329 | 0.02166 | |
21 | VEGF_signaling_pathway_hsa04370 | 6 | 59 | 0.01266 | 0.03135 | |
22 | Apoptosis_hsa04210 | 10 | 138 | 0.01579 | 0.03732 | |
23 | TGF_beta_signaling_pathway_hsa04350 | 7 | 84 | 0.02048 | 0.04594 | |
24 | Oocyte_meiosis_hsa04114 | 9 | 124 | 0.0212 | 0.04594 | |
25 | Apoptosis_multiple_species_hsa04215 | 4 | 33 | 0.02219 | 0.04616 | |
26 | Ferroptosis_hsa04216 | 4 | 40 | 0.04147 | 0.08295 | |
27 | HIF_1_signaling_pathway_hsa04066 | 7 | 100 | 0.0466 | 0.08974 | |
28 | Tight_junction_hsa04530 | 10 | 170 | 0.0544 | 0.101 | |
29 | Mitophagy_animal_hsa04137 | 5 | 65 | 0.06217 | 0.1115 | |
30 | TNF_signaling_pathway_hsa04668 | 7 | 108 | 0.06525 | 0.1131 | |
31 | Ras_signaling_pathway_hsa04014 | 12 | 232 | 0.08184 | 0.1373 | |
32 | cAMP_signaling_pathway_hsa04024 | 10 | 198 | 0.1183 | 0.1923 | |
33 | Hedgehog_signaling_pathway_hsa04340 | 3 | 47 | 0.2001 | 0.3138 | |
34 | Phospholipase_D_signaling_pathway_hsa04072 | 7 | 146 | 0.2052 | 0.3138 | |
35 | Phosphatidylinositol_signaling_system_hsa04070 | 5 | 99 | 0.2261 | 0.3359 | |
36 | Hippo_signaling_pathway_multiple_species_hsa04392 | 2 | 29 | 0.2465 | 0.356 | |
37 | ECM_receptor_interaction_hsa04512 | 4 | 82 | 0.2832 | 0.398 | |
38 | Apelin_signaling_pathway_hsa04371 | 6 | 137 | 0.2954 | 0.4042 | |
39 | Gap_junction_hsa04540 | 4 | 88 | 0.3278 | 0.4371 | |
40 | Notch_signaling_pathway_hsa04330 | 2 | 48 | 0.4709 | 0.6122 | |
41 | Calcium_signaling_pathway_hsa04020 | 6 | 182 | 0.5542 | 0.6957 | |
42 | Phagosome_hsa04145 | 5 | 152 | 0.5619 | 0.6957 | |
43 | Necroptosis_hsa04217 | 5 | 164 | 0.6293 | 0.761 | |
44 | Peroxisome_hsa04146 | 2 | 83 | 0.7619 | 0.8794 | |
45 | NF_kappa_B_signaling_pathway_hsa04064 | 2 | 95 | 0.8237 | 0.9113 | |
46 | Neuroactive_ligand_receptor_interaction_hsa04080 | 6 | 278 | 0.8976 | 0.9725 | |
47 | Cell_adhesion_molecules_.CAMs._hsa04514 | 2 | 145 | 0.9538 | 0.9956 | |
48 | Cytokine_cytokine_receptor_interaction_hsa04060 | 4 | 270 | 0.9789 | 0.9956 |