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-7a-5p | AIFM1 | -0.33 | 0.00046 | -0.39 | 0.00049 | TargetScan; miRNATAP | -0.16 | 0.00689 | NA | |
2 | hsa-let-7d-5p | AIFM1 | 0.05 | 0.70258 | -0.39 | 0.00049 | miRNATAP | -0.23 | 0 | NA | |
3 | hsa-let-7e-5p | AIFM1 | 0.04 | 0.81107 | -0.39 | 0.00049 | miRNATAP | -0.27 | 0 | NA | |
4 | hsa-let-7i-5p | AIFM1 | -0.14 | 0.15414 | -0.39 | 0.00049 | miRNATAP | -0.27 | 0 | NA | |
5 | hsa-miR-125a-5p | AIFM1 | -0.91 | 0 | -0.39 | 0.00049 | miRanda | -0.14 | 0 | NA | |
6 | hsa-miR-20a-3p | AIFM1 | -0.32 | 0.04679 | -0.39 | 0.00049 | miRNATAP | -0.11 | 0.00067 | NA | |
7 | hsa-miR-425-5p | AIFM1 | 0.59 | 2.0E-5 | -0.39 | 0.00049 | miRNATAP | -0.15 | 8.0E-5 | NA | |
8 | hsa-miR-21-5p | AKT2 | 1.51 | 0 | -0.34 | 1.0E-5 | miRNAWalker2 validate | -0.25 | 0 | NA | |
9 | hsa-miR-330-5p | AKT2 | 0.44 | 0.00533 | -0.34 | 1.0E-5 | miRanda | -0.1 | 1.0E-5 | NA | |
10 | hsa-miR-342-3p | AKT2 | -0.32 | 0.04498 | -0.34 | 1.0E-5 | mirMAP | -0.12 | 0 | NA | |
11 | hsa-miR-106b-5p | AKT3 | 0.65 | 0 | -0.66 | 0.00047 | miRNATAP | -0.26 | 0.00148 | NA | |
12 | hsa-miR-107 | AKT3 | 0.24 | 0.01708 | -0.66 | 0.00047 | PITA; miRanda | -0.6 | 0 | NA | |
13 | hsa-miR-122-5p | AKT3 | -1.24 | 0 | -0.66 | 0.00047 | miRNAWalker2 validate; miRTarBase | -0.28 | 0 | 24244539 | miR 122 regulates tumorigenesis in hepatocellular carcinoma by targeting AKT3; Here we identify AKT3 as a novel and direct target of miR-122; Restoration of miR-122 expression in HCC cell lines decreases AKT3 levels inhibits cell migration and proliferation and induces apoptosis; These anti-tumor phenotypes can be rescued by reconstitution of AKT3 expression indicating the essential role of AKT3 in miR-122 mediated HCC transformation; Our data strongly suggest that miR-122 is a tumor suppressor that targets AKT3 to regulate tumorigenesis in HCCs and a potential therapeutic candidate for liver cancer |
14 | hsa-miR-146b-5p | AKT3 | 0.42 | 0.04574 | -0.66 | 0.00047 | miRNAWalker2 validate | -0.16 | 0.00026 | NA | |
15 | hsa-miR-15a-5p | AKT3 | 0.35 | 0.00077 | -0.66 | 0.00047 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.27 | 0.00291 | NA | |
16 | hsa-miR-17-3p | AKT3 | 0.41 | 0.00422 | -0.66 | 0.00047 | miRNATAP | -0.35 | 0 | NA | |
17 | hsa-miR-17-5p | AKT3 | 0.7 | 2.0E-5 | -0.66 | 0.00047 | TargetScan; miRNATAP | -0.29 | 0 | NA | |
18 | hsa-miR-20a-5p | AKT3 | 0.85 | 0 | -0.66 | 0.00047 | miRNATAP | -0.29 | 0 | NA | |
19 | hsa-miR-32-3p | AKT3 | 0.22 | 0.20722 | -0.66 | 0.00047 | mirMAP | -0.23 | 4.0E-5 | NA | |
20 | hsa-miR-33a-3p | AKT3 | -0.68 | 1.0E-5 | -0.66 | 0.00047 | mirMAP | -0.23 | 0.0001 | NA | |
21 | hsa-miR-362-3p | AKT3 | 0.81 | 0 | -0.66 | 0.00047 | miRanda | -0.22 | 0.00083 | NA | |
22 | hsa-miR-362-5p | AKT3 | 0.72 | 2.0E-5 | -0.66 | 0.00047 | PITA; TargetScan; miRNATAP | -0.15 | 0.00734 | NA | |
23 | hsa-miR-374a-5p | AKT3 | 0.02 | 0.86978 | -0.66 | 0.00047 | mirMAP | -0.28 | 0.00294 | NA | |
24 | hsa-miR-502-3p | AKT3 | 0.66 | 0 | -0.66 | 0.00047 | miRNATAP | -0.26 | 0.0008 | NA | |
25 | hsa-miR-616-5p | AKT3 | 0.15 | 0.40284 | -0.66 | 0.00047 | mirMAP | -0.2 | 0.0001 | NA | |
26 | hsa-miR-93-5p | AKT3 | 1.4 | 0 | -0.66 | 0.00047 | miRNATAP | -0.28 | 1.0E-5 | NA | |
27 | hsa-miR-30d-3p | ATM | -0.12 | 0.32955 | -0.24 | 0.01738 | mirMAP | -0.14 | 0.00043 | 24345332 | miR-30d has been observed to be significantly down-regulated in human anaplastic thyroid carcinoma ATC and is believed to be an important event in thyroid cell transformation; In this study we found that miR-30d has a critical role in modulating sensitivity of ATC cells to cisplatin a commonly used chemotherapeutic drug for treatment of this neoplasm; Using a mimic of miR-30d we demonstrated that miR-30d could negatively regulate the expression of beclin 1 a key autophagy gene leading to suppression of the cisplatin-activated autophagic response that protects ATC cells from apoptosis; We further showed that inhibition of the beclin 1-mediated autophagy by the miR-30d mimic sensitized ATC cells to cisplatin both in vitro cell culture and in vivo animal xenograft model; These results suggest that dysregulation of miR-30d in ATC cells is responsible for the insensitivity to cisplatin by promoting autophagic survival; Thus miR-30d may be exploited as a potential target for therapeutic intervention in the treatment of ATC |
28 | hsa-miR-339-5p | ATM | 0.28 | 0.03557 | -0.24 | 0.01738 | miRanda | -0.1 | 0.00399 | NA | |
29 | hsa-miR-455-5p | ATM | -0.27 | 0.05813 | -0.24 | 0.01738 | miRanda | -0.12 | 0.00045 | NA | |
30 | hsa-miR-30a-5p | BAX | -0.63 | 0.00011 | 0.8 | 0 | miRNAWalker2 validate | -0.12 | 0.00058 | NA | |
31 | hsa-miR-365a-3p | BAX | 0.16 | 0.15325 | 0.8 | 0 | miRNAWalker2 validate | -0.23 | 0 | 24216611 | MiR 365 induces gemcitabine resistance in pancreatic cancer cells by targeting the adaptor protein SHC1 and pro apoptotic regulator BAX |
32 | hsa-miR-103a-3p | BCL2 | 0.77 | 0 | -0.35 | 0.02497 | miRNAWalker2 validate | -0.28 | 4.0E-5 | NA | |
33 | hsa-miR-130b-5p | BCL2 | 0.17 | 0.33761 | -0.35 | 0.02497 | mirMAP | -0.17 | 7.0E-5 | 27364335 | The level of microRNA-130b in relationship with the expression of PPARĪ³ VEGF-A BCL-2 and apoptosis were analyzed in 91 lung cancer patient samples using immunohistochemistry and terminal deoxynucleotidyl transferase dUTP nick end labeling TUNEL assay on tissue microarrays; In vitro and in vivo miR-130b enrichment associated with down-regulation of PPARĪ³ up-regulation of VEGF-A and BCL-2 and decreased apoptosis |
34 | hsa-miR-148a-3p | BCL2 | -0.75 | 0 | -0.35 | 0.02497 | miRNAWalker2 validate; miRTarBase | -0.31 | 0 | 21455217; 23975374 | MiR 148a promotes apoptosis by targeting Bcl 2 in colorectal cancer;MiR 148a regulates the growth and apoptosis in pancreatic cancer by targeting CCKBR and Bcl 2; Using western blot and luciferase activity assay CCKBR and Bcl-2 were identified as targets of miR-148a; Moreover we also found that the expression of Bcl-2 lacking in 3'UTR could abrogate the pro-apoptosis function of miR-148a |
35 | hsa-miR-17-5p | BCL2 | 0.7 | 2.0E-5 | -0.35 | 0.02497 | miRNAWalker2 validate; miRTarBase | -0.31 | 0 | 25435430 | Combined overexpression of miR-16 and miR-17 greatly reduced Beclin-1 and Bcl-2 expressions respectively; miR-17 overexpression reduced cytoprotective autophagy by targeting Beclin-1 whereas overexpression of miR-16 potentiated paclitaxel induced apoptotic cell death by inhibiting anti-apoptotic protein Bcl-2 |
36 | hsa-miR-186-5p | BCL2 | -0.06 | 0.53529 | -0.35 | 0.02497 | mirMAP | -0.25 | 0.00125 | NA | |
37 | hsa-miR-192-5p | BCL2 | -0.5 | 0.00345 | -0.35 | 0.02497 | miRNAWalker2 validate | -0.34 | 0 | 26550150 | MicroRNA 192 regulates chemo resistance of lung adenocarcinoma for gemcitabine and cisplatin combined therapy by targeting Bcl 2; In this paper we try to test whether miR-192 regulates chemo-resistance in human carcinoma A549 mice model by targeting Bcl-2; MTT assay real-time RT-PCR western blotting assay were used to investigate miR-192 expression levels cell viability ratio and Bcl-2 protein expression levels; Bcl-2 mRNA and protein expression levels up-regulated in miR-192 inhibitor treated tumor; Bcl-2 is a key regulator for miR-192 related chemotherapy resistance; In this study we demonstrate that miR-192 regulates chemoresistance for gemcitabine and cisplatin combined chemotherapy in human adenocarcinoma lung cancer A549 cells and Bcl-2 is the target of miR-192 |
38 | hsa-miR-20a-3p | BCL2 | -0.32 | 0.04679 | -0.35 | 0.02497 | mirMAP | -0.24 | 0 | NA | |
39 | hsa-miR-20a-5p | BCL2 | 0.85 | 0 | -0.35 | 0.02497 | miRNAWalker2 validate; miRTarBase | -0.31 | 0 | NA | |
40 | hsa-miR-32-3p | BCL2 | 0.22 | 0.20722 | -0.35 | 0.02497 | mirMAP | -0.2 | 1.0E-5 | NA | |
41 | hsa-miR-365a-3p | BCL2 | 0.16 | 0.15325 | -0.35 | 0.02497 | miRNAWalker2 validate; miRTarBase | -0.33 | 0 | NA | |
42 | hsa-miR-455-5p | BCL2 | -0.27 | 0.05813 | -0.35 | 0.02497 | mirMAP | -0.19 | 0.00037 | NA | |
43 | hsa-miR-590-5p | BCL2 | -0.1 | 0.31003 | -0.35 | 0.02497 | miRanda | -0.29 | 0.00011 | NA | |
44 | hsa-miR-616-5p | BCL2 | 0.15 | 0.40284 | -0.35 | 0.02497 | mirMAP | -0.28 | 0 | NA | |
45 | hsa-miR-618 | BCL2 | 0.14 | 0.51715 | -0.35 | 0.02497 | mirMAP | -0.21 | 0 | NA | |
46 | hsa-miR-330-5p | BCL2L1 | 0.44 | 0.00533 | 0.02 | 0.82745 | PITA; miRanda; miRNATAP | -0.15 | 0 | NA | |
47 | hsa-miR-342-3p | BCL2L1 | -0.32 | 0.04498 | 0.02 | 0.82745 | PITA; miRanda; miRNATAP | -0.12 | 8.0E-5 | NA | |
48 | hsa-miR-342-5p | BCL2L1 | -0.78 | 0 | 0.02 | 0.82745 | miRNATAP | -0.11 | 0.00084 | NA | |
49 | hsa-miR-484 | BCL2L1 | 0.09 | 0.45398 | 0.02 | 0.82745 | miRNAWalker2 validate | -0.21 | 0 | NA | |
50 | hsa-miR-140-5p | BID | -0.22 | 0.01407 | 0.21 | 0.07516 | miRanda | -0.21 | 0.00101 | NA | |
51 | hsa-miR-24-1-5p | BIRC3 | -1.32 | 0 | 0.35 | 0.15976 | MirTarget | -0.3 | 0.0004 | NA | |
52 | hsa-miR-26b-5p | BIRC3 | -1.11 | 0 | 0.35 | 0.15976 | mirMAP | -0.35 | 0.00041 | NA | |
53 | hsa-miR-374a-5p | BIRC3 | 0.02 | 0.86978 | 0.35 | 0.15976 | mirMAP | -0.56 | 0 | NA | |
54 | hsa-miR-374b-5p | BIRC3 | -0.31 | 0.00301 | 0.35 | 0.15976 | mirMAP | -0.3 | 0.0093 | NA | |
55 | hsa-miR-651-5p | BIRC3 | -0.24 | 0.08175 | 0.35 | 0.15976 | MirTarget | -0.28 | 0.00126 | NA | |
56 | hsa-miR-664a-3p | BIRC3 | 0.49 | 0.00073 | 0.35 | 0.15976 | mirMAP | -0.27 | 0.00118 | NA | |
57 | hsa-miR-140-5p | CAPN1 | -0.22 | 0.01407 | 0.2 | 0.01338 | miRanda; miRNATAP | -0.15 | 0.00087 | NA | |
58 | hsa-miR-101-3p | CAPN2 | -1.48 | 0 | 0.66 | 0 | miRNAWalker2 validate; MirTarget | -0.21 | 0 | NA | |
59 | hsa-miR-107 | CAPN2 | 0.24 | 0.01708 | 0.66 | 0 | miRanda | -0.2 | 0.00125 | NA | |
60 | hsa-miR-16-2-3p | CAPN2 | -0.03 | 0.80516 | 0.66 | 0 | mirMAP | -0.15 | 0.0006 | NA | |
61 | hsa-miR-20a-3p | CAPN2 | -0.32 | 0.04679 | 0.66 | 0 | MirTarget | -0.13 | 0.00067 | NA | |
62 | hsa-miR-33a-3p | CAPN2 | -0.68 | 1.0E-5 | 0.66 | 0 | mirMAP | -0.13 | 0.00096 | NA | |
63 | hsa-miR-590-3p | CAPN2 | -0.47 | 2.0E-5 | 0.66 | 0 | miRanda | -0.22 | 5.0E-5 | NA | |
64 | hsa-miR-590-5p | CAPN2 | -0.1 | 0.31003 | 0.66 | 0 | miRanda | -0.24 | 5.0E-5 | NA | |
65 | hsa-let-7g-5p | CASP3 | -0.46 | 2.0E-5 | 0.31 | 0.00047 | MirTarget; miRNATAP | -0.11 | 0.00694 | NA | |
66 | hsa-miR-374b-5p | CASP3 | -0.31 | 0.00301 | 0.31 | 0.00047 | mirMAP | -0.14 | 0.00058 | NA | |
67 | hsa-miR-455-5p | CASP8 | -0.27 | 0.05813 | 0.33 | 0.00029 | miRanda | -0.15 | 0 | NA | |
68 | hsa-miR-542-3p | CASP8 | -1.31 | 0 | 0.33 | 0.00029 | miRanda | -0.13 | 4.0E-5 | NA | |
69 | hsa-miR-107 | CFLAR | 0.24 | 0.01708 | -0.33 | 0 | miRanda | -0.15 | 1.0E-5 | NA | |
70 | hsa-miR-455-5p | CFLAR | -0.27 | 0.05813 | -0.33 | 0 | miRanda | -0.11 | 0 | NA | |
71 | hsa-miR-660-5p | CFLAR | 0.99 | 0 | -0.33 | 0 | mirMAP | -0.13 | 0 | NA | |
72 | hsa-miR-15a-5p | CHUK | 0.35 | 0.00077 | -0.2 | 0.00863 | miRNAWalker2 validate; miRTarBase; MirTarget | -0.12 | 0.00057 | NA | |
73 | hsa-miR-15b-5p | CHUK | 0.23 | 0.08248 | -0.2 | 0.00863 | MirTarget | -0.12 | 2.0E-5 | NA | |
74 | hsa-miR-16-5p | CHUK | -0.4 | 0.0001 | -0.2 | 0.00863 | miRNAWalker2 validate; miRTarBase; MirTarget | -0.15 | 3.0E-5 | NA | |
75 | hsa-miR-23a-3p | CHUK | -0.18 | 0.13598 | -0.2 | 0.00863 | MirTarget | -0.1 | 0.00114 | NA | |
76 | hsa-miR-339-5p | CHUK | 0.28 | 0.03557 | -0.2 | 0.00863 | miRanda | -0.12 | 1.0E-5 | NA | |
77 | hsa-miR-590-5p | CHUK | -0.1 | 0.31003 | -0.2 | 0.00863 | miRanda | -0.12 | 0.00129 | NA | |
78 | hsa-miR-19a-3p | CSF2RB | 1.02 | 0 | -0.51 | 0.00683 | MirTarget | -0.12 | 0.00885 | NA | |
79 | hsa-miR-19b-3p | CSF2RB | 0.6 | 0.00017 | -0.51 | 0.00683 | MirTarget | -0.15 | 0.00713 | NA | |
80 | hsa-miR-204-5p | CSF2RB | -0.54 | 0.03309 | -0.51 | 0.00683 | MirTarget | -0.11 | 0.00224 | NA | |
81 | hsa-miR-30b-3p | CSF2RB | -0.44 | 0.00095 | -0.51 | 0.00683 | MirTarget | -0.2 | 0.00366 | NA | |
82 | hsa-miR-455-5p | CSF2RB | -0.27 | 0.05813 | -0.51 | 0.00683 | miRanda | -0.37 | 0 | NA | |
83 | hsa-miR-532-5p | CSF2RB | 1.03 | 0 | -0.51 | 0.00683 | MirTarget | -0.33 | 0 | NA | |
84 | hsa-miR-361-5p | CYCS | 0.23 | 0.00962 | 0.26 | 0.01519 | miRNAWalker2 validate | -0.17 | 0.00331 | NA | |
85 | hsa-let-7b-5p | DFFA | -0.96 | 0 | 0.07 | 0.4191 | miRNAWalker2 validate | -0.11 | 8.0E-5 | NA | |
86 | hsa-miR-26a-5p | DFFA | -0.96 | 0 | 0.07 | 0.4191 | mirMAP | -0.16 | 4.0E-5 | NA | |
87 | hsa-miR-365a-3p | DFFB | 0.16 | 0.15325 | 0.3 | 0.00331 | MirTarget | -0.12 | 0.00456 | NA | |
88 | hsa-miR-130b-3p | ENDOD1 | 0.69 | 0.00011 | -1 | 0 | MirTarget | -0.31 | 0 | NA | |
89 | hsa-miR-16-1-3p | ENDOD1 | 0.39 | 0.00112 | -1 | 0 | mirMAP | -0.45 | 0 | NA | |
90 | hsa-miR-192-5p | ENDOD1 | -0.5 | 0.00345 | -1 | 0 | miRNAWalker2 validate | -0.46 | 0 | NA | |
91 | hsa-miR-193b-3p | ENDOD1 | -0.17 | 0.27202 | -1 | 0 | miRNAWalker2 validate | -0.22 | 0.0003 | NA | |
92 | hsa-miR-19a-3p | ENDOD1 | 1.02 | 0 | -1 | 0 | mirMAP | -0.28 | 0 | NA | |
93 | hsa-miR-19b-3p | ENDOD1 | 0.6 | 0.00017 | -1 | 0 | mirMAP | -0.34 | 0 | NA | |
94 | hsa-miR-20a-3p | ENDOD1 | -0.32 | 0.04679 | -1 | 0 | MirTarget | -0.28 | 0 | NA | |
95 | hsa-miR-224-3p | ENDOD1 | 1.41 | 0 | -1 | 0 | mirMAP | -0.1 | 0.0066 | NA | |
96 | hsa-miR-361-5p | ENDOD1 | 0.23 | 0.00962 | -1 | 0 | MirTarget; miRanda | -0.62 | 0 | NA | |
97 | hsa-miR-3613-5p | ENDOD1 | 0.11 | 0.42651 | -1 | 0 | MirTarget | -0.21 | 0.00254 | NA | |
98 | hsa-miR-362-3p | ENDOD1 | 0.81 | 0 | -1 | 0 | miRanda | -0.34 | 0 | NA | |
99 | hsa-miR-589-3p | ENDOD1 | 1.17 | 0 | -1 | 0 | mirMAP | -0.21 | 5.0E-5 | NA | |
100 | hsa-miR-589-5p | ENDOD1 | 1.19 | 0 | -1 | 0 | MirTarget | -0.56 | 0 | NA | |
101 | hsa-miR-542-3p | EXOG | -1.31 | 0 | 0.81 | 0 | miRanda | -0.11 | 0.0009 | NA | |
102 | hsa-miR-106a-5p | FAS | -0.46 | 0.00972 | -1.02 | 0 | miRNAWalker2 validate; miRTarBase | -0.3 | 0 | 22431000; 27142596 | miR 106a is frequently upregulated in gastric cancer and inhibits the extrinsic apoptotic pathway by targeting FAS; Bioinformatic analysis combining with validation experiments identified FAS as a direct target of miR-106a; Moreover a significant inverse correlation was found between miR-106a and FAS expression not only in gastric cancer cell lines but also in gastric cancer specimens; Taken together these findings suggest that ectopicly overexpressed miR-106a may play an oncogenic role in gastric carcinogenesis and impair extrinsic apoptotic pathway through targeting FAS;Functional experiment ascertained that miR-106a interacted with FAS and mediated caspase3 pathway |
103 | hsa-miR-21-5p | FAS | 1.51 | 0 | -1.02 | 0 | miRNAWalker2 validate | -0.35 | 0 | 24710931 | miR 21 targets Fas ligand mediated apoptosis in breast cancer cell line MCF 7 |
104 | hsa-miR-338-3p | FAS | 0.54 | 0.00461 | -1.02 | 0 | miRanda | -0.23 | 0 | NA | |
105 | hsa-miR-361-5p | FAS | 0.23 | 0.00962 | -1.02 | 0 | miRanda | -0.4 | 0.00016 | NA | |
106 | hsa-miR-590-5p | FAS | -0.1 | 0.31003 | -1.02 | 0 | miRanda | -0.56 | 0 | NA | |
107 | hsa-miR-98-5p | FAS | -0.05 | 0.71591 | -1.02 | 0 | miRNAWalker2 validate | -0.18 | 0.00981 | NA | |
108 | hsa-miR-25-3p | FASLG | 0.63 | 0 | -0.79 | 0.00091 | miRNATAP | -0.41 | 0.00032 | NA | |
109 | hsa-miR-125a-5p | IKBKG | -0.91 | 0 | 0.66 | 0 | miRanda | -0.22 | 0 | NA | |
110 | hsa-miR-143-3p | IKBKG | -0.58 | 0.00091 | 0.66 | 0 | mirMAP | -0.17 | 1.0E-5 | NA | |
111 | hsa-miR-200a-3p | IKBKG | -1.5 | 3.0E-5 | 0.66 | 0 | mirMAP | -0.1 | 0 | NA | |
112 | hsa-miR-24-3p | IKBKG | -0.26 | 0.0069 | 0.66 | 0 | mirMAP | -0.29 | 6.0E-5 | NA | |
113 | hsa-miR-3065-3p | IKBKG | -1.04 | 5.0E-5 | 0.66 | 0 | mirMAP | -0.12 | 1.0E-5 | NA | |
114 | hsa-miR-320a | IKBKG | 0.33 | 0.02214 | 0.66 | 0 | mirMAP | -0.18 | 0.00013 | NA | |
115 | hsa-miR-320b | IKBKG | 0.09 | 0.60798 | 0.66 | 0 | mirMAP | -0.13 | 0.00052 | NA | |
116 | hsa-miR-335-5p | IKBKG | -1.61 | 0 | 0.66 | 0 | mirMAP | -0.27 | 0 | NA | |
117 | hsa-miR-338-5p | IKBKG | -0.22 | 0.25239 | 0.66 | 0 | mirMAP | -0.21 | 0 | NA | |
118 | hsa-miR-376c-3p | IKBKG | -1.79 | 0 | 0.66 | 0 | mirMAP | -0.14 | 0 | NA | |
119 | hsa-miR-542-3p | IKBKG | -1.31 | 0 | 0.66 | 0 | mirMAP | -0.29 | 0 | NA | |
120 | hsa-miR-17-3p | IL1R1 | 0.41 | 0.00422 | -1.01 | 0 | mirMAP | -0.39 | 0 | NA | |
121 | hsa-miR-181a-5p | IL1R1 | 0.25 | 0.05519 | -1.01 | 0 | mirMAP | -0.23 | 1.0E-5 | NA | |
122 | hsa-miR-181b-5p | IL1R1 | 0.49 | 0.00105 | -1.01 | 0 | mirMAP | -0.25 | 0 | NA | |
123 | hsa-miR-29b-3p | IL1RAP | -0.35 | 0.01214 | -2.29 | 0 | MirTarget; miRNATAP | -0.24 | 0.00132 | NA | |
124 | hsa-miR-421 | IL1RAP | 0.94 | 0 | -2.29 | 0 | MirTarget; miRanda | -0.18 | 0.00237 | NA | |
125 | hsa-miR-93-5p | IL1RAP | 1.4 | 0 | -2.29 | 0 | MirTarget | -0.29 | 7.0E-5 | NA | |
126 | hsa-miR-142-3p | IRAK1 | -1.42 | 0 | 1.22 | 0 | PITA; miRanda; miRNATAP | -0.1 | 0.00154 | NA | |
127 | hsa-miR-328-3p | IRAK1 | -0.55 | 1.0E-5 | 1.22 | 0 | miRNAWalker2 validate | -0.17 | 0.00081 | NA | |
128 | hsa-miR-188-5p | IRAK3 | 1.12 | 0 | -1.13 | 0 | mirMAP | -0.16 | 0.0029 | NA | |
129 | hsa-miR-20a-3p | IRAK3 | -0.32 | 0.04679 | -1.13 | 0 | mirMAP | -0.18 | 0.00282 | NA | |
130 | hsa-miR-224-3p | IRAK3 | 1.41 | 0 | -1.13 | 0 | mirMAP | -0.13 | 0.00062 | NA | |
131 | hsa-miR-25-3p | IRAK3 | 0.63 | 0 | -1.13 | 0 | mirMAP | -0.5 | 0 | NA | |
132 | hsa-miR-32-5p | IRAK3 | 0.08 | 0.54898 | -1.13 | 0 | mirMAP | -0.2 | 0.00353 | NA | |
133 | hsa-miR-3200-3p | IRAK3 | 1.4 | 0 | -1.13 | 0 | mirMAP | -0.14 | 6.0E-5 | NA | |
134 | hsa-miR-324-5p | IRAK3 | 0.37 | 0.00592 | -1.13 | 0 | miRanda | -0.19 | 0.00586 | NA | |
135 | hsa-miR-33a-5p | IRAK3 | -0.77 | 1.0E-5 | -1.13 | 0 | mirMAP | -0.17 | 0.00159 | NA | |
136 | hsa-miR-361-5p | IRAK3 | 0.23 | 0.00962 | -1.13 | 0 | miRanda; mirMAP | -0.37 | 0.00049 | NA | |
137 | hsa-miR-452-3p | IRAK3 | 1.77 | 0 | -1.13 | 0 | mirMAP | -0.11 | 0.00056 | NA | |
138 | hsa-miR-589-3p | IRAK3 | 1.17 | 0 | -1.13 | 0 | mirMAP | -0.2 | 0.00011 | NA | |
139 | hsa-miR-616-5p | IRAK3 | 0.15 | 0.40284 | -1.13 | 0 | mirMAP | -0.2 | 0.00013 | NA | |
140 | hsa-miR-660-5p | IRAK3 | 0.99 | 0 | -1.13 | 0 | mirMAP | -0.28 | 6.0E-5 | NA | |
141 | hsa-miR-92a-3p | IRAK3 | 0.21 | 0.13429 | -1.13 | 0 | mirMAP | -0.29 | 1.0E-5 | NA | |
142 | hsa-miR-30d-3p | IRAK4 | -0.12 | 0.32955 | 0.02 | 0.75053 | mirMAP | -0.13 | 0 | NA | |
143 | hsa-miR-17-3p | MAP3K14 | 0.41 | 0.00422 | -0.26 | 0.0806 | MirTarget | -0.13 | 0.00706 | NA | |
144 | hsa-miR-17-5p | MAP3K14 | 0.7 | 2.0E-5 | -0.26 | 0.0806 | MirTarget | -0.2 | 0 | NA | |
145 | hsa-miR-20a-5p | MAP3K14 | 0.85 | 0 | -0.26 | 0.0806 | MirTarget | -0.16 | 0.00014 | NA | |
146 | hsa-miR-874-3p | MAP3K14 | -1.07 | 0 | -0.26 | 0.0806 | MirTarget | -0.12 | 0.00031 | NA | |
147 | hsa-miR-330-5p | MYD88 | 0.44 | 0.00533 | -1.1 | 0 | MirTarget; miRanda | -0.16 | 0 | NA | |
148 | hsa-miR-660-5p | MYD88 | 0.99 | 0 | -1.1 | 0 | MirTarget | -0.17 | 0 | NA | |
149 | hsa-miR-15a-5p | NFKB1 | 0.35 | 0.00077 | -0.54 | 0 | miRNAWalker2 validate | -0.15 | 0.00073 | NA | |
150 | hsa-miR-548j-5p | NFKB1 | 0.25 | 0.17136 | -0.54 | 0 | MirTarget | -0.11 | 5.0E-5 | NA |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | INTRACELLULAR SIGNAL TRANSDUCTION | 37 | 1572 | 2.326e-27 | 1.082e-23 |
2 | POSITIVE REGULATION OF RESPONSE TO STIMULUS | 39 | 1929 | 9.347e-27 | 2.175e-23 |
3 | EXTRINSIC APOPTOTIC SIGNALING PATHWAY VIA DEATH DOMAIN RECEPTORS | 13 | 39 | 1.439e-24 | 2.232e-21 |
4 | APOPTOTIC SIGNALING PATHWAY | 20 | 289 | 6.092e-23 | 7.086e-20 |
5 | EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 15 | 99 | 1.614e-22 | 1.502e-19 |
6 | CELLULAR RESPONSE TO ORGANIC SUBSTANCE | 35 | 1848 | 2.141e-22 | 1.66e-19 |
7 | REGULATION OF CELL DEATH | 32 | 1472 | 6.509e-22 | 4.327e-19 |
8 | CELL DEATH | 28 | 1001 | 9.917e-22 | 5.768e-19 |
9 | RESPONSE TO OXYGEN CONTAINING COMPOUND | 31 | 1381 | 1.582e-21 | 8.181e-19 |
10 | POSITIVE REGULATION OF PROTEIN METABOLIC PROCESS | 31 | 1492 | 1.535e-20 | 7.141e-18 |
11 | POSITIVE REGULATION OF MOLECULAR FUNCTION | 33 | 1791 | 1.764e-20 | 7.462e-18 |
12 | REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 32 | 1656 | 2.303e-20 | 8.928e-18 |
13 | POSITIVE REGULATION OF CELL COMMUNICATION | 31 | 1532 | 3.328e-20 | 1.191e-17 |
14 | NEGATIVE REGULATION OF CELL DEATH | 25 | 872 | 1.826e-19 | 6.068e-17 |
15 | POSITIVE REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 25 | 876 | 2.037e-19 | 6.319e-17 |
16 | ACTIVATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY | 13 | 95 | 5.511e-19 | 1.603e-16 |
17 | REGULATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY | 16 | 213 | 6.11e-19 | 1.672e-16 |
18 | POSITIVE REGULATION OF I KAPPAB KINASE NF KAPPAB SIGNALING | 15 | 179 | 1.661e-18 | 4.293e-16 |
19 | IMMUNE SYSTEM PROCESS | 32 | 1984 | 5.085e-18 | 1.148e-15 |
20 | POSITIVE REGULATION OF CATALYTIC ACTIVITY | 29 | 1518 | 4.863e-18 | 1.148e-15 |
21 | ZYMOGEN ACTIVATION | 13 | 112 | 5.182e-18 | 1.148e-15 |
22 | RESPONSE TO NITROGEN COMPOUND | 23 | 859 | 3.594e-17 | 7.601e-15 |
23 | REGULATION OF I KAPPAB KINASE NF KAPPAB SIGNALING | 15 | 233 | 8.981e-17 | 1.741e-14 |
24 | ACTIVATION OF IMMUNE RESPONSE | 18 | 427 | 8.608e-17 | 1.741e-14 |
25 | REGULATION OF IMMUNE SYSTEM PROCESS | 27 | 1403 | 9.843e-17 | 1.832e-14 |
26 | POSITIVE REGULATION OF CELL DEATH | 20 | 605 | 1.286e-16 | 2.302e-14 |
27 | RESPONSE TO CYTOKINE | 21 | 714 | 1.924e-16 | 3.316e-14 |
28 | POSITIVE REGULATION OF PEPTIDASE ACTIVITY | 13 | 154 | 3.657e-16 | 6.077e-14 |
29 | REGULATION OF IMMUNE RESPONSE | 22 | 858 | 5.289e-16 | 8.486e-14 |
30 | PROTEIN MATURATION | 15 | 265 | 6.146e-16 | 9.225e-14 |
31 | POSITIVE REGULATION OF IMMUNE RESPONSE | 19 | 563 | 6.057e-16 | 9.225e-14 |
32 | POSITIVE REGULATION OF APOPTOTIC SIGNALING PATHWAY | 13 | 171 | 1.453e-15 | 2.112e-13 |
33 | ACTIVATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 7 | 13 | 1.765e-15 | 2.489e-13 |
34 | REGULATION OF TRANSFERASE ACTIVITY | 22 | 946 | 3.986e-15 | 5.455e-13 |
35 | REGULATION OF PEPTIDASE ACTIVITY | 16 | 392 | 9.742e-15 | 1.295e-12 |
36 | REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 12 | 153 | 1.365e-14 | 1.764e-12 |
37 | REGULATION OF KINASE ACTIVITY | 20 | 776 | 1.469e-14 | 1.799e-12 |
38 | POSITIVE REGULATION OF PROTEIN MODIFICATION PROCESS | 23 | 1135 | 1.464e-14 | 1.799e-12 |
39 | POSITIVE REGULATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 7 | 17 | 1.983e-14 | 2.366e-12 |
40 | RESPONSE TO ENDOGENOUS STIMULUS | 25 | 1450 | 2.723e-14 | 3.167e-12 |
41 | REGULATION OF PHOSPHORUS METABOLIC PROCESS | 26 | 1618 | 3.461e-14 | 3.928e-12 |
42 | REGULATION OF PROTEOLYSIS | 19 | 711 | 4.138e-14 | 4.584e-12 |
43 | NEURON APOPTOTIC PROCESS | 8 | 35 | 5.783e-14 | 6.258e-12 |
44 | REGULATION OF APOPTOTIC SIGNALING PATHWAY | 15 | 363 | 6.332e-14 | 6.696e-12 |
45 | PHOSPHORYLATION | 23 | 1228 | 7.765e-14 | 8.029e-12 |
46 | POSITIVE REGULATION OF IMMUNE SYSTEM PROCESS | 20 | 867 | 1.173e-13 | 1.187e-11 |
47 | REGULATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 7 | 22 | 1.72e-13 | 1.703e-11 |
48 | NEGATIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 10 | 98 | 1.779e-13 | 1.725e-11 |
49 | IMMUNE RESPONSE REGULATING CELL SURFACE RECEPTOR SIGNALING PATHWAY | 14 | 323 | 2.554e-13 | 2.425e-11 |
50 | POSITIVE REGULATION OF PHOSPHATE METABOLIC PROCESS | 21 | 1036 | 2.947e-13 | 2.689e-11 |
51 | POSITIVE REGULATION OF PHOSPHORUS METABOLIC PROCESS | 21 | 1036 | 2.947e-13 | 2.689e-11 |
52 | CELLULAR RESPONSE TO OXYGEN CONTAINING COMPOUND | 19 | 799 | 3.311e-13 | 2.963e-11 |
53 | PHOSPHATE CONTAINING COMPOUND METABOLIC PROCESS | 27 | 1977 | 4.521e-13 | 3.969e-11 |
54 | INTRINSIC APOPTOTIC SIGNALING PATHWAY | 11 | 152 | 4.631e-13 | 3.99e-11 |
55 | CELLULAR RESPONSE TO NITROGEN COMPOUND | 16 | 505 | 4.816e-13 | 4.074e-11 |
56 | NEURON DEATH | 8 | 47 | 7.527e-13 | 6.254e-11 |
57 | ACTIVATION OF PROTEIN KINASE ACTIVITY | 13 | 279 | 8.114e-13 | 6.624e-11 |
58 | REGULATION OF PROTEIN MODIFICATION PROCESS | 25 | 1710 | 1.128e-12 | 9.047e-11 |
59 | RESPONSE TO TUMOR NECROSIS FACTOR | 12 | 233 | 2.096e-12 | 1.653e-10 |
60 | RESPONSE TO HORMONE | 19 | 893 | 2.35e-12 | 1.823e-10 |
61 | RESPONSE TO ABIOTIC STIMULUS | 20 | 1024 | 2.537e-12 | 1.935e-10 |
62 | POSITIVE REGULATION OF KINASE ACTIVITY | 15 | 482 | 3.775e-12 | 2.833e-10 |
63 | NEGATIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY VIA DEATH DOMAIN RECEPTORS | 7 | 34 | 5.284e-12 | 3.903e-10 |
64 | PROTEIN PHOSPHORYLATION | 19 | 944 | 6.199e-12 | 4.507e-10 |
65 | CELLULAR RESPONSE TO CYTOKINE STIMULUS | 16 | 606 | 7.593e-12 | 5.436e-10 |
66 | POSITIVE REGULATION OF MITOCHONDRIAL OUTER MEMBRANE PERMEABILIZATION INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 7 | 36 | 8.164e-12 | 5.755e-10 |
67 | CELLULAR RESPONSE TO ABIOTIC STIMULUS | 12 | 263 | 8.705e-12 | 6.046e-10 |
68 | NEGATIVE REGULATION OF APOPTOTIC SIGNALING PATHWAY | 11 | 200 | 9.371e-12 | 6.412e-10 |
69 | ACTIVATION OF INNATE IMMUNE RESPONSE | 11 | 204 | 1.162e-11 | 7.835e-10 |
70 | I KAPPAB KINASE NF KAPPAB SIGNALING | 8 | 70 | 2.149e-11 | 1.408e-09 |
71 | REGULATION OF MEMBRANE PERMEABILITY | 8 | 70 | 2.149e-11 | 1.408e-09 |
72 | POSITIVE REGULATION OF PROTEOLYSIS | 13 | 363 | 2.231e-11 | 1.442e-09 |
73 | POSITIVE REGULATION OF DEFENSE RESPONSE | 13 | 364 | 2.309e-11 | 1.472e-09 |
74 | CYTOKINE MEDIATED SIGNALING PATHWAY | 14 | 452 | 2.354e-11 | 1.48e-09 |
75 | INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO DNA DAMAGE | 8 | 71 | 2.417e-11 | 1.499e-09 |
76 | REGULATION OF RESPONSE TO STRESS | 22 | 1468 | 2.728e-11 | 1.67e-09 |
77 | POSITIVE REGULATION OF INTRACELLULAR TRANSPORT | 13 | 370 | 2.831e-11 | 1.711e-09 |
78 | REGULATION OF MITOCHONDRIAL OUTER MEMBRANE PERMEABILIZATION INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 7 | 43 | 3.103e-11 | 1.851e-09 |
79 | PHOSPHATIDYLINOSITOL 3 PHOSPHATE BIOSYNTHETIC PROCESS | 7 | 49 | 8.165e-11 | 4.809e-09 |
80 | POSITIVE REGULATION OF INNATE IMMUNE RESPONSE | 11 | 246 | 8.737e-11 | 5.07e-09 |
81 | RESPONSE TO MOLECULE OF BACTERIAL ORIGIN | 12 | 321 | 8.825e-11 | 5.07e-09 |
82 | REGULATION OF TUMOR NECROSIS FACTOR MEDIATED SIGNALING PATHWAY | 7 | 50 | 9.473e-11 | 5.375e-09 |
83 | TOLL LIKE RECEPTOR SIGNALING PATHWAY | 8 | 85 | 1.06e-10 | 5.944e-09 |
84 | REGULATION OF NEURON DEATH | 11 | 252 | 1.131e-10 | 6.263e-09 |
85 | POSITIVE REGULATION OF TRANSFERASE ACTIVITY | 15 | 616 | 1.198e-10 | 6.561e-09 |
86 | REGULATION OF NEURON APOPTOTIC PROCESS | 10 | 192 | 1.534e-10 | 8.302e-09 |
87 | ANTIGEN RECEPTOR MEDIATED SIGNALING PATHWAY | 10 | 195 | 1.787e-10 | 9.557e-09 |
88 | REGULATION OF PROTEIN INSERTION INTO MITOCHONDRIAL MEMBRANE INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 6 | 29 | 1.845e-10 | 9.648e-09 |
89 | POSITIVE REGULATION OF PROTEIN INSERTION INTO MITOCHONDRIAL MEMBRANE INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 6 | 29 | 1.845e-10 | 9.648e-09 |
90 | REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY VIA DEATH DOMAIN RECEPTORS | 7 | 55 | 1.904e-10 | 9.842e-09 |
91 | MITOCHONDRIAL MEMBRANE ORGANIZATION | 8 | 92 | 2.02e-10 | 1.033e-08 |
92 | RESPONSE TO BIOTIC STIMULUS | 17 | 886 | 2.201e-10 | 1.113e-08 |
93 | FC EPSILON RECEPTOR SIGNALING PATHWAY | 9 | 142 | 2.391e-10 | 1.197e-08 |
94 | REGULATION OF RESPONSE TO CYTOKINE STIMULUS | 9 | 144 | 2.71e-10 | 1.342e-08 |
95 | CELLULAR RESPONSE TO PEPTIDE | 11 | 274 | 2.758e-10 | 1.351e-08 |
96 | REGULATION OF INNATE IMMUNE RESPONSE | 12 | 357 | 2.992e-10 | 1.45e-08 |
97 | POSITIVE REGULATION OF CELLULAR PROTEIN LOCALIZATION | 12 | 360 | 3.293e-10 | 1.58e-08 |
98 | REGULATION OF PROTEIN SERINE THREONINE KINASE ACTIVITY | 13 | 470 | 5.398e-10 | 2.563e-08 |
99 | CELLULAR RESPONSE TO STRESS | 21 | 1565 | 6.963e-10 | 3.273e-08 |
100 | IMMUNE RESPONSE | 18 | 1100 | 7.429e-10 | 3.457e-08 |
101 | PATTERN RECOGNITION RECEPTOR SIGNALING PATHWAY | 8 | 109 | 7.942e-10 | 3.659e-08 |
102 | ACTIVATION OF PROTEIN KINASE A ACTIVITY | 5 | 17 | 9.471e-10 | 4.321e-08 |
103 | RESPONSE TO PEPTIDE | 12 | 404 | 1.222e-09 | 5.521e-08 |
104 | TUMOR NECROSIS FACTOR MEDIATED SIGNALING PATHWAY | 8 | 118 | 1.499e-09 | 6.709e-08 |
105 | CHEMICAL HOMEOSTASIS | 16 | 874 | 1.66e-09 | 7.357e-08 |
106 | PHOSPHATIDYLINOSITOL BIOSYNTHETIC PROCESS | 8 | 120 | 1.715e-09 | 7.457e-08 |
107 | RESPONSE TO EXTERNAL STIMULUS | 22 | 1821 | 1.702e-09 | 7.457e-08 |
108 | CELLULAR GLUCOSE HOMEOSTASIS | 7 | 75 | 1.782e-09 | 7.678e-08 |
109 | REGULATION OF HYDROLASE ACTIVITY | 19 | 1327 | 2.04e-09 | 8.708e-08 |
110 | RESPONSE TO LIPID | 16 | 888 | 2.086e-09 | 8.825e-08 |
111 | REGULATION OF DEFENSE RESPONSE | 15 | 759 | 2.123e-09 | 8.9e-08 |
112 | REGULATION OF CELL PROLIFERATION | 20 | 1496 | 2.19e-09 | 9.097e-08 |
113 | RESPONSE TO BACTERIUM | 13 | 528 | 2.212e-09 | 9.109e-08 |
114 | HOMEOSTATIC PROCESS | 19 | 1337 | 2.31e-09 | 9.43e-08 |
115 | POSITIVE REGULATION OF HYDROLASE ACTIVITY | 16 | 905 | 2.738e-09 | 1.108e-07 |
116 | CELLULAR RESPONSE TO MECHANICAL STIMULUS | 7 | 80 | 2.821e-09 | 1.132e-07 |
117 | PROTEOLYSIS | 18 | 1208 | 3.292e-09 | 1.309e-07 |
118 | CELLULAR RESPONSE TO EXTERNAL STIMULUS | 10 | 264 | 3.39e-09 | 1.337e-07 |
119 | POSITIVE REGULATION OF NF KAPPAB TRANSCRIPTION FACTOR ACTIVITY | 8 | 132 | 3.661e-09 | 1.431e-07 |
120 | CELLULAR RESPONSE TO HORMONE STIMULUS | 13 | 552 | 3.775e-09 | 1.452e-07 |
121 | REGULATION OF CELLULAR PROTEIN LOCALIZATION | 13 | 552 | 3.775e-09 | 1.452e-07 |
122 | POSITIVE REGULATION OF NEURON APOPTOTIC PROCESS | 6 | 47 | 4.01e-09 | 1.53e-07 |
123 | RESPONSE TO WOUNDING | 13 | 563 | 4.781e-09 | 1.809e-07 |
124 | FC RECEPTOR SIGNALING PATHWAY | 9 | 206 | 6.426e-09 | 2.392e-07 |
125 | REGULATION OF EXECUTION PHASE OF APOPTOSIS | 5 | 24 | 6.408e-09 | 2.392e-07 |
126 | PHOSPHATIDYLINOSITOL 3 KINASE SIGNALING | 5 | 25 | 7.992e-09 | 2.951e-07 |
127 | T CELL RECEPTOR SIGNALING PATHWAY | 8 | 146 | 8.122e-09 | 2.976e-07 |
128 | REGULATION OF MITOCHONDRION ORGANIZATION | 9 | 218 | 1.052e-08 | 3.826e-07 |
129 | REGULATION OF CATABOLIC PROCESS | 14 | 731 | 1.202e-08 | 4.334e-07 |
130 | CELLULAR RESPONSE TO ENDOGENOUS STIMULUS | 16 | 1008 | 1.267e-08 | 4.533e-07 |
131 | REGULATION OF INTRACELLULAR TRANSPORT | 13 | 621 | 1.535e-08 | 5.454e-07 |
132 | POSITIVE REGULATION OF SEQUENCE SPECIFIC DNA BINDING TRANSCRIPTION FACTOR ACTIVITY | 9 | 228 | 1.553e-08 | 5.467e-07 |
133 | RENAL SYSTEM PROCESS | 7 | 102 | 1.563e-08 | 5.467e-07 |
134 | REGULATION OF ORGANELLE ORGANIZATION | 17 | 1178 | 1.63e-08 | 5.659e-07 |
135 | POSITIVE REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION | 12 | 514 | 1.806e-08 | 6.224e-07 |
136 | POSITIVE REGULATION OF MITOCHONDRION ORGANIZATION | 8 | 167 | 2.331e-08 | 7.974e-07 |
137 | RESPONSE TO ORGANIC CYCLIC COMPOUND | 15 | 917 | 2.689e-08 | 9.133e-07 |
138 | POSITIVE REGULATION OF GLUCOSE IMPORT IN RESPONSE TO INSULIN STIMULUS | 4 | 12 | 2.884e-08 | 9.726e-07 |
139 | RESPONSE TO AMINO ACID | 7 | 112 | 2.999e-08 | 1.004e-06 |
140 | NEGATIVE REGULATION OF MOLECULAR FUNCTION | 16 | 1079 | 3.288e-08 | 1.093e-06 |
141 | SIGNAL TRANSDUCTION IN ABSENCE OF LIGAND | 5 | 33 | 3.509e-08 | 1.15e-06 |
142 | EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 5 | 33 | 3.509e-08 | 1.15e-06 |
143 | POSITIVE REGULATION OF NEURON DEATH | 6 | 67 | 3.568e-08 | 1.161e-06 |
144 | MITOCHONDRIAL TRANSPORT | 8 | 177 | 3.667e-08 | 1.185e-06 |
145 | RENAL WATER HOMEOSTASIS | 5 | 34 | 4.105e-08 | 1.317e-06 |
146 | POSITIVE REGULATION OF NUCLEOCYTOPLASMIC TRANSPORT | 7 | 121 | 5.125e-08 | 1.633e-06 |
147 | INFLAMMATORY RESPONSE | 11 | 454 | 5.265e-08 | 1.667e-06 |
148 | INOSITOL LIPID MEDIATED SIGNALING | 7 | 124 | 6.07e-08 | 1.908e-06 |
149 | CELLULAR RESPONSE TO CARBOHYDRATE STIMULUS | 6 | 74 | 6.522e-08 | 2.037e-06 |
150 | PHOSPHATIDYLINOSITOL METABOLIC PROCESS | 8 | 193 | 7.171e-08 | 2.225e-06 |
151 | CELLULAR RESPONSE TO GLUCAGON STIMULUS | 5 | 38 | 7.341e-08 | 2.262e-06 |
152 | WOUND HEALING | 11 | 470 | 7.479e-08 | 2.289e-06 |
153 | T CELL APOPTOTIC PROCESS | 4 | 15 | 7.904e-08 | 2.404e-06 |
154 | MITOCHONDRION ORGANIZATION | 12 | 594 | 8.802e-08 | 2.659e-06 |
155 | NIK NF KAPPAB SIGNALING | 6 | 83 | 1.303e-07 | 3.886e-06 |
156 | NEGATIVE REGULATION OF CELL COMMUNICATION | 16 | 1192 | 1.301e-07 | 3.886e-06 |
157 | NEGATIVE REGULATION OF RESPONSE TO STIMULUS | 17 | 1360 | 1.324e-07 | 3.925e-06 |
158 | REGULATION OF GLUCOSE IMPORT IN RESPONSE TO INSULIN STIMULUS | 4 | 17 | 1.372e-07 | 4.041e-06 |
159 | GLYCEROLIPID BIOSYNTHETIC PROCESS | 8 | 211 | 1.425e-07 | 4.17e-06 |
160 | REGULATION OF RELEASE OF CYTOCHROME C FROM MITOCHONDRIA | 5 | 44 | 1.568e-07 | 4.559e-06 |
161 | LYMPHOCYTE APOPTOTIC PROCESS | 4 | 18 | 1.761e-07 | 5.088e-06 |
162 | REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 5 | 46 | 1.97e-07 | 5.659e-06 |
163 | HEMOSTASIS | 9 | 311 | 2.213e-07 | 6.317e-06 |
164 | RESPONSE TO GLUCAGON | 5 | 48 | 2.45e-07 | 6.952e-06 |
165 | POSITIVE REGULATION OF TRANSPORT | 14 | 936 | 2.572e-07 | 7.253e-06 |
166 | RESPONSE TO GAMMA RADIATION | 5 | 50 | 3.019e-07 | 8.462e-06 |
167 | PHOSPHOLIPID BIOSYNTHETIC PROCESS | 8 | 235 | 3.246e-07 | 9.043e-06 |
168 | POSITIVE REGULATION OF TRANSCRIPTION FACTOR IMPORT INTO NUCLEUS | 5 | 51 | 3.34e-07 | 9.25e-06 |
169 | CELLULAR HOMEOSTASIS | 12 | 676 | 3.538e-07 | 9.742e-06 |
170 | POSITIVE REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY | 5 | 52 | 3.687e-07 | 1.009e-05 |
171 | LIPID PHOSPHORYLATION | 6 | 99 | 3.735e-07 | 1.016e-05 |
172 | RESPONSE TO TOXIC SUBSTANCE | 8 | 241 | 3.931e-07 | 1.063e-05 |
173 | POSITIVE REGULATION OF PROTEIN OLIGOMERIZATION | 4 | 22 | 4.173e-07 | 1.116e-05 |
174 | RELEASE OF CYTOCHROME C FROM MITOCHONDRIA | 4 | 22 | 4.173e-07 | 1.116e-05 |
175 | NEGATIVE REGULATION OF CATALYTIC ACTIVITY | 13 | 829 | 4.381e-07 | 1.165e-05 |
176 | STRESS ACTIVATED PROTEIN KINASE SIGNALING CASCADE | 6 | 103 | 4.724e-07 | 1.249e-05 |
177 | RESPONSE TO CARBOHYDRATE | 7 | 168 | 4.835e-07 | 1.271e-05 |
178 | EXECUTION PHASE OF APOPTOSIS | 5 | 55 | 4.903e-07 | 1.282e-05 |
179 | CELL ACTIVATION | 11 | 568 | 4.968e-07 | 1.292e-05 |
180 | POSITIVE REGULATION OF CELLULAR RESPONSE TO INSULIN STIMULUS | 4 | 23 | 5.041e-07 | 1.296e-05 |
181 | LEUKOCYTE APOPTOTIC PROCESS | 4 | 23 | 5.041e-07 | 1.296e-05 |
182 | CELLULAR CHEMICAL HOMEOSTASIS | 11 | 570 | 5.144e-07 | 1.315e-05 |
183 | GLUCOSE HOMEOSTASIS | 7 | 170 | 5.237e-07 | 1.324e-05 |
184 | CARBOHYDRATE HOMEOSTASIS | 7 | 170 | 5.237e-07 | 1.324e-05 |
185 | POSITIVE REGULATION OF ORGANELLE ORGANIZATION | 11 | 573 | 5.417e-07 | 1.363e-05 |
186 | RESPONSE TO OXIDATIVE STRESS | 9 | 352 | 6.254e-07 | 1.565e-05 |
187 | MULTICELLULAR ORGANISMAL WATER HOMEOSTASIS | 5 | 58 | 6.417e-07 | 1.597e-05 |
188 | POSITIVE REGULATION OF INTRACELLULAR PROTEIN TRANSPORT | 8 | 258 | 6.585e-07 | 1.63e-05 |
189 | CELLULAR RESPONSE TO DNA DAMAGE STIMULUS | 12 | 720 | 6.909e-07 | 1.701e-05 |
190 | REGULATION OF GLUCOSE IMPORT | 5 | 60 | 7.615e-07 | 1.865e-05 |
191 | POSITIVE REGULATION OF GENE EXPRESSION | 18 | 1733 | 8.064e-07 | 1.964e-05 |
192 | REGULATION OF NECROTIC CELL DEATH | 4 | 26 | 8.457e-07 | 2.039e-05 |
193 | REGULATION OF SEQUENCE SPECIFIC DNA BINDING TRANSCRIPTION FACTOR ACTIVITY | 9 | 365 | 8.458e-07 | 2.039e-05 |
194 | RESPONSE TO INTERLEUKIN 1 | 6 | 115 | 9.056e-07 | 2.172e-05 |
195 | MULTICELLULAR ORGANISMAL HOMEOSTASIS | 8 | 272 | 9.802e-07 | 2.339e-05 |
196 | DNA CATABOLIC PROCESS | 4 | 27 | 9.906e-07 | 2.352e-05 |
197 | NUCLEOTIDE BINDING DOMAIN LEUCINE RICH REPEAT CONTAINING RECEPTOR SIGNALING PATHWAY | 4 | 28 | 1.153e-06 | 2.697e-05 |
198 | NECROTIC CELL DEATH | 4 | 28 | 1.153e-06 | 2.697e-05 |
199 | POSITIVE REGULATION OF RELEASE OF CYTOCHROME C FROM MITOCHONDRIA | 4 | 28 | 1.153e-06 | 2.697e-05 |
200 | POSITIVE REGULATION OF CYTOPLASMIC TRANSPORT | 8 | 282 | 1.285e-06 | 2.974e-05 |
201 | REGULATION OF LIPID METABOLIC PROCESS | 8 | 282 | 1.285e-06 | 2.974e-05 |
202 | MYD88 INDEPENDENT TOLL LIKE RECEPTOR SIGNALING PATHWAY | 4 | 30 | 1.537e-06 | 3.54e-05 |
203 | NEGATIVE REGULATION OF PROTEIN METABOLIC PROCESS | 14 | 1087 | 1.544e-06 | 3.54e-05 |
204 | WATER HOMEOSTASIS | 5 | 70 | 1.651e-06 | 3.767e-05 |
205 | LEUKOCYTE DIFFERENTIATION | 8 | 292 | 1.667e-06 | 3.783e-05 |
206 | REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION TO MITOCHONDRION | 6 | 128 | 1.697e-06 | 3.832e-05 |
207 | GLYCEROPHOSPHOLIPID METABOLIC PROCESS | 8 | 297 | 1.892e-06 | 4.252e-05 |
208 | MYD88 DEPENDENT TOLL LIKE RECEPTOR SIGNALING PATHWAY | 4 | 32 | 2.008e-06 | 4.471e-05 |
209 | INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO ENDOPLASMIC RETICULUM STRESS | 4 | 32 | 2.008e-06 | 4.471e-05 |
210 | REGULATION OF PROTEIN LOCALIZATION | 13 | 950 | 2.019e-06 | 4.473e-05 |
211 | B CELL ACTIVATION | 6 | 132 | 2.03e-06 | 4.477e-05 |
212 | RESPONSE TO MECHANICAL STIMULUS | 7 | 210 | 2.157e-06 | 4.734e-05 |
213 | CYTOPLASMIC PATTERN RECOGNITION RECEPTOR SIGNALING PATHWAY | 4 | 33 | 2.281e-06 | 4.982e-05 |
214 | RESPONSE TO ALKALOID | 6 | 137 | 2.521e-06 | 5.481e-05 |
215 | T CELL HOMEOSTASIS | 4 | 34 | 2.579e-06 | 5.582e-05 |
216 | RESPONSE TO OXYGEN LEVELS | 8 | 311 | 2.663e-06 | 5.737e-05 |
217 | REGULATION OF PROTEIN OLIGOMERIZATION | 4 | 35 | 2.906e-06 | 6.231e-05 |
218 | REGULATION OF NUCLEOCYTOPLASMIC TRANSPORT | 7 | 220 | 2.936e-06 | 6.266e-05 |
219 | POSITIVE REGULATION OF CELLULAR COMPONENT ORGANIZATION | 14 | 1152 | 3.054e-06 | 6.489e-05 |
220 | INSULIN RECEPTOR SIGNALING PATHWAY | 5 | 80 | 3.21e-06 | 6.767e-05 |
221 | REGULATION OF MAP KINASE ACTIVITY | 8 | 319 | 3.214e-06 | 6.767e-05 |
222 | NEGATIVE REGULATION OF CELL CYCLE | 9 | 433 | 3.447e-06 | 7.224e-05 |
223 | RESPONSE TO IONIZING RADIATION | 6 | 145 | 3.504e-06 | 7.31e-05 |
224 | POSITIVE REGULATION OF NFAT PROTEIN IMPORT INTO NUCLEUS | 3 | 11 | 3.563e-06 | 7.402e-05 |
225 | PEPTIDYL SERINE MODIFICATION | 6 | 148 | 3.944e-06 | 8.157e-05 |
226 | RESPONSE TO ENDOPLASMIC RETICULUM STRESS | 7 | 233 | 4.288e-06 | 8.828e-05 |
227 | REGULATION OF PHOSPHATIDYLINOSITOL 3 KINASE ACTIVITY | 4 | 40 | 5.018e-06 | 0.0001029 |
228 | IMMUNE SYSTEM DEVELOPMENT | 10 | 582 | 5.08e-06 | 0.0001037 |
229 | CELLULAR RESPONSE TO INTERLEUKIN 1 | 5 | 88 | 5.141e-06 | 0.000104 |
230 | NEGATIVE REGULATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY | 5 | 88 | 5.141e-06 | 0.000104 |
231 | LYMPHOCYTE ACTIVATION | 8 | 342 | 5.366e-06 | 0.0001081 |
232 | HEPATOCYTE APOPTOTIC PROCESS | 3 | 13 | 6.151e-06 | 0.0001218 |
233 | POSITIVE REGULATION OF GLUCOSE TRANSPORT | 4 | 42 | 6.12e-06 | 0.0001218 |
234 | INTERLEUKIN 1 MEDIATED SIGNALING PATHWAY | 3 | 13 | 6.151e-06 | 0.0001218 |
235 | RESPONSE TO COBALT ION | 3 | 13 | 6.151e-06 | 0.0001218 |
236 | DEFENSE RESPONSE | 14 | 1231 | 6.582e-06 | 0.0001298 |
237 | REGULATION OF AUTOPHAGY | 7 | 249 | 6.629e-06 | 0.0001302 |
238 | CELLULAR COMPONENT DISASSEMBLY INVOLVED IN EXECUTION PHASE OF APOPTOSIS | 4 | 43 | 6.734e-06 | 0.0001316 |
239 | GLYCEROLIPID METABOLIC PROCESS | 8 | 356 | 7.197e-06 | 0.0001401 |
240 | REGULATION OF TRANSCRIPTION FACTOR IMPORT INTO NUCLEUS | 5 | 95 | 7.489e-06 | 0.0001452 |
241 | TOLL LIKE RECEPTOR 9 SIGNALING PATHWAY | 3 | 14 | 7.813e-06 | 0.000149 |
242 | RESPONSE TO INORGANIC SUBSTANCE | 9 | 479 | 7.796e-06 | 0.000149 |
243 | LEUKOCYTE CELL CELL ADHESION | 7 | 255 | 7.745e-06 | 0.000149 |
244 | REGULATION OF CAMP DEPENDENT PROTEIN KINASE ACTIVITY | 3 | 14 | 7.813e-06 | 0.000149 |
245 | REGULATION OF CYTOPLASMIC TRANSPORT | 9 | 481 | 8.062e-06 | 0.0001531 |
246 | PHOSPHOLIPID METABOLIC PROCESS | 8 | 364 | 8.462e-06 | 0.0001601 |
247 | LEUKOCYTE MIGRATION | 7 | 259 | 8.572e-06 | 0.0001615 |
248 | NEGATIVE REGULATION OF NEURON DEATH | 6 | 171 | 9.048e-06 | 0.0001698 |
249 | REGULATION OF GLUCOSE TRANSPORT | 5 | 100 | 9.626e-06 | 0.0001799 |
250 | APOPTOTIC DNA FRAGMENTATION | 3 | 15 | 9.747e-06 | 0.0001814 |
251 | REGULATION OF CELLULAR LOCALIZATION | 14 | 1277 | 1.001e-05 | 0.0001856 |
252 | REGULATION OF LIPID KINASE ACTIVITY | 4 | 48 | 1.051e-05 | 0.000194 |
253 | RESPONSE TO CORTICOSTEROID | 6 | 176 | 1.067e-05 | 0.0001962 |
254 | POSITIVE REGULATION OF PROTEIN IMPORT | 5 | 104 | 1.166e-05 | 0.0002135 |
255 | REGULATION OF INTRACELLULAR PROTEIN TRANSPORT | 8 | 381 | 1.179e-05 | 0.0002151 |
256 | REGULATION OF BODY FLUID LEVELS | 9 | 506 | 1.209e-05 | 0.0002197 |
257 | LYMPHOCYTE HOMEOSTASIS | 4 | 50 | 1.238e-05 | 0.0002242 |
258 | INNATE IMMUNE RESPONSE ACTIVATING CELL SURFACE RECEPTOR SIGNALING PATHWAY | 5 | 106 | 1.279e-05 | 0.0002307 |
259 | RESPONSE TO NICOTINE | 4 | 51 | 1.341e-05 | 0.0002409 |
260 | PROTEIN COMPLEX BIOGENESIS | 13 | 1132 | 1.358e-05 | 0.0002421 |
261 | PROTEIN COMPLEX ASSEMBLY | 13 | 1132 | 1.358e-05 | 0.0002421 |
262 | REGULATION OF CELL CYCLE ARREST | 5 | 108 | 1.401e-05 | 0.0002488 |
263 | REGULATION OF NFAT PROTEIN IMPORT INTO NUCLEUS | 3 | 17 | 1.451e-05 | 0.0002557 |
264 | NEGATIVE REGULATION OF ANOIKIS | 3 | 17 | 1.451e-05 | 0.0002557 |
265 | CELLULAR RESPONSE TO AMINO ACID STIMULUS | 4 | 53 | 1.564e-05 | 0.0002736 |
266 | POSITIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 4 | 53 | 1.564e-05 | 0.0002736 |
267 | RESPONSE TO REACTIVE OXYGEN SPECIES | 6 | 191 | 1.698e-05 | 0.0002959 |
268 | SIGNAL TRANSDUCTION BY PROTEIN PHOSPHORYLATION | 8 | 404 | 1.799e-05 | 0.0003123 |
269 | REGULATION OF INFLAMMATORY RESPONSE | 7 | 294 | 1.947e-05 | 0.0003367 |
270 | NEGATIVE REGULATION OF MEIOTIC CELL CYCLE | 3 | 19 | 2.059e-05 | 0.0003535 |
271 | DNA CATABOLIC PROCESS ENDONUCLEOLYTIC | 3 | 19 | 2.059e-05 | 0.0003535 |
272 | NEGATIVE REGULATION OF CELLULAR COMPONENT ORGANIZATION | 10 | 684 | 2.07e-05 | 0.0003541 |
273 | APOPTOTIC MITOCHONDRIAL CHANGES | 4 | 57 | 2.092e-05 | 0.0003566 |
274 | RESPONSE TO RADIATION | 8 | 413 | 2.107e-05 | 0.0003578 |
275 | LEUKOCYTE ACTIVATION | 8 | 414 | 2.144e-05 | 0.0003627 |
276 | REGULATION OF PEPTIDYL SERINE PHOSPHORYLATION | 5 | 118 | 2.152e-05 | 0.0003627 |
277 | REGULATION OF CELLULAR RESPONSE TO INSULIN STIMULUS | 4 | 59 | 2.401e-05 | 0.0004018 |
278 | NEGATIVE REGULATION OF CATABOLIC PROCESS | 6 | 203 | 2.395e-05 | 0.0004018 |
279 | POSITIVE REGULATION OF LYMPHOCYTE APOPTOTIC PROCESS | 3 | 20 | 2.417e-05 | 0.0004032 |
280 | LEUKOCYTE HOMEOSTASIS | 4 | 60 | 2.567e-05 | 0.0004265 |
281 | REGULATION OF PHOSPHOLIPID METABOLIC PROCESS | 4 | 61 | 2.741e-05 | 0.0004539 |
282 | B CELL HOMEOSTASIS | 3 | 21 | 2.815e-05 | 0.0004622 |
283 | NECROPTOTIC PROCESS | 3 | 21 | 2.815e-05 | 0.0004622 |
284 | LYMPHOCYTE DIFFERENTIATION | 6 | 209 | 2.821e-05 | 0.0004622 |
285 | RESPONSE TO DRUG | 8 | 431 | 2.857e-05 | 0.0004664 |
286 | LIPID MODIFICATION | 6 | 210 | 2.898e-05 | 0.0004715 |
287 | REGULATION OF TRANSPORT | 16 | 1804 | 2.908e-05 | 0.0004715 |
288 | POSITIVE REGULATION OF BIOSYNTHETIC PROCESS | 16 | 1805 | 2.928e-05 | 0.0004731 |
289 | RESPONSE TO UV | 5 | 126 | 2.952e-05 | 0.0004736 |
290 | NEGATIVE REGULATION OF PROTEIN SERINE THREONINE KINASE ACTIVITY | 5 | 126 | 2.952e-05 | 0.0004736 |
291 | PROTEIN OLIGOMERIZATION | 8 | 434 | 3.002e-05 | 0.0004799 |
292 | RESPONSE TO ACID CHEMICAL | 7 | 319 | 3.281e-05 | 0.0005229 |
293 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO NUCLEUS | 5 | 129 | 3.305e-05 | 0.0005249 |
294 | EMBRYO DEVELOPMENT | 11 | 894 | 3.743e-05 | 0.0005924 |
295 | ORGANOPHOSPHATE BIOSYNTHETIC PROCESS | 8 | 450 | 3.88e-05 | 0.0006121 |
296 | MEMBRANE ORGANIZATION | 11 | 899 | 3.938e-05 | 0.0006191 |
297 | NEGATIVE REGULATION OF NEURON APOPTOTIC PROCESS | 5 | 135 | 4.11e-05 | 0.0006438 |
298 | REGULATION OF ANOIKIS | 3 | 24 | 4.257e-05 | 0.0006647 |
299 | RESPONSE TO METAL ION | 7 | 333 | 4.31e-05 | 0.0006707 |
300 | CELLULAR RESPONSE TO RADIATION | 5 | 137 | 4.409e-05 | 0.0006838 |
301 | SINGLE ORGANISM CELL ADHESION | 8 | 459 | 4.463e-05 | 0.0006899 |
302 | CELLULAR LIPID METABOLIC PROCESS | 11 | 913 | 4.533e-05 | 0.0006984 |
303 | REGULATION OF PHOSPHATIDYLINOSITOL 3 KINASE SIGNALING | 5 | 138 | 4.565e-05 | 0.000701 |
304 | APOPTOTIC NUCLEAR CHANGES | 3 | 25 | 4.828e-05 | 0.0007366 |
305 | EPITHELIAL CELL APOPTOTIC PROCESS | 3 | 25 | 4.828e-05 | 0.0007366 |
306 | REGULATION OF MULTICELLULAR ORGANISMAL DEVELOPMENT | 15 | 1672 | 4.852e-05 | 0.0007378 |
307 | CELLULAR RESPONSE TO ORGANIC CYCLIC COMPOUND | 8 | 465 | 4.891e-05 | 0.0007413 |
308 | ESTABLISHMENT OF LOCALIZATION IN CELL | 15 | 1676 | 4.988e-05 | 0.0007536 |
309 | POSITIVE REGULATION OF MAPK CASCADE | 8 | 470 | 5.273e-05 | 0.000794 |
310 | CELLULAR RESPONSE TO OXYGEN LEVELS | 5 | 143 | 5.409e-05 | 0.0008119 |
311 | REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY | 5 | 145 | 5.779e-05 | 0.0008646 |
312 | VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 4 | 74 | 5.88e-05 | 0.0008768 |
313 | CELLULAR RESPONSE TO INSULIN STIMULUS | 5 | 146 | 5.971e-05 | 0.0008876 |
314 | REGULATION OF CELL CYCLE G1 S PHASE TRANSITION | 5 | 147 | 6.168e-05 | 0.000914 |
315 | REGULATION OF CELL CYCLE | 11 | 949 | 6.43e-05 | 0.0009498 |
316 | REGULATION OF CELL ACTIVATION | 8 | 484 | 6.478e-05 | 0.0009539 |
317 | REGULATION OF CELL ADHESION | 9 | 629 | 6.638e-05 | 0.0009744 |
318 | IMMUNE EFFECTOR PROCESS | 8 | 486 | 6.668e-05 | 0.0009756 |
319 | POSITIVE REGULATION OF LEUKOCYTE APOPTOTIC PROCESS | 3 | 28 | 6.835e-05 | 0.000997 |
320 | ANATOMICAL STRUCTURE FORMATION INVOLVED IN MORPHOGENESIS | 11 | 957 | 6.934e-05 | 0.001008 |
321 | RESPONSE TO VIRUS | 6 | 247 | 7.154e-05 | 0.001037 |
322 | PROTEIN COMPLEX SUBUNIT ORGANIZATION | 14 | 1527 | 7.297e-05 | 0.001051 |
323 | RESPONSE TO ALCOHOL | 7 | 362 | 7.293e-05 | 0.001051 |
324 | POSITIVE REGULATION OF NIK NF KAPPAB SIGNALING | 3 | 29 | 7.609e-05 | 0.001093 |
325 | RESPONSE TO STEROID HORMONE | 8 | 497 | 7.795e-05 | 0.001116 |
326 | TRANSMEMBRANE RECEPTOR PROTEIN TYROSINE KINASE SIGNALING PATHWAY | 8 | 498 | 7.905e-05 | 0.001128 |
327 | NEGATIVE REGULATION OF B CELL ACTIVATION | 3 | 30 | 8.437e-05 | 0.001201 |
328 | NEGATIVE REGULATION OF IMMUNE SYSTEM PROCESS | 7 | 372 | 8.648e-05 | 0.001227 |
329 | JNK CASCADE | 4 | 82 | 8.787e-05 | 0.001239 |
330 | REGULATION OF PROTEIN MATURATION | 4 | 82 | 8.787e-05 | 0.001239 |
331 | REGULATION OF MAPK CASCADE | 9 | 660 | 9.589e-05 | 0.001348 |
332 | POSITIVE REGULATION OF CELL CYCLE ARREST | 4 | 85 | 0.0001011 | 0.001417 |
333 | NEGATIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 3 | 32 | 0.0001027 | 0.00143 |
334 | NEGATIVE REGULATION OF SIGNAL TRANSDUCTION IN ABSENCE OF LIGAND | 3 | 32 | 0.0001027 | 0.00143 |
335 | AGING | 6 | 264 | 0.0001032 | 0.001433 |
336 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 11 | 1004 | 0.0001064 | 0.001473 |
337 | POSITIVE REGULATION OF PEPTIDYL SERINE PHOSPHORYLATION | 4 | 88 | 0.0001157 | 0.001597 |
338 | B CELL DIFFERENTIATION | 4 | 89 | 0.0001209 | 0.001658 |
339 | MACROMOLECULAR COMPLEX ASSEMBLY | 13 | 1398 | 0.0001212 | 0.001658 |
340 | EPITHELIAL CELL PROLIFERATION | 4 | 89 | 0.0001209 | 0.001658 |
341 | PROTEIN KINASE B SIGNALING | 3 | 34 | 0.0001233 | 0.001678 |
342 | CELLULAR RESPONSE TO ALKALOID | 3 | 34 | 0.0001233 | 0.001678 |
343 | NEGATIVE REGULATION OF HYDROLASE ACTIVITY | 7 | 397 | 0.0001295 | 0.001757 |
344 | STRIATED MUSCLE CELL DIFFERENTIATION | 5 | 173 | 0.000133 | 0.001794 |
345 | ENZYME LINKED RECEPTOR PROTEIN SIGNALING PATHWAY | 9 | 689 | 0.0001328 | 0.001794 |
346 | LIPID BIOSYNTHETIC PROCESS | 8 | 539 | 0.0001366 | 0.001837 |
347 | CELL DEVELOPMENT | 13 | 1426 | 0.0001478 | 0.001982 |
348 | FC GAMMA RECEPTOR SIGNALING PATHWAY | 4 | 95 | 0.0001556 | 0.002081 |
349 | SIGNAL TRANSDUCTION IN RESPONSE TO DNA DAMAGE | 4 | 96 | 0.000162 | 0.00216 |
350 | REGULATION OF RESPONSE TO WOUNDING | 7 | 413 | 0.0001652 | 0.002197 |
351 | POSITIVE REGULATION OF PROTEIN SERINE THREONINE KINASE ACTIVITY | 6 | 289 | 0.000169 | 0.00224 |
352 | REGULATION OF PROTEIN IMPORT | 5 | 183 | 0.0001729 | 0.002283 |
353 | REGULATION OF CELL CYCLE PROCESS | 8 | 558 | 0.0001732 | 0.002283 |
354 | NEGATIVE REGULATION OF CELL CYCLE G1 S PHASE TRANSITION | 4 | 98 | 0.0001754 | 0.002306 |
355 | REGULATION OF MEIOTIC CELL CYCLE | 3 | 40 | 0.0002012 | 0.00263 |
356 | MYELOID CELL DIFFERENTIATION | 5 | 189 | 0.000201 | 0.00263 |
357 | PROTEIN DEPHOSPHORYLATION | 5 | 190 | 0.0002059 | 0.002684 |
358 | PROTEIN AUTOPHOSPHORYLATION | 5 | 192 | 0.0002162 | 0.00281 |
359 | REGULATION OF CELL DIFFERENTIATION | 13 | 1492 | 0.0002316 | 0.003002 |
360 | REGULATION OF NIK NF KAPPAB SIGNALING | 3 | 42 | 0.0002328 | 0.00301 |
361 | REGULATION OF PROTEIN TARGETING | 6 | 307 | 0.0002341 | 0.003018 |
362 | POSITIVE REGULATION OF PROTEIN COMPLEX ASSEMBLY | 5 | 197 | 0.0002435 | 0.00313 |
363 | NEGATIVE REGULATION OF MITOTIC CELL CYCLE | 5 | 199 | 0.0002552 | 0.003271 |
364 | REGULATION OF RESPONSE TO EXTERNAL STIMULUS | 10 | 926 | 0.0002568 | 0.003283 |
365 | RESPONSE TO HYDROGEN PEROXIDE | 4 | 109 | 0.000264 | 0.003365 |
366 | GAMETE GENERATION | 8 | 595 | 0.0002677 | 0.003403 |
367 | MITOTIC CELL CYCLE | 9 | 766 | 0.0002926 | 0.0037 |
368 | RESPONSE TO INSULIN | 5 | 205 | 0.0002927 | 0.0037 |
369 | REGULATION OF CELLULAR COMPONENT BIOGENESIS | 9 | 767 | 0.0002954 | 0.003725 |
370 | OVULATION CYCLE | 4 | 113 | 0.000303 | 0.00381 |
371 | POSITIVE REGULATION OF MAP KINASE ACTIVITY | 5 | 207 | 0.000306 | 0.003838 |
372 | CELL CELL ADHESION | 8 | 608 | 0.0003096 | 0.003872 |
373 | GERM CELL DEVELOPMENT | 5 | 209 | 0.0003199 | 0.00399 |
374 | RESPONSE TO ANTIBIOTIC | 3 | 47 | 0.0003256 | 0.004051 |
375 | FEMALE SEX DIFFERENTIATION | 4 | 116 | 0.0003348 | 0.004154 |
376 | NEGATIVE REGULATION OF PROTEOLYSIS | 6 | 329 | 0.0003391 | 0.004197 |
377 | INNATE IMMUNE RESPONSE | 8 | 619 | 0.0003491 | 0.004308 |
378 | NEGATIVE REGULATION OF CELL CYCLE PROCESS | 5 | 214 | 0.0003566 | 0.004389 |
379 | LIPID METABOLIC PROCESS | 11 | 1158 | 0.0003683 | 0.004522 |
380 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 14 | 1784 | 0.0003756 | 0.004599 |
381 | RESPONSE TO ESTROGEN | 5 | 218 | 0.0003881 | 0.004728 |
382 | REGULATION OF PROTEIN LOCALIZATION TO NUCLEUS | 5 | 218 | 0.0003881 | 0.004728 |
383 | REGULATION OF B CELL ACTIVATION | 4 | 121 | 0.0003931 | 0.004775 |
384 | REGULATION OF DNA METABOLIC PROCESS | 6 | 340 | 0.0004039 | 0.004894 |
385 | REGULATION OF EPITHELIAL CELL DIFFERENTIATION | 4 | 122 | 0.0004055 | 0.004901 |
386 | REGULATION OF CERAMIDE BIOSYNTHETIC PROCESS | 2 | 11 | 0.0004317 | 0.005178 |
387 | POSITIVE REGULATION OF HAIR CYCLE | 2 | 11 | 0.0004317 | 0.005178 |
388 | REGULATION OF NECROPTOTIC PROCESS | 2 | 11 | 0.0004317 | 0.005178 |
389 | CELLULAR RESPONSE TO IONIZING RADIATION | 3 | 52 | 0.0004393 | 0.005255 |
390 | POSITIVE REGULATION OF MULTICELLULAR ORGANISMAL PROCESS | 12 | 1395 | 0.0004735 | 0.005649 |
391 | NEGATIVE REGULATION OF TRANSFERASE ACTIVITY | 6 | 351 | 0.000478 | 0.005688 |
392 | NEGATIVE REGULATION OF REPRODUCTIVE PROCESS | 3 | 54 | 0.0004911 | 0.005784 |
393 | REGULATION OF LYMPHOCYTE APOPTOTIC PROCESS | 3 | 54 | 0.0004911 | 0.005784 |
394 | REGULATION OF MITOCHONDRIAL MEMBRANE POTENTIAL | 3 | 54 | 0.0004911 | 0.005784 |
395 | B CELL RECEPTOR SIGNALING PATHWAY | 3 | 54 | 0.0004911 | 0.005784 |
396 | REGULATION OF VITAMIN METABOLIC PROCESS | 2 | 12 | 0.0005171 | 0.006014 |
397 | REGULATION OF ENDOTHELIAL CELL DEVELOPMENT | 2 | 12 | 0.0005171 | 0.006014 |
398 | REGULATION OF ESTABLISHMENT OF ENDOTHELIAL BARRIER | 2 | 12 | 0.0005171 | 0.006014 |
399 | REGULATION OF B CELL PROLIFERATION | 3 | 55 | 0.0005183 | 0.006014 |
400 | REPLICATIVE SENESCENCE | 2 | 12 | 0.0005171 | 0.006014 |
401 | POSITIVE REGULATION OF EXECUTION PHASE OF APOPTOSIS | 2 | 12 | 0.0005171 | 0.006014 |
402 | INTERSPECIES INTERACTION BETWEEN ORGANISMS | 8 | 662 | 0.0005451 | 0.006293 |
403 | SYMBIOSIS ENCOMPASSING MUTUALISM THROUGH PARASITISM | 8 | 662 | 0.0005451 | 0.006293 |
404 | CELL MOTILITY | 9 | 835 | 0.0005486 | 0.006303 |
405 | LOCALIZATION OF CELL | 9 | 835 | 0.0005486 | 0.006303 |
406 | MUSCLE CELL DIFFERENTIATION | 5 | 237 | 0.0005679 | 0.006508 |
407 | CELL PROLIFERATION | 8 | 672 | 0.0006015 | 0.006877 |
408 | REGULATION OF SPHINGOLIPID BIOSYNTHETIC PROCESS | 2 | 13 | 0.00061 | 0.00689 |
409 | REGULATION OF MEMBRANE LIPID METABOLIC PROCESS | 2 | 13 | 0.00061 | 0.00689 |
410 | POSITIVE REGULATION OF ENDOPLASMIC RETICULUM UNFOLDED PROTEIN RESPONSE | 2 | 13 | 0.00061 | 0.00689 |
411 | PROTEIN AUTOPROCESSING | 2 | 13 | 0.00061 | 0.00689 |
412 | REGULATION OF BICELLULAR TIGHT JUNCTION ASSEMBLY | 2 | 13 | 0.00061 | 0.00689 |
413 | CELLULAR COMPONENT DISASSEMBLY | 7 | 515 | 0.0006255 | 0.007048 |
414 | ACTIVATION OF MAPK ACTIVITY | 4 | 137 | 0.0006282 | 0.007061 |
415 | NEGATIVE REGULATION OF PEPTIDASE ACTIVITY | 5 | 245 | 0.0006598 | 0.007398 |
416 | MITOTIC CELL CYCLE CHECKPOINT | 4 | 139 | 0.0006633 | 0.007419 |
417 | POSITIVE REGULATION OF SMOOTH MUSCLE CELL PROLIFERATION | 3 | 60 | 0.0006693 | 0.007468 |
418 | OVARIAN FOLLICLE DEVELOPMENT | 3 | 61 | 0.0007025 | 0.00782 |
419 | POSITIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 2 | 14 | 0.0007104 | 0.00787 |
420 | DETERMINATION OF ADULT LIFESPAN | 2 | 14 | 0.0007104 | 0.00787 |
421 | PLATELET ACTIVATION | 4 | 142 | 0.0007186 | 0.007942 |
422 | NEGATIVE REGULATION OF KINASE ACTIVITY | 5 | 250 | 0.0007227 | 0.007969 |
423 | REGULATION OF CELL CELL ADHESION | 6 | 380 | 0.0007248 | 0.007973 |
424 | CELLULAR PROCESS INVOLVED IN REPRODUCTION IN MULTICELLULAR ORGANISM | 5 | 252 | 0.0007491 | 0.008221 |
425 | RESPONSE TO OSMOTIC STRESS | 3 | 63 | 0.000772 | 0.008452 |
426 | NUCLEIC ACID PHOSPHODIESTER BOND HYDROLYSIS | 5 | 254 | 0.0007762 | 0.008478 |
427 | RESPONSE TO ESTRADIOL | 4 | 146 | 0.0007972 | 0.008667 |
428 | NEGATIVE REGULATION OF CELL CYCLE PHASE TRANSITION | 4 | 146 | 0.0007972 | 0.008667 |
429 | REGULATION OF HAIR FOLLICLE DEVELOPMENT | 2 | 15 | 0.0008182 | 0.008813 |
430 | NEGATIVE REGULATION OF INTERLEUKIN 12 PRODUCTION | 2 | 15 | 0.0008182 | 0.008813 |
431 | NEGATIVE REGULATION OF B CELL PROLIFERATION | 2 | 15 | 0.0008182 | 0.008813 |
432 | NEUROTROPHIN TRK RECEPTOR SIGNALING PATHWAY | 2 | 15 | 0.0008182 | 0.008813 |
433 | ORGANOPHOSPHATE METABOLIC PROCESS | 9 | 885 | 0.0008315 | 0.008936 |
434 | NEGATIVE REGULATION OF PHOSPHORUS METABOLIC PROCESS | 7 | 541 | 0.0008357 | 0.008939 |
435 | NEGATIVE REGULATION OF PHOSPHATE METABOLIC PROCESS | 7 | 541 | 0.0008357 | 0.008939 |
436 | CELL CYCLE PROCESS | 10 | 1081 | 0.0008656 | 0.009237 |
437 | CELLULAR RESPONSE TO UV | 3 | 66 | 0.0008843 | 0.009415 |
438 | GLAND DEVELOPMENT | 6 | 395 | 0.0008862 | 0.009415 |
439 | CELL AGING | 3 | 67 | 0.0009239 | 0.00977 |
440 | SINGLE ORGANISM CELLULAR LOCALIZATION | 9 | 898 | 0.000922 | 0.00977 |
441 | REGULATION OF REACTIVE OXYGEN SPECIES METABOLIC PROCESS | 4 | 152 | 0.0009264 | 0.009774 |
442 | REGULATION OF PROTEIN HOMOOLIGOMERIZATION | 2 | 16 | 0.0009334 | 0.009804 |
443 | REGULATION OF DEVELOPMENTAL PIGMENTATION | 2 | 16 | 0.0009334 | 0.009804 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY BINDING | 10 | 47 | 7.337e-17 | 6.816e-14 |
2 | DEATH RECEPTOR BINDING | 7 | 18 | 3.237e-14 | 1.504e-11 |
3 | CYTOKINE RECEPTOR BINDING | 13 | 271 | 5.603e-13 | 1.735e-10 |
4 | KINASE ACTIVITY | 19 | 842 | 8.363e-13 | 1.942e-10 |
5 | TRANSFERASE ACTIVITY TRANSFERRING PHOSPHORUS CONTAINING GROUPS | 19 | 992 | 1.466e-11 | 2.724e-09 |
6 | PHOSPHATIDYLINOSITOL 3 KINASE ACTIVITY | 8 | 70 | 2.149e-11 | 3.327e-09 |
7 | X1 PHOSPHATIDYLINOSITOL 3 KINASE ACTIVITY | 7 | 43 | 3.103e-11 | 4.119e-09 |
8 | PHOSPHATIDYLINOSITOL KINASE ACTIVITY | 7 | 51 | 1.096e-10 | 1.272e-08 |
9 | PROTEIN HETERODIMERIZATION ACTIVITY | 13 | 468 | 5.125e-10 | 5.29e-08 |
10 | ENZYME BINDING | 22 | 1737 | 6.974e-10 | 6.479e-08 |
11 | KINASE REGULATOR ACTIVITY | 9 | 186 | 2.625e-09 | 2.217e-07 |
12 | UBIQUITIN LIKE PROTEIN LIGASE BINDING | 10 | 264 | 3.39e-09 | 2.594e-07 |
13 | PROTEIN SERINE THREONINE KINASE ACTIVITY | 12 | 445 | 3.63e-09 | 2.594e-07 |
14 | PROTEASE BINDING | 7 | 104 | 1.79e-08 | 1.188e-06 |
15 | PROTEIN KINASE ACTIVITY | 13 | 640 | 2.192e-08 | 1.272e-06 |
16 | TUMOR NECROSIS FACTOR RECEPTOR BINDING | 5 | 30 | 2.121e-08 | 1.272e-06 |
17 | ADENYL NUCLEOTIDE BINDING | 18 | 1514 | 1.08e-07 | 5.9e-06 |
18 | RECEPTOR BINDING | 17 | 1476 | 4.253e-07 | 2.195e-05 |
19 | PROTEIN DIMERIZATION ACTIVITY | 15 | 1149 | 5.039e-07 | 2.464e-05 |
20 | DEATH RECEPTOR ACTIVITY | 4 | 24 | 6.036e-07 | 2.804e-05 |
21 | KINASE BINDING | 11 | 606 | 9.393e-07 | 4.155e-05 |
22 | PROTEIN SERINE THREONINE KINASE INHIBITOR ACTIVITY | 4 | 30 | 1.537e-06 | 6.491e-05 |
23 | RIBONUCLEOTIDE BINDING | 18 | 1860 | 2.249e-06 | 8.704e-05 |
24 | ENZYME REGULATOR ACTIVITY | 13 | 959 | 2.241e-06 | 8.704e-05 |
25 | INSULIN RECEPTOR SUBSTRATE BINDING | 3 | 11 | 3.563e-06 | 0.0001324 |
26 | MOLECULAR FUNCTION REGULATOR | 15 | 1353 | 3.888e-06 | 0.0001389 |
27 | CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY | 5 | 86 | 4.59e-06 | 0.0001579 |
28 | PROTEIN KINASE A BINDING | 4 | 42 | 6.12e-06 | 0.0002031 |
29 | PROTEIN KINASE A CATALYTIC SUBUNIT BINDING | 3 | 15 | 9.747e-06 | 0.0003018 |
30 | CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY INVOLVED IN APOPTOTIC PROCESS | 3 | 15 | 9.747e-06 | 0.0003018 |
31 | PHOSPHATIDYLINOSITOL PHOSPHATE KINASE ACTIVITY | 3 | 16 | 1.197e-05 | 0.0003588 |
32 | IDENTICAL PROTEIN BINDING | 13 | 1209 | 2.723e-05 | 0.0007907 |
33 | CAMP BINDING | 3 | 23 | 3.733e-05 | 0.001051 |
34 | PROTEIN DOMAIN SPECIFIC BINDING | 9 | 624 | 6.243e-05 | 0.001706 |
35 | ENZYME INHIBITOR ACTIVITY | 7 | 378 | 9.555e-05 | 0.002536 |
36 | KINASE INHIBITOR ACTIVITY | 4 | 89 | 0.0001209 | 0.003119 |
37 | CYCLIC NUCLEOTIDE BINDING | 3 | 36 | 0.0001466 | 0.00368 |
38 | CYSTEINE TYPE PEPTIDASE ACTIVITY | 5 | 184 | 0.0001774 | 0.004337 |
39 | CYSTEINE TYPE ENDOPEPTIDASE REGULATOR ACTIVITY INVOLVED IN APOPTOTIC PROCESS | 3 | 42 | 0.0002328 | 0.005546 |
40 | SIGNAL TRANSDUCER ACTIVITY | 14 | 1731 | 0.0002754 | 0.006288 |
41 | PROTEIN COMPLEX BINDING | 10 | 935 | 0.0002775 | 0.006288 |
42 | PROTEIN PHOSPHATASE BINDING | 4 | 120 | 0.0003809 | 0.008425 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | TRANSFERASE COMPLEX TRANSFERRING PHOSPHORUS CONTAINING GROUPS | 15 | 237 | 1.159e-16 | 6.77e-14 |
2 | MEMBRANE MICRODOMAIN | 14 | 288 | 5.314e-14 | 1.528e-11 |
3 | PHOSPHATIDYLINOSITOL 3 KINASE COMPLEX | 7 | 20 | 7.852e-14 | 1.528e-11 |
4 | CATALYTIC COMPLEX | 20 | 1038 | 3.252e-12 | 4.748e-10 |
5 | MEMBRANE PROTEIN COMPLEX | 18 | 1020 | 2.203e-10 | 2.574e-08 |
6 | TRANSFERASE COMPLEX | 15 | 703 | 7.45e-10 | 7.251e-08 |
7 | CILIARY BASE | 5 | 23 | 5.084e-09 | 4.241e-07 |
8 | PROTEIN KINASE COMPLEX | 7 | 90 | 6.491e-09 | 4.739e-07 |
9 | MEMBRANE REGION | 15 | 1134 | 4.262e-07 | 2.765e-05 |
10 | MITOCHONDRION | 17 | 1633 | 1.743e-06 | 0.0001018 |
11 | EXTRINSIC COMPONENT OF MEMBRANE | 7 | 252 | 7.169e-06 | 0.0003806 |
12 | PERINUCLEAR REGION OF CYTOPLASM | 9 | 642 | 7.765e-05 | 0.003779 |
13 | PLASMA MEMBRANE PROTEIN COMPLEX | 8 | 510 | 9.327e-05 | 0.00419 |
14 | PLASMA MEMBRANE RAFT | 4 | 86 | 0.0001058 | 0.004413 |
15 | MITOCHONDRIAL ENVELOPE | 9 | 691 | 0.0001357 | 0.005285 |
16 | OUTER MEMBRANE | 5 | 190 | 0.0002059 | 0.007517 |
Num | Pathway | Pathview | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|---|
1 | hsa04210_Apoptosis | 57 | 89 | 4.715e-145 | 8.487e-143 | |
2 | hsa04722_Neurotrophin_signaling_pathway | 18 | 127 | 2.033e-26 | 1.402e-24 | |
3 | hsa04380_Osteoclast_differentiation | 18 | 128 | 2.362e-26 | 1.402e-24 | |
4 | hsa04620_Toll.like_receptor_signaling_pathway | 17 | 102 | 3.116e-26 | 1.402e-24 | |
5 | hsa04650_Natural_killer_cell_mediated_cytotoxicity | 18 | 136 | 7.486e-26 | 2.653e-24 | |
6 | hsa04660_T_cell_receptor_signaling_pathway | 17 | 108 | 8.844e-26 | 2.653e-24 | |
7 | hsa04662_B_cell_receptor_signaling_pathway | 15 | 75 | 1.792e-24 | 4.608e-23 | |
8 | hsa04010_MAPK_signaling_pathway | 20 | 268 | 1.325e-23 | 2.982e-22 | |
9 | hsa04910_Insulin_signaling_pathway | 15 | 138 | 3.022e-20 | 6.044e-19 | |
10 | hsa04370_VEGF_signaling_pathway | 12 | 76 | 2.253e-18 | 4.056e-17 | |
11 | hsa04014_Ras_signaling_pathway | 16 | 236 | 3.192e-18 | 5.224e-17 | |
12 | hsa04062_Chemokine_signaling_pathway | 15 | 189 | 3.803e-18 | 5.704e-17 | |
13 | hsa04914_Progesterone.mediated_oocyte_maturation | 12 | 87 | 1.259e-17 | 1.743e-16 | |
14 | hsa04151_PI3K_AKT_signaling_pathway | 17 | 351 | 7.134e-17 | 9.172e-16 | |
15 | hsa04973_Carbohydrate_digestion_and_absorption | 9 | 44 | 4.198e-15 | 5.038e-14 | |
16 | hsa04510_Focal_adhesion | 13 | 200 | 1.124e-14 | 1.265e-13 | |
17 | hsa04664_Fc_epsilon_RI_signaling_pathway | 10 | 79 | 1.906e-14 | 2.018e-13 | |
18 | hsa04150_mTOR_signaling_pathway | 9 | 52 | 2.141e-14 | 2.141e-13 | |
19 | hsa04115_p53_signaling_pathway | 9 | 69 | 3.179e-13 | 3.012e-12 | |
20 | hsa04630_Jak.STAT_signaling_pathway | 11 | 155 | 5.747e-13 | 5.173e-12 | |
21 | hsa04012_ErbB_signaling_pathway | 9 | 87 | 2.767e-12 | 2.372e-11 | |
22 | hsa04666_Fc_gamma_R.mediated_phagocytosis | 9 | 95 | 6.23e-12 | 5.097e-11 | |
23 | hsa04920_Adipocytokine_signaling_pathway | 8 | 68 | 1.69e-11 | 1.323e-10 | |
24 | hsa04960_Aldosterone.regulated_sodium_reabsorption | 7 | 42 | 2.604e-11 | 1.953e-10 | |
25 | hsa04621_NOD.like_receptor_signaling_pathway | 7 | 59 | 3.172e-10 | 2.284e-09 | |
26 | hsa04070_Phosphatidylinositol_signaling_system | 7 | 78 | 2.356e-09 | 1.631e-08 | |
27 | hsa04670_Leukocyte_transendothelial_migration | 7 | 117 | 4.061e-08 | 2.707e-07 | |
28 | hsa04720_Long.term_potentiation | 6 | 70 | 4.657e-08 | 2.994e-07 | |
29 | hsa04622_RIG.I.like_receptor_signaling_pathway | 6 | 71 | 5.075e-08 | 3.15e-07 | |
30 | hsa04310_Wnt_signaling_pathway | 7 | 151 | 2.344e-07 | 1.406e-06 | |
31 | hsa04114_Oocyte_meiosis | 6 | 114 | 8.602e-07 | 4.995e-06 | |
32 | hsa04810_Regulation_of_actin_cytoskeleton | 7 | 214 | 2.445e-06 | 1.375e-05 | |
33 | hsa04020_Calcium_signaling_pathway | 6 | 177 | 1.102e-05 | 6.009e-05 | |
34 | hsa04962_Vasopressin.regulated_water_reabsorption | 3 | 44 | 0.0002675 | 0.001416 | |
35 | hsa04742_Taste_transduction | 3 | 52 | 0.0004393 | 0.002259 | |
36 | hsa04340_Hedgehog_signaling_pathway | 3 | 56 | 0.0005466 | 0.002659 | |
37 | hsa04623_Cytosolic_DNA.sensing_pathway | 3 | 56 | 0.0005466 | 0.002659 | |
38 | hsa00562_Inositol_phosphate_metabolism | 3 | 57 | 0.0005758 | 0.002727 | |
39 | hsa04976_Bile_secretion | 3 | 71 | 0.001093 | 0.005046 | |
40 | hsa04971_Gastric_acid_secretion | 3 | 74 | 0.001233 | 0.005547 | |
41 | hsa04141_Protein_processing_in_endoplasmic_reticulum | 4 | 168 | 0.001342 | 0.005891 | |
42 | hsa04970_Salivary_secretion | 3 | 89 | 0.002095 | 0.00898 | |
43 | hsa04540_Gap_junction | 3 | 90 | 0.002163 | 0.009055 | |
44 | hsa04912_GnRH_signaling_pathway | 3 | 101 | 0.003001 | 0.01201 | |
45 | hsa04916_Melanogenesis | 3 | 101 | 0.003001 | 0.01201 | |
46 | hsa04270_Vascular_smooth_muscle_contraction | 3 | 116 | 0.00443 | 0.01733 | |
47 | hsa04360_Axon_guidance | 3 | 130 | 0.00608 | 0.02328 | |
48 | hsa04640_Hematopoietic_cell_lineage | 2 | 88 | 0.02612 | 0.09796 | |
49 | hsa04110_Cell_cycle | 2 | 128 | 0.05162 | 0.1896 | |
50 | hsa04530_Tight_junction | 2 | 133 | 0.05525 | 0.1989 | |
51 | hsa04120_Ubiquitin_mediated_proteolysis | 2 | 139 | 0.05973 | 0.2108 | |
52 | hsa04740_Olfactory_transduction | 3 | 388 | 0.0987 | 0.3417 |
Num | lncRNA | miRNAs | miRNAs count | Gene | Sponge regulatory network | lncRNA log2FC | lncRNA pvalue | Gene log2FC | Gene pvalue | lncRNA-gene Pearson correlation |
---|---|---|---|---|---|---|---|---|---|---|
1 | HCG11 |
hsa-miR-106b-5p;hsa-miR-107;hsa-miR-15a-5p;hsa-miR-17-3p;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-33a-3p;hsa-miR-362-3p;hsa-miR-502-3p;hsa-miR-93-5p | 10 | AKT3 | Sponge network | -0.781 | 0 | -0.659 | 0.00047 | 0.574 |
2 | DHRS4-AS1 | hsa-miR-106b-5p;hsa-miR-1301-3p;hsa-miR-132-3p;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-582-5p;hsa-miR-589-3p | 10 | PIK3R1 | Sponge network | -0.646 | 0.01829 | -0.892 | 0 | 0.557 |
3 | LINC00261 | hsa-miR-106b-5p;hsa-miR-1301-3p;hsa-miR-132-3p;hsa-miR-188-5p;hsa-miR-21-5p;hsa-miR-212-3p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-324-3p;hsa-miR-330-3p;hsa-miR-629-3p | 11 | PIK3R1 | Sponge network | -1.194 | 0 | -0.892 | 0 | 0.513 |
4 | RP11-12A2.3 | hsa-miR-103a-3p;hsa-miR-106b-5p;hsa-miR-1301-3p;hsa-miR-132-3p;hsa-miR-17-5p;hsa-miR-188-5p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-93-5p | 12 | PIK3R1 | Sponge network | -4.779 | 0 | -0.892 | 0 | 0.489 |
5 | LINC01018 | hsa-miR-103a-3p;hsa-miR-106b-5p;hsa-miR-1301-3p;hsa-miR-132-3p;hsa-miR-17-5p;hsa-miR-200c-3p;hsa-miR-21-5p;hsa-miR-212-3p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-324-3p;hsa-miR-338-5p;hsa-miR-589-3p;hsa-miR-629-3p;hsa-miR-93-5p | 15 | PIK3R1 | Sponge network | -3.231 | 0 | -0.892 | 0 | 0.472 |
6 | LDLRAD4-AS1 | hsa-miR-103a-3p;hsa-miR-106b-5p;hsa-miR-1301-3p;hsa-miR-132-3p;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-93-5p | 10 | PIK3R1 | Sponge network | -3.366 | 0 | -0.892 | 0 | 0.45 |
7 | RP11-119D9.1 | hsa-miR-106b-5p;hsa-miR-1301-3p;hsa-miR-132-3p;hsa-miR-188-5p;hsa-miR-200c-3p;hsa-miR-21-5p;hsa-miR-212-3p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-629-3p;hsa-miR-93-5p | 11 | PIK3R1 | Sponge network | -2.765 | 0 | -0.892 | 0 | 0.418 |
8 | RP11-290F5.1 | hsa-miR-103a-3p;hsa-miR-106b-5p;hsa-miR-1301-3p;hsa-miR-132-3p;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-212-3p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-324-3p | 11 | PIK3R1 | Sponge network | -1.679 | 5.0E-5 | -0.892 | 0 | 0.402 |
9 | LINC00238 | hsa-miR-106b-5p;hsa-miR-1301-3p;hsa-miR-132-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-188-5p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-212-3p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-629-3p | 12 | PIK3R1 | Sponge network | -4.997 | 0 | -0.892 | 0 | 0.369 |
10 | AC004862.6 | hsa-miR-106b-5p;hsa-miR-1301-3p;hsa-miR-132-3p;hsa-miR-17-5p;hsa-miR-188-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-212-3p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-629-3p;hsa-miR-93-5p | 12 | PIK3R1 | Sponge network | -2.202 | 0.00081 | -0.892 | 0 | 0.357 |
11 | RP11-407B7.1 | hsa-miR-1301-3p;hsa-miR-132-3p;hsa-miR-21-5p;hsa-miR-212-3p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-324-3p;hsa-miR-338-5p;hsa-miR-629-3p;hsa-miR-93-5p | 10 | PIK3R1 | Sponge network | -0.818 | 0.00584 | -0.892 | 0 | 0.324 |
12 | RP11-166D19.1 | hsa-miR-106b-5p;hsa-miR-1301-3p;hsa-miR-17-5p;hsa-miR-185-5p;hsa-miR-188-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-324-3p;hsa-miR-589-3p;hsa-miR-590-5p;hsa-miR-629-3p | 11 | PIK3R1 | Sponge network | -0.244 | 0.28835 | -0.892 | 0 | 0.32 |
13 | RP11-7F17.3 | hsa-miR-103a-3p;hsa-miR-106b-5p;hsa-miR-1301-3p;hsa-miR-132-3p;hsa-miR-17-5p;hsa-miR-188-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-324-3p | 11 | PIK3R1 | Sponge network | -0.873 | 0.00204 | -0.892 | 0 | 0.271 |
14 | SMIM2-AS1 | hsa-miR-103a-3p;hsa-miR-106b-5p;hsa-miR-1301-3p;hsa-miR-132-3p;hsa-miR-17-5p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-212-3p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-629-3p | 12 | PIK3R1 | Sponge network | -0.66 | 0.00587 | -0.892 | 0 | 0.27 |