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-7b-5p | AIFM1 | 0.06 | 0.7814 | -0.33 | 0.06746 | miRNATAP | -0.19 | 0.00202 | NA | |
2 | hsa-let-7i-5p | AIFM1 | 0.8 | 3.0E-5 | -0.33 | 0.06746 | miRNATAP | -0.23 | 0.00049 | NA | |
3 | hsa-miR-125b-5p | AIFM1 | -0.51 | 0.13327 | -0.33 | 0.06746 | miRNATAP | -0.22 | 0 | NA | |
4 | hsa-miR-199a-5p | AIFM1 | 0.37 | 0.23266 | -0.33 | 0.06746 | miRanda | -0.21 | 0 | NA | |
5 | hsa-miR-21-5p | AKT2 | 1.75 | 0 | -0.01 | 0.9227 | miRNAWalker2 validate | -0.15 | 0.00352 | NA | |
6 | hsa-miR-29b-3p | AKT2 | -0.23 | 0.36746 | -0.01 | 0.9227 | MirTarget | -0.14 | 0.00022 | 26512921; 26564501; 24076586 | MicroRNA 29B mir 29b regulates the Warburg effect in ovarian cancer by targeting AKT2 and AKT3;The expression of miR-29b was significantly upregualted by cisplatin treatmentwhile its target gene AKT2 was downregulated;Furthermore a feed-back loop comprising of c-Myc miR-29 family and Akt2 were found in myeloid leukemogenesis |
7 | hsa-miR-106b-5p | AKT3 | 1.71 | 0 | -0.75 | 0.06936 | miRNATAP | -0.37 | 7.0E-5 | NA | |
8 | hsa-miR-107 | AKT3 | 0.9 | 5.0E-5 | -0.75 | 0.06936 | PITA; miRanda | -0.6 | 0 | NA | |
9 | hsa-miR-15b-5p | AKT3 | 1.62 | 0 | -0.75 | 0.06936 | miRNATAP | -0.36 | 0.00041 | NA | |
10 | hsa-miR-16-5p | AKT3 | 1.01 | 1.0E-5 | -0.75 | 0.06936 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.47 | 0.00031 | NA | |
11 | hsa-miR-17-3p | AKT3 | 1.31 | 0 | -0.75 | 0.06936 | miRNATAP | -0.52 | 0 | NA | |
12 | hsa-miR-17-5p | AKT3 | 1.66 | 0 | -0.75 | 0.06936 | TargetScan; miRNATAP | -0.28 | 0.0027 | NA | |
13 | hsa-miR-29a-3p | AKT3 | -0.11 | 0.61501 | -0.75 | 0.06936 | miRNATAP | -0.41 | 0.00212 | NA | |
14 | hsa-miR-29b-3p | AKT3 | -0.23 | 0.36746 | -0.75 | 0.06936 | miRNATAP | -0.34 | 0.00361 | 26512921 | MicroRNA 29B mir 29b regulates the Warburg effect in ovarian cancer by targeting AKT2 and AKT3 |
15 | hsa-miR-32-3p | AKT3 | 0.58 | 0.11837 | -0.75 | 0.06936 | mirMAP | -0.32 | 0.00023 | NA | |
16 | hsa-miR-320b | AKT3 | 1.11 | 0.0005 | -0.75 | 0.06936 | PITA; miRanda; miRNATAP | -0.26 | 0.0039 | NA | |
17 | hsa-miR-335-3p | AKT3 | 2.52 | 0 | -0.75 | 0.06936 | mirMAP | -0.22 | 0.00074 | NA | |
18 | hsa-miR-33a-3p | AKT3 | 0.35 | 0.32171 | -0.75 | 0.06936 | mirMAP | -0.38 | 2.0E-5 | NA | |
19 | hsa-miR-362-3p | AKT3 | -0.03 | 0.91378 | -0.75 | 0.06936 | miRanda | -0.38 | 4.0E-5 | NA | |
20 | hsa-miR-362-5p | AKT3 | -0.35 | 0.35491 | -0.75 | 0.06936 | PITA; TargetScan; miRNATAP | -0.23 | 0.00253 | NA | |
21 | hsa-miR-501-3p | AKT3 | 0.73 | 0.02704 | -0.75 | 0.06936 | miRNATAP | -0.39 | 1.0E-5 | NA | |
22 | hsa-miR-502-3p | AKT3 | -0.16 | 0.55747 | -0.75 | 0.06936 | miRNATAP | -0.5 | 0 | NA | |
23 | hsa-miR-505-3p | AKT3 | 0.83 | 0.00112 | -0.75 | 0.06936 | mirMAP | -0.35 | 0.00235 | 22051041 | We also find that Akt3 correlate inversely with miR-505 modulates drug sensitivity in MCF7-ADR |
24 | hsa-miR-548v | AKT3 | -0.16 | 0.70867 | -0.75 | 0.06936 | miRNATAP | -0.27 | 0.00031 | NA | |
25 | hsa-miR-577 | AKT3 | 0.91 | 0.22561 | -0.75 | 0.06936 | mirMAP | -0.23 | 0 | NA | |
26 | hsa-miR-616-5p | AKT3 | 0.83 | 0.03478 | -0.75 | 0.06936 | mirMAP | -0.27 | 0.00041 | NA | |
27 | hsa-miR-23a-3p | APAF1 | 1.11 | 0 | 0.3 | 0.22769 | miRNATAP | -0.49 | 0 | 24992592; 24249161 | Luciferase assay was performed to verify a putative target site of miR-23a in the 3'-UTR of apoptosis protease activating factor 1 APAF1 mRNA; The expression levels of miR-23a and APAF1 in CRC cell lines SW480 and SW620 and clinical samples were assessed using reverse transcription-quantitative real-time PCR RT-qPCR and Western blot; Moreover miR-23a up-regulation was coupled with APAF1 down-regulation in CRC tissue samples;We found that the expression of miR-23a was increased and the level of apoptosis-activating factor-1 APAF-1 was decreased in 5-FU-treated colon cancer cells compared to untreated cells; APAF-1 as a target gene of miR-23a was identified and miR-23a antisense-induced increase in the activation of caspase-9 was observed |
28 | hsa-miR-23b-3p | APAF1 | -0.29 | 0.18665 | 0.3 | 0.22769 | miRNATAP | -0.54 | 0 | NA | |
29 | hsa-miR-27a-3p | APAF1 | 1.3 | 0 | 0.3 | 0.22769 | miRNATAP | -0.39 | 0 | NA | |
30 | hsa-miR-27b-3p | APAF1 | 0.08 | 0.72527 | 0.3 | 0.22769 | miRNATAP | -0.48 | 0 | NA | |
31 | hsa-miR-708-3p | APAF1 | 0.62 | 0.27536 | 0.3 | 0.22769 | mirMAP | -0.24 | 0 | NA | |
32 | hsa-miR-944 | APAF1 | 3.33 | 0.01778 | 0.3 | 0.22769 | miRNATAP | -0.13 | 0 | NA | |
33 | hsa-miR-125a-3p | ATM | 1.2 | 0.00164 | -0.39 | 0.08341 | miRanda | -0.13 | 0.00188 | NA | |
34 | hsa-miR-203a-3p | ATM | 1.45 | 0.03941 | -0.39 | 0.08341 | MirTarget | -0.14 | 0 | 24145123; 27542403 | miR 203 induces oxaliplatin resistance in colorectal cancer cells by negatively regulating ATM kinase; In silico analysis identified ataxia telangiectasia mutated ATM a primary mediator of the DNA damage response as a potential target of miR-203; Using TCGA database we identified a significant reverse correlation of miR-203 and ATM expression in CRC tissues; We validated ATM as a bona fide target of miR-203 in CRC cells; Mutation of the putative miR-203 binding site in the 3' untranslated region 3'UTR of the ATM mRNA abolished the inhibitory effect of miR-203 on ATM;MiR 203 inhibits tumor invasion and metastasis in gastric cancer by ATM; Our results showed that miR-203 was significantly downregulated in gastric cancer tissues and cells while ataxia telangiectasia mutated kinase ATM was upregulated in gastric cancer tissues and cells and was directly regulated by miR-203; ATM knockdown phenocopied the effect of miR-203 overexpression |
35 | hsa-miR-590-5p | ATM | 1.04 | 0.00027 | -0.39 | 0.08341 | mirMAP | -0.17 | 0.00247 | NA | |
36 | hsa-miR-30a-5p | BAX | -1.72 | 0 | 1.23 | 0 | miRNAWalker2 validate | -0.15 | 0.00018 | NA | |
37 | hsa-miR-365a-3p | BAX | -0.89 | 0.00255 | 1.23 | 0 | miRNAWalker2 validate | -0.19 | 6.0E-5 | 24216611 | MiR 365 induces gemcitabine resistance in pancreatic cancer cells by targeting the adaptor protein SHC1 and pro apoptotic regulator BAX |
38 | hsa-miR-15b-3p | BCL2 | 1.76 | 0 | -1.09 | 0.00317 | mirMAP | -0.24 | 0.00334 | 25594541; 26915294; 26884837; 18449891 | MicroRNAs miRNAs encoded by the miR-15 cluster are known to induce G1 arrest and apoptosis by targeting G1 checkpoints and the anti-apoptotic B cell lymphoma 2 BCL-2 gene;As a result transcript levels of the tumor-suppressive miR-15 and let-7 families increased which targeted and decreased the expression of the crucial prosurvival genes BCL-2 and BCL-XL respectively;MiR 15b mediates liver cancer cells proliferation through targeting BCL 2; MiR-15b overexpression downregulated BCL2 mRNA and protein expression obviously P < 0.05; On the contrary miR-15b inhibitor transfection markedly reduced miR-15b expression in liver cancer cells P < 0.05 promoted tumor cell proliferation and increased BCL2 mRNA and protein expression; MiR-15b can inhibit HepG2 cell proliferation and down-regulate BCL2 mRNA and protein expression;miR 15b and miR 16 modulate multidrug resistance by targeting BCL2 in human gastric cancer cells; The downregulation of miR-15b and miR-16 in SGC7901/VCR cells was concurrent with the upregulation of Bcl-2 protein; Taken together our findings suggest that miR-15b and miR-16 could play a role in the development of MDR in gastric cancer cells at least in part by modulation of apoptosis via targeting BCL2 |
39 | hsa-miR-16-2-3p | BCL2 | 1.8 | 0 | -1.09 | 0.00317 | mirMAP | -0.26 | 0.0023 | NA | |
40 | hsa-miR-200a-5p | BCL2 | 1.5 | 0.00264 | -1.09 | 0.00317 | mirMAP | -0.21 | 5.0E-5 | NA | |
41 | hsa-miR-200b-3p | BCL2 | 0.97 | 0.0595 | -1.09 | 0.00317 | miRNAWalker2 validate; miRTarBase; TargetScan; mirMAP | -0.18 | 0.00034 | NA | |
42 | hsa-miR-200b-5p | BCL2 | 0.97 | 0.05305 | -1.09 | 0.00317 | mirMAP | -0.21 | 0.00019 | NA | |
43 | hsa-miR-200c-3p | BCL2 | 1.28 | 0.0037 | -1.09 | 0.00317 | miRNAWalker2 validate; miRTarBase; mirMAP | -0.23 | 0.00013 | NA | |
44 | hsa-miR-20a-3p | BCL2 | 1.14 | 0.00045 | -1.09 | 0.00317 | mirMAP | -0.22 | 0.00669 | NA | |
45 | hsa-miR-21-5p | BCL2 | 1.75 | 0 | -1.09 | 0.00317 | miRNAWalker2 validate; miRTarBase | -0.57 | 2.0E-5 | 21468550; 25994220; 25381586; 26555418; 23359184; 22964582; 21376256 | BCL-2 up-regulation could be achieved by miR-21 overexpression which prevented T24 cells from apoptosis induced by doxorubicin; Furthermore the miR-21 induced BCL-2 up-regulation could be cancelled by the PI3K inhibitor LY294002;Meanwhile miR-21 loss reduced STAT3 and Bcl-2 activation causing an increase in the apoptosis of tumour cells in CAC mice;Changes in the sensitivity of osteosarcoma cells to CDDP were examined after transfection with miR-21 mimics or anti-miR-21 or bcl-2 siRNA in combination with CDDP;The expression of Bax Bcl-2 and miR-21 in parental and paclitaxel-resistant cells was detected by RT-PCR and Western blotting;Resveratrol induces apoptosis of pancreatic cancers cells by inhibiting miR 21 regulation of BCL 2 expression; We also used Western blot to measure BCL-2 protein levels after down-regulation of miR-21 expression; Besides down-regulation of miR-21 expression can inhibit BCL-2 expression in PANC-1 CFPAC-1 and MIA Paca-2 cells; Over-expression of miR-21 expression can reverse down-regulation of BCL-2 expression and apoptosis induced by resveratrol; In this study we demonstrated that the effect of resveratrol on apoptosis is due to inhibiting miR-21 regulation of BCL-2 expression;Tumors harvested from these lungs have elevated levels of oncogenic miRNAs miR-21 and miR-155; are deficient for p53-regulated miRNAs; and have heightened expression of miR-34 target genes such as Met and Bcl-2;Bcl 2 upregulation induced by miR 21 via a direct interaction is associated with apoptosis and chemoresistance in MIA PaCa 2 pancreatic cancer cells; However the roles and mechanisms of miRNA miR-21 in regulation of Bcl-2 in pancreatic cancer remain to be elucidated; Then luciferase activity was observed after miR-21 mimics and pRL-TK plasmids containing wild-type and mutant 3'UTRs of Bcl-2 mRNA were co-transfected; Cells transfected with miR-21 inhibitor revealed an opposite trend. There was a significant increase in luciferase activity in the cells transfected with the wild-type pRL-TK plasmid in contrast to those transfected with the mutant one indicating that miR-21 promotes Bcl-2 expression by binding directly to the 3'UTR of Bcl-2 mRNA; Upregulation of Bcl-2 directly induced by miR-21 is associated with apoptosis chemoresistance and proliferation of MIA PaCa-2 pancreatic cancer cells |
46 | hsa-miR-29a-5p | BCL2 | 0.59 | 0.02301 | -1.09 | 0.00317 | mirMAP | -0.28 | 0.00622 | 20041405 | Subsequent investigation characterized two antiapoptotic molecules Bcl-2 and Mcl-1 as direct targets of miR-29; Furthermore silencing of Bcl-2 and Mcl-1 phenocopied the proapoptotic effect of miR-29 whereas overexpression of these proteins attenuated the effect of miR-29 |
47 | hsa-miR-335-3p | BCL2 | 2.52 | 0 | -1.09 | 0.00317 | mirMAP | -0.17 | 0.00598 | NA | |
48 | hsa-miR-429 | BCL2 | 1.4 | 0.009 | -1.09 | 0.00317 | miRNAWalker2 validate; miRTarBase; PITA; mirMAP | -0.2 | 3.0E-5 | 23999873; 26513239; 26511969 | MiR 429 up regulation induces apoptosis and suppresses invasion by targeting Bcl 2 and SP 1 in esophageal carcinoma; Subsequent Western blotting and luciferase reporter assays showed that miR-429 can bind to putative binding sites within the Bcl-2 and SP1 mRNA 3' untranslated regions UTRs to reduce their expression; Up-regulation of miR-429 inhibits invasion and promotes apoptosis in EC cells by targeting Bcl-2 and SP1; Our findings suggest that Bcl-2 and SP1 may serve as major targets of miR-429;MiR 429 Induces Gastric Carcinoma Cell Apoptosis Through Bcl 2; Here we studied the levels of miR-429 and anti-apoptotic protein Bcl-2 in GC specimens; We performed bioinformatics analyses and used luciferase-reporter assay to analyze the relationship between miR-429 and Bcl-2 in GC cells; MiR-429 levels were significantly decreased and Bcl-2 levels were significantly increased in GC specimens compared to the paired adjacent non-tumor gastric tissue; Moreover the levels of miR-429 and Bcl-2 inversely correlated in GC specimens; Bioinformatics analyses showed that miR-429 targeted the 3'-UTR of Bcl-2 mRNA to inhibit its translation which was confirmed by luciferase-reporter assay;MiR 429 induces apoptosis of glioblastoma cell through Bcl 2; Here we analyzed the levels of miR-429 and anti-apoptotic protein Bcl-2 in GBM specimens; We combined bioinformatics analyses and luciferase reporter assay to determine the relationship between miR-429 and Bcl-2 in GBM cells; We found that miR-429 levels were significantly decreased and Bcl-2 levels were significantly increased in GBM specimens compared to the paired adjacent non-tumor brain tissue; Moreover the levels of miR-429 and Bcl-2 inversely correlated; MiR-429 targeted the 3'-UTR of Bcl-2 mRNA to inhibit its translation |
49 | hsa-miR-455-5p | BCL2 | 1.2 | 7.0E-5 | -1.09 | 0.00317 | mirMAP | -0.35 | 4.0E-5 | NA | |
50 | hsa-miR-577 | BCL2 | 0.91 | 0.22561 | -1.09 | 0.00317 | PITA | -0.1 | 0.00537 | NA | |
51 | hsa-miR-7-5p | BCL2 | 1.64 | 0.01244 | -1.09 | 0.00317 | miRNAWalker2 validate; miRTarBase; mirMAP | -0.14 | 0.00068 | 26464649; 25862909; 21750649 | Western blotting was used to evaluate the effect of miR-7 on Bcl2 in A549 and H460 cells; Moreover subsequent experiments showed that BCL-2 was downregulated by miR-7 at both transcriptional and translational levels; This study further extends the biological role of miR-7 in NSCLC A549 and H460 cells and identifies BCL-2 as a novel target possibly involved in miR-7-mediated growth suppression and apoptosis induction of NSCLC cells;miR-7 overexpression correlated with diminished BCL2 expression but there was no relationship between miR-7 and EGFR expression neither in tumour samples nor in the cell lines; Of the two postulated miR-7 target genes we examined BCL2 but not EGFR seems to be a possible miR-7 target in OC;Bioinformatics predictions revealed a potential binding site of miR-7 on 3'UTR of BCL-2 and it was further confirmed by luciferase assay; Moreover subsequent experiments showed that BCL-2 was downregulated by miR-7 at both transcriptional and translational levels; These results suggest that miR-7 regulates the expression of BCL-2 through direct 3'UTR interactions |
52 | hsa-let-7b-5p | BCL2L1 | 0.06 | 0.7814 | 0.21 | 0.39578 | miRNATAP | -0.31 | 0.00027 | 26915294; 20347499 | As a result transcript levels of the tumor-suppressive miR-15 and let-7 families increased which targeted and decreased the expression of the crucial prosurvival genes BCL-2 and BCL-XL respectively;The let 7 family of microRNAs inhibits Bcl xL expression and potentiates sorafenib induced apoptosis in human hepatocellular carcinoma; The effect of let-7 on Bcl-xL expression was examined by Western blot and a reporter assay; Microarray analysis followed by in silico target prediction identified let-7 microRNAs as being downregulated in Huh7 hepatoma cells in comparison with primary human hepatocytes as well as possessing a putative target site in the bcl-xl mRNA |
53 | hsa-let-7c-5p | BCL2L1 | -0.5 | 0.20685 | 0.21 | 0.39578 | miRNAWalker2 validate; miRTarBase | -0.2 | 1.0E-5 | 20347499 | Over-expression of let-7c or let-7g led to a clear decrease of Bcl-xL expression in Huh7 and HepG2 cell lines; Reporter assays revealed direct post-transcriptional regulation involving let-7c or let-7g and the 3'-untranslated region of bcl-xl mRNA |
54 | hsa-miR-149-5p | BCL2L1 | 0.71 | 0.29685 | 0.21 | 0.39578 | mirMAP | -0.17 | 0 | NA | |
55 | hsa-miR-214-3p | BCL2L1 | 1.01 | 0.00625 | 0.21 | 0.39578 | mirMAP | -0.13 | 0.00824 | NA | |
56 | hsa-miR-23b-3p | BCL2L1 | -0.29 | 0.18665 | 0.21 | 0.39578 | miRNAWalker2 validate | -0.39 | 0 | NA | |
57 | hsa-miR-491-5p | CAPN1 | -0.69 | 0.03136 | 0.47 | 0.04786 | miRanda | -0.18 | 0.0005 | NA | |
58 | hsa-miR-107 | CAPN2 | 0.9 | 5.0E-5 | -0.59 | 0.00617 | miRanda | -0.2 | 0.00395 | NA | |
59 | hsa-miR-320a | CAPN2 | 0.59 | 0.0119 | -0.59 | 0.00617 | miRanda | -0.26 | 6.0E-5 | NA | |
60 | hsa-miR-320b | CAPN2 | 1.11 | 0.0005 | -0.59 | 0.00617 | miRanda | -0.16 | 0.00048 | NA | |
61 | hsa-miR-421 | CAPN2 | 1.81 | 0 | -0.59 | 0.00617 | miRanda | -0.18 | 2.0E-5 | NA | |
62 | hsa-miR-125b-5p | CASP10 | -0.51 | 0.13327 | 0.32 | 0.44988 | mirMAP | -0.45 | 0 | NA | |
63 | hsa-miR-129-5p | CASP10 | -2.57 | 0 | 0.32 | 0.44988 | mirMAP | -0.15 | 0.0057 | NA | |
64 | hsa-miR-145-3p | CASP10 | -1.65 | 2.0E-5 | 0.32 | 0.44988 | mirMAP | -0.22 | 0.00525 | NA | |
65 | hsa-miR-145-5p | CASP10 | -1.75 | 2.0E-5 | 0.32 | 0.44988 | mirMAP | -0.21 | 0.00404 | NA | |
66 | hsa-miR-34c-3p | CASP10 | 2.25 | 9.0E-5 | 0.32 | 0.44988 | mirMAP | -0.32 | 0 | NA | |
67 | hsa-miR-452-5p | CASP10 | 2.09 | 0.00026 | 0.32 | 0.44988 | mirMAP | -0.28 | 0 | NA | |
68 | hsa-miR-744-3p | CASP10 | 1.4 | 0.00097 | 0.32 | 0.44988 | mirMAP | -0.35 | 0 | NA | |
69 | hsa-miR-23b-3p | CASP7 | -0.29 | 0.18665 | 0.22 | 0.30127 | MirTarget | -0.19 | 0.00671 | NA | |
70 | hsa-miR-9-3p | CASP7 | 0.33 | 0.54111 | 0.22 | 0.30127 | MirTarget | -0.1 | 0.00051 | NA | |
71 | hsa-miR-129-5p | CASP8 | -2.57 | 0 | 1.08 | 0 | miRanda | -0.14 | 0 | NA | |
72 | hsa-miR-143-3p | CASP8 | -0.66 | 0.04832 | 1.08 | 0 | MirTarget | -0.19 | 3.0E-5 | NA | |
73 | hsa-miR-193b-3p | CASP9 | 0.28 | 0.45126 | -0.31 | 0.11004 | miRNAWalker2 validate | -0.17 | 0 | NA | |
74 | hsa-miR-130a-3p | CFLAR | 0.15 | 0.63374 | 0.07 | 0.73819 | mirMAP | -0.14 | 0.00421 | NA | |
75 | hsa-miR-130b-3p | CFLAR | 1.33 | 5.0E-5 | 0.07 | 0.73819 | mirMAP | -0.21 | 0 | NA | |
76 | hsa-miR-15b-5p | CFLAR | 1.62 | 0 | 0.07 | 0.73819 | mirMAP | -0.22 | 4.0E-5 | NA | |
77 | hsa-miR-301a-3p | CFLAR | 1.45 | 1.0E-5 | 0.07 | 0.73819 | mirMAP | -0.2 | 1.0E-5 | NA | |
78 | hsa-miR-9-5p | CFLAR | -0.2 | 0.76147 | 0.07 | 0.73819 | mirMAP | -0.13 | 0 | NA | |
79 | hsa-miR-152-3p | CHUK | 0.44 | 0.1617 | -0.11 | 0.43611 | MirTarget | -0.17 | 0 | NA | |
80 | hsa-miR-195-5p | CHUK | -0.91 | 0.00151 | -0.11 | 0.43611 | miRNAWalker2 validate; MirTarget | -0.13 | 0.00012 | NA | |
81 | hsa-miR-23a-3p | CHUK | 1.11 | 0 | -0.11 | 0.43611 | MirTarget | -0.17 | 0.00056 | NA | |
82 | hsa-miR-23b-3p | CHUK | -0.29 | 0.18665 | -0.11 | 0.43611 | miRNAWalker2 validate; miRTarBase; MirTarget; miRNATAP | -0.19 | 6.0E-5 | NA | |
83 | hsa-miR-342-3p | CHUK | 0.32 | 0.26915 | -0.11 | 0.43611 | miRanda | -0.19 | 0 | NA | |
84 | hsa-miR-497-5p | CHUK | -0.8 | 0.0036 | -0.11 | 0.43611 | MirTarget | -0.11 | 0.00273 | NA | |
85 | hsa-miR-15b-3p | CSF2RB | 1.76 | 0 | -0.2 | 0.59657 | mirMAP | -0.31 | 0.00012 | NA | |
86 | hsa-miR-30b-3p | CSF2RB | -0.27 | 0.40085 | -0.2 | 0.59657 | MirTarget | -0.25 | 0.00393 | NA | |
87 | hsa-miR-452-3p | CSF2RB | 2.2 | 0.00185 | -0.2 | 0.59657 | mirMAP | -0.13 | 0.00156 | NA | |
88 | hsa-miR-342-3p | CYCS | 0.32 | 0.26915 | 0.2 | 0.35913 | mirMAP | -0.21 | 8.0E-5 | NA | |
89 | hsa-miR-342-3p | DFFA | 0.32 | 0.26915 | 0.01 | 0.93424 | mirMAP | -0.1 | 0.0044 | NA | |
90 | hsa-miR-199a-5p | DFFB | 0.37 | 0.23266 | 0.21 | 0.40784 | miRanda | -0.2 | 0.00056 | NA | |
91 | hsa-miR-199b-5p | DFFB | 0.12 | 0.67816 | 0.21 | 0.40784 | miRanda | -0.16 | 0.0085 | NA | |
92 | hsa-miR-365a-3p | DFFB | -0.89 | 0.00255 | 0.21 | 0.40784 | MirTarget | -0.41 | 0 | NA | |
93 | hsa-miR-130b-3p | ENDOD1 | 1.33 | 5.0E-5 | 0.17 | 0.52052 | MirTarget | -0.22 | 0.00011 | NA | |
94 | hsa-miR-16-1-3p | ENDOD1 | 1.43 | 0 | 0.17 | 0.52052 | mirMAP | -0.21 | 0.0029 | NA | |
95 | hsa-miR-181b-5p | ENDOD1 | 1.64 | 0 | 0.17 | 0.52052 | MirTarget | -0.17 | 0.00661 | NA | |
96 | hsa-miR-181c-5p | ENDOD1 | 0.34 | 0.11293 | 0.17 | 0.52052 | MirTarget | -0.27 | 0.00393 | NA | |
97 | hsa-miR-181d-5p | ENDOD1 | 0.65 | 0.01434 | 0.17 | 0.52052 | MirTarget | -0.21 | 0.00307 | NA | |
98 | hsa-miR-19a-3p | ENDOD1 | 1.27 | 0.00011 | 0.17 | 0.52052 | mirMAP | -0.27 | 0 | NA | |
99 | hsa-miR-19b-3p | ENDOD1 | 0.76 | 0.00653 | 0.17 | 0.52052 | mirMAP | -0.33 | 0 | NA | |
100 | hsa-miR-20a-3p | ENDOD1 | 1.14 | 0.00045 | 0.17 | 0.52052 | MirTarget | -0.24 | 4.0E-5 | NA | |
101 | hsa-miR-26b-3p | ENDOD1 | -0.01 | 0.96577 | 0.17 | 0.52052 | mirMAP | -0.39 | 0 | NA | |
102 | hsa-miR-301a-3p | ENDOD1 | 1.45 | 1.0E-5 | 0.17 | 0.52052 | MirTarget | -0.17 | 0.00291 | NA | |
103 | hsa-miR-326 | ENDOD1 | -0.43 | 0.26299 | 0.17 | 0.52052 | miRanda | -0.18 | 0.00037 | NA | |
104 | hsa-miR-335-3p | ENDOD1 | 2.52 | 0 | 0.17 | 0.52052 | MirTarget | -0.18 | 4.0E-5 | NA | |
105 | hsa-miR-3607-3p | ENDOD1 | 0.52 | 0.08425 | 0.17 | 0.52052 | MirTarget; miRNATAP | -0.25 | 7.0E-5 | NA | |
106 | hsa-miR-361-5p | ENDOD1 | 0.41 | 0.01813 | 0.17 | 0.52052 | MirTarget; miRanda | -0.42 | 0.00025 | NA | |
107 | hsa-miR-3613-5p | ENDOD1 | 1.12 | 0.00025 | 0.17 | 0.52052 | MirTarget | -0.25 | 4.0E-5 | NA | |
108 | hsa-miR-450b-5p | ENDOD1 | 0.46 | 0.13274 | 0.17 | 0.52052 | MirTarget; mirMAP | -0.17 | 0.00608 | NA | |
109 | hsa-miR-454-3p | ENDOD1 | 0.63 | 0.01349 | 0.17 | 0.52052 | MirTarget | -0.41 | 0 | NA | |
110 | hsa-miR-589-3p | ENDOD1 | 1.02 | 0.00578 | 0.17 | 0.52052 | mirMAP | -0.23 | 1.0E-5 | NA | |
111 | hsa-miR-589-5p | ENDOD1 | 0.7 | 0.00396 | 0.17 | 0.52052 | MirTarget | -0.32 | 5.0E-5 | NA | |
112 | hsa-miR-590-3p | ENDOD1 | 1.12 | 0.00016 | 0.17 | 0.52052 | miRanda | -0.27 | 2.0E-5 | NA | |
113 | hsa-miR-149-5p | EXOG | 0.71 | 0.29685 | -0.16 | 0.33475 | MirTarget | -0.1 | 0 | NA | |
114 | hsa-miR-24-3p | EXOG | 1.09 | 0 | -0.16 | 0.33475 | MirTarget | -0.21 | 0.00012 | NA | |
115 | hsa-miR-129-5p | FADD | -2.57 | 0 | 1.34 | 0.00032 | miRanda | -0.17 | 0.00032 | NA | |
116 | hsa-miR-7-5p | FADD | 1.64 | 0.01244 | 1.34 | 0.00032 | miRNAWalker2 validate | -0.12 | 0.00377 | NA | |
117 | hsa-miR-106a-5p | FAS | -0.17 | 0.64287 | 0.66 | 0.0207 | miRNAWalker2 validate; miRTarBase | -0.16 | 0.00429 | 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 |
118 | hsa-miR-129-5p | FAS | -2.57 | 0 | 0.66 | 0.0207 | miRanda | -0.12 | 0.0007 | NA | |
119 | hsa-miR-92b-3p | FASLG | 1.34 | 0 | 0.49 | 0.39 | miRNATAP | -0.54 | 0.00016 | NA | |
120 | hsa-miR-125a-3p | IKBKB | 1.2 | 0.00164 | 0.13 | 0.50747 | miRanda | -0.13 | 0.00065 | NA | |
121 | hsa-miR-543 | IKBKB | 0.03 | 0.92946 | 0.13 | 0.50747 | miRanda | -0.13 | 0.00308 | NA | |
122 | hsa-miR-125a-5p | IKBKG | -0.88 | 0.00021 | 0.48 | 0.00797 | miRanda | -0.24 | 1.0E-5 | NA | |
123 | hsa-miR-148a-3p | IKBKG | -1.54 | 4.0E-5 | 0.48 | 0.00797 | mirMAP | -0.12 | 0.00063 | NA | |
124 | hsa-miR-191-5p | IL1A | 0.96 | 0.00071 | 3.99 | 1.0E-5 | miRNAWalker2 validate | -0.7 | 0.00262 | NA | |
125 | hsa-miR-200a-3p | IL1A | 0.72 | 0.19391 | 3.99 | 1.0E-5 | MirTarget | -0.34 | 0.00439 | NA | |
126 | hsa-miR-30a-5p | IL1A | -1.72 | 0 | 3.99 | 1.0E-5 | MirTarget | -0.81 | 2.0E-5 | NA | |
127 | hsa-miR-30b-5p | IL1A | -0.43 | 0.05936 | 3.99 | 1.0E-5 | MirTarget | -0.95 | 0.00124 | NA | |
128 | hsa-miR-30c-5p | IL1A | -0.98 | 5.0E-5 | 3.99 | 1.0E-5 | MirTarget | -1.12 | 3.0E-5 | NA | |
129 | hsa-miR-30d-5p | IL1A | -0.55 | 0.01401 | 3.99 | 1.0E-5 | MirTarget | -1.7 | 0 | NA | |
130 | hsa-miR-30e-5p | IL1A | -0.57 | 0.01125 | 3.99 | 1.0E-5 | MirTarget | -0.83 | 0.00482 | NA | |
131 | hsa-miR-532-5p | IL1A | 0.31 | 0.25225 | 3.99 | 1.0E-5 | MirTarget | -1.08 | 1.0E-5 | NA | |
132 | hsa-miR-664a-3p | IL1A | -0.83 | 0.00014 | 3.99 | 1.0E-5 | MirTarget | -0.9 | 0.00323 | NA | |
133 | hsa-miR-30a-3p | IL1B | -1.73 | 0 | 1.27 | 0.03288 | MirTarget | -0.44 | 0.00032 | NA | |
134 | hsa-miR-126-5p | IL1R1 | 0.42 | 0.07532 | -0.91 | 0.00472 | mirMAP | -0.26 | 0.0085 | NA | |
135 | hsa-miR-130b-5p | IL1R1 | 0.7 | 0.05101 | -0.91 | 0.00472 | mirMAP | -0.37 | 0 | NA | |
136 | hsa-miR-17-3p | IL1R1 | 1.31 | 0 | -0.91 | 0.00472 | mirMAP | -0.69 | 0 | NA | |
137 | hsa-miR-186-5p | IL1R1 | 0.15 | 0.43471 | -0.91 | 0.00472 | mirMAP | -0.44 | 0.00029 | NA | |
138 | hsa-miR-197-3p | IL1R1 | 0.89 | 0.0002 | -0.91 | 0.00472 | miRNAWalker2 validate | -0.5 | 0 | NA | |
139 | hsa-miR-24-3p | IL1R1 | 1.09 | 0 | -0.91 | 0.00472 | miRNATAP | -0.42 | 4.0E-5 | NA | |
140 | hsa-miR-26b-5p | IL1R1 | -0.3 | 0.16008 | -0.91 | 0.00472 | mirMAP | -0.46 | 2.0E-5 | NA | |
141 | hsa-miR-30d-3p | IL1R1 | -0.55 | 0.04337 | -0.91 | 0.00472 | mirMAP | -0.23 | 0.0072 | NA | |
142 | hsa-miR-335-3p | IL1R1 | 2.52 | 0 | -0.91 | 0.00472 | mirMAP | -0.32 | 0 | NA | |
143 | hsa-miR-361-5p | IL1R1 | 0.41 | 0.01813 | -0.91 | 0.00472 | miRanda | -0.65 | 0 | NA | |
144 | hsa-miR-3662 | IL1R1 | 1.83 | 0.0054 | -0.91 | 0.00472 | mirMAP | -0.14 | 0.00185 | NA | |
145 | hsa-miR-590-3p | IL1R1 | 1.12 | 0.00016 | -0.91 | 0.00472 | miRanda; miRNATAP | -0.32 | 2.0E-5 | NA | |
146 | hsa-miR-107 | IL1RAP | 0.9 | 5.0E-5 | 1.2 | 0.00709 | miRanda | -0.72 | 0 | NA | |
147 | hsa-miR-139-5p | IL1RAP | -1.83 | 0 | 1.2 | 0.00709 | miRanda | -0.27 | 0.00747 | NA | |
148 | hsa-miR-140-5p | IL1RAP | 0.21 | 0.303 | 1.2 | 0.00709 | miRanda | -0.51 | 0.0015 | NA | |
149 | hsa-miR-186-5p | IL1RAP | 0.15 | 0.43471 | 1.2 | 0.00709 | mirMAP | -0.54 | 0.00161 | NA | |
150 | hsa-miR-190a-5p | IL1RAP | -0.74 | 0.06624 | 1.2 | 0.00709 | MirTarget | -0.39 | 0 | NA |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | POSITIVE REGULATION OF RESPONSE TO STIMULUS | 41 | 1929 | 1.747e-28 | 8.127e-25 |
2 | INTRACELLULAR SIGNAL TRANSDUCTION | 37 | 1572 | 1.475e-26 | 3.431e-23 |
3 | POSITIVE REGULATION OF MOLECULAR FUNCTION | 37 | 1791 | 1.501e-24 | 2.329e-21 |
4 | CELLULAR RESPONSE TO ORGANIC SUBSTANCE | 36 | 1848 | 7.322e-23 | 8.517e-20 |
5 | APOPTOTIC SIGNALING PATHWAY | 20 | 289 | 1.371e-22 | 1.276e-19 |
6 | EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 15 | 99 | 2.897e-22 | 1.925e-19 |
7 | POSITIVE REGULATION OF PROTEIN METABOLIC PROCESS | 33 | 1492 | 2.657e-22 | 1.925e-19 |
8 | REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 34 | 1656 | 4.635e-22 | 2.696e-19 |
9 | REGULATION OF CELL DEATH | 32 | 1472 | 2.745e-21 | 1.419e-18 |
10 | CELL DEATH | 28 | 1001 | 3.314e-21 | 1.542e-18 |
11 | POSITIVE REGULATION OF CELL COMMUNICATION | 32 | 1532 | 9.18e-21 | 3.883e-18 |
12 | IMMUNE SYSTEM PROCESS | 35 | 1984 | 1.138e-20 | 4.385e-18 |
13 | ACTIVATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY | 14 | 95 | 1.225e-20 | 4.385e-18 |
14 | POSITIVE REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 26 | 876 | 3.318e-20 | 1.103e-17 |
15 | POSITIVE REGULATION OF I KAPPAB KINASE NF KAPPAB SIGNALING | 16 | 179 | 6.732e-20 | 2.088e-17 |
16 | EXTRINSIC APOPTOTIC SIGNALING PATHWAY VIA DEATH DOMAIN RECEPTORS | 11 | 39 | 8.619e-20 | 2.507e-17 |
17 | RESPONSE TO OXYGEN CONTAINING COMPOUND | 30 | 1381 | 9.246e-20 | 2.531e-17 |
18 | POSITIVE REGULATION OF CATALYTIC ACTIVITY | 31 | 1518 | 9.919e-20 | 2.564e-17 |
19 | REGULATION OF I KAPPAB KINASE NF KAPPAB SIGNALING | 17 | 233 | 1.339e-19 | 3.232e-17 |
20 | ZYMOGEN ACTIVATION | 14 | 112 | 1.389e-19 | 3.232e-17 |
21 | ACTIVATION OF IMMUNE RESPONSE | 20 | 427 | 3.238e-19 | 7.175e-17 |
22 | REGULATION OF IMMUNE RESPONSE | 25 | 858 | 3.481e-19 | 7.363e-17 |
23 | REGULATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY | 16 | 213 | 1.136e-18 | 2.299e-16 |
24 | NEGATIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 13 | 98 | 1.383e-18 | 2.682e-16 |
25 | REGULATION OF IMMUNE SYSTEM PROCESS | 29 | 1403 | 1.962e-18 | 3.652e-16 |
26 | POSITIVE REGULATION OF IMMUNE RESPONSE | 21 | 563 | 3.646e-18 | 6.526e-16 |
27 | ACTIVATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 8 | 13 | 4.45e-18 | 7.669e-16 |
28 | NEGATIVE REGULATION OF CELL DEATH | 24 | 872 | 8.277e-18 | 1.375e-15 |
29 | REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 14 | 153 | 1.269e-17 | 2.036e-15 |
30 | POSITIVE REGULATION OF PEPTIDASE ACTIVITY | 14 | 154 | 1.393e-17 | 2.16e-15 |
31 | POSITIVE REGULATION OF CELL DEATH | 21 | 605 | 1.569e-17 | 2.355e-15 |
32 | IMMUNE RESPONSE REGULATING CELL SURFACE RECEPTOR SIGNALING PATHWAY | 17 | 323 | 3.415e-17 | 4.965e-15 |
33 | PROTEIN MATURATION | 16 | 265 | 3.779e-17 | 5.329e-15 |
34 | POSITIVE REGULATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 8 | 17 | 8.33e-17 | 1.14e-14 |
35 | RESPONSE TO NITROGEN COMPOUND | 23 | 859 | 8.994e-17 | 1.196e-14 |
36 | RESPONSE TO CYTOKINE | 21 | 714 | 4.379e-16 | 5.66e-14 |
37 | NEGATIVE REGULATION OF APOPTOTIC SIGNALING PATHWAY | 14 | 200 | 5.663e-16 | 7.122e-14 |
38 | REGULATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 8 | 22 | 1.083e-15 | 1.327e-13 |
39 | POSITIVE REGULATION OF IMMUNE SYSTEM PROCESS | 22 | 867 | 1.554e-15 | 1.854e-13 |
40 | CELLULAR RESPONSE TO OXYGEN CONTAINING COMPOUND | 21 | 799 | 4.09e-15 | 4.758e-13 |
41 | REGULATION OF APOPTOTIC SIGNALING PATHWAY | 16 | 363 | 5.39e-15 | 6.117e-13 |
42 | REGULATION OF PROTEOLYSIS | 20 | 711 | 6.07e-15 | 6.725e-13 |
43 | RESPONSE TO ENDOGENOUS STIMULUS | 26 | 1450 | 7.2e-15 | 7.791e-13 |
44 | FC EPSILON RECEPTOR SIGNALING PATHWAY | 12 | 142 | 8.611e-15 | 9.107e-13 |
45 | PATTERN RECOGNITION RECEPTOR SIGNALING PATHWAY | 11 | 109 | 1.691e-14 | 1.748e-12 |
46 | REGULATION OF PEPTIDASE ACTIVITY | 16 | 392 | 1.781e-14 | 1.776e-12 |
47 | PHOSPHORYLATION | 24 | 1228 | 1.794e-14 | 1.776e-12 |
48 | ACTIVATION OF INNATE IMMUNE RESPONSE | 13 | 204 | 2.361e-14 | 2.288e-12 |
49 | SIGNAL TRANSDUCTION IN ABSENCE OF LIGAND | 8 | 33 | 4.588e-14 | 4.269e-12 |
50 | EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 8 | 33 | 4.588e-14 | 4.269e-12 |
51 | TOLL LIKE RECEPTOR SIGNALING PATHWAY | 10 | 85 | 5.906e-14 | 5.356e-12 |
52 | NEGATIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY VIA DEATH DOMAIN RECEPTORS | 8 | 34 | 5.986e-14 | 5.356e-12 |
53 | NEURON APOPTOTIC PROCESS | 8 | 35 | 7.742e-14 | 6.797e-12 |
54 | POSITIVE REGULATION OF APOPTOTIC SIGNALING PATHWAY | 12 | 171 | 8.168e-14 | 7.038e-12 |
55 | POSITIVE REGULATION OF PROTEOLYSIS | 15 | 363 | 1.108e-13 | 9.376e-12 |
56 | POSITIVE REGULATION OF INNATE IMMUNE RESPONSE | 13 | 246 | 2.631e-13 | 2.186e-11 |
57 | ANTIGEN RECEPTOR MEDIATED SIGNALING PATHWAY | 12 | 195 | 3.938e-13 | 3.215e-11 |
58 | REGULATION OF KINASE ACTIVITY | 19 | 776 | 4.02e-13 | 3.225e-11 |
59 | RESPONSE TO ABIOTIC STIMULUS | 21 | 1024 | 5.191e-13 | 4.094e-11 |
60 | FC RECEPTOR SIGNALING PATHWAY | 12 | 206 | 7.569e-13 | 5.87e-11 |
61 | REGULATION OF PHOSPHORUS METABOLIC PROCESS | 25 | 1618 | 8.494e-13 | 6.479e-11 |
62 | REGULATION OF RESPONSE TO STRESS | 24 | 1468 | 8.79e-13 | 6.492e-11 |
63 | CELLULAR RESPONSE TO NITROGEN COMPOUND | 16 | 505 | 8.71e-13 | 6.492e-11 |
64 | NEURON DEATH | 8 | 47 | 1.007e-12 | 7.318e-11 |
65 | PROTEIN PHOSPHORYLATION | 20 | 944 | 1.2e-12 | 8.592e-11 |
66 | REGULATION OF TRANSFERASE ACTIVITY | 20 | 946 | 1.248e-12 | 8.797e-11 |
67 | PHOSPHATE CONTAINING COMPOUND METABOLIC PROCESS | 27 | 1977 | 1.281e-12 | 8.893e-11 |
68 | ACTIVATION OF PROTEIN KINASE ACTIVITY | 13 | 279 | 1.308e-12 | 8.953e-11 |
69 | NUCLEOTIDE BINDING DOMAIN LEUCINE RICH REPEAT CONTAINING RECEPTOR SIGNALING PATHWAY | 7 | 28 | 1.518e-12 | 1.024e-10 |
70 | REGULATION OF INNATE IMMUNE RESPONSE | 14 | 357 | 1.664e-12 | 1.106e-10 |
71 | POSITIVE REGULATION OF DEFENSE RESPONSE | 14 | 364 | 2.163e-12 | 1.417e-10 |
72 | POSITIVE REGULATION OF PROTEIN MODIFICATION PROCESS | 21 | 1135 | 3.723e-12 | 2.406e-10 |
73 | REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY VIA DEATH DOMAIN RECEPTORS | 8 | 55 | 3.827e-12 | 2.439e-10 |
74 | POSITIVE REGULATION OF NF KAPPAB TRANSCRIPTION FACTOR ACTIVITY | 10 | 132 | 5.302e-12 | 3.334e-10 |
75 | CYTOPLASMIC PATTERN RECOGNITION RECEPTOR SIGNALING PATHWAY | 7 | 33 | 5.414e-12 | 3.359e-10 |
76 | POSITIVE REGULATION OF KINASE ACTIVITY | 15 | 482 | 6.532e-12 | 3.917e-10 |
77 | POSITIVE REGULATION OF PHOSPHATE METABOLIC PROCESS | 20 | 1036 | 6.566e-12 | 3.917e-10 |
78 | POSITIVE REGULATION OF PHOSPHORUS METABOLIC PROCESS | 20 | 1036 | 6.566e-12 | 3.917e-10 |
79 | RESPONSE TO PEPTIDE | 14 | 404 | 8.767e-12 | 5.164e-10 |
80 | HOMEOSTATIC PROCESS | 22 | 1337 | 9.797e-12 | 5.698e-10 |
81 | CELLULAR RESPONSE TO CYTOKINE STIMULUS | 16 | 606 | 1.36e-11 | 7.718e-10 |
82 | CELLULAR RESPONSE TO ABIOTIC STIMULUS | 12 | 263 | 1.346e-11 | 7.718e-10 |
83 | T CELL RECEPTOR SIGNALING PATHWAY | 10 | 146 | 1.457e-11 | 8.169e-10 |
84 | CYTOKINE MEDIATED SIGNALING PATHWAY | 14 | 452 | 3.904e-11 | 2.163e-09 |
85 | RESPONSE TO BIOTIC STIMULUS | 18 | 886 | 4.239e-11 | 2.321e-09 |
86 | RESPONSE TO HORMONE | 18 | 893 | 4.822e-11 | 2.609e-09 |
87 | CELLULAR GLUCOSE HOMEOSTASIS | 8 | 75 | 5.068e-11 | 2.71e-09 |
88 | POSITIVE REGULATION OF SEQUENCE SPECIFIC DNA BINDING TRANSCRIPTION FACTOR ACTIVITY | 11 | 228 | 5.746e-11 | 3.038e-09 |
89 | NEGATIVE REGULATION OF CELL COMMUNICATION | 20 | 1192 | 8.202e-11 | 4.288e-09 |
90 | PHOSPHATIDYLINOSITOL 3 PHOSPHATE BIOSYNTHETIC PROCESS | 7 | 49 | 1.05e-10 | 5.427e-09 |
91 | RESPONSE TO MOLECULE OF BACTERIAL ORIGIN | 12 | 321 | 1.357e-10 | 6.94e-09 |
92 | REGULATION OF PROTEIN MODIFICATION PROCESS | 23 | 1710 | 1.654e-10 | 8.366e-09 |
93 | REGULATION OF NEURON DEATH | 11 | 252 | 1.677e-10 | 8.392e-09 |
94 | POSITIVE REGULATION OF TRANSFERASE ACTIVITY | 15 | 616 | 2.048e-10 | 1.014e-08 |
95 | CHEMICAL HOMEOSTASIS | 17 | 874 | 3.263e-10 | 1.598e-08 |
96 | CELLULAR RESPONSE TO ENDOGENOUS STIMULUS | 18 | 1008 | 3.449e-10 | 1.672e-08 |
97 | REGULATION OF DEFENSE RESPONSE | 16 | 759 | 3.777e-10 | 1.812e-08 |
98 | CELLULAR RESPONSE TO PEPTIDE | 11 | 274 | 4.084e-10 | 1.939e-08 |
99 | CELLULAR RESPONSE TO HORMONE STIMULUS | 14 | 552 | 5.368e-10 | 2.523e-08 |
100 | POSITIVE REGULATION OF HYDROLASE ACTIVITY | 17 | 905 | 5.567e-10 | 2.59e-08 |
101 | RESPONSE TO EXTERNAL STIMULUS | 23 | 1821 | 5.76e-10 | 2.654e-08 |
102 | INTRINSIC APOPTOTIC SIGNALING PATHWAY | 9 | 152 | 6.057e-10 | 2.763e-08 |
103 | RESPONSE TO WOUNDING | 14 | 563 | 6.934e-10 | 3.132e-08 |
104 | PROTEOLYSIS | 19 | 1208 | 8.285e-10 | 3.707e-08 |
105 | NEGATIVE REGULATION OF RESPONSE TO STIMULUS | 20 | 1360 | 8.401e-10 | 3.723e-08 |
106 | ACTIVATION OF PROTEIN KINASE A ACTIVITY | 5 | 17 | 1.131e-09 | 4.966e-08 |
107 | REGULATION OF CATABOLIC PROCESS | 15 | 731 | 2.149e-09 | 9.345e-08 |
108 | PHOSPHATIDYLINOSITOL BIOSYNTHETIC PROCESS | 8 | 120 | 2.278e-09 | 9.816e-08 |
109 | RESPONSE TO BACTERIUM | 13 | 528 | 3.485e-09 | 1.488e-07 |
110 | CELLULAR RESPONSE TO MECHANICAL STIMULUS | 7 | 80 | 3.617e-09 | 1.53e-07 |
111 | REGULATION OF HYDROLASE ACTIVITY | 19 | 1327 | 3.938e-09 | 1.651e-07 |
112 | REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 6 | 46 | 4.338e-09 | 1.802e-07 |
113 | REGULATION OF NEURON APOPTOTIC PROCESS | 9 | 192 | 4.767e-09 | 1.963e-07 |
114 | MULTICELLULAR ORGANISMAL HOMEOSTASIS | 10 | 272 | 6.414e-09 | 2.618e-07 |
115 | INFLAMMATORY RESPONSE | 12 | 454 | 6.901e-09 | 2.792e-07 |
116 | REGULATION OF EXECUTION PHASE OF APOPTOSIS | 5 | 24 | 7.649e-09 | 3.068e-07 |
117 | POSITIVE REGULATION OF TRANSCRIPTION FACTOR IMPORT INTO NUCLEUS | 6 | 51 | 8.247e-09 | 3.252e-07 |
118 | REGULATION OF SEQUENCE SPECIFIC DNA BINDING TRANSCRIPTION FACTOR ACTIVITY | 11 | 365 | 8.229e-09 | 3.252e-07 |
119 | CELL ACTIVATION | 13 | 568 | 8.341e-09 | 3.261e-07 |
120 | POSITIVE REGULATION OF GENE EXPRESSION | 21 | 1733 | 9.035e-09 | 3.503e-07 |
121 | POSITIVE REGULATION OF INTRACELLULAR TRANSPORT | 11 | 370 | 9.472e-09 | 3.609e-07 |
122 | CELLULAR RESPONSE TO STRESS | 20 | 1565 | 9.448e-09 | 3.609e-07 |
123 | PHOSPHATIDYLINOSITOL 3 KINASE SIGNALING | 5 | 25 | 9.54e-09 | 3.609e-07 |
124 | REGULATION OF RESPONSE TO CYTOKINE STIMULUS | 8 | 144 | 9.659e-09 | 3.625e-07 |
125 | WOUND HEALING | 12 | 470 | 1.015e-08 | 3.747e-07 |
126 | REGULATION OF PROTEIN SERINE THREONINE KINASE ACTIVITY | 12 | 470 | 1.015e-08 | 3.747e-07 |
127 | RESPONSE TO MECHANICAL STIMULUS | 9 | 210 | 1.042e-08 | 3.819e-07 |
128 | IMMUNE RESPONSE | 17 | 1100 | 1.054e-08 | 3.83e-07 |
129 | REGULATION OF TRANSCRIPTION FACTOR IMPORT INTO NUCLEUS | 7 | 95 | 1.216e-08 | 4.386e-07 |
130 | LEUKOCYTE DIFFERENTIATION | 10 | 292 | 1.261e-08 | 4.514e-07 |
131 | RENAL SYSTEM PROCESS | 7 | 102 | 2e-08 | 7.103e-07 |
132 | REGULATION OF CELLULAR RESPONSE TO INSULIN STIMULUS | 6 | 59 | 2.026e-08 | 7.142e-07 |
133 | MYD88 INDEPENDENT TOLL LIKE RECEPTOR SIGNALING PATHWAY | 5 | 30 | 2.53e-08 | 8.852e-07 |
134 | INNATE IMMUNE RESPONSE ACTIVATING CELL SURFACE RECEPTOR SIGNALING PATHWAY | 7 | 106 | 2.615e-08 | 9.081e-07 |
135 | REGULATION OF CELL PROLIFERATION | 19 | 1496 | 2.77e-08 | 9.547e-07 |
136 | RESPONSE TO LIPID | 15 | 888 | 2.921e-08 | 9.995e-07 |
137 | POSITIVE REGULATION OF GLUCOSE IMPORT IN RESPONSE TO INSULIN STIMULUS | 4 | 12 | 3.321e-08 | 1.128e-06 |
138 | RESPONSE TO TOXIC SUBSTANCE | 9 | 241 | 3.432e-08 | 1.157e-06 |
139 | GLUCOSE HOMEOSTASIS | 8 | 170 | 3.542e-08 | 1.177e-06 |
140 | CARBOHYDRATE HOMEOSTASIS | 8 | 170 | 3.542e-08 | 1.177e-06 |
141 | POSITIVE REGULATION OF NEURON DEATH | 6 | 67 | 4.407e-08 | 1.454e-06 |
142 | RESPONSE TO ORGANIC CYCLIC COMPOUND | 15 | 917 | 4.463e-08 | 1.463e-06 |
143 | RESPONSE TO INTERLEUKIN 1 | 7 | 115 | 4.606e-08 | 1.499e-06 |
144 | INTERLEUKIN 1 MEDIATED SIGNALING PATHWAY | 4 | 13 | 4.787e-08 | 1.547e-06 |
145 | T CELL HOMEOSTASIS | 5 | 34 | 4.896e-08 | 1.56e-06 |
146 | RENAL WATER HOMEOSTASIS | 5 | 34 | 4.896e-08 | 1.56e-06 |
147 | LYMPHOCYTE ACTIVATION | 10 | 342 | 5.602e-08 | 1.761e-06 |
148 | LEUKOCYTE CELL CELL ADHESION | 9 | 255 | 5.574e-08 | 1.761e-06 |
149 | I KAPPAB KINASE NF KAPPAB SIGNALING | 6 | 70 | 5.75e-08 | 1.796e-06 |
150 | REGULATION OF CELLULAR PROTEIN LOCALIZATION | 12 | 552 | 5.956e-08 | 1.848e-06 |
151 | INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO DNA DAMAGE | 6 | 71 | 6.267e-08 | 1.931e-06 |
152 | CELLULAR HOMEOSTASIS | 13 | 676 | 6.473e-08 | 1.982e-06 |
153 | POSITIVE REGULATION OF NUCLEOCYTOPLASMIC TRANSPORT | 7 | 121 | 6.548e-08 | 1.991e-06 |
154 | CELLULAR RESPONSE TO EXTERNAL STIMULUS | 9 | 264 | 7.499e-08 | 2.266e-06 |
155 | INOSITOL LIPID MEDIATED SIGNALING | 7 | 124 | 7.753e-08 | 2.327e-06 |
156 | CELLULAR RESPONSE TO CARBOHYDRATE STIMULUS | 6 | 74 | 8.051e-08 | 2.401e-06 |
157 | CELLULAR CHEMICAL HOMEOSTASIS | 12 | 570 | 8.444e-08 | 2.503e-06 |
158 | CELLULAR RESPONSE TO GLUCAGON STIMULUS | 5 | 38 | 8.753e-08 | 2.578e-06 |
159 | POSITIVE REGULATION OF CELLULAR PROTEIN LOCALIZATION | 10 | 360 | 9.045e-08 | 2.646e-06 |
160 | T CELL APOPTOTIC PROCESS | 4 | 15 | 9.098e-08 | 2.646e-06 |
161 | PHOSPHATIDYLINOSITOL METABOLIC PROCESS | 8 | 193 | 9.466e-08 | 2.736e-06 |
162 | IMMUNE SYSTEM DEVELOPMENT | 12 | 582 | 1.058e-07 | 3.04e-06 |
163 | RESPONSE TO INORGANIC SUBSTANCE | 11 | 479 | 1.316e-07 | 3.757e-06 |
164 | REGULATION OF GLUCOSE IMPORT IN RESPONSE TO INSULIN STIMULUS | 4 | 17 | 1.579e-07 | 4.481e-06 |
165 | REGULATION OF MULTICELLULAR ORGANISMAL DEVELOPMENT | 19 | 1672 | 1.621e-07 | 4.572e-06 |
166 | LYMPHOCYTE DIFFERENTIATION | 8 | 209 | 1.746e-07 | 4.894e-06 |
167 | GLYCEROLIPID BIOSYNTHETIC PROCESS | 8 | 211 | 1.878e-07 | 5.233e-06 |
168 | LYMPHOCYTE APOPTOTIC PROCESS | 4 | 18 | 2.026e-07 | 5.612e-06 |
169 | REGULATION OF INTRACELLULAR TRANSPORT | 12 | 621 | 2.13e-07 | 5.863e-06 |
170 | CELLULAR RESPONSE TO INTERLEUKIN 1 | 6 | 88 | 2.281e-07 | 6.244e-06 |
171 | REGULATION OF NUCLEOCYTOPLASMIC TRANSPORT | 8 | 220 | 2.584e-07 | 7.032e-06 |
172 | PEPTIDYL SERINE MODIFICATION | 7 | 148 | 2.605e-07 | 7.048e-06 |
173 | POSITIVE REGULATION OF NEURON APOPTOTIC PROCESS | 5 | 47 | 2.621e-07 | 7.05e-06 |
174 | POSITIVE REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION | 11 | 514 | 2.665e-07 | 7.125e-06 |
175 | RESPONSE TO GLUCAGON | 5 | 48 | 2.919e-07 | 7.762e-06 |
176 | HEMOSTASIS | 9 | 311 | 3.008e-07 | 7.952e-06 |
177 | LEUKOCYTE ACTIVATION | 10 | 414 | 3.294e-07 | 8.66e-06 |
178 | LYMPHOCYTE HOMEOSTASIS | 5 | 50 | 3.596e-07 | 9.296e-06 |
179 | REGULATION OF TUMOR NECROSIS FACTOR MEDIATED SIGNALING PATHWAY | 5 | 50 | 3.596e-07 | 9.296e-06 |
180 | RESPONSE TO GAMMA RADIATION | 5 | 50 | 3.596e-07 | 9.296e-06 |
181 | RESPONSE TO TUMOR NECROSIS FACTOR | 8 | 233 | 4e-07 | 1.028e-05 |
182 | POSITIVE REGULATION OF TRANSPORT | 14 | 936 | 4.073e-07 | 1.041e-05 |
183 | PHOSPHOLIPID BIOSYNTHETIC PROCESS | 8 | 235 | 4.268e-07 | 1.085e-05 |
184 | CELL DEVELOPMENT | 17 | 1426 | 4.523e-07 | 1.144e-05 |
185 | LIPID PHOSPHORYLATION | 6 | 99 | 4.601e-07 | 1.157e-05 |
186 | RESPONSE TO DRUG | 10 | 431 | 4.762e-07 | 1.191e-05 |
187 | POSITIVE REGULATION OF BIOSYNTHETIC PROCESS | 19 | 1805 | 5.325e-07 | 1.325e-05 |
188 | POSITIVE REGULATION OF CELLULAR RESPONSE TO INSULIN STIMULUS | 4 | 23 | 5.799e-07 | 1.428e-05 |
189 | LEUKOCYTE APOPTOTIC PROCESS | 4 | 23 | 5.799e-07 | 1.428e-05 |
190 | EXECUTION PHASE OF APOPTOSIS | 5 | 55 | 5.838e-07 | 1.43e-05 |
191 | INTRACELLULAR RECEPTOR SIGNALING PATHWAY | 7 | 168 | 6.151e-07 | 1.493e-05 |
192 | POSITIVE REGULATION OF PROTEIN IMPORT | 6 | 104 | 6.16e-07 | 1.493e-05 |
193 | RESPONSE TO VIRUS | 8 | 247 | 6.223e-07 | 1.5e-05 |
194 | MULTICELLULAR ORGANISMAL WATER HOMEOSTASIS | 5 | 58 | 7.638e-07 | 1.832e-05 |
195 | SINGLE ORGANISM CELL ADHESION | 10 | 459 | 8.443e-07 | 2.015e-05 |
196 | POSITIVE REGULATION OF INTRACELLULAR PROTEIN TRANSPORT | 8 | 258 | 8.642e-07 | 2.052e-05 |
197 | LEUKOCYTE HOMEOSTASIS | 5 | 60 | 9.064e-07 | 2.141e-05 |
198 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 14 | 1004 | 9.439e-07 | 2.218e-05 |
199 | RESPONSE TO AMINO ACID | 6 | 112 | 9.537e-07 | 2.23e-05 |
200 | DEVELOPMENTAL PROGRAMMED CELL DEATH | 4 | 26 | 9.727e-07 | 2.252e-05 |
201 | REGULATION OF NECROTIC CELL DEATH | 4 | 26 | 9.727e-07 | 2.252e-05 |
202 | AGING | 8 | 264 | 1.027e-06 | 2.366e-05 |
203 | RESPONSE TO KETONE | 7 | 182 | 1.054e-06 | 2.415e-05 |
204 | REGULATION OF PROTEIN IMPORT | 7 | 183 | 1.093e-06 | 2.493e-05 |
205 | REGULATION OF CYTOPLASMIC TRANSPORT | 10 | 481 | 1.289e-06 | 2.926e-05 |
206 | NECROTIC CELL DEATH | 4 | 28 | 1.326e-06 | 2.996e-05 |
207 | IMMUNE EFFECTOR PROCESS | 10 | 486 | 1.415e-06 | 3.18e-05 |
208 | RESPONSE TO REACTIVE OXYGEN SPECIES | 7 | 191 | 1.455e-06 | 3.255e-05 |
209 | REGULATION OF INTRACELLULAR PROTEIN TRANSPORT | 9 | 381 | 1.63e-06 | 3.629e-05 |
210 | POSITIVE REGULATION OF CYTOPLASMIC TRANSPORT | 8 | 282 | 1.683e-06 | 3.728e-05 |
211 | DEFENSE RESPONSE | 15 | 1231 | 1.938e-06 | 4.274e-05 |
212 | WATER HOMEOSTASIS | 5 | 70 | 1.964e-06 | 4.29e-05 |
213 | REGULATION OF MEMBRANE PERMEABILITY | 5 | 70 | 1.964e-06 | 4.29e-05 |
214 | POSITIVE REGULATION OF PROTEIN LOCALIZATION TO NUCLEUS | 6 | 129 | 2.181e-06 | 4.726e-05 |
215 | NEGATIVE REGULATION OF CATABOLIC PROCESS | 7 | 203 | 2.184e-06 | 4.726e-05 |
216 | NEGATIVE REGULATION OF MOLECULAR FUNCTION | 14 | 1079 | 2.211e-06 | 4.763e-05 |
217 | MYD88 DEPENDENT TOLL LIKE RECEPTOR SIGNALING PATHWAY | 4 | 32 | 2.309e-06 | 4.883e-05 |
218 | NEGATIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 4 | 32 | 2.309e-06 | 4.883e-05 |
219 | INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO ENDOPLASMIC RETICULUM STRESS | 4 | 32 | 2.309e-06 | 4.883e-05 |
220 | NEGATIVE REGULATION OF SIGNAL TRANSDUCTION IN ABSENCE OF LIGAND | 4 | 32 | 2.309e-06 | 4.883e-05 |
221 | GLYCEROPHOSPHOLIPID METABOLIC PROCESS | 8 | 297 | 2.474e-06 | 5.209e-05 |
222 | B CELL ACTIVATION | 6 | 132 | 2.494e-06 | 5.227e-05 |
223 | REGULATION OF PROTEIN LOCALIZATION | 13 | 950 | 3.056e-06 | 6.376e-05 |
224 | RESPONSE TO RADIATION | 9 | 413 | 3.155e-06 | 6.539e-05 |
225 | REGULATION OF PROTEIN TARGETING | 8 | 307 | 3.162e-06 | 6.539e-05 |
226 | ANATOMICAL STRUCTURE FORMATION INVOLVED IN MORPHOGENESIS | 13 | 957 | 3.312e-06 | 6.82e-05 |
227 | REGULATION OF PROTEIN LOCALIZATION TO NUCLEUS | 7 | 218 | 3.501e-06 | 7.176e-05 |
228 | POSITIVE REGULATION OF MITOCHONDRIAL OUTER MEMBRANE PERMEABILIZATION INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 4 | 36 | 3.749e-06 | 7.651e-05 |
229 | INSULIN RECEPTOR SIGNALING PATHWAY | 5 | 80 | 3.814e-06 | 7.75e-05 |
230 | POSITIVE REGULATION OF NFAT PROTEIN IMPORT INTO NUCLEUS | 3 | 11 | 3.957e-06 | 8.004e-05 |
231 | RESPONSE TO ACID CHEMICAL | 8 | 319 | 4.196e-06 | 8.415e-05 |
232 | REGULATION OF MAP KINASE ACTIVITY | 8 | 319 | 4.196e-06 | 8.415e-05 |
233 | REGULATION OF PHOSPHATIDYLINOSITOL 3 KINASE ACTIVITY | 4 | 40 | 5.766e-06 | 0.0001151 |
234 | REGULATION OF ORGANELLE ORGANIZATION | 14 | 1178 | 6.127e-06 | 0.0001218 |
235 | RESPONSE TO COBALT ION | 3 | 13 | 6.829e-06 | 0.0001352 |
236 | POSITIVE REGULATION OF GLUCOSE TRANSPORT | 4 | 42 | 7.03e-06 | 0.0001386 |
237 | MITOCHONDRIAL MEMBRANE ORGANIZATION | 5 | 92 | 7.594e-06 | 0.0001491 |
238 | REGULATION OF MITOCHONDRIAL OUTER MEMBRANE PERMEABILIZATION INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 4 | 43 | 7.734e-06 | 0.0001506 |
239 | CELLULAR COMPONENT DISASSEMBLY INVOLVED IN EXECUTION PHASE OF APOPTOSIS | 4 | 43 | 7.734e-06 | 0.0001506 |
240 | CELLULAR RESPONSE TO ORGANIC CYCLIC COMPOUND | 9 | 465 | 8.232e-06 | 0.0001596 |
241 | TOLL LIKE RECEPTOR 9 SIGNALING PATHWAY | 3 | 14 | 8.673e-06 | 0.0001661 |
242 | REGULATION OF CAMP DEPENDENT PROTEIN KINASE ACTIVITY | 3 | 14 | 8.673e-06 | 0.0001661 |
243 | RESPONSE TO OXIDATIVE STRESS | 8 | 352 | 8.625e-06 | 0.0001661 |
244 | POSITIVE REGULATION OF MAPK CASCADE | 9 | 470 | 8.969e-06 | 0.000171 |
245 | CELLULAR PROCESS INVOLVED IN REPRODUCTION IN MULTICELLULAR ORGANISM | 7 | 252 | 9.055e-06 | 0.000172 |
246 | GLYCEROLIPID METABOLIC PROCESS | 8 | 356 | 9.363e-06 | 0.0001771 |
247 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 17 | 1784 | 9.723e-06 | 0.0001832 |
248 | RESPONSE TO CARBOHYDRATE | 6 | 168 | 1.001e-05 | 0.0001879 |
249 | CELL CELL ADHESION | 10 | 608 | 1.027e-05 | 0.000192 |
250 | LEUKOCYTE MIGRATION | 7 | 259 | 1.082e-05 | 0.0002014 |
251 | PHOSPHOLIPID METABOLIC PROCESS | 8 | 364 | 1.1e-05 | 0.000204 |
252 | NEGATIVE REGULATION OF NEURON DEATH | 6 | 171 | 1.108e-05 | 0.0002045 |
253 | REGULATION OF CELL ACTIVATION | 9 | 484 | 1.134e-05 | 0.0002086 |
254 | REGULATION OF GLUCOSE TRANSPORT | 5 | 100 | 1.142e-05 | 0.0002092 |
255 | REGULATION OF LIPID KINASE ACTIVITY | 4 | 48 | 1.206e-05 | 0.0002201 |
256 | NEGATIVE REGULATION OF IMMUNE SYSTEM PROCESS | 8 | 372 | 1.288e-05 | 0.000234 |
257 | RESPONSE TO CORTICOSTEROID | 6 | 176 | 1.305e-05 | 0.0002363 |
258 | NEGATIVE REGULATION OF PROTEIN METABOLIC PROCESS | 13 | 1087 | 1.314e-05 | 0.0002369 |
259 | STRESS ACTIVATED PROTEIN KINASE SIGNALING CASCADE | 5 | 103 | 1.319e-05 | 0.0002369 |
260 | REGULATION OF CELLULAR LOCALIZATION | 14 | 1277 | 1.535e-05 | 0.0002746 |
261 | REGULATION OF NFAT PROTEIN IMPORT INTO NUCLEUS | 3 | 17 | 1.61e-05 | 0.0002856 |
262 | REGULATION OF BODY FLUID LEVELS | 9 | 506 | 1.614e-05 | 0.0002856 |
263 | NEGATIVE REGULATION OF ANOIKIS | 3 | 17 | 1.61e-05 | 0.0002856 |
264 | POSITIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY | 4 | 53 | 1.795e-05 | 0.0003164 |
265 | INOSITOL PHOSPHATE MEDIATED SIGNALING | 3 | 18 | 1.928e-05 | 0.0003385 |
266 | REGULATION OF CELL DIFFERENTIATION | 15 | 1492 | 1.996e-05 | 0.0003491 |
267 | REGULATION OF MAPK CASCADE | 10 | 660 | 2.087e-05 | 0.0003637 |
268 | NEGATIVE REGULATION OF MEIOTIC CELL CYCLE | 3 | 19 | 2.285e-05 | 0.0003967 |
269 | SIGNAL TRANSDUCTION BY PROTEIN PHOSPHORYLATION | 8 | 404 | 2.33e-05 | 0.0004031 |
270 | POSITIVE REGULATION OF CELLULAR COMPONENT ORGANIZATION | 13 | 1152 | 2.429e-05 | 0.0004187 |
271 | TUMOR NECROSIS FACTOR MEDIATED SIGNALING PATHWAY | 5 | 118 | 2.549e-05 | 0.0004376 |
272 | REGULATION OF GLUCOSE IMPORT | 4 | 60 | 2.944e-05 | 0.0005036 |
273 | RESPONSE TO INSULIN | 6 | 205 | 3.09e-05 | 0.0005266 |
274 | NECROPTOTIC PROCESS | 3 | 21 | 3.123e-05 | 0.0005284 |
275 | T CELL DIFFERENTIATION | 5 | 123 | 3.112e-05 | 0.0005284 |
276 | REGULATION OF PHOSPHOLIPID METABOLIC PROCESS | 4 | 61 | 3.144e-05 | 0.00053 |
277 | RESPONSE TO UV | 5 | 126 | 3.494e-05 | 0.0005848 |
278 | NEGATIVE REGULATION OF PROTEIN SERINE THREONINE KINASE ACTIVITY | 5 | 126 | 3.494e-05 | 0.0005848 |
279 | RESPONSE TO OXYGEN LEVELS | 7 | 311 | 3.507e-05 | 0.0005848 |
280 | LIPID MODIFICATION | 6 | 210 | 3.536e-05 | 0.0005876 |
281 | RELEASE OF CYTOCHROME C FROM MITOCHONDRIA | 3 | 22 | 3.608e-05 | 0.0005975 |
282 | NEGATIVE REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 8 | 437 | 4.072e-05 | 0.0006719 |
283 | POSITIVE REGULATION OF MULTICELLULAR ORGANISMAL PROCESS | 14 | 1395 | 4.102e-05 | 0.0006744 |
284 | POSITIVE REGULATION OF ORGANELLE ORGANIZATION | 9 | 573 | 4.28e-05 | 0.0007012 |
285 | REGULATION OF MITOCHONDRION ORGANIZATION | 6 | 218 | 4.357e-05 | 0.0007114 |
286 | REGULATION OF ANOIKIS | 3 | 24 | 4.723e-05 | 0.0007683 |
287 | NEGATIVE REGULATION OF NEURON APOPTOTIC PROCESS | 5 | 135 | 4.861e-05 | 0.0007881 |
288 | ORGANOPHOSPHATE BIOSYNTHETIC PROCESS | 8 | 450 | 5.007e-05 | 0.000809 |
289 | RESPONSE TO ALKALOID | 5 | 137 | 5.214e-05 | 0.0008366 |
290 | CELLULAR RESPONSE TO RADIATION | 5 | 137 | 5.214e-05 | 0.0008366 |
291 | EMBRYO DEVELOPMENT | 11 | 894 | 5.233e-05 | 0.0008367 |
292 | REGULATION OF PHOSPHATIDYLINOSITOL 3 KINASE SIGNALING | 5 | 138 | 5.398e-05 | 0.0008584 |
293 | RESPONSE TO METAL ION | 7 | 333 | 5.406e-05 | 0.0008584 |
294 | MITOCHONDRION ORGANIZATION | 9 | 594 | 5.654e-05 | 0.0008948 |
295 | DEVELOPMENTAL PROCESS INVOLVED IN REPRODUCTION | 9 | 602 | 6.267e-05 | 0.0009885 |
296 | RESPONSE TO ENDOPLASMIC RETICULUM STRESS | 6 | 233 | 6.306e-05 | 0.0009911 |
297 | CELLULAR LIPID METABOLIC PROCESS | 11 | 913 | 6.326e-05 | 0.0009911 |
298 | VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 4 | 74 | 6.737e-05 | 0.001052 |
299 | DNA CATABOLIC PROCESS | 3 | 27 | 6.782e-05 | 0.001055 |
300 | RESPONSE TO IONIZING RADIATION | 5 | 145 | 6.83e-05 | 0.001059 |
301 | CELLULAR RESPONSE TO INSULIN STIMULUS | 5 | 146 | 7.056e-05 | 0.001091 |
302 | RESPONSE TO TEMPERATURE STIMULUS | 5 | 148 | 7.526e-05 | 0.00116 |
303 | REGULATION OF PROTEIN INSERTION INTO MITOCHONDRIAL MEMBRANE INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 3 | 29 | 8.437e-05 | 0.001287 |
304 | POSITIVE REGULATION OF PROTEIN INSERTION INTO MITOCHONDRIAL MEMBRANE INVOLVED IN APOPTOTIC SIGNALING PATHWAY | 3 | 29 | 8.437e-05 | 0.001287 |
305 | MUSCLE ADAPTATION | 3 | 29 | 8.437e-05 | 0.001287 |
306 | REGULATION OF CELL ADHESION | 9 | 629 | 8.769e-05 | 0.001333 |
307 | REGULATION OF AUTOPHAGY | 6 | 249 | 9.096e-05 | 0.001378 |
308 | RESPONSE TO ALCOHOL | 7 | 362 | 9.124e-05 | 0.001378 |
309 | RESPONSE TO STEROID HORMONE | 8 | 497 | 0.0001002 | 0.001508 |
310 | LIPOPOLYSACCHARIDE MEDIATED SIGNALING PATHWAY | 3 | 31 | 0.0001034 | 0.001551 |
311 | CELLULAR RESPONSE TO BIOTIC STIMULUS | 5 | 163 | 0.0001187 | 0.001775 |
312 | POSITIVE REGULATION OF CELL PROLIFERATION | 10 | 814 | 0.0001214 | 0.00181 |
313 | INTERSPECIES INTERACTION BETWEEN ORGANISMS | 9 | 662 | 0.0001292 | 0.001915 |
314 | SYMBIOSIS ENCOMPASSING MUTUALISM THROUGH PARASITISM | 9 | 662 | 0.0001292 | 0.001915 |
315 | NEGATIVE REGULATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY | 4 | 88 | 0.0001324 | 0.001956 |
316 | POSITIVE REGULATION OF MITOCHONDRION ORGANIZATION | 5 | 167 | 0.000133 | 0.001958 |
317 | PROTEIN KINASE B SIGNALING | 3 | 34 | 0.0001367 | 0.002007 |
318 | B CELL DIFFERENTIATION | 4 | 89 | 0.0001383 | 0.002024 |
319 | NEGATIVE REGULATION OF CATALYTIC ACTIVITY | 10 | 829 | 0.0001409 | 0.002056 |
320 | CALCIUM MEDIATED SIGNALING | 4 | 90 | 0.0001444 | 0.0021 |
321 | STRIATED MUSCLE CELL DIFFERENTIATION | 5 | 173 | 0.0001568 | 0.002266 |
322 | GLAND DEVELOPMENT | 7 | 395 | 0.0001566 | 0.002266 |
323 | HOMEOSTASIS OF NUMBER OF CELLS | 5 | 175 | 0.0001655 | 0.002376 |
324 | NEGATIVE REGULATION OF CELLULAR COMPONENT ORGANIZATION | 9 | 684 | 0.0001652 | 0.002376 |
325 | MITOCHONDRIAL TRANSPORT | 5 | 177 | 0.0001745 | 0.002496 |
326 | LIPID BIOSYNTHETIC PROCESS | 8 | 539 | 0.0001749 | 0.002496 |
327 | REGULATION OF TRANSPORT | 15 | 1804 | 0.0001757 | 0.0025 |
328 | FC GAMMA RECEPTOR SIGNALING PATHWAY | 4 | 95 | 0.000178 | 0.002525 |
329 | REGULATION OF LIPID METABOLIC PROCESS | 6 | 282 | 0.0001794 | 0.002529 |
330 | MUSCLE SYSTEM PROCESS | 6 | 282 | 0.0001794 | 0.002529 |
331 | FEMALE GAMETE GENERATION | 4 | 96 | 0.0001853 | 0.002605 |
332 | BIOLOGICAL ADHESION | 11 | 1032 | 0.0001873 | 0.002625 |
333 | REGULATION OF MYELOID CELL DIFFERENTIATION | 5 | 183 | 0.0002038 | 0.002847 |
334 | POSITIVE REGULATION OF PROTEIN SERINE THREONINE KINASE ACTIVITY | 6 | 289 | 0.0002048 | 0.002853 |
335 | WNT SIGNALING PATHWAY CALCIUM MODULATING PATHWAY | 3 | 39 | 0.0002066 | 0.002862 |
336 | SPLEEN DEVELOPMENT | 3 | 39 | 0.0002066 | 0.002862 |
337 | EMBRYO DEVELOPMENT ENDING IN BIRTH OR EGG HATCHING | 8 | 554 | 0.0002108 | 0.002911 |
338 | REGULATION OF CELL CYCLE PROCESS | 8 | 558 | 0.0002214 | 0.003047 |
339 | REGULATION OF MEIOTIC CELL CYCLE | 3 | 40 | 0.0002229 | 0.00306 |
340 | MYELOID CELL DIFFERENTIATION | 5 | 189 | 0.0002366 | 0.003238 |
341 | PROTEIN DEPHOSPHORYLATION | 5 | 190 | 0.0002425 | 0.003309 |
342 | NEGATIVE REGULATION OF CELL CYCLE | 7 | 433 | 0.0002744 | 0.003734 |
343 | REGULATION OF HOMOTYPIC CELL CELL ADHESION | 6 | 307 | 0.0002834 | 0.003844 |
344 | REGULATION OF CELL CYCLE ARREST | 4 | 108 | 0.0002912 | 0.003939 |
345 | REGULATION OF RELEASE OF CYTOCHROME C FROM MITOCHONDRIA | 3 | 44 | 0.0002963 | 0.003997 |
346 | RESPONSE TO HYDROGEN PEROXIDE | 4 | 109 | 0.0003016 | 0.004057 |
347 | POSITIVE REGULATION OF CELL ACTIVATION | 6 | 311 | 0.0003037 | 0.004072 |
348 | THYMOCYTE AGGREGATION | 3 | 45 | 0.0003168 | 0.004224 |
349 | T CELL DIFFERENTIATION IN THYMUS | 3 | 45 | 0.0003168 | 0.004224 |
350 | REGULATION OF HEMOPOIESIS | 6 | 314 | 0.0003196 | 0.004249 |
351 | REGULATION OF HOMEOSTATIC PROCESS | 7 | 447 | 0.0003326 | 0.004409 |
352 | GAMETE GENERATION | 8 | 595 | 0.000341 | 0.004508 |
353 | OVULATION CYCLE | 4 | 113 | 0.0003461 | 0.004562 |
354 | REGULATION OF LEUKOCYTE PROLIFERATION | 5 | 206 | 0.000352 | 0.004626 |
355 | POSITIVE REGULATION OF MAP KINASE ACTIVITY | 5 | 207 | 0.0003599 | 0.004712 |
356 | RESPONSE TO ANTIBIOTIC | 3 | 47 | 0.0003605 | 0.004712 |
357 | TUBE MORPHOGENESIS | 6 | 323 | 0.0003715 | 0.004843 |
358 | GERM CELL DEVELOPMENT | 5 | 209 | 0.0003761 | 0.004888 |
359 | CELLULAR RESPONSE TO LIPID | 7 | 457 | 0.00038 | 0.004925 |
360 | FEMALE SEX DIFFERENTIATION | 4 | 116 | 0.0003823 | 0.004942 |
361 | MULTICELLULAR ORGANISM REPRODUCTION | 9 | 768 | 0.0003891 | 0.005015 |
362 | TISSUE DEVELOPMENT | 13 | 1518 | 0.0003935 | 0.005058 |
363 | REGULATION OF PEPTIDYL SERINE PHOSPHORYLATION | 4 | 118 | 0.000408 | 0.005229 |
364 | REGULATION OF CELL CYCLE | 10 | 949 | 0.0004173 | 0.005335 |
365 | INNATE IMMUNE RESPONSE | 8 | 619 | 0.0004437 | 0.005657 |
366 | POSITIVE REGULATION OF DEVELOPMENTAL PROCESS | 11 | 1142 | 0.0004469 | 0.005681 |
367 | RESPONSE TO ESTROGEN | 5 | 218 | 0.000456 | 0.005781 |
368 | REGULATION OF EPITHELIAL CELL DIFFERENTIATION | 4 | 122 | 0.0004629 | 0.005837 |
369 | REGULATION OF NECROPTOTIC PROCESS | 2 | 11 | 0.0004626 | 0.005837 |
370 | REGULATION OF DNA METABOLIC PROCESS | 6 | 340 | 0.0004875 | 0.006097 |
371 | REGULATION OF T CELL MEDIATED IMMUNITY | 3 | 52 | 0.0004863 | 0.006097 |
372 | POSITIVE REGULATION OF INTRINSIC APOPTOTIC SIGNALING PATHWAY | 3 | 52 | 0.0004863 | 0.006097 |
373 | LIPID METABOLIC PROCESS | 11 | 1158 | 0.0005025 | 0.006269 |
374 | CELLULAR RESPONSE TO AMINO ACID STIMULUS | 3 | 53 | 0.0005144 | 0.0064 |
375 | NEGATIVE REGULATION OF DEVELOPMENTAL PROCESS | 9 | 801 | 0.0005279 | 0.006551 |
376 | NEGATIVE REGULATION OF REPRODUCTIVE PROCESS | 3 | 54 | 0.0005435 | 0.006673 |
377 | REGULATION OF LYMPHOCYTE APOPTOTIC PROCESS | 3 | 54 | 0.0005435 | 0.006673 |
378 | REGULATION OF MITOCHONDRIAL MEMBRANE POTENTIAL | 3 | 54 | 0.0005435 | 0.006673 |
379 | B CELL RECEPTOR SIGNALING PATHWAY | 3 | 54 | 0.0005435 | 0.006673 |
380 | REGULATION OF ENDOTHELIAL CELL DEVELOPMENT | 2 | 12 | 0.000554 | 0.006713 |
381 | SYSTEM PROCESS | 14 | 1785 | 0.0005513 | 0.006713 |
382 | I KAPPAB PHOSPHORYLATION | 2 | 12 | 0.000554 | 0.006713 |
383 | REGULATION OF ESTABLISHMENT OF ENDOTHELIAL BARRIER | 2 | 12 | 0.000554 | 0.006713 |
384 | POSITIVE REGULATION OF INTERLEUKIN 2 BIOSYNTHETIC PROCESS | 2 | 12 | 0.000554 | 0.006713 |
385 | REGULATION OF LEUKOCYTE DIFFERENTIATION | 5 | 232 | 0.0006049 | 0.007311 |
386 | TRANSMEMBRANE RECEPTOR PROTEIN TYROSINE KINASE SIGNALING PATHWAY | 7 | 498 | 0.0006338 | 0.007641 |
387 | APOPTOTIC MITOCHONDRIAL CHANGES | 3 | 57 | 0.0006371 | 0.00766 |
388 | HEPATOCYTE APOPTOTIC PROCESS | 2 | 13 | 0.0006535 | 0.007737 |
389 | POSITIVE REGULATION OF ENDOPLASMIC RETICULUM UNFOLDED PROTEIN RESPONSE | 2 | 13 | 0.0006535 | 0.007737 |
390 | REGULATION OF HISTONE PHOSPHORYLATION | 2 | 13 | 0.0006535 | 0.007737 |
391 | PROTEIN AUTOPROCESSING | 2 | 13 | 0.0006535 | 0.007737 |
392 | POSITIVE REGULATION OF MACROPHAGE DIFFERENTIATION | 2 | 13 | 0.0006535 | 0.007737 |
393 | REGULATION OF BICELLULAR TIGHT JUNCTION ASSEMBLY | 2 | 13 | 0.0006535 | 0.007737 |
394 | MUSCLE CELL DIFFERENTIATION | 5 | 237 | 0.0006661 | 0.007866 |
395 | POSITIVE REGULATION OF CYTOKINE BIOSYNTHETIC PROCESS | 3 | 58 | 0.0006705 | 0.007898 |
396 | CELL MOTILITY | 9 | 835 | 0.0007114 | 0.008338 |
397 | LOCALIZATION OF CELL | 9 | 835 | 0.0007114 | 0.008338 |
398 | ACTIVATION OF MAPK ACTIVITY | 4 | 137 | 0.0007162 | 0.008373 |
399 | POSITIVE REGULATION OF CELL CELL ADHESION | 5 | 243 | 0.0007455 | 0.008694 |
400 | CELL PROLIFERATION | 8 | 672 | 0.0007612 | 0.00881 |
401 | POSITIVE REGULATION OF EXTRINSIC APOPTOTIC SIGNALING PATHWAY IN ABSENCE OF LIGAND | 2 | 14 | 0.000761 | 0.00881 |
402 | POSITIVE REGULATION OF CYTOKINE PRODUCTION | 6 | 370 | 0.0007591 | 0.00881 |
403 | CELLULAR COMPONENT DISASSEMBLY | 7 | 515 | 0.0007723 | 0.008917 |
404 | OVARIAN FOLLICLE DEVELOPMENT | 3 | 61 | 0.0007772 | 0.008929 |
405 | CELLULAR RESPONSE TO HYDROGEN PEROXIDE | 3 | 61 | 0.0007772 | 0.008929 |
406 | POSITIVE REGULATION OF CELL CYCLE PROCESS | 5 | 247 | 0.0008022 | 0.009194 |
407 | PLATELET ACTIVATION | 4 | 142 | 0.0008189 | 0.009362 |
408 | NEGATIVE REGULATION OF KINASE ACTIVITY | 5 | 250 | 0.0008469 | 0.009658 |
409 | REGULATION OF CELL CELL ADHESION | 6 | 380 | 0.0008718 | 0.009918 |
410 | RESPONSE TO MURAMYL DIPEPTIDE | 2 | 15 | 0.0008764 | 0.009922 |
411 | APOPTOTIC DNA FRAGMENTATION | 2 | 15 | 0.0008764 | 0.009922 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | KINASE ACTIVITY | 20 | 842 | 1.449e-13 | 1.346e-10 |
2 | ENZYME BINDING | 26 | 1737 | 5.001e-13 | 2.323e-10 |
3 | CYTOKINE RECEPTOR BINDING | 13 | 271 | 9.043e-13 | 2.338e-10 |
4 | TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY BINDING | 8 | 47 | 1.007e-12 | 2.338e-10 |
5 | TRANSFERASE ACTIVITY TRANSFERRING PHOSPHORUS CONTAINING GROUPS | 20 | 992 | 2.978e-12 | 5.533e-10 |
6 | DEATH RECEPTOR BINDING | 6 | 18 | 9.164e-12 | 1.419e-09 |
7 | PHOSPHATIDYLINOSITOL 3 KINASE ACTIVITY | 8 | 70 | 2.868e-11 | 3.806e-09 |
8 | X1 PHOSPHATIDYLINOSITOL 3 KINASE ACTIVITY | 7 | 43 | 3.992e-11 | 4.636e-09 |
9 | PHOSPHATIDYLINOSITOL KINASE ACTIVITY | 7 | 51 | 1.408e-10 | 1.454e-08 |
10 | UBIQUITIN LIKE PROTEIN LIGASE BINDING | 11 | 264 | 2.752e-10 | 2.557e-08 |
11 | PROTEIN SERINE THREONINE KINASE ACTIVITY | 13 | 445 | 4.394e-10 | 3.711e-08 |
12 | CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY INVOLVED IN APOPTOTIC PROCESS | 5 | 15 | 5.515e-10 | 4.27e-08 |
13 | PROTEIN HETERODIMERIZATION ACTIVITY | 13 | 468 | 8.119e-10 | 5.802e-08 |
14 | PROTEIN DOMAIN SPECIFIC BINDING | 14 | 624 | 2.609e-09 | 1.731e-07 |
15 | PROTEIN KINASE ACTIVITY | 14 | 640 | 3.606e-09 | 2.234e-07 |
16 | CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY | 7 | 86 | 6.035e-09 | 3.504e-07 |
17 | KINASE BINDING | 13 | 606 | 1.797e-08 | 9.821e-07 |
18 | TUMOR NECROSIS FACTOR RECEPTOR BINDING | 5 | 30 | 2.53e-08 | 1.306e-06 |
19 | ADENYL NUCLEOTIDE BINDING | 19 | 1514 | 3.357e-08 | 1.641e-06 |
20 | KINASE REGULATOR ACTIVITY | 8 | 186 | 7.117e-08 | 3.306e-06 |
21 | INTERLEUKIN 1 RECEPTOR BINDING | 4 | 16 | 1.21e-07 | 5.355e-06 |
22 | PROTEIN DIMERIZATION ACTIVITY | 16 | 1149 | 1.335e-07 | 5.638e-06 |
23 | PROTEASE BINDING | 6 | 104 | 6.16e-07 | 2.488e-05 |
24 | RIBONUCLEOTIDE BINDING | 19 | 1860 | 8.434e-07 | 3.265e-05 |
25 | CYSTEINE TYPE PEPTIDASE ACTIVITY | 7 | 184 | 1.134e-06 | 4.213e-05 |
26 | IDENTICAL PROTEIN BINDING | 15 | 1209 | 1.548e-06 | 5.533e-05 |
27 | ENZYME REGULATOR ACTIVITY | 13 | 959 | 3.389e-06 | 0.0001166 |
28 | RECEPTOR BINDING | 16 | 1476 | 3.74e-06 | 0.0001241 |
29 | INSULIN RECEPTOR SUBSTRATE BINDING | 3 | 11 | 3.957e-06 | 0.0001267 |
30 | MOLECULAR FUNCTION REGULATOR | 15 | 1353 | 6.187e-06 | 0.0001916 |
31 | PROTEIN KINASE A BINDING | 4 | 42 | 7.03e-06 | 0.0002107 |
32 | PROTEIN KINASE A CATALYTIC SUBUNIT BINDING | 3 | 15 | 1.082e-05 | 0.0003141 |
33 | PHOSPHATIDYLINOSITOL PHOSPHATE KINASE ACTIVITY | 3 | 16 | 1.329e-05 | 0.0003741 |
34 | PROTEIN COMPLEX BINDING | 12 | 935 | 1.489e-05 | 0.0004069 |
35 | PROTEIN SERINE THREONINE PHOSPHATASE ACTIVITY | 4 | 64 | 3.803e-05 | 0.001009 |
36 | GROWTH FACTOR RECEPTOR BINDING | 5 | 129 | 3.911e-05 | 0.001009 |
37 | CAMP BINDING | 3 | 23 | 4.141e-05 | 0.00104 |
38 | PROTEIN SERINE THREONINE KINASE INHIBITOR ACTIVITY | 3 | 30 | 9.355e-05 | 0.002287 |
39 | CYCLIC NUCLEOTIDE BINDING | 3 | 36 | 0.0001625 | 0.00387 |
40 | PROTEIN HOMODIMERIZATION ACTIVITY | 9 | 722 | 0.0002471 | 0.00574 |
41 | SCAFFOLD PROTEIN BINDING | 3 | 45 | 0.0003168 | 0.007179 |
42 | ENDOPEPTIDASE ACTIVITY | 7 | 448 | 0.0003371 | 0.007457 |
43 | PROTEIN PHOSPHATASE BINDING | 4 | 120 | 0.0004348 | 0.009394 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | TRANSFERASE COMPLEX TRANSFERRING PHOSPHORUS CONTAINING GROUPS | 15 | 237 | 2.053e-16 | 1.199e-13 |
2 | CATALYTIC COMPLEX | 23 | 1038 | 5.332e-15 | 1.557e-12 |
3 | PHOSPHATIDYLINOSITOL 3 KINASE COMPLEX | 7 | 20 | 1.012e-13 | 1.97e-11 |
4 | MEMBRANE MICRODOMAIN | 12 | 288 | 3.875e-11 | 5.513e-09 |
5 | MEMBRANE PROTEIN COMPLEX | 19 | 1020 | 4.72e-11 | 5.513e-09 |
6 | PROTEIN KINASE COMPLEX | 8 | 90 | 2.25e-10 | 2.19e-08 |
7 | TRANSFERASE COMPLEX | 15 | 703 | 1.262e-09 | 1.053e-07 |
8 | CILIARY BASE | 5 | 23 | 6.069e-09 | 4.431e-07 |
9 | CYTOSOLIC PART | 9 | 223 | 1.756e-08 | 1.139e-06 |
10 | IKAPPAB KINASE COMPLEX | 3 | 11 | 3.957e-06 | 0.0002311 |
11 | EXTRINSIC COMPONENT OF MEMBRANE | 7 | 252 | 9.055e-06 | 0.0004807 |
12 | PHOSPHATASE COMPLEX | 4 | 48 | 1.206e-05 | 0.000587 |
13 | PLASMA MEMBRANE PROTEIN COMPLEX | 9 | 510 | 1.718e-05 | 0.0007719 |
14 | MEMBRANE REGION | 13 | 1134 | 2.058e-05 | 0.0008586 |
15 | PERINUCLEAR REGION OF CYTOPLASM | 9 | 642 | 0.0001025 | 0.003989 |
16 | PLASMA MEMBRANE RAFT | 4 | 86 | 0.0001211 | 0.00442 |
Num | Pathway | Pathview | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|---|
1 | hsa04210_Apoptosis | 59 | 89 | 1.176e-150 | 2.117e-148 | |
2 | hsa04620_Toll.like_receptor_signaling_pathway | 19 | 102 | 5.591e-30 | 3.842e-28 | |
3 | hsa04380_Osteoclast_differentiation | 20 | 128 | 6.404e-30 | 3.842e-28 | |
4 | hsa04662_B_cell_receptor_signaling_pathway | 17 | 75 | 2.005e-28 | 9.021e-27 | |
5 | hsa04722_Neurotrophin_signaling_pathway | 19 | 127 | 4.975e-28 | 1.791e-26 | |
6 | hsa04660_T_cell_receptor_signaling_pathway | 18 | 108 | 1.862e-27 | 5.586e-26 | |
7 | hsa04910_Insulin_signaling_pathway | 16 | 138 | 9.207e-22 | 2.368e-20 | |
8 | hsa04010_MAPK_signaling_pathway | 19 | 268 | 1.184e-21 | 2.664e-20 | |
9 | hsa04062_Chemokine_signaling_pathway | 17 | 189 | 3.611e-21 | 7.222e-20 | |
10 | hsa04370_VEGF_signaling_pathway | 13 | 76 | 4.122e-20 | 7.419e-19 | |
11 | hsa04014_Ras_signaling_pathway | 17 | 236 | 1.668e-19 | 2.729e-18 | |
12 | hsa04650_Natural_killer_cell_mediated_cytotoxicity | 14 | 136 | 2.336e-18 | 3.504e-17 | |
13 | hsa04151_PI3K_AKT_signaling_pathway | 18 | 351 | 5.441e-18 | 7.533e-17 | |
14 | hsa04914_Progesterone.mediated_oocyte_maturation | 12 | 87 | 1.979e-17 | 2.544e-16 | |
15 | hsa04973_Carbohydrate_digestion_and_absorption | 9 | 44 | 5.845e-15 | 7.014e-14 | |
16 | hsa04150_mTOR_signaling_pathway | 9 | 52 | 2.979e-14 | 3.352e-13 | |
17 | hsa04510_Focal_adhesion | 12 | 200 | 5.325e-13 | 5.639e-12 | |
18 | hsa04622_RIG.I.like_receptor_signaling_pathway | 9 | 71 | 5.778e-13 | 5.778e-12 | |
19 | hsa04630_Jak.STAT_signaling_pathway | 11 | 155 | 8.603e-13 | 8.15e-12 | |
20 | hsa04664_Fc_epsilon_RI_signaling_pathway | 9 | 79 | 1.568e-12 | 1.411e-11 | |
21 | hsa04012_ErbB_signaling_pathway | 9 | 87 | 3.838e-12 | 3.29e-11 | |
22 | hsa04621_NOD.like_receptor_signaling_pathway | 8 | 59 | 6.907e-12 | 5.651e-11 | |
23 | hsa04666_Fc_gamma_R.mediated_phagocytosis | 9 | 95 | 8.635e-12 | 6.758e-11 | |
24 | hsa04920_Adipocytokine_signaling_pathway | 8 | 68 | 2.256e-11 | 1.692e-10 | |
25 | hsa04960_Aldosterone.regulated_sodium_reabsorption | 7 | 42 | 3.35e-11 | 2.412e-10 | |
26 | hsa04115_p53_signaling_pathway | 7 | 69 | 1.26e-09 | 8.72e-09 | |
27 | hsa04070_Phosphatidylinositol_signaling_system | 7 | 78 | 3.022e-09 | 2.015e-08 | |
28 | hsa04623_Cytosolic_DNA.sensing_pathway | 6 | 56 | 1.47e-08 | 9.45e-08 | |
29 | hsa04670_Leukocyte_transendothelial_migration | 7 | 117 | 5.19e-08 | 3.221e-07 | |
30 | hsa04720_Long.term_potentiation | 6 | 70 | 5.75e-08 | 3.45e-07 | |
31 | hsa04114_Oocyte_meiosis | 6 | 114 | 1.058e-06 | 6.145e-06 | |
32 | hsa04810_Regulation_of_actin_cytoskeleton | 7 | 214 | 3.098e-06 | 1.743e-05 | |
33 | hsa04310_Wnt_signaling_pathway | 6 | 151 | 5.431e-06 | 2.963e-05 | |
34 | hsa04020_Calcium_signaling_pathway | 6 | 177 | 1.348e-05 | 7.137e-05 | |
35 | hsa04962_Vasopressin.regulated_water_reabsorption | 3 | 44 | 0.0002963 | 0.001524 | |
36 | hsa04742_Taste_transduction | 3 | 52 | 0.0004863 | 0.002431 | |
37 | hsa04340_Hedgehog_signaling_pathway | 3 | 56 | 0.0006049 | 0.002943 | |
38 | hsa00562_Inositol_phosphate_metabolism | 3 | 57 | 0.0006371 | 0.003018 | |
39 | hsa04976_Bile_secretion | 3 | 71 | 0.001209 | 0.005578 | |
40 | hsa04971_Gastric_acid_secretion | 3 | 74 | 0.001362 | 0.00613 | |
41 | hsa04141_Protein_processing_in_endoplasmic_reticulum | 4 | 168 | 0.001526 | 0.006699 | |
42 | hsa04640_Hematopoietic_cell_lineage | 3 | 88 | 0.00224 | 0.009599 | |
43 | hsa04970_Salivary_secretion | 3 | 89 | 0.002313 | 0.009683 | |
44 | hsa04540_Gap_junction | 3 | 90 | 0.002388 | 0.009768 | |
45 | hsa04912_GnRH_signaling_pathway | 3 | 101 | 0.003311 | 0.01295 | |
46 | hsa04916_Melanogenesis | 3 | 101 | 0.003311 | 0.01295 | |
47 | hsa04270_Vascular_smooth_muscle_contraction | 3 | 116 | 0.00488 | 0.01869 | |
48 | hsa04360_Axon_guidance | 3 | 130 | 0.006691 | 0.02509 | |
49 | hsa04530_Tight_junction | 2 | 133 | 0.05873 | 0.2158 | |
50 | hsa04740_Olfactory_transduction | 3 | 388 | 0.1067 | 0.3841 |
Num | lncRNA | miRNAs | miRNAs count | Gene | Sponge regulatory network | lncRNA log2FC | lncRNA pvalue | Gene log2FC | Gene pvalue | lncRNA-gene Pearson correlation |
---|---|---|---|---|---|---|---|---|---|---|
1 | DGCR5 | hsa-miR-107;hsa-miR-139-5p;hsa-miR-140-5p;hsa-miR-190a-5p;hsa-miR-192-5p;hsa-miR-215-5p;hsa-miR-29a-3p;hsa-miR-29c-3p;hsa-miR-362-3p;hsa-miR-375;hsa-miR-577 | 11 | IL1RAP | Sponge network | 1.383 | 0.01835 | 1.199 | 0.00709 | 0.476 |
2 | RFPL1S |
hsa-miR-106b-5p;hsa-miR-107;hsa-miR-17-3p;hsa-miR-29a-3p;hsa-miR-29b-3p;hsa-miR-320b;hsa-miR-33a-3p;hsa-miR-362-3p;hsa-miR-501-3p;hsa-miR-502-3p;hsa-miR-505-3p | 11 | AKT3 | Sponge network | -0.223 | 0.70704 | -0.749 | 0.06936 | 0.466 |
3 | EMX2OS |
hsa-miR-107;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-3p;hsa-miR-17-5p;hsa-miR-32-3p;hsa-miR-335-3p;hsa-miR-362-3p;hsa-miR-501-3p;hsa-miR-502-3p;hsa-miR-505-3p;hsa-miR-577 | 12 | AKT3 | Sponge network | -1.088 | 0.10042 | -0.749 | 0.06936 | 0.354 |
4 | MEG3 |
hsa-miR-106b-5p;hsa-miR-107;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-3p;hsa-miR-17-5p;hsa-miR-320b;hsa-miR-335-3p;hsa-miR-33a-3p;hsa-miR-577;hsa-miR-616-5p | 11 | AKT3 | Sponge network | -1.645 | 0.00049 | -0.749 | 0.06936 | 0.312 |
5 | PCA3 |
hsa-miR-103a-3p;hsa-miR-106b-5p;hsa-miR-107;hsa-miR-128-3p;hsa-miR-144-3p;hsa-miR-15b-5p;hsa-miR-16-2-3p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-185-5p;hsa-miR-188-5p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-22-5p;hsa-miR-221-3p;hsa-miR-222-3p;hsa-miR-32-3p;hsa-miR-320b;hsa-miR-324-3p;hsa-miR-330-3p;hsa-miR-424-5p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-629-3p;hsa-miR-96-5p | 28 | PIK3R1 | Sponge network | -2.778 | 8.0E-5 | -1.094 | 2.0E-5 | 0.309 |
6 | PCA3 |
hsa-let-7f-1-3p;hsa-miR-141-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-183-5p;hsa-miR-18a-5p;hsa-miR-200c-3p;hsa-miR-330-3p;hsa-miR-590-5p;hsa-miR-93-5p;hsa-miR-96-5p | 11 | PRKACB | Sponge network | -2.778 | 8.0E-5 | -2.003 | 0 | 0.257 |