Schematic overview of the cellular and molecular mechanisms involved in the cancer progression, including the proposed cellular and molecular mechanisms in cancer cells trajectory. AT1: alveolar type 1 cells; AT2: alveolar type 2 cells; AAH: atypical adenomatous hyperplasia; AIS: adenocarcinoma in situ; MIA: minimally invasive adenocarcinoma; IA: invasive adenocarcinoma; EMT: epithelial-mesenchymal transition

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Center for Computational Systems Medicine
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Gene summary

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Malignant transformation analysis

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Malignant transformation related pathway analysis

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Cell-cell communication analysis

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Single-cell gene regulatory network inference analysis

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Somatic mutation of malignant transformation related genes

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Related drugs of malignant transformation related genes

Gene: F5

Gene summary for F5

check button Gene summary.

Gene informationSpeciesHuman
Gene symbol

F5

Gene ID

2153

Gene namecoagulation factor V
Gene AliasFVL
Cytomap1q24.2
Gene Typeprotein-coding
GO ID

GO:0003008

UniProtAcc

P12259


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Malignant transformation analysis

check button Identification of the aberrant gene expression in precancerous and cancerous lesions by comparing the gene expression of stem-like cells in diseased tissues with normal stem cells
check button Malignant transformation involving gene list.
Entrez IDSymbolReplicatesSpeciesOrganTissueAdj P-valueLog2FCMalignancy
2153F5NAFLD1HumanLiverNAFLD2.36e-141.30e+00-0.04
2153F5S43HumanLiverCirrhotic7.16e-061.41e-01-0.0187
2153F5HCC1_MengHumanLiverHCC5.06e-97-7.26e-020.0246
2153F5HCC2_MengHumanLiverHCC1.66e-27-1.89e-010.0107
2153F5cirrhotic1HumanLiverCirrhotic4.04e-09-3.08e-010.0202
2153F5cirrhotic2HumanLiverCirrhotic3.27e-10-2.70e-010.0201
2153F5cirrhotic3HumanLiverCirrhotic2.56e-07-1.14e-010.0215
2153F5HCC1HumanLiverHCC1.21e-346.43e+000.5336
2153F5HCC2HumanLiverHCC4.56e-344.38e+000.5341
2153F5HCC5HumanLiverHCC7.21e-043.72e+000.4932
2153F5Pt13.aHumanLiverHCC5.64e-06-1.36e-010.021
2153F5Pt13.bHumanLiverHCC1.32e-06-1.78e-010.0251
2153F5Pt14.aHumanLiverHCC4.03e-067.07e-020.0169
2153F5Pt14.bHumanLiverHCC2.04e-026.43e-020.018
2153F5Pt14.dHumanLiverHCC3.40e-06-7.53e-020.0143
2153F5S014HumanLiverHCC1.60e-201.49e+000.2254
2153F5S015HumanLiverHCC1.05e-151.38e+000.2375
2153F5S016HumanLiverHCC5.00e-191.25e+000.2243
2153F5S027HumanLiverHCC1.52e-111.18e+000.2446
2153F5S028HumanLiverHCC1.29e-251.29e+000.2503
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check button Transcriptomic changes along malignancy continuum.
TissueExpression DynamicsAbbreviation
LiverThe image shows the transcriptomic changes along malignancy continuum.log2FC in expression of this searched gene in stem-like cells from each diseased tissue sample relative to stem-like cells in normal samples in each tissue plotted against the malignancy continuum. Samples are colored based on if they are from different disease stage.HCC: Hepatocellular carcinoma
NAFLD: Non-alcoholic fatty liver disease
∗log2FC in expression of this searched gene in stem-like cells from each diseased tissue sample relative to stem-like cells in normal samples in each tissue plotted against the malignancy continuum. Samples are colored based on if they are from different disease stage.

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Malignant transformation related pathway analysis

check buttonFind out the enriched GO biological processes and KEGG pathways involved in transition from healthy to precancer to cancer
check button Figure of enriched GO biological processes.
TissueDisease StageEnriched GO biological Processes
ColorectumADGO analysis - Figure of enriched GO biological processes: Top 15 enriched GO BP terms are showed in the bar plot of each disease state in each tissue. Each row represents a significant GO biological process which is colored according to the -log10(p.adjust).
ColorectumSERGO analysis - Figure of enriched GO biological processes: Top 15 enriched GO BP terms are showed in the bar plot of each disease state in each tissue. Each row represents a significant GO biological process which is colored according to the -log10(p.adjust).
ColorectumMSSGO analysis - Figure of enriched GO biological processes: Top 15 enriched GO BP terms are showed in the bar plot of each disease state in each tissue. Each row represents a significant GO biological process which is colored according to the -log10(p.adjust).
ColorectumMSI-HGO analysis - Figure of enriched GO biological processes: Top 15 enriched GO BP terms are showed in the bar plot of each disease state in each tissue. Each row represents a significant GO biological process which is colored according to the -log10(p.adjust).
ColorectumFAPGO analysis - Figure of enriched GO biological processes: Top 15 enriched GO BP terms are showed in the bar plot of each disease state in each tissue. Each row represents a significant GO biological process which is colored according to the -log10(p.adjust).
∗Top 15 enriched GO BP terms are showed in the bar plot of each disease state in each tissue. Each row represents a significant GO biological process which is colored according to the -log10(p.adjust).
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check button Enriched GO biological processes.
GO IDTissueDisease StageDescriptionGene RatioBg Ratiopvaluep.adjustCount
GO:190458918ThyroidATCregulation of protein import41/629363/187233.19e-074.76e-0641
GO:006145827ThyroidATCreproductive system development193/6293427/187233.32e-074.92e-06193
GO:007137524ThyroidATCcellular response to peptide hormone stimulus138/6293290/187234.90e-077.05e-06138
GO:004851124ThyroidATCrhythmic process141/6293298/187235.58e-077.93e-06141
GO:012003223ThyroidATCregulation of plasma membrane bounded cell projection assembly95/6293186/187236.13e-078.49e-0695
GO:005164818ThyroidATCvesicle localization91/6293177/187237.21e-079.64e-0691
GO:004860825ThyroidATCreproductive structure development190/6293424/187238.40e-071.11e-05190
GO:0060491111ThyroidATCregulation of cell projection assembly95/6293188/187231.14e-061.47e-0595
GO:003286824ThyroidATCresponse to insulin126/6293264/187231.24e-061.59e-05126
GO:006053724ThyroidATCmuscle tissue development181/6293403/187231.27e-061.62e-05181
GO:003150316ThyroidATCprotein-containing complex localization108/6293220/187231.33e-061.69e-05108
GO:003286923ThyroidATCcellular response to insulin stimulus101/6293203/187231.34e-061.69e-05101
GO:005105618ThyroidATCregulation of small GTPase mediated signal transduction141/6293302/187231.43e-061.77e-05141
GO:003103226ThyroidATCactomyosin structure organization98/6293196/187231.44e-061.77e-0598
GO:001063231ThyroidATCregulation of epithelial cell migration137/6293292/187231.44e-061.77e-05137
GO:005110133ThyroidATCregulation of DNA binding64/6293118/187233.10e-063.54e-0564
GO:003288613ThyroidATCregulation of microtubule-based process114/6293240/187235.17e-065.59e-05114
GO:003312033ThyroidATCpositive regulation of RNA splicing26/629337/187235.64e-066.00e-0526
GO:1905477111ThyroidATCpositive regulation of protein localization to membrane58/6293106/187236.14e-066.42e-0558
GO:003223128ThyroidATCregulation of actin filament bundle assembly57/6293105/187231.01e-051.00e-0457
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check button Enriched KEGG pathways.
Pathway IDTissueDisease StageDescriptionGene RatioBg Ratiopvaluep.adjustqvalueCount
hsa04610LiverNAFLDComplement and coagulation cascades35/104386/84652.48e-112.04e-091.64e-0935
hsa046101LiverNAFLDComplement and coagulation cascades35/104386/84652.48e-112.04e-091.64e-0935
hsa046102LiverCirrhoticComplement and coagulation cascades48/253086/84654.41e-075.44e-063.35e-0648
hsa046103LiverCirrhoticComplement and coagulation cascades48/253086/84654.41e-075.44e-063.35e-0648
hsa046104LiverHCCComplement and coagulation cascades57/402086/84653.19e-041.45e-038.04e-0457
hsa046105LiverHCCComplement and coagulation cascades57/402086/84653.19e-041.45e-038.04e-0457
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Cell-cell communication analysis

check buttonIdentification of potential cell-cell interactions between two cell types and their ligand-receptor pairs for different disease states
LigandReceptorLRpairPathwayTissueDisease Stage
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Single-cell gene regulatory network inference analysis

check buttonFind out the significant the regulons (TFs) and the target genes of each regulon across cell types for different disease states
TFCell TypeTissueDisease StageTarget GeneRSSRegulon Activity
∗The dot plots of a searched regulon are shown for all cell subpopulations in each disease state of each tissue based on the regulon specific score inferred using pySCENIC and by calculating the average expression.
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Somatic mutation of malignant transformation related genes

check buttonAnnotation of somatic variants for genes involved in malignant transformation
Hugo SymbolVariant ClassVariant ClassificationdbSNP RSHGVScHGVSpHGVSp ShortSWISSPROTBIOTYPESIFTPolyPhenTumor Sample BarcodeTissueHistologySexAgeStageTherapy TypesDrugsOutcome
F5SNVMissense_Mutationnovelc.4241N>Tp.Asp1414Valp.D1414VP12259protein_codingdeleterious_low_confidence(0.04)benign(0.209)TCGA-A2-A4RW-01Breastbreast invasive carcinomaFemale<65III/IVUnknownUnknownSD
F5SNVMissense_Mutationnovelc.3913N>Gp.Pro1305Alap.P1305AP12259protein_codingdeleterious_low_confidence(0.03)benign(0.265)TCGA-A2-A4RW-01Breastbreast invasive carcinomaFemale<65III/IVUnknownUnknownSD
F5SNVMissense_Mutationnovelc.1495C>Ap.Gln499Lysp.Q499KP12259protein_codingdeleterious(0.02)possibly_damaging(0.541)TCGA-A7-A0DB-01Breastbreast invasive carcinomaFemale<65I/IIHormone TherapyarimidexSD
F5SNVMissense_Mutationc.6397N>Tp.Ile2133Leup.I2133LP12259protein_codingdeleterious(0.02)possibly_damaging(0.622)TCGA-A8-A06Z-01Breastbreast invasive carcinomaFemale>=65I/IIUnknownUnknownSD
F5SNVMissense_Mutationc.6396N>Tp.Lys2132Asnp.K2132NP12259protein_codingdeleterious(0)probably_damaging(0.996)TCGA-A8-A07L-01Breastbreast invasive carcinomaFemale<65III/IVChemotherapyCR
F5SNVMissense_Mutationnovelc.4087N>Ap.His1363Asnp.H1363NP12259protein_codingtolerated_low_confidence(0.14)benign(0.023)TCGA-A8-A08R-01Breastbreast invasive carcinomaFemale<65I/IIUnknownUnknownSD
F5SNVMissense_Mutationnovelc.4086N>Ap.Ser1362Argp.S1362RP12259protein_codingtolerated_low_confidence(0.09)benign(0.168)TCGA-A8-A08R-01Breastbreast invasive carcinomaFemale<65I/IIUnknownUnknownSD
F5SNVMissense_Mutationc.622G>Cp.Asp208Hisp.D208HP12259protein_codingtolerated(0.13)benign(0.123)TCGA-A8-A09G-01Breastbreast invasive carcinomaFemale>=65III/IVUnknownUnknownSD
F5SNVMissense_Mutationc.1447N>Ap.Tyr483Asnp.Y483NP12259protein_codingdeleterious(0)probably_damaging(0.998)TCGA-A8-A09I-01Breastbreast invasive carcinomaFemale>=65I/IIHormone TherapyanastrozoleSD
F5SNVMissense_Mutationnovelc.5676N>Cp.Gln1892Hisp.Q1892HP12259protein_codingdeleterious(0.04)probably_damaging(0.999)TCGA-AC-A3BB-01Breastbreast invasive carcinomaFemale<65III/IVChemotherapycytoxanCR
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Related drugs of malignant transformation related genes

check buttonIdentification of chemicals and drugs interact with genes involved in malignant transfromation
(DGIdb 4.0)
Entrez IDSymbolCategoryInteraction TypesDrug Claim NameDrug NamePMIDs
2153F5DRUGGABLE GENOMEdrotrecogin alfa15118525
2153F5DRUGGABLE GENOMErivaroxabanRIVAROXABAN
2153F5DRUGGABLE GENOMERivaroxabanRIVAROXABAN
2153F5DRUGGABLE GENOMEestrogensESTRONE SODIUM SULFATE11532625,16113779,12067913,12869355,16301339,9459317,10073976,15467059,11859850,10943572,12069454,12138364,14551147,7968118,11703344
2153F5DRUGGABLE GENOMEDrotrecogin alfa
2153F5DRUGGABLE GENOMEEltrombopagELTROMBOPAG
2153F5DRUGGABLE GENOMEDROTRECOGIN ALFA
2153F5DRUGGABLE GENOMEhormonal contraceptives for systemic use11532625,16113779,15208046,15946211,12869355,16301339,9459317,10073976,15467059,11859850,10943572,12069454,16769590,12138364,14551147,7968118
2153F5DRUGGABLE GENOMEinhibitorCHEMBL2109065DROTRECOGIN ALFA (ACTIVATED)
2153F5DRUGGABLE GENOMETHROMBINTHROMBIN
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