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: CYP4X1

Gene summary for CYP4X1

check button Gene summary.

Gene informationSpeciesHuman
Gene symbol

CYP4X1

Gene ID

260293

Gene namecytochrome P450 family 4 subfamily X member 1
Gene AliasCYPIVX1
Cytomap1p33
Gene Typeprotein-coding
GO ID

GO:0005575

UniProtAcc

Q8N118


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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
260293CYP4X1HTA11_866_3004761011HumanColorectumAD8.57e-083.42e-010.096
260293CYP4X1HTA11_7696_3000711011HumanColorectumAD1.70e-082.02e-010.0674
260293CYP4X1HTA11_99999970781_79442HumanColorectumMSS3.35e-297.96e-010.294
260293CYP4X1A002-C-010HumanColorectumFAP5.22e-032.62e-010.242
260293CYP4X1A002-C-021HumanColorectumFAP5.06e-205.09e-010.1171
260293CYP4X1LZE8THumanEsophagusESCC1.59e-104.35e-010.067
260293CYP4X1LZE24THumanEsophagusESCC9.35e-166.72e-010.0596
260293CYP4X1P2T-EHumanEsophagusESCC2.34e-204.89e-010.1177
260293CYP4X1P4T-EHumanEsophagusESCC2.89e-022.22e-020.1323
260293CYP4X1P8T-EHumanEsophagusESCC6.59e-234.26e-010.0889
260293CYP4X1P16T-EHumanEsophagusESCC2.48e-04-1.07e-020.1153
260293CYP4X1P20T-EHumanEsophagusESCC1.96e-246.94e-010.1124
260293CYP4X1P22T-EHumanEsophagusESCC1.22e-066.65e-020.1236
260293CYP4X1P23T-EHumanEsophagusESCC2.56e-036.38e-020.108
260293CYP4X1P27T-EHumanEsophagusESCC6.83e-132.93e-010.1055
260293CYP4X1P28T-EHumanEsophagusESCC2.45e-02-5.20e-020.1149
260293CYP4X1P32T-EHumanEsophagusESCC2.34e-02-5.66e-020.1666
260293CYP4X1P40T-EHumanEsophagusESCC6.26e-041.54e-010.109
260293CYP4X1P42T-EHumanEsophagusESCC8.24e-104.30e-010.1175
260293CYP4X1P48T-EHumanEsophagusESCC3.26e-132.44e-010.0959
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check button Transcriptomic changes along malignancy continuum.
TissueExpression DynamicsAbbreviation
Colorectum (GSE201348)The 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.FAP: Familial adenomatous polyposis
CRC: Colorectal cancer
Colorectum (HTA11)The 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.AD: Adenomas
SER: Sessile serrated lesions
MSI-H: Microsatellite-high colorectal cancer
MSS: Microsatellite stable colorectal cancer
EsophagusThe 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.ESCC: Esophageal squamous cell carcinoma
HGIN: High-grade intraepithelial neoplasias
LGIN: Low-grade intraepithelial neoplasias
Oral CavityThe 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.EOLP: Erosive Oral lichen planus
LP: leukoplakia
NEOLP: Non-erosive oral lichen planus
OSCC: Oral squamous cell carcinoma
∗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
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check button Enriched KEGG pathways.
Pathway IDTissueDisease StageDescriptionGene RatioBg Ratiopvaluep.adjustqvalueCount
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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
CYP4X1SNVMissense_Mutationrs778935923c.671N>Gp.Phe224Cysp.F224CQ8N118protein_codingtolerated(0.15)possibly_damaging(0.886)TCGA-BH-A0DZ-01Breastbreast invasive carcinomaFemale<65I/IIChemotherapydocetaxelSD
CYP4X1SNVMissense_Mutationrs751651489c.836N>Gp.Pro279Argp.P279RQ8N118protein_codingtolerated(0.56)benign(0.009)TCGA-BH-A1FC-01Breastbreast invasive carcinomaFemale>=65I/IIUnknownUnknownSD
CYP4X1SNVMissense_Mutationc.664A>Gp.Ile222Valp.I222VQ8N118protein_codingdeleterious(0.02)possibly_damaging(0.574)TCGA-D8-A1J8-01Breastbreast invasive carcinomaFemale>=65I/IIHormone TherapynolvadexSD
CYP4X1SNVMissense_Mutationnovelc.349N>Ap.Ser117Thrp.S117TQ8N118protein_codingdeleterious(0.01)benign(0)TCGA-OL-A66K-01Breastbreast invasive carcinomaFemale>=65I/IIUnknownUnknownSD
CYP4X1SNVMissense_Mutationnovelc.1219N>Tp.Val407Phep.V407FQ8N118protein_codingtolerated(0.75)benign(0.03)TCGA-OL-A6VO-01Breastbreast invasive carcinomaFemale<65I/IIChemotherapytaxotereCR
CYP4X1insertionIn_Frame_Insnovelc.977_978insAAGAAAp.Ser326_Trp327insArgAsnp.S326_W327insRNQ8N118protein_codingTCGA-A8-A08H-01Breastbreast invasive carcinomaFemale>=65I/IIUnknownUnknownSD
CYP4X1insertionIn_Frame_Insnovelc.978_979insTTCCCTTCAAAACATTTATTTGTAAAATCACTTp.Ser326_Trp327insPheProSerLysHisLeuPheValLysSerLeup.S326_W327insFPSKHLFVKSLQ8N118protein_codingTCGA-A8-A08H-01Breastbreast invasive carcinomaFemale>=65I/IIUnknownUnknownSD
CYP4X1insertionNonsense_Mutationnovelc.749_750insTAAGACCTATCGGTCGACCTGAACTTTTAAAATTTCp.Leu250delinsPheLysThrTyrArgSerThrTerThrPheLysIleSerp.L250delinsFKTYRST*TFKISQ8N118protein_codingTCGA-B6-A0RG-01Breastbreast invasive carcinomaFemale<65I/IIUnknownUnknownSD
CYP4X1SNVMissense_Mutationnovelc.638C>Tp.Ala213Valp.A213VQ8N118protein_codingtolerated(0.32)benign(0.001)TCGA-2W-A8YY-01Cervixcervical & endocervical cancerFemale<65I/IIChemotherapycisplatinCR
CYP4X1SNVMissense_Mutationc.160T>Cp.Phe54Leup.F54LQ8N118protein_codingtolerated(1)benign(0.013)TCGA-FU-A3HZ-01Cervixcervical & endocervical cancerFemale<65I/IIChemotherapycisplatinCR
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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
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