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Gene: IRF6 |
Gene summary for IRF6 |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | IRF6 | Gene ID | 3664 |
| Gene name | interferon regulatory factor 6 | |
| Gene Alias | LPS | |
| Cytomap | 1q32.2 | |
| Gene Type | protein-coding | GO ID | GO:0002376 | UniProtAcc | O14896 |
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Malignant transformation analysis |
| 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 |
| Malignant transformation involving gene list. |
| Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
| 3664 | IRF6 | CA_HPV_1 | Human | Cervix | CC | 6.46e-03 | -1.63e-01 | 0.0264 |
| 3664 | IRF6 | CA_HPV_2 | Human | Cervix | CC | 2.76e-02 | 2.19e-01 | 0.0391 |
| 3664 | IRF6 | CCI_1 | Human | Cervix | CC | 1.46e-02 | 9.11e-01 | 0.528 |
| 3664 | IRF6 | Tumor | Human | Cervix | CC | 1.43e-23 | 5.34e-01 | 0.1241 |
| 3664 | IRF6 | sample1 | Human | Cervix | CC | 3.26e-08 | 5.58e-01 | 0.0959 |
| 3664 | IRF6 | sample3 | Human | Cervix | CC | 8.57e-41 | 6.45e-01 | 0.1387 |
| 3664 | IRF6 | T1 | Human | Cervix | CC | 4.31e-13 | 4.83e-01 | 0.0918 |
| 3664 | IRF6 | T3 | Human | Cervix | CC | 1.33e-28 | 6.32e-01 | 0.1389 |
| 3664 | IRF6 | HTA11_2487_2000001011 | Human | Colorectum | SER | 1.65e-03 | 3.23e-01 | -0.1808 |
| 3664 | IRF6 | HTA11_1938_2000001011 | Human | Colorectum | AD | 2.37e-04 | 3.17e-01 | -0.0811 |
| 3664 | IRF6 | HTA11_78_2000001011 | Human | Colorectum | AD | 2.10e-09 | 5.13e-01 | -0.1088 |
| 3664 | IRF6 | HTA11_347_2000001011 | Human | Colorectum | AD | 1.77e-16 | 4.70e-01 | -0.1954 |
| 3664 | IRF6 | HTA11_411_2000001011 | Human | Colorectum | SER | 3.37e-06 | 8.34e-01 | -0.2602 |
| 3664 | IRF6 | HTA11_83_2000001011 | Human | Colorectum | SER | 9.38e-05 | 2.77e-01 | -0.1526 |
| 3664 | IRF6 | HTA11_2992_2000001011 | Human | Colorectum | SER | 1.27e-04 | 4.51e-01 | -0.1706 |
| 3664 | IRF6 | HTA11_5212_2000001011 | Human | Colorectum | AD | 3.63e-02 | 3.83e-01 | -0.2061 |
| 3664 | IRF6 | HTA11_6801_2000001011 | Human | Colorectum | SER | 1.33e-02 | 3.75e-01 | 0.0171 |
| 3664 | IRF6 | HTA11_99999965104_69814 | Human | Colorectum | MSS | 1.32e-03 | 2.95e-01 | 0.281 |
| 3664 | IRF6 | HTA11_99999971662_82457 | Human | Colorectum | MSS | 1.77e-09 | 2.52e-01 | 0.3859 |
| 3664 | IRF6 | LZE4T | Human | Esophagus | ESCC | 8.10e-08 | 5.81e-01 | 0.0811 |
| Page: 1 2 3 4 5 6 |
| Transcriptomic changes along malignancy continuum. |
| Tissue | Expression Dynamics | Abbreviation |
| Cervix |  | CC: Cervix cancer |
| HSIL_HPV: HPV-infected high-grade squamous intraepithelial lesions | ||
| N_HPV: HPV-infected normal cervix | ||
| Colorectum (GSE201348) |  | FAP: Familial adenomatous polyposis |
| CRC: Colorectal cancer | ||
| Colorectum (HTA11) |  | AD: Adenomas |
| SER: Sessile serrated lesions | ||
| MSI-H: Microsatellite-high colorectal cancer | ||
| MSS: Microsatellite stable colorectal cancer | ||
| Esophagus |  | ESCC: Esophageal squamous cell carcinoma |
| HGIN: High-grade intraepithelial neoplasias | ||
| LGIN: Low-grade intraepithelial neoplasias | ||
| Liver |  | HCC: Hepatocellular carcinoma |
| NAFLD: Non-alcoholic fatty liver disease | ||
| Oral Cavity |  | EOLP: Erosive Oral lichen planus |
| LP: leukoplakia | ||
| NEOLP: Non-erosive oral lichen planus | ||
| OSCC: Oral squamous cell carcinoma | ||
| Skin |  | AK: Actinic keratosis |
| cSCC: Cutaneous squamous cell carcinoma | ||
| SCCIS:squamous cell carcinoma in situ |
| ∗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 |
| Find out the enriched GO biological processes and KEGG pathways involved in transition from healthy to precancer to cancer |
| Figure of enriched GO biological processes. |
| Tissue | Disease Stage | Enriched GO biological Processes |
| Colorectum | AD |  |
| Colorectum | SER |  |
| Colorectum | MSS |  |
| Colorectum | MSI-H |  |
| Colorectum | FAP |  |
| ∗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). |
| Page: 1 2 3 4 5 6 7 8 9 |
| Enriched GO biological processes. |
| GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
| GO:00085446 | Cervix | CC | epidermis development | 83/2311 | 324/18723 | 3.91e-11 | 8.54e-09 | 83 |
| GO:00435884 | Cervix | CC | skin development | 71/2311 | 263/18723 | 8.04e-11 | 1.46e-08 | 71 |
| GO:00506737 | Cervix | CC | epithelial cell proliferation | 98/2311 | 437/18723 | 2.01e-09 | 2.15e-07 | 98 |
| GO:00302164 | Cervix | CC | keratinocyte differentiation | 42/2311 | 139/18723 | 1.74e-08 | 1.28e-06 | 42 |
| GO:00099137 | Cervix | CC | epidermal cell differentiation | 53/2311 | 202/18723 | 5.48e-08 | 3.25e-06 | 53 |
| GO:004873210 | Cervix | CC | gland development | 84/2311 | 436/18723 | 1.93e-05 | 3.54e-04 | 84 |
| GO:00436164 | Cervix | CC | keratinocyte proliferation | 15/2311 | 46/18723 | 2.70e-04 | 2.97e-03 | 15 |
| GO:00487365 | Cervix | CC | appendage development | 35/2311 | 172/18723 | 1.88e-03 | 1.39e-02 | 35 |
| GO:00601735 | Cervix | CC | limb development | 35/2311 | 172/18723 | 1.88e-03 | 1.39e-02 | 35 |
| GO:00308797 | Cervix | CC | mammary gland development | 28/2311 | 137/18723 | 4.74e-03 | 2.83e-02 | 28 |
| GO:0048732 | Colorectum | AD | gland development | 149/3918 | 436/18723 | 6.07e-11 | 6.33e-09 | 149 |
| GO:0030879 | Colorectum | AD | mammary gland development | 53/3918 | 137/18723 | 1.46e-06 | 4.58e-05 | 53 |
| GO:0061180 | Colorectum | AD | mammary gland epithelium development | 28/3918 | 67/18723 | 8.74e-05 | 1.35e-03 | 28 |
| GO:0050673 | Colorectum | AD | epithelial cell proliferation | 119/3918 | 437/18723 | 8.75e-04 | 8.51e-03 | 119 |
| GO:0043616 | Colorectum | AD | keratinocyte proliferation | 19/3918 | 46/18723 | 1.36e-03 | 1.19e-02 | 19 |
| GO:0048736 | Colorectum | AD | appendage development | 51/3918 | 172/18723 | 4.20e-03 | 2.89e-02 | 51 |
| GO:0060173 | Colorectum | AD | limb development | 51/3918 | 172/18723 | 4.20e-03 | 2.89e-02 | 51 |
| GO:0009913 | Colorectum | AD | epidermal cell differentiation | 58/3918 | 202/18723 | 5.16e-03 | 3.42e-02 | 58 |
| GO:0008544 | Colorectum | AD | epidermis development | 87/3918 | 324/18723 | 5.99e-03 | 3.76e-02 | 87 |
| GO:00487321 | Colorectum | SER | gland development | 112/2897 | 436/18723 | 1.75e-08 | 1.28e-06 | 112 |
| Page: 1 2 3 4 5 |
| Enriched KEGG pathways. |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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Cell-cell communication analysis |
| Identification of potential cell-cell interactions between two cell types and their ligand-receptor pairs for different disease states |
| Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
| Page: 1 |
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Single-cell gene regulatory network inference analysis |
| Find out the significant the regulons (TFs) and the target genes of each regulon across cell types for different disease states |
| TF | Cell Type | Tissue | Disease Stage | Target Gene | RSS | Regulon Activity |
| IRF6 | CAF | Breast | ADJ | KRT17,SFN,KRT14, etc. | 9.99e-02 |  |
| IRF6 | pDC | Prostate | Healthy | ANXA2,TRAF4,TACSTD2, etc. | 2.47e-01 |  |
| IRF6 | FIB | Prostate | ADJ | KLF5,LAMC2,PERP, etc. | 8.32e-02 |  |
| IRF6 | INFIB | Prostate | ADJ | KLF5,LAMC2,PERP, etc. | 1.11e-01 | |
| IRF6 | INFIB | Prostate | BPH | KLF5,LAMC2,PERP, etc. | 2.67e-01 |  |
| IRF6 | INFIB | Prostate | Healthy | KLF5,LAMC2,PERP, etc. | 3.74e-01 | |
| IRF6 | INFIB | Prostate | Tumor | KLF5,LAMC2,PERP, etc. | 7.40e-02 |  |
| IRF6 | KER | Skin | Healthy | SFN,SERPINB5,LYPD3, etc. | 1.99e-01 |  |
| ∗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. |
| Page: 1 |
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Somatic mutation of malignant transformation related genes |
| Annotation of somatic variants for genes involved in malignant transformation |
| Hugo Symbol | Variant Class | Variant Classification | dbSNP RS | HGVSc | HGVSp | HGVSp Short | SWISSPROT | BIOTYPE | SIFT | PolyPhen | Tumor Sample Barcode | Tissue | Histology | Sex | Age | Stage | Therapy Types | Drugs | Outcome |
| IRF6 | SNV | Missense_Mutation | rs201017955 | c.781N>C | p.Asp261His | p.D261H | O14896 | protein_coding | deleterious(0.01) | probably_damaging(0.951) | TCGA-A8-A08R-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
| IRF6 | SNV | Missense_Mutation | c.250N>A | p.Arg84Ser | p.R84S | O14896 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-C8-A1HL-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | |
| IRF6 | SNV | Missense_Mutation | c.899N>C | p.Arg300Thr | p.R300T | O14896 | protein_coding | deleterious(0.04) | probably_damaging(1) | TCGA-D8-A1JA-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | adriamycin | PD | |
| IRF6 | SNV | Missense_Mutation | c.38G>C | p.Trp13Ser | p.W13S | O14896 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-E2-A10C-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | SD | |
| IRF6 | SNV | Missense_Mutation | c.214N>A | p.Asp72Asn | p.D72N | O14896 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-DR-A0ZM-01 | Cervix | cervical & endocervical cancer | Female | <65 | III/IV | Unspecific | Cisplatin | SD | |
| IRF6 | SNV | Missense_Mutation | c.1296N>G | p.Ile432Met | p.I432M | O14896 | protein_coding | tolerated(0.88) | benign(0.201) | TCGA-IR-A3LH-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
| IRF6 | SNV | Missense_Mutation | c.315G>T | p.Met105Ile | p.M105I | O14896 | protein_coding | tolerated(0.5) | possibly_damaging(0.593) | TCGA-AA-3510-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
| IRF6 | SNV | Missense_Mutation | c.301N>G | p.Lys101Glu | p.K101E | O14896 | protein_coding | deleterious(0) | possibly_damaging(0.648) | TCGA-AA-3715-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |
| IRF6 | SNV | Missense_Mutation | c.772N>T | p.Pro258Ser | p.P258S | O14896 | protein_coding | deleterious(0) | probably_damaging(0.949) | TCGA-AA-3930-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | capecitabine | PD | |
| IRF6 | SNV | Missense_Mutation | c.274G>A | p.Glu92Lys | p.E92K | O14896 | protein_coding | deleterious(0.03) | probably_damaging(0.988) | TCGA-AA-A00N-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
| Page: 1 2 3 4 5 6 7 8 |
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Related drugs of malignant transformation related genes |
| Identification of chemicals and drugs interact with genes involved in malignant transfromation |
| (DGIdb 4.0) |
| Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
| 3664 | IRF6 | TRANSCRIPTION FACTOR | interferon beta-1b | 30013178 | ||
| 3664 | IRF6 | TRANSCRIPTION FACTOR | interferon beta-1a | 30013178 |
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