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Gene: IL1RN |
Gene summary for IL1RN |
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Gene information | Species | Human | Gene symbol | IL1RN | Gene ID | 3557 |
Gene name | interleukin 1 receptor antagonist | |
Gene Alias | DIRA | |
Cytomap | 2q14.1 | |
Gene Type | protein-coding | GO ID | GO:0001959 | UniProtAcc | P18510 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
3557 | IL1RN | LZE24D1 | Human | Esophagus | HGIN | 3.84e-03 | 5.45e-01 | 0.054 |
3557 | IL1RN | P5T-E | Human | Esophagus | ESCC | 2.40e-03 | -1.47e-01 | 0.1327 |
3557 | IL1RN | P9T-E | Human | Esophagus | ESCC | 1.26e-02 | -2.50e-02 | 0.1131 |
3557 | IL1RN | P10T-E | Human | Esophagus | ESCC | 3.78e-02 | 6.16e-02 | 0.116 |
3557 | IL1RN | P16T-E | Human | Esophagus | ESCC | 3.75e-03 | -2.16e-01 | 0.1153 |
3557 | IL1RN | P21T-E | Human | Esophagus | ESCC | 1.58e-14 | 5.64e-01 | 0.1617 |
3557 | IL1RN | P22T-E | Human | Esophagus | ESCC | 3.85e-13 | 1.62e-01 | 0.1236 |
3557 | IL1RN | P23T-E | Human | Esophagus | ESCC | 5.78e-27 | 2.27e+00 | 0.108 |
3557 | IL1RN | P27T-E | Human | Esophagus | ESCC | 1.09e-07 | 2.89e-02 | 0.1055 |
3557 | IL1RN | P28T-E | Human | Esophagus | ESCC | 7.74e-07 | 5.02e-01 | 0.1149 |
3557 | IL1RN | P32T-E | Human | Esophagus | ESCC | 9.70e-04 | -1.95e-01 | 0.1666 |
3557 | IL1RN | P54T-E | Human | Esophagus | ESCC | 5.39e-20 | 1.20e+00 | 0.0975 |
3557 | IL1RN | P82T-E | Human | Esophagus | ESCC | 1.21e-05 | 1.22e+00 | 0.1072 |
3557 | IL1RN | P83T-E | Human | Esophagus | ESCC | 5.63e-11 | 1.50e+00 | 0.1738 |
3557 | IL1RN | P130T-E | Human | Esophagus | ESCC | 5.63e-15 | 8.18e-01 | 0.1676 |
3557 | IL1RN | C04 | Human | Oral cavity | OSCC | 5.68e-21 | 1.80e+00 | 0.2633 |
3557 | IL1RN | C21 | Human | Oral cavity | OSCC | 1.08e-21 | 2.32e+00 | 0.2678 |
3557 | IL1RN | C43 | Human | Oral cavity | OSCC | 3.98e-44 | 1.98e+00 | 0.1704 |
3557 | IL1RN | C46 | Human | Oral cavity | OSCC | 1.65e-11 | 4.58e-01 | 0.1673 |
3557 | IL1RN | C57 | Human | Oral cavity | OSCC | 2.86e-63 | 2.98e+00 | 0.1679 |
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∗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 |
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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). |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:00027903 | Stomach | GC | peptide secretion | 26/1159 | 242/18723 | 4.39e-03 | 3.60e-02 | 26 |
GO:00224083 | Stomach | GC | negative regulation of cell-cell adhesion | 22/1159 | 196/18723 | 5.02e-03 | 3.98e-02 | 22 |
GO:00300723 | Stomach | GC | peptide hormone secretion | 25/1159 | 236/18723 | 6.15e-03 | 4.64e-02 | 25 |
GO:00319601 | Stomach | CAG with IM | response to corticosteroid | 27/1050 | 167/18723 | 6.35e-07 | 3.36e-05 | 27 |
GO:00513841 | Stomach | CAG with IM | response to glucocorticoid | 24/1050 | 148/18723 | 2.49e-06 | 1.07e-04 | 24 |
GO:00224071 | Stomach | CAG with IM | regulation of cell-cell adhesion | 49/1050 | 448/18723 | 6.02e-06 | 2.23e-04 | 49 |
GO:004854511 | Stomach | CAG with IM | response to steroid hormone | 40/1050 | 339/18723 | 7.19e-06 | 2.57e-04 | 40 |
GO:007169211 | Stomach | CAG with IM | protein localization to extracellular region | 38/1050 | 368/18723 | 2.15e-04 | 3.94e-03 | 38 |
GO:000930611 | Stomach | CAG with IM | protein secretion | 37/1050 | 359/18723 | 2.69e-04 | 4.73e-03 | 37 |
GO:003559211 | Stomach | CAG with IM | establishment of protein localization to extracellular region | 37/1050 | 360/18723 | 2.84e-04 | 4.96e-03 | 37 |
GO:001583311 | Stomach | CAG with IM | peptide transport | 27/1050 | 264/18723 | 1.92e-03 | 2.02e-02 | 27 |
GO:003007311 | Stomach | CAG with IM | insulin secretion | 21/1050 | 195/18723 | 3.17e-03 | 2.95e-02 | 21 |
GO:00319602 | Stomach | CSG | response to corticosteroid | 27/1034 | 167/18723 | 4.71e-07 | 2.77e-05 | 27 |
GO:00513842 | Stomach | CSG | response to glucocorticoid | 24/1034 | 148/18723 | 1.91e-06 | 8.78e-05 | 24 |
GO:004854521 | Stomach | CSG | response to steroid hormone | 40/1034 | 339/18723 | 4.99e-06 | 1.94e-04 | 40 |
GO:00224072 | Stomach | CSG | regulation of cell-cell adhesion | 48/1034 | 448/18723 | 8.67e-06 | 3.05e-04 | 48 |
GO:007169221 | Stomach | CSG | protein localization to extracellular region | 35/1034 | 368/18723 | 1.25e-03 | 1.50e-02 | 35 |
GO:000930621 | Stomach | CSG | protein secretion | 34/1034 | 359/18723 | 1.57e-03 | 1.75e-02 | 34 |
GO:003559221 | Stomach | CSG | establishment of protein localization to extracellular region | 34/1034 | 360/18723 | 1.64e-03 | 1.81e-02 | 34 |
GO:001583321 | Stomach | CSG | peptide transport | 26/1034 | 264/18723 | 3.14e-03 | 2.92e-02 | 26 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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Cell-cell communication analysis |
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Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
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Single-cell gene regulatory network inference analysis |
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TF | Cell Type | Tissue | Disease Stage | Target Gene | RSS | Regulon 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 |
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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 |
IL1RN | SNV | Missense_Mutation | c.301N>T | p.Gly101Cys | p.G101C | P18510 | protein_coding | deleterious(0) | probably_damaging(0.994) | TCGA-B6-A0IE-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | PD | |
IL1RN | SNV | Missense_Mutation | novel | c.359N>A | p.Arg120Lys | p.R120K | P18510 | protein_coding | tolerated(1) | benign(0.001) | TCGA-BH-A0EE-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | docetaxel | SD |
IL1RN | SNV | Missense_Mutation | rs764209607 | c.307N>A | p.Glu103Lys | p.E103K | P18510 | protein_coding | tolerated(0.38) | benign(0.031) | TCGA-C8-A26V-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Hormone Therapy | tamoxiphen | CR |
IL1RN | SNV | Missense_Mutation | c.392C>T | p.Ser131Leu | p.S131L | P18510 | protein_coding | tolerated(0.09) | benign(0.073) | TCGA-AA-3663-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
IL1RN | SNV | Missense_Mutation | c.317T>G | p.Leu106Arg | p.L106R | P18510 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AA-3864-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
IL1RN | SNV | Missense_Mutation | rs780956028 | c.389N>A | p.Arg130His | p.R130H | P18510 | protein_coding | tolerated(0.07) | probably_damaging(0.999) | TCGA-F4-6854-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
IL1RN | SNV | Missense_Mutation | rs373101669 | c.374N>A | p.Arg125His | p.R125H | P18510 | protein_coding | deleterious(0.01) | possibly_damaging(0.771) | TCGA-AG-3887-01 | Colorectum | rectum adenocarcinoma | Male | >=65 | I/II | Chemotherapy | irinotecan | SD |
IL1RN | SNV | Missense_Mutation | novel | c.149N>G | p.Thr50Ser | p.T50S | P18510 | protein_coding | tolerated(0.53) | benign(0.009) | TCGA-AG-A00Y-01 | Colorectum | rectum adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
IL1RN | SNV | Missense_Mutation | rs143208167 | c.505N>A | p.Val169Ile | p.V169I | P18510 | protein_coding | tolerated(0.48) | benign(0) | TCGA-A5-A0GG-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
IL1RN | SNV | Missense_Mutation | novel | c.157N>A | p.Leu53Met | p.L53M | P18510 | protein_coding | deleterious(0.05) | benign(0.191) | TCGA-AJ-A5DW-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
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Related drugs of malignant transformation related genes |
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(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
3557 | IL1RN | DRUGGABLE GENOME | AC-201 | DIACEREIN | ||
3557 | IL1RN | DRUGGABLE GENOME | haloperidol | HALOPERIDOL | 27023437 | |
3557 | IL1RN | DRUGGABLE GENOME | Tumor necrosis factor alpha (TNF-alpha) inhibitors | 24776844 | ||
3557 | IL1RN | DRUGGABLE GENOME | MTX | METHOTREXATE | 8877917 |
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