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Gene: MED4 |
Gene summary for MED4 |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | MED4 | Gene ID | 29079 |
| Gene name | mediator complex subunit 4 | |
| Gene Alias | ARC36 | |
| Cytomap | 13q14.2 | |
| Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | Q9NPJ6 |
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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 |
| 29079 | MED4 | LZE4T | Human | Esophagus | ESCC | 7.93e-13 | 1.35e-01 | 0.0811 |
| 29079 | MED4 | LZE7T | Human | Esophagus | ESCC | 3.21e-06 | 2.27e-01 | 0.0667 |
| 29079 | MED4 | LZE8T | Human | Esophagus | ESCC | 2.95e-06 | 6.39e-02 | 0.067 |
| 29079 | MED4 | LZE20T | Human | Esophagus | ESCC | 3.18e-06 | 6.75e-02 | 0.0662 |
| 29079 | MED4 | LZE22D1 | Human | Esophagus | HGIN | 5.79e-05 | 7.09e-02 | 0.0595 |
| 29079 | MED4 | LZE22T | Human | Esophagus | ESCC | 1.08e-04 | 1.92e-01 | 0.068 |
| 29079 | MED4 | LZE24T | Human | Esophagus | ESCC | 8.26e-16 | 1.84e-01 | 0.0596 |
| 29079 | MED4 | LZE6T | Human | Esophagus | ESCC | 8.30e-05 | -4.12e-02 | 0.0845 |
| 29079 | MED4 | P1T-E | Human | Esophagus | ESCC | 1.18e-08 | 2.77e-01 | 0.0875 |
| 29079 | MED4 | P2T-E | Human | Esophagus | ESCC | 6.15e-20 | 4.66e-01 | 0.1177 |
| 29079 | MED4 | P4T-E | Human | Esophagus | ESCC | 6.84e-22 | 1.15e-01 | 0.1323 |
| 29079 | MED4 | P5T-E | Human | Esophagus | ESCC | 3.48e-09 | 1.02e-01 | 0.1327 |
| 29079 | MED4 | P8T-E | Human | Esophagus | ESCC | 8.58e-43 | 6.68e-01 | 0.0889 |
| 29079 | MED4 | P9T-E | Human | Esophagus | ESCC | 3.17e-17 | 3.14e-01 | 0.1131 |
| 29079 | MED4 | P10T-E | Human | Esophagus | ESCC | 6.93e-20 | 4.36e-01 | 0.116 |
| 29079 | MED4 | P11T-E | Human | Esophagus | ESCC | 8.81e-15 | 2.39e-01 | 0.1426 |
| 29079 | MED4 | P12T-E | Human | Esophagus | ESCC | 3.31e-23 | 4.38e-01 | 0.1122 |
| 29079 | MED4 | P15T-E | Human | Esophagus | ESCC | 5.61e-24 | 4.60e-01 | 0.1149 |
| 29079 | MED4 | P16T-E | Human | Esophagus | ESCC | 7.02e-24 | 5.31e-01 | 0.1153 |
| 29079 | MED4 | P17T-E | Human | Esophagus | ESCC | 9.56e-04 | 3.92e-01 | 0.1278 |
| Page: 1 2 3 4 5 6 |
| Transcriptomic changes along malignancy continuum. |
| Tissue | Expression Dynamics | Abbreviation |
| 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 | ||
| Thyroid |  | ATC: Anaplastic thyroid cancer |
| HT: Hashimoto's thyroiditis | ||
| PTC: Papillary thyroid cancer |
| ∗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:0048193 | Colorectum | AD | Golgi vesicle transport | 109/3918 | 296/18723 | 1.80e-10 | 1.68e-08 | 109 |
| GO:0043123 | Colorectum | AD | positive regulation of I-kappaB kinase/NF-kappaB signaling | 60/3918 | 186/18723 | 1.91e-04 | 2.56e-03 | 60 |
| GO:0043122 | Colorectum | AD | regulation of I-kappaB kinase/NF-kappaB signaling | 76/3918 | 249/18723 | 2.17e-04 | 2.85e-03 | 76 |
| GO:0006888 | Colorectum | AD | endoplasmic reticulum to Golgi vesicle-mediated transport | 44/3918 | 130/18723 | 4.13e-04 | 4.68e-03 | 44 |
| GO:0007249 | Colorectum | AD | I-kappaB kinase/NF-kappaB signaling | 82/3918 | 281/18723 | 6.09e-04 | 6.40e-03 | 82 |
| GO:00481931 | Colorectum | SER | Golgi vesicle transport | 79/2897 | 296/18723 | 4.20e-07 | 2.15e-05 | 79 |
| GO:00068881 | Colorectum | SER | endoplasmic reticulum to Golgi vesicle-mediated transport | 34/2897 | 130/18723 | 1.13e-03 | 1.29e-02 | 34 |
| GO:00481932 | Colorectum | MSS | Golgi vesicle transport | 101/3467 | 296/18723 | 9.09e-11 | 9.77e-09 | 101 |
| GO:00068882 | Colorectum | MSS | endoplasmic reticulum to Golgi vesicle-mediated transport | 44/3467 | 130/18723 | 2.17e-05 | 4.60e-04 | 44 |
| GO:00431221 | Colorectum | MSS | regulation of I-kappaB kinase/NF-kappaB signaling | 71/3467 | 249/18723 | 7.12e-05 | 1.21e-03 | 71 |
| GO:00072491 | Colorectum | MSS | I-kappaB kinase/NF-kappaB signaling | 77/3467 | 281/18723 | 1.51e-04 | 2.19e-03 | 77 |
| GO:00431231 | Colorectum | MSS | positive regulation of I-kappaB kinase/NF-kappaB signaling | 55/3467 | 186/18723 | 1.60e-04 | 2.29e-03 | 55 |
| GO:00068883 | Colorectum | MSI-H | endoplasmic reticulum to Golgi vesicle-mediated transport | 22/1319 | 130/18723 | 1.05e-04 | 3.24e-03 | 22 |
| GO:00481933 | Colorectum | MSI-H | Golgi vesicle transport | 39/1319 | 296/18723 | 1.17e-04 | 3.51e-03 | 39 |
| GO:00481934 | Colorectum | FAP | Golgi vesicle transport | 77/2622 | 296/18723 | 2.86e-08 | 2.62e-06 | 77 |
| GO:00431222 | Colorectum | FAP | regulation of I-kappaB kinase/NF-kappaB signaling | 56/2622 | 249/18723 | 1.82e-04 | 2.69e-03 | 56 |
| GO:00431232 | Colorectum | FAP | positive regulation of I-kappaB kinase/NF-kappaB signaling | 42/2622 | 186/18723 | 1.01e-03 | 9.89e-03 | 42 |
| GO:00072492 | Colorectum | FAP | I-kappaB kinase/NF-kappaB signaling | 58/2622 | 281/18723 | 1.37e-03 | 1.24e-02 | 58 |
| GO:00068884 | Colorectum | FAP | endoplasmic reticulum to Golgi vesicle-mediated transport | 30/2622 | 130/18723 | 3.51e-03 | 2.53e-02 | 30 |
| GO:00481939 | Endometrium | AEH | Golgi vesicle transport | 60/2100 | 296/18723 | 3.65e-06 | 9.79e-05 | 60 |
| Page: 1 2 3 4 5 6 7 |
| Enriched KEGG pathways. |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
| hsa0491928 | Esophagus | ESCC | Thyroid hormone signaling pathway | 78/4205 | 121/8465 | 6.79e-04 | 2.23e-03 | 1.14e-03 | 78 |
| hsa04919113 | Esophagus | ESCC | Thyroid hormone signaling pathway | 78/4205 | 121/8465 | 6.79e-04 | 2.23e-03 | 1.14e-03 | 78 |
| hsa0491912 | Liver | HCC | Thyroid hormone signaling pathway | 75/4020 | 121/8465 | 8.76e-04 | 3.38e-03 | 1.88e-03 | 75 |
| hsa0491913 | Liver | HCC | Thyroid hormone signaling pathway | 75/4020 | 121/8465 | 8.76e-04 | 3.38e-03 | 1.88e-03 | 75 |
| hsa0491926 | Oral cavity | OSCC | Thyroid hormone signaling pathway | 73/3704 | 121/8465 | 1.63e-04 | 5.52e-04 | 2.81e-04 | 73 |
| hsa04919112 | Oral cavity | OSCC | Thyroid hormone signaling pathway | 73/3704 | 121/8465 | 1.63e-04 | 5.52e-04 | 2.81e-04 | 73 |
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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 |
| ∗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 |
| MED4 | SNV | Missense_Mutation | rs775421698 | c.533N>T | p.Thr178Ile | p.T178I | Q9NPJ6 | protein_coding | deleterious(0.03) | probably_damaging(0.995) | TCGA-BH-A0HF-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | arimidex | SD |
| MED4 | SNV | Missense_Mutation | c.479N>A | p.Ala160Asp | p.A160D | Q9NPJ6 | protein_coding | deleterious(0) | probably_damaging(0.954) | TCGA-AA-3672-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
| MED4 | SNV | Missense_Mutation | c.193G>A | p.Val65Ile | p.V65I | Q9NPJ6 | protein_coding | tolerated(0.41) | benign(0.001) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR | |
| MED4 | SNV | Missense_Mutation | c.373N>A | p.Val125Ile | p.V125I | Q9NPJ6 | protein_coding | tolerated(1) | benign(0.045) | TCGA-CK-5916-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
| MED4 | SNV | Missense_Mutation | rs144201204 | c.592N>A | p.Val198Met | p.V198M | Q9NPJ6 | protein_coding | tolerated(0.22) | benign(0.326) | TCGA-G4-6586-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| MED4 | SNV | Missense_Mutation | c.229C>G | p.Gln77Glu | p.Q77E | Q9NPJ6 | protein_coding | tolerated(0.12) | benign(0.003) | TCGA-A5-A0GU-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
| MED4 | SNV | Missense_Mutation | novel | c.768N>T | p.Glu256Asp | p.E256D | Q9NPJ6 | protein_coding | tolerated(0.06) | probably_damaging(0.931) | TCGA-B5-A1MR-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
| MED4 | SNV | Missense_Mutation | novel | c.151N>C | p.Ser51Pro | p.S51P | Q9NPJ6 | protein_coding | tolerated(0.47) | benign(0.328) | TCGA-B5-A3FC-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
| MED4 | SNV | Missense_Mutation | rs199856249 | c.215N>A | p.Arg72Gln | p.R72Q | Q9NPJ6 | protein_coding | deleterious(0.01) | benign(0.147) | TCGA-DI-A1BU-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | paclitaxel | SD |
| MED4 | SNV | Missense_Mutation | c.506N>A | p.Pro169Gln | p.P169Q | Q9NPJ6 | protein_coding | tolerated(0.53) | probably_damaging(0.999) | TCGA-55-6971-01 | Lung | lung adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
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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 |
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