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Gene: MED9 |
Gene summary for MED9 |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | MED9 | Gene ID | 55090 |
| Gene name | mediator complex subunit 9 | |
| Gene Alias | MED25 | |
| Cytomap | 17p11.2 | |
| Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | Q9NWA0 |
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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 |
| 55090 | MED9 | LZE4T | Human | Esophagus | ESCC | 1.26e-05 | 1.82e-01 | 0.0811 |
| 55090 | MED9 | LZE7T | Human | Esophagus | ESCC | 8.41e-09 | 4.61e-01 | 0.0667 |
| 55090 | MED9 | LZE24T | Human | Esophagus | ESCC | 3.58e-13 | 1.95e-01 | 0.0596 |
| 55090 | MED9 | P1T-E | Human | Esophagus | ESCC | 8.31e-10 | 3.51e-01 | 0.0875 |
| 55090 | MED9 | P2T-E | Human | Esophagus | ESCC | 4.13e-19 | 2.91e-01 | 0.1177 |
| 55090 | MED9 | P4T-E | Human | Esophagus | ESCC | 2.86e-11 | 2.42e-01 | 0.1323 |
| 55090 | MED9 | P5T-E | Human | Esophagus | ESCC | 6.21e-11 | 1.51e-01 | 0.1327 |
| 55090 | MED9 | P8T-E | Human | Esophagus | ESCC | 1.50e-10 | 1.72e-01 | 0.0889 |
| 55090 | MED9 | P10T-E | Human | Esophagus | ESCC | 9.25e-17 | 1.73e-01 | 0.116 |
| 55090 | MED9 | P11T-E | Human | Esophagus | ESCC | 2.91e-08 | 2.78e-01 | 0.1426 |
| 55090 | MED9 | P12T-E | Human | Esophagus | ESCC | 8.28e-26 | 3.01e-01 | 0.1122 |
| 55090 | MED9 | P15T-E | Human | Esophagus | ESCC | 3.06e-07 | 1.33e-01 | 0.1149 |
| 55090 | MED9 | P16T-E | Human | Esophagus | ESCC | 1.42e-24 | 5.08e-01 | 0.1153 |
| 55090 | MED9 | P19T-E | Human | Esophagus | ESCC | 4.69e-02 | 2.52e-01 | 0.1662 |
| 55090 | MED9 | P20T-E | Human | Esophagus | ESCC | 1.83e-06 | 1.66e-01 | 0.1124 |
| 55090 | MED9 | P21T-E | Human | Esophagus | ESCC | 1.09e-07 | 1.48e-01 | 0.1617 |
| 55090 | MED9 | P22T-E | Human | Esophagus | ESCC | 5.80e-20 | 3.69e-01 | 0.1236 |
| 55090 | MED9 | P23T-E | Human | Esophagus | ESCC | 4.87e-07 | 2.26e-01 | 0.108 |
| 55090 | MED9 | P24T-E | Human | Esophagus | ESCC | 2.70e-09 | 1.58e-01 | 0.1287 |
| 55090 | MED9 | P26T-E | Human | Esophagus | ESCC | 2.46e-16 | 2.90e-01 | 0.1276 |
| Page: 1 2 3 |
| 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 |
| ∗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:00516506 | Lung | IAC | establishment of vesicle localization | 32/2061 | 161/18723 | 6.53e-04 | 8.87e-03 | 32 |
| GO:00516566 | Lung | IAC | establishment of organelle localization | 64/2061 | 390/18723 | 7.12e-04 | 9.50e-03 | 64 |
| GO:00516486 | Lung | IAC | vesicle localization | 34/2061 | 177/18723 | 8.53e-04 | 1.09e-02 | 34 |
| GO:00069008 | Lung | IAC | vesicle budding from membrane | 15/2061 | 61/18723 | 2.08e-03 | 2.07e-02 | 15 |
| GO:00481937 | Lung | IAC | Golgi vesicle transport | 49/2061 | 296/18723 | 2.35e-03 | 2.28e-02 | 49 |
| GO:005165012 | Lung | AIS | establishment of vesicle localization | 31/1849 | 161/18723 | 2.15e-04 | 4.36e-03 | 31 |
| GO:005164812 | Lung | AIS | vesicle localization | 33/1849 | 177/18723 | 2.56e-04 | 4.96e-03 | 33 |
| GO:000703011 | Lung | AIS | Golgi organization | 30/1849 | 157/18723 | 3.09e-04 | 5.63e-03 | 30 |
| GO:005165612 | Lung | AIS | establishment of organelle localization | 59/1849 | 390/18723 | 6.08e-04 | 9.24e-03 | 59 |
| GO:004819312 | Lung | AIS | Golgi vesicle transport | 46/1849 | 296/18723 | 1.32e-03 | 1.64e-02 | 46 |
| GO:000690013 | Lung | AIS | vesicle budding from membrane | 14/1849 | 61/18723 | 2.09e-03 | 2.28e-02 | 14 |
| GO:004819315 | Oral cavity | OSCC | Golgi vesicle transport | 209/7305 | 296/18723 | 1.39e-28 | 6.30e-26 | 209 |
| GO:005165610 | Oral cavity | OSCC | establishment of organelle localization | 239/7305 | 390/18723 | 2.46e-19 | 3.31e-17 | 239 |
| GO:00160508 | Oral cavity | OSCC | vesicle organization | 189/7305 | 300/18723 | 2.40e-17 | 2.14e-15 | 189 |
| GO:00068888 | Oral cavity | OSCC | endoplasmic reticulum to Golgi vesicle-mediated transport | 97/7305 | 130/18723 | 1.42e-16 | 1.15e-14 | 97 |
| GO:000690019 | Oral cavity | OSCC | vesicle budding from membrane | 49/7305 | 61/18723 | 4.73e-11 | 1.50e-09 | 49 |
| GO:00069037 | Oral cavity | OSCC | vesicle targeting | 38/7305 | 45/18723 | 4.49e-10 | 1.19e-08 | 38 |
| GO:00516509 | Oral cavity | OSCC | establishment of vesicle localization | 101/7305 | 161/18723 | 8.79e-10 | 2.17e-08 | 101 |
| GO:00516489 | Oral cavity | OSCC | vesicle localization | 105/7305 | 177/18723 | 3.30e-08 | 6.30e-07 | 105 |
| GO:00070307 | Oral cavity | OSCC | Golgi organization | 92/7305 | 157/18723 | 4.96e-07 | 7.27e-06 | 92 |
| Page: 1 2 3 4 5 6 7 8 9 10 |
| Enriched KEGG pathways. |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
| Page: 1 |
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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 |
| MED9 | SNV | Missense_Mutation | novel | c.419N>A | p.Met140Lys | p.M140K | Q9NWA0 | protein_coding | deleterious(0.03) | possibly_damaging(0.478) | TCGA-C5-A8XH-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
| MED9 | SNV | Missense_Mutation | c.124C>G | p.Gln42Glu | p.Q42E | Q9NWA0 | protein_coding | tolerated_low_confidence(0.78) | benign(0.015) | TCGA-DS-A0VN-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | SD | |
| MED9 | SNV | Missense_Mutation | c.424N>A | p.Glu142Lys | p.E142K | Q9NWA0 | protein_coding | deleterious(0.01) | possibly_damaging(0.771) | TCGA-AA-3977-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
| MED9 | SNV | Missense_Mutation | novel | c.221N>C | p.Lys74Thr | p.K74T | Q9NWA0 | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-AJ-A3EL-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
| MED9 | SNV | Missense_Mutation | novel | c.256N>A | p.Asp86Asn | p.D86N | Q9NWA0 | protein_coding | deleterious(0.04) | benign(0.38) | TCGA-AP-A1DV-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
| MED9 | SNV | Missense_Mutation | c.334N>A | p.Glu112Lys | p.E112K | Q9NWA0 | protein_coding | deleterious(0.01) | possibly_damaging(0.454) | TCGA-AX-A06H-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | paclitaxel | SD | |
| MED9 | SNV | Missense_Mutation | novel | c.304N>G | p.Ser102Gly | p.S102G | Q9NWA0 | protein_coding | tolerated(0.4) | benign(0.005) | TCGA-AX-A0J0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
| MED9 | SNV | Missense_Mutation | rs137951481 | c.350N>T | p.Gln117Leu | p.Q117L | Q9NWA0 | protein_coding | tolerated(0.06) | benign(0.003) | TCGA-AX-A1C9-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| MED9 | SNV | Missense_Mutation | c.293N>A | p.Arg98His | p.R98H | Q9NWA0 | protein_coding | deleterious(0.01) | probably_damaging(0.999) | TCGA-FI-A2D5-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatinum | PD | |
| MED9 | SNV | Missense_Mutation | novel | c.215N>A | p.Ile72Asn | p.I72N | Q9NWA0 | protein_coding | deleterious(0) | possibly_damaging(0.776) | TCGA-21-1081-01 | Lung | lung squamous cell carcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
| Page: 1 2 |
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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 |
| Page: 1 |
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