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Gene: MAVS |
Gene summary for MAVS |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | MAVS | Gene ID | 57506 |
| Gene name | mitochondrial antiviral signaling protein | |
| Gene Alias | CARDIF | |
| Cytomap | 20p13 | |
| Gene Type | protein-coding | GO ID | GO:0001816 | UniProtAcc | Q7Z434 |
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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 |
| 57506 | MAVS | HTA11_2487_2000001011 | Human | Colorectum | SER | 6.18e-07 | 6.14e-01 | -0.1808 |
| 57506 | MAVS | HTA11_1938_2000001011 | Human | Colorectum | AD | 3.49e-05 | 5.62e-01 | -0.0811 |
| 57506 | MAVS | HTA11_347_2000001011 | Human | Colorectum | AD | 9.59e-27 | 9.03e-01 | -0.1954 |
| 57506 | MAVS | HTA11_411_2000001011 | Human | Colorectum | SER | 1.32e-02 | 7.91e-01 | -0.2602 |
| 57506 | MAVS | HTA11_3361_2000001011 | Human | Colorectum | AD | 5.34e-07 | 6.83e-01 | -0.1207 |
| 57506 | MAVS | HTA11_83_2000001011 | Human | Colorectum | SER | 5.76e-12 | 9.28e-01 | -0.1526 |
| 57506 | MAVS | HTA11_696_2000001011 | Human | Colorectum | AD | 9.58e-22 | 9.12e-01 | -0.1464 |
| 57506 | MAVS | HTA11_866_2000001011 | Human | Colorectum | AD | 6.46e-10 | 5.31e-01 | -0.1001 |
| 57506 | MAVS | HTA11_1391_2000001011 | Human | Colorectum | AD | 1.81e-09 | 6.82e-01 | -0.059 |
| 57506 | MAVS | HTA11_2992_2000001011 | Human | Colorectum | SER | 5.22e-03 | 6.74e-01 | -0.1706 |
| 57506 | MAVS | HTA11_546_2000001011 | Human | Colorectum | AD | 8.52e-04 | 6.09e-01 | -0.0842 |
| 57506 | MAVS | HTA11_866_3004761011 | Human | Colorectum | AD | 9.37e-03 | 3.96e-01 | 0.096 |
| 57506 | MAVS | HTA11_9408_2000001011 | Human | Colorectum | AD | 8.16e-03 | 2.17e-01 | 0.0451 |
| 57506 | MAVS | HTA11_7663_2000001011 | Human | Colorectum | SER | 8.30e-04 | 6.18e-01 | 0.0131 |
| 57506 | MAVS | HTA11_99999973899_84307 | Human | Colorectum | MSS | 4.42e-02 | 5.61e-01 | 0.2585 |
| 57506 | MAVS | HTA11_99999974143_84620 | Human | Colorectum | MSS | 1.06e-08 | 4.61e-01 | 0.3005 |
| 57506 | MAVS | A002-C-010 | Human | Colorectum | FAP | 7.67e-04 | -3.06e-01 | 0.242 |
| 57506 | MAVS | A015-C-203 | Human | Colorectum | FAP | 1.62e-14 | -1.09e-01 | -0.1294 |
| 57506 | MAVS | A002-C-201 | Human | Colorectum | FAP | 6.04e-05 | -1.91e-01 | 0.0324 |
| 57506 | MAVS | A001-C-108 | Human | Colorectum | FAP | 9.92e-10 | -2.04e-01 | -0.0272 |
| Page: 1 2 3 4 5 6 7 8 |
| Transcriptomic changes along malignancy continuum. |
| Tissue | Expression Dynamics | Abbreviation |
| 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 | ||
| Prostate |  | BPH: Benign Prostatic Hyperplasia |
| 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:0016032 | Colorectum | AD | viral process | 168/3918 | 415/18723 | 4.67e-20 | 3.66e-17 | 168 |
| GO:1903829 | Colorectum | AD | positive regulation of cellular protein localization | 110/3918 | 276/18723 | 4.58e-13 | 8.44e-11 | 110 |
| GO:0019058 | Colorectum | AD | viral life cycle | 119/3918 | 317/18723 | 6.18e-12 | 8.23e-10 | 119 |
| GO:0072594 | Colorectum | AD | establishment of protein localization to organelle | 148/3918 | 422/18723 | 7.95e-12 | 1.04e-09 | 148 |
| GO:1904951 | Colorectum | AD | positive regulation of establishment of protein localization | 112/3918 | 319/18723 | 2.55e-09 | 1.80e-07 | 112 |
| GO:0051222 | Colorectum | AD | positive regulation of protein transport | 106/3918 | 303/18723 | 8.45e-09 | 5.08e-07 | 106 |
| GO:0006913 | Colorectum | AD | nucleocytoplasmic transport | 102/3918 | 301/18723 | 1.00e-07 | 4.85e-06 | 102 |
| GO:0051169 | Colorectum | AD | nuclear transport | 102/3918 | 301/18723 | 1.00e-07 | 4.85e-06 | 102 |
| GO:1900180 | Colorectum | AD | regulation of protein localization to nucleus | 55/3918 | 136/18723 | 1.70e-07 | 7.34e-06 | 55 |
| GO:0090316 | Colorectum | AD | positive regulation of intracellular protein transport | 62/3918 | 160/18723 | 1.82e-07 | 7.79e-06 | 62 |
| GO:0032388 | Colorectum | AD | positive regulation of intracellular transport | 74/3918 | 202/18723 | 1.83e-07 | 7.80e-06 | 74 |
| GO:0032386 | Colorectum | AD | regulation of intracellular transport | 109/3918 | 337/18723 | 5.33e-07 | 1.95e-05 | 109 |
| GO:0033157 | Colorectum | AD | regulation of intracellular protein transport | 80/3918 | 229/18723 | 5.81e-07 | 2.09e-05 | 80 |
| GO:1900182 | Colorectum | AD | positive regulation of protein localization to nucleus | 38/3918 | 87/18723 | 1.43e-06 | 4.52e-05 | 38 |
| GO:0019079 | Colorectum | AD | viral genome replication | 51/3918 | 131/18723 | 1.83e-06 | 5.51e-05 | 51 |
| GO:0034504 | Colorectum | AD | protein localization to nucleus | 94/3918 | 290/18723 | 2.83e-06 | 8.09e-05 | 94 |
| GO:0050792 | Colorectum | AD | regulation of viral process | 59/3918 | 164/18723 | 5.95e-06 | 1.52e-04 | 59 |
| GO:0046822 | Colorectum | AD | regulation of nucleocytoplasmic transport | 41/3918 | 106/18723 | 2.17e-05 | 4.33e-04 | 41 |
| GO:0046824 | Colorectum | AD | positive regulation of nucleocytoplasmic transport | 27/3918 | 62/18723 | 4.91e-05 | 8.43e-04 | 27 |
| GO:0017038 | Colorectum | AD | protein import | 67/3918 | 206/18723 | 6.34e-05 | 1.05e-03 | 67 |
| Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 |
| Enriched KEGG pathways. |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
| hsa046223 | Oral cavity | LP | RIG-I-like receptor signaling pathway | 30/2418 | 71/8465 | 9.09e-03 | 3.33e-02 | 2.14e-02 | 30 |
| hsa046233 | Oral cavity | LP | Cytosolic DNA-sensing pathway | 31/2418 | 75/8465 | 1.17e-02 | 3.91e-02 | 2.52e-02 | 31 |
| hsa0517129 | Prostate | Tumor | Coronavirus disease - COVID-19 | 118/1791 | 232/8465 | 3.58e-24 | 1.69e-22 | 1.05e-22 | 118 |
| hsa0516927 | Prostate | Tumor | Epstein-Barr virus infection | 72/1791 | 202/8465 | 1.15e-06 | 1.09e-05 | 6.73e-06 | 72 |
| hsa0516023 | Prostate | Tumor | Hepatitis C | 51/1791 | 157/8465 | 5.67e-04 | 2.89e-03 | 1.79e-03 | 51 |
| hsa0516121 | Prostate | Tumor | Hepatitis B | 50/1791 | 162/8465 | 2.23e-03 | 8.68e-03 | 5.38e-03 | 50 |
| hsa051622 | Prostate | Tumor | Measles | 44/1791 | 139/8465 | 2.33e-03 | 8.85e-03 | 5.49e-03 | 44 |
| hsa0516423 | Prostate | Tumor | Influenza A | 49/1791 | 171/8465 | 1.18e-02 | 3.64e-02 | 2.26e-02 | 49 |
| hsa0517137 | Prostate | Tumor | Coronavirus disease - COVID-19 | 118/1791 | 232/8465 | 3.58e-24 | 1.69e-22 | 1.05e-22 | 118 |
| hsa0516935 | Prostate | Tumor | Epstein-Barr virus infection | 72/1791 | 202/8465 | 1.15e-06 | 1.09e-05 | 6.73e-06 | 72 |
| hsa0516033 | Prostate | Tumor | Hepatitis C | 51/1791 | 157/8465 | 5.67e-04 | 2.89e-03 | 1.79e-03 | 51 |
| hsa051613 | Prostate | Tumor | Hepatitis B | 50/1791 | 162/8465 | 2.23e-03 | 8.68e-03 | 5.38e-03 | 50 |
| hsa051623 | Prostate | Tumor | Measles | 44/1791 | 139/8465 | 2.33e-03 | 8.85e-03 | 5.49e-03 | 44 |
| hsa0516433 | Prostate | Tumor | Influenza A | 49/1791 | 171/8465 | 1.18e-02 | 3.64e-02 | 2.26e-02 | 49 |
| Page: 1 2 3 4 5 |
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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 |
| MAVS | SNV | Missense_Mutation | novel | c.967C>A | p.Pro323Thr | p.P323T | Q7Z434 | protein_coding | deleterious(0.02) | benign(0.047) | TCGA-A2-A0CP-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | SD |
| MAVS | SNV | Missense_Mutation | novel | c.841N>G | p.Ile281Val | p.I281V | Q7Z434 | protein_coding | tolerated(0.1) | benign(0) | TCGA-A2-A0YM-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| MAVS | SNV | Missense_Mutation | rs762014329 | c.1460N>T | p.Ala487Val | p.A487V | Q7Z434 | protein_coding | tolerated(0.18) | benign(0.087) | TCGA-AC-A62X-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| MAVS | SNV | Missense_Mutation | novel | c.1249G>C | p.Glu417Gln | p.E417Q | Q7Z434 | protein_coding | deleterious(0.02) | possibly_damaging(0.728) | TCGA-E9-A3QA-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
| MAVS | SNV | Missense_Mutation | novel | c.1216N>C | p.Asp406His | p.D406H | Q7Z434 | protein_coding | deleterious(0) | probably_damaging(0.958) | TCGA-LL-A5YO-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | taxotere | CR |
| MAVS | insertion | Frame_Shift_Ins | novel | c.965_966insCCCTCAGAAATATATAGTTGTCCATCTG | p.Ser324GlnfsTer15 | p.S324Qfs*15 | Q7Z434 | protein_coding | TCGA-A2-A0CP-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | SD | ||
| MAVS | SNV | Missense_Mutation | c.545N>G | p.Ser182Cys | p.S182C | Q7Z434 | protein_coding | deleterious(0.04) | possibly_damaging(0.826) | TCGA-Q1-A73O-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
| MAVS | SNV | Missense_Mutation | c.1438N>C | p.Glu480Gln | p.E480Q | Q7Z434 | protein_coding | tolerated(0.22) | possibly_damaging(0.605) | TCGA-Q1-A73O-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
| MAVS | SNV | Missense_Mutation | novel | c.835N>A | p.Glu279Lys | p.E279K | Q7Z434 | protein_coding | tolerated(0.33) | benign(0.02) | TCGA-AA-3994-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | capecitabine | CR |
| MAVS | SNV | Missense_Mutation | c.1459N>A | p.Ala487Thr | p.A487T | Q7Z434 | protein_coding | tolerated(0.27) | benign(0.034) | TCGA-AZ-4615-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | xeloda | PD |
| Page: 1 2 3 4 5 |
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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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