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Gene: MEN1 |
Gene summary for MEN1 |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | MEN1 | Gene ID | 4221 |
| Gene name | menin 1 | |
| Gene Alias | MEAI | |
| Cytomap | 11q13.1 | |
| Gene Type | protein-coding | GO ID | GO:0000003 | UniProtAcc | A0A024R5D2 |
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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 |
| 4221 | MEN1 | LZE7T | Human | Esophagus | ESCC | 4.28e-04 | 1.71e-01 | 0.0667 |
| 4221 | MEN1 | LZE24T | Human | Esophagus | ESCC | 4.41e-10 | 2.62e-01 | 0.0596 |
| 4221 | MEN1 | LZE21T | Human | Esophagus | ESCC | 1.56e-02 | 1.64e-01 | 0.0655 |
| 4221 | MEN1 | P1T-E | Human | Esophagus | ESCC | 8.21e-03 | 2.17e-01 | 0.0875 |
| 4221 | MEN1 | P2T-E | Human | Esophagus | ESCC | 1.99e-21 | 3.48e-01 | 0.1177 |
| 4221 | MEN1 | P4T-E | Human | Esophagus | ESCC | 7.62e-16 | 4.22e-01 | 0.1323 |
| 4221 | MEN1 | P5T-E | Human | Esophagus | ESCC | 1.61e-07 | 1.00e-01 | 0.1327 |
| 4221 | MEN1 | P8T-E | Human | Esophagus | ESCC | 9.05e-11 | 1.81e-01 | 0.0889 |
| 4221 | MEN1 | P9T-E | Human | Esophagus | ESCC | 5.20e-08 | 1.53e-01 | 0.1131 |
| 4221 | MEN1 | P10T-E | Human | Esophagus | ESCC | 1.23e-12 | 2.08e-01 | 0.116 |
| 4221 | MEN1 | P11T-E | Human | Esophagus | ESCC | 9.72e-05 | 2.37e-01 | 0.1426 |
| 4221 | MEN1 | P12T-E | Human | Esophagus | ESCC | 1.37e-08 | 2.44e-01 | 0.1122 |
| 4221 | MEN1 | P15T-E | Human | Esophagus | ESCC | 2.76e-03 | 5.63e-02 | 0.1149 |
| 4221 | MEN1 | P16T-E | Human | Esophagus | ESCC | 1.24e-15 | 2.53e-01 | 0.1153 |
| 4221 | MEN1 | P17T-E | Human | Esophagus | ESCC | 2.75e-03 | 1.64e-01 | 0.1278 |
| 4221 | MEN1 | P19T-E | Human | Esophagus | ESCC | 2.10e-03 | 2.71e-01 | 0.1662 |
| 4221 | MEN1 | P20T-E | Human | Esophagus | ESCC | 2.61e-03 | 8.45e-02 | 0.1124 |
| 4221 | MEN1 | P21T-E | Human | Esophagus | ESCC | 1.39e-08 | 1.85e-01 | 0.1617 |
| 4221 | MEN1 | P22T-E | Human | Esophagus | ESCC | 3.16e-03 | 5.95e-02 | 0.1236 |
| 4221 | MEN1 | P23T-E | Human | Esophagus | ESCC | 7.07e-10 | 2.13e-01 | 0.108 |
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| 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 |
| ∗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:00160557 | Cervix | CC | Wnt signaling pathway | 98/2311 | 444/18723 | 4.82e-09 | 4.65e-07 | 98 |
| GO:01987387 | Cervix | CC | cell-cell signaling by wnt | 98/2311 | 446/18723 | 6.16e-09 | 5.58e-07 | 98 |
| GO:00301117 | Cervix | CC | regulation of Wnt signaling pathway | 76/2311 | 328/18723 | 3.05e-08 | 2.08e-06 | 76 |
| GO:19030349 | Cervix | CC | regulation of response to wounding | 44/2311 | 167/18723 | 6.33e-07 | 2.31e-05 | 44 |
| GO:00608287 | Cervix | CC | regulation of canonical Wnt signaling pathway | 58/2311 | 253/18723 | 1.83e-06 | 5.89e-05 | 58 |
| GO:00600707 | Cervix | CC | canonical Wnt signaling pathway | 66/2311 | 303/18723 | 2.47e-06 | 7.35e-05 | 66 |
| GO:00109757 | Cervix | CC | regulation of neuron projection development | 88/2311 | 445/18723 | 4.26e-06 | 1.09e-04 | 88 |
| GO:00310996 | Cervix | CC | regeneration | 46/2311 | 198/18723 | 1.43e-05 | 2.84e-04 | 46 |
| GO:00615647 | Cervix | CC | axon development | 89/2311 | 467/18723 | 1.71e-05 | 3.27e-04 | 89 |
| GO:00313456 | Cervix | CC | negative regulation of cell projection organization | 39/2311 | 186/18723 | 5.86e-04 | 5.57e-03 | 39 |
| GO:00321022 | Cervix | CC | negative regulation of response to external stimulus | 75/2311 | 420/18723 | 5.96e-04 | 5.61e-03 | 75 |
| GO:00301784 | Cervix | CC | negative regulation of Wnt signaling pathway | 35/2311 | 170/18723 | 1.52e-03 | 1.17e-02 | 35 |
| GO:00015037 | Cervix | CC | ossification | 71/2311 | 408/18723 | 1.67e-03 | 1.28e-02 | 71 |
| 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:00900901 | Cervix | CC | negative regulation of canonical Wnt signaling pathway | 29/2311 | 137/18723 | 2.40e-03 | 1.70e-02 | 29 |
| GO:00109775 | Cervix | CC | negative regulation of neuron projection development | 28/2311 | 137/18723 | 4.74e-03 | 2.83e-02 | 28 |
| GO:00486782 | Cervix | CC | response to axon injury | 19/2311 | 83/18723 | 5.25e-03 | 3.08e-02 | 19 |
| GO:0048679 | Cervix | CC | regulation of axon regeneration | 9/2311 | 29/18723 | 6.49e-03 | 3.61e-02 | 9 |
| GO:00302781 | Cervix | CC | regulation of ossification | 24/2311 | 115/18723 | 6.51e-03 | 3.61e-02 | 24 |
| Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 |
| Enriched KEGG pathways. |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
| hsa052028 | Esophagus | ESCC | Transcriptional misregulation in cancer | 116/4205 | 193/8465 | 2.08e-03 | 5.95e-03 | 3.05e-03 | 116 |
| hsa0520213 | Esophagus | ESCC | Transcriptional misregulation in cancer | 116/4205 | 193/8465 | 2.08e-03 | 5.95e-03 | 3.05e-03 | 116 |
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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 |
| MEN1 | SNV | Missense_Mutation | novel | c.676N>A | p.Leu226Met | p.L226M | O00255 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-A2-A04N-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | cytoxan | SD |
| MEN1 | SNV | Missense_Mutation | c.1817C>G | p.Ser606Cys | p.S606C | O00255 | protein_coding | deleterious(0.01) | possibly_damaging(0.82) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
| MEN1 | SNV | Missense_Mutation | c.323G>C | p.Arg108Pro | p.R108P | O00255 | protein_coding | tolerated(0.07) | possibly_damaging(0.7) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
| MEN1 | SNV | Missense_Mutation | c.1084G>C | p.Asp362His | p.D362H | O00255 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AC-A6IX-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | |
| MEN1 | SNV | Missense_Mutation | rs377715802 | c.1040N>T | p.Ala347Val | p.A347V | O00255 | protein_coding | deleterious(0) | possibly_damaging(0.726) | TCGA-AN-A0AK-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| MEN1 | SNV | Missense_Mutation | c.479N>T | p.Ser160Phe | p.S160F | O00255 | protein_coding | tolerated(1) | benign(0.009) | TCGA-BH-A0DK-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD | |
| MEN1 | SNV | Missense_Mutation | c.550G>A | p.Glu184Lys | p.E184K | O00255 | protein_coding | deleterious(0) | probably_damaging(0.934) | TCGA-C8-A8HQ-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
| MEN1 | deletion | Frame_Shift_Del | c.1700_1706delNNNNNNN | p.Lys567SerfsTer24 | p.K567Sfs*24 | O00255 | protein_coding | TCGA-BH-A18R-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |||
| MEN1 | deletion | Frame_Shift_Del | c.225_229delNNNNN | p.Thr76LeufsTer39 | p.T76Lfs*39 | O00255 | protein_coding | TCGA-E9-A1N5-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin | SD | |||
| MEN1 | insertion | Frame_Shift_Ins | rs767319284 | c.1561_1562insC | p.Arg521ProfsTer15 | p.R521Pfs*15 | O00255 | protein_coding | TCGA-E9-A228-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin | SD |
| 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 |
| 4221 | MEN1 | CLINICALLY ACTIONABLE, DNA REPAIR | CHLORHEXIDINE HYDROCHLORIDE | CHLORHEXIDINE HYDROCHLORIDE | ||
| 4221 | MEN1 | CLINICALLY ACTIONABLE, DNA REPAIR | FURAFYLLINE | FURAFYLLINE | ||
| 4221 | MEN1 | CLINICALLY ACTIONABLE, DNA REPAIR | TCMDC-123591 | CHEMBL588234 | ||
| 4221 | MEN1 | CLINICALLY ACTIONABLE, DNA REPAIR | CYCLIRAMINE MALEATE | CYCLIRAMINE MALEATE | ||
| 4221 | MEN1 | CLINICALLY ACTIONABLE, DNA REPAIR | METHYLENE BLUE | METHYLENE BLUE | ||
| 4221 | MEN1 | CLINICALLY ACTIONABLE, DNA REPAIR | TANNIC ACID | TANNIC ACID | ||
| 4221 | MEN1 | CLINICALLY ACTIONABLE, DNA REPAIR | SJ000029700 | CHEMBL591864 | ||
| 4221 | MEN1 | CLINICALLY ACTIONABLE, DNA REPAIR | TRIMETREXATE | TRIMETREXATE | ||
| 4221 | MEN1 | CLINICALLY ACTIONABLE, DNA REPAIR | TCMDC-124518 | CHEMBL527584 | ||
| 4221 | MEN1 | CLINICALLY ACTIONABLE, DNA REPAIR | TRACAZOLATE | TRACAZOLATE |
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