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Gene: ELF2 |
Gene summary for ELF2 |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | ELF2 | Gene ID | 1998 |
| Gene name | E74 like ETS transcription factor 2 | |
| Gene Alias | EU32 | |
| Cytomap | 4q31.1 | |
| Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | Q15723 |
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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 |
| 1998 | ELF2 | CA_HPV_3 | Human | Cervix | CC | 4.54e-02 | -3.67e-02 | 0.0414 |
| 1998 | ELF2 | CCI_1 | Human | Cervix | CC | 1.96e-10 | 1.36e+00 | 0.528 |
| 1998 | ELF2 | CCI_2 | Human | Cervix | CC | 5.36e-12 | 1.25e+00 | 0.5249 |
| 1998 | ELF2 | CCI_3 | Human | Cervix | CC | 7.47e-09 | 8.79e-01 | 0.516 |
| 1998 | ELF2 | HTA11_3410_2000001011 | Human | Colorectum | AD | 2.91e-03 | -3.17e-01 | 0.0155 |
| 1998 | ELF2 | HTA11_347_2000001011 | Human | Colorectum | AD | 1.87e-03 | 3.75e-01 | -0.1954 |
| 1998 | ELF2 | HTA11_8622_2000001021 | Human | Colorectum | SER | 2.46e-03 | -4.91e-01 | 0.0528 |
| 1998 | ELF2 | HTA11_99999973899_84307 | Human | Colorectum | MSS | 1.09e-02 | -3.85e-01 | 0.2585 |
| 1998 | ELF2 | HTA11_99999974143_84620 | Human | Colorectum | MSS | 2.06e-09 | -4.13e-01 | 0.3005 |
| 1998 | ELF2 | F007 | Human | Colorectum | FAP | 2.59e-02 | -2.51e-01 | 0.1176 |
| 1998 | ELF2 | A001-C-207 | Human | Colorectum | FAP | 2.13e-04 | -3.24e-01 | 0.1278 |
| 1998 | ELF2 | A015-C-203 | Human | Colorectum | FAP | 5.66e-25 | -3.83e-01 | -0.1294 |
| 1998 | ELF2 | A015-C-204 | Human | Colorectum | FAP | 4.74e-07 | -4.17e-01 | -0.0228 |
| 1998 | ELF2 | A014-C-040 | Human | Colorectum | FAP | 8.30e-06 | -5.89e-01 | -0.1184 |
| 1998 | ELF2 | A002-C-201 | Human | Colorectum | FAP | 7.79e-13 | -4.02e-01 | 0.0324 |
| 1998 | ELF2 | A001-C-119 | Human | Colorectum | FAP | 1.78e-06 | -3.34e-01 | -0.1557 |
| 1998 | ELF2 | A001-C-108 | Human | Colorectum | FAP | 6.60e-14 | -3.62e-01 | -0.0272 |
| 1998 | ELF2 | A002-C-205 | Human | Colorectum | FAP | 3.89e-25 | -4.91e-01 | -0.1236 |
| 1998 | ELF2 | A001-C-104 | Human | Colorectum | FAP | 6.58e-05 | -3.01e-01 | 0.0184 |
| 1998 | ELF2 | A015-C-005 | Human | Colorectum | FAP | 1.81e-04 | -3.17e-01 | -0.0336 |
| Page: 1 2 3 4 5 6 7 8 9 10 |
| Transcriptomic changes along malignancy continuum. |
| Tissue | Expression Dynamics | Abbreviation |
| Cervix |  | CC: Cervix cancer |
| HSIL_HPV: HPV-infected high-grade squamous intraepithelial lesions | ||
| N_HPV: HPV-infected normal cervix | ||
| 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 | ||
| Endometrium |  | AEH: Atypical endometrial hyperplasia |
| EEC: Endometrioid 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 | ||
| Lung |  | AAH: Atypical adenomatous hyperplasia |
| AIS: Adenocarcinoma in situ | ||
| IAC: Invasive lung adenocarcinoma | ||
| MIA: Minimally invasive adenocarcinoma | ||
| Prostate |  | BPH: Benign Prostatic Hyperplasia |
| 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:0022618111 | Esophagus | ESCC | ribonucleoprotein complex assembly | 159/8552 | 220/18723 | 8.19e-16 | 5.71e-14 | 159 |
| GO:0048024111 | Esophagus | ESCC | regulation of mRNA splicing, via spliceosome | 78/8552 | 101/18723 | 8.72e-11 | 2.66e-09 | 78 |
| GO:000038019 | Esophagus | ESCC | alternative mRNA splicing, via spliceosome | 55/8552 | 77/18723 | 4.07e-06 | 4.38e-05 | 55 |
| GO:000038119 | Esophagus | ESCC | regulation of alternative mRNA splicing, via spliceosome | 40/8552 | 60/18723 | 8.30e-04 | 4.28e-03 | 40 |
| GO:000024514 | Esophagus | ESCC | spliceosomal complex assembly | 48/8552 | 79/18723 | 4.93e-03 | 1.89e-02 | 48 |
| GO:00434848 | Lung | IAC | regulation of RNA splicing | 49/2061 | 148/18723 | 4.76e-13 | 7.06e-10 | 49 |
| GO:19033117 | Lung | IAC | regulation of mRNA metabolic process | 71/2061 | 288/18723 | 3.76e-11 | 1.24e-08 | 71 |
| GO:00480248 | Lung | IAC | regulation of mRNA splicing, via spliceosome | 34/2061 | 101/18723 | 1.05e-09 | 1.95e-07 | 34 |
| GO:00506847 | Lung | IAC | regulation of mRNA processing | 41/2061 | 137/18723 | 1.23e-09 | 2.15e-07 | 41 |
| GO:00003817 | Lung | IAC | regulation of alternative mRNA splicing, via spliceosome | 19/2061 | 60/18723 | 1.36e-05 | 4.05e-04 | 19 |
| GO:00003807 | Lung | IAC | alternative mRNA splicing, via spliceosome | 22/2061 | 77/18723 | 1.85e-05 | 5.22e-04 | 22 |
| GO:00718268 | Lung | IAC | ribonucleoprotein complex subunit organization | 46/2061 | 227/18723 | 3.02e-05 | 7.79e-04 | 46 |
| GO:00083808 | Lung | IAC | RNA splicing | 75/2061 | 434/18723 | 4.89e-05 | 1.12e-03 | 75 |
| GO:00226188 | Lung | IAC | ribonucleoprotein complex assembly | 44/2061 | 220/18723 | 6.16e-05 | 1.34e-03 | 44 |
| GO:00003778 | Lung | IAC | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 52/2061 | 320/18723 | 2.64e-03 | 2.44e-02 | 52 |
| GO:00003988 | Lung | IAC | mRNA splicing, via spliceosome | 52/2061 | 320/18723 | 2.64e-03 | 2.44e-02 | 52 |
| GO:19035222 | Lung | IAC | regulation of blood circulation | 43/2061 | 256/18723 | 3.18e-03 | 2.77e-02 | 43 |
| GO:00003758 | Lung | IAC | RNA splicing, via transesterification reactions | 52/2061 | 324/18723 | 3.43e-03 | 2.93e-02 | 52 |
| GO:004348413 | Lung | AIS | regulation of RNA splicing | 45/1849 | 148/18723 | 2.75e-12 | 2.67e-09 | 45 |
| GO:004802413 | Lung | AIS | regulation of mRNA splicing, via spliceosome | 32/1849 | 101/18723 | 1.20e-09 | 2.42e-07 | 32 |
| Page: 1 2 3 4 5 6 7 8 9 10 11 |
| 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 |
| ELF2 | STM | Esophagus | Healthy | F3,DYNC1LI1,RALGDS, etc. | 4.73e-01 |  |
| ELF2 | INMON | Oral cavity | NEOLP | BTRC,COQ8A,TXNDC16, etc. | 3.29e-02 |  |
| ELF2 | BAS | Skin | ADJ | NCOA1,SMC5,ATF2, etc. | 1.97e-01 |  |
| ELF2 | BAS | Skin | cSCC | NCOA1,SMC5,ATF2, etc. | 1.41e-01 |  |
| ELF2 | BAS | Skin | SCCIS | NCOA1,SMC5,ATF2, etc. | 1.82e-01 |  |
| ∗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 |
| ELF2 | SNV | Missense_Mutation | c.1436N>G | p.Thr479Ser | p.T479S | Q15723 | protein_coding | tolerated(0.8) | benign(0) | TCGA-BH-A0EE-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | docetaxel | SD | |
| ELF2 | SNV | Missense_Mutation | rs772612721 | c.1244N>T | p.Ala415Val | p.A415V | Q15723 | protein_coding | tolerated(0.11) | benign(0.009) | TCGA-EW-A1PB-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
| ELF2 | SNV | Missense_Mutation | novel | c.878N>A | p.Pro293Gln | p.P293Q | Q15723 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-EW-A2FR-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | epirubicin | SD |
| ELF2 | SNV | Missense_Mutation | novel | c.791T>G | p.Met264Arg | p.M264R | Q15723 | protein_coding | deleterious(0) | probably_damaging(0.996) | TCGA-5M-AAT6-01 | Colorectum | colon adenocarcinoma | Female | <65 | III/IV | Unknown | Unknown | PD |
| ELF2 | SNV | Missense_Mutation | c.857N>C | p.Val286Ala | p.V286A | Q15723 | protein_coding | tolerated(0.23) | possibly_damaging(0.773) | TCGA-AA-3672-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
| ELF2 | SNV | Missense_Mutation | novel | c.1309N>G | p.Thr437Ala | p.T437A | Q15723 | protein_coding | tolerated(0.83) | benign(0.007) | TCGA-CA-6717-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | oxaliplatin | CR |
| ELF2 | SNV | Missense_Mutation | c.1702N>A | p.Val568Ile | p.V568I | Q15723 | protein_coding | tolerated(0.05) | possibly_damaging(0.764) | TCGA-EI-6882-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
| ELF2 | SNV | Missense_Mutation | novel | c.829C>A | p.Leu277Ile | p.L277I | Q15723 | protein_coding | deleterious(0) | probably_damaging(0.98) | TCGA-F5-6814-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
| ELF2 | SNV | Missense_Mutation | novel | c.698G>T | p.Arg233Ile | p.R233I | Q15723 | protein_coding | deleterious(0) | probably_damaging(0.944) | TCGA-F5-6814-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
| ELF2 | insertion | Nonsense_Mutation | novel | c.1190_1191insCTG | p.Val397_Met398insTer | p.V397_M398ins* | Q15723 | protein_coding | TCGA-AM-5821-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| 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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