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Gene: SRSF11 |
Gene summary for SRSF11 |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | SRSF11 | Gene ID | 9295 |
| Gene name | serine and arginine rich splicing factor 11 | |
| Gene Alias | NET2 | |
| Cytomap | 1p31.1 | |
| Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | Q05519 |
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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 |
| 9295 | SRSF11 | HTA11_3410_2000001011 | Human | Colorectum | AD | 3.74e-30 | -7.79e-01 | 0.0155 |
| 9295 | SRSF11 | HTA11_2487_2000001011 | Human | Colorectum | SER | 2.21e-04 | -4.51e-01 | -0.1808 |
| 9295 | SRSF11 | HTA11_3361_2000001011 | Human | Colorectum | AD | 2.17e-14 | -7.72e-01 | -0.1207 |
| 9295 | SRSF11 | HTA11_696_2000001011 | Human | Colorectum | AD | 1.64e-14 | -5.08e-01 | -0.1464 |
| 9295 | SRSF11 | HTA11_866_2000001011 | Human | Colorectum | AD | 6.66e-06 | -3.69e-01 | -0.1001 |
| 9295 | SRSF11 | HTA11_5212_2000001011 | Human | Colorectum | AD | 9.12e-05 | -6.90e-01 | -0.2061 |
| 9295 | SRSF11 | HTA11_866_3004761011 | Human | Colorectum | AD | 1.32e-03 | -4.02e-01 | 0.096 |
| 9295 | SRSF11 | HTA11_4255_2000001011 | Human | Colorectum | SER | 4.89e-03 | -6.71e-01 | 0.0446 |
| 9295 | SRSF11 | HTA11_8622_2000001021 | Human | Colorectum | SER | 2.57e-02 | -6.02e-01 | 0.0528 |
| 9295 | SRSF11 | HTA11_10711_2000001011 | Human | Colorectum | AD | 6.02e-08 | -6.05e-01 | 0.0338 |
| 9295 | SRSF11 | HTA11_7696_3000711011 | Human | Colorectum | AD | 8.11e-04 | -3.28e-01 | 0.0674 |
| 9295 | SRSF11 | HTA11_11156_2000001011 | Human | Colorectum | AD | 8.42e-03 | -9.25e-01 | 0.0397 |
| 9295 | SRSF11 | HTA11_6818_2000001021 | Human | Colorectum | AD | 1.13e-02 | -4.81e-01 | 0.0588 |
| 9295 | SRSF11 | HTA11_99999973899_84307 | Human | Colorectum | MSS | 2.89e-02 | -5.05e-01 | 0.2585 |
| 9295 | SRSF11 | HTA11_99999974143_84620 | Human | Colorectum | MSS | 3.91e-12 | -4.14e-01 | 0.3005 |
| 9295 | SRSF11 | A002-C-010 | Human | Colorectum | FAP | 4.23e-04 | -2.22e-01 | 0.242 |
| 9295 | SRSF11 | A001-C-207 | Human | Colorectum | FAP | 1.01e-02 | -2.16e-01 | 0.1278 |
| 9295 | SRSF11 | A015-C-203 | Human | Colorectum | FAP | 1.36e-34 | 9.27e-03 | -0.1294 |
| 9295 | SRSF11 | A015-C-204 | Human | Colorectum | FAP | 3.94e-05 | -1.66e-01 | -0.0228 |
| 9295 | SRSF11 | A014-C-040 | Human | Colorectum | FAP | 1.08e-04 | -1.88e-01 | -0.1184 |
| Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 |
| 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 | ||
| 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 | ||
| 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 |
| 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:0008380 | Colorectum | AD | RNA splicing | 169/3918 | 434/18723 | 3.59e-18 | 2.04e-15 | 169 |
| GO:00083801 | Colorectum | SER | RNA splicing | 123/2897 | 434/18723 | 3.84e-12 | 8.41e-10 | 123 |
| GO:00083802 | Colorectum | MSS | RNA splicing | 159/3467 | 434/18723 | 1.75e-19 | 1.22e-16 | 159 |
| GO:00083804 | Colorectum | FAP | RNA splicing | 108/2622 | 434/18723 | 7.90e-10 | 1.86e-07 | 108 |
| GO:00083805 | Colorectum | CRC | RNA splicing | 90/2078 | 434/18723 | 2.80e-09 | 7.97e-07 | 90 |
| GO:000838016 | Endometrium | AEH | RNA splicing | 111/2100 | 434/18723 | 2.42e-17 | 1.12e-14 | 111 |
| GO:000838017 | Endometrium | EEC | RNA splicing | 111/2168 | 434/18723 | 2.45e-16 | 1.13e-13 | 111 |
| GO:000838026 | Esophagus | HGIN | RNA splicing | 160/2587 | 434/18723 | 3.74e-34 | 1.12e-30 | 160 |
| GO:0008380111 | Esophagus | ESCC | RNA splicing | 336/8552 | 434/18723 | 1.74e-42 | 3.67e-39 | 336 |
| GO:000838012 | Liver | Cirrhotic | RNA splicing | 229/4634 | 434/18723 | 9.13e-37 | 2.86e-33 | 229 |
| GO:000838022 | Liver | HCC | RNA splicing | 313/7958 | 434/18723 | 1.36e-36 | 1.73e-33 | 313 |
| GO:00083808 | Lung | IAC | RNA splicing | 75/2061 | 434/18723 | 4.89e-05 | 1.12e-03 | 75 |
| GO:000838013 | Lung | AIS | RNA splicing | 68/1849 | 434/18723 | 8.50e-05 | 2.11e-03 | 68 |
| GO:000838023 | Lung | MIAC | RNA splicing | 44/967 | 434/18723 | 1.56e-05 | 1.07e-03 | 44 |
| GO:000838020 | Oral cavity | OSCC | RNA splicing | 308/7305 | 434/18723 | 2.43e-42 | 7.70e-39 | 308 |
| GO:0008380110 | Oral cavity | LP | RNA splicing | 237/4623 | 434/18723 | 1.82e-41 | 3.79e-38 | 237 |
| GO:000838025 | Oral cavity | EOLP | RNA splicing | 115/2218 | 434/18723 | 2.24e-17 | 3.04e-14 | 115 |
| GO:000838033 | Oral cavity | NEOLP | RNA splicing | 110/2005 | 434/18723 | 2.29e-18 | 2.72e-15 | 110 |
| GO:000838018 | Prostate | BPH | RNA splicing | 147/3107 | 434/18723 | 5.17e-19 | 2.29e-16 | 147 |
| GO:000838019 | Prostate | Tumor | RNA splicing | 153/3246 | 434/18723 | 9.15e-20 | 5.79e-17 | 153 |
| Page: 1 2 |
| 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 |
| SRSF11 | SNV | Missense_Mutation | c.1441N>A | p.Asp481Asn | p.D481N | Q05519 | protein_coding | deleterious_low_confidence(0) | benign(0.307) | TCGA-A2-A0SW-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Hormone Therapy | arimidex | PD | |
| SRSF11 | SNV | Missense_Mutation | c.511N>C | p.Gly171Arg | p.G171R | Q05519 | protein_coding | deleterious(0) | possibly_damaging(0.71) | TCGA-AR-A0TZ-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unspecific | Doxorubicin | PD | |
| SRSF11 | SNV | Missense_Mutation | c.275N>T | p.Ala92Val | p.A92V | Q05519 | protein_coding | deleterious(0) | possibly_damaging(0.687) | TCGA-BH-A0E9-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | taxotere | CR | |
| SRSF11 | SNV | Missense_Mutation | c.965N>C | p.Arg322Pro | p.R322P | Q05519 | protein_coding | deleterious(0.01) | possibly_damaging(0.769) | TCGA-D8-A1JF-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
| SRSF11 | SNV | Missense_Mutation | c.553N>A | p.Asp185Asn | p.D185N | Q05519 | protein_coding | deleterious(0.04) | possibly_damaging(0.681) | TCGA-D8-A1Y1-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Hormone Therapy | tamoxiphen | PD | |
| SRSF11 | insertion | Frame_Shift_Ins | novel | c.115_116insCTTTTGC | p.Asn39ThrfsTer9 | p.N39Tfs*9 | Q05519 | protein_coding | TCGA-AO-A0JB-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | cyclophosphamide | SD | ||
| SRSF11 | insertion | Nonsense_Mutation | novel | c.116_117insGGAGGATGAATGCTTTTTTTAAAAAAAAAGTTTATACG | p.Asn39LysfsTer8 | p.N39Kfs*8 | Q05519 | protein_coding | TCGA-AO-A0JB-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | cyclophosphamide | SD | ||
| SRSF11 | SNV | Missense_Mutation | novel | c.1342G>A | p.Gly448Ser | p.G448S | Q05519 | protein_coding | tolerated_low_confidence(0.7) | benign(0.023) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
| SRSF11 | SNV | Missense_Mutation | novel | c.1147N>A | p.Asp383Asn | p.D383N | Q05519 | protein_coding | deleterious(0.02) | benign(0.07) | TCGA-MA-AA41-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
| SRSF11 | SNV | Missense_Mutation | c.823N>T | p.Arg275Trp | p.R275W | Q05519 | protein_coding | deleterious(0) | probably_damaging(0.99) | TCGA-AA-3950-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| Page: 1 2 3 4 5 6 |
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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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