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Gene: COL11A1 |
Gene summary for COL11A1 |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | COL11A1 | Gene ID | 1301 |
| Gene name | collagen type XI alpha 1 chain | |
| Gene Alias | CO11A1 | |
| Cytomap | 1p21.1 | |
| Gene Type | protein-coding | GO ID | GO:0001501 | UniProtAcc | P12107 |
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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 |
| 1301 | COL11A1 | P4T-E | Human | Esophagus | ESCC | 2.20e-02 | 2.73e-01 | 0.1323 |
| 1301 | COL11A1 | P9T-E | Human | Esophagus | ESCC | 4.01e-04 | 7.07e-01 | 0.1131 |
| 1301 | COL11A1 | P10T-E | Human | Esophagus | ESCC | 2.02e-06 | 3.94e-01 | 0.116 |
| 1301 | COL11A1 | P22T-E | Human | Esophagus | ESCC | 1.66e-02 | 2.68e-01 | 0.1236 |
| 1301 | COL11A1 | P32T-E | Human | Esophagus | ESCC | 9.53e-09 | 7.25e-01 | 0.1666 |
| 1301 | COL11A1 | P42T-E | Human | Esophagus | ESCC | 9.46e-03 | 3.79e-01 | 0.1175 |
| 1301 | COL11A1 | P44T-E | Human | Esophagus | ESCC | 1.25e-08 | 1.26e+00 | 0.1096 |
| 1301 | COL11A1 | P47T-E | Human | Esophagus | ESCC | 4.17e-05 | 4.84e-01 | 0.1067 |
| 1301 | COL11A1 | P76T-E | Human | Esophagus | ESCC | 1.96e-05 | 2.04e-01 | 0.1207 |
| 1301 | COL11A1 | P128T-E | Human | Esophagus | ESCC | 3.90e-02 | 1.35e-01 | 0.1241 |
| 1301 | COL11A1 | ATC13 | Human | Thyroid | ATC | 2.48e-11 | 3.77e-01 | 0.34 |
| 1301 | COL11A1 | ATC2 | Human | Thyroid | ATC | 4.44e-15 | 2.14e+00 | 0.34 |
| 1301 | COL11A1 | ATC5 | Human | Thyroid | ATC | 2.12e-13 | 4.03e-01 | 0.34 |
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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 | ||
| 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:000320612 | Thyroid | ATC | cardiac chamber morphogenesis | 57/6293 | 121/18723 | 1.39e-03 | 7.20e-03 | 57 |
| GO:00485688 | Thyroid | ATC | embryonic organ development | 172/6293 | 427/18723 | 2.08e-03 | 9.84e-03 | 172 |
| GO:00512163 | Thyroid | ATC | cartilage development | 81/6293 | 190/18723 | 5.70e-03 | 2.30e-02 | 81 |
| GO:000910011 | Thyroid | ATC | glycoprotein metabolic process | 153/6293 | 387/18723 | 7.90e-03 | 3.06e-02 | 153 |
| GO:00032291 | Thyroid | ATC | ventricular cardiac muscle tissue development | 27/6293 | 55/18723 | 1.24e-02 | 4.38e-02 | 27 |
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| Enriched KEGG pathways. |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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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 |
| COL11A1 | SNV | Missense_Mutation | c.3193N>A | p.Ala1065Thr | p.A1065T | P12107 | protein_coding | deleterious(0.05) | probably_damaging(0.989) | TCGA-A2-A0YK-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | SD | |
| COL11A1 | SNV | Missense_Mutation | novel | c.1307C>A | p.Pro436His | p.P436H | P12107 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-A2-A25A-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unspecific | Cytoxan | SD |
| COL11A1 | SNV | Missense_Mutation | c.3187N>C | p.Gly1063Arg | p.G1063R | P12107 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-A8-A06X-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
| COL11A1 | SNV | Missense_Mutation | novel | c.3863G>C | p.Gly1288Ala | p.G1288A | P12107 | protein_coding | deleterious(0) | probably_damaging(0.996) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
| COL11A1 | SNV | Missense_Mutation | c.2288G>C | p.Gly763Ala | p.G763A | P12107 | protein_coding | deleterious(0) | probably_damaging(0.996) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
| COL11A1 | SNV | Missense_Mutation | novel | c.4106G>A | p.Gly1369Asp | p.G1369D | P12107 | protein_coding | deleterious(0) | possibly_damaging(0.541) | TCGA-AC-A2BM-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
| COL11A1 | SNV | Missense_Mutation | c.3184N>T | p.Arg1062Cys | p.R1062C | P12107 | protein_coding | deleterious(0) | probably_damaging(0.99) | TCGA-AN-A0AK-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
| COL11A1 | SNV | Missense_Mutation | c.5295N>C | p.Lys1765Asn | p.K1765N | P12107 | protein_coding | deleterious(0.01) | benign(0.007) | TCGA-D8-A1JA-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | adriamycin | PD | |
| COL11A1 | SNV | Missense_Mutation | c.545N>T | p.Cys182Phe | p.C182F | P12107 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-D8-A1XJ-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Hormone Therapy | tamoxiphen | SD | |
| COL11A1 | SNV | Missense_Mutation | c.3973C>T | p.Pro1325Ser | p.P1325S | P12107 | protein_coding | deleterious(0.05) | benign(0.395) | TCGA-E2-A10C-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | SD |
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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 |
| 1301 | COL11A1 | DRUGGABLE GENOME | CHEMBL2095222 | OCRIPLASMIN | ||
| 1301 | COL11A1 | DRUGGABLE GENOME | CHEMBL2108709 | COLLAGENASE CLOSTRIDIUM HISTOLYTICUM |
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