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Gene: CLU |
Gene summary for CLU |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | CLU | Gene ID | 1191 |
| Gene name | clusterin | |
| Gene Alias | AAG4 | |
| Cytomap | 8p21.1 | |
| Gene Type | protein-coding | GO ID | GO:0000902 | UniProtAcc | P10909 |
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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 |
| 1191 | CLU | GSM4909282 | Human | Breast | IDC | 3.33e-34 | -8.49e-01 | -0.0288 |
| 1191 | CLU | GSM4909285 | Human | Breast | IDC | 5.64e-39 | -8.76e-01 | 0.21 |
| 1191 | CLU | GSM4909288 | Human | Breast | IDC | 3.98e-03 | -3.45e-01 | 0.0988 |
| 1191 | CLU | GSM4909290 | Human | Breast | IDC | 2.17e-38 | -9.43e-01 | 0.2096 |
| 1191 | CLU | GSM4909293 | Human | Breast | IDC | 2.68e-14 | -5.99e-01 | 0.1581 |
| 1191 | CLU | GSM4909294 | Human | Breast | IDC | 1.78e-10 | -4.40e-01 | 0.2022 |
| 1191 | CLU | GSM4909296 | Human | Breast | IDC | 6.83e-33 | -7.74e-01 | 0.1524 |
| 1191 | CLU | GSM4909297 | Human | Breast | IDC | 3.03e-10 | -2.40e-01 | 0.1517 |
| 1191 | CLU | GSM4909298 | Human | Breast | IDC | 1.61e-07 | -5.29e-01 | 0.1551 |
| 1191 | CLU | GSM4909299 | Human | Breast | IDC | 3.59e-17 | 5.67e-01 | 0.035 |
| 1191 | CLU | GSM4909300 | Human | Breast | IDC | 9.03e-05 | 4.60e-01 | 0.0334 |
| 1191 | CLU | GSM4909301 | Human | Breast | IDC | 1.76e-22 | -7.36e-01 | 0.1577 |
| 1191 | CLU | GSM4909304 | Human | Breast | IDC | 8.74e-22 | -7.57e-01 | 0.1636 |
| 1191 | CLU | GSM4909311 | Human | Breast | IDC | 5.72e-38 | -7.49e-01 | 0.1534 |
| 1191 | CLU | GSM4909312 | Human | Breast | IDC | 1.55e-32 | -7.91e-01 | 0.1552 |
| 1191 | CLU | GSM4909313 | Human | Breast | IDC | 3.75e-02 | 1.83e-01 | 0.0391 |
| 1191 | CLU | GSM4909315 | Human | Breast | IDC | 2.63e-04 | -3.33e-01 | 0.21 |
| 1191 | CLU | GSM4909316 | Human | Breast | IDC | 4.55e-04 | -5.96e-01 | 0.21 |
| 1191 | CLU | GSM4909318 | Human | Breast | IDC | 2.93e-05 | -7.64e-01 | 0.2031 |
| 1191 | CLU | GSM4909319 | Human | Breast | IDC | 2.47e-39 | -4.32e-01 | 0.1563 |
| Page: 1 2 3 4 5 6 7 8 9 10 11 12 |
| Transcriptomic changes along malignancy continuum. |
| Tissue | Expression Dynamics | Abbreviation |
| Breast |  | IDC: Invasive ductal carcinoma |
| DCIS: Ductal carcinoma in situ | ||
| Precancer(BRCA1-mut): Precancerous lesion from BRCA1 mutation carriers | ||
| Cervix |  | CC: Cervix cancer |
| HSIL_HPV: HPV-infected high-grade squamous intraepithelial lesions | ||
| N_HPV: HPV-infected normal cervix | ||
| Endometrium |  | AEH: Atypical endometrial hyperplasia |
| EEC: Endometrioid Cancer | ||
| Esophagus |  | ESCC: Esophageal squamous cell carcinoma |
| HGIN: High-grade intraepithelial neoplasias | ||
| LGIN: Low-grade intraepithelial neoplasias | ||
| GC |  | CAG: Chronic atrophic gastritis |
| CAG with IM: Chronic atrophic gastritis with intestinal metaplasia | ||
| CSG: Chronic superficial gastritis | ||
| GC: Gastric cancer | ||
| SIM: Severe intestinal metaplasia | ||
| WIM: Wild intestinal metaplasia | ||
| 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 |
| 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:000961518 | Esophagus | ESCC | response to virus | 238/8552 | 367/18723 | 6.65e-14 | 3.32e-12 | 238 |
| GO:1901800110 | Esophagus | ESCC | positive regulation of proteasomal protein catabolic process | 91/8552 | 114/18723 | 6.74e-14 | 3.34e-12 | 91 |
| GO:1903052110 | Esophagus | ESCC | positive regulation of proteolysis involved in cellular protein catabolic process | 101/8552 | 133/18723 | 9.58e-13 | 4.19e-11 | 101 |
| GO:0010821110 | Esophagus | ESCC | regulation of mitochondrion organization | 107/8552 | 144/18723 | 2.31e-12 | 9.41e-11 | 107 |
| GO:2001243111 | Esophagus | ESCC | negative regulation of intrinsic apoptotic signaling pathway | 78/8552 | 98/18723 | 5.50e-12 | 2.10e-10 | 78 |
| GO:0008630110 | Esophagus | ESCC | intrinsic apoptotic signaling pathway in response to DNA damage | 78/8552 | 99/18723 | 1.43e-11 | 5.08e-10 | 78 |
| GO:0008637110 | Esophagus | ESCC | apoptotic mitochondrial changes | 83/8552 | 107/18723 | 1.43e-11 | 5.08e-10 | 83 |
| GO:0032436111 | Esophagus | ESCC | positive regulation of proteasomal ubiquitin-dependent protein catabolic process | 72/8552 | 90/18723 | 2.30e-11 | 7.87e-10 | 72 |
| GO:1902905111 | Esophagus | ESCC | positive regulation of supramolecular fiber organization | 142/8552 | 209/18723 | 5.51e-11 | 1.76e-09 | 142 |
| GO:1902903111 | Esophagus | ESCC | regulation of supramolecular fiber organization | 237/8552 | 383/18723 | 9.06e-11 | 2.75e-09 | 237 |
| GO:0061077110 | Esophagus | ESCC | chaperone-mediated protein folding | 56/8552 | 67/18723 | 1.52e-10 | 4.36e-09 | 56 |
| GO:2000060111 | Esophagus | ESCC | positive regulation of ubiquitin-dependent protein catabolic process | 81/8552 | 107/18723 | 2.23e-10 | 6.34e-09 | 81 |
| GO:2001020110 | Esophagus | ESCC | regulation of response to DNA damage stimulus | 145/8552 | 219/18723 | 5.97e-10 | 1.50e-08 | 145 |
| GO:0010639110 | Esophagus | ESCC | negative regulation of organelle organization | 215/8552 | 348/18723 | 8.20e-10 | 2.01e-08 | 215 |
| GO:00070419 | Esophagus | ESCC | lysosomal transport | 83/8552 | 114/18723 | 3.52e-09 | 7.41e-08 | 83 |
| GO:1905897111 | Esophagus | ESCC | regulation of response to endoplasmic reticulum stress | 63/8552 | 82/18723 | 8.16e-09 | 1.66e-07 | 63 |
| GO:0070997111 | Esophagus | ESCC | neuron death | 216/8552 | 361/18723 | 3.49e-08 | 6.45e-07 | 216 |
| GO:003010018 | Esophagus | ESCC | regulation of endocytosis | 135/8552 | 211/18723 | 5.75e-08 | 1.02e-06 | 135 |
| GO:000183619 | Esophagus | ESCC | release of cytochrome c from mitochondria | 47/8552 | 59/18723 | 9.02e-08 | 1.51e-06 | 47 |
| GO:00726659 | Esophagus | ESCC | protein localization to vacuole | 52/8552 | 67/18723 | 9.14e-08 | 1.52e-06 | 52 |
| 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 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 |
| Enriched KEGG pathways. |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
| hsa04610 | Liver | NAFLD | Complement and coagulation cascades | 35/1043 | 86/8465 | 2.48e-11 | 2.04e-09 | 1.64e-09 | 35 |
| hsa046101 | Liver | NAFLD | Complement and coagulation cascades | 35/1043 | 86/8465 | 2.48e-11 | 2.04e-09 | 1.64e-09 | 35 |
| hsa046102 | Liver | Cirrhotic | Complement and coagulation cascades | 48/2530 | 86/8465 | 4.41e-07 | 5.44e-06 | 3.35e-06 | 48 |
| hsa046103 | Liver | Cirrhotic | Complement and coagulation cascades | 48/2530 | 86/8465 | 4.41e-07 | 5.44e-06 | 3.35e-06 | 48 |
| hsa046104 | Liver | HCC | Complement and coagulation cascades | 57/4020 | 86/8465 | 3.19e-04 | 1.45e-03 | 8.04e-04 | 57 |
| hsa046105 | Liver | HCC | Complement and coagulation cascades | 57/4020 | 86/8465 | 3.19e-04 | 1.45e-03 | 8.04e-04 | 57 |
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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 |
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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 |
| CLU | SNV | Missense_Mutation | novel | c.1199C>T | p.Ser400Phe | p.S400F | P10909 | protein_coding | deleterious(0) | possibly_damaging(0.708) | TCGA-3C-AALI-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unspecific | Poly E | Complete Response |
| CLU | SNV | Missense_Mutation | novel | c.862N>G | p.Ile288Val | p.I288V | P10909 | protein_coding | deleterious(0.04) | possibly_damaging(0.524) | TCGA-D8-A1JF-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
| CLU | SNV | Missense_Mutation | novel | c.58N>T | p.Val20Phe | p.V20F | P10909 | protein_coding | deleterious(0.01) | probably_damaging(0.991) | TCGA-V7-A7HQ-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Hormone Therapy | letrozole | CR |
| CLU | SNV | Missense_Mutation | c.139N>A | p.Gln47Lys | p.Q47K | P10909 | protein_coding | tolerated(0.31) | benign(0.005) | TCGA-AA-3510-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
| CLU | SNV | Missense_Mutation | c.1027N>A | p.Glu343Lys | p.E343K | P10909 | protein_coding | tolerated(0.23) | possibly_damaging(0.503) | TCGA-AA-3672-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
| CLU | SNV | Missense_Mutation | rs769830551 | c.679C>T | p.Arg227Cys | p.R227C | P10909 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AA-A01K-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Chemotherapy | folinic | CR |
| CLU | SNV | Missense_Mutation | rs146625005 | c.1135N>A | p.Glu379Lys | p.E379K | P10909 | protein_coding | tolerated(0.5) | benign(0.195) | TCGA-AA-A01R-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | 5-fluorouracil | PD |
| CLU | SNV | Missense_Mutation | c.236N>T | p.Lys79Met | p.K79M | P10909 | protein_coding | tolerated(0.08) | probably_damaging(0.995) | TCGA-AA-A02O-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
| CLU | SNV | Missense_Mutation | novel | c.98N>G | p.Glu33Gly | p.E33G | P10909 | protein_coding | deleterious(0) | probably_damaging(0.949) | TCGA-AZ-4315-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
| CLU | SNV | Missense_Mutation | c.657N>G | p.Phe219Leu | p.F219L | P10909 | protein_coding | tolerated(0.77) | benign(0.015) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
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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 |
| 1191 | CLU | CELL SURFACE, DRUGGABLE GENOME | OGX-011 | CUSTIRSEN SODIUM | ||
| 1191 | CLU | CELL SURFACE, DRUGGABLE GENOME | antisense oligonucleotide | CUSTIRSEN | CUSTIRSEN | |
| 1191 | CLU | CELL SURFACE, DRUGGABLE GENOME | PMSG | 1547735 | ||
| 1191 | CLU | CELL SURFACE, DRUGGABLE GENOME | inhibitor | OGX-011 | CUSTIRSEN SODIUM | |
| 1191 | CLU | CELL SURFACE, DRUGGABLE GENOME | LUBIPROSTONE | LUBIPROSTONE |
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