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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 |
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Transcriptomic changes along malignancy continuum. |
∗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). |
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Enriched GO biological processes. |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:00313346 | Stomach | GC | positive regulation of protein-containing complex assembly | 39/1159 | 237/18723 | 2.00e-08 | 1.63e-06 | 39 |
GO:19029036 | Stomach | GC | regulation of supramolecular fiber organization | 53/1159 | 383/18723 | 3.07e-08 | 2.39e-06 | 53 |
GO:20012346 | Stomach | GC | negative regulation of apoptotic signaling pathway | 37/1159 | 224/18723 | 4.14e-08 | 2.85e-06 | 37 |
GO:00971936 | Stomach | GC | intrinsic apoptotic signaling pathway | 43/1159 | 288/18723 | 7.09e-08 | 4.62e-06 | 43 |
GO:00610776 | Stomach | GC | chaperone-mediated protein folding | 18/1159 | 67/18723 | 8.05e-08 | 5.15e-06 | 18 |
GO:00359666 | Stomach | GC | response to topologically incorrect protein | 29/1159 | 159/18723 | 1.37e-07 | 8.14e-06 | 29 |
GO:00086376 | Stomach | GC | apoptotic mitochondrial changes | 22/1159 | 107/18723 | 5.25e-07 | 2.67e-05 | 22 |
GO:19029056 | Stomach | GC | positive regulation of supramolecular fiber organization | 32/1159 | 209/18723 | 1.88e-06 | 8.30e-05 | 32 |
GO:0006959 | Stomach | GC | humoral immune response | 42/1159 | 317/18723 | 2.59e-06 | 1.10e-04 | 42 |
GO:20012426 | Stomach | GC | regulation of intrinsic apoptotic signaling pathway | 27/1159 | 164/18723 | 2.91e-06 | 1.23e-04 | 27 |
GO:00316476 | Stomach | GC | regulation of protein stability | 40/1159 | 298/18723 | 3.23e-06 | 1.31e-04 | 40 |
GO:00508216 | Stomach | GC | protein stabilization | 29/1159 | 191/18723 | 6.65e-06 | 2.54e-04 | 29 |
GO:00018365 | Stomach | GC | release of cytochrome c from mitochondria | 14/1159 | 59/18723 | 1.08e-05 | 3.57e-04 | 14 |
GO:00342506 | Stomach | GC | positive regulation of cellular amide metabolic process | 25/1159 | 162/18723 | 2.12e-05 | 6.44e-04 | 25 |
GO:0061684 | Stomach | GC | chaperone-mediated autophagy | 7/1159 | 16/18723 | 2.38e-05 | 6.93e-04 | 7 |
GO:00458626 | Stomach | GC | positive regulation of proteolysis | 44/1159 | 372/18723 | 2.81e-05 | 7.88e-04 | 44 |
GO:20012436 | Stomach | GC | negative regulation of intrinsic apoptotic signaling pathway | 18/1159 | 98/18723 | 2.85e-05 | 7.90e-04 | 18 |
GO:00462096 | Stomach | GC | nitric oxide metabolic process | 16/1159 | 81/18723 | 3.09e-05 | 8.48e-04 | 16 |
GO:20010576 | Stomach | GC | reactive nitrogen species metabolic process | 16/1159 | 82/18723 | 3.62e-05 | 9.51e-04 | 16 |
GO:00421766 | Stomach | GC | regulation of protein catabolic process | 45/1159 | 391/18723 | 4.48e-05 | 1.09e-03 | 45 |
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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. |
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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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