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Gene: CGN |
Gene summary for CGN |
Gene summary. |
Gene information | Species | Human | Gene symbol | CGN | Gene ID | 57530 |
Gene name | cingulin | |
Gene Alias | CGN | |
Cytomap | 1q21.3 | |
Gene Type | protein-coding | GO ID | GO:0008150 | UniProtAcc | Q9P2M7 |
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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 |
57530 | CGN | HTA11_2487_2000001011 | Human | Colorectum | SER | 1.56e-06 | 6.72e-01 | -0.1808 |
57530 | CGN | HTA11_1938_2000001011 | Human | Colorectum | AD | 1.39e-02 | 3.36e-01 | -0.0811 |
57530 | CGN | HTA11_347_2000001011 | Human | Colorectum | AD | 7.93e-20 | 7.34e-01 | -0.1954 |
57530 | CGN | HTA11_411_2000001011 | Human | Colorectum | SER | 1.20e-03 | 9.71e-01 | -0.2602 |
57530 | CGN | HTA11_3361_2000001011 | Human | Colorectum | AD | 6.17e-04 | 4.66e-01 | -0.1207 |
57530 | CGN | HTA11_83_2000001011 | Human | Colorectum | SER | 3.37e-03 | 5.89e-01 | -0.1526 |
57530 | CGN | HTA11_696_2000001011 | Human | Colorectum | AD | 1.00e-23 | 6.83e-01 | -0.1464 |
57530 | CGN | HTA11_866_2000001011 | Human | Colorectum | AD | 1.11e-10 | 4.04e-01 | -0.1001 |
57530 | CGN | HTA11_1391_2000001011 | Human | Colorectum | AD | 1.72e-06 | 5.68e-01 | -0.059 |
57530 | CGN | HTA11_5212_2000001011 | Human | Colorectum | AD | 2.53e-03 | 4.56e-01 | -0.2061 |
57530 | CGN | HTA11_7696_3000711011 | Human | Colorectum | AD | 1.16e-05 | 2.38e-01 | 0.0674 |
57530 | CGN | HTA11_99999971662_82457 | Human | Colorectum | MSS | 3.94e-13 | 4.64e-01 | 0.3859 |
57530 | CGN | HTA11_99999974143_84620 | Human | Colorectum | MSS | 1.80e-03 | 2.18e-01 | 0.3005 |
57530 | CGN | A002-C-205 | Human | Colorectum | FAP | 7.59e-03 | -6.12e-02 | -0.1236 |
57530 | CGN | A015-C-002 | Human | Colorectum | FAP | 5.14e-03 | -2.25e-01 | -0.0763 |
57530 | CGN | LZE24T | Human | Esophagus | ESCC | 8.06e-06 | 1.11e-01 | 0.0596 |
57530 | CGN | P1T-E | Human | Esophagus | ESCC | 1.62e-03 | 2.92e-01 | 0.0875 |
57530 | CGN | P2T-E | Human | Esophagus | ESCC | 4.11e-19 | 2.02e-01 | 0.1177 |
57530 | CGN | P8T-E | Human | Esophagus | ESCC | 3.67e-22 | 4.47e-01 | 0.0889 |
57530 | CGN | P10T-E | Human | Esophagus | ESCC | 4.70e-07 | 1.08e-01 | 0.116 |
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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:00070157 | Liver | NAFLD | actin filament organization | 78/1882 | 442/18723 | 5.44e-07 | 3.21e-05 | 78 |
GO:00310326 | Liver | NAFLD | actomyosin structure organization | 41/1882 | 196/18723 | 4.26e-06 | 1.66e-04 | 41 |
GO:00510564 | Liver | NAFLD | regulation of small GTPase mediated signal transduction | 56/1882 | 302/18723 | 4.62e-06 | 1.75e-04 | 56 |
GO:19029037 | Liver | NAFLD | regulation of supramolecular fiber organization | 66/1882 | 383/18723 | 8.97e-06 | 2.96e-04 | 66 |
GO:00329707 | Liver | NAFLD | regulation of actin filament-based process | 66/1882 | 397/18723 | 2.92e-05 | 7.72e-04 | 66 |
GO:00329567 | Liver | NAFLD | regulation of actin cytoskeleton organization | 60/1882 | 358/18723 | 5.20e-05 | 1.20e-03 | 60 |
GO:01100537 | Liver | NAFLD | regulation of actin filament organization | 49/1882 | 278/18723 | 6.88e-05 | 1.46e-03 | 49 |
GO:00510583 | Liver | NAFLD | negative regulation of small GTPase mediated signal transduction | 16/1882 | 56/18723 | 8.53e-05 | 1.72e-03 | 16 |
GO:00300387 | Liver | NAFLD | contractile actin filament bundle assembly | 24/1882 | 106/18723 | 1.10e-04 | 2.13e-03 | 24 |
GO:00431497 | Liver | NAFLD | stress fiber assembly | 24/1882 | 106/18723 | 1.10e-04 | 2.13e-03 | 24 |
GO:01100207 | Liver | NAFLD | regulation of actomyosin structure organization | 22/1882 | 100/18723 | 3.22e-04 | 4.98e-03 | 22 |
GO:00514927 | Liver | NAFLD | regulation of stress fiber assembly | 20/1882 | 91/18723 | 5.98e-04 | 7.95e-03 | 20 |
GO:00615727 | Liver | NAFLD | actin filament bundle organization | 29/1882 | 161/18723 | 1.37e-03 | 1.54e-02 | 29 |
GO:00322317 | Liver | NAFLD | regulation of actin filament bundle assembly | 21/1882 | 105/18723 | 1.60e-03 | 1.71e-02 | 21 |
GO:00510177 | Liver | NAFLD | actin filament bundle assembly | 28/1882 | 157/18723 | 1.91e-03 | 1.93e-02 | 28 |
GO:000701512 | Liver | Cirrhotic | actin filament organization | 171/4634 | 442/18723 | 3.93e-11 | 2.30e-09 | 171 |
GO:190290312 | Liver | Cirrhotic | regulation of supramolecular fiber organization | 148/4634 | 383/18723 | 8.85e-10 | 4.08e-08 | 148 |
GO:003297012 | Liver | Cirrhotic | regulation of actin filament-based process | 152/4634 | 397/18723 | 1.12e-09 | 5.00e-08 | 152 |
GO:003295612 | Liver | Cirrhotic | regulation of actin cytoskeleton organization | 136/4634 | 358/18723 | 1.47e-08 | 5.49e-07 | 136 |
GO:005101712 | Liver | Cirrhotic | actin filament bundle assembly | 69/4634 | 157/18723 | 1.06e-07 | 3.05e-06 | 69 |
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Enriched KEGG pathways. |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa04530 | Colorectum | AD | Tight junction | 76/2092 | 169/8465 | 5.49e-09 | 9.69e-08 | 6.18e-08 | 76 |
hsa045301 | Colorectum | AD | Tight junction | 76/2092 | 169/8465 | 5.49e-09 | 9.69e-08 | 6.18e-08 | 76 |
hsa045302 | Colorectum | SER | Tight junction | 59/1580 | 169/8465 | 3.24e-07 | 5.98e-06 | 4.34e-06 | 59 |
hsa045303 | Colorectum | SER | Tight junction | 59/1580 | 169/8465 | 3.24e-07 | 5.98e-06 | 4.34e-06 | 59 |
hsa045304 | Colorectum | MSS | Tight junction | 66/1875 | 169/8465 | 4.10e-07 | 6.25e-06 | 3.83e-06 | 66 |
hsa045305 | Colorectum | MSS | Tight junction | 66/1875 | 169/8465 | 4.10e-07 | 6.25e-06 | 3.83e-06 | 66 |
hsa045308 | Colorectum | FAP | Tight junction | 60/1404 | 169/8465 | 1.40e-09 | 9.33e-08 | 5.67e-08 | 60 |
hsa045309 | Colorectum | FAP | Tight junction | 60/1404 | 169/8465 | 1.40e-09 | 9.33e-08 | 5.67e-08 | 60 |
hsa04530211 | Esophagus | ESCC | Tight junction | 105/4205 | 169/8465 | 6.73e-04 | 2.23e-03 | 1.14e-03 | 105 |
hsa04530310 | Esophagus | ESCC | Tight junction | 105/4205 | 169/8465 | 6.73e-04 | 2.23e-03 | 1.14e-03 | 105 |
hsa0453022 | Liver | Cirrhotic | Tight junction | 82/2530 | 169/8465 | 2.14e-07 | 2.85e-06 | 1.76e-06 | 82 |
hsa0453032 | Liver | Cirrhotic | Tight junction | 82/2530 | 169/8465 | 2.14e-07 | 2.85e-06 | 1.76e-06 | 82 |
hsa0453042 | Liver | HCC | Tight junction | 110/4020 | 169/8465 | 2.45e-06 | 2.28e-05 | 1.27e-05 | 110 |
hsa0453052 | Liver | HCC | Tight junction | 110/4020 | 169/8465 | 2.45e-06 | 2.28e-05 | 1.27e-05 | 110 |
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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 |
CGN | SNV | Missense_Mutation | novel | c.1184N>G | p.Gln395Arg | p.Q395R | Q9P2M7 | protein_coding | tolerated(0.46) | benign(0.015) | TCGA-AA-3833-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
CGN | SNV | Missense_Mutation | rs761721175 | c.1286N>A | p.Arg429His | p.R429H | Q9P2M7 | protein_coding | tolerated(0.19) | benign(0.001) | TCGA-AA-3947-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
CGN | SNV | Missense_Mutation | rs762534512 | c.1072N>A | p.Val358Met | p.V358M | Q9P2M7 | protein_coding | tolerated(0.12) | benign(0.005) | TCGA-AA-3966-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
CGN | SNV | Missense_Mutation | c.181G>A | p.Ala61Thr | p.A61T | Q9P2M7 | protein_coding | deleterious(0.03) | probably_damaging(0.999) | TCGA-AA-3977-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
CGN | SNV | Missense_Mutation | c.2853N>T | p.Glu951Asp | p.E951D | Q9P2M7 | protein_coding | tolerated(0.15) | benign(0.028) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR | |
CGN | SNV | Missense_Mutation | rs765530896 | c.1555N>T | p.Arg519Trp | p.R519W | Q9P2M7 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-AA-A01R-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | 5-fluorouracil | PD |
CGN | SNV | Missense_Mutation | novel | c.1226T>C | p.Leu409Pro | p.L409P | Q9P2M7 | protein_coding | tolerated(0.21) | probably_damaging(0.921) | TCGA-AD-6964-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | folfox | PD |
CGN | SNV | Missense_Mutation | novel | c.488N>G | p.Val163Gly | p.V163G | Q9P2M7 | protein_coding | tolerated(0.38) | benign(0) | TCGA-AY-4070-01 | Colorectum | colon adenocarcinoma | Female | <65 | III/IV | Chemotherapy | 5-fu | PD |
CGN | SNV | Missense_Mutation | rs753255750 | c.1853N>A | p.Arg618Gln | p.R618Q | Q9P2M7 | protein_coding | tolerated(0.11) | benign(0.027) | TCGA-CA-6717-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | oxaliplatin | CR |
CGN | SNV | Missense_Mutation | c.686N>A | p.Arg229His | p.R229H | Q9P2M7 | protein_coding | tolerated(0.22) | benign(0.007) | TCGA-D5-6930-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | 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 |
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