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Gene: CLASP2 |
Gene summary for CLASP2 |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | CLASP2 | Gene ID | 23122 |
| Gene name | cytoplasmic linker associated protein 2 | |
| Gene Alias | CLASP2 | |
| Cytomap | 3p22.3 | |
| Gene Type | protein-coding | GO ID | GO:0000226 | UniProtAcc | O75122 |
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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 |
| 23122 | CLASP2 | CCI_2 | Human | Cervix | CC | 5.33e-04 | 6.80e-01 | 0.5249 |
| 23122 | CLASP2 | CCI_3 | Human | Cervix | CC | 1.79e-13 | 8.49e-01 | 0.516 |
| 23122 | CLASP2 | HTA11_3410_2000001011 | Human | Colorectum | AD | 5.80e-09 | -3.32e-01 | 0.0155 |
| 23122 | CLASP2 | HTA11_3361_2000001011 | Human | Colorectum | AD | 4.94e-06 | -4.43e-01 | -0.1207 |
| 23122 | CLASP2 | HTA11_5212_2000001011 | Human | Colorectum | AD | 1.36e-02 | -4.70e-01 | -0.2061 |
| 23122 | CLASP2 | HTA11_866_3004761011 | Human | Colorectum | AD | 1.77e-04 | -2.49e-01 | 0.096 |
| 23122 | CLASP2 | F007 | Human | Colorectum | FAP | 5.10e-03 | -2.64e-01 | 0.1176 |
| 23122 | CLASP2 | A001-C-207 | Human | Colorectum | FAP | 1.01e-02 | -1.35e-01 | 0.1278 |
| 23122 | CLASP2 | A015-C-203 | Human | Colorectum | FAP | 1.78e-26 | -2.89e-01 | -0.1294 |
| 23122 | CLASP2 | A015-C-204 | Human | Colorectum | FAP | 5.98e-09 | -3.28e-01 | -0.0228 |
| 23122 | CLASP2 | A014-C-040 | Human | Colorectum | FAP | 1.49e-02 | -1.90e-01 | -0.1184 |
| 23122 | CLASP2 | A002-C-201 | Human | Colorectum | FAP | 5.94e-17 | -3.25e-01 | 0.0324 |
| 23122 | CLASP2 | A002-C-203 | Human | Colorectum | FAP | 7.13e-03 | -1.04e-01 | 0.2786 |
| 23122 | CLASP2 | A001-C-119 | Human | Colorectum | FAP | 1.01e-05 | -9.76e-02 | -0.1557 |
| 23122 | CLASP2 | A001-C-108 | Human | Colorectum | FAP | 1.85e-17 | -1.99e-01 | -0.0272 |
| 23122 | CLASP2 | A002-C-205 | Human | Colorectum | FAP | 5.98e-27 | -4.16e-01 | -0.1236 |
| 23122 | CLASP2 | A015-C-005 | Human | Colorectum | FAP | 4.19e-02 | -8.08e-02 | -0.0336 |
| 23122 | CLASP2 | A015-C-006 | Human | Colorectum | FAP | 1.63e-16 | -3.93e-01 | -0.0994 |
| 23122 | CLASP2 | A015-C-106 | Human | Colorectum | FAP | 8.85e-09 | -1.16e-01 | -0.0511 |
| 23122 | CLASP2 | A002-C-114 | Human | Colorectum | FAP | 2.34e-19 | -3.36e-01 | -0.1561 |
| Page: 1 2 3 4 |
| Transcriptomic changes along malignancy continuum. |
| Tissue | Expression Dynamics | Abbreviation |
| Cervix |  | CC: Cervix cancer |
| HSIL_HPV: HPV-infected high-grade squamous intraepithelial lesions | ||
| N_HPV: HPV-infected normal cervix | ||
| 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 | ||
| Lung |  | AAH: Atypical adenomatous hyperplasia |
| AIS: Adenocarcinoma in situ | ||
| IAC: Invasive lung adenocarcinoma | ||
| MIA: Minimally invasive adenocarcinoma | ||
| Skin |  | AK: Actinic keratosis |
| cSCC: Cutaneous squamous cell carcinoma | ||
| SCCIS:squamous cell carcinoma in situ |
| ∗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:00070206 | Skin | cSCC | microtubule nucleation | 20/4864 | 35/18723 | 9.08e-05 | 8.48e-04 | 20 |
| GO:009050421 | Skin | cSCC | epiboly | 20/4864 | 35/18723 | 9.08e-05 | 8.48e-04 | 20 |
| GO:00310234 | Skin | cSCC | microtubule organizing center organization | 58/4864 | 143/18723 | 9.47e-05 | 8.83e-04 | 58 |
| GO:000716024 | Skin | cSCC | cell-matrix adhesion | 85/4864 | 233/18723 | 2.43e-04 | 1.98e-03 | 85 |
| GO:00400012 | Skin | cSCC | establishment of mitotic spindle localization | 19/4864 | 35/18723 | 3.37e-04 | 2.67e-03 | 19 |
| GO:005101729 | Skin | cSCC | actin filament bundle assembly | 60/4864 | 157/18723 | 4.86e-04 | 3.66e-03 | 60 |
| GO:00516534 | Skin | cSCC | spindle localization | 26/4864 | 56/18723 | 7.59e-04 | 5.27e-03 | 26 |
| GO:004678513 | Skin | cSCC | microtubule polymerization | 35/4864 | 83/18723 | 9.52e-04 | 6.47e-03 | 35 |
| GO:006157229 | Skin | cSCC | actin filament bundle organization | 60/4864 | 161/18723 | 1.02e-03 | 6.86e-03 | 60 |
| GO:000201114 | Skin | cSCC | morphogenesis of an epithelial sheet | 26/4864 | 57/18723 | 1.05e-03 | 7.06e-03 | 26 |
| GO:00512931 | Skin | cSCC | establishment of spindle localization | 23/4864 | 51/18723 | 2.41e-03 | 1.38e-02 | 23 |
| GO:003288612 | Skin | cSCC | regulation of microtubule-based process | 82/4864 | 240/18723 | 2.82e-03 | 1.58e-02 | 82 |
| GO:190290425 | Skin | cSCC | negative regulation of supramolecular fiber organization | 59/4864 | 167/18723 | 4.56e-03 | 2.33e-02 | 59 |
| GO:001063125 | Skin | cSCC | epithelial cell migration | 115/4864 | 357/18723 | 4.64e-03 | 2.37e-02 | 115 |
| GO:003110911 | Skin | cSCC | microtubule polymerization or depolymerization | 45/4864 | 122/18723 | 5.05e-03 | 2.56e-02 | 45 |
| GO:004362411 | Skin | cSCC | cellular protein complex disassembly | 49/4864 | 136/18723 | 6.00e-03 | 2.95e-02 | 49 |
| GO:009013225 | Skin | cSCC | epithelium migration | 115/4864 | 360/18723 | 6.20e-03 | 3.04e-02 | 115 |
| GO:004599521 | Skin | cSCC | regulation of embryonic development | 26/4864 | 64/18723 | 7.34e-03 | 3.47e-02 | 26 |
| GO:000716224 | Skin | cSCC | negative regulation of cell adhesion | 98/4864 | 303/18723 | 7.45e-03 | 3.50e-02 | 98 |
| GO:0032231111 | Skin | cSCC | regulation of actin filament bundle assembly | 39/4864 | 105/18723 | 7.56e-03 | 3.53e-02 | 39 |
| 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 |
| 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 |
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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 |
| CLASP2 | SNV | Missense_Mutation | c.1111N>A | p.Asp371Asn | p.D371N | protein_coding | deleterious(0.02) | probably_damaging(0.993) | TCGA-A2-A0CT-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | cytoxan | SD | ||
| CLASP2 | SNV | Missense_Mutation | c.293N>C | p.Ile98Thr | p.I98T | protein_coding | tolerated(0.23) | benign(0.234) | TCGA-A8-A09A-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD | ||
| CLASP2 | SNV | Missense_Mutation | c.1355T>C | p.Val452Ala | p.V452A | protein_coding | tolerated(0.06) | probably_damaging(0.954) | TCGA-A8-A09Z-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | ||
| CLASP2 | SNV | Missense_Mutation | rs554149266 | c.1343N>A | p.Arg448Gln | p.R448Q | protein_coding | deleterious(0.01) | probably_damaging(0.964) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
| CLASP2 | SNV | Missense_Mutation | novel | c.3842G>T | p.Gly1281Val | p.G1281V | protein_coding | deleterious(0.03) | possibly_damaging(0.531) | TCGA-AR-A2LE-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | tamoxiphen | PD | |
| CLASP2 | SNV | Missense_Mutation | novel | c.179N>A | p.Gly60Glu | p.G60E | protein_coding | deleterious(0.01) | probably_damaging(0.998) | TCGA-B6-A0I8-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | PD | |
| CLASP2 | SNV | Missense_Mutation | c.2793N>A | p.Met931Ile | p.M931I | protein_coding | deleterious(0.01) | benign(0.233) | TCGA-BH-A18T-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | ||
| CLASP2 | SNV | Missense_Mutation | c.2897C>G | p.Ser966Cys | p.S966C | protein_coding | deleterious(0.03) | possibly_damaging(0.54) | TCGA-D8-A73U-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | tamoxiphen | SD | ||
| CLASP2 | SNV | Missense_Mutation | novel | c.2311N>G | p.Leu771Val | p.L771V | protein_coding | tolerated(0.17) | possibly_damaging(0.875) | TCGA-E2-A14V-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cyclophosphamide | SD | |
| CLASP2 | insertion | Nonsense_Mutation | novel | c.2873_2874insCTAGGGATGAGGCCTACATGACCATGGTG | p.Met958IlefsTer2 | p.M958Ifs*2 | protein_coding | TCGA-AO-A03R-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin | SD |
| Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 |
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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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