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Gene: TACSTD2 |
Gene summary for TACSTD2 |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | TACSTD2 | Gene ID | 4070 |
| Gene name | tumor associated calcium signal transducer 2 | |
| Gene Alias | EGP-1 | |
| Cytomap | 1p32.1 | |
| Gene Type | protein-coding | GO ID | GO:0000902 | UniProtAcc | P09758 |
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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 |
| 4070 | TACSTD2 | GSM4909281 | Human | Breast | IDC | 8.47e-31 | -8.82e-01 | 0.21 |
| 4070 | TACSTD2 | GSM4909282 | Human | Breast | IDC | 1.32e-21 | 4.71e-01 | -0.0288 |
| 4070 | TACSTD2 | GSM4909285 | Human | Breast | IDC | 7.61e-09 | 1.01e-01 | 0.21 |
| 4070 | TACSTD2 | GSM4909286 | Human | Breast | IDC | 1.90e-83 | -1.49e+00 | 0.1081 |
| 4070 | TACSTD2 | GSM4909288 | Human | Breast | IDC | 2.86e-06 | -7.81e-01 | 0.0988 |
| 4070 | TACSTD2 | GSM4909290 | Human | Breast | IDC | 2.22e-26 | -8.21e-01 | 0.2096 |
| 4070 | TACSTD2 | GSM4909291 | Human | Breast | IDC | 1.10e-24 | -1.00e+00 | 0.1753 |
| 4070 | TACSTD2 | GSM4909292 | Human | Breast | IDC | 3.41e-04 | -9.50e-01 | 0.1236 |
| 4070 | TACSTD2 | GSM4909293 | Human | Breast | IDC | 1.83e-33 | -7.57e-01 | 0.1581 |
| 4070 | TACSTD2 | GSM4909294 | Human | Breast | IDC | 1.34e-26 | -8.61e-01 | 0.2022 |
| 4070 | TACSTD2 | GSM4909296 | Human | Breast | IDC | 2.23e-23 | -7.87e-01 | 0.1524 |
| 4070 | TACSTD2 | GSM4909297 | Human | Breast | IDC | 3.79e-07 | -5.30e-01 | 0.1517 |
| 4070 | TACSTD2 | GSM4909298 | Human | Breast | IDC | 4.47e-27 | -6.79e-01 | 0.1551 |
| 4070 | TACSTD2 | GSM4909300 | Human | Breast | IDC | 2.04e-02 | 3.32e-01 | 0.0334 |
| 4070 | TACSTD2 | GSM4909301 | Human | Breast | IDC | 7.48e-20 | -6.41e-01 | 0.1577 |
| 4070 | TACSTD2 | GSM4909302 | Human | Breast | IDC | 9.22e-18 | -6.63e-01 | 0.1545 |
| 4070 | TACSTD2 | GSM4909304 | Human | Breast | IDC | 5.32e-47 | -1.01e+00 | 0.1636 |
| 4070 | TACSTD2 | GSM4909305 | Human | Breast | IDC | 7.21e-04 | 1.61e-01 | 0.0436 |
| 4070 | TACSTD2 | GSM4909306 | Human | Breast | IDC | 2.82e-11 | -3.19e-01 | 0.1564 |
| 4070 | TACSTD2 | GSM4909307 | Human | Breast | IDC | 1.86e-18 | -7.36e-01 | 0.1569 |
| Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 |
| 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 | ||
| Lung |  | AAH: Atypical adenomatous hyperplasia |
| AIS: Adenocarcinoma in situ | ||
| IAC: Invasive lung adenocarcinoma | ||
| MIA: Minimally invasive adenocarcinoma | ||
| 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:001081031 | Stomach | WIM | regulation of cell-substrate adhesion | 12/426 | 221/18723 | 4.85e-03 | 4.37e-02 | 12 |
| GO:190290351 | Stomach | SIM | regulation of supramolecular fiber organization | 37/708 | 383/18723 | 1.84e-07 | 1.40e-05 | 37 |
| GO:00510175 | Stomach | SIM | actin filament bundle assembly | 20/708 | 157/18723 | 2.03e-06 | 1.04e-04 | 20 |
| GO:000701541 | Stomach | SIM | actin filament organization | 38/708 | 442/18723 | 2.29e-06 | 1.15e-04 | 38 |
| GO:00615725 | Stomach | SIM | actin filament bundle organization | 20/708 | 161/18723 | 3.01e-06 | 1.45e-04 | 20 |
| GO:011005351 | Stomach | SIM | regulation of actin filament organization | 27/708 | 278/18723 | 7.56e-06 | 2.92e-04 | 27 |
| GO:003297041 | Stomach | SIM | regulation of actin filament-based process | 34/708 | 397/18723 | 8.43e-06 | 3.18e-04 | 34 |
| GO:00322315 | Stomach | SIM | regulation of actin filament bundle assembly | 15/708 | 105/18723 | 9.40e-06 | 3.47e-04 | 15 |
| GO:003295651 | Stomach | SIM | regulation of actin cytoskeleton organization | 31/708 | 358/18723 | 1.69e-05 | 5.45e-04 | 31 |
| GO:00514925 | Stomach | SIM | regulation of stress fiber assembly | 13/708 | 91/18723 | 3.67e-05 | 1.05e-03 | 13 |
| GO:00300385 | Stomach | SIM | contractile actin filament bundle assembly | 14/708 | 106/18723 | 4.55e-05 | 1.26e-03 | 14 |
| GO:00431495 | Stomach | SIM | stress fiber assembly | 14/708 | 106/18723 | 4.55e-05 | 1.26e-03 | 14 |
| GO:190002451 | Stomach | SIM | regulation of substrate adhesion-dependent cell spreading | 10/708 | 57/18723 | 4.85e-05 | 1.30e-03 | 10 |
| GO:01100205 | Stomach | SIM | regulation of actomyosin structure organization | 13/708 | 100/18723 | 9.96e-05 | 2.43e-03 | 13 |
| GO:003444651 | Stomach | SIM | substrate adhesion-dependent cell spreading | 13/708 | 108/18723 | 2.19e-04 | 4.45e-03 | 13 |
| GO:002260451 | Stomach | SIM | regulation of cell morphogenesis | 25/708 | 309/18723 | 3.09e-04 | 5.72e-03 | 25 |
| GO:00106395 | Stomach | SIM | negative regulation of organelle organization | 27/708 | 348/18723 | 3.53e-04 | 6.34e-03 | 27 |
| GO:003103231 | Stomach | SIM | actomyosin structure organization | 17/708 | 196/18723 | 1.28e-03 | 1.59e-02 | 17 |
| GO:000716221 | Stomach | SIM | negative regulation of cell adhesion | 22/708 | 303/18723 | 2.76e-03 | 2.69e-02 | 22 |
| GO:001076941 | Stomach | SIM | regulation of cell morphogenesis involved in differentiation | 10/708 | 96/18723 | 3.39e-03 | 3.20e-02 | 10 |
| 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 |
| Enriched KEGG pathways. |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
| Page: 1 |
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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 |
| TACSTD2 | deletion | Frame_Shift_Del | novel | c.534delG | p.Leu179SerfsTer92 | p.L179Sfs*92 | P09758 | protein_coding | TCGA-D8-A27V-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD | ||
| TACSTD2 | SNV | Missense_Mutation | novel | c.476N>A | p.Arg159His | p.R159H | P09758 | protein_coding | deleterious(0) | probably_damaging(0.94) | TCGA-AA-3947-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
| TACSTD2 | SNV | Missense_Mutation | novel | c.884T>C | p.Leu295Pro | p.L295P | P09758 | protein_coding | deleterious(0) | probably_damaging(0.96) | TCGA-AD-6964-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | folfox | PD |
| TACSTD2 | SNV | Missense_Mutation | c.763C>T | p.Arg255Cys | p.R255C | P09758 | protein_coding | deleterious(0) | benign(0.353) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
| TACSTD2 | SNV | Missense_Mutation | novel | c.745G>A | p.Glu249Lys | p.E249K | P09758 | protein_coding | tolerated(0.12) | benign(0.01) | TCGA-AX-A2HC-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | paclitaxel | PD |
| TACSTD2 | SNV | Missense_Mutation | novel | c.821C>T | p.Thr274Ile | p.T274I | P09758 | protein_coding | tolerated(0.09) | benign(0.373) | TCGA-B5-A3FC-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
| TACSTD2 | SNV | Missense_Mutation | novel | c.334G>A | p.Gly112Ser | p.G112S | P09758 | protein_coding | deleterious(0) | probably_damaging(0.977) | TCGA-B5-A3FC-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
| TACSTD2 | SNV | Missense_Mutation | novel | c.578N>T | p.Ala193Val | p.A193V | P09758 | protein_coding | tolerated(0.08) | possibly_damaging(0.769) | TCGA-D1-A15X-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
| TACSTD2 | SNV | Missense_Mutation | novel | c.908N>T | p.Ser303Leu | p.S303L | P09758 | protein_coding | tolerated(0.1) | benign(0.001) | TCGA-EO-A22R-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
| TACSTD2 | SNV | Missense_Mutation | novel | c.866N>C | p.Val289Ala | p.V289A | P09758 | protein_coding | tolerated(0.73) | benign(0.056) | TCGA-EO-A3AV-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatin | CR |
| Page: 1 2 |
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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 |
| 4070 | TACSTD2 | NA | antibody | 249565933 | ||
| 4070 | TACSTD2 | NA | N/A |
| Page: 1 |
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