|
|||||
|
 | |
| |
| |
| |
| |
| |
|
Gene: ENTPD5 |
Gene summary for ENTPD5 |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | ENTPD5 | Gene ID | 957 |
| Gene name | ectonucleoside triphosphate diphosphohydrolase 5 (inactive) | |
| Gene Alias | CD39L4 | |
| Cytomap | 14q24.3 | |
| Gene Type | protein-coding | GO ID | GO:0005975 | UniProtAcc | A0A024R6D3 |
Top |
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 |
| 957 | ENTPD5 | HTA11_3410_2000001011 | Human | Colorectum | AD | 5.15e-09 | -4.60e-01 | 0.0155 |
| 957 | ENTPD5 | HTA11_347_2000001011 | Human | Colorectum | AD | 3.69e-10 | 5.71e-01 | -0.1954 |
| 957 | ENTPD5 | HTA11_866_3004761011 | Human | Colorectum | AD | 4.88e-07 | -4.30e-01 | 0.096 |
| 957 | ENTPD5 | HTA11_7696_3000711011 | Human | Colorectum | AD | 4.03e-02 | -2.66e-01 | 0.0674 |
| 957 | ENTPD5 | HTA11_6818_2000001021 | Human | Colorectum | AD | 1.61e-05 | -5.64e-01 | 0.0588 |
| 957 | ENTPD5 | HTA11_99999970781_79442 | Human | Colorectum | MSS | 7.26e-17 | -5.12e-01 | 0.294 |
| 957 | ENTPD5 | HTA11_99999965104_69814 | Human | Colorectum | MSS | 4.43e-04 | -5.01e-01 | 0.281 |
| 957 | ENTPD5 | HTA11_99999971662_82457 | Human | Colorectum | MSS | 1.33e-17 | -5.06e-01 | 0.3859 |
| 957 | ENTPD5 | HTA11_99999973899_84307 | Human | Colorectum | MSS | 2.19e-03 | -5.48e-01 | 0.2585 |
| 957 | ENTPD5 | HTA11_99999974143_84620 | Human | Colorectum | MSS | 1.96e-22 | -5.54e-01 | 0.3005 |
| 957 | ENTPD5 | F007 | Human | Colorectum | FAP | 2.12e-02 | -2.97e-01 | 0.1176 |
| 957 | ENTPD5 | A002-C-010 | Human | Colorectum | FAP | 2.02e-03 | -2.40e-01 | 0.242 |
| 957 | ENTPD5 | A001-C-207 | Human | Colorectum | FAP | 2.23e-04 | -3.93e-01 | 0.1278 |
| 957 | ENTPD5 | A015-C-203 | Human | Colorectum | FAP | 3.03e-24 | -4.65e-01 | -0.1294 |
| 957 | ENTPD5 | A015-C-204 | Human | Colorectum | FAP | 2.23e-06 | -3.14e-01 | -0.0228 |
| 957 | ENTPD5 | A014-C-040 | Human | Colorectum | FAP | 1.84e-03 | -4.17e-01 | -0.1184 |
| 957 | ENTPD5 | A002-C-201 | Human | Colorectum | FAP | 4.29e-13 | -4.38e-01 | 0.0324 |
| 957 | ENTPD5 | A002-C-203 | Human | Colorectum | FAP | 6.02e-08 | -2.96e-01 | 0.2786 |
| 957 | ENTPD5 | A001-C-119 | Human | Colorectum | FAP | 1.54e-11 | -5.33e-01 | -0.1557 |
| 957 | ENTPD5 | A001-C-108 | Human | Colorectum | FAP | 5.23e-19 | -3.84e-01 | -0.0272 |
| Page: 1 2 3 4 5 6 |
| Transcriptomic changes along malignancy continuum. |
| Tissue | Expression Dynamics | Abbreviation |
| 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 | ||
| Esophagus |  | ESCC: Esophageal squamous cell carcinoma |
| HGIN: High-grade intraepithelial neoplasias | ||
| LGIN: Low-grade intraepithelial neoplasias | ||
| Liver |  | HCC: Hepatocellular carcinoma |
| NAFLD: Non-alcoholic fatty liver disease | ||
| Prostate |  | BPH: Benign Prostatic Hyperplasia |
| ∗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. |
Top |
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:00091354 | Colorectum | FAP | purine nucleoside diphosphate metabolic process | 37/2622 | 103/18723 | 2.00e-08 | 1.98e-06 | 37 |
| GO:00091794 | Colorectum | FAP | purine ribonucleoside diphosphate metabolic process | 37/2622 | 103/18723 | 2.00e-08 | 1.98e-06 | 37 |
| GO:00091854 | Colorectum | FAP | ribonucleoside diphosphate metabolic process | 37/2622 | 106/18723 | 4.79e-08 | 3.86e-06 | 37 |
| GO:00442704 | Colorectum | FAP | cellular nitrogen compound catabolic process | 101/2622 | 451/18723 | 7.42e-07 | 3.44e-05 | 101 |
| GO:00469394 | Colorectum | FAP | nucleotide phosphorylation | 33/2622 | 101/18723 | 1.40e-06 | 6.17e-05 | 33 |
| GO:00346554 | Colorectum | FAP | nucleobase-containing compound catabolic process | 92/2622 | 407/18723 | 1.50e-06 | 6.49e-05 | 92 |
| GO:00160523 | Colorectum | FAP | carbohydrate catabolic process | 44/2622 | 154/18723 | 1.82e-06 | 7.42e-05 | 44 |
| GO:00467004 | Colorectum | FAP | heterocycle catabolic process | 98/2622 | 445/18723 | 2.36e-06 | 9.21e-05 | 98 |
| GO:00061654 | Colorectum | FAP | nucleoside diphosphate phosphorylation | 32/2622 | 99/18723 | 2.61e-06 | 9.94e-05 | 32 |
| GO:00091174 | Colorectum | FAP | nucleotide metabolic process | 105/2622 | 489/18723 | 3.52e-06 | 1.25e-04 | 105 |
| GO:00091324 | Colorectum | FAP | nucleoside diphosphate metabolic process | 37/2622 | 124/18723 | 3.86e-06 | 1.32e-04 | 37 |
| GO:00194394 | Colorectum | FAP | aromatic compound catabolic process | 100/2622 | 467/18723 | 6.75e-06 | 2.08e-04 | 100 |
| GO:00067534 | Colorectum | FAP | nucleoside phosphate metabolic process | 105/2622 | 497/18723 | 7.47e-06 | 2.25e-04 | 105 |
| GO:00061092 | Colorectum | FAP | regulation of carbohydrate metabolic process | 46/2622 | 178/18723 | 1.99e-05 | 4.90e-04 | 46 |
| GO:19035802 | Colorectum | FAP | positive regulation of ATP metabolic process | 16/2622 | 38/18723 | 2.16e-05 | 5.18e-04 | 16 |
| GO:00620122 | Colorectum | FAP | regulation of small molecule metabolic process | 74/2622 | 334/18723 | 3.15e-05 | 7.13e-04 | 74 |
| GO:00459812 | Colorectum | FAP | positive regulation of nucleotide metabolic process | 17/2622 | 43/18723 | 3.23e-05 | 7.20e-04 | 17 |
| GO:19005442 | Colorectum | FAP | positive regulation of purine nucleotide metabolic process | 17/2622 | 43/18723 | 3.23e-05 | 7.20e-04 | 17 |
| GO:19013614 | Colorectum | FAP | organic cyclic compound catabolic process | 101/2622 | 495/18723 | 4.87e-05 | 9.93e-04 | 101 |
| GO:19035784 | Colorectum | FAP | regulation of ATP metabolic process | 26/2622 | 87/18723 | 9.84e-05 | 1.66e-03 | 26 |
| Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 |
| Enriched KEGG pathways. |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
| hsa012325 | Esophagus | ESCC | Nucleotide metabolism | 59/4205 | 85/8465 | 1.67e-04 | 6.58e-04 | 3.37e-04 | 59 |
| hsa002405 | Esophagus | ESCC | Pyrimidine metabolism | 41/4205 | 58/8465 | 9.14e-04 | 2.92e-03 | 1.49e-03 | 41 |
| hsa0123212 | Esophagus | ESCC | Nucleotide metabolism | 59/4205 | 85/8465 | 1.67e-04 | 6.58e-04 | 3.37e-04 | 59 |
| hsa0024012 | Esophagus | ESCC | Pyrimidine metabolism | 41/4205 | 58/8465 | 9.14e-04 | 2.92e-03 | 1.49e-03 | 41 |
| hsa002402 | Liver | HCC | Pyrimidine metabolism | 44/4020 | 58/8465 | 9.34e-06 | 7.11e-05 | 3.95e-05 | 44 |
| hsa012322 | Liver | HCC | Nucleotide metabolism | 59/4020 | 85/8465 | 3.30e-05 | 1.88e-04 | 1.04e-04 | 59 |
| hsa002403 | Liver | HCC | Pyrimidine metabolism | 44/4020 | 58/8465 | 9.34e-06 | 7.11e-05 | 3.95e-05 | 44 |
| hsa012323 | Liver | HCC | Nucleotide metabolism | 59/4020 | 85/8465 | 3.30e-05 | 1.88e-04 | 1.04e-04 | 59 |
| Page: 1 |
Top |
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 |
Top |
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 |
Top |
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 |
| ENTPD5 | SNV | Missense_Mutation | c.1183N>C | p.Asp395His | p.D395H | O75356 | protein_coding | deleterious(0.04) | possibly_damaging(0.781) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
| ENTPD5 | SNV | Missense_Mutation | c.412G>C | p.Glu138Gln | p.E138Q | O75356 | protein_coding | tolerated(0.21) | possibly_damaging(0.751) | TCGA-AN-A0XU-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
| ENTPD5 | SNV | Missense_Mutation | novel | c.804N>G | p.Phe268Leu | p.F268L | O75356 | protein_coding | tolerated(1) | probably_damaging(0.998) | TCGA-GM-A3NW-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | fluorouracil | SD |
| ENTPD5 | insertion | Nonsense_Mutation | novel | c.519_520insTATTTAGAGCTGGCTCTCATTTGACAGGTCAGCTGCATG | p.Gly173_Ile174insTyrLeuGluLeuAlaLeuIleTerGlnValSerCysMet | p.G173_I174insYLELALI*QVSCM | O75356 | protein_coding | TCGA-A8-A07U-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Chemotherapy | 5-fluorouracil | SD | ||
| ENTPD5 | SNV | Missense_Mutation | rs757235389 | c.134N>T | p.Ala45Val | p.A45V | O75356 | protein_coding | tolerated(0.27) | benign(0.037) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
| ENTPD5 | SNV | Missense_Mutation | novel | c.596A>T | p.Asp199Val | p.D199V | O75356 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-VS-A9UD-01 | Cervix | cervical & endocervical cancer | Female | >=65 | III/IV | Chemotherapy | cisplatin | CR |
| ENTPD5 | SNV | Missense_Mutation | novel | c.987C>A | p.Phe329Leu | p.F329L | O75356 | protein_coding | tolerated(0.07) | probably_damaging(0.998) | TCGA-A5-A2K5-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| ENTPD5 | SNV | Missense_Mutation | novel | c.987N>A | p.Phe329Leu | p.F329L | O75356 | protein_coding | tolerated(0.07) | probably_damaging(0.998) | TCGA-AP-A0LM-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | cisplatin | SD |
| ENTPD5 | SNV | Missense_Mutation | novel | c.1241N>C | p.Leu414Ser | p.L414S | O75356 | protein_coding | deleterious(0) | possibly_damaging(0.883) | TCGA-B5-A1MW-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | PD |
| ENTPD5 | SNV | Missense_Mutation | novel | c.983C>T | p.Ala328Val | p.A328V | O75356 | protein_coding | deleterious(0.04) | probably_damaging(0.999) | TCGA-B5-A3FC-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
| Page: 1 2 3 |
Top |
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 |
Copyright 2023-Present -The University of Texas Health Science Center at Houston |