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Gene: PTK6 |
Gene summary for PTK6 |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | PTK6 | Gene ID | 5753 |
| Gene name | protein tyrosine kinase 6 | |
| Gene Alias | BRK | |
| Cytomap | 20q13.33 | |
| Gene Type | protein-coding | GO ID | GO:0001932 | UniProtAcc | Q13882 |
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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 |
| 5753 | PTK6 | HTA11_2487_2000001011 | Human | Colorectum | SER | 3.00e-24 | 8.09e-01 | -0.1808 |
| 5753 | PTK6 | HTA11_1938_2000001011 | Human | Colorectum | AD | 3.53e-04 | 3.62e-01 | -0.0811 |
| 5753 | PTK6 | HTA11_78_2000001011 | Human | Colorectum | AD | 1.60e-04 | 3.62e-01 | -0.1088 |
| 5753 | PTK6 | HTA11_347_2000001011 | Human | Colorectum | AD | 3.97e-29 | 7.29e-01 | -0.1954 |
| 5753 | PTK6 | HTA11_411_2000001011 | Human | Colorectum | SER | 3.46e-08 | 1.14e+00 | -0.2602 |
| 5753 | PTK6 | HTA11_2112_2000001011 | Human | Colorectum | SER | 4.86e-09 | 8.82e-01 | -0.2196 |
| 5753 | PTK6 | HTA11_3361_2000001011 | Human | Colorectum | AD | 2.95e-10 | 5.49e-01 | -0.1207 |
| 5753 | PTK6 | HTA11_83_2000001011 | Human | Colorectum | SER | 6.18e-18 | 7.71e-01 | -0.1526 |
| 5753 | PTK6 | HTA11_696_2000001011 | Human | Colorectum | AD | 3.99e-18 | 6.83e-01 | -0.1464 |
| 5753 | PTK6 | HTA11_866_2000001011 | Human | Colorectum | AD | 9.50e-10 | 3.54e-01 | -0.1001 |
| 5753 | PTK6 | HTA11_1391_2000001011 | Human | Colorectum | AD | 1.40e-14 | 6.20e-01 | -0.059 |
| 5753 | PTK6 | HTA11_2992_2000001011 | Human | Colorectum | SER | 1.03e-02 | 6.66e-01 | -0.1706 |
| 5753 | PTK6 | HTA11_5212_2000001011 | Human | Colorectum | AD | 8.05e-07 | 6.62e-01 | -0.2061 |
| 5753 | PTK6 | HTA11_10623_2000001011 | Human | Colorectum | AD | 1.41e-02 | 4.61e-01 | -0.0177 |
| 5753 | PTK6 | HTA11_10711_2000001011 | Human | Colorectum | AD | 2.00e-03 | 2.77e-01 | 0.0338 |
| 5753 | PTK6 | HTA11_7696_3000711011 | Human | Colorectum | AD | 7.73e-05 | 2.70e-01 | 0.0674 |
| 5753 | PTK6 | HTA11_99999971662_82457 | Human | Colorectum | MSS | 1.75e-19 | 7.74e-01 | 0.3859 |
| 5753 | PTK6 | HTA11_99999974143_84620 | Human | Colorectum | MSS | 9.29e-08 | 2.85e-01 | 0.3005 |
| 5753 | PTK6 | A015-C-202 | Human | Colorectum | FAP | 1.38e-02 | 2.45e-01 | -0.0849 |
| 5753 | PTK6 | LZE4T | Human | Esophagus | ESCC | 3.46e-08 | 1.81e-01 | 0.0811 |
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| 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 | ||
| Oral Cavity |  | EOLP: Erosive Oral lichen planus |
| LP: leukoplakia | ||
| NEOLP: Non-erosive oral lichen planus | ||
| OSCC: Oral squamous cell carcinoma |
| ∗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:00457872 | Colorectum | FAP | positive regulation of cell cycle | 66/2622 | 313/18723 | 3.66e-04 | 4.63e-03 | 66 |
| GO:00610992 | Colorectum | FAP | negative regulation of protein tyrosine kinase activity | 11/2622 | 31/18723 | 2.26e-03 | 1.84e-02 | 11 |
| GO:0048565 | Colorectum | FAP | digestive tract development | 29/2622 | 127/18723 | 4.75e-03 | 3.20e-02 | 29 |
| GO:0055123 | Colorectum | FAP | digestive system development | 30/2622 | 137/18723 | 7.75e-03 | 4.60e-02 | 30 |
| GO:0010563111 | Esophagus | ESCC | negative regulation of phosphorus metabolic process | 274/8552 | 442/18723 | 2.32e-12 | 9.41e-11 | 274 |
| GO:0045936111 | Esophagus | ESCC | negative regulation of phosphate metabolic process | 273/8552 | 441/18723 | 3.18e-12 | 1.25e-10 | 273 |
| GO:0051348111 | Esophagus | ESCC | negative regulation of transferase activity | 177/8552 | 268/18723 | 1.08e-11 | 4.00e-10 | 177 |
| GO:0042326111 | Esophagus | ESCC | negative regulation of phosphorylation | 237/8552 | 385/18723 | 1.86e-10 | 5.33e-09 | 237 |
| GO:0001933111 | Esophagus | ESCC | negative regulation of protein phosphorylation | 213/8552 | 342/18723 | 3.54e-10 | 9.76e-09 | 213 |
| GO:004578710 | Esophagus | ESCC | positive regulation of cell cycle | 196/8552 | 313/18723 | 9.27e-10 | 2.24e-08 | 196 |
| GO:003367319 | Esophagus | ESCC | negative regulation of kinase activity | 154/8552 | 237/18723 | 1.38e-09 | 3.27e-08 | 154 |
| GO:000646920 | Esophagus | ESCC | negative regulation of protein kinase activity | 140/8552 | 212/18723 | 1.53e-09 | 3.56e-08 | 140 |
| GO:003812718 | Esophagus | ESCC | ERBB signaling pathway | 82/8552 | 121/18723 | 7.23e-07 | 9.40e-06 | 82 |
| GO:004677710 | Esophagus | ESCC | protein autophosphorylation | 138/8552 | 227/18723 | 2.98e-06 | 3.38e-05 | 138 |
| GO:000717318 | Esophagus | ESCC | epidermal growth factor receptor signaling pathway | 73/8552 | 108/18723 | 3.36e-06 | 3.73e-05 | 73 |
| GO:00459267 | Esophagus | ESCC | negative regulation of growth | 148/8552 | 249/18723 | 7.88e-06 | 7.73e-05 | 148 |
| GO:003134616 | Esophagus | ESCC | positive regulation of cell projection organization | 201/8552 | 353/18723 | 1.19e-05 | 1.11e-04 | 201 |
| GO:190118413 | Esophagus | ESCC | regulation of ERBB signaling pathway | 54/8552 | 79/18723 | 3.81e-05 | 3.08e-04 | 54 |
| GO:00507322 | Esophagus | ESCC | negative regulation of peptidyl-tyrosine phosphorylation | 42/8552 | 59/18723 | 6.35e-05 | 4.84e-04 | 42 |
| GO:00420588 | Esophagus | ESCC | regulation of epidermal growth factor receptor signaling pathway | 50/8552 | 73/18723 | 6.75e-05 | 5.12e-04 | 50 |
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| 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. |
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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 |
| PTK6 | SNV | Missense_Mutation | c.119N>C | p.Lys40Thr | p.K40T | Q13882 | protein_coding | tolerated(0.17) | possibly_damaging(0.661) | TCGA-AA-3492-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
| PTK6 | SNV | Missense_Mutation | rs770065818 | c.832N>A | p.Asp278Asn | p.D278N | Q13882 | protein_coding | tolerated(0.43) | benign(0.001) | TCGA-AZ-6601-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
| PTK6 | SNV | Missense_Mutation | c.802G>A | p.Ala268Thr | p.A268T | Q13882 | protein_coding | tolerated(0.26) | benign(0.011) | TCGA-CK-5913-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
| PTK6 | SNV | Missense_Mutation | c.340T>C | p.Tyr114His | p.Y114H | Q13882 | protein_coding | tolerated(0.06) | benign(0.397) | TCGA-EI-6882-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
| PTK6 | SNV | Missense_Mutation | rs761742593 | c.1313N>A | p.Arg438Gln | p.R438Q | Q13882 | protein_coding | tolerated(1) | benign(0.003) | TCGA-A5-A0G1-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| PTK6 | SNV | Missense_Mutation | rs200723492 | c.619N>A | p.Glu207Lys | p.E207K | Q13882 | protein_coding | tolerated(0.1) | benign(0.135) | TCGA-A5-A2K5-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| PTK6 | SNV | Missense_Mutation | rs757318592 | c.109N>A | p.Val37Met | p.V37M | Q13882 | protein_coding | deleterious(0) | probably_damaging(0.954) | TCGA-AJ-A3OL-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatin | PD |
| PTK6 | SNV | Missense_Mutation | novel | c.638G>A | p.Arg213Gln | p.R213Q | Q13882 | protein_coding | tolerated(0.55) | benign(0.001) | TCGA-AP-A059-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| PTK6 | SNV | Missense_Mutation | novel | c.1137N>T | p.Glu379Asp | p.E379D | Q13882 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-AP-A0LM-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | cisplatin | SD |
| PTK6 | SNV | Missense_Mutation | novel | c.1222N>C | p.Cys408Arg | p.C408R | Q13882 | protein_coding | tolerated(0.45) | benign(0.007) | TCGA-AP-A1DK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <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 |
| 5753 | PTK6 | DRUGGABLE GENOME, TRANSCRIPTION FACTOR, KINASE, TYROSINE KINASE, ENZYME | inhibitor | 249565866 | ||
| 5753 | PTK6 | DRUGGABLE GENOME, TRANSCRIPTION FACTOR, KINASE, TYROSINE KINASE, ENZYME | inhibitor | 315661136 | ||
| 5753 | PTK6 | DRUGGABLE GENOME, TRANSCRIPTION FACTOR, KINASE, TYROSINE KINASE, ENZYME | TAE-684 | TAE-684 | ||
| 5753 | PTK6 | DRUGGABLE GENOME, TRANSCRIPTION FACTOR, KINASE, TYROSINE KINASE, ENZYME | OSI-632 | OSI-632 | ||
| 5753 | PTK6 | DRUGGABLE GENOME, TRANSCRIPTION FACTOR, KINASE, TYROSINE KINASE, ENZYME | CEDIRANIB | CEDIRANIB | ||
| 5753 | PTK6 | DRUGGABLE GENOME, TRANSCRIPTION FACTOR, KINASE, TYROSINE KINASE, ENZYME | SB-202190 | SB-202190 | 22951114 | |
| 5753 | PTK6 | DRUGGABLE GENOME, TRANSCRIPTION FACTOR, KINASE, TYROSINE KINASE, ENZYME | inhibitor | CHEMBL24828 | VANDETANIB | |
| 5753 | PTK6 | DRUGGABLE GENOME, TRANSCRIPTION FACTOR, KINASE, TYROSINE KINASE, ENZYME | DASATINIB | DASATINIB | ||
| 5753 | PTK6 | DRUGGABLE GENOME, TRANSCRIPTION FACTOR, KINASE, TYROSINE KINASE, ENZYME | TAMATINIB | R-406 | ||
| 5753 | PTK6 | DRUGGABLE GENOME, TRANSCRIPTION FACTOR, KINASE, TYROSINE KINASE, ENZYME | ISIS-CRP |
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