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Gene: MESP1 |
Gene summary for MESP1 |
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Gene information | Species | Human | Gene symbol | MESP1 | Gene ID | 55897 |
Gene name | mesoderm posterior bHLH transcription factor 1 | |
Gene Alias | bHLHc5 | |
Cytomap | 15q26.1 | |
Gene Type | protein-coding | GO ID | GO:0000578 | UniProtAcc | Q9BRJ9 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
55897 | MESP1 | GSM4909294 | Human | Breast | IDC | 1.76e-04 | 3.66e-01 | 0.2022 |
55897 | MESP1 | GSM4909295 | Human | Breast | IDC | 9.10e-04 | 3.48e-01 | 0.0898 |
55897 | MESP1 | GSM4909301 | Human | Breast | IDC | 1.16e-14 | 6.02e-01 | 0.1577 |
55897 | MESP1 | GSM4909304 | Human | Breast | IDC | 1.16e-02 | -1.28e-01 | 0.1636 |
55897 | MESP1 | GSM4909305 | Human | Breast | IDC | 8.53e-03 | 2.56e-01 | 0.0436 |
55897 | MESP1 | GSM4909306 | Human | Breast | IDC | 5.94e-29 | 7.97e-01 | 0.1564 |
55897 | MESP1 | GSM4909308 | Human | Breast | IDC | 3.00e-04 | -1.71e-01 | 0.158 |
55897 | MESP1 | GSM4909309 | Human | Breast | IDC | 1.24e-02 | 2.39e-01 | 0.0483 |
55897 | MESP1 | GSM4909311 | Human | Breast | IDC | 1.78e-05 | -1.61e-01 | 0.1534 |
55897 | MESP1 | GSM4909312 | Human | Breast | IDC | 7.25e-03 | -1.38e-01 | 0.1552 |
55897 | MESP1 | GSM4909315 | Human | Breast | IDC | 6.28e-05 | -1.60e-01 | 0.21 |
55897 | MESP1 | GSM4909319 | Human | Breast | IDC | 6.53e-07 | -1.28e-01 | 0.1563 |
55897 | MESP1 | GSM4909320 | Human | Breast | IDC | 1.82e-03 | 1.60e-01 | 0.1575 |
55897 | MESP1 | GSM4909321 | Human | Breast | IDC | 1.61e-11 | 4.40e-01 | 0.1559 |
55897 | MESP1 | M2 | Human | Breast | IDC | 9.20e-03 | 2.69e-01 | 0.21 |
55897 | MESP1 | NCCBC14 | Human | Breast | DCIS | 3.33e-02 | -1.08e-01 | 0.2021 |
55897 | MESP1 | NCCBC6 | Human | Breast | DCIS | 1.42e-03 | 3.43e-01 | 0.2095 |
55897 | MESP1 | DCIS2 | Human | Breast | DCIS | 1.35e-35 | 2.17e-01 | 0.0085 |
55897 | MESP1 | LZE5T | Human | Esophagus | ESCC | 1.60e-07 | 7.54e-01 | 0.0514 |
55897 | MESP1 | P2T-E | Human | Esophagus | ESCC | 6.35e-16 | 2.56e-01 | 0.1177 |
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∗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 |
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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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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:000188922 | Liver | HCC | liver development | 108/7958 | 147/18723 | 2.16e-14 | 1.41e-12 | 108 |
GO:006100822 | Liver | HCC | hepaticobiliary system development | 109/7958 | 150/18723 | 5.72e-14 | 3.42e-12 | 109 |
GO:019873821 | Liver | HCC | cell-cell signaling by wnt | 247/7958 | 446/18723 | 2.11e-08 | 4.96e-07 | 247 |
GO:004873222 | Liver | HCC | gland development | 242/7958 | 436/18723 | 2.26e-08 | 5.28e-07 | 242 |
GO:001605521 | Liver | HCC | Wnt signaling pathway | 245/7958 | 444/18723 | 3.68e-08 | 8.09e-07 | 245 |
GO:003011121 | Liver | HCC | regulation of Wnt signaling pathway | 180/7958 | 328/18723 | 3.62e-06 | 4.72e-05 | 180 |
GO:006007021 | Liver | HCC | canonical Wnt signaling pathway | 162/7958 | 303/18723 | 7.00e-05 | 6.32e-04 | 162 |
GO:006082821 | Liver | HCC | regulation of canonical Wnt signaling pathway | 137/7958 | 253/18723 | 1.15e-04 | 9.70e-04 | 137 |
GO:006056011 | Liver | HCC | developmental growth involved in morphogenesis | 124/7958 | 234/18723 | 7.37e-04 | 4.47e-03 | 124 |
GO:00074921 | Liver | HCC | endoderm development | 43/7958 | 77/18723 | 1.24e-02 | 4.51e-02 | 43 |
GO:000166721 | Liver | HCC | ameboidal-type cell migration | 226/7958 | 475/18723 | 1.35e-02 | 4.81e-02 | 226 |
GO:004873219 | Prostate | Tumor | gland development | 132/3246 | 436/18723 | 1.40e-11 | 1.04e-09 | 132 |
GO:001605514 | Prostate | Tumor | Wnt signaling pathway | 131/3246 | 444/18723 | 1.16e-10 | 7.11e-09 | 131 |
GO:019873814 | Prostate | Tumor | cell-cell signaling by wnt | 131/3246 | 446/18723 | 1.61e-10 | 9.69e-09 | 131 |
GO:003011114 | Prostate | Tumor | regulation of Wnt signaling pathway | 99/3246 | 328/18723 | 5.92e-09 | 2.34e-07 | 99 |
GO:000166718 | Prostate | Tumor | ameboidal-type cell migration | 130/3246 | 475/18723 | 2.36e-08 | 8.09e-07 | 130 |
GO:006082814 | Prostate | Tumor | regulation of canonical Wnt signaling pathway | 79/3246 | 253/18723 | 4.01e-08 | 1.25e-06 | 79 |
GO:000315815 | Prostate | Tumor | endothelium development | 50/3246 | 136/18723 | 4.60e-08 | 1.42e-06 | 50 |
GO:004544614 | Prostate | Tumor | endothelial cell differentiation | 45/3246 | 118/18723 | 6.08e-08 | 1.80e-06 | 45 |
GO:006007014 | Prostate | Tumor | canonical Wnt signaling pathway | 87/3246 | 303/18723 | 5.49e-07 | 1.17e-05 | 87 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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Cell-cell communication analysis |
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Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
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Single-cell gene regulatory network inference analysis |
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∗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 |
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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 |
MESP1 | insertion | Nonsense_Mutation | novel | c.727_728insATTATTGAGTATTTATTGT | p.Leu243HisfsTer3 | p.L243Hfs*3 | Q9BRJ9 | protein_coding | TCGA-BH-A0DP-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | arimidex | SD | ||
MESP1 | SNV | Missense_Mutation | c.391C>T | p.Arg131Cys | p.R131C | Q9BRJ9 | protein_coding | deleterious(0) | probably_damaging(0.995) | TCGA-44-8117-01 | Lung | lung adenocarcinoma | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
MESP1 | SNV | Missense_Mutation | novel | c.461N>T | p.Arg154Leu | p.R154L | Q9BRJ9 | protein_coding | tolerated(0.34) | benign(0) | TCGA-58-8391-01 | Lung | lung squamous cell carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatin | PD |
MESP1 | SNV | Missense_Mutation | novel | c.74N>T | p.Pro25Leu | p.P25L | Q9BRJ9 | protein_coding | tolerated_low_confidence(0.19) | benign(0.003) | TCGA-58-8391-01 | Lung | lung squamous cell carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatin | PD |
MESP1 | SNV | Missense_Mutation | novel | c.754N>A | p.Glu252Lys | p.E252K | Q9BRJ9 | protein_coding | deleterious_low_confidence(0) | possibly_damaging(0.826) | TCGA-ET-A25R-01 | Thyroid | thyroid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
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Related drugs of malignant transformation related genes |
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(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
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