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Gene: MBD3 |
Gene summary for MBD3 |
Gene summary. |
Gene information | Species | Human | Gene symbol | MBD3 | Gene ID | 53615 |
Gene name | methyl-CpG binding domain protein 3 | |
Gene Alias | MBD3 | |
Cytomap | 19p13.3 | |
Gene Type | protein-coding | GO ID | GO:0000122 | UniProtAcc | O95983 |
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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 |
53615 | MBD3 | LZE7T | Human | Esophagus | ESCC | 1.34e-05 | 1.95e-01 | 0.0667 |
53615 | MBD3 | LZE24T | Human | Esophagus | ESCC | 4.58e-07 | 7.55e-02 | 0.0596 |
53615 | MBD3 | LZE21T | Human | Esophagus | ESCC | 7.00e-05 | 2.34e-01 | 0.0655 |
53615 | MBD3 | P1T-E | Human | Esophagus | ESCC | 2.14e-04 | 2.07e-01 | 0.0875 |
53615 | MBD3 | P2T-E | Human | Esophagus | ESCC | 8.80e-08 | 5.43e-02 | 0.1177 |
53615 | MBD3 | P4T-E | Human | Esophagus | ESCC | 2.10e-09 | 1.53e-01 | 0.1323 |
53615 | MBD3 | P5T-E | Human | Esophagus | ESCC | 5.46e-06 | 8.58e-03 | 0.1327 |
53615 | MBD3 | P8T-E | Human | Esophagus | ESCC | 2.59e-05 | 5.58e-02 | 0.0889 |
53615 | MBD3 | P9T-E | Human | Esophagus | ESCC | 4.42e-07 | 1.83e-01 | 0.1131 |
53615 | MBD3 | P10T-E | Human | Esophagus | ESCC | 9.68e-22 | 3.67e-01 | 0.116 |
53615 | MBD3 | P11T-E | Human | Esophagus | ESCC | 1.58e-03 | 1.49e-01 | 0.1426 |
53615 | MBD3 | P12T-E | Human | Esophagus | ESCC | 2.17e-08 | 3.52e-02 | 0.1122 |
53615 | MBD3 | P15T-E | Human | Esophagus | ESCC | 1.09e-02 | -7.29e-03 | 0.1149 |
53615 | MBD3 | P16T-E | Human | Esophagus | ESCC | 7.41e-09 | 5.46e-03 | 0.1153 |
53615 | MBD3 | P20T-E | Human | Esophagus | ESCC | 2.12e-03 | 6.54e-03 | 0.1124 |
53615 | MBD3 | P21T-E | Human | Esophagus | ESCC | 5.23e-12 | 9.22e-02 | 0.1617 |
53615 | MBD3 | P22T-E | Human | Esophagus | ESCC | 3.65e-06 | 8.52e-02 | 0.1236 |
53615 | MBD3 | P23T-E | Human | Esophagus | ESCC | 2.06e-07 | 1.68e-01 | 0.108 |
53615 | MBD3 | P24T-E | Human | Esophagus | ESCC | 1.41e-03 | -3.02e-03 | 0.1287 |
53615 | MBD3 | P26T-E | Human | Esophagus | ESCC | 1.85e-10 | 9.47e-02 | 0.1276 |
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Transcriptomic changes along malignancy continuum. |
∗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). |
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Enriched GO biological processes. |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:001657015 | Esophagus | ESCC | histone modification | 323/8552 | 463/18723 | 2.61e-26 | 7.88e-24 | 323 |
GO:001820514 | Esophagus | ESCC | peptidyl-lysine modification | 259/8552 | 376/18723 | 3.90e-20 | 5.26e-18 | 259 |
GO:000170119 | Esophagus | ESCC | in utero embryonic development | 243/8552 | 367/18723 | 1.00e-15 | 6.86e-14 | 243 |
GO:005105215 | Esophagus | ESCC | regulation of DNA metabolic process | 232/8552 | 359/18723 | 2.40e-13 | 1.13e-11 | 232 |
GO:001839413 | Esophagus | ESCC | peptidyl-lysine acetylation | 123/8552 | 169/18723 | 6.58e-13 | 2.94e-11 | 123 |
GO:004354313 | Esophagus | ESCC | protein acylation | 165/8552 | 243/18723 | 1.69e-12 | 7.14e-11 | 165 |
GO:000647313 | Esophagus | ESCC | protein acetylation | 140/8552 | 201/18723 | 4.37e-12 | 1.69e-10 | 140 |
GO:0031667111 | Esophagus | ESCC | response to nutrient levels | 289/8552 | 474/18723 | 9.25e-12 | 3.47e-10 | 289 |
GO:001839313 | Esophagus | ESCC | internal peptidyl-lysine acetylation | 114/8552 | 158/18723 | 1.16e-11 | 4.24e-10 | 114 |
GO:000647513 | Esophagus | ESCC | internal protein amino acid acetylation | 115/8552 | 160/18723 | 1.43e-11 | 5.08e-10 | 115 |
GO:00165735 | Esophagus | ESCC | histone acetylation | 110/8552 | 152/18723 | 1.95e-11 | 6.81e-10 | 110 |
GO:00434143 | Esophagus | ESCC | macromolecule methylation | 199/8552 | 316/18723 | 3.44e-10 | 9.57e-09 | 199 |
GO:00322592 | Esophagus | ESCC | methylation | 222/8552 | 364/18723 | 2.26e-09 | 5.09e-08 | 222 |
GO:000632517 | Esophagus | ESCC | chromatin organization | 240/8552 | 409/18723 | 6.52e-08 | 1.14e-06 | 240 |
GO:00400295 | Esophagus | ESCC | regulation of gene expression, epigenetic | 74/8552 | 105/18723 | 2.24e-07 | 3.42e-06 | 74 |
GO:000756820 | Esophagus | ESCC | aging | 201/8552 | 339/18723 | 2.64e-07 | 3.94e-06 | 201 |
GO:00485687 | Esophagus | ESCC | embryonic organ development | 228/8552 | 427/18723 | 7.28e-04 | 3.79e-03 | 228 |
GO:00708281 | Esophagus | ESCC | heterochromatin organization | 31/8552 | 46/18723 | 2.42e-03 | 1.06e-02 | 31 |
GO:0045814 | Esophagus | ESCC | negative regulation of gene expression, epigenetic | 32/8552 | 50/18723 | 6.90e-03 | 2.52e-02 | 32 |
GO:0006304 | Esophagus | ESCC | DNA modification | 68/8552 | 120/18723 | 9.95e-03 | 3.42e-02 | 68 |
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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 |
MBD3 | SNV | Missense_Mutation | c.530N>A | p.Leu177Gln | p.L177Q | O95983 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
MBD3 | SNV | Missense_Mutation | novel | c.335N>A | p.Val112Glu | p.V112E | O95983 | protein_coding | deleterious(0.03) | probably_damaging(0.993) | TCGA-D8-A1XK-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicine+cyclophosphamide | SD |
MBD3 | SNV | Missense_Mutation | c.260N>G | p.Asn87Ser | p.N87S | O95983 | protein_coding | tolerated(0.61) | benign(0.009) | TCGA-E2-A15C-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | arimidex | SD | |
MBD3 | deletion | Frame_Shift_Del | novel | c.640delN | p.Leu214CysfsTer7 | p.L214Cfs*7 | O95983 | protein_coding | TCGA-D8-A27V-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD | ||
MBD3 | SNV | Missense_Mutation | novel | c.775N>C | p.Glu259Gln | p.E259Q | O95983 | protein_coding | tolerated_low_confidence(0.06) | benign(0.039) | TCGA-VS-A9UC-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | SD |
MBD3 | SNV | Missense_Mutation | novel | c.593N>G | p.Ala198Gly | p.A198G | O95983 | protein_coding | tolerated(0.06) | possibly_damaging(0.643) | TCGA-AA-3930-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | capecitabine | PD |
MBD3 | SNV | Missense_Mutation | c.193N>A | p.Arg65Ser | p.R65S | O95983 | protein_coding | deleterious(0.02) | possibly_damaging(0.5) | TCGA-DM-A28C-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |
MBD3 | SNV | Missense_Mutation | c.245G>A | p.Arg82His | p.R82H | O95983 | protein_coding | tolerated(0.1) | probably_damaging(0.943) | TCGA-QG-A5YV-01 | Colorectum | colon adenocarcinoma | Female | <65 | III/IV | Chemotherapy | xeloda | CR | |
MBD3 | SNV | Missense_Mutation | c.19N>A | p.Glu7Lys | p.E7K | O95983 | protein_coding | deleterious(0.01) | benign(0.133) | TCGA-DY-A1DF-01 | Colorectum | rectum adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
MBD3 | SNV | Missense_Mutation | novel | c.239N>A | p.Arg80His | p.R80H | O95983 | protein_coding | tolerated(0.06) | possibly_damaging(0.902) | TCGA-A5-A2K3-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Chemotherapy | carboplatin | 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 |
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