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Gene: ZBTB7B |
Gene summary for ZBTB7B |
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Gene information | Species | Human | Gene symbol | ZBTB7B | Gene ID | 51043 |
Gene name | zinc finger and BTB domain containing 7B | |
Gene Alias | CKROX | |
Cytomap | 1q21.3 | |
Gene Type | protein-coding | GO ID | GO:0000122 | UniProtAcc | O15156 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
51043 | ZBTB7B | HTA11_7663_2000001011 | Human | Colorectum | SER | 6.48e-06 | 6.39e-01 | 0.0131 |
51043 | ZBTB7B | HTA11_10623_2000001011 | Human | Colorectum | AD | 1.59e-06 | 6.76e-01 | -0.0177 |
51043 | ZBTB7B | HTA11_10711_2000001011 | Human | Colorectum | AD | 6.85e-16 | 7.16e-01 | 0.0338 |
51043 | ZBTB7B | HTA11_7696_3000711011 | Human | Colorectum | AD | 1.19e-02 | 2.42e-01 | 0.0674 |
51043 | ZBTB7B | HTA11_6818_2000001011 | Human | Colorectum | AD | 9.00e-27 | 1.61e+00 | 0.0112 |
51043 | ZBTB7B | HTA11_6818_2000001021 | Human | Colorectum | AD | 7.53e-18 | 1.02e+00 | 0.0588 |
51043 | ZBTB7B | HTA11_99999974143_84620 | Human | Colorectum | MSS | 1.45e-57 | 1.40e+00 | 0.3005 |
51043 | ZBTB7B | LZE7T | Human | Esophagus | ESCC | 2.17e-11 | 1.79e-01 | 0.0667 |
51043 | ZBTB7B | LZE20T | Human | Esophagus | ESCC | 4.95e-09 | 6.50e-02 | 0.0662 |
51043 | ZBTB7B | LZE24T | Human | Esophagus | ESCC | 4.44e-07 | 2.46e-01 | 0.0596 |
51043 | ZBTB7B | P1T-E | Human | Esophagus | ESCC | 8.18e-04 | 4.04e-01 | 0.0875 |
51043 | ZBTB7B | P2T-E | Human | Esophagus | ESCC | 3.30e-12 | 2.77e-02 | 0.1177 |
51043 | ZBTB7B | P4T-E | Human | Esophagus | ESCC | 7.44e-10 | 5.52e-02 | 0.1323 |
51043 | ZBTB7B | P5T-E | Human | Esophagus | ESCC | 1.92e-17 | 1.58e-01 | 0.1327 |
51043 | ZBTB7B | P8T-E | Human | Esophagus | ESCC | 2.68e-10 | 6.64e-02 | 0.0889 |
51043 | ZBTB7B | P9T-E | Human | Esophagus | ESCC | 1.65e-09 | 2.76e-02 | 0.1131 |
51043 | ZBTB7B | P10T-E | Human | Esophagus | ESCC | 9.30e-11 | -6.31e-03 | 0.116 |
51043 | ZBTB7B | P11T-E | Human | Esophagus | ESCC | 2.17e-03 | 8.62e-02 | 0.1426 |
51043 | ZBTB7B | P12T-E | Human | Esophagus | ESCC | 7.17e-09 | 1.32e-01 | 0.1122 |
51043 | ZBTB7B | P15T-E | Human | Esophagus | ESCC | 8.10e-13 | 2.35e-01 | 0.1149 |
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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). |
Page: 1 2 3 4 5 6 7 8 9 |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:0048732 | Colorectum | AD | gland development | 149/3918 | 436/18723 | 6.07e-11 | 6.33e-09 | 149 |
GO:0032868 | Colorectum | AD | response to insulin | 91/3918 | 264/18723 | 2.02e-07 | 8.48e-06 | 91 |
GO:1901653 | Colorectum | AD | cellular response to peptide | 114/3918 | 359/18723 | 8.32e-07 | 2.88e-05 | 114 |
GO:0032869 | Colorectum | AD | cellular response to insulin stimulus | 72/3918 | 203/18723 | 1.10e-06 | 3.68e-05 | 72 |
GO:0030879 | Colorectum | AD | mammary gland development | 53/3918 | 137/18723 | 1.46e-06 | 4.58e-05 | 53 |
GO:0071375 | Colorectum | AD | cellular response to peptide hormone stimulus | 95/3918 | 290/18723 | 1.50e-06 | 4.66e-05 | 95 |
GO:0043434 | Colorectum | AD | response to peptide hormone | 126/3918 | 414/18723 | 2.70e-06 | 7.86e-05 | 126 |
GO:0006984 | Colorectum | AD | ER-nucleus signaling pathway | 21/3918 | 46/18723 | 1.47e-04 | 2.08e-03 | 21 |
GO:0050878 | Colorectum | AD | regulation of body fluid levels | 108/3918 | 379/18723 | 2.54e-04 | 3.20e-03 | 108 |
GO:0045785 | Colorectum | AD | positive regulation of cell adhesion | 122/3918 | 437/18723 | 2.65e-04 | 3.28e-03 | 122 |
GO:0007589 | Colorectum | AD | body fluid secretion | 33/3918 | 93/18723 | 8.26e-04 | 8.13e-03 | 33 |
GO:0032933 | Colorectum | AD | SREBP signaling pathway | 9/3918 | 15/18723 | 1.11e-03 | 1.01e-02 | 9 |
GO:0071501 | Colorectum | AD | cellular response to sterol depletion | 9/3918 | 16/18723 | 2.06e-03 | 1.64e-02 | 9 |
GO:1903706 | Colorectum | AD | regulation of hemopoiesis | 99/3918 | 367/18723 | 3.08e-03 | 2.28e-02 | 99 |
GO:0120162 | Colorectum | AD | positive regulation of cold-induced thermogenesis | 32/3918 | 97/18723 | 3.74e-03 | 2.63e-02 | 32 |
GO:0007595 | Colorectum | AD | lactation | 18/3918 | 47/18723 | 4.81e-03 | 3.25e-02 | 18 |
GO:0006991 | Colorectum | AD | response to sterol depletion | 9/3918 | 18/18723 | 5.82e-03 | 3.67e-02 | 9 |
GO:0031056 | Colorectum | AD | regulation of histone modification | 45/3918 | 152/18723 | 7.05e-03 | 4.31e-02 | 45 |
GO:0106106 | Colorectum | AD | cold-induced thermogenesis | 43/3918 | 144/18723 | 7.05e-03 | 4.31e-02 | 43 |
GO:0120161 | Colorectum | AD | regulation of cold-induced thermogenesis | 43/3918 | 144/18723 | 7.05e-03 | 4.31e-02 | 43 |
Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 |
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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 |
ZBTB7B | SNV | Missense_Mutation | rs150590726 | c.706N>T | p.Arg236Cys | p.R236C | O15156 | protein_coding | deleterious(0.02) | probably_damaging(0.996) | TCGA-B7-5816-01 | Stomach | stomach adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
ZBTB7B | SNV | Missense_Mutation | c.218N>A | p.Arg73Gln | p.R73Q | O15156 | protein_coding | deleterious(0.04) | benign(0.295) | TCGA-BR-4362-01 | Stomach | stomach adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
ZBTB7B | SNV | Missense_Mutation | novel | c.427N>A | p.Ala143Thr | p.A143T | O15156 | protein_coding | deleterious(0) | probably_damaging(0.916) | TCGA-BR-8361-01 | Stomach | stomach adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
ZBTB7B | SNV | Missense_Mutation | novel | c.1286N>G | p.Lys429Arg | p.K429R | O15156 | protein_coding | deleterious(0) | probably_damaging(0.98) | TCGA-D7-A6EY-01 | Stomach | stomach adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | PD |
ZBTB7B | SNV | Missense_Mutation | c.810N>T | p.Glu270Asp | p.E270D | O15156 | protein_coding | tolerated(0.34) | benign(0) | TCGA-HF-7132-01 | Stomach | stomach adenocarcinoma | Male | Unknown | I/II | Chemotherapy | fluorouracil | SD | |
ZBTB7B | SNV | Missense_Mutation | novel | c.1619N>T | p.Ala540Val | p.A540V | O15156 | protein_coding | tolerated_low_confidence(0.45) | benign(0.003) | TCGA-VQ-A91E-01 | Stomach | stomach adenocarcinoma | Female | >=65 | III/IV | Chemotherapy | fluorouracil | CR |
ZBTB7B | SNV | Missense_Mutation | novel | c.829G>T | p.Gly277Cys | p.G277C | O15156 | protein_coding | deleterious(0.01) | probably_damaging(0.998) | TCGA-VQ-A91K-01 | Stomach | stomach adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | fluorouracil | CR |
ZBTB7B | SNV | Missense_Mutation | c.447N>A | p.Ser149Arg | p.S149R | O15156 | protein_coding | tolerated(0.08) | benign(0.289) | TCGA-DJ-A2Q2-01 | Thyroid | thyroid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | |
ZBTB7B | SNV | Missense_Mutation | c.1316N>A | p.Pro439Gln | p.P439Q | O15156 | protein_coding | tolerated(0.67) | benign(0.013) | TCGA-ET-A39R-01 | Thyroid | thyroid carcinoma | Female | <65 | I/II | 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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