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Gene: BCL7A |
Gene summary for BCL7A |
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Gene information | Species | Human | Gene symbol | BCL7A | Gene ID | 605 |
Gene name | BAF chromatin remodeling complex subunit BCL7A | |
Gene Alias | BCL7 | |
Cytomap | 12q24.31 | |
Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | Q4VC05 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
605 | BCL7A | LZE4T | Human | Esophagus | ESCC | 1.49e-07 | 1.64e-01 | 0.0811 |
605 | BCL7A | LZE24T | Human | Esophagus | ESCC | 2.44e-06 | 2.14e-01 | 0.0596 |
605 | BCL7A | LZE21T | Human | Esophagus | ESCC | 2.88e-06 | 3.91e-01 | 0.0655 |
605 | BCL7A | P1T-E | Human | Esophagus | ESCC | 2.57e-04 | 2.53e-01 | 0.0875 |
605 | BCL7A | P2T-E | Human | Esophagus | ESCC | 2.91e-65 | 1.14e+00 | 0.1177 |
605 | BCL7A | P4T-E | Human | Esophagus | ESCC | 3.24e-14 | 3.59e-01 | 0.1323 |
605 | BCL7A | P5T-E | Human | Esophagus | ESCC | 2.81e-15 | 2.10e-01 | 0.1327 |
605 | BCL7A | P8T-E | Human | Esophagus | ESCC | 4.51e-17 | 2.68e-01 | 0.0889 |
605 | BCL7A | P9T-E | Human | Esophagus | ESCC | 8.62e-10 | 1.94e-01 | 0.1131 |
605 | BCL7A | P10T-E | Human | Esophagus | ESCC | 9.97e-30 | 5.07e-01 | 0.116 |
605 | BCL7A | P11T-E | Human | Esophagus | ESCC | 1.97e-04 | 4.60e-01 | 0.1426 |
605 | BCL7A | P12T-E | Human | Esophagus | ESCC | 1.16e-23 | 5.21e-01 | 0.1122 |
605 | BCL7A | P15T-E | Human | Esophagus | ESCC | 3.44e-24 | 5.68e-01 | 0.1149 |
605 | BCL7A | P16T-E | Human | Esophagus | ESCC | 1.41e-32 | 6.02e-01 | 0.1153 |
605 | BCL7A | P17T-E | Human | Esophagus | ESCC | 1.50e-05 | 2.22e-01 | 0.1278 |
605 | BCL7A | P20T-E | Human | Esophagus | ESCC | 1.46e-14 | 3.07e-01 | 0.1124 |
605 | BCL7A | P21T-E | Human | Esophagus | ESCC | 7.75e-16 | 3.04e-01 | 0.1617 |
605 | BCL7A | P22T-E | Human | Esophagus | ESCC | 3.40e-12 | 2.32e-01 | 0.1236 |
605 | BCL7A | P23T-E | Human | Esophagus | ESCC | 5.45e-09 | 1.29e-01 | 0.108 |
605 | BCL7A | P24T-E | Human | Esophagus | ESCC | 2.54e-07 | 1.04e-01 | 0.1287 |
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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 |
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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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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 |
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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 |
BCL7A | SNV | Missense_Mutation | c.618N>T | p.Leu206Phe | p.L206F | Q4VC05 | protein_coding | deleterious_low_confidence(0.02) | benign(0.001) | TCGA-A8-A09A-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD | |
BCL7A | SNV | Missense_Mutation | novel | c.514C>G | p.Pro172Ala | p.P172A | Q4VC05 | protein_coding | deleterious(0.02) | benign(0.107) | TCGA-D8-A1XQ-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
BCL7A | SNV | Missense_Mutation | rs763960478 | c.51N>A | p.Asp17Glu | p.D17E | Q4VC05 | protein_coding | deleterious(0.03) | benign(0.391) | TCGA-OL-A66P-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | cytoxan | CR |
BCL7A | SNV | Missense_Mutation | rs749055080 | c.155N>T | p.Thr52Met | p.T52M | Q4VC05 | protein_coding | deleterious(0.02) | probably_damaging(0.989) | TCGA-AA-A01R-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | 5-fluorouracil | PD |
BCL7A | SNV | Missense_Mutation | rs767784265 | c.620N>T | p.Ser207Leu | p.S207L | Q4VC05 | protein_coding | tolerated_low_confidence(0.96) | benign(0) | TCGA-AG-A002-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
BCL7A | SNV | Missense_Mutation | rs780831032 | c.112N>A | p.Val38Ile | p.V38I | Q4VC05 | protein_coding | tolerated(0.07) | possibly_damaging(0.51) | TCGA-AJ-A3BH-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | Unknown | I/II | Unknown | Unknown | SD |
BCL7A | SNV | Missense_Mutation | c.498N>T | p.Glu166Asp | p.E166D | Q4VC05 | protein_coding | tolerated(0.14) | probably_damaging(0.99) | TCGA-AX-A05Z-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | adriamycin | SD | |
BCL7A | SNV | Missense_Mutation | novel | c.104N>T | p.Trp35Leu | p.W35L | Q4VC05 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-AX-A1CE-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unspecific | Paclitaxel | SD |
BCL7A | SNV | Missense_Mutation | c.157G>A | p.Glu53Lys | p.E53K | Q4VC05 | protein_coding | deleterious(0.01) | benign(0.062) | TCGA-B5-A0JY-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | doxorubicin | SD | |
BCL7A | SNV | Missense_Mutation | novel | c.637N>A | p.Val213Met | p.V213M | Q4VC05 | protein_coding | deleterious_low_confidence(0.04) | benign(0.444) | TCGA-B5-A11R-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | paclitaxel | 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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