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Gene: GTF2IRD2B |
Gene summary for GTF2IRD2B |
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Gene information | Species | Human | Gene symbol | GTF2IRD2B | Gene ID | 389524 |
Gene name | GTF2I repeat domain containing 2B | |
Gene Alias | GTF2IRD2 | |
Cytomap | 7q11.23 | |
Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | Q6EKJ0 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
389524 | GTF2IRD2B | HTA11_3410_2000001011 | Human | Colorectum | AD | 6.24e-06 | 3.26e-01 | 0.0155 |
389524 | GTF2IRD2B | HTA11_1938_2000001011 | Human | Colorectum | AD | 1.18e-04 | 4.12e-01 | -0.0811 |
389524 | GTF2IRD2B | HTA11_78_2000001011 | Human | Colorectum | AD | 3.19e-10 | 5.79e-01 | -0.1088 |
389524 | GTF2IRD2B | HTA11_347_2000001011 | Human | Colorectum | AD | 8.59e-20 | 6.69e-01 | -0.1954 |
389524 | GTF2IRD2B | HTA11_3361_2000001011 | Human | Colorectum | AD | 1.53e-09 | 5.32e-01 | -0.1207 |
389524 | GTF2IRD2B | HTA11_83_2000001011 | Human | Colorectum | SER | 2.97e-02 | 3.61e-01 | -0.1526 |
389524 | GTF2IRD2B | HTA11_696_2000001011 | Human | Colorectum | AD | 2.43e-14 | 6.73e-01 | -0.1464 |
389524 | GTF2IRD2B | HTA11_866_2000001011 | Human | Colorectum | AD | 2.98e-23 | 6.96e-01 | -0.1001 |
389524 | GTF2IRD2B | HTA11_1391_2000001011 | Human | Colorectum | AD | 2.99e-16 | 6.98e-01 | -0.059 |
389524 | GTF2IRD2B | HTA11_2992_2000001011 | Human | Colorectum | SER | 2.56e-02 | 3.68e-01 | -0.1706 |
389524 | GTF2IRD2B | HTA11_546_2000001011 | Human | Colorectum | AD | 1.35e-18 | 1.04e+00 | -0.0842 |
389524 | GTF2IRD2B | HTA11_9341_2000001011 | Human | Colorectum | SER | 4.31e-02 | 4.35e-01 | -0.00410000000000005 |
389524 | GTF2IRD2B | HTA11_866_3004761011 | Human | Colorectum | AD | 2.63e-06 | 3.43e-01 | 0.096 |
389524 | GTF2IRD2B | HTA11_4255_2000001011 | Human | Colorectum | SER | 5.11e-06 | 6.38e-01 | 0.0446 |
389524 | GTF2IRD2B | HTA11_7663_2000001011 | Human | Colorectum | SER | 2.17e-02 | 5.79e-01 | 0.0131 |
389524 | GTF2IRD2B | HTA11_10623_2000001011 | Human | Colorectum | AD | 3.51e-03 | 5.04e-01 | -0.0177 |
389524 | GTF2IRD2B | HTA11_10711_2000001011 | Human | Colorectum | AD | 8.27e-11 | 6.32e-01 | 0.0338 |
389524 | GTF2IRD2B | HTA11_7696_3000711011 | Human | Colorectum | AD | 1.78e-11 | 4.95e-01 | 0.0674 |
389524 | GTF2IRD2B | HTA11_6818_2000001011 | Human | Colorectum | AD | 2.19e-11 | 8.88e-01 | 0.0112 |
389524 | GTF2IRD2B | HTA11_11156_2000001011 | Human | Colorectum | AD | 1.04e-04 | 9.09e-01 | 0.0397 |
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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 |
GTF2IRD2B | SNV | Missense_Mutation | novel | c.1445N>A | p.Arg482His | p.R482H | Q6EKJ0 | protein_coding | deleterious(0) | probably_damaging(0.98) | TCGA-HU-A4GQ-01 | Stomach | stomach adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | SD |
GTF2IRD2B | SNV | Missense_Mutation | novel | c.209C>T | p.Thr70Met | p.T70M | Q6EKJ0 | protein_coding | tolerated_low_confidence(0.28) | benign(0.007) | TCGA-VQ-A91K-01 | Stomach | stomach adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | fluorouracil | CR |
GTF2IRD2B | SNV | Missense_Mutation | novel | c.1664C>T | p.Thr555Met | p.T555M | Q6EKJ0 | protein_coding | deleterious(0.01) | probably_damaging(0.991) | TCGA-VQ-A94U-01 | Stomach | stomach adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
GTF2IRD2B | SNV | Missense_Mutation | novel | c.2114T>A | p.Leu705His | p.L705H | Q6EKJ0 | protein_coding | deleterious(0) | probably_damaging(0.993) | TCGA-FY-A4B0-01 | Thyroid | thyroid carcinoma | Male | >=65 | I/II | Hormone Therapy | synthroid | SD |
GTF2IRD2B | insertion | Frame_Shift_Ins | novel | c.2116_2117insA | p.Leu706HisfsTer7 | p.L706Hfs*7 | Q6EKJ0 | protein_coding | TCGA-FY-A4B0-01 | Thyroid | thyroid carcinoma | Male | >=65 | I/II | Hormone Therapy | synthroid | 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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