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Gene: HIC2 |
Gene summary for HIC2 |
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Gene information | Species | Human | Gene symbol | HIC2 | Gene ID | 23119 |
Gene name | HIC ZBTB transcriptional repressor 2 | |
Gene Alias | HRG22 | |
Cytomap | 22q11.21 | |
Gene Type | protein-coding | GO ID | GO:0000122 | UniProtAcc | Q96JB3 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
23119 | HIC2 | LZE7T | Human | Esophagus | ESCC | 2.48e-05 | 3.58e-01 | 0.0667 |
23119 | HIC2 | LZE24T | Human | Esophagus | ESCC | 3.07e-05 | 1.08e-01 | 0.0596 |
23119 | HIC2 | P1T-E | Human | Esophagus | ESCC | 3.06e-03 | 3.24e-01 | 0.0875 |
23119 | HIC2 | P2T-E | Human | Esophagus | ESCC | 2.65e-17 | 1.04e-01 | 0.1177 |
23119 | HIC2 | P4T-E | Human | Esophagus | ESCC | 4.00e-12 | 2.98e-01 | 0.1323 |
23119 | HIC2 | P5T-E | Human | Esophagus | ESCC | 4.12e-02 | 5.54e-02 | 0.1327 |
23119 | HIC2 | P8T-E | Human | Esophagus | ESCC | 5.47e-04 | 6.91e-02 | 0.0889 |
23119 | HIC2 | P9T-E | Human | Esophagus | ESCC | 4.72e-04 | 1.93e-01 | 0.1131 |
23119 | HIC2 | P10T-E | Human | Esophagus | ESCC | 5.48e-11 | 2.16e-01 | 0.116 |
23119 | HIC2 | P11T-E | Human | Esophagus | ESCC | 4.31e-03 | 2.10e-01 | 0.1426 |
23119 | HIC2 | P12T-E | Human | Esophagus | ESCC | 7.38e-10 | 2.32e-01 | 0.1122 |
23119 | HIC2 | P15T-E | Human | Esophagus | ESCC | 1.65e-03 | 6.95e-02 | 0.1149 |
23119 | HIC2 | P16T-E | Human | Esophagus | ESCC | 6.25e-10 | 1.40e-01 | 0.1153 |
23119 | HIC2 | P21T-E | Human | Esophagus | ESCC | 2.05e-09 | 3.53e-01 | 0.1617 |
23119 | HIC2 | P22T-E | Human | Esophagus | ESCC | 3.76e-04 | 8.21e-02 | 0.1236 |
23119 | HIC2 | P23T-E | Human | Esophagus | ESCC | 2.08e-06 | 2.35e-01 | 0.108 |
23119 | HIC2 | P24T-E | Human | Esophagus | ESCC | 3.97e-05 | 5.76e-02 | 0.1287 |
23119 | HIC2 | P26T-E | Human | Esophagus | ESCC | 4.75e-24 | 3.66e-01 | 0.1276 |
23119 | HIC2 | P27T-E | Human | Esophagus | ESCC | 7.79e-08 | 1.99e-01 | 0.1055 |
23119 | HIC2 | P28T-E | Human | Esophagus | ESCC | 1.79e-23 | 6.08e-01 | 0.1149 |
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Tissue | Expression Dynamics | Abbreviation |
Esophagus | ![]() | ESCC: Esophageal squamous cell carcinoma |
HGIN: High-grade intraepithelial neoplasias | ||
LGIN: Low-grade intraepithelial neoplasias |
∗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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∗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 |
HIC2 | SNV | Missense_Mutation | c.394G>A | p.Ala132Thr | p.A132T | Q96JB3 | protein_coding | deleterious(0.01) | probably_damaging(0.999) | TCGA-D7-A4YY-01 | Stomach | stomach adenocarcinoma | Male | <65 | III/IV | Chemotherapy | 5-fluorouracil | SD | |
HIC2 | SNV | Missense_Mutation | c.58N>T | p.Gly20Trp | p.G20W | Q96JB3 | protein_coding | deleterious_low_confidence(0.03) | probably_damaging(0.97) | TCGA-F1-6874-01 | Stomach | stomach adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
HIC2 | SNV | Missense_Mutation | rs137951777 | c.1267G>A | p.Ala423Thr | p.A423T | Q96JB3 | protein_coding | tolerated(0.34) | benign(0.007) | TCGA-HU-A4GU-01 | Stomach | stomach adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
HIC2 | SNV | Missense_Mutation | novel | c.269C>T | p.Ser90Phe | p.S90F | Q96JB3 | protein_coding | deleterious(0) | benign(0.003) | TCGA-VQ-A8P2-01 | Stomach | stomach adenocarcinoma | Male | >=65 | III/IV | Unspecific | Complete Response | |
HIC2 | insertion | Frame_Shift_Ins | rs781520412 | c.481dupC | p.Arg161ProfsTer40 | p.R161Pfs*40 | Q96JB3 | protein_coding | TCGA-VQ-A8PP-01 | Stomach | stomach adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | fluorouracil | PD |
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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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