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Gene: ZFHX4 |
Gene summary for ZFHX4 |
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Gene information | Species | Human | Gene symbol | ZFHX4 | Gene ID | 79776 |
Gene name | zinc finger homeobox 4 | |
Gene Alias | ZFH4 | |
Cytomap | 8q21.13 | |
Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | Q86UP3 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
79776 | ZFHX4 | P1T-E | Human | Esophagus | ESCC | 5.20e-08 | 3.43e-01 | 0.0875 |
79776 | ZFHX4 | P5T-E | Human | Esophagus | ESCC | 3.76e-04 | 9.90e-02 | 0.1327 |
79776 | ZFHX4 | P9T-E | Human | Esophagus | ESCC | 5.23e-05 | 1.38e-01 | 0.1131 |
79776 | ZFHX4 | P10T-E | Human | Esophagus | ESCC | 3.29e-21 | 4.45e-01 | 0.116 |
79776 | ZFHX4 | P11T-E | Human | Esophagus | ESCC | 3.25e-05 | 2.03e-01 | 0.1426 |
79776 | ZFHX4 | P15T-E | Human | Esophagus | ESCC | 8.45e-04 | 1.24e-01 | 0.1149 |
79776 | ZFHX4 | P16T-E | Human | Esophagus | ESCC | 2.22e-05 | 8.99e-02 | 0.1153 |
79776 | ZFHX4 | P23T-E | Human | Esophagus | ESCC | 6.91e-16 | 4.27e-01 | 0.108 |
79776 | ZFHX4 | P24T-E | Human | Esophagus | ESCC | 8.72e-07 | 1.08e-01 | 0.1287 |
79776 | ZFHX4 | P26T-E | Human | Esophagus | ESCC | 1.63e-05 | 1.11e-01 | 0.1276 |
79776 | ZFHX4 | P27T-E | Human | Esophagus | ESCC | 8.49e-09 | 2.07e-01 | 0.1055 |
79776 | ZFHX4 | P30T-E | Human | Esophagus | ESCC | 2.31e-10 | 3.75e-01 | 0.137 |
79776 | ZFHX4 | P36T-E | Human | Esophagus | ESCC | 4.17e-05 | 2.13e-01 | 0.1187 |
79776 | ZFHX4 | P37T-E | Human | Esophagus | ESCC | 3.53e-03 | 1.09e-01 | 0.1371 |
79776 | ZFHX4 | P42T-E | Human | Esophagus | ESCC | 1.02e-24 | 6.57e-01 | 0.1175 |
79776 | ZFHX4 | P47T-E | Human | Esophagus | ESCC | 1.94e-02 | 6.53e-02 | 0.1067 |
79776 | ZFHX4 | P49T-E | Human | Esophagus | ESCC | 3.75e-07 | 6.69e-01 | 0.1768 |
79776 | ZFHX4 | P62T-E | Human | Esophagus | ESCC | 1.57e-81 | 1.32e+00 | 0.1302 |
79776 | ZFHX4 | P74T-E | Human | Esophagus | ESCC | 2.69e-24 | 5.65e-01 | 0.1479 |
79776 | ZFHX4 | P75T-E | Human | Esophagus | ESCC | 2.25e-19 | 3.95e-01 | 0.1125 |
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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 |
ZFHX4 | SNV | Missense_Mutation | c.3745N>T | p.Pro1249Ser | p.P1249S | Q86UP3 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-EY-A1G7-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
ZFHX4 | SNV | Missense_Mutation | rs756374230 | c.4565N>A | p.Pro1522His | p.P1522H | Q86UP3 | protein_coding | deleterious(0) | probably_damaging(0.991) | TCGA-EY-A1G8-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
ZFHX4 | SNV | Missense_Mutation | c.9715N>A | p.Asp3239Asn | p.D3239N | Q86UP3 | protein_coding | deleterious(0) | probably_damaging(0.982) | TCGA-EY-A1G8-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
ZFHX4 | SNV | Missense_Mutation | novel | c.2012N>C | p.Gly671Ala | p.G671A | Q86UP3 | protein_coding | deleterious(0.01) | possibly_damaging(0.679) | TCGA-EY-A1GD-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
ZFHX4 | SNV | Missense_Mutation | c.7921N>A | p.Glu2641Lys | p.E2641K | Q86UP3 | protein_coding | deleterious(0) | possibly_damaging(0.895) | TCGA-EY-A1GD-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
ZFHX4 | SNV | Missense_Mutation | c.8855N>A | p.Arg2952Gln | p.R2952Q | Q86UP3 | protein_coding | deleterious(0) | probably_damaging(0.982) | TCGA-EY-A1GD-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
ZFHX4 | SNV | Missense_Mutation | novel | c.7621N>A | p.Asp2541Asn | p.D2541N | Q86UP3 | protein_coding | deleterious(0.01) | probably_damaging(0.931) | TCGA-EY-A1GI-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
ZFHX4 | SNV | Missense_Mutation | c.8414N>T | p.Ser2805Leu | p.S2805L | Q86UP3 | protein_coding | deleterious(0) | probably_damaging(0.991) | TCGA-EY-A1GI-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
ZFHX4 | SNV | Missense_Mutation | c.6625G>C | p.Asp2209His | p.D2209H | Q86UP3 | protein_coding | deleterious(0) | possibly_damaging(0.826) | TCGA-EY-A1GS-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Chemotherapy | taxol | PD | |
ZFHX4 | SNV | Missense_Mutation | novel | c.1840N>A | p.Glu614Lys | p.E614K | Q86UP3 | protein_coding | deleterious(0.01) | probably_damaging(0.994) | TCGA-EY-A215-01 | Endometrium | uterine corpus endometrioid 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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