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Gene: ZNF146 |
Gene summary for ZNF146 |
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Gene information | Species | Human | Gene symbol | ZNF146 | Gene ID | 7705 |
Gene name | zinc finger protein 146 | |
Gene Alias | OZF | |
Cytomap | 19q13.12 | |
Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | Q15072 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
7705 | ZNF146 | P127T-E | Human | Esophagus | ESCC | 3.12e-21 | 3.74e-01 | 0.0826 |
7705 | ZNF146 | P128T-E | Human | Esophagus | ESCC | 2.24e-35 | 1.14e+00 | 0.1241 |
7705 | ZNF146 | P130T-E | Human | Esophagus | ESCC | 3.44e-50 | 1.08e+00 | 0.1676 |
7705 | ZNF146 | HCC1_Meng | Human | Liver | HCC | 8.37e-71 | 1.30e-01 | 0.0246 |
7705 | ZNF146 | HCC2_Meng | Human | Liver | HCC | 7.46e-18 | 4.47e-02 | 0.0107 |
7705 | ZNF146 | HCC1 | Human | Liver | HCC | 1.28e-06 | 3.44e+00 | 0.5336 |
7705 | ZNF146 | HCC2 | Human | Liver | HCC | 1.97e-13 | 3.72e+00 | 0.5341 |
7705 | ZNF146 | S014 | Human | Liver | HCC | 4.50e-06 | 3.73e-01 | 0.2254 |
7705 | ZNF146 | S015 | Human | Liver | HCC | 4.53e-05 | 5.74e-01 | 0.2375 |
7705 | ZNF146 | S016 | Human | Liver | HCC | 5.64e-04 | 3.56e-01 | 0.2243 |
7705 | ZNF146 | S027 | Human | Liver | HCC | 2.82e-03 | 6.79e-01 | 0.2446 |
7705 | ZNF146 | S028 | Human | Liver | HCC | 5.43e-13 | 7.48e-01 | 0.2503 |
7705 | ZNF146 | S029 | Human | Liver | HCC | 2.68e-11 | 7.06e-01 | 0.2581 |
7705 | ZNF146 | C04 | Human | Oral cavity | OSCC | 1.55e-15 | 9.48e-01 | 0.2633 |
7705 | ZNF146 | C21 | Human | Oral cavity | OSCC | 2.73e-13 | 5.52e-01 | 0.2678 |
7705 | ZNF146 | C30 | Human | Oral cavity | OSCC | 1.68e-22 | 1.09e+00 | 0.3055 |
7705 | ZNF146 | C38 | Human | Oral cavity | OSCC | 7.87e-07 | 7.49e-01 | 0.172 |
7705 | ZNF146 | C43 | Human | Oral cavity | OSCC | 7.58e-31 | 5.36e-01 | 0.1704 |
7705 | ZNF146 | C46 | Human | Oral cavity | OSCC | 2.45e-11 | 3.70e-01 | 0.1673 |
7705 | ZNF146 | C51 | Human | Oral cavity | OSCC | 2.42e-05 | 3.83e-01 | 0.2674 |
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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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∗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 |
ZNF146 | SNV | Missense_Mutation | c.769N>G | p.Leu257Val | p.L257V | Q15072 | protein_coding | tolerated(0.52) | possibly_damaging(0.469) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
ZNF146 | SNV | Missense_Mutation | c.323N>T | p.Ala108Val | p.A108V | Q15072 | protein_coding | deleterious(0.02) | probably_damaging(0.989) | TCGA-BH-A0HF-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | arimidex | SD | |
ZNF146 | SNV | Missense_Mutation | c.266N>T | p.Thr89Met | p.T89M | Q15072 | protein_coding | tolerated(0.13) | benign(0.007) | TCGA-A6-2686-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
ZNF146 | SNV | Missense_Mutation | c.737G>A | p.Gly246Glu | p.G246E | Q15072 | protein_coding | deleterious(0.02) | probably_damaging(1) | TCGA-D5-6931-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | SD | |
ZNF146 | SNV | Missense_Mutation | c.217G>A | p.Glu73Lys | p.E73K | Q15072 | protein_coding | tolerated(0.53) | benign(0) | TCGA-F5-6814-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
ZNF146 | SNV | Missense_Mutation | c.386T>C | p.Val129Ala | p.V129A | Q15072 | protein_coding | tolerated(0.16) | benign(0.254) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | |
ZNF146 | SNV | Missense_Mutation | novel | c.542A>G | p.Glu181Gly | p.E181G | Q15072 | protein_coding | deleterious(0) | probably_damaging(0.993) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
ZNF146 | SNV | Missense_Mutation | novel | c.716C>A | p.Pro239His | p.P239H | Q15072 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
ZNF146 | SNV | Missense_Mutation | novel | c.677C>T | p.Ser226Phe | p.S226F | Q15072 | protein_coding | tolerated(0.17) | probably_damaging(0.997) | TCGA-A5-A2K5-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
ZNF146 | SNV | Missense_Mutation | novel | c.352C>T | p.His118Tyr | p.H118Y | Q15072 | protein_coding | deleterious(0) | possibly_damaging(0.649) | TCGA-AJ-A3EK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | CR |
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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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