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Gene: ZFP64 |
Gene summary for ZFP64 |
| Gene information | Species | Human | Gene symbol | ZFP64 | Gene ID | 55734 |
| Gene name | ZFP64 zinc finger protein | |
| Gene Alias | ZNF338 | |
| Cytomap | 20q13.2 | |
| Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | Q9NTW7 |
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Malignant transformation analysis |
Identification of the aberrant gene expression in precancerous and cancerous lesions by comparing the gene expression of stem-like cells in diseased tissues with normal stem cells |
| Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
| 55734 | ZFP64 | LZE2T | Human | Esophagus | ESCC | 6.63e-03 | 2.73e-01 | 0.082 |
| 55734 | ZFP64 | LZE4T | Human | Esophagus | ESCC | 2.16e-10 | 2.73e-01 | 0.0811 |
| 55734 | ZFP64 | LZE5T | Human | Esophagus | ESCC | 1.15e-02 | 1.57e-01 | 0.0514 |
| 55734 | ZFP64 | LZE7T | Human | Esophagus | ESCC | 3.14e-13 | 4.41e-01 | 0.0667 |
| 55734 | ZFP64 | LZE8T | Human | Esophagus | ESCC | 1.78e-02 | 6.24e-02 | 0.067 |
| 55734 | ZFP64 | LZE20T | Human | Esophagus | ESCC | 4.41e-07 | 1.18e-01 | 0.0662 |
| 55734 | ZFP64 | LZE24T | Human | Esophagus | ESCC | 2.60e-17 | 3.80e-01 | 0.0596 |
| 55734 | ZFP64 | LZE22D3 | Human | Esophagus | HGIN | 4.80e-02 | 3.27e-01 | 0.0653 |
| 55734 | ZFP64 | LZE21T | Human | Esophagus | ESCC | 1.59e-05 | 3.30e-01 | 0.0655 |
| 55734 | ZFP64 | P1T-E | Human | Esophagus | ESCC | 9.57e-14 | 4.28e-01 | 0.0875 |
| 55734 | ZFP64 | P2T-E | Human | Esophagus | ESCC | 1.02e-24 | 4.60e-01 | 0.1177 |
| 55734 | ZFP64 | P4T-E | Human | Esophagus | ESCC | 2.36e-51 | 1.08e+00 | 0.1323 |
| 55734 | ZFP64 | P5T-E | Human | Esophagus | ESCC | 6.87e-15 | 2.87e-01 | 0.1327 |
| 55734 | ZFP64 | P8T-E | Human | Esophagus | ESCC | 2.90e-24 | 3.41e-01 | 0.0889 |
| 55734 | ZFP64 | P9T-E | Human | Esophagus | ESCC | 1.70e-20 | 4.81e-01 | 0.1131 |
| 55734 | ZFP64 | P10T-E | Human | Esophagus | ESCC | 8.51e-48 | 7.70e-01 | 0.116 |
| 55734 | ZFP64 | P11T-E | Human | Esophagus | ESCC | 9.72e-20 | 5.38e-01 | 0.1426 |
| 55734 | ZFP64 | P12T-E | Human | Esophagus | ESCC | 1.18e-44 | 9.09e-01 | 0.1122 |
| 55734 | ZFP64 | P15T-E | Human | Esophagus | ESCC | 6.80e-38 | 7.84e-01 | 0.1149 |
| 55734 | ZFP64 | P16T-E | Human | Esophagus | ESCC | 9.87e-25 | 5.66e-01 | 0.1153 |
| Page: 1 2 3 4 5 |
| ∗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 |
Find out the enriched GO biological processes and KEGG pathways involved in transition from healthy to precancer to cancer |
| 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). |
| Page: 1 2 3 4 5 6 7 8 9 |
| GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
| Page: 1 |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
| Page: 1 |
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Cell-cell communication analysis |
Identification of potential cell-cell interactions between two cell types and their ligand-receptor pairs for different disease states |
| Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
| Page: 1 |
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Single-cell gene regulatory network inference analysis |
Find out the significant the regulons (TFs) and the target genes of each regulon across cell types for different disease states |
| ∗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. |
| Page: 1 2 3 4 |
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Somatic mutation of malignant transformation related genes |
Annotation of somatic variants for genes involved in malignant transformation |
| 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 |
| ZFP64 | SNV | Missense_Mutation | novel | c.831N>T | p.Lys277Asn | p.K277N | Q9NTW7 | protein_coding | tolerated(0.38) | benign(0.014) | TCGA-BR-6452-01 | Stomach | stomach adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| ZFP64 | SNV | Missense_Mutation | c.640G>A | p.Asp214Asn | p.D214N | Q9NPA5 | protein_coding | deleterious(0) | possibly_damaging(0.719) | TCGA-BR-8078-01 | Stomach | stomach adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
| ZFP64 | SNV | Missense_Mutation | c.1562G>T | p.Arg521Leu | p.R521L | Q9NTW7 | protein_coding | deleterious(0) | probably_damaging(0.992) | TCGA-BR-8297-01 | Stomach | stomach adenocarcinoma | Male | <65 | III/IV | Chemotherapy | etoposide | SD | |
| ZFP64 | SNV | Missense_Mutation | rs371226164 | c.1435N>T | p.Arg479Trp | p.R479W | Q9NTW7 | protein_coding | deleterious(0) | probably_damaging(0.988) | TCGA-CD-A4MJ-01 | Stomach | stomach adenocarcinoma | Male | <65 | I/II | Chemotherapy | cisplatin | CR |
| ZFP64 | SNV | Missense_Mutation | c.1699C>T | p.Pro567Ser | p.P567S | Q9NPA5 | protein_coding | tolerated(0.13) | benign(0.01) | TCGA-CG-4305-01 | Stomach | stomach adenocarcinoma | Male | >=65 | I/II | Chemotherapy | cisplatin | CR | |
| ZFP64 | SNV | Missense_Mutation | rs760668340 | c.1132N>T | p.Arg378Trp | p.R378W | Q9NTW7 | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-CG-4442-01 | Stomach | stomach adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
| ZFP64 | SNV | Missense_Mutation | c.1103N>G | p.Asp368Gly | p.D368G | Q9NPA5 | protein_coding | deleterious(0.01) | benign(0.149) | TCGA-CG-4442-01 | Stomach | stomach adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
| ZFP64 | SNV | Missense_Mutation | c.801G>C | p.Lys267Asn | p.K267N | Q9NPA5 | protein_coding | deleterious(0) | probably_damaging(0.946) | TCGA-CG-4443-01 | Stomach | stomach adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
| ZFP64 | SNV | Missense_Mutation | c.1013N>A | p.Cys338Tyr | p.C338Y | Q9NTW7 | protein_coding | tolerated(0.09) | probably_damaging(0.986) | TCGA-CG-5721-01 | Stomach | stomach adenocarcinoma | Male | <65 | III/IV | Unknown | Unknown | SD | |
| ZFP64 | SNV | Missense_Mutation | c.1910N>G | p.Asn637Ser | p.N637S | Q9NPA5 | protein_coding | tolerated(1) | benign(0) | TCGA-CG-5723-01 | Stomach | stomach adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
| Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 |
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Related drugs of malignant transformation related genes |
Identification of chemicals and drugs interact with genes involved in malignant transfromation |
| (DGIdb 4.0) |
| Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
| Page: 1 |