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Gene: ZNF579 |
Gene summary for ZNF579 |
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Gene information | Species | Human | Gene symbol | ZNF579 | Gene ID | 163033 |
Gene name | zinc finger protein 579 | |
Gene Alias | ZNF579 | |
Cytomap | 19q13.42 | |
Gene Type | protein-coding | GO ID | GO:0005575 | UniProtAcc | Q8NAF0 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
163033 | ZNF579 | HCC1_Meng | Human | Liver | HCC | 1.76e-35 | 8.76e-02 | 0.0246 |
163033 | ZNF579 | HCC2_Meng | Human | Liver | HCC | 5.47e-09 | 7.02e-02 | 0.0107 |
163033 | ZNF579 | HCC1 | Human | Liver | HCC | 1.03e-02 | 2.07e+00 | 0.5336 |
163033 | ZNF579 | S014 | Human | Liver | HCC | 1.89e-02 | 2.32e-01 | 0.2254 |
163033 | ZNF579 | S016 | Human | Liver | HCC | 3.91e-02 | 1.83e-01 | 0.2243 |
163033 | ZNF579 | S027 | Human | Liver | HCC | 2.00e-06 | 4.86e-01 | 0.2446 |
163033 | ZNF579 | S028 | Human | Liver | HCC | 1.16e-16 | 6.87e-01 | 0.2503 |
163033 | ZNF579 | S029 | Human | Liver | HCC | 3.16e-09 | 5.20e-01 | 0.2581 |
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Tissue | Expression Dynamics | Abbreviation |
Liver | ![]() | HCC: Hepatocellular carcinoma |
NAFLD: Non-alcoholic fatty liver disease |
∗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 |
ZNF579 | SNV | Missense_Mutation | rs192618440 | c.1588N>T | p.Ala530Ser | p.A530S | Q8NAF0 | protein_coding | tolerated(0.14) | possibly_damaging(0.718) | TCGA-MA-AA42-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Unknown | Unknown | SD |
ZNF579 | SNV | Missense_Mutation | novel | c.1354C>T | p.Arg452Cys | p.R452C | Q8NAF0 | protein_coding | deleterious(0) | probably_damaging(0.971) | TCGA-VS-A94X-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | PD |
ZNF579 | SNV | Missense_Mutation | c.929N>T | p.Ala310Val | p.A310V | Q8NAF0 | protein_coding | tolerated(0.1) | possibly_damaging(0.533) | TCGA-AD-6964-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | folfox | PD | |
ZNF579 | SNV | Missense_Mutation | c.1537T>A | p.Ser513Thr | p.S513T | Q8NAF0 | protein_coding | deleterious_low_confidence(0.03) | benign(0.255) | TCGA-AD-6965-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | oxaliplatin | PD | |
ZNF579 | SNV | Missense_Mutation | c.788N>T | p.Pro263Leu | p.P263L | Q8NAF0 | protein_coding | deleterious(0.02) | benign(0.031) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
ZNF579 | SNV | Missense_Mutation | c.1478N>T | p.Ala493Val | p.A493V | Q8NAF0 | protein_coding | tolerated_low_confidence(0.28) | benign(0.003) | TCGA-F4-6856-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Ancillary | leucovorin | CR | |
ZNF579 | SNV | Missense_Mutation | novel | c.962N>A | p.Gly321Asp | p.G321D | Q8NAF0 | protein_coding | deleterious(0.01) | possibly_damaging(0.878) | TCGA-BG-A222-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
ZNF579 | SNV | Missense_Mutation | novel | c.82N>T | p.Arg28Trp | p.R28W | Q8NAF0 | protein_coding | deleterious_low_confidence(0) | probably_damaging(0.948) | TCGA-D1-A175-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | paclitaxel | SD |
ZNF579 | SNV | Missense_Mutation | c.1502C>T | p.Pro501Leu | p.P501L | Q8NAF0 | protein_coding | tolerated_low_confidence(0.08) | benign(0.013) | TCGA-D1-A17A-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
ZNF579 | SNV | Missense_Mutation | novel | c.1666N>T | p.Gly556Trp | p.G556W | Q8NAF0 | protein_coding | deleterious_low_confidence(0) | probably_damaging(0.983) | TCGA-D1-A2G0-01 | 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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