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Gene: ZNF586 |
Gene summary for ZNF586 |
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Gene information | Species | Human | Gene symbol | ZNF586 | Gene ID | 54807 |
Gene name | zinc finger protein 586 | |
Gene Alias | ZNF586 | |
Cytomap | 19q13.43 | |
Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | Q9NXT0 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
54807 | ZNF586 | HTA11_347_2000001011 | Human | Colorectum | AD | 1.55e-09 | 4.74e-01 | -0.1954 |
54807 | ZNF586 | HTA11_866_2000001011 | Human | Colorectum | AD | 2.91e-02 | 2.39e-01 | -0.1001 |
54807 | ZNF586 | HTA11_1391_2000001011 | Human | Colorectum | AD | 4.28e-03 | 3.91e-01 | -0.059 |
54807 | ZNF586 | HTA11_546_2000001011 | Human | Colorectum | AD | 5.30e-04 | 4.46e-01 | -0.0842 |
54807 | ZNF586 | HTA11_7696_3000711011 | Human | Colorectum | AD | 9.51e-09 | 4.82e-01 | 0.0674 |
54807 | ZNF586 | A015-C-203 | Human | Colorectum | FAP | 2.09e-10 | -2.89e-01 | -0.1294 |
54807 | ZNF586 | A002-C-201 | Human | Colorectum | FAP | 1.57e-03 | -2.27e-01 | 0.0324 |
54807 | ZNF586 | A002-C-203 | Human | Colorectum | FAP | 2.21e-05 | -2.81e-01 | 0.2786 |
54807 | ZNF586 | A001-C-108 | Human | Colorectum | FAP | 4.34e-05 | -1.51e-01 | -0.0272 |
54807 | ZNF586 | A002-C-205 | Human | Colorectum | FAP | 7.46e-06 | -1.97e-01 | -0.1236 |
54807 | ZNF586 | A015-C-006 | Human | Colorectum | FAP | 1.14e-03 | -1.40e-01 | -0.0994 |
54807 | ZNF586 | A015-C-106 | Human | Colorectum | FAP | 2.56e-03 | -1.07e-01 | -0.0511 |
54807 | ZNF586 | A002-C-114 | Human | Colorectum | FAP | 5.78e-05 | -3.87e-02 | -0.1561 |
54807 | ZNF586 | A015-C-104 | Human | Colorectum | FAP | 1.37e-09 | -1.40e-01 | -0.1899 |
54807 | ZNF586 | A001-C-014 | Human | Colorectum | FAP | 1.12e-06 | -2.64e-01 | 0.0135 |
54807 | ZNF586 | A002-C-016 | Human | Colorectum | FAP | 3.65e-13 | -2.51e-01 | 0.0521 |
54807 | ZNF586 | A015-C-002 | Human | Colorectum | FAP | 4.90e-05 | -3.82e-01 | -0.0763 |
54807 | ZNF586 | A001-C-203 | Human | Colorectum | FAP | 4.45e-04 | -1.20e-01 | -0.0481 |
54807 | ZNF586 | A002-C-116 | Human | Colorectum | FAP | 1.52e-15 | -1.63e-01 | -0.0452 |
54807 | ZNF586 | A014-C-008 | Human | Colorectum | FAP | 3.52e-03 | -1.38e-01 | -0.191 |
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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 |
ZNF586 | SNV | Missense_Mutation | novel | c.859G>C | p.Glu287Gln | p.E287Q | Q9NXT0 | protein_coding | deleterious(0.01) | probably_damaging(0.991) | TCGA-AC-A5XS-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | femara | SD |
ZNF586 | SNV | Missense_Mutation | novel | c.947G>A | p.Arg316Lys | p.R316K | Q9NXT0 | protein_coding | tolerated(0.31) | benign(0.241) | TCGA-C8-A26X-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | 5-fluorouracil | CR |
ZNF586 | SNV | Missense_Mutation | c.551N>C | p.Gly184Ala | p.G184A | Q9NXT0 | protein_coding | deleterious(0.01) | probably_damaging(0.985) | TCGA-D8-A1JA-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | adriamycin | PD | |
ZNF586 | SNV | Missense_Mutation | rs767980205 | c.409C>T | p.Leu137Phe | p.L137F | Q9NXT0 | protein_coding | tolerated(0.38) | probably_damaging(0.914) | TCGA-D8-A1JK-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
ZNF586 | insertion | Frame_Shift_Ins | novel | c.747dupT | p.Ile250TyrfsTer2 | p.I250Yfs*2 | Q9NXT0 | protein_coding | TCGA-AN-A03Y-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | ||
ZNF586 | insertion | Frame_Shift_Ins | novel | c.1061_1062insCGGAGGC | p.Ala355GlyfsTer4 | p.A355Gfs*4 | Q9NXT0 | protein_coding | TCGA-AO-A0JB-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | cyclophosphamide | SD | ||
ZNF586 | insertion | Frame_Shift_Ins | novel | c.1063_1064insAGGTGGGCGGATCA | p.Ala355GlufsTer15 | p.A355Efs*15 | Q9NXT0 | protein_coding | TCGA-AO-A0JB-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | cyclophosphamide | SD | ||
ZNF586 | SNV | Missense_Mutation | c.491N>T | p.Ser164Leu | p.S164L | Q9NXT0 | protein_coding | tolerated(0.24) | possibly_damaging(0.459) | TCGA-IR-A3LA-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
ZNF586 | SNV | Missense_Mutation | c.602C>T | p.Ser201Phe | p.S201F | Q9NXT0 | protein_coding | deleterious(0) | probably_damaging(0.979) | TCGA-JW-A5VL-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | |
ZNF586 | SNV | Missense_Mutation | c.52N>A | p.Glu18Lys | p.E18K | Q9NXT0 | protein_coding | deleterious(0) | benign(0.048) | TCGA-LP-A5U2-01 | Cervix | cervical & endocervical cancer | Female | <65 | III/IV | 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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