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Gene: ZNF224 |
Gene summary for ZNF224 |
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Gene information | Species | Human | Gene symbol | ZNF224 | Gene ID | 7767 |
Gene name | zinc finger protein 224 | |
Gene Alias | BMZF-2 | |
Cytomap | 19q13.31 | |
Gene Type | protein-coding | GO ID | GO:0000122 | UniProtAcc | Q9NZL3 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
7767 | ZNF224 | P65T-E | Human | Esophagus | ESCC | 1.46e-09 | 1.66e-01 | 0.0978 |
7767 | ZNF224 | P74T-E | Human | Esophagus | ESCC | 8.12e-10 | 2.06e-01 | 0.1479 |
7767 | ZNF224 | P75T-E | Human | Esophagus | ESCC | 1.00e-24 | 3.70e-01 | 0.1125 |
7767 | ZNF224 | P76T-E | Human | Esophagus | ESCC | 2.02e-06 | 1.33e-01 | 0.1207 |
7767 | ZNF224 | P79T-E | Human | Esophagus | ESCC | 3.52e-19 | 2.85e-01 | 0.1154 |
7767 | ZNF224 | P82T-E | Human | Esophagus | ESCC | 3.86e-11 | 5.09e-01 | 0.1072 |
7767 | ZNF224 | P83T-E | Human | Esophagus | ESCC | 2.43e-08 | 2.29e-01 | 0.1738 |
7767 | ZNF224 | P84T-E | Human | Esophagus | ESCC | 1.31e-09 | 3.10e-01 | 0.0933 |
7767 | ZNF224 | P89T-E | Human | Esophagus | ESCC | 2.64e-08 | 3.46e-01 | 0.1752 |
7767 | ZNF224 | P91T-E | Human | Esophagus | ESCC | 1.74e-03 | 3.40e-01 | 0.1828 |
7767 | ZNF224 | P107T-E | Human | Esophagus | ESCC | 7.54e-10 | 1.88e-01 | 0.171 |
7767 | ZNF224 | P127T-E | Human | Esophagus | ESCC | 9.06e-09 | 2.09e-01 | 0.0826 |
7767 | ZNF224 | P128T-E | Human | Esophagus | ESCC | 2.71e-13 | 3.40e-01 | 0.1241 |
7767 | ZNF224 | P130T-E | Human | Esophagus | ESCC | 1.76e-12 | 2.08e-01 | 0.1676 |
7767 | ZNF224 | male-WTA | Human | Thyroid | PTC | 1.75e-05 | 6.98e-02 | 0.1037 |
7767 | ZNF224 | PTC01 | Human | Thyroid | PTC | 4.26e-17 | 1.86e-01 | 0.1899 |
7767 | ZNF224 | PTC03 | Human | Thyroid | PTC | 5.89e-09 | 2.84e-01 | 0.1784 |
7767 | ZNF224 | PTC04 | Human | Thyroid | PTC | 2.25e-05 | 1.97e-01 | 0.1927 |
7767 | ZNF224 | PTC05 | Human | Thyroid | PTC | 6.51e-14 | 4.80e-01 | 0.2065 |
7767 | ZNF224 | PTC06 | Human | Thyroid | PTC | 9.81e-22 | 4.01e-01 | 0.2057 |
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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 |
ZNF224 | SNV | Missense_Mutation | rs3746323 | c.1516N>G | p.His506Asp | p.H506D | Q9NZL3 | protein_coding | deleterious(0) | probably_damaging(0.969) | TCGA-AN-A0XW-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
ZNF224 | SNV | Missense_Mutation | c.905G>C | p.Arg302Thr | p.R302T | Q9NZL3 | protein_coding | tolerated(0.41) | benign(0.215) | TCGA-B6-A0RE-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
ZNF224 | SNV | Missense_Mutation | c.1826C>T | p.Ser609Leu | p.S609L | Q9NZL3 | protein_coding | tolerated(0.12) | probably_damaging(0.987) | TCGA-BH-A202-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | CR | |
ZNF224 | insertion | In_Frame_Ins | novel | c.1084_1085insGCTCCAACTCCTGGGTTCTTGCCATTCTCCTGCCTCAGCCTCCCGAGT | p.His362delinsArgSerAsnSerTrpValLeuAlaIleLeuLeuProGlnProProGluTyr | p.H362delinsRSNSWVLAILLPQPPEY | Q9NZL3 | protein_coding | TCGA-AN-A03X-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | ||
ZNF224 | SNV | Missense_Mutation | c.1200N>G | p.Phe400Leu | p.F400L | Q9NZL3 | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-DS-A1OC-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | gemcitabine | SD | |
ZNF224 | SNV | Missense_Mutation | c.399N>C | p.Gln133His | p.Q133H | Q9NZL3 | protein_coding | tolerated(0.24) | benign(0.127) | TCGA-IR-A3LK-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Chemotherapy | cisplatin | PD | |
ZNF224 | SNV | Missense_Mutation | novel | c.240N>A | p.Asp80Glu | p.D80E | Q9NZL3 | protein_coding | tolerated(0.83) | benign(0.029) | TCGA-VS-A8EI-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
ZNF224 | SNV | Missense_Mutation | rs763079230 | c.976N>T | p.Arg326Cys | p.R326C | Q9NZL3 | protein_coding | tolerated(0.1) | probably_damaging(0.93) | TCGA-AA-3510-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
ZNF224 | SNV | Missense_Mutation | c.1684N>T | p.His562Tyr | p.H562Y | Q9NZL3 | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-AA-3715-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |
ZNF224 | SNV | Missense_Mutation | rs3208192 | c.1613G>A | p.Arg538Lys | p.R538K | Q9NZL3 | protein_coding | tolerated(1) | benign(0.03) | TCGA-AA-A00N-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
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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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