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Gene: ZNF185 |
Gene summary for ZNF185 |
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Gene information | Species | Human | Gene symbol | ZNF185 | Gene ID | 7739 |
Gene name | zinc finger protein 185 with LIM domain | |
Gene Alias | SCELL | |
Cytomap | Xq28 | |
Gene Type | protein-coding | GO ID | GO:0005575 | UniProtAcc | B3KPM4 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
7739 | ZNF185 | C04 | Human | Oral cavity | OSCC | 5.08e-07 | 3.98e-01 | 0.2633 |
7739 | ZNF185 | C21 | Human | Oral cavity | OSCC | 1.56e-39 | 1.22e+00 | 0.2678 |
7739 | ZNF185 | C30 | Human | Oral cavity | OSCC | 1.77e-16 | 7.75e-01 | 0.3055 |
7739 | ZNF185 | C43 | Human | Oral cavity | OSCC | 7.81e-17 | 4.10e-01 | 0.1704 |
7739 | ZNF185 | C46 | Human | Oral cavity | OSCC | 3.60e-12 | 2.77e-01 | 0.1673 |
7739 | ZNF185 | C51 | Human | Oral cavity | OSCC | 4.86e-14 | 5.45e-01 | 0.2674 |
7739 | ZNF185 | C57 | Human | Oral cavity | OSCC | 9.77e-28 | 9.34e-01 | 0.1679 |
7739 | ZNF185 | C08 | Human | Oral cavity | OSCC | 1.69e-02 | 1.52e-01 | 0.1919 |
7739 | ZNF185 | C09 | Human | Oral cavity | OSCC | 1.74e-04 | 1.17e-01 | 0.1431 |
7739 | ZNF185 | SYSMH1 | Human | Oral cavity | OSCC | 4.27e-07 | 2.51e-01 | 0.1127 |
7739 | ZNF185 | SYSMH3 | Human | Oral cavity | OSCC | 2.09e-11 | 2.77e-01 | 0.2442 |
7739 | ZNF185 | SYSMH4 | Human | Oral cavity | OSCC | 2.38e-02 | 1.38e-01 | 0.1226 |
7739 | ZNF185 | SYSMH5 | Human | Oral cavity | OSCC | 2.21e-07 | 1.95e-01 | 0.0647 |
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Tissue | Expression Dynamics | Abbreviation |
Oral Cavity | ![]() | EOLP: Erosive Oral lichen planus |
LP: leukoplakia | ||
NEOLP: Non-erosive oral lichen planus | ||
OSCC: Oral squamous cell carcinoma |
∗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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TF | Cell Type | Tissue | Disease Stage | Target Gene | RSS | Regulon Activity |
∗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 |
ZNF185 | SNV | Missense_Mutation | novel | c.1516N>G | p.Phe506Val | p.F506V | O15231 | protein_coding | tolerated(0.49) | benign(0.048) | TCGA-EO-A3B0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
ZNF185 | SNV | Missense_Mutation | novel | c.542N>T | p.Ala181Val | p.A181V | O15231 | protein_coding | deleterious(0.01) | probably_damaging(0.992) | TCGA-EO-A3KX-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
ZNF185 | SNV | Missense_Mutation | novel | c.1487N>G | p.Glu496Gly | p.E496G | O15231 | protein_coding | deleterious(0.02) | benign(0.163) | TCGA-2Y-A9GZ-01 | Liver | liver hepatocellular carcinoma | Female | >=65 | I/II | Targeted Molecular therapy | sorafenib | PD |
ZNF185 | SNV | Missense_Mutation | c.1582G>T | p.Gly528Cys | p.G528C | O15231 | protein_coding | tolerated(0.23) | benign(0.207) | TCGA-DD-AACC-01 | Liver | liver hepatocellular carcinoma | Male | <65 | I/II | Unknown | Unknown | PD | |
ZNF185 | SNV | Missense_Mutation | novel | c.700N>T | p.Pro234Ser | p.P234S | O15231 | protein_coding | tolerated(0.09) | benign(0.108) | TCGA-DD-AAE4-01 | Liver | liver hepatocellular carcinoma | Female | <65 | I/II | Unknown | Unknown | PD |
ZNF185 | SNV | Missense_Mutation | c.1286N>T | p.Ala429Val | p.A429V | O15231 | protein_coding | tolerated(0.18) | benign(0.003) | TCGA-EP-A2KC-01 | Liver | liver hepatocellular carcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
ZNF185 | SNV | Missense_Mutation | c.8N>G | p.Ile3Ser | p.I3S | O15231 | protein_coding | deleterious(0) | possibly_damaging(0.716) | TCGA-05-4382-01 | Lung | lung adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |
ZNF185 | SNV | Missense_Mutation | c.87N>A | p.Met29Ile | p.M29I | O15231 | protein_coding | deleterious(0) | possibly_damaging(0.492) | TCGA-44-5644-01 | Lung | lung adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
ZNF185 | SNV | Missense_Mutation | novel | c.486G>T | p.Glu162Asp | p.E162D | O15231 | protein_coding | tolerated(0.11) | benign(0.163) | TCGA-49-6761-01 | Lung | lung adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
ZNF185 | SNV | Missense_Mutation | c.1697N>C | p.Ser566Thr | p.S566T | O15231 | protein_coding | tolerated(0.23) | benign(0.229) | TCGA-86-A4D0-01 | Lung | lung adenocarcinoma | Male | <65 | I/II | Chemotherapy | etoposide | 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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