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Gene: UHRF1 |
Gene summary for UHRF1 |
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Gene information | Species | Human | Gene symbol | UHRF1 | Gene ID | 29128 |
Gene name | ubiquitin like with PHD and ring finger domains 1 | |
Gene Alias | ICBP90 | |
Cytomap | 19p13.3 | |
Gene Type | protein-coding | GO ID | GO:0000122 | UniProtAcc | Q96T88 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
29128 | UHRF1 | LZE7T | Human | Esophagus | ESCC | 2.07e-09 | 5.97e-01 | 0.0667 |
29128 | UHRF1 | LZE21T | Human | Esophagus | ESCC | 6.52e-03 | 1.97e-01 | 0.0655 |
29128 | UHRF1 | P1T-E | Human | Esophagus | ESCC | 7.11e-04 | 3.39e-01 | 0.0875 |
29128 | UHRF1 | P2T-E | Human | Esophagus | ESCC | 7.40e-11 | 3.98e-01 | 0.1177 |
29128 | UHRF1 | P4T-E | Human | Esophagus | ESCC | 9.47e-14 | 3.25e-01 | 0.1323 |
29128 | UHRF1 | P5T-E | Human | Esophagus | ESCC | 4.40e-09 | 1.94e-01 | 0.1327 |
29128 | UHRF1 | P8T-E | Human | Esophagus | ESCC | 4.40e-09 | 2.86e-01 | 0.0889 |
29128 | UHRF1 | P10T-E | Human | Esophagus | ESCC | 2.06e-08 | 2.68e-01 | 0.116 |
29128 | UHRF1 | P12T-E | Human | Esophagus | ESCC | 8.40e-04 | 1.08e-01 | 0.1122 |
29128 | UHRF1 | P15T-E | Human | Esophagus | ESCC | 3.38e-04 | 2.10e-01 | 0.1149 |
29128 | UHRF1 | P16T-E | Human | Esophagus | ESCC | 2.06e-08 | 2.35e-01 | 0.1153 |
29128 | UHRF1 | P17T-E | Human | Esophagus | ESCC | 4.79e-04 | 3.20e-01 | 0.1278 |
29128 | UHRF1 | P19T-E | Human | Esophagus | ESCC | 5.57e-05 | 3.96e-01 | 0.1662 |
29128 | UHRF1 | P20T-E | Human | Esophagus | ESCC | 1.17e-04 | 1.81e-01 | 0.1124 |
29128 | UHRF1 | P21T-E | Human | Esophagus | ESCC | 9.44e-07 | 2.49e-01 | 0.1617 |
29128 | UHRF1 | P22T-E | Human | Esophagus | ESCC | 1.88e-04 | 2.09e-01 | 0.1236 |
29128 | UHRF1 | P24T-E | Human | Esophagus | ESCC | 3.89e-12 | 3.74e-01 | 0.1287 |
29128 | UHRF1 | P26T-E | Human | Esophagus | ESCC | 1.97e-10 | 3.23e-01 | 0.1276 |
29128 | UHRF1 | P27T-E | Human | Esophagus | ESCC | 4.31e-06 | 2.60e-01 | 0.1055 |
29128 | UHRF1 | P28T-E | Human | Esophagus | ESCC | 2.56e-16 | 4.40e-01 | 0.1149 |
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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). |
Page: 1 2 3 4 5 6 7 8 9 |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:001657015 | Esophagus | ESCC | histone modification | 323/8552 | 463/18723 | 2.61e-26 | 7.88e-24 | 323 |
GO:00065136 | Esophagus | ESCC | protein monoubiquitination | 53/8552 | 67/18723 | 2.11e-08 | 4.03e-07 | 53 |
GO:001657414 | Esophagus | ESCC | histone ubiquitination | 40/8552 | 47/18723 | 2.40e-08 | 4.55e-07 | 40 |
GO:00103904 | Esophagus | ESCC | histone monoubiquitination | 25/8552 | 29/18723 | 7.24e-06 | 7.20e-05 | 25 |
GO:005067318 | Esophagus | ESCC | epithelial cell proliferation | 238/8552 | 437/18723 | 1.19e-04 | 8.20e-04 | 238 |
GO:005067817 | Esophagus | ESCC | regulation of epithelial cell proliferation | 206/8552 | 381/18723 | 5.51e-04 | 3.02e-03 | 206 |
GO:00518658 | Esophagus | ESCC | protein autoubiquitination | 47/8552 | 73/18723 | 9.72e-04 | 4.93e-03 | 47 |
GO:00165707 | Oral cavity | OSCC | histone modification | 270/7305 | 463/18723 | 1.59e-17 | 1.50e-15 | 270 |
GO:00165746 | Oral cavity | OSCC | histone ubiquitination | 38/7305 | 47/18723 | 5.22e-09 | 1.14e-07 | 38 |
GO:00065135 | Oral cavity | OSCC | protein monoubiquitination | 47/7305 | 67/18723 | 2.32e-07 | 3.68e-06 | 47 |
GO:00103903 | Oral cavity | OSCC | histone monoubiquitination | 24/7305 | 29/18723 | 1.74e-06 | 2.26e-05 | 24 |
GO:005067310 | Oral cavity | OSCC | epithelial cell proliferation | 212/7305 | 437/18723 | 2.82e-05 | 2.61e-04 | 212 |
GO:005067810 | Oral cavity | OSCC | regulation of epithelial cell proliferation | 180/7305 | 381/18723 | 5.88e-04 | 3.35e-03 | 180 |
GO:00518657 | Oral cavity | OSCC | protein autoubiquitination | 40/7305 | 73/18723 | 4.45e-03 | 1.79e-02 | 40 |
GO:001657014 | Oral cavity | LP | histone modification | 152/4623 | 463/18723 | 4.04e-05 | 5.90e-04 | 152 |
GO:000651313 | Oral cavity | LP | protein monoubiquitination | 29/4623 | 67/18723 | 6.51e-04 | 5.90e-03 | 29 |
GO:001657413 | Oral cavity | LP | histone ubiquitination | 22/4623 | 47/18723 | 8.02e-04 | 7.05e-03 | 22 |
GO:00103901 | Oral cavity | LP | histone monoubiquitination | 15/4623 | 29/18723 | 1.55e-03 | 1.20e-02 | 15 |
GO:005186512 | Oral cavity | LP | protein autoubiquitination | 29/4623 | 73/18723 | 3.20e-03 | 2.18e-02 | 29 |
GO:001657017 | Thyroid | ATC | histone modification | 243/6293 | 463/18723 | 2.23e-17 | 2.27e-15 | 243 |
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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 |
UHRF1 | SNV | Missense_Mutation | novel | c.1417C>A | p.Leu473Ile | p.L473I | protein_coding | tolerated(0.5) | benign(0.188) | TCGA-FI-A2F4-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
UHRF1 | SNV | Missense_Mutation | rs760435882 | c.2149C>T | p.Arg717Trp | p.R717W | protein_coding | deleterious(0) | benign(0) | TCGA-QS-A5YR-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | |
UHRF1 | insertion | Frame_Shift_Ins | novel | c.1954_1955insC | p.Arg654GlnfsTer56 | p.R654Qfs*56 | protein_coding | TCGA-EO-A3KX-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |||
UHRF1 | SNV | Missense_Mutation | novel | c.41T>C | p.Met14Thr | p.M14T | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-DD-AAW2-01 | Liver | liver hepatocellular carcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |
UHRF1 | SNV | Missense_Mutation | novel | c.1927G>A | p.Glu643Lys | p.E643K | protein_coding | tolerated(0.7) | benign(0.003) | TCGA-55-8510-01 | Lung | lung adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
UHRF1 | SNV | Missense_Mutation | novel | c.1292A>G | p.Tyr431Cys | p.Y431C | protein_coding | deleterious(0) | possibly_damaging(0.87) | TCGA-55-A490-01 | Lung | lung adenocarcinoma | Male | >=65 | I/II | Chemotherapy | carboplatin | SD | |
UHRF1 | SNV | Missense_Mutation | novel | c.2078A>G | p.Gln693Arg | p.Q693R | protein_coding | deleterious(0.05) | possibly_damaging(0.578) | TCGA-55-A490-01 | Lung | lung adenocarcinoma | Male | >=65 | I/II | Chemotherapy | carboplatin | SD | |
UHRF1 | SNV | Missense_Mutation | novel | c.521N>T | p.Arg174Leu | p.R174L | protein_coding | tolerated(0.09) | benign(0.015) | TCGA-86-8358-01 | Lung | lung adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
UHRF1 | SNV | Missense_Mutation | novel | c.379N>T | p.Ala127Ser | p.A127S | protein_coding | tolerated(0.79) | benign(0.007) | TCGA-18-3408-01 | Lung | lung squamous cell carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
UHRF1 | SNV | Missense_Mutation | novel | c.917N>T | p.Pro306Leu | p.P306L | protein_coding | tolerated(0.18) | benign(0.044) | TCGA-21-1079-01 | Lung | lung squamous cell carcinoma | Male | >=65 | III/IV | 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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