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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:001657416 | Thyroid | ATC | histone ubiquitination | 30/6293 | 47/18723 | 2.16e-05 | 1.92e-04 | 30 |
GO:005186513 | Thyroid | ATC | protein autoubiquitination | 41/6293 | 73/18723 | 6.14e-05 | 4.69e-04 | 41 |
GO:000651314 | Thyroid | ATC | protein monoubiquitination | 35/6293 | 67/18723 | 1.26e-03 | 6.58e-03 | 35 |
GO:0050673111 | Thyroid | ATC | epithelial cell proliferation | 174/6293 | 437/18723 | 3.49e-03 | 1.55e-02 | 174 |
GO:0050678110 | Thyroid | ATC | regulation of epithelial cell proliferation | 151/6293 | 381/18723 | 7.47e-03 | 2.92e-02 | 151 |
GO:00103905 | Thyroid | ATC | histone monoubiquitination | 16/6293 | 29/18723 | 1.37e-02 | 4.77e-02 | 16 |
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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.1526N>G | p.Ser509Cys | p.S509C | protein_coding | deleterious(0.02) | probably_damaging(0.995) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
UHRF1 | SNV | Missense_Mutation | novel | c.2181N>A | p.Phe727Leu | p.F727L | protein_coding | deleterious(0.02) | possibly_damaging(0.767) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
UHRF1 | SNV | Missense_Mutation | novel | c.2212A>G | p.Ile738Val | p.I738V | protein_coding | tolerated(0.42) | possibly_damaging(0.514) | TCGA-AN-A0XV-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
UHRF1 | SNV | Missense_Mutation | novel | c.2246C>T | p.Thr749Met | p.T749M | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-BH-A0DO-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
UHRF1 | SNV | Missense_Mutation | novel | c.829N>T | p.Asp277Tyr | p.D277Y | protein_coding | deleterious(0) | possibly_damaging(0.459) | TCGA-C8-A1HM-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | doxorubicin | CR | |
UHRF1 | SNV | Missense_Mutation | novel | c.901N>T | p.Pro301Ser | p.P301S | protein_coding | tolerated(0.3) | benign(0.02) | TCGA-E2-A9RU-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Hormone Therapy | arimidex | SD | |
UHRF1 | SNV | Missense_Mutation | novel | c.1456G>T | p.Gly486Trp | p.G486W | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-OL-A6VR-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
UHRF1 | insertion | Nonsense_Mutation | novel | c.1604_1605insATAATCTCGGCT | p.Ala535_Glu536insTer | p.A535_E536ins* | protein_coding | TCGA-A8-A06P-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unspecific | SD | ||||
UHRF1 | insertion | Frame_Shift_Ins | novel | c.761_762insCCTGCCTGGATTTCCAGCTTCTCTTGACAAAT | p.Glu255LeufsTer36 | p.E255Lfs*36 | protein_coding | TCGA-A8-A08R-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |||
UHRF1 | insertion | In_Frame_Ins | novel | c.1696_1697insCGCGCC | p.Asn566delinsThrArgHis | p.N566delinsTRH | protein_coding | TCGA-B6-A0IM-01 | Breast | breast invasive 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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