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Gene: UFM1 |
Gene summary for UFM1 |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | UFM1 | Gene ID | 51569 |
| Gene name | ubiquitin fold modifier 1 | |
| Gene Alias | BM-002 | |
| Cytomap | 13q13.3 | |
| Gene Type | protein-coding | GO ID | GO:0006464 | UniProtAcc | P61960 |
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Malignant transformation analysis |
| Identification of the aberrant gene expression in precancerous and cancerous lesions by comparing the gene expression of stem-like cells in diseased tissues with normal stem cells |
| Malignant transformation involving gene list. |
| Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
| 51569 | UFM1 | LZE8T | Human | Esophagus | ESCC | 7.00e-05 | 4.21e-01 | 0.067 |
| 51569 | UFM1 | LZE20T | Human | Esophagus | ESCC | 5.27e-04 | 2.88e-02 | 0.0662 |
| 51569 | UFM1 | LZE22D1 | Human | Esophagus | HGIN | 6.56e-05 | 3.22e-02 | 0.0595 |
| 51569 | UFM1 | LZE22T | Human | Esophagus | ESCC | 6.95e-03 | 7.22e-01 | 0.068 |
| 51569 | UFM1 | LZE24T | Human | Esophagus | ESCC | 2.37e-18 | 6.07e-01 | 0.0596 |
| 51569 | UFM1 | LZE22D3 | Human | Esophagus | HGIN | 8.29e-04 | 1.53e-01 | 0.0653 |
| 51569 | UFM1 | LZE6T | Human | Esophagus | ESCC | 5.27e-09 | 6.30e-02 | 0.0845 |
| 51569 | UFM1 | P1T-E | Human | Esophagus | ESCC | 4.90e-06 | 6.17e-01 | 0.0875 |
| 51569 | UFM1 | P2T-E | Human | Esophagus | ESCC | 6.01e-27 | 5.87e-01 | 0.1177 |
| 51569 | UFM1 | P4T-E | Human | Esophagus | ESCC | 7.79e-22 | 6.61e-01 | 0.1323 |
| 51569 | UFM1 | P5T-E | Human | Esophagus | ESCC | 6.80e-28 | 6.28e-01 | 0.1327 |
| 51569 | UFM1 | P8T-E | Human | Esophagus | ESCC | 5.78e-32 | 8.93e-01 | 0.0889 |
| 51569 | UFM1 | P9T-E | Human | Esophagus | ESCC | 3.89e-29 | 7.50e-01 | 0.1131 |
| 51569 | UFM1 | P10T-E | Human | Esophagus | ESCC | 5.34e-39 | 8.66e-01 | 0.116 |
| 51569 | UFM1 | P11T-E | Human | Esophagus | ESCC | 1.64e-16 | 7.62e-01 | 0.1426 |
| 51569 | UFM1 | P12T-E | Human | Esophagus | ESCC | 1.31e-16 | 2.01e-01 | 0.1122 |
| 51569 | UFM1 | P15T-E | Human | Esophagus | ESCC | 1.56e-26 | 6.32e-01 | 0.1149 |
| 51569 | UFM1 | P16T-E | Human | Esophagus | ESCC | 1.08e-15 | 2.70e-01 | 0.1153 |
| 51569 | UFM1 | P17T-E | Human | Esophagus | ESCC | 8.90e-14 | 9.68e-01 | 0.1278 |
| 51569 | UFM1 | P19T-E | Human | Esophagus | ESCC | 6.53e-08 | 1.14e+00 | 0.1662 |
| Page: 1 2 3 4 5 6 7 8 9 |
| Transcriptomic changes along malignancy continuum. |
| Tissue | Expression Dynamics | Abbreviation |
| Colorectum (GSE201348) |  | FAP: Familial adenomatous polyposis |
| CRC: Colorectal cancer | ||
| Colorectum (HTA11) |  | AD: Adenomas |
| SER: Sessile serrated lesions | ||
| MSI-H: Microsatellite-high colorectal cancer | ||
| MSS: Microsatellite stable colorectal cancer | ||
| Endometrium |  | AEH: Atypical endometrial hyperplasia |
| EEC: Endometrioid Cancer | ||
| Esophagus |  | ESCC: Esophageal squamous cell carcinoma |
| HGIN: High-grade intraepithelial neoplasias | ||
| LGIN: Low-grade intraepithelial neoplasias | ||
| Liver |  | HCC: Hepatocellular carcinoma |
| NAFLD: Non-alcoholic fatty liver disease | ||
| Oral Cavity |  | EOLP: Erosive Oral lichen planus |
| LP: leukoplakia | ||
| NEOLP: Non-erosive oral lichen planus | ||
| OSCC: Oral squamous cell carcinoma | ||
| Skin |  | AK: Actinic keratosis |
| cSCC: Cutaneous squamous cell carcinoma | ||
| SCCIS:squamous cell carcinoma in situ | ||
| Thyroid |  | ATC: Anaplastic thyroid cancer |
| HT: Hashimoto's thyroiditis | ||
| PTC: Papillary thyroid cancer |
| ∗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 |
| Find out the enriched GO biological processes and KEGG pathways involved in transition from healthy to precancer to cancer |
| Figure of enriched GO biological processes. |
| 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 |
| Enriched GO biological processes. |
| GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
| GO:00725942 | Colorectum | MSS | establishment of protein localization to organelle | 139/3467 | 422/18723 | 5.75e-13 | 1.12e-10 | 139 |
| GO:00069132 | Colorectum | MSS | nucleocytoplasmic transport | 99/3467 | 301/18723 | 1.35e-09 | 1.03e-07 | 99 |
| GO:00511692 | Colorectum | MSS | nuclear transport | 99/3467 | 301/18723 | 1.35e-09 | 1.03e-07 | 99 |
| GO:19001802 | Colorectum | MSS | regulation of protein localization to nucleus | 54/3467 | 136/18723 | 6.20e-09 | 3.95e-07 | 54 |
| GO:00713832 | Colorectum | MSS | cellular response to steroid hormone stimulus | 72/3467 | 204/18723 | 8.87e-09 | 5.43e-07 | 72 |
| GO:00224112 | Colorectum | MSS | cellular component disassembly | 130/3467 | 443/18723 | 1.44e-08 | 8.46e-07 | 130 |
| GO:00162362 | Colorectum | MSS | macroautophagy | 93/3467 | 291/18723 | 2.08e-08 | 1.17e-06 | 93 |
| GO:00345042 | Colorectum | MSS | protein localization to nucleus | 92/3467 | 290/18723 | 3.66e-08 | 1.98e-06 | 92 |
| GO:00331572 | Colorectum | MSS | regulation of intracellular protein transport | 76/3467 | 229/18723 | 7.03e-08 | 3.56e-06 | 76 |
| GO:00323862 | Colorectum | MSS | regulation of intracellular transport | 102/3467 | 337/18723 | 9.73e-08 | 4.71e-06 | 102 |
| GO:00434012 | Colorectum | MSS | steroid hormone mediated signaling pathway | 51/3467 | 136/18723 | 1.43e-07 | 6.67e-06 | 51 |
| GO:00305222 | Colorectum | MSS | intracellular receptor signaling pathway | 84/3467 | 265/18723 | 1.47e-07 | 6.79e-06 | 84 |
| GO:00485452 | Colorectum | MSS | response to steroid hormone | 101/3467 | 339/18723 | 2.60e-07 | 1.10e-05 | 101 |
| GO:00349762 | Colorectum | MSS | response to endoplasmic reticulum stress | 81/3467 | 256/18723 | 2.65e-07 | 1.10e-05 | 81 |
| GO:00305182 | Colorectum | MSS | intracellular steroid hormone receptor signaling pathway | 44/3467 | 116/18723 | 6.95e-07 | 2.49e-05 | 44 |
| GO:00097552 | Colorectum | MSS | hormone-mediated signaling pathway | 63/3467 | 190/18723 | 9.26e-07 | 3.23e-05 | 63 |
| GO:00468222 | Colorectum | MSS | regulation of nucleocytoplasmic transport | 40/3467 | 106/18723 | 2.55e-06 | 7.75e-05 | 40 |
| GO:19030082 | Colorectum | MSS | organelle disassembly | 42/3467 | 114/18723 | 2.98e-06 | 8.91e-05 | 42 |
| GO:00170382 | Colorectum | MSS | protein import | 65/3467 | 206/18723 | 4.28e-06 | 1.22e-04 | 65 |
| GO:00511702 | Colorectum | MSS | import into nucleus | 52/3467 | 159/18723 | 1.23e-05 | 2.87e-04 | 52 |
| Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 |
| Enriched KEGG pathways. |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
| Page: 1 |
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Cell-cell communication analysis |
| Identification of potential cell-cell interactions between two cell types and their ligand-receptor pairs for different disease states |
| Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
| Page: 1 |
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Single-cell gene regulatory network inference analysis |
| Find out the significant the regulons (TFs) and the target genes of each regulon across cell types for different disease states |
| 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. |
| Page: 1 |
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Somatic mutation of malignant transformation related genes |
| Annotation of somatic variants for genes involved in malignant transformation |
| 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 |
| UFM1 | SNV | Missense_Mutation | c.68N>T | p.Ala23Val | p.A23V | P61960 | protein_coding | deleterious_low_confidence(0.03) | possibly_damaging(0.691) | TCGA-AA-A01P-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | PD | |
| UFM1 | SNV | Missense_Mutation | novel | c.253N>G | p.Phe85Val | p.F85V | P61960 | protein_coding | deleterious_low_confidence(0) | possibly_damaging(0.804) | TCGA-AJ-A3EK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | CR |
| UFM1 | SNV | Missense_Mutation | novel | c.278N>T | p.Arg93Leu | p.R93L | P61960 | protein_coding | deleterious_low_confidence(0.02) | possibly_damaging(0.875) | TCGA-EY-A1GK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| UFM1 | SNV | Missense_Mutation | rs368429371 | c.277N>T | p.Arg93Trp | p.R93W | P61960 | protein_coding | deleterious_low_confidence(0.01) | probably_damaging(0.988) | TCGA-FI-A2D5-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatinum | PD |
| UFM1 | SNV | Missense_Mutation | novel | c.191N>A | p.Thr64Lys | p.T64K | P61960 | protein_coding | deleterious_low_confidence(0) | probably_damaging(1) | TCGA-ZQ-A9CR-01 | Stomach | stomach adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
| Page: 1 |
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Related drugs of malignant transformation related genes |
| Identification of chemicals and drugs interact with genes involved in malignant transfromation |
| (DGIdb 4.0) |
| Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
| Page: 1 |
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