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Gene: UGT2B11 |
Gene summary for UGT2B11 |
| Gene information | Species | Human | Gene symbol | UGT2B11 | Gene ID | 10720 |
| Gene name | UDP glucuronosyltransferase family 2 member B11 | |
| Gene Alias | UGT2B11 | |
| Cytomap | 4q13.2 | |
| Gene Type | protein-coding | GO ID | GO:0006063 | UniProtAcc | O75310 |
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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 |
| Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
| 10720 | UGT2B11 | HCC1_Meng | Human | Liver | HCC | 1.15e-60 | 3.47e-01 | 0.0246 |
| 10720 | UGT2B11 | HCC2 | Human | Liver | HCC | 6.22e-11 | 2.94e+00 | 0.5341 |
| 10720 | UGT2B11 | Pt14.a | Human | Liver | HCC | 2.21e-17 | 7.98e-01 | 0.0169 |
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| Tissue | Expression Dynamics | Abbreviation |
| Liver | ![]() | HCC: Hepatocellular carcinoma |
| NAFLD: Non-alcoholic fatty liver disease |
| ∗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 |
| Tissue | Disease Stage | Enriched GO biological Processes |
| Stomach | WIM | ![]() |
| Stomach | SIM | ![]() |
| Liver | NAFLD | ![]() |
| Liver | Cirrhotic | ![]() |
| Liver | HCC | ![]() |
| ∗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 |
| GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
| GO:00082022 | Liver | HCC | steroid metabolic process | 188/7958 | 319/18723 | 1.96e-09 | 5.63e-08 | 188 |
| GO:000941022 | Liver | HCC | response to xenobiotic stimulus | 248/7958 | 462/18723 | 6.47e-07 | 1.02e-05 | 248 |
| GO:00714662 | Liver | HCC | cellular response to xenobiotic stimulus | 93/7958 | 177/18723 | 4.35e-03 | 1.89e-02 | 93 |
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| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
| hsa012402 | Liver | HCC | Biosynthesis of cofactors | 103/4020 | 153/8465 | 4.67e-07 | 5.05e-06 | 2.81e-06 | 103 |
| hsa009832 | Liver | HCC | Drug metabolism - other enzymes | 54/4020 | 80/8465 | 2.25e-04 | 1.09e-03 | 6.08e-04 | 54 |
| hsa012403 | Liver | HCC | Biosynthesis of cofactors | 103/4020 | 153/8465 | 4.67e-07 | 5.05e-06 | 2.81e-06 | 103 |
| hsa009833 | Liver | HCC | Drug metabolism - other enzymes | 54/4020 | 80/8465 | 2.25e-04 | 1.09e-03 | 6.08e-04 | 54 |
| 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 |
| UGT2B11 | SNV | Missense_Mutation | novel | c.1537C>A | p.Leu513Met | p.L513M | O75310 | protein_coding | deleterious(0.04) | benign(0.363) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
| UGT2B11 | SNV | Missense_Mutation | c.205N>T | p.Ala69Ser | p.A69S | O75310 | protein_coding | tolerated(1) | benign(0) | TCGA-DS-A1OA-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Chemotherapy | carboplatin | PD | |
| UGT2B11 | SNV | Missense_Mutation | c.411N>A | p.Met137Ile | p.M137I | O75310 | protein_coding | tolerated(0.13) | benign(0.06) | TCGA-EK-A2PG-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Unknown | Unknown | SD | |
| UGT2B11 | SNV | Missense_Mutation | c.193N>A | p.Asp65Asn | p.D65N | O75310 | protein_coding | tolerated(0.25) | benign(0.013) | TCGA-IR-A3LL-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
| UGT2B11 | SNV | Missense_Mutation | c.880N>A | p.Glu294Lys | p.E294K | O75310 | protein_coding | tolerated(0.07) | benign(0.142) | TCGA-JW-A5VL-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | |
| UGT2B11 | SNV | Missense_Mutation | novel | c.1136N>A | p.Gly379Asp | p.G379D | O75310 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-VS-A94Z-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
| UGT2B11 | SNV | Missense_Mutation | rs367971286 | c.442N>A | p.Val148Ile | p.V148I | O75310 | protein_coding | tolerated(0.46) | benign(0.015) | TCGA-A6-6653-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
| UGT2B11 | SNV | Missense_Mutation | rs760333531 | c.1191T>G | p.Phe397Leu | p.F397L | O75310 | protein_coding | deleterious(0.04) | benign(0) | TCGA-AA-3866-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| UGT2B11 | SNV | Missense_Mutation | novel | c.1127N>T | p.Gly376Val | p.G376V | O75310 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AA-3950-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| UGT2B11 | SNV | Missense_Mutation | c.1469N>A | p.Ser490Tyr | p.S490Y | O75310 | protein_coding | deleterious(0) | probably_damaging(0.98) | 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 |
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 |
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