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Gene: B4GAT1 |
Gene summary for B4GAT1 |
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Gene information | Species | Human | Gene symbol | B4GAT1 | Gene ID | 11041 |
Gene name | beta-1,4-glucuronyltransferase 1 | |
Gene Alias | B3GN-T1 | |
Cytomap | 11q13.2 | |
Gene Type | protein-coding | GO ID | GO:0006022 | UniProtAcc | A0A024R5F9 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
11041 | B4GAT1 | P2T-E | Human | Esophagus | ESCC | 1.49e-18 | 3.81e-01 | 0.1177 |
11041 | B4GAT1 | P4T-E | Human | Esophagus | ESCC | 2.68e-16 | 3.36e-01 | 0.1323 |
11041 | B4GAT1 | P5T-E | Human | Esophagus | ESCC | 5.35e-04 | 1.05e-01 | 0.1327 |
11041 | B4GAT1 | P8T-E | Human | Esophagus | ESCC | 2.04e-05 | 1.36e-01 | 0.0889 |
11041 | B4GAT1 | P9T-E | Human | Esophagus | ESCC | 2.15e-04 | 1.54e-01 | 0.1131 |
11041 | B4GAT1 | P10T-E | Human | Esophagus | ESCC | 4.91e-16 | 2.69e-01 | 0.116 |
11041 | B4GAT1 | P11T-E | Human | Esophagus | ESCC | 1.47e-12 | 4.69e-01 | 0.1426 |
11041 | B4GAT1 | P12T-E | Human | Esophagus | ESCC | 1.01e-18 | 3.19e-01 | 0.1122 |
11041 | B4GAT1 | P15T-E | Human | Esophagus | ESCC | 2.64e-09 | 2.41e-01 | 0.1149 |
11041 | B4GAT1 | P16T-E | Human | Esophagus | ESCC | 7.95e-29 | 5.22e-01 | 0.1153 |
11041 | B4GAT1 | P19T-E | Human | Esophagus | ESCC | 2.66e-07 | 4.97e-01 | 0.1662 |
11041 | B4GAT1 | P21T-E | Human | Esophagus | ESCC | 2.45e-04 | 1.76e-01 | 0.1617 |
11041 | B4GAT1 | P22T-E | Human | Esophagus | ESCC | 7.87e-09 | 1.23e-01 | 0.1236 |
11041 | B4GAT1 | P24T-E | Human | Esophagus | ESCC | 2.54e-03 | 9.44e-02 | 0.1287 |
11041 | B4GAT1 | P26T-E | Human | Esophagus | ESCC | 5.55e-07 | 1.04e-01 | 0.1276 |
11041 | B4GAT1 | P28T-E | Human | Esophagus | ESCC | 1.24e-03 | 8.65e-02 | 0.1149 |
11041 | B4GAT1 | P30T-E | Human | Esophagus | ESCC | 3.09e-02 | 1.67e-01 | 0.137 |
11041 | B4GAT1 | P31T-E | Human | Esophagus | ESCC | 9.99e-06 | 5.42e-02 | 0.1251 |
11041 | B4GAT1 | P32T-E | Human | Esophagus | ESCC | 3.79e-10 | 2.72e-01 | 0.1666 |
11041 | B4GAT1 | P36T-E | Human | Esophagus | ESCC | 2.17e-03 | 1.57e-01 | 0.1187 |
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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). |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:00091002 | Esophagus | ESCC | glycoprotein metabolic process | 226/8552 | 387/18723 | 2.64e-07 | 3.94e-06 | 226 |
GO:00067906 | Esophagus | ESCC | sulfur compound metabolic process | 201/8552 | 339/18723 | 2.64e-07 | 3.94e-06 | 201 |
GO:00442725 | Esophagus | ESCC | sulfur compound biosynthetic process | 96/8552 | 148/18723 | 1.86e-06 | 2.16e-05 | 96 |
GO:00700854 | Esophagus | ESCC | glycosylation | 144/8552 | 240/18723 | 5.12e-06 | 5.38e-05 | 144 |
GO:00064865 | Esophagus | ESCC | protein glycosylation | 135/8552 | 226/18723 | 1.36e-05 | 1.24e-04 | 135 |
GO:00434135 | Esophagus | ESCC | macromolecule glycosylation | 135/8552 | 226/18723 | 1.36e-05 | 1.24e-04 | 135 |
GO:00091012 | Esophagus | ESCC | glycoprotein biosynthetic process | 181/8552 | 317/18723 | 2.54e-05 | 2.15e-04 | 181 |
GO:00064931 | Esophagus | ESCC | protein O-linked glycosylation | 51/8552 | 86/18723 | 7.54e-03 | 2.70e-02 | 51 |
GO:0006024 | Esophagus | ESCC | glycosaminoglycan biosynthetic process | 45/8552 | 75/18723 | 8.75e-03 | 3.08e-02 | 45 |
GO:0006023 | Esophagus | ESCC | aminoglycan biosynthetic process | 47/8552 | 79/18723 | 9.29e-03 | 3.23e-02 | 47 |
GO:000679021 | Liver | HCC | sulfur compound metabolic process | 212/7958 | 339/18723 | 5.60e-14 | 3.39e-12 | 212 |
GO:00442722 | Liver | HCC | sulfur compound biosynthetic process | 95/7958 | 148/18723 | 7.89e-08 | 1.58e-06 | 95 |
GO:00064862 | Liver | HCC | protein glycosylation | 122/7958 | 226/18723 | 3.11e-04 | 2.21e-03 | 122 |
GO:00434132 | Liver | HCC | macromolecule glycosylation | 122/7958 | 226/18723 | 3.11e-04 | 2.21e-03 | 122 |
GO:00700852 | Liver | HCC | glycosylation | 128/7958 | 240/18723 | 4.35e-04 | 2.92e-03 | 128 |
GO:0009100 | Liver | HCC | glycoprotein metabolic process | 193/7958 | 387/18723 | 1.89e-03 | 9.62e-03 | 193 |
GO:00442724 | Oral cavity | OSCC | sulfur compound biosynthetic process | 82/7305 | 148/18723 | 3.71e-05 | 3.31e-04 | 82 |
GO:00067905 | Oral cavity | OSCC | sulfur compound metabolic process | 168/7305 | 339/18723 | 4.50e-05 | 3.84e-04 | 168 |
GO:00091001 | Oral cavity | OSCC | glycoprotein metabolic process | 185/7305 | 387/18723 | 2.37e-04 | 1.54e-03 | 185 |
GO:00091011 | Oral cavity | OSCC | glycoprotein biosynthetic process | 151/7305 | 317/18723 | 1.01e-03 | 5.26e-03 | 151 |
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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 |
B4GAT1 | SNV | Missense_Mutation | rs756392214 | c.144C>A | p.Phe48Leu | p.F48L | O43505 | protein_coding | tolerated(1) | benign(0) | TCGA-B5-A1MR-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
B4GAT1 | SNV | Missense_Mutation | novel | c.545N>A | p.Cys182Tyr | p.C182Y | O43505 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-B5-A1MX-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Hormone Therapy | megace | SD |
B4GAT1 | SNV | Missense_Mutation | c.781N>A | p.Glu261Lys | p.E261K | O43505 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-BS-A0UV-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | |
B4GAT1 | SNV | Missense_Mutation | novel | c.484C>T | p.Arg162Cys | p.R162C | O43505 | protein_coding | tolerated(0.06) | possibly_damaging(0.684) | TCGA-E6-A2P8-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | PD |
B4GAT1 | SNV | Missense_Mutation | novel | c.428G>A | p.Ser143Asn | p.S143N | O43505 | protein_coding | tolerated(0.15) | benign(0.158) | TCGA-EO-A22U-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
B4GAT1 | SNV | Missense_Mutation | novel | c.538C>T | p.Arg180Trp | p.R180W | O43505 | protein_coding | deleterious(0.01) | benign(0.379) | TCGA-EO-A3KX-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
B4GAT1 | deletion | Frame_Shift_Del | novel | c.696delN | p.Ser233AlafsTer38 | p.S233Afs*38 | O43505 | protein_coding | TCGA-EY-A2OP-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | ||
B4GAT1 | SNV | Missense_Mutation | novel | c.827N>A | p.Val276Glu | p.V276E | O43505 | protein_coding | deleterious(0) | benign(0.044) | TCGA-DD-AAD5-01 | Liver | liver hepatocellular carcinoma | Male | <65 | I/II | Unknown | Unknown | PD |
B4GAT1 | SNV | Missense_Mutation | c.514N>A | p.Glu172Lys | p.E172K | O43505 | protein_coding | tolerated(0.41) | benign(0.044) | TCGA-44-6146-01 | Lung | lung adenocarcinoma | Male | <65 | I/II | Chemotherapy | alimta | PD | |
B4GAT1 | SNV | Missense_Mutation | novel | c.104G>T | p.Gly35Val | p.G35V | O43505 | protein_coding | tolerated(0.11) | possibly_damaging(0.636) | TCGA-86-8674-01 | Lung | lung adenocarcinoma | Male | <65 | I/II | Chemotherapy | vinblastine | 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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