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Gene: B3GALT6 |
Gene summary for B3GALT6 |
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Gene information | Species | Human | Gene symbol | B3GALT6 | Gene ID | 126792 |
Gene name | beta-1,3-galactosyltransferase 6 | |
Gene Alias | ALGAZ | |
Cytomap | 1p36.33 | |
Gene Type | protein-coding | GO ID | GO:0006022 | UniProtAcc | Q96L58 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
126792 | B3GALT6 | P2T-E | Human | Esophagus | ESCC | 5.19e-08 | 1.63e-01 | 0.1177 |
126792 | B3GALT6 | P4T-E | Human | Esophagus | ESCC | 3.17e-23 | 5.77e-01 | 0.1323 |
126792 | B3GALT6 | P5T-E | Human | Esophagus | ESCC | 1.15e-24 | 2.65e-01 | 0.1327 |
126792 | B3GALT6 | P8T-E | Human | Esophagus | ESCC | 4.44e-06 | 8.65e-02 | 0.0889 |
126792 | B3GALT6 | P10T-E | Human | Esophagus | ESCC | 1.37e-10 | 1.11e-01 | 0.116 |
126792 | B3GALT6 | P11T-E | Human | Esophagus | ESCC | 1.35e-02 | 1.25e-01 | 0.1426 |
126792 | B3GALT6 | P12T-E | Human | Esophagus | ESCC | 9.66e-08 | 7.71e-02 | 0.1122 |
126792 | B3GALT6 | P15T-E | Human | Esophagus | ESCC | 5.45e-05 | 1.03e-01 | 0.1149 |
126792 | B3GALT6 | P16T-E | Human | Esophagus | ESCC | 6.57e-07 | 9.17e-02 | 0.1153 |
126792 | B3GALT6 | P17T-E | Human | Esophagus | ESCC | 1.13e-02 | 1.36e-01 | 0.1278 |
126792 | B3GALT6 | P20T-E | Human | Esophagus | ESCC | 1.35e-03 | 6.38e-02 | 0.1124 |
126792 | B3GALT6 | P21T-E | Human | Esophagus | ESCC | 1.49e-18 | 2.77e-01 | 0.1617 |
126792 | B3GALT6 | P22T-E | Human | Esophagus | ESCC | 1.22e-05 | 1.67e-02 | 0.1236 |
126792 | B3GALT6 | P23T-E | Human | Esophagus | ESCC | 1.02e-06 | 1.84e-01 | 0.108 |
126792 | B3GALT6 | P24T-E | Human | Esophagus | ESCC | 7.10e-03 | 4.42e-02 | 0.1287 |
126792 | B3GALT6 | P26T-E | Human | Esophagus | ESCC | 1.04e-15 | 1.23e-01 | 0.1276 |
126792 | B3GALT6 | P27T-E | Human | Esophagus | ESCC | 5.63e-07 | 4.20e-02 | 0.1055 |
126792 | B3GALT6 | P28T-E | Human | Esophagus | ESCC | 5.67e-10 | 1.10e-01 | 0.1149 |
126792 | B3GALT6 | P31T-E | Human | Esophagus | ESCC | 2.17e-25 | 2.66e-01 | 0.1251 |
126792 | B3GALT6 | P32T-E | Human | Esophagus | ESCC | 5.97e-06 | 5.76e-02 | 0.1666 |
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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 |
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). |
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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:0006029 | Esophagus | ESCC | proteoglycan metabolic process | 48/8552 | 79/18723 | 4.93e-03 | 1.89e-02 | 48 |
GO:0030166 | Esophagus | ESCC | proteoglycan biosynthetic process | 35/8552 | 56/18723 | 8.30e-03 | 2.94e-02 | 35 |
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:0030201 | Esophagus | ESCC | heparan sulfate proteoglycan metabolic process | 21/8552 | 31/18723 | 1.10e-02 | 3.70e-02 | 21 |
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 |
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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 |
B3GALT6 | SNV | Missense_Mutation | c.946N>A | p.Ala316Thr | p.A316T | Q96L58 | protein_coding | deleterious(0.05) | possibly_damaging(0.484) | TCGA-NH-A5IV-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
B3GALT6 | SNV | Missense_Mutation | c.371N>G | p.Ala124Gly | p.A124G | Q96L58 | protein_coding | tolerated(0.37) | benign(0.01) | TCGA-55-8207-01 | Lung | lung adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
B3GALT6 | SNV | Missense_Mutation | novel | c.349G>T | p.Gly117Trp | p.G117W | Q96L58 | protein_coding | deleterious(0.01) | probably_damaging(0.998) | TCGA-CX-7082-01 | Oral cavity | head & neck squamous cell carcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
B3GALT6 | SNV | Missense_Mutation | rs749438460 | c.371C>T | p.Ala124Val | p.A124V | Q96L58 | protein_coding | tolerated(0.23) | benign(0.227) | TCGA-F7-A624-01 | Oral cavity | head & neck squamous cell carcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
B3GALT6 | SNV | Missense_Mutation | c.484N>T | p.Arg162Trp | p.R162W | Q96L58 | protein_coding | deleterious(0) | probably_damaging(0.995) | TCGA-BR-7851-01 | Stomach | stomach adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
B3GALT6 | SNV | Missense_Mutation | c.626N>G | p.Tyr209Cys | p.Y209C | Q96L58 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-BR-8591-01 | Stomach | stomach adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | SD | |
B3GALT6 | SNV | Missense_Mutation | c.529N>A | p.Arg177Ser | p.R177S | Q96L58 | protein_coding | tolerated(0.27) | benign(0.101) | TCGA-D7-A6EY-01 | Stomach | stomach adenocarcinoma | Female | >=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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