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Gene: VPS52 |
Gene summary for VPS52 |
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Gene information | Species | Human | Gene symbol | VPS52 | Gene ID | 6293 |
Gene name | VPS52 subunit of GARP complex | |
Gene Alias | ARE1 | |
Cytomap | 6p21.32 | |
Gene Type | protein-coding | GO ID | GO:0006810 | UniProtAcc | B4DS44 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
6293 | VPS52 | LZE4T | Human | Esophagus | ESCC | 5.27e-06 | 1.89e-01 | 0.0811 |
6293 | VPS52 | LZE7T | Human | Esophagus | ESCC | 2.17e-05 | 3.14e-01 | 0.0667 |
6293 | VPS52 | LZE8T | Human | Esophagus | ESCC | 2.19e-05 | 1.58e-01 | 0.067 |
6293 | VPS52 | LZE20T | Human | Esophagus | ESCC | 2.64e-08 | 3.08e-01 | 0.0662 |
6293 | VPS52 | LZE22T | Human | Esophagus | ESCC | 1.98e-04 | 2.82e-01 | 0.068 |
6293 | VPS52 | LZE24T | Human | Esophagus | ESCC | 1.75e-06 | 1.92e-01 | 0.0596 |
6293 | VPS52 | LZE21T | Human | Esophagus | ESCC | 1.62e-04 | 2.46e-01 | 0.0655 |
6293 | VPS52 | P1T-E | Human | Esophagus | ESCC | 1.21e-06 | 2.77e-01 | 0.0875 |
6293 | VPS52 | P2T-E | Human | Esophagus | ESCC | 4.75e-22 | 4.24e-01 | 0.1177 |
6293 | VPS52 | P4T-E | Human | Esophagus | ESCC | 7.72e-09 | 2.13e-01 | 0.1323 |
6293 | VPS52 | P5T-E | Human | Esophagus | ESCC | 1.14e-06 | 1.34e-01 | 0.1327 |
6293 | VPS52 | P8T-E | Human | Esophagus | ESCC | 2.60e-12 | 2.34e-01 | 0.0889 |
6293 | VPS52 | P9T-E | Human | Esophagus | ESCC | 4.05e-10 | 1.74e-01 | 0.1131 |
6293 | VPS52 | P10T-E | Human | Esophagus | ESCC | 3.30e-10 | 2.02e-01 | 0.116 |
6293 | VPS52 | P11T-E | Human | Esophagus | ESCC | 1.82e-10 | 4.12e-01 | 0.1426 |
6293 | VPS52 | P12T-E | Human | Esophagus | ESCC | 5.90e-16 | 3.68e-01 | 0.1122 |
6293 | VPS52 | P15T-E | Human | Esophagus | ESCC | 1.05e-14 | 2.77e-01 | 0.1149 |
6293 | VPS52 | P16T-E | Human | Esophagus | ESCC | 5.30e-25 | 4.55e-01 | 0.1153 |
6293 | VPS52 | P17T-E | Human | Esophagus | ESCC | 3.16e-03 | 2.46e-01 | 0.1278 |
6293 | VPS52 | P19T-E | Human | Esophagus | ESCC | 2.34e-05 | 4.38e-01 | 0.1662 |
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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:004819318 | Esophagus | ESCC | Golgi vesicle transport | 231/8552 | 296/18723 | 1.82e-30 | 9.63e-28 | 231 |
GO:001619715 | Esophagus | ESCC | endosomal transport | 168/8552 | 230/18723 | 2.28e-17 | 1.93e-15 | 168 |
GO:000703417 | Esophagus | ESCC | vacuolar transport | 119/8552 | 157/18723 | 1.16e-14 | 6.30e-13 | 119 |
GO:001648210 | Esophagus | ESCC | cytosolic transport | 124/8552 | 168/18723 | 9.69e-14 | 4.69e-12 | 124 |
GO:000689215 | Esophagus | ESCC | post-Golgi vesicle-mediated transport | 82/8552 | 104/18723 | 4.00e-12 | 1.55e-10 | 82 |
GO:009887615 | Esophagus | ESCC | vesicle-mediated transport to the plasma membrane | 99/8552 | 136/18723 | 1.13e-10 | 3.39e-09 | 99 |
GO:00070419 | Esophagus | ESCC | lysosomal transport | 83/8552 | 114/18723 | 3.52e-09 | 7.41e-08 | 83 |
GO:00421477 | Esophagus | ESCC | retrograde transport, endosome to Golgi | 63/8552 | 91/18723 | 4.58e-06 | 4.87e-05 | 63 |
GO:00324565 | Esophagus | ESCC | endocytic recycling | 51/8552 | 73/18723 | 2.47e-05 | 2.10e-04 | 51 |
GO:00485687 | Esophagus | ESCC | embryonic organ development | 228/8552 | 427/18723 | 7.28e-04 | 3.79e-03 | 228 |
GO:00068963 | Esophagus | ESCC | Golgi to vacuole transport | 16/8552 | 20/18723 | 1.85e-03 | 8.40e-03 | 16 |
GO:004819321 | Liver | HCC | Golgi vesicle transport | 217/7958 | 296/18723 | 2.58e-27 | 1.02e-24 | 217 |
GO:001619721 | Liver | HCC | endosomal transport | 154/7958 | 230/18723 | 4.74e-14 | 2.95e-12 | 154 |
GO:001648221 | Liver | HCC | cytosolic transport | 117/7958 | 168/18723 | 8.83e-13 | 4.48e-11 | 117 |
GO:000703421 | Liver | HCC | vacuolar transport | 108/7958 | 157/18723 | 2.22e-11 | 8.69e-10 | 108 |
GO:000689221 | Liver | HCC | post-Golgi vesicle-mediated transport | 77/7958 | 104/18723 | 6.14e-11 | 2.24e-09 | 77 |
GO:009887621 | Liver | HCC | vesicle-mediated transport to the plasma membrane | 92/7958 | 136/18723 | 2.57e-09 | 7.07e-08 | 92 |
GO:000704121 | Liver | HCC | lysosomal transport | 76/7958 | 114/18723 | 1.56e-07 | 2.88e-06 | 76 |
GO:004214721 | Liver | HCC | retrograde transport, endosome to Golgi | 61/7958 | 91/18723 | 1.94e-06 | 2.68e-05 | 61 |
GO:00324562 | Liver | HCC | endocytic recycling | 48/7958 | 73/18723 | 5.07e-05 | 4.83e-04 | 48 |
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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 |
VPS52 | SNV | Missense_Mutation | rs780463214 | c.1655C>G | p.Ala552Gly | p.A552G | Q8N1B4 | protein_coding | tolerated(0.09) | benign(0.333) | TCGA-EJ-5498-01 | Prostate | prostate adenocarcinoma | Male | <65 | 7 | Unknown | Unknown | SD |
VPS52 | SNV | Missense_Mutation | rs775407704 | c.1015N>T | p.Arg339Cys | p.R339C | Q8N1B4 | protein_coding | deleterious(0) | probably_damaging(0.939) | TCGA-B7-A5TI-01 | Stomach | stomach adenocarcinoma | Male | <65 | III/IV | Chemotherapy | eloxatin | CR |
VPS52 | SNV | Missense_Mutation | c.1910G>T | p.Arg637Leu | p.R637L | Q8N1B4 | protein_coding | tolerated(0.14) | benign(0.031) | TCGA-BR-6456-01 | Stomach | stomach adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
VPS52 | SNV | Missense_Mutation | c.1284N>C | p.Lys428Asn | p.K428N | Q8N1B4 | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-BR-8487-01 | Stomach | stomach adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
VPS52 | SNV | Missense_Mutation | rs147423039 | c.691N>T | p.Arg231Trp | p.R231W | Q8N1B4 | protein_coding | deleterious(0) | probably_damaging(0.986) | TCGA-HF-7132-01 | Stomach | stomach adenocarcinoma | Male | Unknown | I/II | Chemotherapy | fluorouracil | SD |
VPS52 | SNV | Missense_Mutation | rs768171623 | c.1049N>A | p.Arg350His | p.R350H | Q8N1B4 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-HF-A5NB-01 | Stomach | stomach adenocarcinoma | Female | >=65 | III/IV | Chemotherapy | fluorouracil | SD |
VPS52 | SNV | Missense_Mutation | c.1709N>C | p.Met570Thr | p.M570T | Q8N1B4 | protein_coding | deleterious(0.05) | benign(0.288) | TCGA-HU-A4H2-01 | Stomach | stomach adenocarcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | |
VPS52 | SNV | Missense_Mutation | c.1508N>G | p.Asp503Gly | p.D503G | Q8N1B4 | protein_coding | deleterious(0.01) | probably_damaging(0.99) | TCGA-IN-7806-01 | Stomach | stomach adenocarcinoma | Male | <65 | I/II | Chemotherapy | epirubicin | CR | |
VPS52 | SNV | Missense_Mutation | rs370857138 | c.374G>A | p.Arg125Gln | p.R125Q | Q8N1B4 | protein_coding | tolerated(0.12) | possibly_damaging(0.476) | TCGA-MX-A5UJ-01 | Stomach | stomach adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
VPS52 | insertion | Frame_Shift_Ins | novel | c.1832_1833insG | p.Leu612PhefsTer9 | p.L612Ffs*9 | Q8N1B4 | protein_coding | TCGA-BR-8487-01 | Stomach | stomach adenocarcinoma | 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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