|
Gene: VPS26A |
Gene summary for VPS26A |
Gene summary. |
Gene information | Species | Human | Gene symbol | VPS26A | Gene ID | 9559 |
Gene name | VPS26, retromer complex component A | |
Gene Alias | HB58 | |
Cytomap | 10q22.1 | |
Gene Type | protein-coding | GO ID | GO:0006810 | UniProtAcc | O75436 |
Top |
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 |
9559 | VPS26A | LZE4T | Human | Esophagus | ESCC | 1.31e-28 | 7.43e-01 | 0.0811 |
9559 | VPS26A | LZE5T | Human | Esophagus | ESCC | 1.74e-03 | 5.09e-01 | 0.0514 |
9559 | VPS26A | LZE7T | Human | Esophagus | ESCC | 2.84e-03 | 3.22e-01 | 0.0667 |
9559 | VPS26A | LZE8T | Human | Esophagus | ESCC | 1.39e-07 | 2.88e-01 | 0.067 |
9559 | VPS26A | LZE20T | Human | Esophagus | ESCC | 1.20e-05 | 3.29e-02 | 0.0662 |
9559 | VPS26A | LZE22T | Human | Esophagus | ESCC | 1.67e-05 | 4.24e-01 | 0.068 |
9559 | VPS26A | LZE24T | Human | Esophagus | ESCC | 1.96e-24 | 8.71e-01 | 0.0596 |
9559 | VPS26A | LZE21T | Human | Esophagus | ESCC | 2.24e-04 | 1.80e-01 | 0.0655 |
9559 | VPS26A | LZE6T | Human | Esophagus | ESCC | 1.78e-15 | 4.57e-01 | 0.0845 |
9559 | VPS26A | P1T-E | Human | Esophagus | ESCC | 2.33e-06 | 4.96e-01 | 0.0875 |
9559 | VPS26A | P2T-E | Human | Esophagus | ESCC | 3.50e-47 | 8.59e-01 | 0.1177 |
9559 | VPS26A | P4T-E | Human | Esophagus | ESCC | 1.60e-42 | 1.06e+00 | 0.1323 |
9559 | VPS26A | P5T-E | Human | Esophagus | ESCC | 1.80e-23 | 6.47e-01 | 0.1327 |
9559 | VPS26A | P8T-E | Human | Esophagus | ESCC | 1.65e-24 | 4.95e-01 | 0.0889 |
9559 | VPS26A | P9T-E | Human | Esophagus | ESCC | 3.30e-10 | 2.18e-01 | 0.1131 |
9559 | VPS26A | P10T-E | Human | Esophagus | ESCC | 7.21e-22 | 3.74e-01 | 0.116 |
9559 | VPS26A | P11T-E | Human | Esophagus | ESCC | 5.20e-22 | 8.55e-01 | 0.1426 |
9559 | VPS26A | P12T-E | Human | Esophagus | ESCC | 6.87e-42 | 9.74e-01 | 0.1122 |
9559 | VPS26A | P15T-E | Human | Esophagus | ESCC | 6.20e-27 | 6.20e-01 | 0.1149 |
9559 | VPS26A | P16T-E | Human | Esophagus | ESCC | 1.43e-30 | 6.94e-01 | 0.1153 |
Page: 1 2 3 4 5 6 |
Transcriptomic changes along malignancy continuum. |
∗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. |
Top |
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 | CRC | |
Stomach | GC | |
Stomach | CAG with IM | |
Stomach | CSG | |
Stomach | CAG |
∗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:001623617 | Esophagus | ESCC | macroautophagy | 216/8552 | 291/18723 | 1.94e-23 | 4.57e-21 | 216 |
GO:001050617 | Esophagus | ESCC | regulation of autophagy | 220/8552 | 317/18723 | 6.72e-18 | 6.36e-16 | 220 |
GO:001619715 | Esophagus | ESCC | endosomal transport | 168/8552 | 230/18723 | 2.28e-17 | 1.93e-15 | 168 |
GO:001648210 | Esophagus | ESCC | cytosolic transport | 124/8552 | 168/18723 | 9.69e-14 | 4.69e-12 | 124 |
GO:001624114 | Esophagus | ESCC | regulation of macroautophagy | 102/8552 | 141/18723 | 1.09e-10 | 3.27e-09 | 102 |
GO:009887615 | Esophagus | ESCC | vesicle-mediated transport to the plasma membrane | 99/8552 | 136/18723 | 1.13e-10 | 3.39e-09 | 99 |
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:001623611 | Liver | Cirrhotic | macroautophagy | 129/4634 | 291/18723 | 1.75e-13 | 1.41e-11 | 129 |
GO:001050611 | Liver | Cirrhotic | regulation of autophagy | 132/4634 | 317/18723 | 2.17e-11 | 1.33e-09 | 132 |
GO:001648211 | Liver | Cirrhotic | cytosolic transport | 74/4634 | 168/18723 | 3.34e-08 | 1.12e-06 | 74 |
GO:001619711 | Liver | Cirrhotic | endosomal transport | 93/4634 | 230/18723 | 1.01e-07 | 2.93e-06 | 93 |
GO:009887611 | Liver | Cirrhotic | vesicle-mediated transport to the plasma membrane | 59/4634 | 136/18723 | 1.46e-06 | 2.88e-05 | 59 |
GO:00162414 | Liver | Cirrhotic | regulation of macroautophagy | 60/4634 | 141/18723 | 2.57e-06 | 4.63e-05 | 60 |
GO:004214711 | Liver | Cirrhotic | retrograde transport, endosome to Golgi | 34/4634 | 91/18723 | 5.01e-03 | 2.60e-02 | 34 |
GO:001623621 | Liver | HCC | macroautophagy | 204/7958 | 291/18723 | 8.66e-22 | 1.41e-19 | 204 |
GO:001050621 | Liver | HCC | regulation of autophagy | 210/7958 | 317/18723 | 7.59e-18 | 8.45e-16 | 210 |
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:001624111 | Liver | HCC | regulation of macroautophagy | 96/7958 | 141/18723 | 6.82e-10 | 2.14e-08 | 96 |
Page: 1 2 3 4 |
Enriched KEGG pathways. |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa04144210 | Esophagus | ESCC | Endocytosis | 186/4205 | 251/8465 | 9.74e-16 | 4.66e-14 | 2.39e-14 | 186 |
hsa0414437 | Esophagus | ESCC | Endocytosis | 186/4205 | 251/8465 | 9.74e-16 | 4.66e-14 | 2.39e-14 | 186 |
hsa0414412 | Liver | Cirrhotic | Endocytosis | 119/2530 | 251/8465 | 2.33e-09 | 4.56e-08 | 2.81e-08 | 119 |
hsa0414413 | Liver | Cirrhotic | Endocytosis | 119/2530 | 251/8465 | 2.33e-09 | 4.56e-08 | 2.81e-08 | 119 |
hsa0414422 | Liver | HCC | Endocytosis | 178/4020 | 251/8465 | 2.03e-14 | 5.22e-13 | 2.91e-13 | 178 |
hsa0414432 | Liver | HCC | Endocytosis | 178/4020 | 251/8465 | 2.03e-14 | 5.22e-13 | 2.91e-13 | 178 |
hsa0414427 | Oral cavity | OSCC | Endocytosis | 174/3704 | 251/8465 | 9.42e-17 | 4.51e-15 | 2.29e-15 | 174 |
hsa04144112 | Oral cavity | OSCC | Endocytosis | 174/3704 | 251/8465 | 9.42e-17 | 4.51e-15 | 2.29e-15 | 174 |
hsa0414428 | Oral cavity | LP | Endocytosis | 121/2418 | 251/8465 | 1.89e-11 | 3.70e-10 | 2.38e-10 | 121 |
hsa0414436 | Oral cavity | LP | Endocytosis | 121/2418 | 251/8465 | 1.89e-11 | 3.70e-10 | 2.38e-10 | 121 |
hsa0414461 | Oral cavity | NEOLP | Endocytosis | 62/1112 | 251/8465 | 3.56e-07 | 4.92e-06 | 3.09e-06 | 62 |
hsa0414471 | Oral cavity | NEOLP | Endocytosis | 62/1112 | 251/8465 | 3.56e-07 | 4.92e-06 | 3.09e-06 | 62 |
Page: 1 |
Top |
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 |
Top |
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 |
Top |
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 |
VPS26A | SNV | Missense_Mutation | c.206G>A | p.Arg69Lys | p.R69K | O75436 | protein_coding | tolerated(1) | benign(0.003) | TCGA-A8-A0A7-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
VPS26A | SNV | Missense_Mutation | rs766824852 | c.407T>C | p.Ile136Thr | p.I136T | O75436 | protein_coding | tolerated(0.06) | benign(0.125) | TCGA-BH-A1EU-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
VPS26A | SNV | Missense_Mutation | c.133N>A | p.Gly45Arg | p.G45R | O75436 | protein_coding | deleterious(0.02) | probably_damaging(0.983) | TCGA-D8-A140-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin+cyclophosphamid | SD | |
VPS26A | SNV | Missense_Mutation | c.328N>C | p.Glu110Gln | p.E110Q | O75436 | protein_coding | deleterious(0.02) | possibly_damaging(0.649) | TCGA-D8-A1JA-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | adriamycin | PD | |
VPS26A | SNV | Missense_Mutation | c.416N>A | p.Arg139Lys | p.R139K | O75436 | protein_coding | tolerated(0.29) | benign(0.095) | TCGA-E9-A228-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin | SD | |
VPS26A | insertion | Frame_Shift_Ins | novel | c.598_599insATTATAGGCATGAGCCACCGCGCCCAACATATTTTTT | p.Val200AspfsTer47 | p.V200Dfs*47 | O75436 | protein_coding | TCGA-AN-A0FX-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | ||
VPS26A | SNV | Missense_Mutation | rs140007940 | c.981N>A | p.Met327Ile | p.M327I | O75436 | protein_coding | tolerated_low_confidence(0.08) | benign(0) | TCGA-DM-A1HA-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | SD |
VPS26A | SNV | Missense_Mutation | c.860T>C | p.Phe287Ser | p.F287S | O75436 | protein_coding | deleterious(0) | probably_damaging(0.995) | TCGA-DM-A28M-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
VPS26A | SNV | Missense_Mutation | novel | c.227N>G | p.Ile76Ser | p.I76S | O75436 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AG-A002-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
VPS26A | SNV | Missense_Mutation | rs761116648 | c.472N>A | p.Pro158Thr | p.P158T | O75436 | protein_coding | deleterious(0.02) | possibly_damaging(0.78) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
Page: 1 2 3 |
Top |
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 |