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Gene: VASN |
Gene summary for VASN |
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Gene information | Species | Human | Gene symbol | VASN | Gene ID | 114990 |
Gene name | vasorin | |
Gene Alias | SLITL2 | |
Cytomap | 16p13.3 | |
Gene Type | protein-coding | GO ID | GO:0001666 | UniProtAcc | Q6EMK4 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
114990 | VASN | P2T-E | Human | Esophagus | ESCC | 4.33e-62 | 1.19e+00 | 0.1177 |
114990 | VASN | P4T-E | Human | Esophagus | ESCC | 4.42e-02 | 1.97e-01 | 0.1323 |
114990 | VASN | P8T-E | Human | Esophagus | ESCC | 3.66e-12 | 4.33e-01 | 0.0889 |
114990 | VASN | P10T-E | Human | Esophagus | ESCC | 3.78e-04 | 1.53e-01 | 0.116 |
114990 | VASN | P11T-E | Human | Esophagus | ESCC | 2.34e-12 | 9.45e-01 | 0.1426 |
114990 | VASN | P12T-E | Human | Esophagus | ESCC | 4.44e-10 | 3.26e-01 | 0.1122 |
114990 | VASN | P15T-E | Human | Esophagus | ESCC | 4.77e-05 | 1.69e-01 | 0.1149 |
114990 | VASN | P16T-E | Human | Esophagus | ESCC | 3.55e-16 | 3.82e-01 | 0.1153 |
114990 | VASN | P21T-E | Human | Esophagus | ESCC | 3.64e-02 | 8.45e-02 | 0.1617 |
114990 | VASN | P22T-E | Human | Esophagus | ESCC | 4.68e-02 | 6.00e-02 | 0.1236 |
114990 | VASN | P26T-E | Human | Esophagus | ESCC | 2.36e-04 | 8.87e-02 | 0.1276 |
114990 | VASN | P27T-E | Human | Esophagus | ESCC | 2.57e-03 | 7.75e-02 | 0.1055 |
114990 | VASN | P31T-E | Human | Esophagus | ESCC | 4.76e-12 | 2.09e-01 | 0.1251 |
114990 | VASN | P39T-E | Human | Esophagus | ESCC | 4.11e-07 | 6.32e-02 | 0.0894 |
114990 | VASN | P42T-E | Human | Esophagus | ESCC | 3.41e-02 | 2.69e-01 | 0.1175 |
114990 | VASN | P44T-E | Human | Esophagus | ESCC | 3.00e-02 | 1.76e-01 | 0.1096 |
114990 | VASN | P47T-E | Human | Esophagus | ESCC | 1.31e-04 | 1.32e-01 | 0.1067 |
114990 | VASN | P48T-E | Human | Esophagus | ESCC | 7.66e-06 | 3.52e-02 | 0.0959 |
114990 | VASN | P52T-E | Human | Esophagus | ESCC | 1.27e-06 | 1.90e-01 | 0.1555 |
114990 | VASN | P54T-E | Human | Esophagus | ESCC | 3.36e-02 | 1.41e-01 | 0.0975 |
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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:0070482111 | Esophagus | ESCC | response to oxygen levels | 218/8552 | 347/18723 | 6.91e-11 | 2.17e-09 | 218 |
GO:0036293111 | Esophagus | ESCC | response to decreased oxygen levels | 201/8552 | 322/18723 | 8.37e-10 | 2.04e-08 | 201 |
GO:0001666111 | Esophagus | ESCC | response to hypoxia | 192/8552 | 307/18723 | 1.59e-09 | 3.69e-08 | 192 |
GO:00715599 | Esophagus | ESCC | response to transforming growth factor beta | 157/8552 | 256/18723 | 2.95e-07 | 4.23e-06 | 157 |
GO:0071453110 | Esophagus | ESCC | cellular response to oxygen levels | 114/8552 | 177/18723 | 3.63e-07 | 5.06e-06 | 114 |
GO:0036294110 | Esophagus | ESCC | cellular response to decreased oxygen levels | 105/8552 | 161/18723 | 4.20e-07 | 5.73e-06 | 105 |
GO:00715609 | Esophagus | ESCC | cellular response to transforming growth factor beta stimulus | 151/8552 | 250/18723 | 1.78e-06 | 2.10e-05 | 151 |
GO:007145616 | Esophagus | ESCC | cellular response to hypoxia | 97/8552 | 151/18723 | 3.12e-06 | 3.51e-05 | 97 |
GO:00071799 | Esophagus | ESCC | transforming growth factor beta receptor signaling pathway | 121/8552 | 198/18723 | 8.26e-06 | 8.03e-05 | 121 |
GO:00018378 | Esophagus | ESCC | epithelial to mesenchymal transition | 95/8552 | 157/18723 | 1.25e-04 | 8.56e-04 | 95 |
GO:000717810 | Esophagus | ESCC | transmembrane receptor protein serine/threonine kinase signaling pathway | 195/8552 | 355/18723 | 2.58e-04 | 1.58e-03 | 195 |
GO:00487628 | Esophagus | ESCC | mesenchymal cell differentiation | 133/8552 | 236/18723 | 5.94e-04 | 3.22e-03 | 133 |
GO:00107174 | Esophagus | ESCC | regulation of epithelial to mesenchymal transition | 61/8552 | 99/18723 | 1.01e-03 | 5.09e-03 | 61 |
GO:00170156 | Esophagus | ESCC | regulation of transforming growth factor beta receptor signaling pathway | 75/8552 | 128/18723 | 2.19e-03 | 9.71e-03 | 75 |
GO:19038447 | Esophagus | ESCC | regulation of cellular response to transforming growth factor beta stimulus | 76/8552 | 131/18723 | 2.96e-03 | 1.24e-02 | 76 |
GO:00604856 | Esophagus | ESCC | mesenchyme development | 156/8552 | 291/18723 | 3.76e-03 | 1.53e-02 | 156 |
GO:00704827 | Liver | Cirrhotic | response to oxygen levels | 125/4634 | 347/18723 | 1.55e-06 | 3.02e-05 | 125 |
GO:007155911 | Liver | Cirrhotic | response to transforming growth factor beta | 96/4634 | 256/18723 | 3.55e-06 | 6.09e-05 | 96 |
GO:007156011 | Liver | Cirrhotic | cellular response to transforming growth factor beta stimulus | 93/4634 | 250/18723 | 7.34e-06 | 1.13e-04 | 93 |
GO:00362937 | Liver | Cirrhotic | response to decreased oxygen levels | 113/4634 | 322/18723 | 1.87e-05 | 2.52e-04 | 113 |
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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 |
VASN | SNV | Missense_Mutation | novel | c.350N>G | p.Asn117Ser | p.N117S | Q6EMK4 | protein_coding | tolerated(0.08) | possibly_damaging(0.621) | TCGA-GM-A3NY-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | arimidex | SD |
VASN | SNV | Missense_Mutation | novel | c.1816G>A | p.Ala606Thr | p.A606T | Q6EMK4 | protein_coding | tolerated(0.18) | benign(0.003) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
VASN | SNV | Missense_Mutation | novel | c.1817N>T | p.Ala606Val | p.A606V | Q6EMK4 | protein_coding | deleterious(0.04) | benign(0.115) | TCGA-AA-A022-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
VASN | SNV | Missense_Mutation | rs755829190 | c.952N>A | p.Val318Ile | p.V318I | Q6EMK4 | protein_coding | tolerated(0.31) | benign(0.007) | TCGA-AD-6964-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | folfox | PD |
VASN | SNV | Missense_Mutation | c.80G>A | p.Gly27Asp | p.G27D | Q6EMK4 | protein_coding | tolerated(0.43) | benign(0.076) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
VASN | SNV | Missense_Mutation | c.1591T>A | p.Tyr531Asn | p.Y531N | Q6EMK4 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
VASN | SNV | Missense_Mutation | rs199795973 | c.409C>T | p.Arg137Cys | p.R137C | Q6EMK4 | protein_coding | deleterious(0.04) | benign(0.013) | TCGA-CK-6746-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
VASN | SNV | Missense_Mutation | rs113954688 | c.647N>A | p.Arg216His | p.R216H | Q6EMK4 | protein_coding | tolerated(0.19) | benign(0.005) | TCGA-CM-6674-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
VASN | SNV | Missense_Mutation | c.1187N>A | p.Ala396Asp | p.A396D | Q6EMK4 | protein_coding | tolerated(0.17) | benign(0.235) | TCGA-DC-4749-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
VASN | insertion | Frame_Shift_Ins | novel | c.340_341insA | p.Ile115AsnfsTer4 | p.I115Nfs*4 | Q6EMK4 | protein_coding | TCGA-AZ-6606-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | folfiri | 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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