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Gene: SOX2 |
Gene summary for SOX2 |
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Gene information | Species | Human | Gene symbol | SOX2 | Gene ID | 6657 |
Gene name | SRY-box transcription factor 2 | |
Gene Alias | ANOP3 | |
Cytomap | 3q26.33 | |
Gene Type | protein-coding | GO ID | GO:0000122 | UniProtAcc | A0A0U3FYV6 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
6657 | SOX2 | LZE2T | Human | Esophagus | ESCC | 9.01e-06 | 1.33e+00 | 0.082 |
6657 | SOX2 | LZE4T | Human | Esophagus | ESCC | 6.78e-19 | 9.94e-01 | 0.0811 |
6657 | SOX2 | LZE5T | Human | Esophagus | ESCC | 2.93e-05 | 5.15e-01 | 0.0514 |
6657 | SOX2 | LZE7T | Human | Esophagus | ESCC | 2.09e-27 | 2.04e+00 | 0.0667 |
6657 | SOX2 | LZE20T | Human | Esophagus | ESCC | 6.79e-12 | 7.05e-01 | 0.0662 |
6657 | SOX2 | LZE22D1 | Human | Esophagus | HGIN | 6.20e-05 | 2.23e-01 | 0.0595 |
6657 | SOX2 | LZE22T | Human | Esophagus | ESCC | 9.69e-11 | 8.28e-01 | 0.068 |
6657 | SOX2 | LZE24T | Human | Esophagus | ESCC | 3.95e-30 | 1.05e+00 | 0.0596 |
6657 | SOX2 | LZE22D3 | Human | Esophagus | HGIN | 2.69e-02 | 5.15e-01 | 0.0653 |
6657 | SOX2 | LZE21T | Human | Esophagus | ESCC | 6.47e-17 | 1.77e+00 | 0.0655 |
6657 | SOX2 | P1T-E | Human | Esophagus | ESCC | 4.96e-18 | 1.10e+00 | 0.0875 |
6657 | SOX2 | P2T-E | Human | Esophagus | ESCC | 7.74e-83 | 1.99e+00 | 0.1177 |
6657 | SOX2 | P4T-E | Human | Esophagus | ESCC | 3.83e-60 | 1.87e+00 | 0.1323 |
6657 | SOX2 | P5T-E | Human | Esophagus | ESCC | 3.67e-98 | 2.57e+00 | 0.1327 |
6657 | SOX2 | P8T-E | Human | Esophagus | ESCC | 8.06e-70 | 1.53e+00 | 0.0889 |
6657 | SOX2 | P9T-E | Human | Esophagus | ESCC | 1.72e-81 | 2.57e+00 | 0.1131 |
6657 | SOX2 | P10T-E | Human | Esophagus | ESCC | 1.38e-109 | 2.78e+00 | 0.116 |
6657 | SOX2 | P11T-E | Human | Esophagus | ESCC | 1.79e-18 | 8.97e-01 | 0.1426 |
6657 | SOX2 | P12T-E | Human | Esophagus | ESCC | 1.10e-116 | 3.35e+00 | 0.1122 |
6657 | SOX2 | P15T-E | Human | Esophagus | ESCC | 3.11e-87 | 3.08e+00 | 0.1149 |
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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:000150331 | Oral cavity | NEOLP | ossification | 81/2005 | 408/18723 | 2.67e-08 | 1.15e-06 | 81 |
GO:004328132 | Oral cavity | NEOLP | regulation of cysteine-type endopeptidase activity involved in apoptotic process | 49/2005 | 209/18723 | 8.94e-08 | 3.36e-06 | 49 |
GO:006082831 | Oral cavity | NEOLP | regulation of canonical Wnt signaling pathway | 55/2005 | 253/18723 | 2.23e-07 | 7.28e-06 | 55 |
GO:006007031 | Oral cavity | NEOLP | canonical Wnt signaling pathway | 62/2005 | 303/18723 | 3.79e-07 | 1.15e-05 | 62 |
GO:001982721 | Oral cavity | NEOLP | stem cell population maintenance | 34/2005 | 131/18723 | 6.89e-07 | 1.93e-05 | 34 |
GO:003109931 | Oral cavity | NEOLP | regeneration | 45/2005 | 198/18723 | 7.52e-07 | 2.10e-05 | 45 |
GO:009872721 | Oral cavity | NEOLP | maintenance of cell number | 34/2005 | 134/18723 | 1.21e-06 | 3.13e-05 | 34 |
GO:002240724 | Oral cavity | NEOLP | regulation of cell-cell adhesion | 81/2005 | 448/18723 | 1.54e-06 | 3.83e-05 | 81 |
GO:01500631 | Oral cavity | NEOLP | visual system development | 70/2005 | 375/18723 | 2.46e-06 | 5.64e-05 | 70 |
GO:000165411 | Oral cavity | NEOLP | eye development | 69/2005 | 371/18723 | 3.30e-06 | 7.40e-05 | 69 |
GO:00488801 | Oral cavity | NEOLP | sensory system development | 70/2005 | 381/18723 | 4.38e-06 | 9.42e-05 | 70 |
GO:000164931 | Oral cavity | NEOLP | osteoblast differentiation | 47/2005 | 229/18723 | 8.59e-06 | 1.66e-04 | 47 |
GO:000749221 | Oral cavity | NEOLP | endoderm development | 22/2005 | 77/18723 | 1.19e-05 | 2.17e-04 | 22 |
GO:004873232 | Oral cavity | NEOLP | gland development | 76/2005 | 436/18723 | 1.25e-05 | 2.25e-04 | 76 |
GO:003090013 | Oral cavity | NEOLP | forebrain development | 67/2005 | 379/18723 | 2.54e-05 | 3.99e-04 | 67 |
GO:000170621 | Oral cavity | NEOLP | endoderm formation | 17/2005 | 54/18723 | 2.91e-05 | 4.46e-04 | 17 |
GO:003598711 | Oral cavity | NEOLP | endodermal cell differentiation | 15/2005 | 45/18723 | 4.02e-05 | 5.71e-04 | 15 |
GO:000632521 | Oral cavity | NEOLP | chromatin organization | 70/2005 | 409/18723 | 4.97e-05 | 6.83e-04 | 70 |
GO:000736921 | Oral cavity | NEOLP | gastrulation | 38/2005 | 185/18723 | 5.90e-05 | 7.93e-04 | 38 |
GO:000170421 | Oral cavity | NEOLP | formation of primary germ layer | 28/2005 | 121/18723 | 6.25e-05 | 8.31e-04 | 28 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0439018 | Esophagus | ESCC | Hippo signaling pathway | 92/4205 | 157/8465 | 1.46e-02 | 3.31e-02 | 1.69e-02 | 92 |
hsa0439019 | Esophagus | ESCC | Hippo signaling pathway | 92/4205 | 157/8465 | 1.46e-02 | 3.31e-02 | 1.69e-02 | 92 |
hsa0439016 | Oral cavity | OSCC | Hippo signaling pathway | 86/3704 | 157/8465 | 3.30e-03 | 8.24e-03 | 4.20e-03 | 86 |
hsa0439017 | Oral cavity | OSCC | Hippo signaling pathway | 86/3704 | 157/8465 | 3.30e-03 | 8.24e-03 | 4.20e-03 | 86 |
hsa0439025 | Oral cavity | NEOLP | Hippo signaling pathway | 35/1112 | 157/8465 | 9.91e-04 | 4.85e-03 | 3.05e-03 | 35 |
hsa0439035 | Oral cavity | NEOLP | Hippo signaling pathway | 35/1112 | 157/8465 | 9.91e-04 | 4.85e-03 | 3.05e-03 | 35 |
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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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∗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 |
SOX2 | SNV | Missense_Mutation | c.466C>T | p.Arg156Cys | p.R156C | P48431 | protein_coding | deleterious(0.01) | probably_damaging(0.993) | TCGA-A8-A09Z-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
SOX2 | SNV | Missense_Mutation | c.250N>A | p.Glu84Lys | p.E84K | P48431 | protein_coding | deleterious(0) | probably_damaging(0.989) | TCGA-E2-A10C-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | SD | |
SOX2 | SNV | Missense_Mutation | c.277G>A | p.Glu93Lys | p.E93K | P48431 | protein_coding | deleterious(0) | probably_damaging(0.991) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
SOX2 | SNV | Missense_Mutation | c.796N>G | p.Gln266Glu | p.Q266E | P48431 | protein_coding | tolerated(0.25) | benign(0.072) | TCGA-C5-A7UC-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | |
SOX2 | SNV | Missense_Mutation | c.472N>A | p.Asp158Asn | p.D158N | P48431 | protein_coding | deleterious(0.01) | benign(0.326) | TCGA-DS-A0VM-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | PD | |
SOX2 | SNV | Missense_Mutation | novel | c.198N>A | p.Met66Ile | p.M66I | P48431 | protein_coding | deleterious(0) | possibly_damaging(0.543) | TCGA-EA-A3HU-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
SOX2 | SNV | Missense_Mutation | c.602N>G | p.Asp201Gly | p.D201G | P48431 | protein_coding | deleterious(0) | probably_damaging(0.961) | TCGA-AA-A00N-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |
SOX2 | SNV | Missense_Mutation | novel | c.838N>A | p.Gly280Ser | p.G280S | P48431 | protein_coding | tolerated(0.13) | benign(0.013) | TCGA-AD-6901-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Chemotherapy | xeloda | PD |
SOX2 | SNV | Missense_Mutation | c.644N>T | p.Thr215Ile | p.T215I | P48431 | protein_coding | deleterious(0.05) | benign(0.439) | TCGA-AD-6964-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | folfox | PD | |
SOX2 | SNV | Missense_Mutation | novel | c.829N>C | p.Tyr277His | p.Y277H | P48431 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-AZ-4315-01 | Colorectum | colon adenocarcinoma | Male | <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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