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Gene: SEPT10 |
Gene summary for SEPT10 |
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Gene information | Species | Human | Gene symbol | SEPT10 | Gene ID | 151011 |
Gene name | septin 10 | |
Gene Alias | SEPT10 | |
Cytomap | 2q13 | |
Gene Type | protein-coding | GO ID | GO:0000910 | UniProtAcc | B7Z371 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
151011 | SEPT10 | LP15 | Human | Oral cavity | LP | 1.22e-02 | 1.05e+00 | 0.2174 |
151011 | SEPT10 | LP17 | Human | Oral cavity | LP | 2.52e-02 | 8.23e-01 | 0.2349 |
151011 | SEPT10 | EOLP-1 | Human | Oral cavity | EOLP | 1.86e-04 | -2.01e-01 | -0.0202 |
151011 | SEPT10 | EOLP-2 | Human | Oral cavity | EOLP | 3.94e-04 | -2.01e-01 | -0.0203 |
151011 | SEPT10 | NEOLP-1 | Human | Oral cavity | NEOLP | 3.94e-04 | -2.01e-01 | -0.0194 |
151011 | SEPT10 | NEOLP-2 | Human | Oral cavity | NEOLP | 1.86e-04 | -2.01e-01 | -0.0196 |
151011 | SEPT10 | NEOLP-3 | Human | Oral cavity | NEOLP | 1.86e-04 | -2.01e-01 | -0.0191 |
151011 | SEPT10 | SYSMH1 | Human | Oral cavity | OSCC | 3.71e-19 | 5.85e-01 | 0.1127 |
151011 | SEPT10 | SYSMH2 | Human | Oral cavity | OSCC | 1.15e-32 | 9.78e-01 | 0.2326 |
151011 | SEPT10 | SYSMH3 | Human | Oral cavity | OSCC | 4.13e-25 | 6.62e-01 | 0.2442 |
151011 | SEPT10 | SYSMH4 | Human | Oral cavity | OSCC | 9.11e-11 | 3.21e-01 | 0.1226 |
151011 | SEPT10 | SYSMH5 | Human | Oral cavity | OSCC | 1.27e-04 | 2.02e-01 | 0.0647 |
151011 | SEPT10 | SYSMH6 | Human | Oral cavity | OSCC | 1.93e-02 | 2.59e-01 | 0.1275 |
151011 | SEPT10 | P1_S1_AK | Human | Skin | AK | 8.79e-12 | -2.85e-01 | -0.3399 |
151011 | SEPT10 | P2_S3_AK | Human | Skin | AK | 4.25e-11 | -2.85e-01 | -0.3287 |
151011 | SEPT10 | P2_S4_SCCIS | Human | Skin | SCCIS | 1.80e-12 | -2.85e-01 | -0.3043 |
151011 | SEPT10 | P3_S6_AK | Human | Skin | AK | 4.25e-11 | -2.85e-01 | -0.3256 |
151011 | SEPT10 | P4_S8_cSCC | Human | Skin | cSCC | 8.96e-09 | -2.85e-01 | -0.3095 |
151011 | SEPT10 | P5_S10_cSCC | Human | Skin | cSCC | 1.93e-11 | -2.85e-01 | -0.299 |
151011 | SEPT10 | P1_cSCC | Human | Skin | cSCC | 2.01e-21 | 9.85e-01 | 0.0292 |
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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 |
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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 |
SEPT10 | SNV | Missense_Mutation | novel | c.1177G>A | p.Glu393Lys | p.E393K | protein_coding | tolerated(0.06) | possibly_damaging(0.887) | TCGA-5L-AAT1-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Hormone Therapy | letrozol | SD | |
SEPT10 | SNV | Missense_Mutation | rs200598502 | c.1555N>G | p.Phe519Val | p.F519V | protein_coding | tolerated_low_confidence(0.14) | benign(0.003) | TCGA-A1-A0SD-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
SEPT10 | SNV | Missense_Mutation | rs200598502 | c.1555T>G | p.Phe519Val | p.F519V | protein_coding | tolerated_low_confidence(0.14) | benign(0.003) | TCGA-A8-A097-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | tamoxiphen | SD | |
SEPT10 | SNV | Missense_Mutation | novel | c.1292N>C | p.His431Pro | p.H431P | protein_coding | deleterious(0.04) | benign(0) | TCGA-A8-A0A2-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | tamoxiphen | SD | |
SEPT10 | SNV | Missense_Mutation | c.104N>T | p.Arg35Ile | p.R35I | protein_coding | tolerated(0.07) | benign(0.169) | TCGA-AO-A03T-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cyclophosphamide | SD | ||
SEPT10 | SNV | Missense_Mutation | rs200598502 | c.1555N>G | p.Phe519Val | p.F519V | protein_coding | tolerated_low_confidence(0.14) | benign(0.003) | TCGA-B6-A0IC-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
SEPT10 | SNV | Missense_Mutation | rs200598502 | c.1555T>G | p.Phe519Val | p.F519V | protein_coding | tolerated_low_confidence(0.14) | benign(0.003) | TCGA-B6-A0RT-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | |
SEPT10 | SNV | Missense_Mutation | rs200598502 | c.1555T>G | p.Phe519Val | p.F519V | protein_coding | tolerated_low_confidence(0.14) | benign(0.003) | TCGA-BH-A0C7-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | CR | |
SEPT10 | SNV | Missense_Mutation | rs200598502 | c.1555N>G | p.Phe519Val | p.F519V | protein_coding | tolerated_low_confidence(0.14) | benign(0.003) | TCGA-BH-A0DE-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
SEPT10 | SNV | Missense_Mutation | rs200598502 | c.1555T>G | p.Phe519Val | p.F519V | protein_coding | tolerated_low_confidence(0.14) | benign(0.003) | TCGA-C8-A12M-01 | Breast | breast invasive carcinoma | 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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