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Gene: SUDS3 |
Gene summary for SUDS3 |
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Gene information | Species | Human | Gene symbol | SUDS3 | Gene ID | 64426 |
Gene name | SDS3 homolog, SIN3A corepressor complex component | |
Gene Alias | SAP45 | |
Cytomap | 12q24.23 | |
Gene Type | protein-coding | GO ID | GO:0000122 | UniProtAcc | Q9H7L9 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
64426 | SUDS3 | LZE2T | Human | Esophagus | ESCC | 3.48e-05 | 5.45e-01 | 0.082 |
64426 | SUDS3 | LZE4T | Human | Esophagus | ESCC | 3.37e-13 | 3.42e-01 | 0.0811 |
64426 | SUDS3 | LZE5T | Human | Esophagus | ESCC | 4.30e-09 | 5.67e-01 | 0.0514 |
64426 | SUDS3 | LZE7T | Human | Esophagus | ESCC | 3.20e-09 | 3.08e-01 | 0.0667 |
64426 | SUDS3 | LZE8T | Human | Esophagus | ESCC | 2.21e-09 | 1.68e-01 | 0.067 |
64426 | SUDS3 | LZE20T | Human | Esophagus | ESCC | 1.25e-09 | 3.75e-01 | 0.0662 |
64426 | SUDS3 | LZE22D1 | Human | Esophagus | HGIN | 9.10e-04 | 2.19e-01 | 0.0595 |
64426 | SUDS3 | LZE22T | Human | Esophagus | ESCC | 1.26e-09 | 3.83e-01 | 0.068 |
64426 | SUDS3 | LZE24T | Human | Esophagus | ESCC | 5.37e-25 | 6.25e-01 | 0.0596 |
64426 | SUDS3 | LZE21T | Human | Esophagus | ESCC | 2.54e-02 | 3.01e-01 | 0.0655 |
64426 | SUDS3 | P1T-E | Human | Esophagus | ESCC | 1.42e-25 | 1.05e+00 | 0.0875 |
64426 | SUDS3 | P2T-E | Human | Esophagus | ESCC | 2.12e-61 | 1.16e+00 | 0.1177 |
64426 | SUDS3 | P4T-E | Human | Esophagus | ESCC | 1.96e-45 | 9.77e-01 | 0.1323 |
64426 | SUDS3 | P5T-E | Human | Esophagus | ESCC | 1.91e-25 | 6.52e-01 | 0.1327 |
64426 | SUDS3 | P8T-E | Human | Esophagus | ESCC | 7.05e-42 | 8.35e-01 | 0.0889 |
64426 | SUDS3 | P9T-E | Human | Esophagus | ESCC | 8.31e-22 | 3.56e-01 | 0.1131 |
64426 | SUDS3 | P10T-E | Human | Esophagus | ESCC | 2.91e-19 | 4.38e-01 | 0.116 |
64426 | SUDS3 | P11T-E | Human | Esophagus | ESCC | 3.28e-16 | 5.88e-01 | 0.1426 |
64426 | SUDS3 | P12T-E | Human | Esophagus | ESCC | 2.32e-20 | 4.94e-01 | 0.1122 |
64426 | SUDS3 | P15T-E | Human | Esophagus | ESCC | 1.90e-34 | 8.04e-01 | 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:00165708 | Esophagus | HGIN | histone modification | 92/2587 | 463/18723 | 1.70e-04 | 3.30e-03 | 92 |
GO:002176220 | Esophagus | HGIN | substantia nigra development | 14/2587 | 44/18723 | 1.75e-03 | 1.90e-02 | 14 |
GO:001657015 | Esophagus | ESCC | histone modification | 323/8552 | 463/18723 | 2.61e-26 | 7.88e-24 | 323 |
GO:00356015 | Esophagus | ESCC | protein deacylation | 79/8552 | 112/18723 | 8.30e-08 | 1.42e-06 | 79 |
GO:00987325 | Esophagus | ESCC | macromolecule deacylation | 80/8552 | 116/18723 | 3.19e-07 | 4.50e-06 | 80 |
GO:00165754 | Esophagus | ESCC | histone deacetylation | 60/8552 | 82/18723 | 3.85e-07 | 5.32e-06 | 60 |
GO:00064765 | Esophagus | ESCC | protein deacetylation | 70/8552 | 101/18723 | 1.29e-06 | 1.58e-05 | 70 |
GO:0021762111 | Esophagus | ESCC | substantia nigra development | 35/8552 | 44/18723 | 4.40e-06 | 4.69e-05 | 35 |
GO:004885718 | Esophagus | ESCC | neural nucleus development | 44/8552 | 64/18723 | 1.59e-04 | 1.05e-03 | 44 |
GO:003090118 | Esophagus | ESCC | midbrain development | 58/8552 | 90/18723 | 2.52e-04 | 1.55e-03 | 58 |
GO:002176212 | Liver | Cirrhotic | substantia nigra development | 25/4634 | 44/18723 | 5.57e-06 | 9.10e-05 | 25 |
GO:001657011 | Liver | Cirrhotic | histone modification | 154/4634 | 463/18723 | 1.92e-05 | 2.57e-04 | 154 |
GO:004885712 | Liver | Cirrhotic | neural nucleus development | 28/4634 | 64/18723 | 6.78e-04 | 5.08e-03 | 28 |
GO:003090111 | Liver | Cirrhotic | midbrain development | 35/4634 | 90/18723 | 2.06e-03 | 1.28e-02 | 35 |
GO:0035601 | Liver | Cirrhotic | protein deacylation | 39/4634 | 112/18723 | 1.08e-02 | 4.75e-02 | 39 |
GO:001657021 | Liver | HCC | histone modification | 283/7958 | 463/18723 | 2.68e-16 | 2.33e-14 | 283 |
GO:002176222 | Liver | HCC | substantia nigra development | 33/7958 | 44/18723 | 1.21e-05 | 1.38e-04 | 33 |
GO:003090121 | Liver | HCC | midbrain development | 54/7958 | 90/18723 | 6.04e-04 | 3.79e-03 | 54 |
GO:0098732 | Liver | HCC | macromolecule deacylation | 67/7958 | 116/18723 | 6.46e-04 | 3.99e-03 | 67 |
GO:00356011 | Liver | HCC | protein deacylation | 64/7958 | 112/18723 | 1.23e-03 | 6.83e-03 | 64 |
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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 |
SUDS3 | SNV | Missense_Mutation | c.743N>T | p.Ser248Phe | p.S248F | Q9H7L9 | protein_coding | tolerated(0.06) | benign(0.364) | TCGA-GM-A2D9-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | arimidex | SD | |
SUDS3 | SNV | Missense_Mutation | novel | c.297N>C | p.Met99Ile | p.M99I | Q9H7L9 | protein_coding | tolerated(0.08) | benign(0.003) | TCGA-HN-A2NL-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cyclophosphamide | SD |
SUDS3 | SNV | Missense_Mutation | novel | c.293N>T | p.Arg98Ile | p.R98I | Q9H7L9 | protein_coding | deleterious(0.02) | probably_damaging(0.985) | TCGA-F5-6814-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
SUDS3 | insertion | Frame_Shift_Ins | novel | c.303dupA | p.Leu102ThrfsTer21 | p.L102Tfs*21 | Q9H7L9 | protein_coding | TCGA-AA-A01P-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | PD | ||
SUDS3 | SNV | Missense_Mutation | c.973C>T | p.Arg325Cys | p.R325C | Q9H7L9 | protein_coding | deleterious(0) | probably_damaging(0.982) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | |
SUDS3 | SNV | Missense_Mutation | novel | c.914G>A | p.Ser305Asn | p.S305N | Q9H7L9 | protein_coding | tolerated(0.35) | possibly_damaging(0.878) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
SUDS3 | SNV | Missense_Mutation | novel | c.604N>T | p.Pro202Ser | p.P202S | Q9H7L9 | protein_coding | deleterious(0.04) | probably_damaging(0.992) | TCGA-AJ-A3EK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | CR |
SUDS3 | SNV | Missense_Mutation | c.439A>G | p.Lys147Glu | p.K147E | Q9H7L9 | protein_coding | deleterious(0.01) | probably_damaging(0.982) | TCGA-AP-A056-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
SUDS3 | SNV | Missense_Mutation | c.328N>G | p.Ile110Val | p.I110V | Q9H7L9 | protein_coding | tolerated(0.18) | benign(0.025) | TCGA-AP-A0LM-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | cisplatin | SD | |
SUDS3 | SNV | Missense_Mutation | c.383N>G | p.Tyr128Cys | p.Y128C | Q9H7L9 | protein_coding | tolerated(0.16) | probably_damaging(0.997) | TCGA-AP-A0LM-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | cisplatin | 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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