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Gene: GSDMC |
Gene summary for GSDMC |
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Gene information | Species | Human | Gene symbol | GSDMC | Gene ID | 56169 |
Gene name | gasdermin C | |
Gene Alias | MLZE | |
Cytomap | 8q24.21 | |
Gene Type | protein-coding | GO ID | GO:0002376 | UniProtAcc | Q9BYG8 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
56169 | GSDMC | LZE4T | Human | Esophagus | ESCC | 6.95e-04 | 3.24e-01 | 0.0811 |
56169 | GSDMC | LZE22T | Human | Esophagus | ESCC | 3.93e-02 | 4.58e-01 | 0.068 |
56169 | GSDMC | P5T-E | Human | Esophagus | ESCC | 7.61e-16 | 5.37e-01 | 0.1327 |
56169 | GSDMC | P8T-E | Human | Esophagus | ESCC | 2.51e-02 | 6.99e-02 | 0.0889 |
56169 | GSDMC | P9T-E | Human | Esophagus | ESCC | 2.60e-12 | 2.52e-01 | 0.1131 |
56169 | GSDMC | P10T-E | Human | Esophagus | ESCC | 1.68e-04 | 1.95e-01 | 0.116 |
56169 | GSDMC | P11T-E | Human | Esophagus | ESCC | 1.13e-09 | 4.58e-01 | 0.1426 |
56169 | GSDMC | P12T-E | Human | Esophagus | ESCC | 7.08e-10 | 2.75e-01 | 0.1122 |
56169 | GSDMC | P15T-E | Human | Esophagus | ESCC | 4.38e-13 | 4.47e-01 | 0.1149 |
56169 | GSDMC | P17T-E | Human | Esophagus | ESCC | 4.40e-06 | 5.28e-01 | 0.1278 |
56169 | GSDMC | P19T-E | Human | Esophagus | ESCC | 1.50e-04 | 6.41e-01 | 0.1662 |
56169 | GSDMC | P21T-E | Human | Esophagus | ESCC | 9.04e-32 | 7.43e-01 | 0.1617 |
56169 | GSDMC | P23T-E | Human | Esophagus | ESCC | 6.95e-04 | 1.65e-01 | 0.108 |
56169 | GSDMC | P24T-E | Human | Esophagus | ESCC | 1.56e-02 | -2.58e-03 | 0.1287 |
56169 | GSDMC | P26T-E | Human | Esophagus | ESCC | 3.76e-06 | 2.29e-01 | 0.1276 |
56169 | GSDMC | P28T-E | Human | Esophagus | ESCC | 7.52e-09 | 7.94e-02 | 0.1149 |
56169 | GSDMC | P30T-E | Human | Esophagus | ESCC | 3.04e-09 | 5.54e-01 | 0.137 |
56169 | GSDMC | P31T-E | Human | Esophagus | ESCC | 7.20e-09 | 2.76e-01 | 0.1251 |
56169 | GSDMC | P36T-E | Human | Esophagus | ESCC | 2.09e-02 | 1.80e-01 | 0.1187 |
56169 | GSDMC | P37T-E | Human | Esophagus | ESCC | 3.77e-11 | 2.42e-01 | 0.1371 |
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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 |
GSDMC | SNV | Missense_Mutation | c.542A>T | p.Lys181Ile | p.K181I | Q9BYG8 | protein_coding | deleterious(0) | possibly_damaging(0.492) | TCGA-AX-A0J0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
GSDMC | SNV | Missense_Mutation | rs114264223 | c.1234G>A | p.Asp412Asn | p.D412N | Q9BYG8 | protein_coding | tolerated(0.41) | benign(0.142) | TCGA-AX-A1CN-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unspecific | Carboplatin | PD |
GSDMC | SNV | Missense_Mutation | novel | c.1516N>A | p.Ala506Thr | p.A506T | Q9BYG8 | protein_coding | tolerated(0.09) | possibly_damaging(0.7) | TCGA-BK-A13B-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | PD |
GSDMC | SNV | Missense_Mutation | novel | c.650N>T | p.Arg217Ile | p.R217I | Q9BYG8 | protein_coding | deleterious(0) | possibly_damaging(0.812) | TCGA-BK-A6W3-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
GSDMC | SNV | Missense_Mutation | rs770331372 | c.892N>A | p.Glu298Lys | p.E298K | Q9BYG8 | protein_coding | tolerated(0.77) | benign(0) | TCGA-D1-A17Q-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
GSDMC | SNV | Missense_Mutation | novel | c.58N>T | p.Asp20Tyr | p.D20Y | Q9BYG8 | protein_coding | deleterious(0) | probably_damaging(0.995) | TCGA-E6-A1LX-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
GSDMC | SNV | Missense_Mutation | c.846N>T | p.Glu282Asp | p.E282D | Q9BYG8 | protein_coding | tolerated(0.63) | benign(0.028) | TCGA-EO-A22R-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
GSDMC | SNV | Missense_Mutation | rs753360215 | c.1360N>A | p.Ala454Thr | p.A454T | Q9BYG8 | protein_coding | deleterious(0.03) | probably_damaging(1) | TCGA-EO-A22X-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unspecific | Carboplatin | Complete Response |
GSDMC | SNV | Missense_Mutation | novel | c.897N>C | p.Gln299His | p.Q299H | Q9BYG8 | protein_coding | tolerated(0.22) | benign(0.392) | TCGA-EO-A22X-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unspecific | Carboplatin | Complete Response |
GSDMC | SNV | Missense_Mutation | novel | c.1073T>C | p.Leu358Pro | p.L358P | Q9BYG8 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-EO-A3AS-01 | Endometrium | uterine corpus endometrioid 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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