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Gene: MRPS23 |
Gene summary for MRPS23 |
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Gene information | Species | Human | Gene symbol | MRPS23 | Gene ID | 51649 |
Gene name | mitochondrial ribosomal protein S23 | |
Gene Alias | CGI-138 | |
Cytomap | 17q22 | |
Gene Type | protein-coding | GO ID | GO:0006412 | UniProtAcc | Q9Y3D9 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
51649 | MRPS23 | GSM4909286 | Human | Breast | IDC | 3.85e-02 | 1.89e-01 | 0.1081 |
51649 | MRPS23 | GSM4909290 | Human | Breast | IDC | 5.96e-09 | 3.76e-01 | 0.2096 |
51649 | MRPS23 | GSM4909294 | Human | Breast | IDC | 4.45e-16 | 5.63e-01 | 0.2022 |
51649 | MRPS23 | GSM4909296 | Human | Breast | IDC | 2.22e-05 | 1.05e-03 | 0.1524 |
51649 | MRPS23 | GSM4909308 | Human | Breast | IDC | 9.71e-05 | 2.35e-01 | 0.158 |
51649 | MRPS23 | GSM4909311 | Human | Breast | IDC | 1.85e-14 | -7.84e-02 | 0.1534 |
51649 | MRPS23 | GSM4909312 | Human | Breast | IDC | 2.47e-07 | 3.91e-02 | 0.1552 |
51649 | MRPS23 | GSM4909317 | Human | Breast | IDC | 4.31e-07 | 2.67e-01 | 0.1355 |
51649 | MRPS23 | GSM4909318 | Human | Breast | IDC | 1.43e-03 | 4.86e-01 | 0.2031 |
51649 | MRPS23 | GSM4909319 | Human | Breast | IDC | 7.92e-18 | 1.02e-03 | 0.1563 |
51649 | MRPS23 | GSM4909320 | Human | Breast | IDC | 2.01e-02 | 8.63e-02 | 0.1575 |
51649 | MRPS23 | GSM4909321 | Human | Breast | IDC | 3.05e-09 | 1.63e-01 | 0.1559 |
51649 | MRPS23 | brca1 | Human | Breast | Precancer | 8.85e-08 | 3.46e-01 | -0.0338 |
51649 | MRPS23 | brca2 | Human | Breast | Precancer | 3.19e-02 | 2.26e-01 | -0.024 |
51649 | MRPS23 | M1 | Human | Breast | IDC | 2.80e-09 | 3.76e-01 | 0.1577 |
51649 | MRPS23 | NCCBC14 | Human | Breast | DCIS | 3.10e-04 | 2.77e-01 | 0.2021 |
51649 | MRPS23 | NCCBC2 | Human | Breast | DCIS | 1.62e-06 | 4.96e-01 | 0.1554 |
51649 | MRPS23 | NCCBC5 | Human | Breast | DCIS | 1.91e-04 | 1.70e-01 | 0.2046 |
51649 | MRPS23 | P1 | Human | Breast | IDC | 9.20e-03 | 4.71e-02 | 0.1527 |
51649 | MRPS23 | P2 | Human | Breast | IDC | 9.01e-10 | 4.80e-01 | 0.21 |
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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 |
MRPS23 | SNV | Missense_Mutation | novel | c.462G>C | p.Leu154Phe | p.L154F | Q9Y3D9 | protein_coding | tolerated(0.07) | benign(0.054) | TCGA-C8-A3M7-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | PD |
MRPS23 | SNV | Missense_Mutation | rs145979934 | c.345N>T | p.Glu115Asp | p.E115D | Q9Y3D9 | protein_coding | tolerated(0.21) | benign(0.057) | TCGA-A6-6141-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | 5-fu | SD |
MRPS23 | SNV | Missense_Mutation | rs761410726 | c.439G>A | p.Val147Ile | p.V147I | Q9Y3D9 | protein_coding | tolerated(0.36) | benign(0) | TCGA-AA-3494-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | folinic | PR |
MRPS23 | SNV | Missense_Mutation | rs371617294 | c.167N>A | p.Ala56Asp | p.A56D | Q9Y3D9 | protein_coding | tolerated(0.16) | probably_damaging(0.959) | TCGA-AP-A051-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
MRPS23 | SNV | Missense_Mutation | rs760880323 | c.337N>T | p.Asp113Tyr | p.D113Y | Q9Y3D9 | protein_coding | deleterious(0) | probably_damaging(0.986) | TCGA-AP-A056-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
MRPS23 | SNV | Missense_Mutation | c.329G>T | p.Gly110Val | p.G110V | Q9Y3D9 | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-AP-A0LF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
MRPS23 | SNV | Missense_Mutation | rs145979934 | c.345N>T | p.Glu115Asp | p.E115D | Q9Y3D9 | protein_coding | tolerated(0.21) | benign(0.057) | TCGA-AP-A1E0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | paclitaxel | SD |
MRPS23 | SNV | Missense_Mutation | novel | c.134T>C | p.Val45Ala | p.V45A | Q9Y3D9 | protein_coding | deleterious(0.01) | possibly_damaging(0.473) | TCGA-AX-A2HC-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | paclitaxel | PD |
MRPS23 | SNV | Missense_Mutation | rs145979934 | c.345G>T | p.Glu115Asp | p.E115D | Q9Y3D9 | protein_coding | tolerated(0.21) | benign(0.057) | TCGA-EO-A3AV-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatin | CR |
MRPS23 | SNV | Missense_Mutation | novel | c.292N>T | p.Arg98Trp | p.R98W | Q9Y3D9 | protein_coding | deleterious(0) | probably_damaging(0.994) | TCGA-FI-A2D0-01 | 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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