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Gene: RPS2 |
Gene summary for RPS2 |
Gene summary. |
Gene information | Species | Human | Gene symbol | RPS2 | Gene ID | 6187 |
Gene name | ribosomal protein S2 | |
Gene Alias | LLREP3 | |
Cytomap | 16p13.3 | |
Gene Type | protein-coding | GO ID | GO:0002181 | UniProtAcc | P15880 |
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Malignant transformation analysis |
Identification of the aberrant gene expression in precancerous and cancerous lesions by comparing the gene expression of stem-like cells in diseased tissues with normal stem cells |
Malignant transformation involving gene list. |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
6187 | RPS2 | CCI_1 | Human | Cervix | CC | 2.56e-66 | -1.91e+00 | 0.528 |
6187 | RPS2 | CCI_2 | Human | Cervix | CC | 1.27e-33 | -1.09e+00 | 0.5249 |
6187 | RPS2 | CCI_3 | Human | Cervix | CC | 1.69e-62 | -1.79e+00 | 0.516 |
6187 | RPS2 | CCII_1 | Human | Cervix | CC | 4.20e-94 | -2.01e+00 | 0.3249 |
6187 | RPS2 | Tumor | Human | Cervix | CC | 7.87e-10 | -1.49e-01 | 0.1241 |
6187 | RPS2 | sample3 | Human | Cervix | CC | 1.88e-39 | -3.03e-01 | 0.1387 |
6187 | RPS2 | H2 | Human | Cervix | HSIL_HPV | 2.01e-56 | -5.69e-01 | 0.0632 |
6187 | RPS2 | T1 | Human | Cervix | CC | 6.50e-14 | -1.94e-01 | 0.0918 |
6187 | RPS2 | T2 | Human | Cervix | CC | 2.70e-05 | -2.25e-01 | 0.0709 |
6187 | RPS2 | T3 | Human | Cervix | CC | 3.73e-35 | -2.99e-01 | 0.1389 |
6187 | RPS2 | HTA11_3410_2000001011 | Human | Colorectum | AD | 8.02e-128 | 3.08e+00 | 0.0155 |
6187 | RPS2 | HTA11_2487_2000001011 | Human | Colorectum | SER | 1.02e-63 | 3.96e+00 | -0.1808 |
6187 | RPS2 | HTA11_2951_2000001011 | Human | Colorectum | AD | 1.85e-37 | 4.33e+00 | 0.0216 |
6187 | RPS2 | HTA11_1938_2000001011 | Human | Colorectum | AD | 1.52e-65 | 3.88e+00 | -0.0811 |
6187 | RPS2 | HTA11_78_2000001011 | Human | Colorectum | AD | 3.20e-74 | 3.01e+00 | -0.1088 |
6187 | RPS2 | HTA11_347_2000001011 | Human | Colorectum | AD | 2.03e-96 | 3.93e+00 | -0.1954 |
6187 | RPS2 | HTA11_411_2000001011 | Human | Colorectum | SER | 7.92e-26 | 4.03e+00 | -0.2602 |
6187 | RPS2 | HTA11_2112_2000001011 | Human | Colorectum | SER | 8.65e-15 | 3.59e+00 | -0.2196 |
6187 | RPS2 | HTA11_3361_2000001011 | Human | Colorectum | AD | 9.53e-64 | 3.74e+00 | -0.1207 |
6187 | RPS2 | HTA11_83_2000001011 | Human | Colorectum | SER | 2.24e-50 | 3.53e+00 | -0.1526 |
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Transcriptomic changes along malignancy continuum. |
∗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 |
Find out the enriched GO biological processes and KEGG pathways involved in transition from healthy to precancer to cancer |
Figure of enriched GO biological processes. |
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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Enriched GO biological processes. |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:0019693112 | Skin | cSCC | ribose phosphate metabolic process | 146/4864 | 396/18723 | 9.28e-07 | 1.68e-05 | 146 |
GO:000675324 | Skin | cSCC | nucleoside phosphate metabolic process | 176/4864 | 497/18723 | 1.55e-06 | 2.62e-05 | 176 |
GO:00004694 | Skin | cSCC | cleavage involved in rRNA processing | 19/4864 | 27/18723 | 1.72e-06 | 2.88e-05 | 19 |
GO:0046390111 | Skin | cSCC | ribose phosphate biosynthetic process | 79/4864 | 190/18723 | 1.86e-06 | 3.10e-05 | 79 |
GO:000911724 | Skin | cSCC | nucleotide metabolic process | 173/4864 | 489/18723 | 2.03e-06 | 3.35e-05 | 173 |
GO:190199114 | Skin | cSCC | negative regulation of mitotic cell cycle phase transition | 75/4864 | 179/18723 | 2.38e-06 | 3.84e-05 | 75 |
GO:0072521112 | Skin | cSCC | purine-containing compound metabolic process | 150/4864 | 416/18723 | 2.88e-06 | 4.54e-05 | 150 |
GO:004593014 | Skin | cSCC | negative regulation of mitotic cell cycle | 93/4864 | 235/18723 | 3.14e-06 | 4.89e-05 | 93 |
GO:003139817 | Skin | cSCC | positive regulation of protein ubiquitination | 54/4864 | 119/18723 | 3.61e-06 | 5.49e-05 | 54 |
GO:004578613 | Skin | cSCC | negative regulation of cell cycle | 140/4864 | 385/18723 | 3.64e-06 | 5.50e-05 | 140 |
GO:000226229 | Skin | cSCC | myeloid cell homeostasis | 67/4864 | 157/18723 | 3.79e-06 | 5.70e-05 | 67 |
GO:0010950112 | Skin | cSCC | positive regulation of endopeptidase activity | 74/4864 | 179/18723 | 4.98e-06 | 7.25e-05 | 74 |
GO:004887229 | Skin | cSCC | homeostasis of number of cells | 104/4864 | 272/18723 | 5.34e-06 | 7.71e-05 | 104 |
GO:003410129 | Skin | cSCC | erythrocyte homeostasis | 57/4864 | 129/18723 | 5.45e-06 | 7.84e-05 | 57 |
GO:000008222 | Skin | cSCC | G1/S transition of mitotic cell cycle | 85/4864 | 214/18723 | 6.90e-06 | 9.60e-05 | 85 |
GO:005143826 | Skin | cSCC | regulation of ubiquitin-protein transferase activity | 29/4864 | 53/18723 | 8.04e-06 | 1.09e-04 | 29 |
GO:0008630111 | Skin | cSCC | intrinsic apoptotic signaling pathway in response to DNA damage | 46/4864 | 99/18723 | 8.60e-06 | 1.14e-04 | 46 |
GO:190466628 | Skin | cSCC | regulation of ubiquitin protein ligase activity | 16/4864 | 23/18723 | 1.47e-05 | 1.82e-04 | 16 |
GO:00091235 | Skin | cSCC | nucleoside monophosphate metabolic process | 37/4864 | 76/18723 | 1.75e-05 | 2.11e-04 | 37 |
GO:0006163112 | Skin | cSCC | purine nucleotide metabolic process | 140/4864 | 396/18723 | 1.93e-05 | 2.27e-04 | 140 |
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Enriched KEGG pathways. |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0517120 | Cervix | CC | Coronavirus disease - COVID-19 | 111/1267 | 232/8465 | 1.82e-33 | 5.90e-31 | 3.49e-31 | 111 |
hsa05171110 | Cervix | CC | Coronavirus disease - COVID-19 | 111/1267 | 232/8465 | 1.82e-33 | 5.90e-31 | 3.49e-31 | 111 |
hsa0301025 | Cervix | HSIL_HPV | Ribosome | 80/459 | 167/8465 | 9.61e-58 | 2.82e-55 | 2.28e-55 | 80 |
hsa0517125 | Cervix | HSIL_HPV | Coronavirus disease - COVID-19 | 91/459 | 232/8465 | 2.14e-56 | 3.13e-54 | 2.53e-54 | 91 |
hsa0301035 | Cervix | HSIL_HPV | Ribosome | 80/459 | 167/8465 | 9.61e-58 | 2.82e-55 | 2.28e-55 | 80 |
hsa0517135 | Cervix | HSIL_HPV | Coronavirus disease - COVID-19 | 91/459 | 232/8465 | 2.14e-56 | 3.13e-54 | 2.53e-54 | 91 |
hsa03010 | Colorectum | AD | Ribosome | 96/2092 | 167/8465 | 8.28e-20 | 5.54e-18 | 3.54e-18 | 96 |
hsa05171 | Colorectum | AD | Coronavirus disease - COVID-19 | 113/2092 | 232/8465 | 9.90e-16 | 2.55e-14 | 1.63e-14 | 113 |
hsa030101 | Colorectum | AD | Ribosome | 96/2092 | 167/8465 | 8.28e-20 | 5.54e-18 | 3.54e-18 | 96 |
hsa051711 | Colorectum | AD | Coronavirus disease - COVID-19 | 113/2092 | 232/8465 | 9.90e-16 | 2.55e-14 | 1.63e-14 | 113 |
hsa030102 | Colorectum | SER | Ribosome | 92/1580 | 167/8465 | 2.21e-26 | 3.66e-24 | 2.66e-24 | 92 |
hsa051712 | Colorectum | SER | Coronavirus disease - COVID-19 | 98/1580 | 232/8465 | 3.33e-17 | 8.50e-16 | 6.17e-16 | 98 |
hsa030103 | Colorectum | SER | Ribosome | 92/1580 | 167/8465 | 2.21e-26 | 3.66e-24 | 2.66e-24 | 92 |
hsa051713 | Colorectum | SER | Coronavirus disease - COVID-19 | 98/1580 | 232/8465 | 3.33e-17 | 8.50e-16 | 6.17e-16 | 98 |
hsa030104 | Colorectum | MSS | Ribosome | 96/1875 | 167/8465 | 1.82e-23 | 2.03e-21 | 1.24e-21 | 96 |
hsa051714 | Colorectum | MSS | Coronavirus disease - COVID-19 | 108/1875 | 232/8465 | 6.50e-17 | 1.67e-15 | 1.03e-15 | 108 |
hsa030105 | Colorectum | MSS | Ribosome | 96/1875 | 167/8465 | 1.82e-23 | 2.03e-21 | 1.24e-21 | 96 |
hsa051715 | Colorectum | MSS | Coronavirus disease - COVID-19 | 108/1875 | 232/8465 | 6.50e-17 | 1.67e-15 | 1.03e-15 | 108 |
hsa030106 | Colorectum | MSI-H | Ribosome | 87/797 | 167/8465 | 5.55e-46 | 1.80e-43 | 1.51e-43 | 87 |
hsa051716 | Colorectum | MSI-H | Coronavirus disease - COVID-19 | 91/797 | 232/8465 | 2.21e-35 | 3.58e-33 | 3.00e-33 | 91 |
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Cell-cell communication analysis |
Identification of potential cell-cell interactions between two cell types and their ligand-receptor pairs for different disease states |
Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
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Single-cell gene regulatory network inference analysis |
Find out the significant the regulons (TFs) and the target genes of each regulon across cell types for different disease states |
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 |
Annotation of somatic variants for genes involved in malignant transformation |
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 |
RPS2 | SNV | Missense_Mutation | c.825N>C | p.Lys275Asn | p.K275N | P15880 | protein_coding | deleterious(0) | benign(0.142) | TCGA-BH-A1FC-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
RPS2 | SNV | Missense_Mutation | novel | c.137G>C | p.Arg46Pro | p.R46P | P15880 | protein_coding | tolerated(0.23) | probably_damaging(0.969) | TCGA-C5-A1BK-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
RPS2 | SNV | Missense_Mutation | c.620N>T | p.Ala207Val | p.A207V | P15880 | protein_coding | deleterious(0.05) | possibly_damaging(0.542) | TCGA-AD-6964-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | folfox | PD | |
RPS2 | SNV | Missense_Mutation | c.728C>T | p.Ala243Val | p.A243V | P15880 | protein_coding | deleterious(0.02) | probably_damaging(0.974) | TCGA-CM-4743-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Chemotherapy | capecitabine | SD | |
RPS2 | SNV | Missense_Mutation | c.580C>T | p.Arg194Cys | p.R194C | P15880 | protein_coding | tolerated(0.19) | benign(0.168) | TCGA-G5-6233-01 | Colorectum | rectum adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | 5-fluorouracil | PD | |
RPS2 | SNV | Missense_Mutation | novel | c.362N>A | p.Arg121His | p.R121H | P15880 | protein_coding | deleterious(0.04) | benign(0.427) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
RPS2 | SNV | Missense_Mutation | rs753906824 | c.820N>A | p.Val274Ile | p.V274I | P15880 | protein_coding | tolerated(0.22) | benign(0.074) | TCGA-AJ-A3EK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | CR |
RPS2 | SNV | Missense_Mutation | novel | c.557N>A | p.Gly186Asp | p.G186D | P15880 | protein_coding | deleterious(0.01) | possibly_damaging(0.905) | TCGA-AJ-A3EK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | CR |
RPS2 | SNV | Missense_Mutation | novel | c.341N>C | p.Lys114Thr | p.K114T | P15880 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-AJ-A3EK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | CR |
RPS2 | SNV | Missense_Mutation | novel | c.655A>T | p.Ile219Phe | p.I219F | P15880 | protein_coding | deleterious(0.01) | benign(0.364) | TCGA-AJ-A3NE-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
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Related drugs of malignant transformation related genes |
Identification of chemicals and drugs interact with genes involved in malignant transfromation |
(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
6187 | RPS2 | NA | FGF3 | 16263090 |
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