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Gene: RPA2 |
Gene summary for RPA2 |
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Gene information | Species | Human | Gene symbol | RPA2 | Gene ID | 6118 |
Gene name | replication protein A2 | |
Gene Alias | REPA2 | |
Cytomap | 1p35.3 | |
Gene Type | protein-coding | GO ID | GO:0000018 | UniProtAcc | B4DUL2 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
6118 | RPA2 | LZE4T | Human | Esophagus | ESCC | 9.39e-08 | 2.63e-01 | 0.0811 |
6118 | RPA2 | LZE7T | Human | Esophagus | ESCC | 1.44e-08 | 4.07e-01 | 0.0667 |
6118 | RPA2 | LZE8T | Human | Esophagus | ESCC | 9.10e-04 | 1.01e-01 | 0.067 |
6118 | RPA2 | LZE20T | Human | Esophagus | ESCC | 6.68e-03 | 1.75e-01 | 0.0662 |
6118 | RPA2 | LZE22T | Human | Esophagus | ESCC | 4.67e-03 | 3.34e-01 | 0.068 |
6118 | RPA2 | LZE24T | Human | Esophagus | ESCC | 4.52e-15 | 3.66e-01 | 0.0596 |
6118 | RPA2 | LZE21T | Human | Esophagus | ESCC | 2.82e-04 | 2.45e-01 | 0.0655 |
6118 | RPA2 | LZE6T | Human | Esophagus | ESCC | 1.71e-04 | 2.41e-01 | 0.0845 |
6118 | RPA2 | P1T-E | Human | Esophagus | ESCC | 4.37e-04 | 4.40e-01 | 0.0875 |
6118 | RPA2 | P2T-E | Human | Esophagus | ESCC | 5.38e-34 | 6.11e-01 | 0.1177 |
6118 | RPA2 | P4T-E | Human | Esophagus | ESCC | 1.87e-20 | 5.30e-01 | 0.1323 |
6118 | RPA2 | P5T-E | Human | Esophagus | ESCC | 3.59e-22 | 4.58e-01 | 0.1327 |
6118 | RPA2 | P8T-E | Human | Esophagus | ESCC | 7.39e-25 | 5.06e-01 | 0.0889 |
6118 | RPA2 | P9T-E | Human | Esophagus | ESCC | 9.65e-06 | 2.05e-01 | 0.1131 |
6118 | RPA2 | P10T-E | Human | Esophagus | ESCC | 6.11e-55 | 1.08e+00 | 0.116 |
6118 | RPA2 | P11T-E | Human | Esophagus | ESCC | 3.35e-11 | 5.86e-01 | 0.1426 |
6118 | RPA2 | P12T-E | Human | Esophagus | ESCC | 4.96e-21 | 3.47e-01 | 0.1122 |
6118 | RPA2 | P15T-E | Human | Esophagus | ESCC | 2.77e-15 | 3.80e-01 | 0.1149 |
6118 | RPA2 | P16T-E | Human | Esophagus | ESCC | 1.42e-15 | 3.30e-01 | 0.1153 |
6118 | RPA2 | P17T-E | Human | Esophagus | ESCC | 1.26e-06 | 3.60e-01 | 0.1278 |
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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). |
Page: 1 2 3 4 5 6 7 8 9 |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:001094811 | Oral cavity | LP | negative regulation of cell cycle process | 95/4623 | 294/18723 | 1.80e-03 | 1.37e-02 | 95 |
GO:200004512 | Oral cavity | LP | regulation of G1/S transition of mitotic cell cycle | 51/4623 | 142/18723 | 1.81e-03 | 1.37e-02 | 51 |
GO:00062841 | Oral cavity | LP | base-excision repair | 19/4623 | 43/18723 | 4.04e-03 | 2.61e-02 | 19 |
GO:190198811 | Oral cavity | LP | negative regulation of cell cycle phase transition | 80/4623 | 249/18723 | 4.63e-03 | 2.94e-02 | 80 |
GO:000007511 | Oral cavity | LP | cell cycle checkpoint | 57/4623 | 169/18723 | 5.05e-03 | 3.14e-02 | 57 |
GO:000630211 | Oral cavity | LP | double-strand break repair | 80/4623 | 251/18723 | 5.81e-03 | 3.46e-02 | 80 |
GO:004477311 | Oral cavity | LP | mitotic DNA damage checkpoint | 30/4623 | 81/18723 | 8.95e-03 | 4.82e-02 | 30 |
GO:000734617 | Skin | cSCC | regulation of mitotic cell cycle | 192/4864 | 457/18723 | 3.47e-14 | 2.31e-12 | 192 |
GO:004477223 | Skin | cSCC | mitotic cell cycle phase transition | 180/4864 | 424/18723 | 7.09e-14 | 4.45e-12 | 180 |
GO:190199014 | Skin | cSCC | regulation of mitotic cell cycle phase transition | 128/4864 | 299/18723 | 1.48e-10 | 6.56e-09 | 128 |
GO:0000723110 | Skin | cSCC | telomere maintenance | 68/4864 | 131/18723 | 1.97e-10 | 8.53e-09 | 68 |
GO:190198714 | Skin | cSCC | regulation of cell cycle phase transition | 150/4864 | 390/18723 | 3.21e-08 | 8.61e-07 | 150 |
GO:000626012 | Skin | cSCC | DNA replication | 106/4864 | 260/18723 | 1.18e-07 | 2.77e-06 | 106 |
GO:005105217 | Skin | cSCC | regulation of DNA metabolic process | 136/4864 | 359/18723 | 3.83e-07 | 7.58e-06 | 136 |
GO:190199114 | Skin | cSCC | negative regulation of mitotic cell cycle phase transition | 75/4864 | 179/18723 | 2.38e-06 | 3.84e-05 | 75 |
GO:003220015 | Skin | cSCC | telomere organization | 68/4864 | 159/18723 | 2.94e-06 | 4.62e-05 | 68 |
GO:004593014 | Skin | cSCC | negative regulation of mitotic cell cycle | 93/4864 | 235/18723 | 3.14e-06 | 4.89e-05 | 93 |
GO:004578613 | Skin | cSCC | negative regulation of cell cycle | 140/4864 | 385/18723 | 3.64e-06 | 5.50e-05 | 140 |
GO:00345025 | Skin | cSCC | protein localization to chromosome | 44/4864 | 92/18723 | 5.27e-06 | 7.64e-05 | 44 |
GO:2001020111 | Skin | cSCC | regulation of response to DNA damage stimulus | 87/4864 | 219/18723 | 5.38e-06 | 7.75e-05 | 87 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0342022 | Esophagus | ESCC | Nucleotide excision repair | 54/4205 | 63/8465 | 2.01e-09 | 2.17e-08 | 1.11e-08 | 54 |
hsa030304 | Esophagus | ESCC | DNA replication | 32/4205 | 36/8465 | 7.71e-07 | 5.06e-06 | 2.59e-06 | 32 |
hsa034304 | Esophagus | ESCC | Mismatch repair | 21/4205 | 23/8465 | 2.85e-05 | 1.35e-04 | 6.90e-05 | 21 |
hsa0342032 | Esophagus | ESCC | Nucleotide excision repair | 54/4205 | 63/8465 | 2.01e-09 | 2.17e-08 | 1.11e-08 | 54 |
hsa0303011 | Esophagus | ESCC | DNA replication | 32/4205 | 36/8465 | 7.71e-07 | 5.06e-06 | 2.59e-06 | 32 |
hsa0343011 | Esophagus | ESCC | Mismatch repair | 21/4205 | 23/8465 | 2.85e-05 | 1.35e-04 | 6.90e-05 | 21 |
hsa03420 | Liver | Cirrhotic | Nucleotide excision repair | 29/2530 | 63/8465 | 4.81e-03 | 1.74e-02 | 1.07e-02 | 29 |
hsa034201 | Liver | Cirrhotic | Nucleotide excision repair | 29/2530 | 63/8465 | 4.81e-03 | 1.74e-02 | 1.07e-02 | 29 |
hsa034202 | Liver | HCC | Nucleotide excision repair | 41/4020 | 63/8465 | 3.59e-03 | 1.12e-02 | 6.22e-03 | 41 |
hsa034203 | Liver | HCC | Nucleotide excision repair | 41/4020 | 63/8465 | 3.59e-03 | 1.12e-02 | 6.22e-03 | 41 |
hsa034204 | Oral cavity | OSCC | Nucleotide excision repair | 49/3704 | 63/8465 | 3.48e-08 | 2.91e-07 | 1.48e-07 | 49 |
hsa03030 | Oral cavity | OSCC | DNA replication | 31/3704 | 36/8465 | 1.70e-07 | 1.19e-06 | 6.03e-07 | 31 |
hsa03430 | Oral cavity | OSCC | Mismatch repair | 19/3704 | 23/8465 | 1.55e-04 | 5.34e-04 | 2.72e-04 | 19 |
hsa0342011 | Oral cavity | OSCC | Nucleotide excision repair | 49/3704 | 63/8465 | 3.48e-08 | 2.91e-07 | 1.48e-07 | 49 |
hsa030301 | Oral cavity | OSCC | DNA replication | 31/3704 | 36/8465 | 1.70e-07 | 1.19e-06 | 6.03e-07 | 31 |
hsa034301 | Oral cavity | OSCC | Mismatch repair | 19/3704 | 23/8465 | 1.55e-04 | 5.34e-04 | 2.72e-04 | 19 |
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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 |
RPA2 | SNV | Missense_Mutation | c.279N>T | p.Lys93Asn | p.K93N | P15927 | protein_coding | deleterious(0.01) | benign(0.44) | TCGA-A2-A25B-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | taxotere | PD | |
RPA2 | SNV | Missense_Mutation | novel | c.215N>A | p.Phe72Tyr | p.F72Y | P15927 | protein_coding | deleterious(0.01) | possibly_damaging(0.906) | TCGA-Z7-A8R6-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | taxol | CR |
RPA2 | SNV | Missense_Mutation | rs755345876 | c.92N>T | p.Ser31Phe | p.S31F | P15927 | protein_coding | deleterious(0) | possibly_damaging(0.907) | TCGA-AA-3984-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
RPA2 | SNV | Missense_Mutation | c.331G>T | p.Asp111Tyr | p.D111Y | P15927 | protein_coding | deleterious(0) | probably_damaging(0.942) | TCGA-G4-6311-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | oxaliplatin | SD | |
RPA2 | SNV | Missense_Mutation | novel | c.307N>T | p.Asp103Tyr | p.D103Y | P15927 | protein_coding | deleterious(0.03) | probably_damaging(0.999) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
RPA2 | SNV | Missense_Mutation | novel | c.758C>A | p.Ala253Asp | p.A253D | P15927 | protein_coding | deleterious(0) | benign(0.319) | TCGA-AJ-A3EK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | CR |
RPA2 | SNV | Missense_Mutation | novel | c.139T>G | p.Ser47Ala | p.S47A | P15927 | protein_coding | tolerated(0.19) | benign(0.022) | TCGA-AP-A1E0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | paclitaxel | SD |
RPA2 | SNV | Missense_Mutation | novel | c.276G>T | p.Glu92Asp | p.E92D | P15927 | protein_coding | tolerated(0.17) | benign(0.003) | TCGA-AX-A2HC-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | paclitaxel | PD |
RPA2 | SNV | Missense_Mutation | c.568N>T | p.Pro190Ser | p.P190S | P15927 | protein_coding | tolerated(0.37) | benign(0.007) | TCGA-B5-A0K6-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
RPA2 | SNV | Missense_Mutation | c.624G>A | p.Met208Ile | p.M208I | P15927 | protein_coding | tolerated(0.48) | benign(0.001) | TCGA-B5-A11E-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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