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Gene: RRP1 |
Gene summary for RRP1 |
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Gene information | Species | Human | Gene symbol | RRP1 | Gene ID | 8568 |
Gene name | ribosomal RNA processing 1 | |
Gene Alias | D21S2056E | |
Cytomap | 21q22.3 | |
Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | P56182 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
8568 | RRP1 | LZE2T | Human | Esophagus | ESCC | 6.82e-03 | 2.10e-01 | 0.082 |
8568 | RRP1 | LZE5T | Human | Esophagus | ESCC | 4.65e-05 | 1.53e-01 | 0.0514 |
8568 | RRP1 | LZE7T | Human | Esophagus | ESCC | 8.87e-14 | 4.22e-01 | 0.0667 |
8568 | RRP1 | LZE8T | Human | Esophagus | ESCC | 1.54e-10 | 2.39e-01 | 0.067 |
8568 | RRP1 | LZE20T | Human | Esophagus | ESCC | 5.48e-11 | 1.31e-01 | 0.0662 |
8568 | RRP1 | LZE22D1 | Human | Esophagus | HGIN | 2.29e-03 | 6.43e-02 | 0.0595 |
8568 | RRP1 | LZE24T | Human | Esophagus | ESCC | 8.01e-26 | 6.53e-01 | 0.0596 |
8568 | RRP1 | LZE6T | Human | Esophagus | ESCC | 3.53e-04 | 8.97e-02 | 0.0845 |
8568 | RRP1 | P1T-E | Human | Esophagus | ESCC | 2.50e-11 | 3.49e-01 | 0.0875 |
8568 | RRP1 | P2T-E | Human | Esophagus | ESCC | 2.11e-22 | 4.87e-01 | 0.1177 |
8568 | RRP1 | P4T-E | Human | Esophagus | ESCC | 2.41e-17 | 4.82e-01 | 0.1323 |
8568 | RRP1 | P5T-E | Human | Esophagus | ESCC | 2.25e-21 | 4.93e-01 | 0.1327 |
8568 | RRP1 | P8T-E | Human | Esophagus | ESCC | 4.70e-09 | 1.44e-01 | 0.0889 |
8568 | RRP1 | P9T-E | Human | Esophagus | ESCC | 1.24e-10 | 2.46e-01 | 0.1131 |
8568 | RRP1 | P10T-E | Human | Esophagus | ESCC | 4.54e-23 | 5.16e-01 | 0.116 |
8568 | RRP1 | P11T-E | Human | Esophagus | ESCC | 2.47e-05 | 3.67e-01 | 0.1426 |
8568 | RRP1 | P12T-E | Human | Esophagus | ESCC | 4.81e-20 | 4.41e-01 | 0.1122 |
8568 | RRP1 | P15T-E | Human | Esophagus | ESCC | 1.66e-15 | 2.12e-01 | 0.1149 |
8568 | RRP1 | P16T-E | Human | Esophagus | ESCC | 5.27e-23 | 4.79e-01 | 0.1153 |
8568 | RRP1 | P17T-E | Human | Esophagus | ESCC | 4.69e-13 | 5.35e-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:002261327 | Esophagus | HGIN | ribonucleoprotein complex biogenesis | 158/2587 | 463/18723 | 2.61e-29 | 5.23e-26 | 158 |
GO:004225426 | Esophagus | HGIN | ribosome biogenesis | 101/2587 | 299/18723 | 8.74e-19 | 4.03e-16 | 101 |
GO:001607219 | Esophagus | HGIN | rRNA metabolic process | 72/2587 | 236/18723 | 2.26e-11 | 2.56e-09 | 72 |
GO:000636419 | Esophagus | HGIN | rRNA processing | 69/2587 | 225/18723 | 4.53e-11 | 5.04e-09 | 69 |
GO:003447010 | Esophagus | HGIN | ncRNA processing | 97/2587 | 395/18723 | 5.92e-09 | 3.90e-07 | 97 |
GO:00346606 | Esophagus | HGIN | ncRNA metabolic process | 104/2587 | 485/18723 | 2.26e-06 | 8.23e-05 | 104 |
GO:0022613111 | Esophagus | ESCC | ribonucleoprotein complex biogenesis | 365/8552 | 463/18723 | 1.74e-49 | 1.11e-45 | 365 |
GO:0042254111 | Esophagus | ESCC | ribosome biogenesis | 252/8552 | 299/18723 | 3.27e-44 | 1.04e-40 | 252 |
GO:0008380111 | Esophagus | ESCC | RNA splicing | 336/8552 | 434/18723 | 1.74e-42 | 3.67e-39 | 336 |
GO:003447015 | Esophagus | ESCC | ncRNA processing | 300/8552 | 395/18723 | 3.09e-35 | 3.26e-32 | 300 |
GO:0016072110 | Esophagus | ESCC | rRNA metabolic process | 197/8552 | 236/18723 | 1.31e-33 | 1.18e-30 | 197 |
GO:0006364110 | Esophagus | ESCC | rRNA processing | 189/8552 | 225/18723 | 4.88e-33 | 3.87e-30 | 189 |
GO:003466012 | Esophagus | ESCC | ncRNA metabolic process | 346/8552 | 485/18723 | 4.35e-31 | 2.51e-28 | 346 |
GO:0016032111 | Esophagus | ESCC | viral process | 301/8552 | 415/18723 | 3.34e-29 | 1.32e-26 | 301 |
GO:0043484111 | Esophagus | ESCC | regulation of RNA splicing | 116/8552 | 148/18723 | 3.18e-16 | 2.38e-14 | 116 |
GO:0042273111 | Esophagus | ESCC | ribosomal large subunit biogenesis | 65/8552 | 72/18723 | 1.53e-15 | 9.82e-14 | 65 |
GO:001908017 | Esophagus | ESCC | viral gene expression | 80/8552 | 94/18723 | 2.04e-15 | 1.28e-13 | 80 |
GO:000961518 | Esophagus | ESCC | response to virus | 238/8552 | 367/18723 | 6.65e-14 | 3.32e-12 | 238 |
GO:0044403111 | Esophagus | ESCC | biological process involved in symbiotic interaction | 186/8552 | 290/18723 | 1.43e-10 | 4.16e-09 | 186 |
GO:000047016 | Esophagus | ESCC | maturation of LSU-rRNA | 27/8552 | 28/18723 | 9.94e-09 | 2.00e-07 | 27 |
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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 |
RRP1 | SNV | Missense_Mutation | novel | c.272N>T | p.Ala91Val | p.A91V | P56182 | protein_coding | deleterious(0.02) | benign(0.255) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
RRP1 | SNV | Missense_Mutation | c.1091N>C | p.Gln364Pro | p.Q364P | P56182 | protein_coding | tolerated(0.28) | benign(0.006) | TCGA-BH-A0HA-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
RRP1 | SNV | Missense_Mutation | c.353N>G | p.Phe118Cys | p.F118C | P56182 | protein_coding | deleterious(0) | possibly_damaging(0.905) | TCGA-BH-A0HY-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | taxotere | CR | |
RRP1 | SNV | Missense_Mutation | c.677N>T | p.Pro226Leu | p.P226L | P56182 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-E2-A15G-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | arimidex | SD | |
RRP1 | SNV | Missense_Mutation | rs376330937 | c.985N>T | p.Arg329Trp | p.R329W | P56182 | protein_coding | deleterious(0) | probably_damaging(0.913) | TCGA-E2-A1BD-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | arimidex | SD |
RRP1 | insertion | Nonsense_Mutation | novel | c.1073_1074insCGCGTGGCGGATGGAACTGGCATAGGTTATCG | p.Gln358HisfsTer9 | p.Q358Hfs*9 | P56182 | protein_coding | TCGA-A2-A0EX-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD | ||
RRP1 | SNV | Missense_Mutation | c.601G>T | p.Ala201Ser | p.A201S | P56182 | protein_coding | deleterious(0) | probably_damaging(0.977) | TCGA-EK-A2RJ-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | |
RRP1 | SNV | Missense_Mutation | novel | c.1305G>C | p.Arg435Ser | p.R435S | P56182 | protein_coding | deleterious_low_confidence(0.03) | benign(0.143) | TCGA-MA-AA41-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
RRP1 | SNV | Missense_Mutation | rs367993051 | c.382N>A | p.Glu128Lys | p.E128K | P56182 | protein_coding | deleterious(0.01) | possibly_damaging(0.833) | TCGA-Q1-A6DW-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | SD |
RRP1 | SNV | Missense_Mutation | novel | c.974N>G | p.Tyr325Cys | p.Y325C | P56182 | protein_coding | tolerated(0.16) | probably_damaging(0.998) | TCGA-AD-6895-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | 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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