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Gene: RRP8 |
Gene summary for RRP8 |
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Gene information | Species | Human | Gene symbol | RRP8 | Gene ID | 23378 |
Gene name | ribosomal RNA processing 8 | |
Gene Alias | KIAA0409 | |
Cytomap | 11p15.4 | |
Gene Type | protein-coding | GO ID | GO:0000183 | UniProtAcc | O43159 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
23378 | RRP8 | LZE4T | Human | Esophagus | ESCC | 4.34e-02 | 1.20e-01 | 0.0811 |
23378 | RRP8 | LZE7T | Human | Esophagus | ESCC | 2.60e-07 | 2.31e-01 | 0.0667 |
23378 | RRP8 | LZE8T | Human | Esophagus | ESCC | 6.02e-05 | 1.59e-01 | 0.067 |
23378 | RRP8 | LZE20T | Human | Esophagus | ESCC | 2.65e-03 | 1.01e-01 | 0.0662 |
23378 | RRP8 | LZE24T | Human | Esophagus | ESCC | 1.39e-08 | 2.33e-01 | 0.0596 |
23378 | RRP8 | P1T-E | Human | Esophagus | ESCC | 2.80e-03 | 1.51e-01 | 0.0875 |
23378 | RRP8 | P2T-E | Human | Esophagus | ESCC | 2.52e-18 | 2.49e-01 | 0.1177 |
23378 | RRP8 | P4T-E | Human | Esophagus | ESCC | 1.34e-07 | 1.95e-01 | 0.1323 |
23378 | RRP8 | P5T-E | Human | Esophagus | ESCC | 1.52e-08 | 1.84e-01 | 0.1327 |
23378 | RRP8 | P8T-E | Human | Esophagus | ESCC | 4.83e-15 | 1.31e-01 | 0.0889 |
23378 | RRP8 | P9T-E | Human | Esophagus | ESCC | 1.72e-11 | 2.62e-01 | 0.1131 |
23378 | RRP8 | P10T-E | Human | Esophagus | ESCC | 1.65e-17 | 2.77e-01 | 0.116 |
23378 | RRP8 | P11T-E | Human | Esophagus | ESCC | 6.58e-10 | 4.62e-01 | 0.1426 |
23378 | RRP8 | P12T-E | Human | Esophagus | ESCC | 8.48e-10 | 1.93e-01 | 0.1122 |
23378 | RRP8 | P15T-E | Human | Esophagus | ESCC | 6.61e-11 | 2.37e-01 | 0.1149 |
23378 | RRP8 | P16T-E | Human | Esophagus | ESCC | 3.83e-12 | 1.35e-01 | 0.1153 |
23378 | RRP8 | P17T-E | Human | Esophagus | ESCC | 2.46e-07 | 3.76e-01 | 0.1278 |
23378 | RRP8 | P19T-E | Human | Esophagus | ESCC | 8.01e-04 | 3.82e-01 | 0.1662 |
23378 | RRP8 | P20T-E | Human | Esophagus | ESCC | 6.22e-11 | 2.55e-01 | 0.1124 |
23378 | RRP8 | P21T-E | Human | Esophagus | ESCC | 1.42e-14 | 1.97e-01 | 0.1617 |
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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:00708281 | Esophagus | ESCC | heterochromatin organization | 31/8552 | 46/18723 | 2.42e-03 | 1.06e-02 | 31 |
GO:0045814 | Esophagus | ESCC | negative regulation of gene expression, epigenetic | 32/8552 | 50/18723 | 6.90e-03 | 2.52e-02 | 32 |
GO:002261322 | Liver | HCC | ribonucleoprotein complex biogenesis | 355/7958 | 463/18723 | 7.76e-52 | 4.92e-48 | 355 |
GO:004225422 | Liver | HCC | ribosome biogenesis | 246/7958 | 299/18723 | 4.99e-46 | 1.58e-42 | 246 |
GO:00344702 | Liver | HCC | ncRNA processing | 293/7958 | 395/18723 | 4.26e-38 | 6.76e-35 | 293 |
GO:001607212 | Liver | HCC | rRNA metabolic process | 193/7958 | 236/18723 | 1.26e-35 | 1.14e-32 | 193 |
GO:000636421 | Liver | HCC | rRNA processing | 185/7958 | 225/18723 | 8.14e-35 | 6.45e-32 | 185 |
GO:00346601 | Liver | HCC | ncRNA metabolic process | 332/7958 | 485/18723 | 1.48e-31 | 7.80e-29 | 332 |
GO:009719322 | Liver | HCC | intrinsic apoptotic signaling pathway | 184/7958 | 288/18723 | 1.50e-13 | 8.32e-12 | 184 |
GO:003166722 | Liver | HCC | response to nutrient levels | 276/7958 | 474/18723 | 2.30e-12 | 1.08e-10 | 276 |
GO:007149622 | Liver | HCC | cellular response to external stimulus | 191/7958 | 320/18723 | 3.40e-10 | 1.13e-08 | 191 |
GO:007233122 | Liver | HCC | signal transduction by p53 class mediator | 108/7958 | 163/18723 | 7.14e-10 | 2.23e-08 | 108 |
GO:003166812 | Liver | HCC | cellular response to extracellular stimulus | 149/7958 | 246/18723 | 7.35e-09 | 1.86e-07 | 149 |
GO:0032259 | Liver | HCC | methylation | 206/7958 | 364/18723 | 3.35e-08 | 7.53e-07 | 206 |
GO:004259421 | Liver | HCC | response to starvation | 121/7958 | 197/18723 | 6.08e-08 | 1.28e-06 | 121 |
GO:003166912 | Liver | HCC | cellular response to nutrient levels | 130/7958 | 215/18723 | 7.52e-08 | 1.51e-06 | 130 |
GO:000926712 | Liver | HCC | cellular response to starvation | 94/7958 | 156/18723 | 5.61e-06 | 6.95e-05 | 94 |
GO:00069971 | Liver | HCC | nucleus organization | 82/7958 | 133/18723 | 6.32e-06 | 7.72e-05 | 82 |
GO:007233212 | Liver | HCC | intrinsic apoptotic signaling pathway by p53 class mediator | 51/7958 | 76/18723 | 1.27e-05 | 1.42e-04 | 51 |
GO:000632511 | Liver | HCC | chromatin organization | 206/7958 | 409/18723 | 7.23e-04 | 4.41e-03 | 206 |
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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 |
RRP8 | insertion | Nonsense_Mutation | novel | c.388_389insGCTGCTCCATATCCCTTTATTTGGATATATTATAATCTAACT | p.Glu130delinsGlyCysSerIleSerLeuTyrLeuAspIleLeuTerSerAsnTer | p.E130delinsGCSISLYLDIL*SN* | O43159 | protein_coding | TCGA-AR-A0TY-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unspecific | Paclitaxel | PD | ||
RRP8 | SNV | Missense_Mutation | rs761872259 | c.1202N>A | p.Arg401Gln | p.R401Q | O43159 | protein_coding | tolerated(0.11) | benign(0.009) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
RRP8 | SNV | Missense_Mutation | novel | c.1042N>A | p.Ala348Thr | p.A348T | O43159 | protein_coding | deleterious(0.05) | possibly_damaging(0.506) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
RRP8 | SNV | Missense_Mutation | c.703N>A | p.Ala235Thr | p.A235T | O43159 | protein_coding | tolerated(0.06) | benign(0.074) | TCGA-AD-5900-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
RRP8 | SNV | Missense_Mutation | rs770567575 | c.718G>A | p.Ala240Thr | p.A240T | O43159 | protein_coding | tolerated(0.06) | benign(0.294) | TCGA-AG-A036-01 | Colorectum | rectum adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | 5-fluorouracil | CR |
RRP8 | SNV | Missense_Mutation | rs763957188 | c.1213C>T | p.Arg405Trp | p.R405W | O43159 | protein_coding | deleterious(0) | possibly_damaging(0.812) | TCGA-CL-5918-01 | Colorectum | rectum adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
RRP8 | SNV | Missense_Mutation | c.791G>A | p.Ser264Asn | p.S264N | O43159 | protein_coding | tolerated(0.06) | benign(0.012) | TCGA-DY-A1DC-01 | Colorectum | rectum adenocarcinoma | Female | >=65 | I/II | Chemotherapy | capecitabine | PR | |
RRP8 | insertion | Frame_Shift_Ins | novel | c.648dupC | p.Thr217HisfsTer16 | p.T217Hfs*16 | O43159 | protein_coding | TCGA-EI-6507-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | ||
RRP8 | SNV | Missense_Mutation | novel | c.889N>A | p.Asp297Asn | p.D297N | O43159 | protein_coding | tolerated(0.15) | possibly_damaging(0.679) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
RRP8 | SNV | Missense_Mutation | novel | c.696N>T | p.Glu232Asp | p.E232D | O43159 | protein_coding | tolerated(0.12) | benign(0.037) | TCGA-A5-A1OF-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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