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Gene: PCNT |
Gene summary for PCNT |
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Gene information | Species | Human | Gene symbol | PCNT | Gene ID | 5116 |
Gene name | pericentrin | |
Gene Alias | KEN | |
Cytomap | 21q22.3 | |
Gene Type | protein-coding | GO ID | GO:0000226 | UniProtAcc | O95613 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
5116 | PCNT | LZE4T | Human | Esophagus | ESCC | 3.15e-02 | 1.17e-01 | 0.0811 |
5116 | PCNT | LZE22T | Human | Esophagus | ESCC | 4.33e-02 | 1.68e-01 | 0.068 |
5116 | PCNT | LZE24T | Human | Esophagus | ESCC | 7.35e-11 | 2.86e-01 | 0.0596 |
5116 | PCNT | P1T-E | Human | Esophagus | ESCC | 4.37e-05 | 3.06e-01 | 0.0875 |
5116 | PCNT | P2T-E | Human | Esophagus | ESCC | 1.03e-07 | 1.53e-01 | 0.1177 |
5116 | PCNT | P4T-E | Human | Esophagus | ESCC | 2.56e-09 | 2.04e-01 | 0.1323 |
5116 | PCNT | P5T-E | Human | Esophagus | ESCC | 3.28e-08 | 1.72e-01 | 0.1327 |
5116 | PCNT | P9T-E | Human | Esophagus | ESCC | 1.29e-04 | 6.20e-02 | 0.1131 |
5116 | PCNT | P10T-E | Human | Esophagus | ESCC | 3.42e-20 | 3.79e-01 | 0.116 |
5116 | PCNT | P12T-E | Human | Esophagus | ESCC | 1.23e-06 | 1.98e-01 | 0.1122 |
5116 | PCNT | P15T-E | Human | Esophagus | ESCC | 1.09e-03 | 6.81e-02 | 0.1149 |
5116 | PCNT | P16T-E | Human | Esophagus | ESCC | 6.17e-11 | 1.93e-01 | 0.1153 |
5116 | PCNT | P17T-E | Human | Esophagus | ESCC | 1.62e-05 | 1.97e-01 | 0.1278 |
5116 | PCNT | P20T-E | Human | Esophagus | ESCC | 3.64e-05 | 8.94e-02 | 0.1124 |
5116 | PCNT | P21T-E | Human | Esophagus | ESCC | 2.34e-11 | 2.13e-01 | 0.1617 |
5116 | PCNT | P22T-E | Human | Esophagus | ESCC | 1.35e-10 | 1.61e-01 | 0.1236 |
5116 | PCNT | P23T-E | Human | Esophagus | ESCC | 1.72e-03 | 1.01e-01 | 0.108 |
5116 | PCNT | P24T-E | Human | Esophagus | ESCC | 3.57e-06 | 1.47e-01 | 0.1287 |
5116 | PCNT | P26T-E | Human | Esophagus | ESCC | 8.43e-05 | 1.25e-01 | 0.1276 |
5116 | PCNT | P27T-E | Human | Esophagus | ESCC | 2.70e-16 | 3.45e-01 | 0.1055 |
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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:003238618 | Esophagus | ESCC | regulation of intracellular transport | 243/8552 | 337/18723 | 3.20e-23 | 7.25e-21 | 243 |
GO:0033157110 | Esophagus | ESCC | regulation of intracellular protein transport | 169/8552 | 229/18723 | 3.31e-18 | 3.23e-16 | 169 |
GO:0032388110 | Esophagus | ESCC | positive regulation of intracellular transport | 152/8552 | 202/18723 | 7.89e-18 | 7.36e-16 | 152 |
GO:190285015 | Esophagus | ESCC | microtubule cytoskeleton organization involved in mitosis | 116/8552 | 147/18723 | 1.25e-16 | 9.91e-15 | 116 |
GO:1904951111 | Esophagus | ESCC | positive regulation of establishment of protein localization | 216/8552 | 319/18723 | 1.01e-15 | 6.86e-14 | 216 |
GO:000705214 | Esophagus | ESCC | mitotic spindle organization | 97/8552 | 120/18723 | 2.17e-15 | 1.33e-13 | 97 |
GO:009031617 | Esophagus | ESCC | positive regulation of intracellular protein transport | 122/8552 | 160/18723 | 2.45e-15 | 1.49e-13 | 122 |
GO:0051222111 | Esophagus | ESCC | positive regulation of protein transport | 204/8552 | 303/18723 | 1.56e-14 | 8.38e-13 | 204 |
GO:000705114 | Esophagus | ESCC | spindle organization | 134/8552 | 184/18723 | 5.70e-14 | 2.87e-12 | 134 |
GO:003238621 | Liver | HCC | regulation of intracellular transport | 231/7958 | 337/18723 | 1.99e-22 | 3.40e-20 | 231 |
GO:003315721 | Liver | HCC | regulation of intracellular protein transport | 165/7958 | 229/18723 | 8.37e-20 | 1.15e-17 | 165 |
GO:003238821 | Liver | HCC | positive regulation of intracellular transport | 148/7958 | 202/18723 | 5.15e-19 | 6.66e-17 | 148 |
GO:009031621 | Liver | HCC | positive regulation of intracellular protein transport | 121/7958 | 160/18723 | 1.27e-17 | 1.39e-15 | 121 |
GO:190495122 | Liver | HCC | positive regulation of establishment of protein localization | 207/7958 | 319/18723 | 3.95e-16 | 3.29e-14 | 207 |
GO:005122222 | Liver | HCC | positive regulation of protein transport | 194/7958 | 303/18723 | 2.41e-14 | 1.56e-12 | 194 |
GO:000705111 | Liver | HCC | spindle organization | 116/7958 | 184/18723 | 1.40e-08 | 3.40e-07 | 116 |
GO:000705211 | Liver | HCC | mitotic spindle organization | 80/7958 | 120/18723 | 7.43e-08 | 1.50e-06 | 80 |
GO:190285011 | Liver | HCC | microtubule cytoskeleton organization involved in mitosis | 93/7958 | 147/18723 | 2.91e-07 | 5.09e-06 | 93 |
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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 |
PCNT | SNV | Missense_Mutation | rs375834635 | c.6095N>T | p.Ser2032Leu | p.S2032L | O95613 | protein_coding | deleterious(0) | possibly_damaging(0.474) | TCGA-BR-8487-01 | Stomach | stomach adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
PCNT | SNV | Missense_Mutation | c.3875N>C | p.Glu1292Ala | p.E1292A | O95613 | protein_coding | tolerated(0.06) | probably_damaging(0.994) | TCGA-BR-8589-01 | Stomach | stomach adenocarcinoma | Male | <65 | III/IV | Unknown | Unknown | SD | |
PCNT | SNV | Missense_Mutation | rs776782829 | c.1406N>A | p.Arg469His | p.R469H | O95613 | protein_coding | tolerated(0.27) | benign(0) | TCGA-BR-8591-01 | Stomach | stomach adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | SD |
PCNT | SNV | Missense_Mutation | rs140173772 | c.7628N>A | p.Arg2543His | p.R2543H | O95613 | protein_coding | tolerated(0.17) | benign(0.001) | TCGA-BR-8680-01 | Stomach | stomach adenocarcinoma | Male | <65 | III/IV | Chemotherapy | oxaliplatin | CR |
PCNT | SNV | Missense_Mutation | rs150279909 | c.3481N>A | p.Ala1161Thr | p.A1161T | O95613 | protein_coding | tolerated(0.39) | benign(0.005) | TCGA-CD-A4MG-01 | Stomach | stomach adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
PCNT | SNV | Missense_Mutation | c.2619N>T | p.Glu873Asp | p.E873D | O95613 | protein_coding | deleterious(0.01) | possibly_damaging(0.791) | TCGA-CG-5721-01 | Stomach | stomach adenocarcinoma | Male | <65 | III/IV | Unknown | Unknown | SD | |
PCNT | SNV | Missense_Mutation | c.4970N>G | p.Asp1657Gly | p.D1657G | O95613 | protein_coding | deleterious(0.02) | benign(0.011) | TCGA-CG-5721-01 | Stomach | stomach adenocarcinoma | Male | <65 | III/IV | Unknown | Unknown | SD | |
PCNT | SNV | Missense_Mutation | c.3595G>A | p.Ala1199Thr | p.A1199T | O95613 | protein_coding | tolerated(0.14) | benign(0.253) | TCGA-CG-5726-01 | Stomach | stomach adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
PCNT | SNV | Missense_Mutation | rs886057194 | c.9211N>G | p.Arg3071Gly | p.R3071G | O95613 | protein_coding | deleterious(0) | benign(0.003) | TCGA-D7-A4YY-01 | Stomach | stomach adenocarcinoma | Male | <65 | III/IV | Chemotherapy | 5-fluorouracil | SD |
PCNT | SNV | Missense_Mutation | rs772942335 | c.5890N>A | p.Ala1964Thr | p.A1964T | O95613 | protein_coding | tolerated(0.34) | benign(0.003) | TCGA-HU-A4G8-01 | Stomach | stomach adenocarcinoma | Female | >=65 | I/II | Chemotherapy | 5-fluorouracil | 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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