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Gene: PDCL |
Gene summary for PDCL |
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Gene information | Species | Human | Gene symbol | PDCL | Gene ID | 5082 |
Gene name | phosducin like | |
Gene Alias | PhLP | |
Cytomap | 9q33.2 | |
Gene Type | protein-coding | GO ID | GO:0003008 | UniProtAcc | Q13371 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
5082 | PDCL | LZE4T | Human | Esophagus | ESCC | 2.56e-14 | 3.66e-01 | 0.0811 |
5082 | PDCL | LZE7T | Human | Esophagus | ESCC | 7.91e-13 | 4.33e-01 | 0.0667 |
5082 | PDCL | LZE20T | Human | Esophagus | ESCC | 1.34e-05 | 2.13e-01 | 0.0662 |
5082 | PDCL | LZE24T | Human | Esophagus | ESCC | 1.52e-16 | 2.66e-01 | 0.0596 |
5082 | PDCL | LZE21T | Human | Esophagus | ESCC | 8.81e-03 | 1.49e-01 | 0.0655 |
5082 | PDCL | LZE6T | Human | Esophagus | ESCC | 3.93e-04 | 1.62e-01 | 0.0845 |
5082 | PDCL | P1T-E | Human | Esophagus | ESCC | 1.29e-05 | 3.07e-01 | 0.0875 |
5082 | PDCL | P2T-E | Human | Esophagus | ESCC | 1.46e-32 | 5.24e-01 | 0.1177 |
5082 | PDCL | P4T-E | Human | Esophagus | ESCC | 1.05e-20 | 4.71e-01 | 0.1323 |
5082 | PDCL | P5T-E | Human | Esophagus | ESCC | 3.96e-03 | 1.20e-01 | 0.1327 |
5082 | PDCL | P8T-E | Human | Esophagus | ESCC | 3.31e-08 | 2.13e-01 | 0.0889 |
5082 | PDCL | P9T-E | Human | Esophagus | ESCC | 1.71e-07 | 2.14e-01 | 0.1131 |
5082 | PDCL | P10T-E | Human | Esophagus | ESCC | 2.52e-19 | 2.52e-01 | 0.116 |
5082 | PDCL | P11T-E | Human | Esophagus | ESCC | 2.34e-15 | 5.94e-01 | 0.1426 |
5082 | PDCL | P12T-E | Human | Esophagus | ESCC | 4.86e-17 | 3.29e-01 | 0.1122 |
5082 | PDCL | P15T-E | Human | Esophagus | ESCC | 1.49e-12 | 3.03e-01 | 0.1149 |
5082 | PDCL | P16T-E | Human | Esophagus | ESCC | 2.15e-12 | 2.09e-01 | 0.1153 |
5082 | PDCL | P17T-E | Human | Esophagus | ESCC | 1.17e-07 | 3.29e-01 | 0.1278 |
5082 | PDCL | P19T-E | Human | Esophagus | ESCC | 3.76e-05 | 2.56e-01 | 0.1662 |
5082 | PDCL | P20T-E | Human | Esophagus | ESCC | 2.56e-09 | 1.44e-01 | 0.1124 |
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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). |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:004217627 | Esophagus | HGIN | regulation of protein catabolic process | 119/2587 | 391/18723 | 8.09e-18 | 2.43e-15 | 119 |
GO:003164727 | Esophagus | HGIN | regulation of protein stability | 96/2587 | 298/18723 | 2.21e-16 | 5.76e-14 | 96 |
GO:000645720 | Esophagus | HGIN | protein folding | 75/2587 | 212/18723 | 1.61e-15 | 3.86e-13 | 75 |
GO:190336227 | Esophagus | HGIN | regulation of cellular protein catabolic process | 81/2587 | 255/18723 | 1.16e-13 | 1.93e-11 | 81 |
GO:005082127 | Esophagus | HGIN | protein stabilization | 64/2587 | 191/18723 | 3.11e-12 | 4.24e-10 | 64 |
GO:190305027 | Esophagus | HGIN | regulation of proteolysis involved in cellular protein catabolic process | 70/2587 | 221/18723 | 6.21e-12 | 7.76e-10 | 70 |
GO:000989520 | Esophagus | HGIN | negative regulation of catabolic process | 87/2587 | 320/18723 | 1.74e-10 | 1.68e-08 | 87 |
GO:003133026 | Esophagus | HGIN | negative regulation of cellular catabolic process | 74/2587 | 262/18723 | 6.27e-10 | 5.30e-08 | 74 |
GO:200005827 | Esophagus | HGIN | regulation of ubiquitin-dependent protein catabolic process | 53/2587 | 164/18723 | 9.89e-10 | 8.13e-08 | 53 |
GO:003460520 | Esophagus | HGIN | cellular response to heat | 30/2587 | 69/18723 | 1.78e-09 | 1.35e-07 | 30 |
GO:006107720 | Esophagus | HGIN | chaperone-mediated protein folding | 27/2587 | 67/18723 | 7.99e-08 | 4.20e-06 | 27 |
GO:004217720 | Esophagus | HGIN | negative regulation of protein catabolic process | 37/2587 | 121/18723 | 1.47e-06 | 5.56e-05 | 37 |
GO:000940819 | Esophagus | HGIN | response to heat | 34/2587 | 110/18723 | 2.94e-06 | 1.01e-04 | 34 |
GO:000926618 | Esophagus | HGIN | response to temperature stimulus | 42/2587 | 178/18723 | 2.91e-04 | 4.98e-03 | 42 |
GO:190336319 | Esophagus | HGIN | negative regulation of cellular protein catabolic process | 22/2587 | 75/18723 | 3.62e-04 | 5.68e-03 | 22 |
GO:200005920 | Esophagus | HGIN | negative regulation of ubiquitin-dependent protein catabolic process | 16/2587 | 48/18723 | 4.73e-04 | 6.93e-03 | 16 |
GO:190305119 | Esophagus | HGIN | negative regulation of proteolysis involved in cellular protein catabolic process | 18/2587 | 64/18723 | 2.03e-03 | 2.13e-02 | 18 |
GO:004586126 | Esophagus | HGIN | negative regulation of proteolysis | 68/2587 | 351/18723 | 2.21e-03 | 2.28e-02 | 68 |
GO:0042176111 | Esophagus | ESCC | regulation of protein catabolic process | 280/8552 | 391/18723 | 8.65e-26 | 2.39e-23 | 280 |
GO:0031647111 | Esophagus | ESCC | regulation of protein stability | 223/8552 | 298/18723 | 5.76e-25 | 1.52e-22 | 223 |
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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 |
PDCL | SNV | Missense_Mutation | novel | c.79N>A | p.His27Asn | p.H27N | Q13371 | protein_coding | tolerated(0.52) | benign(0) | TCGA-A2-A25B-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | taxotere | PD |
PDCL | insertion | In_Frame_Ins | novel | c.832_833insGTCTTGATCCTGTAAAGG | p.Lys277_Glu278insGlyLeuAspProValLys | p.K277_E278insGLDPVK | Q13371 | protein_coding | TCGA-BH-A0HK-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | arimidex | SD | ||
PDCL | SNV | Missense_Mutation | c.506G>T | p.Gly169Val | p.G169V | Q13371 | protein_coding | tolerated(0.09) | benign(0.158) | TCGA-AA-3681-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
PDCL | SNV | Missense_Mutation | rs756766356 | c.82N>A | p.Glu28Lys | p.E28K | Q13371 | protein_coding | tolerated(0.18) | benign(0.003) | TCGA-AA-3864-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
PDCL | SNV | Missense_Mutation | c.857N>A | p.Arg286His | p.R286H | Q13371 | protein_coding | tolerated(0.21) | benign(0.005) | TCGA-AZ-6603-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
PDCL | SNV | Missense_Mutation | novel | c.20A>G | p.Lys7Arg | p.K7R | Q13371 | protein_coding | tolerated(0.14) | benign(0.276) | TCGA-CA-6717-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | oxaliplatin | CR |
PDCL | SNV | Missense_Mutation | novel | c.695N>A | p.Ala232Asp | p.A232D | Q13371 | protein_coding | deleterious(0) | probably_damaging(0.968) | TCGA-AG-A00Y-01 | Colorectum | rectum adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
PDCL | SNV | Missense_Mutation | novel | c.421N>T | p.Arg141Trp | p.R141W | Q13371 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
PDCL | SNV | Missense_Mutation | rs374915234 | c.151N>A | p.Glu51Lys | p.E51K | Q13371 | protein_coding | tolerated(0.05) | benign(0.082) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
PDCL | SNV | Missense_Mutation | novel | c.856N>A | p.Arg286Ser | p.R286S | Q13371 | protein_coding | tolerated(0.21) | benign(0.043) | TCGA-AP-A1DO-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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