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Gene: PLCXD2 |
Gene summary for PLCXD2 |
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Gene information | Species | Human | Gene symbol | PLCXD2 | Gene ID | 257068 |
Gene name | phosphatidylinositol specific phospholipase C X domain containing 2 | |
Gene Alias | PLCXD2 | |
Cytomap | 3q13.2 | |
Gene Type | protein-coding | GO ID | GO:0006629 | UniProtAcc | Q0VAA5 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
257068 | PLCXD2 | LZE4T | Human | Esophagus | ESCC | 6.76e-43 | 1.48e+00 | 0.0811 |
257068 | PLCXD2 | LZE20T | Human | Esophagus | ESCC | 1.10e-04 | 1.86e-01 | 0.0662 |
257068 | PLCXD2 | P1T-E | Human | Esophagus | ESCC | 5.63e-07 | 5.10e-01 | 0.0875 |
257068 | PLCXD2 | P8T-E | Human | Esophagus | ESCC | 1.16e-02 | 1.36e-01 | 0.0889 |
257068 | PLCXD2 | P11T-E | Human | Esophagus | ESCC | 1.50e-14 | 3.78e-01 | 0.1426 |
257068 | PLCXD2 | P20T-E | Human | Esophagus | ESCC | 5.32e-10 | 2.38e-01 | 0.1124 |
257068 | PLCXD2 | P22T-E | Human | Esophagus | ESCC | 3.20e-07 | 2.42e-01 | 0.1236 |
257068 | PLCXD2 | P26T-E | Human | Esophagus | ESCC | 4.96e-23 | 4.96e-01 | 0.1276 |
257068 | PLCXD2 | P28T-E | Human | Esophagus | ESCC | 7.04e-23 | 7.33e-01 | 0.1149 |
257068 | PLCXD2 | P30T-E | Human | Esophagus | ESCC | 1.33e-25 | 8.85e-01 | 0.137 |
257068 | PLCXD2 | P32T-E | Human | Esophagus | ESCC | 9.73e-08 | 4.41e-01 | 0.1666 |
257068 | PLCXD2 | P39T-E | Human | Esophagus | ESCC | 2.11e-02 | 2.22e-02 | 0.0894 |
257068 | PLCXD2 | P42T-E | Human | Esophagus | ESCC | 3.29e-04 | 4.23e-02 | 0.1175 |
257068 | PLCXD2 | P47T-E | Human | Esophagus | ESCC | 3.54e-12 | 2.54e-01 | 0.1067 |
257068 | PLCXD2 | P48T-E | Human | Esophagus | ESCC | 2.43e-03 | 6.64e-03 | 0.0959 |
257068 | PLCXD2 | P52T-E | Human | Esophagus | ESCC | 6.11e-07 | 3.92e-01 | 0.1555 |
257068 | PLCXD2 | P54T-E | Human | Esophagus | ESCC | 3.68e-08 | 2.60e-01 | 0.0975 |
257068 | PLCXD2 | P61T-E | Human | Esophagus | ESCC | 1.88e-03 | 1.14e-01 | 0.099 |
257068 | PLCXD2 | P62T-E | Human | Esophagus | ESCC | 5.77e-09 | 2.37e-01 | 0.1302 |
257068 | PLCXD2 | P65T-E | Human | Esophagus | ESCC | 1.26e-07 | 8.49e-02 | 0.0978 |
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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:00160427 | Esophagus | ESCC | lipid catabolic process | 168/8552 | 320/18723 | 7.97e-03 | 2.84e-02 | 168 |
GO:001604212 | Liver | Cirrhotic | lipid catabolic process | 112/4634 | 320/18723 | 2.31e-05 | 3.03e-04 | 112 |
GO:001604221 | Liver | HCC | lipid catabolic process | 175/7958 | 320/18723 | 6.50e-06 | 7.88e-05 | 175 |
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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 |
PLCXD2 | SNV | Missense_Mutation | c.466N>C | p.Glu156Gln | p.E156Q | Q0VAA5 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-C5-A3HE-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | PD | |
PLCXD2 | SNV | Missense_Mutation | rs147048469 | c.238C>T | p.Arg80Cys | p.R80C | Q0VAA5 | protein_coding | tolerated(0.15) | probably_damaging(0.959) | TCGA-AA-3989-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | PD |
PLCXD2 | SNV | Missense_Mutation | novel | c.137N>C | p.Leu46Pro | p.L46P | Q0VAA5 | protein_coding | deleterious(0.03) | benign(0.211) | TCGA-AM-5821-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
PLCXD2 | SNV | Missense_Mutation | c.820A>G | p.Ile274Val | p.I274V | Q0VAA5 | protein_coding | tolerated(1) | benign(0.026) | TCGA-DC-6682-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
PLCXD2 | SNV | Missense_Mutation | c.443N>T | p.Ser148Leu | p.S148L | Q0VAA5 | protein_coding | tolerated(0.12) | benign(0.04) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | |
PLCXD2 | SNV | Missense_Mutation | rs770445265 | c.593N>T | p.Thr198Met | p.T198M | Q0VAA5 | protein_coding | deleterious(0) | benign(0.072) | TCGA-AJ-A3BH-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | Unknown | I/II | Unknown | Unknown | SD |
PLCXD2 | SNV | Missense_Mutation | rs201638622 | c.346N>T | p.Arg116Cys | p.R116C | Q0VAA5 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-AP-A0LM-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | cisplatin | SD |
PLCXD2 | SNV | Missense_Mutation | rs748891173 | c.244N>A | p.Ala82Thr | p.A82T | Q0VAA5 | protein_coding | deleterious(0.04) | probably_damaging(0.999) | TCGA-AP-A1DV-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
PLCXD2 | SNV | Missense_Mutation | rs754981611 | c.794N>T | p.Ala265Val | p.A265V | Q0VAA5 | protein_coding | tolerated(0.39) | probably_damaging(0.994) | TCGA-AX-A1CE-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unspecific | Paclitaxel | SD |
PLCXD2 | SNV | Missense_Mutation | novel | c.23G>T | p.Arg8Met | p.R8M | Q0VAA5 | protein_coding | deleterious_low_confidence(0.02) | possibly_damaging(0.541) | TCGA-AX-A2HD-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=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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