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Gene: PCMT1 |
Gene summary for PCMT1 |
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Gene information | Species | Human | Gene symbol | PCMT1 | Gene ID | 5110 |
Gene name | protein-L-isoaspartate (D-aspartate) O-methyltransferase | |
Gene Alias | PIMT | |
Cytomap | 6q25.1 | |
Gene Type | protein-coding | GO ID | GO:0006464 | UniProtAcc | H7BY58 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
5110 | PCMT1 | SYSMH3 | Human | Oral cavity | OSCC | 1.65e-42 | 1.30e+00 | 0.2442 |
5110 | PCMT1 | SYSMH4 | Human | Oral cavity | OSCC | 6.86e-10 | 1.78e-01 | 0.1226 |
5110 | PCMT1 | SYSMH5 | Human | Oral cavity | OSCC | 1.38e-18 | 6.09e-01 | 0.0647 |
5110 | PCMT1 | SYSMH6 | Human | Oral cavity | OSCC | 3.06e-15 | 6.83e-01 | 0.1275 |
5110 | PCMT1 | P4_S8_cSCC | Human | Skin | cSCC | 1.23e-08 | -3.85e-02 | -0.3095 |
5110 | PCMT1 | P5_S10_cSCC | Human | Skin | cSCC | 1.16e-06 | -2.08e-01 | -0.299 |
5110 | PCMT1 | P1_cSCC | Human | Skin | cSCC | 1.26e-16 | 1.08e+00 | 0.0292 |
5110 | PCMT1 | P2_cSCC | Human | Skin | cSCC | 1.19e-04 | 6.39e-01 | -0.024 |
5110 | PCMT1 | P4_cSCC | Human | Skin | cSCC | 6.33e-25 | 9.76e-01 | -0.00290000000000005 |
5110 | PCMT1 | P10_cSCC | Human | Skin | cSCC | 7.69e-33 | 1.43e+00 | 0.1017 |
5110 | PCMT1 | cSCC_p3 | Human | Skin | cSCC | 3.05e-04 | -3.46e-01 | -0.2085 |
5110 | PCMT1 | cSCC_p4 | Human | Skin | cSCC | 1.19e-03 | -2.11e-01 | -0.2022 |
5110 | PCMT1 | cSCC_p6 | Human | Skin | cSCC | 1.88e-02 | -2.69e-01 | -0.1989 |
5110 | PCMT1 | cSCC_p7 | Human | Skin | cSCC | 1.92e-07 | -3.59e-01 | -0.2332 |
5110 | PCMT1 | cSCC_p8 | Human | Skin | cSCC | 1.91e-09 | -2.03e-01 | -0.1971 |
5110 | PCMT1 | cSCC_p9 | Human | Skin | cSCC | 9.06e-09 | -1.63e-01 | -0.1991 |
5110 | PCMT1 | male-WTA | Human | Thyroid | PTC | 1.87e-40 | 1.34e-01 | 0.1037 |
5110 | PCMT1 | PTC01 | Human | Thyroid | PTC | 5.19e-22 | 4.94e-01 | 0.1899 |
5110 | PCMT1 | PTC04 | Human | Thyroid | PTC | 9.18e-10 | 4.30e-01 | 0.1927 |
5110 | PCMT1 | PTC05 | Human | Thyroid | PTC | 3.27e-18 | 9.18e-01 | 0.2065 |
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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:00434143 | Esophagus | ESCC | macromolecule methylation | 199/8552 | 316/18723 | 3.44e-10 | 9.57e-09 | 199 |
GO:00322592 | Esophagus | ESCC | methylation | 222/8552 | 364/18723 | 2.26e-09 | 5.09e-08 | 222 |
GO:000647914 | Esophagus | ESCC | protein methylation | 115/8552 | 181/18723 | 9.07e-07 | 1.16e-05 | 115 |
GO:000821314 | Esophagus | ESCC | protein alkylation | 115/8552 | 181/18723 | 9.07e-07 | 1.16e-05 | 115 |
GO:00064791 | Liver | Cirrhotic | protein methylation | 61/4634 | 181/18723 | 4.13e-03 | 2.21e-02 | 61 |
GO:00082131 | Liver | Cirrhotic | protein alkylation | 61/4634 | 181/18723 | 4.13e-03 | 2.21e-02 | 61 |
GO:00434141 | Liver | HCC | macromolecule methylation | 183/7958 | 316/18723 | 2.00e-08 | 4.72e-07 | 183 |
GO:0032259 | Liver | HCC | methylation | 206/7958 | 364/18723 | 3.35e-08 | 7.53e-07 | 206 |
GO:00064792 | Liver | HCC | protein methylation | 111/7958 | 181/18723 | 2.36e-07 | 4.18e-06 | 111 |
GO:00082132 | Liver | HCC | protein alkylation | 111/7958 | 181/18723 | 2.36e-07 | 4.18e-06 | 111 |
GO:00064797 | Oral cavity | OSCC | protein methylation | 92/7305 | 181/18723 | 7.86e-04 | 4.26e-03 | 92 |
GO:00082137 | Oral cavity | OSCC | protein alkylation | 92/7305 | 181/18723 | 7.86e-04 | 4.26e-03 | 92 |
GO:00434142 | Oral cavity | OSCC | macromolecule methylation | 149/7305 | 316/18723 | 1.82e-03 | 8.60e-03 | 149 |
GO:00322591 | Oral cavity | OSCC | methylation | 168/7305 | 364/18723 | 3.03e-03 | 1.31e-02 | 168 |
GO:000647915 | Skin | cSCC | protein methylation | 67/4864 | 181/18723 | 6.65e-04 | 4.75e-03 | 67 |
GO:000821315 | Skin | cSCC | protein alkylation | 67/4864 | 181/18723 | 6.65e-04 | 4.75e-03 | 67 |
GO:004341411 | Skin | cSCC | macromolecule methylation | 107/4864 | 316/18723 | 1.03e-03 | 6.94e-03 | 107 |
GO:00322593 | Skin | cSCC | methylation | 120/4864 | 364/18723 | 1.61e-03 | 9.93e-03 | 120 |
GO:000647910 | Thyroid | PTC | protein methylation | 82/5968 | 181/18723 | 1.01e-04 | 8.21e-04 | 82 |
GO:000821310 | Thyroid | PTC | protein alkylation | 82/5968 | 181/18723 | 1.01e-04 | 8.21e-04 | 82 |
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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 |
PCMT1 | SNV | Missense_Mutation | c.256G>C | p.Val86Leu | p.V86L | protein_coding | deleterious(0) | possibly_damaging(0.826) | TCGA-A8-A07R-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Ancillary | zoledronic | SD | ||
PCMT1 | SNV | Missense_Mutation | c.188N>T | p.Ser63Phe | p.S63F | protein_coding | tolerated(0.08) | probably_damaging(0.979) | TCGA-C8-A26Y-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | ||
PCMT1 | deletion | Frame_Shift_Del | novel | c.801delN | p.Val269Ter | p.V269* | protein_coding | TCGA-D8-A27V-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD | |||
PCMT1 | SNV | Missense_Mutation | rs754551183 | c.200G>A | p.Ser67Asn | p.S67N | protein_coding | tolerated(0.5) | benign(0.001) | TCGA-5M-AAT6-01 | Colorectum | colon adenocarcinoma | Female | <65 | III/IV | Unknown | Unknown | PD | |
PCMT1 | SNV | Missense_Mutation | novel | c.291N>A | p.His97Gln | p.H97Q | protein_coding | tolerated(0.07) | possibly_damaging(0.698) | TCGA-A6-3808-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
PCMT1 | SNV | Missense_Mutation | novel | c.481N>C | p.Thr161Pro | p.T161P | protein_coding | tolerated(0.09) | benign(0.324) | TCGA-AZ-4315-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
PCMT1 | SNV | Missense_Mutation | novel | c.718N>T | p.Pro240Ser | p.P240S | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-F4-6808-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
PCMT1 | SNV | Missense_Mutation | rs769452465 | c.677N>T | p.Ala226Val | p.A226V | protein_coding | deleterious(0.03) | possibly_damaging(0.907) | TCGA-AG-A002-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
PCMT1 | SNV | Missense_Mutation | novel | c.419N>T | p.Ala140Val | p.A140V | protein_coding | tolerated(0.32) | benign(0.239) | TCGA-EI-6917-01 | Colorectum | rectum adenocarcinoma | Male | <65 | III/IV | Chemotherapy | 5fluorouracil+oxaciplatina+l-folinian | SD | |
PCMT1 | SNV | Missense_Mutation | novel | c.611N>A | p.Gly204Glu | p.G204E | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-A5-A0G2-01 | 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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