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Gene: PTTG1 |
Gene summary for PTTG1 |
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Gene information | Species | Human | Gene symbol | PTTG1 | Gene ID | 9232 |
Gene name | PTTG1 regulator of sister chromatid separation, securin | |
Gene Alias | EAP1 | |
Cytomap | 5q33.3 | |
Gene Type | protein-coding | GO ID | GO:0000003 | UniProtAcc | O95997 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
9232 | PTTG1 | P1_cSCC | Human | Skin | cSCC | 2.76e-23 | 1.69e+00 | 0.0292 |
9232 | PTTG1 | P2_cSCC | Human | Skin | cSCC | 1.89e-10 | 1.60e+00 | -0.024 |
9232 | PTTG1 | P4_cSCC | Human | Skin | cSCC | 1.22e-28 | 2.03e+00 | -0.00290000000000005 |
9232 | PTTG1 | P10_cSCC | Human | Skin | cSCC | 1.17e-48 | 2.47e+00 | 0.1017 |
9232 | PTTG1 | cSCC_p11 | Human | Skin | cSCC | 9.93e-04 | -2.92e-01 | -0.2102 |
9232 | PTTG1 | cSCC_p4 | Human | Skin | cSCC | 1.47e-02 | -2.78e-01 | -0.2022 |
9232 | PTTG1 | cSCC_p7 | Human | Skin | cSCC | 1.04e-04 | -3.20e-01 | -0.2332 |
9232 | PTTG1 | Adj_PTCwithHT_6 | Human | Thyroid | HT | 3.23e-10 | -8.04e-01 | 0.02 |
9232 | PTTG1 | Adj_PTCwithHT_8 | Human | Thyroid | HT | 2.43e-07 | -6.54e-01 | 0.0267 |
9232 | PTTG1 | PTCwithHT_1 | Human | Thyroid | HT | 2.36e-05 | -8.07e-01 | 0.0238 |
9232 | PTTG1 | PTCwithHT_6 | Human | Thyroid | HT | 4.96e-10 | -7.40e-01 | 0.02 |
9232 | PTTG1 | PTCwithHT_8 | Human | Thyroid | HT | 4.39e-13 | -8.03e-01 | 0.0351 |
9232 | PTTG1 | PTCwithoutHT_2 | Human | Thyroid | PTC | 4.85e-15 | -8.85e-01 | 0.0419 |
9232 | PTTG1 | male-WTA | Human | Thyroid | PTC | 1.16e-45 | -6.99e-01 | 0.1037 |
9232 | PTTG1 | female-WTA | Human | Thyroid | PTC | 1.91e-02 | -6.67e-01 | 0.0726 |
9232 | PTTG1 | nodule-WTA | Human | Thyroid | goiters | 1.08e-14 | -8.47e-01 | 0.0534 |
9232 | PTTG1 | PTC01 | Human | Thyroid | PTC | 1.47e-03 | -4.99e-01 | 0.1899 |
9232 | PTTG1 | PTC03 | Human | Thyroid | PTC | 2.27e-11 | -9.18e-01 | 0.1784 |
9232 | PTTG1 | PTC05 | Human | Thyroid | PTC | 5.09e-16 | -4.70e-01 | 0.2065 |
9232 | PTTG1 | ATC08 | Human | Thyroid | ATC | 2.58e-14 | -8.35e-01 | 0.0541 |
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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:005254714 | Breast | IDC | regulation of peptidase activity | 96/1434 | 461/18723 | 7.58e-20 | 6.15e-17 | 96 |
GO:005254814 | Breast | IDC | regulation of endopeptidase activity | 88/1434 | 432/18723 | 1.20e-17 | 4.85e-15 | 88 |
GO:004586114 | Breast | IDC | negative regulation of proteolysis | 70/1434 | 351/18723 | 8.21e-14 | 2.22e-11 | 70 |
GO:005134613 | Breast | IDC | negative regulation of hydrolase activity | 71/1434 | 379/18723 | 1.33e-12 | 2.90e-10 | 71 |
GO:001046613 | Breast | IDC | negative regulation of peptidase activity | 56/1434 | 262/18723 | 1.39e-12 | 2.92e-10 | 56 |
GO:001095112 | Breast | IDC | negative regulation of endopeptidase activity | 52/1434 | 252/18723 | 3.53e-11 | 5.57e-09 | 52 |
GO:00330445 | Breast | IDC | regulation of chromosome organization | 26/1434 | 187/18723 | 2.22e-03 | 2.06e-02 | 26 |
GO:005254723 | Breast | DCIS | regulation of peptidase activity | 88/1390 | 461/18723 | 1.18e-16 | 4.78e-14 | 88 |
GO:005254823 | Breast | DCIS | regulation of endopeptidase activity | 83/1390 | 432/18723 | 6.07e-16 | 2.15e-13 | 83 |
GO:004586123 | Breast | DCIS | negative regulation of proteolysis | 63/1390 | 351/18723 | 4.39e-11 | 6.06e-09 | 63 |
GO:005134623 | Breast | DCIS | negative regulation of hydrolase activity | 64/1390 | 379/18723 | 4.32e-10 | 4.80e-08 | 64 |
GO:001046622 | Breast | DCIS | negative regulation of peptidase activity | 49/1390 | 262/18723 | 1.54e-09 | 1.43e-07 | 49 |
GO:001095122 | Breast | DCIS | negative regulation of endopeptidase activity | 47/1390 | 252/18723 | 3.63e-09 | 3.11e-07 | 47 |
GO:003304412 | Breast | DCIS | regulation of chromosome organization | 26/1390 | 187/18723 | 1.44e-03 | 1.47e-02 | 26 |
GO:0042176 | Colorectum | AD | regulation of protein catabolic process | 160/3918 | 391/18723 | 1.06e-19 | 7.34e-17 | 160 |
GO:0009896 | Colorectum | AD | positive regulation of catabolic process | 180/3918 | 492/18723 | 4.33e-16 | 1.94e-13 | 180 |
GO:1903362 | Colorectum | AD | regulation of cellular protein catabolic process | 109/3918 | 255/18723 | 2.14e-15 | 6.08e-13 | 109 |
GO:0031331 | Colorectum | AD | positive regulation of cellular catabolic process | 156/3918 | 427/18723 | 4.68e-14 | 1.05e-11 | 156 |
GO:0072594 | Colorectum | AD | establishment of protein localization to organelle | 148/3918 | 422/18723 | 7.95e-12 | 1.04e-09 | 148 |
GO:0045732 | Colorectum | AD | positive regulation of protein catabolic process | 92/3918 | 231/18723 | 3.85e-11 | 4.47e-09 | 92 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0516624 | Breast | IDC | Human T-cell leukemia virus 1 infection | 40/867 | 222/8465 | 2.52e-04 | 2.21e-03 | 1.66e-03 | 40 |
hsa0516634 | Breast | IDC | Human T-cell leukemia virus 1 infection | 40/867 | 222/8465 | 2.52e-04 | 2.21e-03 | 1.66e-03 | 40 |
hsa0516642 | Breast | DCIS | Human T-cell leukemia virus 1 infection | 41/846 | 222/8465 | 7.03e-05 | 6.88e-04 | 5.07e-04 | 41 |
hsa0516652 | Breast | DCIS | Human T-cell leukemia virus 1 infection | 41/846 | 222/8465 | 7.03e-05 | 6.88e-04 | 5.07e-04 | 41 |
hsa0516639 | Esophagus | HGIN | Human T-cell leukemia virus 1 infection | 51/1383 | 222/8465 | 5.84e-03 | 4.05e-02 | 3.22e-02 | 51 |
hsa041109 | Esophagus | HGIN | Cell cycle | 38/1383 | 157/8465 | 6.70e-03 | 4.37e-02 | 3.47e-02 | 38 |
hsa05166114 | Esophagus | HGIN | Human T-cell leukemia virus 1 infection | 51/1383 | 222/8465 | 5.84e-03 | 4.05e-02 | 3.22e-02 | 51 |
hsa0411016 | Esophagus | HGIN | Cell cycle | 38/1383 | 157/8465 | 6.70e-03 | 4.37e-02 | 3.47e-02 | 38 |
hsa0411023 | Esophagus | ESCC | Cell cycle | 126/4205 | 157/8465 | 1.34e-15 | 5.60e-14 | 2.87e-14 | 126 |
hsa05166211 | Esophagus | ESCC | Human T-cell leukemia virus 1 infection | 164/4205 | 222/8465 | 8.13e-14 | 2.09e-12 | 1.07e-12 | 164 |
hsa041146 | Esophagus | ESCC | Oocyte meiosis | 77/4205 | 131/8465 | 2.19e-02 | 4.80e-02 | 2.46e-02 | 77 |
hsa0411033 | Esophagus | ESCC | Cell cycle | 126/4205 | 157/8465 | 1.34e-15 | 5.60e-14 | 2.87e-14 | 126 |
hsa05166310 | Esophagus | ESCC | Human T-cell leukemia virus 1 infection | 164/4205 | 222/8465 | 8.13e-14 | 2.09e-12 | 1.07e-12 | 164 |
hsa0411411 | Esophagus | ESCC | Oocyte meiosis | 77/4205 | 131/8465 | 2.19e-02 | 4.80e-02 | 2.46e-02 | 77 |
hsa041102 | Liver | HCC | Cell cycle | 106/4020 | 157/8465 | 2.54e-07 | 3.04e-06 | 1.69e-06 | 106 |
hsa0516622 | Liver | HCC | Human T-cell leukemia virus 1 infection | 139/4020 | 222/8465 | 3.17e-06 | 2.79e-05 | 1.55e-05 | 139 |
hsa041103 | Liver | HCC | Cell cycle | 106/4020 | 157/8465 | 2.54e-07 | 3.04e-06 | 1.69e-06 | 106 |
hsa0516632 | Liver | HCC | Human T-cell leukemia virus 1 infection | 139/4020 | 222/8465 | 3.17e-06 | 2.79e-05 | 1.55e-05 | 139 |
hsa041108 | Oral cavity | OSCC | Cell cycle | 118/3704 | 157/8465 | 7.15e-16 | 2.66e-14 | 1.35e-14 | 118 |
hsa0516630 | Oral cavity | OSCC | Human T-cell leukemia virus 1 infection | 150/3704 | 222/8465 | 3.68e-13 | 7.26e-12 | 3.70e-12 | 150 |
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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 |
PTTG1 | SNV | Missense_Mutation | c.385N>A | p.Asp129Asn | p.D129N | O95997 | protein_coding | deleterious(0.03) | benign(0.125) | TCGA-BH-A204-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
PTTG1 | SNV | Missense_Mutation | rs763093561 | c.351N>A | p.Phe117Leu | p.F117L | O95997 | protein_coding | tolerated(0.5) | benign(0.007) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR |
PTTG1 | SNV | Missense_Mutation | novel | c.491C>A | p.Pro164His | p.P164H | O95997 | protein_coding | deleterious(0) | probably_damaging(0.992) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
PTTG1 | SNV | Missense_Mutation | novel | c.551N>A | p.Ser184Asn | p.S184N | O95997 | protein_coding | tolerated(0.31) | possibly_damaging(0.459) | TCGA-AX-A06F-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatin | SD |
PTTG1 | SNV | Missense_Mutation | c.329N>T | p.Ala110Val | p.A110V | O95997 | protein_coding | tolerated(0.2) | benign(0.171) | TCGA-AX-A1CE-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unspecific | Paclitaxel | SD | |
PTTG1 | SNV | Missense_Mutation | c.385N>A | p.Asp129Asn | p.D129N | O95997 | protein_coding | deleterious(0.03) | benign(0.125) | TCGA-B5-A11U-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
PTTG1 | SNV | Missense_Mutation | novel | c.391C>T | p.Pro131Ser | p.P131S | O95997 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-B5-A3FA-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
PTTG1 | SNV | Missense_Mutation | novel | c.584N>T | p.Pro195Leu | p.P195L | O95997 | protein_coding | deleterious(0) | possibly_damaging(0.661) | TCGA-EO-A3KX-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
PTTG1 | SNV | Missense_Mutation | novel | c.583N>A | p.Pro195Thr | p.P195T | O95997 | protein_coding | deleterious(0) | possibly_damaging(0.661) | TCGA-DD-AAC9-01 | Liver | liver hepatocellular carcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
PTTG1 | SNV | Missense_Mutation | c.410C>G | p.Ala137Gly | p.A137G | O95997 | protein_coding | deleterious(0.02) | possibly_damaging(0.715) | TCGA-05-4427-01 | Lung | lung adenocarcinoma | Female | >=65 | I/II | Chemotherapy | cisplatin | CR |
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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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