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Gene: TPPP3 |
Gene summary for TPPP3 |
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Gene information | Species | Human | Gene symbol | TPPP3 | Gene ID | 51673 |
Gene name | tubulin polymerization promoting protein family member 3 | |
Gene Alias | CGI-38 | |
Cytomap | 16q22.1 | |
Gene Type | protein-coding | GO ID | GO:0000003 | UniProtAcc | A0A024R702 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
51673 | TPPP3 | LZE4T | Human | Esophagus | ESCC | 1.21e-09 | 5.24e-01 | 0.0811 |
51673 | TPPP3 | LZE8T | Human | Esophagus | ESCC | 2.75e-07 | 4.37e-01 | 0.067 |
51673 | TPPP3 | P8T-E | Human | Esophagus | ESCC | 3.53e-16 | 7.37e-01 | 0.0889 |
51673 | TPPP3 | P11T-E | Human | Esophagus | ESCC | 8.31e-06 | 5.60e-01 | 0.1426 |
51673 | TPPP3 | P19T-E | Human | Esophagus | ESCC | 2.85e-03 | 9.25e-01 | 0.1662 |
51673 | TPPP3 | P21T-E | Human | Esophagus | ESCC | 2.85e-64 | 2.58e+00 | 0.1617 |
51673 | TPPP3 | P22T-E | Human | Esophagus | ESCC | 1.06e-04 | -2.01e-02 | 0.1236 |
51673 | TPPP3 | P23T-E | Human | Esophagus | ESCC | 1.02e-06 | 3.42e-01 | 0.108 |
51673 | TPPP3 | P26T-E | Human | Esophagus | ESCC | 2.00e-09 | 3.73e-01 | 0.1276 |
51673 | TPPP3 | P31T-E | Human | Esophagus | ESCC | 5.34e-56 | 1.71e+00 | 0.1251 |
51673 | TPPP3 | P48T-E | Human | Esophagus | ESCC | 8.61e-12 | 4.29e-01 | 0.0959 |
51673 | TPPP3 | P54T-E | Human | Esophagus | ESCC | 1.43e-05 | 5.18e-01 | 0.0975 |
51673 | TPPP3 | P74T-E | Human | Esophagus | ESCC | 1.81e-15 | 5.08e-01 | 0.1479 |
51673 | TPPP3 | P82T-E | Human | Esophagus | ESCC | 1.05e-06 | 8.41e-01 | 0.1072 |
51673 | TPPP3 | P89T-E | Human | Esophagus | ESCC | 1.93e-08 | 1.32e+00 | 0.1752 |
51673 | TPPP3 | P91T-E | Human | Esophagus | ESCC | 5.45e-04 | 1.91e+00 | 0.1828 |
51673 | TPPP3 | P104T-E | Human | Esophagus | ESCC | 7.85e-07 | 5.36e-01 | 0.0931 |
51673 | TPPP3 | P107T-E | Human | Esophagus | ESCC | 8.60e-47 | 1.91e+00 | 0.171 |
51673 | TPPP3 | P128T-E | Human | Esophagus | ESCC | 1.70e-02 | 3.08e-01 | 0.1241 |
51673 | TPPP3 | P130T-E | Human | Esophagus | ESCC | 3.14e-22 | 6.49e-01 | 0.1676 |
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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:000756615 | Oral cavity | NEOLP | embryo implantation | 18/2005 | 53/18723 | 5.16e-06 | 1.07e-04 | 18 |
GO:004678531 | Oral cavity | NEOLP | microtubule polymerization | 22/2005 | 83/18723 | 4.31e-05 | 6.10e-04 | 22 |
GO:00311092 | Oral cavity | NEOLP | microtubule polymerization or depolymerization | 26/2005 | 122/18723 | 4.52e-04 | 4.06e-03 | 26 |
GO:000756531 | Oral cavity | NEOLP | female pregnancy | 36/2005 | 193/18723 | 6.47e-04 | 5.47e-03 | 36 |
GO:004470614 | Oral cavity | NEOLP | multi-multicellular organism process | 37/2005 | 220/18723 | 3.69e-03 | 2.15e-02 | 37 |
GO:004860819 | Skin | AK | reproductive structure development | 77/1910 | 424/18723 | 3.56e-07 | 1.36e-05 | 77 |
GO:006145820 | Skin | AK | reproductive system development | 77/1910 | 427/18723 | 4.76e-07 | 1.74e-05 | 77 |
GO:004325428 | Skin | AK | regulation of protein-containing complex assembly | 75/1910 | 428/18723 | 2.05e-06 | 5.98e-05 | 75 |
GO:000189020 | Skin | AK | placenta development | 33/1910 | 144/18723 | 6.49e-06 | 1.47e-04 | 33 |
GO:003133426 | Skin | AK | positive regulation of protein-containing complex assembly | 45/1910 | 237/18723 | 3.01e-05 | 5.15e-04 | 45 |
GO:005125827 | Skin | AK | protein polymerization | 53/1910 | 297/18723 | 3.74e-05 | 6.20e-04 | 53 |
GO:003227127 | Skin | AK | regulation of protein polymerization | 41/1910 | 233/18723 | 3.65e-04 | 3.59e-03 | 41 |
GO:00075658 | Skin | AK | female pregnancy | 34/1910 | 193/18723 | 1.09e-03 | 8.48e-03 | 34 |
GO:003227326 | Skin | AK | positive regulation of protein polymerization | 26/1910 | 138/18723 | 1.50e-03 | 1.08e-02 | 26 |
GO:00075669 | Skin | AK | embryo implantation | 13/1910 | 53/18723 | 2.11e-03 | 1.40e-02 | 13 |
GO:00447068 | Skin | AK | multi-multicellular organism process | 36/1910 | 220/18723 | 2.97e-03 | 1.87e-02 | 36 |
GO:00311095 | Skin | AK | microtubule polymerization or depolymerization | 22/1910 | 122/18723 | 5.74e-03 | 3.13e-02 | 22 |
GO:00467857 | Skin | AK | microtubule polymerization | 16/1910 | 83/18723 | 9.04e-03 | 4.44e-02 | 16 |
GO:0048608110 | Skin | SCCIS | reproductive structure development | 47/919 | 424/18723 | 1.60e-07 | 1.85e-05 | 47 |
GO:0061458111 | Skin | SCCIS | reproductive system development | 47/919 | 427/18723 | 1.98e-07 | 2.10e-05 | 47 |
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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 |
TPPP3 | SNV | Missense_Mutation | rs562124643 | c.412N>T | p.Arg138Cys | p.R138C | Q9BW30 | protein_coding | tolerated(0.08) | probably_damaging(0.999) | TCGA-AC-A3QP-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | femara | SD |
TPPP3 | SNV | Missense_Mutation | c.487G>T | p.Ala163Ser | p.A163S | Q9BW30 | protein_coding | tolerated(0.12) | benign(0.039) | TCGA-BH-A0BL-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | CR | |
TPPP3 | SNV | Missense_Mutation | novel | c.431A>C | p.Lys144Thr | p.K144T | Q9BW30 | protein_coding | deleterious(0) | possibly_damaging(0.846) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
TPPP3 | SNV | Missense_Mutation | c.469G>A | p.Asp157Asn | p.D157N | Q9BW30 | protein_coding | tolerated(1) | benign(0.001) | TCGA-A6-6781-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | oxaliplatin | SD | |
TPPP3 | SNV | Missense_Mutation | novel | c.476N>A | p.Gly159Asp | p.G159D | Q9BW30 | protein_coding | tolerated(0.06) | probably_damaging(0.941) | TCGA-AA-3864-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
TPPP3 | SNV | Missense_Mutation | rs562124643 | c.412C>T | p.Arg138Cys | p.R138C | Q9BW30 | protein_coding | tolerated(0.08) | probably_damaging(0.999) | TCGA-D5-6531-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
TPPP3 | insertion | Frame_Shift_Ins | novel | c.62_63insATGGCTGGGCTGGAGGAGAGCTTCCGCAAGTTTGTCATCCATGG | p.Asp22TrpfsTer24 | p.D22Wfs*24 | Q9BW30 | protein_coding | TCGA-EI-6510-01 | Colorectum | rectum adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | ||
TPPP3 | SNV | Missense_Mutation | rs749753194 | c.511G>A | p.Asp171Asn | p.D171N | Q9BW30 | protein_coding | deleterious(0.04) | benign(0.269) | TCGA-AP-A1DV-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
TPPP3 | SNV | Missense_Mutation | c.125N>A | p.Cys42Tyr | p.C42Y | Q9BW30 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-D1-A0ZO-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
TPPP3 | SNV | Missense_Mutation | rs377234620 | c.44G>A | p.Arg15His | p.R15H | Q9BW30 | protein_coding | tolerated(0.24) | benign(0.021) | TCGA-EO-A22R-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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