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Gene: THUMPD3 |
Gene summary for THUMPD3 |
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Gene information | Species | Human | Gene symbol | THUMPD3 | Gene ID | 25917 |
Gene name | THUMP domain containing 3 | |
Gene Alias | THUMPD3 | |
Cytomap | 3p25.3 | |
Gene Type | protein-coding | GO ID | GO:0001510 | UniProtAcc | A0A024R2F4 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
25917 | THUMPD3 | LZE4T | Human | Esophagus | ESCC | 1.36e-08 | 2.04e-01 | 0.0811 |
25917 | THUMPD3 | LZE7T | Human | Esophagus | ESCC | 7.88e-04 | 1.38e-01 | 0.0667 |
25917 | THUMPD3 | LZE20T | Human | Esophagus | ESCC | 1.81e-02 | 3.92e-02 | 0.0662 |
25917 | THUMPD3 | LZE24T | Human | Esophagus | ESCC | 4.10e-11 | 2.02e-01 | 0.0596 |
25917 | THUMPD3 | LZE21T | Human | Esophagus | ESCC | 1.41e-02 | 1.49e-01 | 0.0655 |
25917 | THUMPD3 | LZE6T | Human | Esophagus | ESCC | 1.59e-03 | 2.09e-01 | 0.0845 |
25917 | THUMPD3 | P1T-E | Human | Esophagus | ESCC | 3.87e-09 | 3.42e-01 | 0.0875 |
25917 | THUMPD3 | P2T-E | Human | Esophagus | ESCC | 5.12e-30 | 4.29e-01 | 0.1177 |
25917 | THUMPD3 | P4T-E | Human | Esophagus | ESCC | 2.55e-28 | 6.15e-01 | 0.1323 |
25917 | THUMPD3 | P5T-E | Human | Esophagus | ESCC | 2.76e-36 | 7.00e-01 | 0.1327 |
25917 | THUMPD3 | P8T-E | Human | Esophagus | ESCC | 6.41e-15 | 2.38e-01 | 0.0889 |
25917 | THUMPD3 | P9T-E | Human | Esophagus | ESCC | 6.42e-05 | 1.58e-01 | 0.1131 |
25917 | THUMPD3 | P10T-E | Human | Esophagus | ESCC | 2.13e-13 | 2.21e-01 | 0.116 |
25917 | THUMPD3 | P11T-E | Human | Esophagus | ESCC | 1.07e-11 | 5.28e-01 | 0.1426 |
25917 | THUMPD3 | P12T-E | Human | Esophagus | ESCC | 5.35e-24 | 4.33e-01 | 0.1122 |
25917 | THUMPD3 | P15T-E | Human | Esophagus | ESCC | 1.40e-12 | 2.33e-01 | 0.1149 |
25917 | THUMPD3 | P16T-E | Human | Esophagus | ESCC | 3.81e-31 | 3.87e-01 | 0.1153 |
25917 | THUMPD3 | P17T-E | Human | Esophagus | ESCC | 8.38e-06 | 1.81e-01 | 0.1278 |
25917 | THUMPD3 | P19T-E | Human | Esophagus | ESCC | 3.09e-10 | 3.77e-01 | 0.1662 |
25917 | THUMPD3 | P20T-E | Human | Esophagus | ESCC | 1.98e-16 | 3.70e-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 |
Breast | Precancer | ![]() |
Breast | IDC | ![]() |
Breast | DCIS | ![]() |
Cervix | CC | ![]() |
Cervix | HSIL_HPV | ![]() |
∗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:003447015 | Esophagus | ESCC | ncRNA processing | 300/8552 | 395/18723 | 3.09e-35 | 3.26e-32 | 300 |
GO:003466012 | Esophagus | ESCC | ncRNA metabolic process | 346/8552 | 485/18723 | 4.35e-31 | 2.51e-28 | 346 |
GO:00434143 | Esophagus | ESCC | macromolecule methylation | 199/8552 | 316/18723 | 3.44e-10 | 9.57e-09 | 199 |
GO:00080333 | Esophagus | ESCC | tRNA processing | 92/8552 | 127/18723 | 7.83e-10 | 1.93e-08 | 92 |
GO:00063992 | Esophagus | ESCC | tRNA metabolic process | 122/8552 | 179/18723 | 9.03e-10 | 2.19e-08 | 122 |
GO:00322592 | Esophagus | ESCC | methylation | 222/8552 | 364/18723 | 2.26e-09 | 5.09e-08 | 222 |
GO:00094512 | Esophagus | ESCC | RNA modification | 114/8552 | 167/18723 | 2.76e-09 | 6.04e-08 | 114 |
GO:00015101 | Esophagus | ESCC | RNA methylation | 58/8552 | 83/18723 | 6.87e-06 | 6.94e-05 | 58 |
GO:00064002 | Esophagus | ESCC | tRNA modification | 62/8552 | 90/18723 | 7.02e-06 | 7.04e-05 | 62 |
GO:00304881 | Esophagus | ESCC | tRNA methylation | 30/8552 | 41/18723 | 3.27e-04 | 1.93e-03 | 30 |
GO:00344702 | Liver | HCC | ncRNA processing | 293/7958 | 395/18723 | 4.26e-38 | 6.76e-35 | 293 |
GO:00346601 | Liver | HCC | ncRNA metabolic process | 332/7958 | 485/18723 | 1.48e-31 | 7.80e-29 | 332 |
GO:0008033 | Liver | HCC | tRNA processing | 87/7958 | 127/18723 | 2.66e-09 | 7.23e-08 | 87 |
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:0006399 | Liver | HCC | tRNA metabolic process | 108/7958 | 179/18723 | 1.07e-06 | 1.59e-05 | 108 |
GO:0009451 | Liver | HCC | RNA modification | 101/7958 | 167/18723 | 2.02e-06 | 2.78e-05 | 101 |
GO:0006400 | Liver | HCC | tRNA modification | 60/7958 | 90/18723 | 3.09e-06 | 4.09e-05 | 60 |
GO:0001510 | Liver | HCC | RNA methylation | 53/7958 | 83/18723 | 6.96e-05 | 6.29e-04 | 53 |
GO:0030488 | Liver | HCC | tRNA methylation | 29/7958 | 41/18723 | 2.38e-04 | 1.79e-03 | 29 |
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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 |
THUMPD3 | SNV | Missense_Mutation | novel | c.991N>T | p.Gly331Trp | p.G331W | Q9BV44 | protein_coding | deleterious(0.01) | probably_damaging(1) | TCGA-A7-A0DB-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | arimidex | SD |
THUMPD3 | SNV | Missense_Mutation | novel | c.120N>G | p.Ile40Met | p.I40M | Q9BV44 | protein_coding | deleterious(0) | possibly_damaging(0.826) | TCGA-A8-A095-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | 5-fluorouracil | CR |
THUMPD3 | SNV | Missense_Mutation | novel | c.1285N>A | p.Glu429Lys | p.E429K | Q9BV44 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-D8-A1JS-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | tamoxiphen | SD |
THUMPD3 | SNV | Missense_Mutation | rs766648779 | c.526A>T | p.Thr176Ser | p.T176S | Q9BV44 | protein_coding | tolerated(0.77) | benign(0) | TCGA-E2-A1L8-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cyclophosphamide | SD |
THUMPD3 | insertion | Nonsense_Mutation | novel | c.166_167insAGATCTTGTGAGACTTATTCACTACCACAAGAACAGTA | p.Val56GlufsTer4 | p.V56Efs*4 | Q9BV44 | protein_coding | TCGA-B6-A0IK-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | PD | ||
THUMPD3 | SNV | Missense_Mutation | novel | c.31N>T | p.Leu11Phe | p.L11F | Q9BV44 | protein_coding | tolerated_low_confidence(0.14) | benign(0.007) | TCGA-C5-A2LV-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
THUMPD3 | SNV | Missense_Mutation | novel | c.977N>A | p.Pro326Gln | p.P326Q | Q9BV44 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-AA-3947-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
THUMPD3 | SNV | Missense_Mutation | c.1114A>T | p.Ile372Phe | p.I372F | Q9BV44 | protein_coding | tolerated(0.05) | possibly_damaging(0.49) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR | |
THUMPD3 | SNV | Missense_Mutation | c.1519G>A | p.Glu507Lys | p.E507K | Q9BV44 | protein_coding | tolerated_low_confidence(0.05) | benign(0) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR | |
THUMPD3 | SNV | Missense_Mutation | rs140248268 | c.541N>T | p.Asp181Tyr | p.D181Y | Q9BV44 | protein_coding | deleterious(0) | possibly_damaging(0.564) | TCGA-CA-6717-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | oxaliplatin | 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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