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Gene: NPM3 |
Gene summary for NPM3 |
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Gene information | Species | Human | Gene symbol | NPM3 | Gene ID | 10360 |
Gene name | nucleophosmin/nucleoplasmin 3 | |
Gene Alias | PORMIN | |
Cytomap | 10q24.32 | |
Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | O75607 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
10360 | NPM3 | LZE2T | Human | Esophagus | ESCC | 1.43e-02 | 3.77e-01 | 0.082 |
10360 | NPM3 | LZE4T | Human | Esophagus | ESCC | 3.29e-08 | 1.41e-01 | 0.0811 |
10360 | NPM3 | LZE5T | Human | Esophagus | ESCC | 6.41e-03 | 9.48e-02 | 0.0514 |
10360 | NPM3 | LZE7T | Human | Esophagus | ESCC | 5.50e-09 | 2.30e-01 | 0.0667 |
10360 | NPM3 | LZE20T | Human | Esophagus | ESCC | 1.69e-07 | 1.17e-01 | 0.0662 |
10360 | NPM3 | LZE22T | Human | Esophagus | ESCC | 8.13e-03 | 1.77e-01 | 0.068 |
10360 | NPM3 | LZE24T | Human | Esophagus | ESCC | 5.03e-16 | 5.28e-01 | 0.0596 |
10360 | NPM3 | LZE21T | Human | Esophagus | ESCC | 9.87e-04 | 1.14e-01 | 0.0655 |
10360 | NPM3 | LZE6T | Human | Esophagus | ESCC | 1.29e-05 | 4.06e-01 | 0.0845 |
10360 | NPM3 | P1T-E | Human | Esophagus | ESCC | 1.80e-02 | 3.55e-01 | 0.0875 |
10360 | NPM3 | P2T-E | Human | Esophagus | ESCC | 4.30e-17 | 3.77e-01 | 0.1177 |
10360 | NPM3 | P4T-E | Human | Esophagus | ESCC | 5.74e-45 | 1.30e+00 | 0.1323 |
10360 | NPM3 | P5T-E | Human | Esophagus | ESCC | 6.96e-29 | 1.06e+00 | 0.1327 |
10360 | NPM3 | P8T-E | Human | Esophagus | ESCC | 6.17e-11 | 3.01e-02 | 0.0889 |
10360 | NPM3 | P9T-E | Human | Esophagus | ESCC | 9.68e-15 | 3.10e-01 | 0.1131 |
10360 | NPM3 | P10T-E | Human | Esophagus | ESCC | 5.77e-20 | 1.01e-01 | 0.116 |
10360 | NPM3 | P11T-E | Human | Esophagus | ESCC | 1.46e-10 | 4.11e-01 | 0.1426 |
10360 | NPM3 | P12T-E | Human | Esophagus | ESCC | 7.61e-31 | 6.70e-01 | 0.1122 |
10360 | NPM3 | P15T-E | Human | Esophagus | ESCC | 1.09e-23 | 6.48e-01 | 0.1149 |
10360 | NPM3 | P16T-E | Human | Esophagus | ESCC | 3.25e-24 | 6.25e-01 | 0.1153 |
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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:0022613111 | Esophagus | ESCC | ribonucleoprotein complex biogenesis | 365/8552 | 463/18723 | 1.74e-49 | 1.11e-45 | 365 |
GO:0042254111 | Esophagus | ESCC | ribosome biogenesis | 252/8552 | 299/18723 | 3.27e-44 | 1.04e-40 | 252 |
GO:003447015 | Esophagus | ESCC | ncRNA processing | 300/8552 | 395/18723 | 3.09e-35 | 3.26e-32 | 300 |
GO:0016072110 | Esophagus | ESCC | rRNA metabolic process | 197/8552 | 236/18723 | 1.31e-33 | 1.18e-30 | 197 |
GO:0006364110 | Esophagus | ESCC | rRNA processing | 189/8552 | 225/18723 | 4.88e-33 | 3.87e-30 | 189 |
GO:003466012 | Esophagus | ESCC | ncRNA metabolic process | 346/8552 | 485/18723 | 4.35e-31 | 2.51e-28 | 346 |
GO:000632517 | Esophagus | ESCC | chromatin organization | 240/8552 | 409/18723 | 6.52e-08 | 1.14e-06 | 240 |
GO:00987812 | Esophagus | ESCC | ncRNA transcription | 45/8552 | 56/18723 | 1.05e-07 | 1.72e-06 | 45 |
GO:00093032 | Esophagus | ESCC | rRNA transcription | 28/8552 | 34/18723 | 1.21e-05 | 1.12e-04 | 28 |
GO:002261312 | Liver | Cirrhotic | ribonucleoprotein complex biogenesis | 231/4634 | 463/18723 | 3.28e-32 | 6.86e-29 | 231 |
GO:004225412 | Liver | Cirrhotic | ribosome biogenesis | 154/4634 | 299/18723 | 1.18e-23 | 6.72e-21 | 154 |
GO:000636412 | Liver | Cirrhotic | rRNA processing | 115/4634 | 225/18723 | 1.12e-17 | 1.64e-15 | 115 |
GO:00160724 | Liver | Cirrhotic | rRNA metabolic process | 119/4634 | 236/18723 | 1.19e-17 | 1.70e-15 | 119 |
GO:00344701 | Liver | Cirrhotic | ncRNA processing | 158/4634 | 395/18723 | 1.09e-11 | 6.96e-10 | 158 |
GO:00346603 | Liver | Cirrhotic | ncRNA metabolic process | 173/4634 | 485/18723 | 3.64e-08 | 1.21e-06 | 173 |
GO:002261322 | Liver | HCC | ribonucleoprotein complex biogenesis | 355/7958 | 463/18723 | 7.76e-52 | 4.92e-48 | 355 |
GO:004225422 | Liver | HCC | ribosome biogenesis | 246/7958 | 299/18723 | 4.99e-46 | 1.58e-42 | 246 |
GO:00344702 | Liver | HCC | ncRNA processing | 293/7958 | 395/18723 | 4.26e-38 | 6.76e-35 | 293 |
GO:001607212 | Liver | HCC | rRNA metabolic process | 193/7958 | 236/18723 | 1.26e-35 | 1.14e-32 | 193 |
GO:000636421 | Liver | HCC | rRNA processing | 185/7958 | 225/18723 | 8.14e-35 | 6.45e-32 | 185 |
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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 |
NPM3 | SNV | Missense_Mutation | novel | c.342C>G | p.Phe114Leu | p.F114L | O75607 | protein_coding | deleterious(0.02) | possibly_damaging(0.545) | TCGA-5L-AAT1-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Hormone Therapy | letrozol | SD |
NPM3 | SNV | Missense_Mutation | rs773885926 | c.114N>A | p.Phe38Leu | p.F38L | O75607 | protein_coding | tolerated(1) | benign(0.009) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR |
NPM3 | SNV | Missense_Mutation | novel | c.325N>A | p.Leu109Ile | p.L109I | O75607 | protein_coding | deleterious(0.03) | possibly_damaging(0.672) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
NPM3 | SNV | Missense_Mutation | novel | c.480N>T | p.Glu160Asp | p.E160D | O75607 | protein_coding | tolerated(0.16) | benign(0) | TCGA-AP-A1DO-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
NPM3 | SNV | Missense_Mutation | rs771883465 | c.377C>T | p.Ser126Leu | p.S126L | O75607 | protein_coding | tolerated(0.07) | probably_damaging(0.957) | TCGA-E6-A1LX-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
NPM3 | SNV | Missense_Mutation | novel | c.422N>T | p.Thr141Met | p.T141M | O75607 | protein_coding | tolerated(0.13) | benign(0.06) | TCGA-EO-A3AY-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | PD |
NPM3 | insertion | Frame_Shift_Ins | novel | c.527_528insG | p.Arg177GlnfsTer21 | p.R177Qfs*21 | O75607 | protein_coding | TCGA-AX-A2HA-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | ||
NPM3 | SNV | Missense_Mutation | c.193N>T | p.Ala65Ser | p.A65S | O75607 | protein_coding | tolerated(0.97) | possibly_damaging(0.76) | TCGA-44-6776-01 | Lung | lung adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
NPM3 | SNV | Missense_Mutation | rs745777576 | c.217N>A | p.Glu73Lys | p.E73K | O75607 | protein_coding | tolerated(0.19) | benign(0.067) | TCGA-CN-A6V1-01 | Oral cavity | head & neck squamous cell carcinoma | Male | <65 | I/II | Immunotherapy | erbitux | CR |
NPM3 | SNV | Missense_Mutation | c.394N>G | p.Arg132Gly | p.R132G | O75607 | protein_coding | deleterious(0.04) | benign(0.259) | TCGA-CV-A461-01 | Oral cavity | head & neck squamous cell carcinoma | Male | >=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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