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Gene: NXN |
Gene summary for NXN |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | NXN | Gene ID | 64359 |
| Gene name | nucleoredoxin | |
| Gene Alias | NRX | |
| Cytomap | 17p13.3 | |
| Gene Type | protein-coding | GO ID | GO:0001701 | UniProtAcc | Q6DKJ4 |
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Malignant transformation analysis |
| Identification of the aberrant gene expression in precancerous and cancerous lesions by comparing the gene expression of stem-like cells in diseased tissues with normal stem cells |
| Malignant transformation involving gene list. |
| Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
| 64359 | NXN | LZE22D3 | Human | Esophagus | HGIN | 4.21e-04 | 4.54e-01 | 0.0653 |
| 64359 | NXN | LZE21T | Human | Esophagus | ESCC | 1.21e-07 | 4.67e-01 | 0.0655 |
| 64359 | NXN | P1T-E | Human | Esophagus | ESCC | 7.17e-03 | 4.02e-01 | 0.0875 |
| 64359 | NXN | P2T-E | Human | Esophagus | ESCC | 4.20e-17 | 3.57e-01 | 0.1177 |
| 64359 | NXN | P4T-E | Human | Esophagus | ESCC | 2.49e-27 | 5.54e-01 | 0.1323 |
| 64359 | NXN | P5T-E | Human | Esophagus | ESCC | 3.49e-22 | 3.82e-01 | 0.1327 |
| 64359 | NXN | P8T-E | Human | Esophagus | ESCC | 1.25e-26 | 5.27e-01 | 0.0889 |
| 64359 | NXN | P9T-E | Human | Esophagus | ESCC | 3.40e-14 | 2.05e-01 | 0.1131 |
| 64359 | NXN | P10T-E | Human | Esophagus | ESCC | 4.54e-13 | 2.85e-01 | 0.116 |
| 64359 | NXN | P11T-E | Human | Esophagus | ESCC | 5.21e-07 | 1.91e-01 | 0.1426 |
| 64359 | NXN | P12T-E | Human | Esophagus | ESCC | 8.28e-26 | 6.02e-01 | 0.1122 |
| 64359 | NXN | P15T-E | Human | Esophagus | ESCC | 6.16e-07 | 2.29e-01 | 0.1149 |
| 64359 | NXN | P16T-E | Human | Esophagus | ESCC | 7.38e-22 | 1.21e-01 | 0.1153 |
| 64359 | NXN | P17T-E | Human | Esophagus | ESCC | 2.14e-02 | 1.61e-01 | 0.1278 |
| 64359 | NXN | P20T-E | Human | Esophagus | ESCC | 2.48e-13 | 2.18e-01 | 0.1124 |
| 64359 | NXN | P21T-E | Human | Esophagus | ESCC | 1.33e-23 | 3.29e-01 | 0.1617 |
| 64359 | NXN | P22T-E | Human | Esophagus | ESCC | 3.39e-08 | 1.73e-01 | 0.1236 |
| 64359 | NXN | P23T-E | Human | Esophagus | ESCC | 6.98e-16 | 4.07e-01 | 0.108 |
| 64359 | NXN | P24T-E | Human | Esophagus | ESCC | 1.84e-17 | 5.09e-01 | 0.1287 |
| 64359 | NXN | P26T-E | Human | Esophagus | ESCC | 8.07e-17 | 2.58e-01 | 0.1276 |
| Page: 1 2 3 4 5 6 7 |
| Transcriptomic changes along malignancy continuum. |
| Tissue | Expression Dynamics | Abbreviation |
| Cervix |  | CC: Cervix cancer |
| HSIL_HPV: HPV-infected high-grade squamous intraepithelial lesions | ||
| N_HPV: HPV-infected normal cervix | ||
| Endometrium |  | AEH: Atypical endometrial hyperplasia |
| EEC: Endometrioid Cancer | ||
| Esophagus |  | ESCC: Esophageal squamous cell carcinoma |
| HGIN: High-grade intraepithelial neoplasias | ||
| LGIN: Low-grade intraepithelial neoplasias | ||
| Lung |  | AAH: Atypical adenomatous hyperplasia |
| AIS: Adenocarcinoma in situ | ||
| IAC: Invasive lung adenocarcinoma | ||
| MIA: Minimally invasive adenocarcinoma | ||
| Oral Cavity |  | EOLP: Erosive Oral lichen planus |
| LP: leukoplakia | ||
| NEOLP: Non-erosive oral lichen planus | ||
| OSCC: Oral squamous cell carcinoma | ||
| Prostate |  | BPH: Benign Prostatic Hyperplasia |
| Skin |  | AK: Actinic keratosis |
| cSCC: Cutaneous squamous cell carcinoma | ||
| SCCIS:squamous cell carcinoma in situ | ||
| Thyroid |  | ATC: Anaplastic thyroid cancer |
| HT: Hashimoto's thyroiditis | ||
| PTC: Papillary thyroid cancer |
| ∗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 |
| Find out the enriched GO biological processes and KEGG pathways involved in transition from healthy to precancer to cancer |
| Figure of enriched GO biological processes. |
| 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 |
| Enriched GO biological processes. |
| GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
| GO:190332010 | Cervix | CC | regulation of protein modification by small protein conjugation or removal | 66/2311 | 242/18723 | 2.31e-10 | 3.46e-08 | 66 |
| GO:003139610 | Cervix | CC | regulation of protein ubiquitination | 59/2311 | 210/18723 | 5.90e-10 | 7.51e-08 | 59 |
| GO:00160557 | Cervix | CC | Wnt signaling pathway | 98/2311 | 444/18723 | 4.82e-09 | 4.65e-07 | 98 |
| GO:01987387 | Cervix | CC | cell-cell signaling by wnt | 98/2311 | 446/18723 | 6.16e-09 | 5.58e-07 | 98 |
| GO:00301117 | Cervix | CC | regulation of Wnt signaling pathway | 76/2311 | 328/18723 | 3.05e-08 | 2.08e-06 | 76 |
| GO:003139710 | Cervix | CC | negative regulation of protein ubiquitination | 28/2311 | 83/18723 | 3.32e-07 | 1.35e-05 | 28 |
| GO:190332110 | Cervix | CC | negative regulation of protein modification by small protein conjugation or removal | 29/2311 | 95/18723 | 2.15e-06 | 6.55e-05 | 29 |
| GO:00988699 | Cervix | CC | cellular oxidant detoxification | 30/2311 | 101/18723 | 2.72e-06 | 7.93e-05 | 30 |
| GO:19907489 | Cervix | CC | cellular detoxification | 30/2311 | 116/18723 | 5.34e-05 | 7.94e-04 | 30 |
| GO:00017018 | Cervix | CC | in utero embryonic development | 71/2311 | 367/18723 | 7.21e-05 | 1.00e-03 | 71 |
| GO:00972379 | Cervix | CC | cellular response to toxic substance | 31/2311 | 124/18723 | 8.09e-05 | 1.10e-03 | 31 |
| GO:00096369 | Cervix | CC | response to toxic substance | 52/2311 | 262/18723 | 3.34e-04 | 3.52e-03 | 52 |
| GO:00987549 | Cervix | CC | detoxification | 33/2311 | 152/18723 | 7.97e-04 | 7.00e-03 | 33 |
| GO:00301784 | Cervix | CC | negative regulation of Wnt signaling pathway | 35/2311 | 170/18723 | 1.52e-03 | 1.17e-02 | 35 |
| GO:190332016 | Endometrium | AEH | regulation of protein modification by small protein conjugation or removal | 67/2100 | 242/18723 | 1.10e-12 | 2.26e-10 | 67 |
| GO:003139616 | Endometrium | AEH | regulation of protein ubiquitination | 57/2100 | 210/18723 | 1.24e-10 | 1.40e-08 | 57 |
| GO:00301118 | Endometrium | AEH | regulation of Wnt signaling pathway | 71/2100 | 328/18723 | 3.31e-08 | 1.87e-06 | 71 |
| GO:003139716 | Endometrium | AEH | negative regulation of protein ubiquitination | 28/2100 | 83/18723 | 4.36e-08 | 2.40e-06 | 28 |
| GO:190332116 | Endometrium | AEH | negative regulation of protein modification by small protein conjugation or removal | 30/2100 | 95/18723 | 7.94e-08 | 4.04e-06 | 30 |
| GO:00160558 | Endometrium | AEH | Wnt signaling pathway | 85/2100 | 444/18723 | 4.99e-07 | 1.97e-05 | 85 |
| Page: 1 2 3 4 5 6 7 8 9 10 11 |
| Enriched KEGG pathways. |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
| Page: 1 |
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Cell-cell communication analysis |
| Identification of potential cell-cell interactions between two cell types and their ligand-receptor pairs for different disease states |
| Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
| Page: 1 |
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Single-cell gene regulatory network inference analysis |
| Find out the significant the regulons (TFs) and the target genes of each regulon across cell types for different disease states |
| 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. |
| Page: 1 |
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Somatic mutation of malignant transformation related genes |
| Annotation of somatic variants for genes involved in malignant transformation |
| 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 |
| NXN | SNV | Missense_Mutation | novel | c.464N>A | p.Arg155Gln | p.R155Q | Q6DKJ4 | protein_coding | tolerated(0.21) | probably_damaging(0.945) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
| NXN | SNV | Missense_Mutation | c.600N>A | p.Phe200Leu | p.F200L | Q6DKJ4 | protein_coding | deleterious(0.04) | probably_damaging(0.977) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
| NXN | SNV | Missense_Mutation | novel | c.1165N>T | p.Pro389Ser | p.P389S | Q6DKJ4 | protein_coding | tolerated(0.22) | probably_damaging(0.999) | TCGA-OL-A66J-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| NXN | SNV | Missense_Mutation | novel | c.1205N>T | p.Ala402Val | p.A402V | Q6DKJ4 | protein_coding | tolerated(0.12) | probably_damaging(0.996) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
| NXN | SNV | Missense_Mutation | c.383G>A | p.Arg128Gln | p.R128Q | Q6DKJ4 | protein_coding | deleterious(0.02) | benign(0.278) | TCGA-IR-A3LL-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
| NXN | SNV | Missense_Mutation | c.600N>A | p.Phe200Leu | p.F200L | Q6DKJ4 | protein_coding | deleterious(0.04) | probably_damaging(0.977) | TCGA-AA-A00N-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |
| NXN | SNV | Missense_Mutation | c.529C>T | p.Pro177Ser | p.P177S | Q6DKJ4 | protein_coding | tolerated(0.33) | probably_damaging(0.986) | TCGA-AD-A5EJ-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
| NXN | SNV | Missense_Mutation | novel | c.1226N>G | p.Asp409Gly | p.D409G | Q6DKJ4 | protein_coding | tolerated(0.1) | probably_damaging(0.997) | TCGA-AZ-4315-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
| NXN | SNV | Missense_Mutation | rs201764402 | c.604N>A | p.Ala202Thr | p.A202T | Q6DKJ4 | protein_coding | deleterious(0) | probably_damaging(0.995) | TCGA-CM-4743-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Chemotherapy | capecitabine | SD |
| NXN | SNV | Missense_Mutation | novel | c.860T>C | p.Val287Ala | p.V287A | Q6DKJ4 | protein_coding | deleterious(0.03) | benign(0.197) | TCGA-G4-6588-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
| Page: 1 2 3 4 |
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Related drugs of malignant transformation related genes |
| Identification of chemicals and drugs interact with genes involved in malignant transfromation |
| (DGIdb 4.0) |
| Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
| Page: 1 |
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