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Gene: NUP205 |
Gene summary for NUP205 |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | NUP205 | Gene ID | 23165 |
| Gene name | nucleoporin 205 | |
| Gene Alias | C7orf14 | |
| Cytomap | 7q33 | |
| Gene Type | protein-coding | GO ID | GO:0006403 | UniProtAcc | Q92621 |
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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 |
| 23165 | NUP205 | P24T-E | Human | Esophagus | ESCC | 8.28e-08 | 1.94e-01 | 0.1287 |
| 23165 | NUP205 | P26T-E | Human | Esophagus | ESCC | 6.67e-15 | 3.17e-01 | 0.1276 |
| 23165 | NUP205 | P27T-E | Human | Esophagus | ESCC | 1.24e-07 | 2.40e-01 | 0.1055 |
| 23165 | NUP205 | P28T-E | Human | Esophagus | ESCC | 1.66e-15 | 2.50e-01 | 0.1149 |
| 23165 | NUP205 | P30T-E | Human | Esophagus | ESCC | 4.40e-09 | 4.24e-01 | 0.137 |
| 23165 | NUP205 | P31T-E | Human | Esophagus | ESCC | 1.50e-08 | 1.80e-01 | 0.1251 |
| 23165 | NUP205 | P32T-E | Human | Esophagus | ESCC | 1.09e-17 | 3.44e-01 | 0.1666 |
| 23165 | NUP205 | P36T-E | Human | Esophagus | ESCC | 1.29e-02 | 1.28e-01 | 0.1187 |
| 23165 | NUP205 | P37T-E | Human | Esophagus | ESCC | 4.60e-13 | 3.08e-01 | 0.1371 |
| 23165 | NUP205 | P38T-E | Human | Esophagus | ESCC | 5.56e-05 | 1.50e-01 | 0.127 |
| 23165 | NUP205 | P39T-E | Human | Esophagus | ESCC | 2.49e-05 | 1.45e-01 | 0.0894 |
| 23165 | NUP205 | P42T-E | Human | Esophagus | ESCC | 4.99e-02 | 2.35e-01 | 0.1175 |
| 23165 | NUP205 | P44T-E | Human | Esophagus | ESCC | 2.80e-06 | 5.97e-02 | 0.1096 |
| 23165 | NUP205 | P47T-E | Human | Esophagus | ESCC | 1.66e-04 | 3.36e-02 | 0.1067 |
| 23165 | NUP205 | P49T-E | Human | Esophagus | ESCC | 8.45e-05 | 5.54e-01 | 0.1768 |
| 23165 | NUP205 | P52T-E | Human | Esophagus | ESCC | 6.15e-12 | 1.95e-01 | 0.1555 |
| 23165 | NUP205 | P54T-E | Human | Esophagus | ESCC | 2.18e-07 | 2.35e-01 | 0.0975 |
| 23165 | NUP205 | P57T-E | Human | Esophagus | ESCC | 4.44e-08 | 1.09e-01 | 0.0926 |
| 23165 | NUP205 | P61T-E | Human | Esophagus | ESCC | 3.67e-08 | 1.79e-01 | 0.099 |
| 23165 | NUP205 | P62T-E | Human | Esophagus | ESCC | 5.57e-09 | 8.56e-02 | 0.1302 |
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| Transcriptomic changes along malignancy continuum. |
| Tissue | Expression Dynamics | Abbreviation |
| Esophagus |  | ESCC: Esophageal squamous cell carcinoma |
| HGIN: High-grade intraepithelial neoplasias | ||
| LGIN: Low-grade intraepithelial neoplasias | ||
| 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:0006913110 | Esophagus | ESCC | nucleocytoplasmic transport | 230/8552 | 301/18723 | 6.04e-28 | 2.02e-25 | 230 |
| GO:0051169110 | Esophagus | ESCC | nuclear transport | 230/8552 | 301/18723 | 6.04e-28 | 2.02e-25 | 230 |
| GO:0006403110 | Esophagus | ESCC | RNA localization | 166/8552 | 201/18723 | 1.95e-27 | 6.18e-25 | 166 |
| GO:005123617 | Esophagus | ESCC | establishment of RNA localization | 134/8552 | 166/18723 | 1.23e-20 | 1.81e-18 | 134 |
| GO:005102815 | Esophagus | ESCC | mRNA transport | 110/8552 | 130/18723 | 2.76e-20 | 3.80e-18 | 110 |
| GO:005065717 | Esophagus | ESCC | nucleic acid transport | 131/8552 | 163/18723 | 6.94e-20 | 8.46e-18 | 131 |
| GO:005065817 | Esophagus | ESCC | RNA transport | 131/8552 | 163/18723 | 6.94e-20 | 8.46e-18 | 131 |
| GO:001593117 | Esophagus | ESCC | nucleobase-containing compound transport | 162/8552 | 222/18723 | 9.87e-17 | 7.93e-15 | 162 |
| GO:000699713 | Esophagus | ESCC | nucleus organization | 96/8552 | 133/18723 | 4.66e-10 | 1.21e-08 | 96 |
| GO:00069994 | Esophagus | ESCC | nuclear pore organization | 14/8552 | 14/18723 | 1.71e-05 | 1.52e-04 | 14 |
| GO:00469316 | Esophagus | ESCC | pore complex assembly | 16/8552 | 20/18723 | 1.85e-03 | 8.40e-03 | 16 |
| GO:0006913112 | Thyroid | PTC | nucleocytoplasmic transport | 181/5968 | 301/18723 | 2.93e-24 | 7.69e-22 | 181 |
| GO:0051169112 | Thyroid | PTC | nuclear transport | 181/5968 | 301/18723 | 2.93e-24 | 7.69e-22 | 181 |
| GO:0006403112 | Thyroid | PTC | RNA localization | 130/5968 | 201/18723 | 9.23e-22 | 1.94e-19 | 130 |
| GO:0051236110 | Thyroid | PTC | establishment of RNA localization | 100/5968 | 166/18723 | 4.26e-14 | 2.58e-12 | 100 |
| GO:0050657110 | Thyroid | PTC | nucleic acid transport | 98/5968 | 163/18723 | 9.08e-14 | 4.90e-12 | 98 |
| GO:0050658110 | Thyroid | PTC | RNA transport | 98/5968 | 163/18723 | 9.08e-14 | 4.90e-12 | 98 |
| GO:0015931110 | Thyroid | PTC | nucleobase-containing compound transport | 120/5968 | 222/18723 | 5.45e-12 | 2.35e-10 | 120 |
| GO:005102817 | Thyroid | PTC | mRNA transport | 78/5968 | 130/18723 | 3.44e-11 | 1.26e-09 | 78 |
| GO:00069977 | Thyroid | PTC | nucleus organization | 65/5968 | 133/18723 | 3.16e-05 | 3.01e-04 | 65 |
| Page: 1 2 |
| Enriched KEGG pathways. |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
| hsa05014210 | Esophagus | ESCC | Amyotrophic lateral sclerosis | 266/4205 | 364/8465 | 1.31e-20 | 2.20e-18 | 1.13e-18 | 266 |
| hsa0301321 | Esophagus | ESCC | Nucleocytoplasmic transport | 89/4205 | 108/8465 | 1.20e-12 | 2.37e-11 | 1.21e-11 | 89 |
| hsa0501438 | Esophagus | ESCC | Amyotrophic lateral sclerosis | 266/4205 | 364/8465 | 1.31e-20 | 2.20e-18 | 1.13e-18 | 266 |
| hsa0301331 | Esophagus | ESCC | Nucleocytoplasmic transport | 89/4205 | 108/8465 | 1.20e-12 | 2.37e-11 | 1.21e-11 | 89 |
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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 |
| NUP205 | SNV | Missense_Mutation | novel | c.1102N>T | p.Val368Phe | p.V368F | Q92621 | protein_coding | deleterious(0) | possibly_damaging(0.694) | TCGA-A8-A06P-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unspecific | SD | |
| NUP205 | SNV | Missense_Mutation | c.3437A>G | p.Asp1146Gly | p.D1146G | Q92621 | protein_coding | deleterious(0) | probably_damaging(0.977) | TCGA-A8-A08R-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
| NUP205 | SNV | Missense_Mutation | rs566054477 | c.5899N>A | p.Ala1967Thr | p.A1967T | Q92621 | protein_coding | tolerated(0.2) | benign(0.003) | TCGA-AO-A0J5-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Other, specify in notesBisphosphonate | zoledronic | PD |
| NUP205 | SNV | Missense_Mutation | rs367553464 | c.4772G>A | p.Arg1591His | p.R1591H | Q92621 | protein_coding | tolerated(0.11) | probably_damaging(0.91) | TCGA-BH-A0HN-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | arimidex | SD |
| NUP205 | SNV | Missense_Mutation | novel | c.118N>T | p.Asp40Tyr | p.D40Y | Q92621 | protein_coding | deleterious(0) | probably_damaging(0.957) | TCGA-BH-A209-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| NUP205 | SNV | Missense_Mutation | c.1425C>G | p.Ile475Met | p.I475M | Q92621 | protein_coding | tolerated(0.29) | benign(0.048) | TCGA-D8-A1J8-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | nolvadex | SD | |
| NUP205 | SNV | Missense_Mutation | rs547020231 | c.1433N>G | p.Ser478Cys | p.S478C | Q92621 | protein_coding | deleterious(0.01) | possibly_damaging(0.853) | TCGA-E2-A152-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Targeted Molecular therapy | trastuzumab | PD |
| NUP205 | insertion | Frame_Shift_Ins | novel | c.4902_4903insTTCTATTCTAAACACAGCATTTTCAATATAGTATATA | p.Met1635PhefsTer32 | p.M1635Ffs*32 | Q92621 | protein_coding | TCGA-A2-A0EO-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD | ||
| NUP205 | insertion | Frame_Shift_Ins | novel | c.4607_4608insCCTCCTTCATTTATTTA | p.Leu1536PhefsTer18 | p.L1536Ffs*18 | Q92621 | protein_coding | TCGA-C8-A134-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | 5-fluorouracil | CR | ||
| NUP205 | SNV | Missense_Mutation | rs554848551 | c.3155C>T | p.Ala1052Val | p.A1052V | Q92621 | protein_coding | tolerated(0.2) | benign(0.058) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
| Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 |
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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 |
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