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Gene: NOC2L |
Gene summary for NOC2L |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | NOC2L | Gene ID | 26155 |
| Gene name | NOC2 like nucleolar associated transcriptional repressor | |
| Gene Alias | NET15 | |
| Cytomap | 1p36.33 | |
| Gene Type | protein-coding | GO ID | GO:0000122 | UniProtAcc | Q9Y3T9 |
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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 |
| 26155 | NOC2L | LZE2T | Human | Esophagus | ESCC | 2.84e-03 | 5.15e-01 | 0.082 |
| 26155 | NOC2L | LZE4T | Human | Esophagus | ESCC | 2.36e-17 | 3.69e-01 | 0.0811 |
| 26155 | NOC2L | LZE7T | Human | Esophagus | ESCC | 3.51e-12 | 7.08e-01 | 0.0667 |
| 26155 | NOC2L | LZE8T | Human | Esophagus | ESCC | 1.18e-04 | 3.15e-01 | 0.067 |
| 26155 | NOC2L | LZE20T | Human | Esophagus | ESCC | 1.25e-07 | 2.62e-01 | 0.0662 |
| 26155 | NOC2L | LZE22T | Human | Esophagus | ESCC | 1.18e-07 | 5.58e-01 | 0.068 |
| 26155 | NOC2L | LZE24T | Human | Esophagus | ESCC | 1.38e-21 | 6.60e-01 | 0.0596 |
| 26155 | NOC2L | P1T-E | Human | Esophagus | ESCC | 5.85e-13 | 6.13e-01 | 0.0875 |
| 26155 | NOC2L | P2T-E | Human | Esophagus | ESCC | 5.52e-39 | 7.13e-01 | 0.1177 |
| 26155 | NOC2L | P4T-E | Human | Esophagus | ESCC | 1.14e-39 | 1.09e+00 | 0.1323 |
| 26155 | NOC2L | P5T-E | Human | Esophagus | ESCC | 2.65e-39 | 7.28e-01 | 0.1327 |
| 26155 | NOC2L | P8T-E | Human | Esophagus | ESCC | 7.74e-47 | 8.52e-01 | 0.0889 |
| 26155 | NOC2L | P9T-E | Human | Esophagus | ESCC | 9.52e-11 | 3.36e-01 | 0.1131 |
| 26155 | NOC2L | P10T-E | Human | Esophagus | ESCC | 5.00e-58 | 9.58e-01 | 0.116 |
| 26155 | NOC2L | P11T-E | Human | Esophagus | ESCC | 4.68e-09 | 6.50e-01 | 0.1426 |
| 26155 | NOC2L | P12T-E | Human | Esophagus | ESCC | 2.40e-27 | 5.49e-01 | 0.1122 |
| 26155 | NOC2L | P15T-E | Human | Esophagus | ESCC | 1.12e-34 | 8.76e-01 | 0.1149 |
| 26155 | NOC2L | P16T-E | Human | Esophagus | ESCC | 6.32e-40 | 5.68e-01 | 0.1153 |
| 26155 | NOC2L | P17T-E | Human | Esophagus | ESCC | 1.25e-13 | 8.99e-01 | 0.1278 |
| 26155 | NOC2L | P19T-E | Human | Esophagus | ESCC | 2.35e-08 | 8.63e-01 | 0.1662 |
| Page: 1 2 3 4 5 6 |
| 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 | ||
| Liver |  | HCC: Hepatocellular carcinoma |
| NAFLD: Non-alcoholic fatty liver disease | ||
| Oral Cavity |  | EOLP: Erosive Oral lichen planus |
| LP: leukoplakia | ||
| NEOLP: Non-erosive oral lichen planus | ||
| OSCC: Oral squamous cell carcinoma | ||
| 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: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:0097193111 | Esophagus | ESCC | intrinsic apoptotic signaling pathway | 222/8552 | 288/18723 | 5.87e-28 | 2.02e-25 | 222 |
| GO:001657015 | Esophagus | ESCC | histone modification | 323/8552 | 463/18723 | 2.61e-26 | 7.88e-24 | 323 |
| GO:2001233111 | Esophagus | ESCC | regulation of apoptotic signaling pathway | 256/8552 | 356/18723 | 4.11e-24 | 1.04e-21 | 256 |
| GO:001820514 | Esophagus | ESCC | peptidyl-lysine modification | 259/8552 | 376/18723 | 3.90e-20 | 5.26e-18 | 259 |
| GO:2001242111 | Esophagus | ESCC | regulation of intrinsic apoptotic signaling pathway | 128/8552 | 164/18723 | 1.75e-17 | 1.50e-15 | 128 |
| GO:2001234111 | Esophagus | ESCC | negative regulation of apoptotic signaling pathway | 161/8552 | 224/18723 | 1.24e-15 | 8.09e-14 | 161 |
| GO:0042273111 | Esophagus | ESCC | ribosomal large subunit biogenesis | 65/8552 | 72/18723 | 1.53e-15 | 9.82e-14 | 65 |
| GO:000941113 | Esophagus | ESCC | response to UV | 115/8552 | 149/18723 | 3.29e-15 | 1.93e-13 | 115 |
| GO:001839413 | Esophagus | ESCC | peptidyl-lysine acetylation | 123/8552 | 169/18723 | 6.58e-13 | 2.94e-11 | 123 |
| GO:004354313 | Esophagus | ESCC | protein acylation | 165/8552 | 243/18723 | 1.69e-12 | 7.14e-11 | 165 |
| GO:000647313 | Esophagus | ESCC | protein acetylation | 140/8552 | 201/18723 | 4.37e-12 | 1.69e-10 | 140 |
| GO:2001243111 | Esophagus | ESCC | negative regulation of intrinsic apoptotic signaling pathway | 78/8552 | 98/18723 | 5.50e-12 | 2.10e-10 | 78 |
| GO:001839313 | Esophagus | ESCC | internal peptidyl-lysine acetylation | 114/8552 | 158/18723 | 1.16e-11 | 4.24e-10 | 114 |
| GO:000647513 | Esophagus | ESCC | internal protein amino acid acetylation | 115/8552 | 160/18723 | 1.43e-11 | 5.08e-10 | 115 |
| GO:00165735 | Esophagus | ESCC | histone acetylation | 110/8552 | 152/18723 | 1.95e-11 | 6.81e-10 | 110 |
| GO:000931419 | Esophagus | ESCC | response to radiation | 277/8552 | 456/18723 | 4.42e-11 | 1.43e-09 | 277 |
| GO:003464413 | Esophagus | ESCC | cellular response to UV | 70/8552 | 90/18723 | 4.59e-10 | 1.20e-08 | 70 |
| GO:007121419 | Esophagus | ESCC | cellular response to abiotic stimulus | 206/8552 | 331/18723 | 7.52e-10 | 1.88e-08 | 206 |
| Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 |
| 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 |
| NOC2L | SNV | Missense_Mutation | c.576N>T | p.Glu192Asp | p.E192D | Q9Y3T9 | protein_coding | tolerated(0.37) | benign(0.015) | TCGA-A8-A08H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
| NOC2L | SNV | Missense_Mutation | rs144525853 | c.469T>C | p.Trp157Arg | p.W157R | Q9Y3T9 | protein_coding | deleterious(0) | probably_damaging(0.99) | TCGA-GM-A2DM-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | taxol | CR |
| NOC2L | SNV | Missense_Mutation | c.468A>T | p.Arg156Ser | p.R156S | Q9Y3T9 | protein_coding | tolerated(0.16) | benign(0.079) | TCGA-GM-A2DM-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | taxol | CR | |
| NOC2L | insertion | Nonsense_Mutation | novel | c.52_53insTATGTTGGTGAGTTGTGCAAAAAT | p.Glu18delinsValCysTrpTerValValGlnLysTer | p.E18delinsVCW*VVQK* | Q9Y3T9 | protein_coding | TCGA-A8-A06P-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unspecific | SD | |||
| NOC2L | insertion | Frame_Shift_Ins | novel | c.535_536insGACACTTT | p.Ala179GlyfsTer110 | p.A179Gfs*110 | Q9Y3T9 | protein_coding | TCGA-A8-A07J-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | 5-fluorouracil | CR | ||
| NOC2L | deletion | Frame_Shift_Del | novel | c.1438delC | p.Leu480TrpfsTer16 | p.L480Wfs*16 | Q9Y3T9 | protein_coding | TCGA-EW-A2FV-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | docetaxel | SD | ||
| NOC2L | SNV | Missense_Mutation | rs777608108 | c.1556G>A | p.Arg519Gln | p.R519Q | Q9Y3T9 | protein_coding | deleterious(0.02) | benign(0.058) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
| NOC2L | SNV | Missense_Mutation | novel | c.133N>C | p.Glu45Gln | p.E45Q | Q9Y3T9 | protein_coding | tolerated(0.53) | benign(0.225) | TCGA-JW-A5VL-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
| NOC2L | SNV | Missense_Mutation | rs112703241 | c.1378N>T | p.Arg460Cys | p.R460C | Q9Y3T9 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-A6-6653-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
| NOC2L | SNV | Missense_Mutation | rs773184606 | c.326N>T | p.Pro109Leu | p.P109L | Q9Y3T9 | protein_coding | tolerated(0.22) | benign(0.031) | TCGA-AY-4071-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
| Page: 1 2 3 4 5 6 |
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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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