HCSGD entry for NBN
1. General information
Official gene symbol | NBN |
---|---|
Entrez ID | 4683 |
Gene full name | nibrin |
Other gene symbols | AT-V1 AT-V2 ATV NBS NBS1 P95 |
Links to Entrez Gene | Links to Entrez Gene |
2. Neighbors in the network

This gene isn't in Literature mining network.
3. Gene ontology annotation
GO ID | GO term | Evidence | Category |
---|---|---|---|
GO:0000077 | DNA damage checkpoint | IDA | biological_process |
GO:0000723 | Telomere maintenance | IMP | biological_process |
GO:0000724 | Double-strand break repair via homologous recombination | TAS | biological_process |
GO:0000784 | Nuclear chromosome, telomeric region | IDA | cellular_component |
GO:0001832 | Blastocyst growth | IEA | biological_process |
GO:0003684 | Damaged DNA binding | IC IEA | molecular_function |
GO:0004003 | ATP-dependent DNA helicase activity | IMP | molecular_function |
GO:0005515 | Protein binding | IPI | molecular_function |
GO:0005634 | Nucleus | IDA IEA | cellular_component |
GO:0005654 | Nucleoplasm | TAS | cellular_component |
GO:0005657 | Replication fork | IEA | cellular_component |
GO:0005730 | Nucleolus | IDA | cellular_component |
GO:0006200 | ATP catabolic process | IMP | biological_process |
GO:0006281 | DNA repair | TAS | biological_process |
GO:0006302 | Double-strand break repair | IDA TAS | biological_process |
GO:0007050 | Cell cycle arrest | TAS | biological_process |
GO:0007093 | Mitotic cell cycle checkpoint | IDA | biological_process |
GO:0007095 | Mitotic G2 DNA damage checkpoint | IDA IEA | biological_process |
GO:0007126 | Meiosis | IEA | biological_process |
GO:0008134 | Transcription factor binding | IPI | molecular_function |
GO:0008283 | Cell proliferation | IEA | biological_process |
GO:0016605 | PML body | IDA | cellular_component |
GO:0030174 | Regulation of DNA-dependent DNA replication initiation | TAS | biological_process |
GO:0030330 | DNA damage response, signal transduction by p53 class mediator | TAS | biological_process |
GO:0030870 | Mre11 complex | IDA | cellular_component |
GO:0031954 | Positive regulation of protein autophosphorylation | IDA | biological_process |
GO:0032508 | DNA duplex unwinding | IMP | biological_process |
GO:0033674 | Positive regulation of kinase activity | IDA | biological_process |
GO:0035861 | Site of double-strand break | IDA | cellular_component |
GO:0042405 | Nuclear inclusion body | IDA | cellular_component |
GO:0045190 | Isotype switching | IEA | biological_process |
GO:0047485 | Protein N-terminus binding | IPI | molecular_function |
GO:0050885 | Neuromuscular process controlling balance | IEA | biological_process |
GO:0097193 | Intrinsic apoptotic signaling pathway | IEA | biological_process |
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4. Expression levels in datasets
- Meta-analysis result
p-value up | p-value down | FDR up | FDR down |
---|---|---|---|
0.1552936629 | 0.0471966415 | 0.7832763929 | 0.4079281024 |
- Individual experiment result
( "-" represent NA in the specific microarray platform )
( "-" represent NA in the specific microarray platform )
Data source | Up or down | Log fold change |
---|---|---|
GSE11954 | Up | 0.5554019762 |
GSE13712_SHEAR | Up | 0.4585939077 |
GSE13712_STATIC | Up | 0.2524701558 |
GSE19018 | Down | -0.3049886470 |
GSE19899_A1 | Up | 0.2963999044 |
GSE19899_A2 | Up | 0.2201989293 |
PubMed_21979375_A1 | Up | 0.2173414012 |
PubMed_21979375_A2 | Up | 0.4532796289 |
GSE35957 | Down | -0.7807658756 |
GSE36640 | Down | -0.4710134192 |
GSE54402 | Up | 0.4909274744 |
GSE9593 | Down | -0.3745827681 |
GSE43922 | Up | 0.1779812560 |
GSE24585 | Down | -1.2438053584 |
GSE37065 | Up | 0.1950577202 |
GSE28863_A1 | Down | -0.0715487188 |
GSE28863_A2 | Down | -0.2203078184 |
GSE28863_A3 | Down | -1.1136542231 |
GSE28863_A4 | Up | 0.2428611709 |
GSE48662 | Down | -0.6636546939 |
5. Regulation relationships with compounds/drugs/microRNAs
- Compounds
Not regulated by compounds
- Drugs
Not regulated by drugs
- MicroRNAs
- mirTarBase
MiRNA_name | mirBase ID | miRTarBase ID | Experiment | Support type | References (Pubmed ID) |
---|---|---|---|---|---|
hsa-miR-132-3p | MIMAT0000426 | MIRT021833 | Microarray | Functional MTI (Weak) | 17612493 |
hsa-miR-215-5p | MIMAT0000272 | MIRT024642 | Microarray | Functional MTI (Weak) | 19074876 |
hsa-miR-192-5p | MIMAT0000222 | MIRT026789 | Microarray | Functional MTI (Weak) | 19074876 |
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- mirRecord
No target information from mirRecord
6. Text-mining results about the gene
Gene occurances in abstracts of cellular senescence-associated articles: 4 abstracts the gene occurs.
PubMed ID of the article | Sentenece the gene occurs |
---|---|
26731175 | We determined associations of frailty phenotype, a T-cell senescence marker (p16(INK4a) expression), age and demographics with exposures of the intracellular metabolites (IM) and endogenous nucleotides (EN) of tenofovir/emtricitabine (TFV/FTC), efavirenz (EFV), atazanavir (ATV) and ritonavir (RTV) |
26731175 | METHODS: Plasma and peripheral blood mononuclear cell samples for drug, IM and EN concentrations were collected at four time points in HIV+ adults receiving TFV/FTC with EFV or ATV/RTV |
26731175 | No associations were observed for EFV, ATV or RTV AUCs |
25948863 | 9% in the ATV/r group vs -3 |
25119968 | The role of nibrin in doxorubicin-induced apoptosis and cell senescence in Nijmegen Breakage Syndrome patients lymphocytes |
25119968 | Nibrin plays an important role in the DNA damage response (DDR) and DNA repair |
25119968 | To verify whether truncated nibrin (p70), causing Nijmegen Breakage Syndrome (NBS), is involved in DDR and cell fate upon DNA damage, we used two (S4 and S3R) spontaneously immortalized T cell lines from NBS patients, with the founding mutation and a control cell line (L5) |
25119968 | S4 and S3R cells have the same level of p70 nibrin, however p70 from S4 cells was able to form more complexes with ATM and BRCA1 |
25119968 | Downregulation of nibrin in normal human vascular smooth muscle cells (VSMCs) did not prevent the activation of DDR and induction of senescence |
25119968 | Our results indicate that a substantially reduced level of nibrin or its truncated p70 form is sufficient to induce DNA-damage dependent senescence in VSMCs and S4 cells, respectively |
19442255 | It is known that telomere length maintenance in ALT+ cells is dependent on the MRN [MRE11 (meiotic recombination 11)-Rad50-NBS1 (Nijmegen breakage syndrome 1)] complex, but knowledge of the role of other genes, including the Werner's (WRN) and Bloom's (BLM) syndrome DNA helicase genes, is still limited |
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