HCSGD entry for IFNB1
1. General information
Official gene symbol | IFNB1 |
---|---|
Entrez ID | 3456 |
Gene full name | interferon, beta 1, fibroblast |
Other gene symbols | IFB IFF IFNB |
Links to Entrez Gene | Links to Entrez Gene |
2. Neighbors in the network

3. Gene ontology annotation
GO ID | GO term | Evidence | Category |
---|---|---|---|
GO:0002250 | Adaptive immune response | IEA | biological_process |
GO:0002286 | T cell activation involved in immune response | IBA | biological_process |
GO:0002312 | B cell activation involved in immune response | IMP | biological_process |
GO:0002323 | Natural killer cell activation involved in immune response | IBA | biological_process |
GO:0005125 | Cytokine activity | IBA IDA | molecular_function |
GO:0005132 | Type I interferon receptor binding | NAS | molecular_function |
GO:0005576 | Extracellular region | IC TAS | cellular_component |
GO:0005615 | Extracellular space | IBA | cellular_component |
GO:0006919 | Activation of cysteine-type endopeptidase activity involved in apoptotic process | IDA NAS | biological_process |
GO:0006959 | Humoral immune response | IBA | biological_process |
GO:0007166 | Cell surface receptor signaling pathway | TAS | biological_process |
GO:0007596 | Blood coagulation | TAS | biological_process |
GO:0009615 | Response to virus | NAS | biological_process |
GO:0019221 | Cytokine-mediated signaling pathway | IBA TAS | biological_process |
GO:0030101 | Natural killer cell activation | NAS | biological_process |
GO:0030183 | B cell differentiation | IBA | biological_process |
GO:0033141 | Positive regulation of peptidyl-serine phosphorylation of STAT protein | IDA | biological_process |
GO:0042100 | B cell proliferation | NAS | biological_process |
GO:0042742 | Defense response to bacterium | IEA | biological_process |
GO:0043330 | Response to exogenous dsRNA | IDA | biological_process |
GO:0045071 | Negative regulation of viral genome replication | IDA | biological_process |
GO:0045087 | Innate immune response | TAS | biological_process |
GO:0045089 | Positive regulation of innate immune response | NAS | biological_process |
GO:0045343 | Regulation of MHC class I biosynthetic process | NAS | biological_process |
GO:0045581 | Negative regulation of T cell differentiation | IDA | biological_process |
GO:0045944 | Positive regulation of transcription from RNA polymerase II promoter | IDA | biological_process |
GO:0046597 | Negative regulation of viral entry into host cell | NAS | biological_process |
GO:0051607 | Defense response to virus | TAS | biological_process |
GO:0060337 | Type I interferon signaling pathway | TAS | biological_process |
GO:0060338 | Regulation of type I interferon-mediated signaling pathway | TAS | biological_process |
GO:0071360 | Cellular response to exogenous dsRNA | TAS | biological_process |
GO:0097194 | Execution phase of apoptosis | IDA | biological_process |
GO:2000552 | Negative regulation of T-helper 2 cell cytokine production | IDA | biological_process |
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4. Expression levels in datasets
- Meta-analysis result
p-value up | p-value down | FDR up | FDR down |
---|---|---|---|
0.5196326583 | 0.7851788686 | 0.9999902473 | 1.0000000000 |
- 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 | Down | -0.0249392766 |
GSE13712_SHEAR | Down | -0.1030767570 |
GSE13712_STATIC | Up | 0.2604059220 |
GSE19018 | Down | -0.0089434040 |
GSE19899_A1 | Down | -0.0070149926 |
GSE19899_A2 | Down | -0.0273641502 |
PubMed_21979375_A1 | Up | 0.0219866784 |
PubMed_21979375_A2 | Down | -0.2949382856 |
GSE35957 | Down | -0.1424927581 |
GSE36640 | Up | 0.0715166536 |
GSE54402 | Up | 0.1141328519 |
GSE9593 | Down | -0.1024507456 |
GSE43922 | Up | 0.0194052339 |
GSE24585 | Up | 0.1089286120 |
GSE37065 | Up | 0.0780541177 |
GSE28863_A1 | Up | 0.1023826505 |
GSE28863_A2 | Up | 0.3140326924 |
GSE28863_A3 | Up | 0.0983308474 |
GSE28863_A4 | Up | 0.0882292139 |
GSE48662 | Up | 0.0250548853 |
5. Regulation relationships with compounds/drugs/microRNAs
- Compounds
Not regulated by compounds
- Drugs
Name | Drug | Accession number |
---|---|---|
Beta-D-Glucose | DB02379 | EXPT00685 | EXPT00455 | EXPT01603 |
- MicroRNAs
- mirTarBase
MiRNA_name | mirBase ID | miRTarBase ID | Experiment | Support type | References (Pubmed ID) |
---|---|---|---|---|---|
hsa-let-7b-5p | MIMAT0000063 | MIRT004614 | ELISA//Luciferase reporter assay//qRT-PCR | Functional MTI | 20130213 |
hsa-miR-26a-5p | MIMAT0000082 | MIRT004615 | ELISA//Luciferase reporter assay//qRT-PCR | Functional MTI | 20130213 |
hsa-miR-145-5p | MIMAT0000437 | MIRT004616 | ELISA//Luciferase reporter assay//qRT-PCR | Functional MTI | 20130213 |
hsa-miR-34a-5p | MIMAT0000255 | MIRT004617 | ELISA//Luciferase reporter assay//qRT-PCR | Functional MTI | 20130213 |
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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: 10 abstracts the gene occurs.
PubMed ID of the article | Sentenece the gene occurs |
---|---|
27063514 | DDR-induced signaling in cells activates the ATM-p53 and ATM-IKKalpha/beta-interferon (IFN)-beta signaling pathways, thus leading to an induction of the p53 and IFN-inducible IFI16 gene |
27063514 | Further, upon DNA-damage, DNA accumulates in the cytoplasm, thereby inducing the IFI16 protein and STING-dependent IFN-beta production and activation of the IFI16 inflammasome, resulting in the production of proinflammatory cytokines (e |
27039820 | We here aimed to investigate cellular senescence in immortalized cholangiocyte and cholangiocarcinoma cell lines using five different inducing agents: 5-aza-2'deoxycytidine, bromodeoxyuridine, interferons (IFNbeta and IFNgamma), and hydrogen peroxide |
22864395 | Significantly, higher IFNbeta and chemokine gene transcripts have been observed, together with increased STAT1 and decreased STAT3 and NF-kappaB signaling activities |
22864395 | The knockdown of Maml1 transcription in the human melanoma cell line M537 also results in senescence, IFNbeta upregulation, increased chemokine gene expression, and greater NK and CD8(+) T cell migration in a transwell system |
22615843 | In particular, upon longer IFN-beta treatments, cutaneous HPV38 expressing cells undergo senescence |
22615843 | IFN-beta appears to induce senescence by upregulating the expression of the tumor suppressor PML, a well known IFN-induced gene |
22615843 | IFN-beta treatment leads to a modulation of p53 phosphorylation and acetylation status and a reduction in the expression of the p53 dominant negative DeltaNp73 |
21471287 | On sensing dsDNA, the IFI16 protein induces the expression of IFN-beta whereas the AIM2 protein forms an inflammasome, which promotes the secretion of IL-1beta |
21471287 | The IFN-beta treatment of the young HDFs, which induced the expression of IFI16 and AIM2 proteins, activated a DNA damage response and also increased basal levels of IL-1beta |
19802007 | JAK1/STAT-activating ligands, interleukin 10 (IL10), IL20, IL24, interferon gamma (IFNgamma), IFNbeta and IL6, were also expressed by senescent cells, supporting autocrine/paracrine activation of JAK1/STAT |
16989575 | PTX1(ERGIC2)-VP22 fusion protein upregulates interferon-beta in prostate cancer cell line PC-3 |
16989575 | Gene expression microarray analyses showed that interferon-beta (IFN-beta) and a number of IFN-inducible genes, among other genes, were upregulated by the PTX1-VP22 fusion protein |
16989575 | Upregulation of IFN-beta was confirmed by RTPCR and promoter-reporter assay |
16989575 | However, the upregulation of IFN-beta by the PTX1-VP22 fusion protein was not due to nuclear translocation of the PTX1 luminal domain |
14563561 | These studies demonstrate that IFN-beta controls hPNPase(old-35) expression by transcriptional modulation rather than by altering mRNA stability |
14563561 | Transcriptional activation of hPNPase(old-35) by IFN-beta is primarily mediated by the interferon stimulatory response element (ISRE) present in its promoter |
9144735 | Non-polarized secretion of mouse interferon-beta from gene-transferred human intestinal Caco-2 cells |
9144735 | To this end, Caco-2 cells derived from human colon carcinoma were transfected with a mouse interferon-beta (IFN-beta) expression vector and several stable sublines were established; this hetero-specific cytokine allows unexpected cellular effects to be avoided |
9144735 | METHODS: The secretion polarity of mouse IFN-beta in its gene-transduced Caco-2 sublines was studied in a bicameral culture system in which the chambers were separated by microporous filters |
9144735 | RESULTS: Mouse IFN-beta was secreted to the same extent from both apical and basolateral surfaces of the transduced cells regardless of cell aging |
8376318 | Effects of tumor necrosis factor and interferon-beta on proliferation and epidermal growth factor binding in young and senescent WI-38 cells |
8376318 | We have examined the effects of TNF and IFN-beta on the proliferation of WI-38 cells in a serum-free, growth factor-supplemented medium and in serum-containing medium |
8376318 | IFN-beta inhibits DNA synthesis 60 to 70% in both young and senescent cells |
8376318 | TNF and IFN-beta together have a synergistic effect and completely inhibit growth factor-stimulated DNA synthesis in young cells |
8376318 | IFN-beta has little or no effect on EGF binding either alone or in combination with TNF |
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