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Fusion Gene Summary | |
Fusion Gene ORF analysis | |
Fusion Genomic Features | |
Fusion Protein Features | |
Fusion Gene Sequence | |
Fusion Gene PPI analysis | |
Related Drugs | |
Related Diseases |
Fusion gene:LBP-F2 (FusionGDB2 ID:HG3929TG2147) |
Fusion Gene Summary for LBP-F2 |
Fusion gene summary |
Fusion gene information | Fusion gene name: LBP-F2 | Fusion gene ID: hg3929tg2147 | Hgene | Tgene | Gene symbol | LBP | F2 | Gene ID | 3929 | 2147 |
Gene name | lipopolysaccharide binding protein | coagulation factor II, thrombin | |
Synonyms | BPIFD2 | PT|RPRGL2|THPH1 | |
Cytomap | ('LBP')('F2') 20q11.23 | 11p11.2 | |
Type of gene | protein-coding | protein-coding | |
Description | lipopolysaccharide-binding proteinBPI fold containing family D, member 2LPS-binding protein | prothrombinprepro-coagulation factor IIprothrombin B-chainserine proteasethrombin factor II | |
Modification date | 20200313 | 20200329 | |
UniProtAcc | P18428 | P00734 | |
Ensembl transtripts involved in fusion gene | ENST00000217407, | ||
Fusion gene scores | * DoF score | 3 X 3 X 2=18 | 3 X 4 X 3=36 |
# samples | 3 | 4 | |
** MAII score | log2(3/18*10)=0.736965594166206 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | log2(4/36*10)=0.15200309344505 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | |
Context | PubMed: LBP [Title/Abstract] AND F2 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | LBP(36993406)-F2(46760598), # samples:1 | ||
Anticipated loss of major functional domain due to fusion event. | LBP-F2 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF. LBP-F2 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF. LBP-F2 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF. |
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types ** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10) |
Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez |
Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | LBP | GO:0015920 | lipopolysaccharide transport | 8985160 |
Hgene | LBP | GO:0031663 | lipopolysaccharide-mediated signaling pathway | 8409400|11739189 |
Hgene | LBP | GO:0032490 | detection of molecule of bacterial origin | 11528597 |
Hgene | LBP | GO:0032496 | response to lipopolysaccharide | 8409400|11739189 |
Hgene | LBP | GO:0032720 | negative regulation of tumor necrosis factor production | 11739189 |
Hgene | LBP | GO:0032755 | positive regulation of interleukin-6 production | 8409400 |
Hgene | LBP | GO:0032757 | positive regulation of interleukin-8 production | 8409400 |
Hgene | LBP | GO:0032760 | positive regulation of tumor necrosis factor production | 8409400|12594207 |
Hgene | LBP | GO:0033036 | macromolecule localization | 15294986 |
Hgene | LBP | GO:0034145 | positive regulation of toll-like receptor 4 signaling pathway | 11528597 |
Hgene | LBP | GO:0043032 | positive regulation of macrophage activation | 8409400 |
Hgene | LBP | GO:0045919 | positive regulation of cytolysis | 15294986 |
Hgene | LBP | GO:0050829 | defense response to Gram-negative bacterium | 11528597 |
Hgene | LBP | GO:0050830 | defense response to Gram-positive bacterium | 12932360 |
Hgene | LBP | GO:0071222 | cellular response to lipopolysaccharide | 12594207 |
Hgene | LBP | GO:0071223 | cellular response to lipoteichoic acid | 12594207 |
Tgene | F2 | GO:0001934 | positive regulation of protein phosphorylation | 7559487 |
Tgene | F2 | GO:0007166 | cell surface receptor signaling pathway | 1672265 |
Tgene | F2 | GO:0009611 | response to wounding | 9639571 |
Tgene | F2 | GO:0030168 | platelet activation | 9038223 |
Tgene | F2 | GO:0030194 | positive regulation of blood coagulation | 9038223 |
Tgene | F2 | GO:0032967 | positive regulation of collagen biosynthetic process | 9639571 |
Tgene | F2 | GO:0042730 | fibrinolysis | 12855810 |
Tgene | F2 | GO:0045861 | negative regulation of proteolysis | 1695900 |
Tgene | F2 | GO:0048712 | negative regulation of astrocyte differentiation | 1691280 |
Tgene | F2 | GO:0051281 | positive regulation of release of sequestered calcium ion into cytosol | 1672265|19052258 |
Tgene | F2 | GO:0051480 | regulation of cytosolic calcium ion concentration | 19052258 |
Tgene | F2 | GO:0051838 | cytolysis by host of symbiont cells | 20421939 |
Tgene | F2 | GO:0061844 | antimicrobial humoral immune response mediated by antimicrobial peptide | 20421939 |
Tgene | F2 | GO:0070945 | neutrophil mediated killing of gram-negative bacterium | 20421939 |
Tgene | F2 | GO:0090218 | positive regulation of lipid kinase activity | 11309392 |
Tgene | F2 | GO:1900016 | negative regulation of cytokine production involved in inflammatory response | 20421939 |
Tgene | F2 | GO:1900182 | positive regulation of protein localization to nucleus | 11309392 |
Tgene | F2 | GO:1900738 | positive regulation of phospholipase C-activating G protein-coupled receptor signaling pathway | 20164183 |
Tgene | F2 | GO:2000379 | positive regulation of reactive oxygen species metabolic process | 17275676 |
Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0) * All genome coordinats were lifted-over on hg19. * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
Source | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
ChimerDB4 | LIHC | TCGA-G3-A3CG-01A | LBP | chr20 | 36993406 | + | F2 | chr11 | 46760598 | + |
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Fusion Gene ORF analysis for LBP-F2 |
Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure. * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
ORF | Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
Frame-shift | ENST00000217407 | ENST00000311907 | LBP | chr20 | 36993406 | + | F2 | chr11 | 46760598 | + |
Frame-shift | ENST00000217407 | ENST00000530231 | LBP | chr20 | 36993406 | + | F2 | chr11 | 46760598 | + |
ORFfinder result based on the fusion transcript sequence of in-frame fusion genes. |
Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | Seq length (transcript) | BP loci (transcript) | Predicted start (transcript) | Predicted stop (transcript) | Seq length (amino acids) |
DeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated. |
Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
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Fusion Genomic Features for LBP-F2 |
FusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints. |
Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | 1-p | p (fusion gene breakpoint) |
LBP | chr20 | 36993406 | + | F2 | chr11 | 46760597 | + | 1.05E-05 | 0.9999895 |
LBP | chr20 | 36993406 | + | F2 | chr11 | 46760597 | + | 1.05E-05 | 0.9999895 |
Distribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page. |
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Fusion Protein Features for LBP-F2 |
Four levels of functional features of fusion genes Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:36993406/:46760598) - FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels. - How to search 1. Put your fusion gene symbol. 2. Press the tab key until there will be shown the breakpoint information filled. 4. Go down and press 'Search' tab twice. 4. Go down to have the hyperlink of the search result. 5. Click the hyperlink. 6. See the FGviewer result for your fusion gene. |
Main function of each fusion partner protein. (from UniProt) |
Hgene | Tgene |
LBP | F2 |
FUNCTION: Plays a role in the innate immune response. Binds to the lipid A moiety of bacterial lipopolysaccharides (LPS), a glycolipid present in the outer membrane of all Gram-negative bacteria (PubMed:7517398, PubMed:24120359). Acts as an affinity enhancer for CD14, facilitating its association with LPS. Promotes the release of cytokines in response to bacterial lipopolysaccharide (PubMed:7517398, PubMed:24120359). {ECO:0000269|PubMed:1698311, ECO:0000269|PubMed:20133493, ECO:0000269|PubMed:24120359, ECO:0000269|PubMed:7517398, ECO:0000305|PubMed:17481951}. | FUNCTION: Thrombin, which cleaves bonds after Arg and Lys, converts fibrinogen to fibrin and activates factors V, VII, VIII, XIII, and, in complex with thrombomodulin, protein C. Functions in blood homeostasis, inflammation and wound healing. {ECO:0000269|PubMed:2856554}. |
Retention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at * Minus value of BPloci means that the break pointn is located before the CDS. |
- In-frame and retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
- In-frame and not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
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Fusion Gene Sequence for LBP-F2 |
For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones. |
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Fusion Gene PPI Analysis for LBP-F2 |
Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in |
Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160) |
Hgene | Hgene's interactors | Tgene | Tgene's interactors |
- Retained PPIs in in-frame fusion. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
- Lost PPIs in in-frame fusion. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
- Retained PPIs, but lost function due to frame-shift fusion. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Related Drugs for LBP-F2 |
Drugs targeting genes involved in this fusion gene. (DrugBank Version 5.1.8 2021-05-08) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Tgene | F2 | P00734 | DB00001 | Lepirudin | Inhibitor | Biotech | Approved |
Tgene | F2 | P00734 | DB01123 | Proflavine | Other/unknown | Small molecule | Approved |
Tgene | F2 | P00734 | DB06404 | Human C1-esterase inhibitor | Inhibitor | Biotech | Approved |
Tgene | F2 | P00734 | DB06695 | Dabigatran etexilate | Inhibitor | Small molecule | Approved |
Tgene | F2 | P00734 | DB09332 | Kappadione | Agonist | Small molecule | Approved |
Tgene | F2 | P00734 | DB13152 | Coagulation Factor IX Human | Biotech | Approved | |
Tgene | F2 | P00734 | DB14738 | Turoctocog alfa pegol | Binder | Biotech | Approved |
Tgene | F2 | P00734 | DB00006 | Bivalirudin | Inhibitor | Small molecule | Approved|Investigational |
Tgene | F2 | P00734 | DB00100 | Coagulation Factor IX (Recombinant) | Biotech | Approved|Investigational | |
Tgene | F2 | P00734 | DB00278 | Argatroban | Inhibitor | Small molecule | Approved|Investigational |
Tgene | F2 | P00734 | DB01593 | Zinc | Small molecule | Approved|Investigational | |
Tgene | F2 | P00734 | DB05777 | Thrombomodulin Alfa | Inhibitor | Biotech | Approved|Investigational |
Tgene | F2 | P00734 | DB09109 | Turoctocog alfa | Binder | Biotech | Approved|Investigational |
Tgene | F2 | P00734 | DB09130 | Copper | Small molecule | Approved|Investigational | |
Tgene | F2 | P00734 | DB09228 | Conestat alfa | Inhibitor | Biotech | Approved|Investigational |
Tgene | F2 | P00734 | DB11166 | Antithrombin Alfa | Inhibitor | Biotech | Approved|Investigational |
Tgene | F2 | P00734 | DB13151 | Anti-inhibitor coagulant complex | Agonist | Biotech | Approved|Investigational |
Tgene | F2 | P00734 | DB14487 | Zinc acetate | Small molecule | Approved|Investigational | |
Tgene | F2 | P00734 | DB00055 | Drotrecogin alfa | Biotech | Approved|Investigational|Withdrawn | |
Tgene | F2 | P00734 | DB04898 | Ximelagatran | Inhibitor | Small molecule | Approved|Investigational|Withdrawn |
Tgene | F2 | P00734 | DB00170 | Menadione | Activator | Small molecule | Approved|Nutraceutical |
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Related Diseases for LBP-F2 |
Diseases associated with fusion partners. (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | LBP | C0023893 | Liver Cirrhosis, Experimental | 2 | CTD_human |
Hgene | LBP | C0001969 | Alcoholic Intoxication | 1 | PSYGENET |
Hgene | LBP | C0019193 | Hepatitis, Toxic | 1 | CTD_human |
Hgene | LBP | C0026766 | Multiple Organ Failure | 1 | CTD_human |
Hgene | LBP | C0028754 | Obesity | 1 | CTD_human |
Hgene | LBP | C0034189 | Pyemia | 1 | CTD_human |
Hgene | LBP | C0036690 | Septicemia | 1 | CTD_human |
Hgene | LBP | C0043094 | Weight Gain | 1 | CTD_human |
Hgene | LBP | C0243026 | Sepsis | 1 | CTD_human |
Hgene | LBP | C0524620 | Metabolic Syndrome X | 1 | CTD_human |
Hgene | LBP | C0860207 | Drug-Induced Liver Disease | 1 | CTD_human |
Hgene | LBP | C1262760 | Hepatitis, Drug-Induced | 1 | CTD_human |
Hgene | LBP | C1719672 | Severe Sepsis | 1 | CTD_human |
Hgene | LBP | C3658290 | Drug-Induced Acute Liver Injury | 1 | CTD_human |
Hgene | LBP | C4277682 | Chemical and Drug Induced Liver Injury | 1 | CTD_human |
Hgene | LBP | C4279912 | Chemically-Induced Liver Toxicity | 1 | CTD_human |
Tgene | C0020640 | Inherited Factor II deficiency | 14 | CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT | |
Tgene | C0040053 | Thrombosis | 4 | CTD_human | |
Tgene | C0087086 | Thrombus | 4 | CTD_human | |
Tgene | C0027051 | Myocardial Infarction | 3 | CTD_human | |
Tgene | C0042487 | Venous Thrombosis | 3 | CTD_human | |
Tgene | C0149871 | Deep Vein Thrombosis | 3 | CTD_human | |
Tgene | C0007786 | Brain Ischemia | 2 | CTD_human | |
Tgene | C0085762 | Alcohol abuse | 2 | PSYGENET | |
Tgene | C0272317 | Hereditary factor II deficiency disease | 2 | ORPHANET | |
Tgene | C0917798 | Cerebral Ischemia | 2 | CTD_human | |
Tgene | C3203356 | Factor II deficiency | 2 | ORPHANET | |
Tgene | C4722227 | Hypoprothrombinemias | 2 | CTD_human;GENOMICS_ENGLAND | |
Tgene | C0002395 | Alzheimer's Disease | 1 | CTD_human | |
Tgene | C0003873 | Rheumatoid Arthritis | 1 | CTD_human | |
Tgene | C0005779 | Blood Coagulation Disorders | 1 | CTD_human | |
Tgene | C0011265 | Presenile dementia | 1 | CTD_human | |
Tgene | C0012739 | Disseminated Intravascular Coagulation | 1 | CTD_human | |
Tgene | C0015695 | Fatty Liver | 1 | CTD_human | |
Tgene | C0019080 | Hemorrhage | 1 | CTD_human | |
Tgene | C0020564 | Hypertrophy | 1 | CTD_human | |
Tgene | C0023890 | Liver Cirrhosis | 1 | CTD_human | |
Tgene | C0027720 | Nephrosis | 1 | CTD_human | |
Tgene | C0027746 | Nerve Degeneration | 1 | CTD_human | |
Tgene | C0028754 | Obesity | 1 | CTD_human | |
Tgene | C0030524 | Paratuberculosis | 1 | CTD_human | |
Tgene | C0036341 | Schizophrenia | 1 | CTD_human | |
Tgene | C0037198 | Sinus Thrombosis, Intracranial | 1 | CTD_human | |
Tgene | C0038454 | Cerebrovascular accident | 1 | CTD_human | |
Tgene | C0040038 | Thromboembolism | 1 | CTD_human | |
Tgene | C0085605 | Liver Failure | 1 | CTD_human | |
Tgene | C0162819 | Skin Diseases, Vascular | 1 | CTD_human | |
Tgene | C0239946 | Fibrosis, Liver | 1 | CTD_human | |
Tgene | C0267412 | Mesenteric Venous Thrombosis | 1 | CTD_human | |
Tgene | C0276496 | Familial Alzheimer Disease (FAD) | 1 | CTD_human | |
Tgene | C0398623 | Thrombophilia | 1 | CTD_human | |
Tgene | C0400966 | Non-alcoholic Fatty Liver Disease | 1 | CTD_human | |
Tgene | C0494463 | Alzheimer Disease, Late Onset | 1 | CTD_human | |
Tgene | C0546126 | Acute Confusional Senile Dementia | 1 | CTD_human | |
Tgene | C0750900 | Alzheimer's Disease, Focal Onset | 1 | CTD_human | |
Tgene | C0750901 | Alzheimer Disease, Early Onset | 1 | CTD_human | |
Tgene | C0751500 | Petrous Sinus Thrombophlebitis | 1 | CTD_human | |
Tgene | C0751501 | Intracranial Sinus Thrombophlebitis | 1 | CTD_human | |
Tgene | C0751502 | Petrous Sinus Thrombosis | 1 | CTD_human | |
Tgene | C0751956 | Acute Cerebrovascular Accidents | 1 | CTD_human | |
Tgene | C1412000 | Mesenteric vascular insufficiency | 1 | CTD_human | |
Tgene | C1861172 | Venous Thromboembolism | 1 | CTD_human | |
Tgene | C2239176 | Liver carcinoma | 1 | CTD_human | |
Tgene | C2711227 | Steatohepatitis | 1 | CTD_human | |
Tgene | C3241937 | Nonalcoholic Steatohepatitis | 1 | CTD_human | |
Tgene | C3852984 | Acute Mesenteric Arterial Embolus | 1 | CTD_human | |
Tgene | C3852985 | Occlusive Mesenteric Arterial Ischemia | 1 | CTD_human | |
Tgene | C3852986 | Nonocclusive Mesenteric Ischemia | 1 | CTD_human | |
Tgene | C3852987 | Acute Mesenteric Arterial Thrombosis | 1 | CTD_human |