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Fusion gene ID: 12400 |
FusionGeneSummary for F3_C11orf80 |
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Fusion gene information | Fusion gene name: F3_C11orf80 | Fusion gene ID: 12400 | Hgene | Tgene | Gene symbol | F3 | C11orf80 | Gene ID | 2152 | 79703 |
Gene name | coagulation factor III, tissue factor | chromosome 11 open reading frame 80 | |
Synonyms | CD142|TF|TFA | TOP6BL|TOPOVIBL | |
Cytomap | 1p21.3 | 11q13.2 | |
Type of gene | protein-coding | protein-coding | |
Description | tissue factorcoagulation factor III (thromboplastin, tissue factor) | type 2 DNA topoisomerase 6 subunit B-liketype 2 DNA topoisomerase VI subunit B-like | |
Modification date | 20180527 | 20180523 | |
UniProtAcc | P13726 | ||
Ensembl transtripts involved in fusion gene | ENST00000334047, ENST00000370207, ENST00000480356, | ENST00000346672, ENST00000360962, ENST00000527634, ENST00000540737, ENST00000532565, ENST00000525449, ENST00000527368, | |
Fusion gene scores | * DoF score | 3 X 3 X 2=18 | 12 X 7 X 8=672 |
# samples | 4 | 15 | |
** MAII score | log2(4/18*10)=1.15200309344505 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | log2(15/672*10)=-2.16349873228288 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: F3 [Title/Abstract] AND C11orf80 [Title/Abstract] AND fusion [Title/Abstract] | ||
Functional or gene categories assigned by FusionGDB annotation |
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types ** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | F3 | GO:0001938 | positive regulation of endothelial cell proliferation | 17898544 |
Hgene | F3 | GO:0002541 | activation of plasma proteins involved in acute inflammatory response | 17469850 |
Hgene | F3 | GO:0006919 | activation of cysteine-type endopeptidase activity involved in apoptotic process | 17898544 |
Hgene | F3 | GO:0007596 | blood coagulation | 8632006|24998411 |
Hgene | F3 | GO:0010641 | positive regulation of platelet-derived growth factor receptor signaling pathway | 17991872 |
Hgene | F3 | GO:0016485 | protein processing | 24998411 |
Hgene | F3 | GO:0045766 | positive regulation of angiogenesis | 17898544 |
![]() (ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018)) * 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. |
Data type | Source | Cancer type | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
TCGA | LD | HNSC | TCGA-D6-6517-01A | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
TCGA | LD | HNSC | TCGA-F7-A620-01A | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
![]() * 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 | ENST00000334047 | ENST00000346672 | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
Frame-shift | ENST00000334047 | ENST00000360962 | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
Frame-shift | ENST00000334047 | ENST00000527634 | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
Frame-shift | ENST00000334047 | ENST00000540737 | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
Frame-shift | ENST00000334047 | ENST00000532565 | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
Frame-shift | ENST00000334047 | ENST00000525449 | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
5CDS-intron | ENST00000334047 | ENST00000527368 | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
Frame-shift | ENST00000370207 | ENST00000346672 | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
Frame-shift | ENST00000370207 | ENST00000360962 | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
Frame-shift | ENST00000370207 | ENST00000527634 | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
Frame-shift | ENST00000370207 | ENST00000540737 | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
Frame-shift | ENST00000370207 | ENST00000532565 | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
Frame-shift | ENST00000370207 | ENST00000525449 | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
5CDS-intron | ENST00000370207 | ENST00000527368 | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
5UTR-3CDS | ENST00000480356 | ENST00000346672 | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
5UTR-3CDS | ENST00000480356 | ENST00000360962 | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
5UTR-3CDS | ENST00000480356 | ENST00000527634 | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
5UTR-3CDS | ENST00000480356 | ENST00000540737 | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
5UTR-3CDS | ENST00000480356 | ENST00000532565 | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
5UTR-3CDS | ENST00000480356 | ENST00000525449 | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
5UTR-intron | ENST00000480356 | ENST00000527368 | F3 | chr1 | 95007093 | - | C11orf80 | chr11 | 66583524 | + |
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FusionProtFeatures for F3_C11orf80 |
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Hgene | Tgene |
F3 | C11orf80 |
Initiates blood coagulation by forming a complex withcirculating factor VII or VIIa. The [TF:VIIa] complex activatesfactors IX or X by specific limited protolysis. TF plays a role innormal hemostasis by initiating the cell-surface assembly andpropagation of the coagulation protease cascade.{ECO:0000269|PubMed:12652293}. | Lectin that binds to various sugars: galactose > mannose= fucose > N-acetylglucosamine > N-acetylgalactosamine(PubMed:10224141). Acts as a chemoattractant, probably involved inthe regulation of cell migration (PubMed:28301481).{ECO:0000269|PubMed:10224141, ECO:0000269|PubMed:28301481}. |
![]() * 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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FusionGeneSequence for F3_C11orf80 |
![]() (nt: nucleotides, aa: amino acids) |
* Fusion amino acid sequences. |
* Fusion transcript sequences (only coding sequence (CDS) region). |
* Fusion transcript sequences (Full-length transcript). |
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FusionGenePPI for F3_C11orf80 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
F3 | F7, FLNA, PLG, ELAVL1, DAD1, TM9SF4, RAB13, STX12, UBE2D1, UBE2D2, UBE2D3, UBE2D4, PPP2R4 | C11orf80 |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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RelatedDrugs for F3_C11orf80 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Hgene | F3 | P13726 | DB00036 | Coagulation factor VIIa Recombinant Human | Tissue factor | biotech | approved |
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RelatedDiseases for F3_C11orf80 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | F3 | C0012739 | Disseminated Intravascular Coagulation | 3 | CTD_human |
Hgene | F3 | C0040053 | Thrombosis | 2 | CTD_human |
Hgene | F3 | C0023487 | Acute Promyelocytic Leukemia | 1 | CTD_human |
Hgene | F3 | C0023890 | Liver Cirrhosis | 1 | CTD_human |
Hgene | F3 | C0027726 | Nephrotic Syndrome | 1 | CTD_human |
Hgene | F3 | C0034155 | Purpura, Thrombotic Thrombocytopenic | 1 | CTD_human |
Hgene | F3 | C0042487 | Venous Thrombosis | 1 | CTD_human |
Hgene | F3 | C0151744 | Myocardial Ischemia | 1 | CTD_human |
Hgene | F3 | C1458155 | Mammary Neoplasms | 1 | CTD_human |