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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:SKIV2L2-F2R (FusionGDB2 ID:82108)

Fusion Gene Summary for SKIV2L2-F2R

check button Fusion gene summary
Fusion gene informationFusion gene name: SKIV2L2-F2R
Fusion gene ID: 82108
HgeneTgene
Gene symbol

SKIV2L2

F2R

Gene ID

23517

2149

Gene nameMtr4 exosome RNA helicasecoagulation factor II thrombin receptor
SynonymsDob1|KIAA0052|Mtr4|SKIV2L2|fSAP118CF2R|HTR|PAR-1|PAR1|TR
Cytomap

5q11.2

5q13.3

Type of geneprotein-codingprotein-coding
Descriptionexosome RNA helicase MTR4ATP-dependent RNA helicase DOB1ATP-dependent RNA helicase SKIV2L2ATP-dependent helicase SKIV2L2Ski2 like RNA helicase 2TRAMP-like complex helicasefunctional spliceosome-associated protein 118superkiller viralicidic activityproteinase-activated receptor 1protease-activated receptor 1
Modification date2020031320200313
UniProtAcc.

P55085

Ensembl transtripts involved in fusion geneENST00000504388, ENST00000230640, 
ENST00000545714, 
ENST00000319211, 
ENST00000505600, 
Fusion gene scores* DoF score34 X 12 X 8=32643 X 3 X 2=18
# samples 153
** MAII scorelog2(15/3264*10)=-4.44360665147561
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: SKIV2L2 [Title/Abstract] AND F2R [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSKIV2L2(54603975)-F2R(76028139), # samples:1
Anticipated loss of major functional domain due to fusion event.SKIV2L2-F2R seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
SKIV2L2-F2R 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)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneSKIV2L2

GO:0006401

RNA catabolic process

29906447

TgeneF2R

GO:0002248

connective tissue replacement involved in inflammatory response wound healing

9639571

TgeneF2R

GO:0006919

activation of cysteine-type endopeptidase activity involved in apoptotic process

10692450

TgeneF2R

GO:0007200

phospholipase C-activating G protein-coupled receptor signaling pathway

20164183

TgeneF2R

GO:0008285

negative regulation of cell proliferation

10692450

TgeneF2R

GO:0009611

response to wounding

9639571

TgeneF2R

GO:0030168

platelet activation

9038223

TgeneF2R

GO:0030193

regulation of blood coagulation

17848177

TgeneF2R

GO:0030194

positive regulation of blood coagulation

9038223

TgeneF2R

GO:0032967

positive regulation of collagen biosynthetic process

9639571

TgeneF2R

GO:0043280

positive regulation of cysteine-type endopeptidase activity involved in apoptotic process

10692450

TgeneF2R

GO:0043410

positive regulation of MAPK cascade

17848177

TgeneF2R

GO:0045893

positive regulation of transcription, DNA-templated

17848177

TgeneF2R

GO:0051281

positive regulation of release of sequestered calcium ion into cytosol

1672265

TgeneF2R

GO:2000484

positive regulation of interleukin-8 secretion

17404307

TgeneF2R

GO:2000778

positive regulation of interleukin-6 secretion

11447194


check buttonFusion gene breakpoints across SKIV2L2 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across F2R (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check button 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4PRADTCGA-J4-A83I-01ASKIV2L2chr5

54603975

-F2Rchr5

76028139

+


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Fusion Gene ORF analysis for SKIV2L2-F2R

check button 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.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
3UTR-3CDSENST00000504388ENST00000319211SKIV2L2chr5

54603975

-F2Rchr5

76028139

+
3UTR-intronENST00000504388ENST00000505600SKIV2L2chr5

54603975

-F2Rchr5

76028139

+
5CDS-intronENST00000230640ENST00000505600SKIV2L2chr5

54603975

-F2Rchr5

76028139

+
5CDS-intronENST00000545714ENST00000505600SKIV2L2chr5

54603975

-F2Rchr5

76028139

+
Frame-shiftENST00000545714ENST00000319211SKIV2L2chr5

54603975

-F2Rchr5

76028139

+
In-frameENST00000230640ENST00000319211SKIV2L2chr5

54603975

-F2Rchr5

76028139

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000230640SKIV2L2chr554603975-ENST00000319211F2Rchr576028139+38563882731577434

check buttonDeepORF 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.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score
ENST00000230640ENST00000319211SKIV2L2chr554603975-F2Rchr576028139+0.001668970.998331

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Fusion Genomic Features for SKIV2L2-F2R


check buttonFusionAI 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.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.
genomic feature

check buttonDistribution 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 SKIV2L2-F2R


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr5:54603975/chr5:76028139)
- 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.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.F2R

P55085

FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.FUNCTION: Receptor for trypsin and trypsin-like enzymes coupled to G proteins (PubMed:28445455). Its function is mediated through the activation of several signaling pathways including phospholipase C (PLC), intracellular calcium, mitogen-activated protein kinase (MAPK), I-kappaB kinase/NF-kappaB and Rho (PubMed:28445455). Can also be transactivated by cleaved F2R/PAR1. Involved in modulation of inflammatory responses and regulation of innate and adaptive immunity, and acts as a sensor for proteolytic enzymes generated during infection. Generally is promoting inflammation. Can signal synergistically with TLR4 and probably TLR2 in inflammatory responses and modulates TLR3 signaling. Has a protective role in establishing the endothelial barrier; the activity involves coagulation factor X. Regulates endothelial cell barrier integrity during neutrophil extravasation, probably following proteolytic cleavage by PRTN3 (PubMed:23202369). Proposed to have a bronchoprotective role in airway epithelium, but also shown to compromise the airway epithelial barrier by interrupting E-cadherin adhesion (PubMed:10086357). Involved in the regulation of vascular tone; activation results in hypotension presumably mediated by vasodilation. Associates with a subset of G proteins alpha subunits such as GNAQ, GNA11, GNA14, GNA12 and GNA13, but probably not with G(o) alpha, G(i) subunit alpha-1 and G(i) subunit alpha-2. However, according to PubMed:21627585 can signal through G(i) subunit alpha. Believed to be a class B receptor which internalizes as a complex with arrestin and traffic with it to endosomal vesicles, presumably as desensitized receptor, for extended periods of time. Mediates inhibition of TNF-alpha stimulated JNK phosphorylation via coupling to GNAQ and GNA11; the function involves dissociation of RIPK1 and TRADD from TNFR1. Mediates phosphorylation of nuclear factor NF-kappa-B RELA subunit at 'Ser-536'; the function involves IKBKB and is predominantly independent of G proteins. Involved in cellular migration. Involved in cytoskeletal rearrangement and chemotaxis through beta-arrestin-promoted scaffolds; the function is independent of GNAQ and GNA11 and involves promotion of cofilin dephosphorylation and actin filament severing. Induces redistribution of COPS5 from the plasma membrane to the cytosol and activation of the JNK cascade is mediated by COPS5. Involved in the recruitment of leukocytes to the sites of inflammation and is the major PAR receptor capable of modulating eosinophil function such as proinflammatory cytokine secretion, superoxide production and degranulation. During inflammation promotes dendritic cell maturation, trafficking to the lymph nodes and subsequent T-cell activation. Involved in antimicrobial response of innate immune cells; activation enhances phagocytosis of Gram-positive and killing of Gram-negative bacteria. Acts synergistically with interferon-gamma in enhancing antiviral responses. Implicated in a number of acute and chronic inflammatory diseases such as of the joints, lungs, brain, gastrointestinal tract, periodontium, skin, and vascular systems, and in autoimmune disorders. {ECO:0000269|PubMed:10086357, ECO:0000269|PubMed:10725339, ECO:0000269|PubMed:11413129, ECO:0000269|PubMed:11441110, ECO:0000269|PubMed:11447194, ECO:0000269|PubMed:11714832, ECO:0000269|PubMed:12832443, ECO:0000269|PubMed:15155775, ECO:0000269|PubMed:16359518, ECO:0000269|PubMed:16410250, ECO:0000269|PubMed:16478888, ECO:0000269|PubMed:16714334, ECO:0000269|PubMed:17404307, ECO:0000269|PubMed:17500066, ECO:0000269|PubMed:18424071, ECO:0000269|PubMed:18453611, ECO:0000269|PubMed:18474671, ECO:0000269|PubMed:18622013, ECO:0000269|PubMed:19494303, ECO:0000269|PubMed:19781631, ECO:0000269|PubMed:19864598, ECO:0000269|PubMed:19865078, ECO:0000269|PubMed:20826780, ECO:0000269|PubMed:21501162, ECO:0000269|PubMed:23202369, ECO:0000269|PubMed:28445455}.

check buttonRetention 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

download page


* 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.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneF2Rchr5:54603975chr5:76028139ENST000003192110257_6029426.0Compositional biasNote=Asp/Glu-rich (acidic)
TgeneF2Rchr5:54603975chr5:76028139ENST0000031921102129_13729426.0Topological domainCytoplasmic
TgeneF2Rchr5:54603975chr5:76028139ENST0000031921102158_17629426.0Topological domainExtracellular
TgeneF2Rchr5:54603975chr5:76028139ENST0000031921102199_21829426.0Topological domainCytoplasmic
TgeneF2Rchr5:54603975chr5:76028139ENST0000031921102240_26829426.0Topological domainExtracellular
TgeneF2Rchr5:54603975chr5:76028139ENST0000031921102289_31129426.0Topological domainCytoplasmic
TgeneF2Rchr5:54603975chr5:76028139ENST0000031921102335_35029426.0Topological domainExtracellular
TgeneF2Rchr5:54603975chr5:76028139ENST0000031921102375_42529426.0Topological domainCytoplasmic
TgeneF2Rchr5:54603975chr5:76028139ENST000003192110242_10229426.0Topological domainExtracellular
TgeneF2Rchr5:54603975chr5:76028139ENST0000031921102103_12829426.0TransmembraneHelical%3B Name%3D1
TgeneF2Rchr5:54603975chr5:76028139ENST0000031921102138_15729426.0TransmembraneHelical%3B Name%3D2
TgeneF2Rchr5:54603975chr5:76028139ENST0000031921102177_19829426.0TransmembraneHelical%3B Name%3D3
TgeneF2Rchr5:54603975chr5:76028139ENST0000031921102219_23929426.0TransmembraneHelical%3B Name%3D4
TgeneF2Rchr5:54603975chr5:76028139ENST0000031921102269_28829426.0TransmembraneHelical%3B Name%3D5
TgeneF2Rchr5:54603975chr5:76028139ENST0000031921102312_33429426.0TransmembraneHelical%3B Name%3D6
TgeneF2Rchr5:54603975chr5:76028139ENST0000031921102351_37429426.0TransmembraneHelical%3B Name%3D7

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneSKIV2L2chr5:54603975chr5:76028139ENST00000230640-127148_304441043.0DomainHelicase ATP-binding
HgeneSKIV2L2chr5:54603975chr5:76028139ENST00000230640-127405_577441043.0DomainHelicase C-terminal
HgeneSKIV2L2chr5:54603975chr5:76028139ENST00000230640-127252_255441043.0MotifNote=DEIH box
HgeneSKIV2L2chr5:54603975chr5:76028139ENST00000230640-127161_168441043.0Nucleotide bindingATP


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Fusion Gene Sequence for SKIV2L2-F2R


check button 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.
>82108_82108_1_SKIV2L2-F2R_SKIV2L2_chr5_54603975_ENST00000230640_F2R_chr5_76028139_ENST00000319211_length(transcript)=3856nt_BP=388nt
GCTGCCTGCCACACGCCAGGCGCCACGCGCCGCCCTCGCTCTTTATCCACTGAGCAGCTTATCCACTTTAGGTCGGAAAGGAAAGGAAAG
AAAAGCAGGAAAAAAAAAAAAAGTCAGGGGAACATTTTTGTCGGCTGCGCGACTCGACTACTTTTGTCTCCTGCGGGCCACTGTTGAGCC
TTCACGAGACGTCACTGTCTTCGGTCGCGGGGCATCGTGGGTAGGAGGGAGATTTGCTCTCACTGCTCCCAAAAATGGCGGACGCATTCG
GAGATGAGCTGTTCAGCGTGTTCGAGGGCGACTCGACCACTGCGGCGGGAACCAAAAAAGACAAGGAAAAGGACAAGGGGAAATGGAAGG
GGCCTCCAGGGTCTGCAGACAAGGCAGGAATCAAAAGCAACAAATGCCACCTTAGATCCCCGGTCATTTCTTCTCAGGAACCCCAATGAT
AAATATGAACCATTTTGGGAGGATGAGGAGAAAAATGAAAGTGGGTTAACTGAATACAGATTAGTCTCCATCAATAAAAGCAGTCCTCTT
CAAAAACAACTTCCTGCATTCATCTCAGAAGATGCCTCCGGATATTTGACCAGCTCCTGGCTGACACTCTTTGTCCCATCTGTGTACACC
GGAGTGTTTGTAGTCAGCCTCCCACTAAACATCATGGCCATCGTTGTGTTCATCCTGAAAATGAAGGTCAAGAAGCCGGCGGTGGTGTAC
ATGCTGCACCTGGCCACGGCAGATGTGCTGTTTGTGTCTGTGCTCCCCTTTAAGATCAGCTATTACTTTTCCGGCAGTGATTGGCAGTTT
GGGTCTGAATTGTGTCGCTTCGTCACTGCAGCATTTTACTGTAACATGTACGCCTCTATCTTGCTCATGACAGTCATAAGCATTGACCGG
TTTCTGGCTGTGGTGTATCCCATGCAGTCCCTCTCCTGGCGTACTCTGGGAAGGGCTTCCTTCACTTGTCTGGCCATCTGGGCTTTGGCC
ATCGCAGGGGTAGTGCCTCTGCTCCTCAAGGAGCAAACCATCCAGGTGCCCGGGCTCAACATCACTACCTGTCATGATGTGCTCAATGAA
ACCCTGCTCGAAGGCTACTATGCCTACTACTTCTCAGCCTTCTCTGCTGTCTTCTTTTTTGTGCCGCTGATCATTTCCACGGTCTGTTAT
GTGTCTATCATTCGATGTCTTAGCTCTTCCGCAGTTGCCAACCGCAGCAAGAAGTCCCGGGCTTTGTTCCTGTCAGCTGCTGTTTTCTGC
ATCTTCATCATTTGCTTCGGACCCACAAACGTCCTCCTGATTGCGCATTACTCATTCCTTTCTCACACTTCCACCACAGAGGCTGCCTAC
TTTGCCTACCTCCTCTGTGTCTGTGTCAGCAGCATAAGCTGCTGCATCGACCCCCTAATTTACTATTACGCTTCCTCTGAGTGCCAGAGG
TACGTCTACAGTATCTTATGCTGCAAAGAAAGTTCCGATCCCAGCAGTTATAACAGCAGTGGGCAGTTGATGGCAAGTAAAATGGATACC
TGCTCTAGTAACCTGAATAACAGCATATACAAAAAGCTGTTAACTTAGGAAAAGGGACTGCTGGGAGGTTAAAAAGAAAAGTTTATAAAA
GTGAATAACCTGAGGATTCTATTAGTCCCCACCCAAACTTTATTGATTCACCTCCTAAAACAACAGATGTACGACTTGCATACCTGCTTT
TTATGGGAGCTGTCAAGCATGTATTTTTGTCAATTACCAGAAAGATAACAGGACGAGATGACGGTGTTATTCCAAGGGAATATTGCCAAT
GCTACAGTAATAAATGAATGTCACTTCTGGATATAGCTAGGTGACATATACATACTTACATGTGTGTATATGTAGATGTATGCACACACA
TATATTATTTGCAGTGCAGTATAGAATAGGCACTTTAAAACACTCTTTCCCCGCACCCCAGCAATTATGAAAATAATCTCTGATTCCCTG
ATTTAATATGCAAAGTCTAGGTTGGTAGAGTTTAGCCCTGAACATTTCATGGTGTTCATCAACAGTGAGAGACTCCATAGTTTGGGCTTG
TACCACTTTTGCAAATAAGTGTATTTTGAAATTGTTTGACGGCAAGGTTTAAGTTATTAAGAGGTAAGACTTAGTACTATCTGTGCGTAG
AAGTTCTAGTGTTTTCAATTTTAAACATATCCAAGTTTGAATTCCTAAAATTATGGAAACAGATGAAAAGCCTCTGTTTTGATATGGGTA
GTATTTTTTACATTTTACACACTGTACACATAAGCCAAAACTGAGCATAAGTCCTCTAGTGAATGTAGGCTGGCTTTCAGAGTAGGCTAT
TCCTGAGAGCTGCATGTGTCCGCCCCCGATGGAGGACTCCAGGCAGCAGACACATGCCAGGGCCATGTCAGACACAGATTGGCCAGAAAC
CTTCCTGCTGAGCCTCACAGCAGTGAGACTGGGGCCACTACATTTGCTCCATCCTCCTGGGATTGGCTGTGAACTGATCATGTTTATGAG
AAACTGGCAAAGCAGAATGTGATATCCTAGGAGGTAATGACCATGAAAGACTTCTCTACCCATCTTAAAAACAACGAAAGAAGGCATGGA
CTTCTGGATGCCCATCCACTGGGTGTAAACACATCTAGTAGTTGTTCTGAAATGTCAGTTCTGATATGGAAGCACCCATTATGCGCTGTG
GCCACTCCAATAGGTGCTGAGTGTACAGAGTGGAATAAGACAGAGACCTGCCCTCAAGAGCAAAGTAGATCATGCATAGAGTGTGATGTA
TGTGTAATAAATATGTTTCACACAAACAAGGCCTGTCAGCTAAAGAAGTTTGAACATTTGGGTTACTATTTCTTGTGGTTATAACTTAAT
GAAAACAATGCAGTACAGGACATATATTTTTTAAAATAAGTCTGATTTAATTGGGCACTATTTATTTACAAATGTTTTGCTCAATAGATT
GCTCAAATCAGGTTTTCTTTTAAGAATCAATCATGTCAGTCTGCTTAGAAATAACAGAAGAAAATAGAATTGACATTGAAATCTAGGAAA
ATTATTCTATAATTTCCATTTACTTAAGACTTAATGAGACTTTAAAAGCATTTTTTAACCTCCTAAGTATCAAGTATAGAAAATCTTCAT
GGAATTCACAAAGTAATTTGGAAATTAGGTTGAAACATATCTCTTATCTTACGAAAAAATGGTAGCATTTTAAACAAAATAGAAAGTTGC
AAGGCAAATGTTTATTTAAAAGAGCAGGCCAGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGTGGATCAC
GAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCGTCTCTACTAAAAATGCAAAAAAAATTAGCCGGGCGTGGTGGCAGG
CACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGACTGGCGTGAACCCAGGAGGCGGACCTTGTAGTGAGCCGAGATCGCGCCAC
TGTGCTCCAGCCTGGGCAACAGAGCAAGACTCCATCTCAAAAAATAAAAATAAATAAAAAATAAAAAAATAAAAGAGCAAACTATTTCCA
AATACCATAGAATAACTTACATAAAAGTAATATAACTGTATTGTAAGTAGAAGCTAGCACTGGTTTTATTAATTTAGTGACTATTCATTT
TATCTAAATCAGTGAAGATTTACTGTCATTGTTTATTAGTCTGTATATATTAAAATATGATATCATTAATGTACTTACAAAATAGTATGT

>82108_82108_1_SKIV2L2-F2R_SKIV2L2_chr5_54603975_ENST00000230640_F2R_chr5_76028139_ENST00000319211_length(amino acids)=434AA_BP=38
MSCSACSRATRPLRREPKKTRKRTRGNGRGLQGLQTRQESKATNATLDPRSFLLRNPNDKYEPFWEDEEKNESGLTEYRLVSINKSSPLQ
KQLPAFISEDASGYLTSSWLTLFVPSVYTGVFVVSLPLNIMAIVVFILKMKVKKPAVVYMLHLATADVLFVSVLPFKISYYFSGSDWQFG
SELCRFVTAAFYCNMYASILLMTVISIDRFLAVVYPMQSLSWRTLGRASFTCLAIWALAIAGVVPLLLKEQTIQVPGLNITTCHDVLNET
LLEGYYAYYFSAFSAVFFFVPLIISTVCYVSIIRCLSSSAVANRSKKSRALFLSAAVFCIFIICFGPTNVLLIAHYSFLSHTSTTEAAYF

--------------------------------------------------------------

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Fusion Gene PPI Analysis for SKIV2L2-F2R


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for SKIV2L2-F2R


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for SKIV2L2-F2R


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource