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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:F11R-LSM14A (FusionGDB2 ID:28147)

Fusion Gene Summary for F11R-LSM14A

check button Fusion gene summary
Fusion gene informationFusion gene name: F11R-LSM14A
Fusion gene ID: 28147
HgeneTgene
Gene symbol

F11R

LSM14A

Gene ID

50848

26065

Gene nameF11 receptorLSM14A mRNA processing body assembly factor
SynonymsCD321|JAM|JAM1|JAMA|JCAM|KAT|PAM-1C19orf13|FAM61A|RAP55|RAP55A
Cytomap

1q23.3

19q13.11

Type of geneprotein-codingprotein-coding
Descriptionjunctional adhesion molecule Ajunctional adhesion molecule 1platelet F11 receptorplatelet adhesion molecule 1protein LSM14 homolog ALSM14 homolog ALSM14A, SCD6 homolog ARNA-associated protein 55RNA-associated protein 55AalphaSNBPfamily with sequence similarity 61, member AhRAP55hRAP55Aprotein SCD6 homologputative alpha-synuclein-binding protein
Modification date2020031320200327
UniProtAcc

Q9Y624

Q8ND56

Ensembl transtripts involved in fusion geneENST00000289779, ENST00000368026, 
ENST00000472573, ENST00000537746, 
ENST00000433627, ENST00000540746, 
ENST00000544216, 
Fusion gene scores* DoF score15 X 9 X 8=108016 X 15 X 8=1920
# samples 1820
** MAII scorelog2(18/1080*10)=-2.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(20/1920*10)=-3.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: F11R [Title/Abstract] AND LSM14A [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointF11R(161008670)-LSM14A(34685383), # samples:1
Anticipated loss of major functional domain due to fusion event.F11R-LSM14A seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
F11R-LSM14A seems lost the major protein functional domain in Tgene partner, which is a CGC 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
HgeneF11R

GO:0008360

regulation of cell shape

15344881

HgeneF11R

GO:0032956

regulation of actin cytoskeleton organization

15344881

HgeneF11R

GO:0035025

positive regulation of Rho protein signal transduction

26985018

HgeneF11R

GO:0035683

memory T cell extravasation

11812992

HgeneF11R

GO:0071260

cellular response to mechanical stimulus

26985018

HgeneF11R

GO:0098609

cell-cell adhesion

14749337

HgeneF11R

GO:1901731

positive regulation of platelet aggregation

15344881

TgeneLSM14A

GO:0033962

cytoplasmic mRNA processing body assembly

16484376


check buttonFusion gene breakpoints across F11R (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across LSM14A (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

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
ChimerDB4BRCATCGA-EW-A1PH-01AF11Rchr1

161008670

-LSM14Achr19

34685383

+


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Fusion Gene ORF analysis for F11R-LSM14A

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
Frame-shiftENST00000289779ENST00000433627F11Rchr1

161008670

-LSM14Achr19

34685383

+
Frame-shiftENST00000289779ENST00000540746F11Rchr1

161008670

-LSM14Achr19

34685383

+
Frame-shiftENST00000289779ENST00000544216F11Rchr1

161008670

-LSM14Achr19

34685383

+
intron-3CDSENST00000368026ENST00000433627F11Rchr1

161008670

-LSM14Achr19

34685383

+
intron-3CDSENST00000368026ENST00000540746F11Rchr1

161008670

-LSM14Achr19

34685383

+
intron-3CDSENST00000368026ENST00000544216F11Rchr1

161008670

-LSM14Achr19

34685383

+
intron-3CDSENST00000472573ENST00000433627F11Rchr1

161008670

-LSM14Achr19

34685383

+
intron-3CDSENST00000472573ENST00000540746F11Rchr1

161008670

-LSM14Achr19

34685383

+
intron-3CDSENST00000472573ENST00000544216F11Rchr1

161008670

-LSM14Achr19

34685383

+
intron-3CDSENST00000537746ENST00000433627F11Rchr1

161008670

-LSM14Achr19

34685383

+
intron-3CDSENST00000537746ENST00000540746F11Rchr1

161008670

-LSM14Achr19

34685383

+
intron-3CDSENST00000537746ENST00000544216F11Rchr1

161008670

-LSM14Achr19

34685383

+

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)

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

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Fusion Genomic Features for F11R-LSM14A


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)
F11Rchr1161008669-LSM14Achr1934685382+1.65E-060.99999833
F11Rchr1161008669-LSM14Achr1934685382+1.65E-060.99999833

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.

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.
genomic feature of top 1%

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Fusion Protein Features for F11R-LSM14A


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/:161008670/:34685383)
- 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
F11R

Q9Y624

LSM14A

Q8ND56

FUNCTION: Seems to play a role in epithelial tight junction formation. Appears early in primordial forms of cell junctions and recruits PARD3 (PubMed:11489913). The association of the PARD6-PARD3 complex may prevent the interaction of PARD3 with JAM1, thereby preventing tight junction assembly (By similarity). Plays a role in regulating monocyte transmigration involved in integrity of epithelial barrier (By similarity). Ligand for integrin alpha-L/beta-2 involved in memory T-cell and neutrophil transmigration (PubMed:11812992). Involved in platelet activation (PubMed:10753840). {ECO:0000250|UniProtKB:O88792, ECO:0000269|PubMed:10753840, ECO:0000269|PubMed:11489913, ECO:0000269|PubMed:11812992}.; FUNCTION: (Microbial infection) Acts as a receptor for Mammalian reovirus sigma-1. {ECO:0000269|PubMed:11239401}.; FUNCTION: (Microbial infection) Acts as a receptor for Human Rotavirus strain Wa. {ECO:0000269|PubMed:25481868}.FUNCTION: Essential for formation of P-bodies, cytoplasmic structures that provide storage sites for translationally inactive mRNAs and protect them from degradation (PubMed:16484376, PubMed:17074753, PubMed:29510985). Acts as a repressor of mRNA translation (PubMed:29510985). May play a role in mitotic spindle assembly (PubMed:26339800). {ECO:0000269|PubMed:16484376, ECO:0000269|PubMed:17074753, ECO:0000269|PubMed:26339800, ECO:0000269|PubMed:29510985}.

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

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for F11R-LSM14A


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.

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Fusion Gene PPI Analysis for F11R-LSM14A


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 F11R-LSM14A


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 F11R-LSM14A


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