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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:FUS-PYCARD (FusionGDB2 ID:31710)

Fusion Gene Summary for FUS-PYCARD

check button Fusion gene summary
Fusion gene informationFusion gene name: FUS-PYCARD
Fusion gene ID: 31710
HgeneTgene
Gene symbol

FUS

PYCARD

Gene ID

2521

29108

Gene nameFUS RNA binding proteinPYD and CARD domain containing
SynonymsALS6|ETM4|FUS1|HNRNPP2|POMP75|TLSASC|CARD5|TMS|TMS-1|TMS1
Cytomap

16p11.2

16p11.2

Type of geneprotein-codingprotein-coding
DescriptionRNA-binding protein FUS75 kDa DNA-pairing proteinfus-like proteinfused in sarcomafusion gene in myxoid liposarcomaheterogeneous nuclear ribonucleoprotein P2oncogene FUSoncogene TLStranslocated in liposarcoma proteinapoptosis-associated speck-like protein containing a CARDcaspase recruitment domain-containing protein 5target of methylation-induced silencing 1
Modification date2020032920200313
UniProtAcc

P35637

.
Ensembl transtripts involved in fusion geneENST00000254108, ENST00000380244, 
ENST00000568685, ENST00000474990, 
ENST00000247470, ENST00000350605, 
Fusion gene scores* DoF score37 X 37 X 16=219041 X 1 X 1=1
# samples 441
** MAII scorelog2(44/21904*10)=-5.63754701773324
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: FUS [Title/Abstract] AND PYCARD [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointFUS(31193743)-PYCARD(31213524), # samples:2
Anticipated loss of major functional domain due to fusion event.FUS-PYCARD seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
FUS-PYCARD seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
FUS-PYCARD seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
FUS-PYCARD seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor due to the frame-shifted ORF.
FUS-PYCARD seems lost the major protein functional domain in Tgene partner, which is a essential gene 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
HgeneFUS

GO:0006355

regulation of transcription, DNA-templated

26124092

HgeneFUS

GO:0006357

regulation of transcription by RNA polymerase II

25453086

HgeneFUS

GO:0008380

RNA splicing

26124092

HgeneFUS

GO:0043484

regulation of RNA splicing

25453086|27731383

HgeneFUS

GO:0048255

mRNA stabilization

27378374

HgeneFUS

GO:0051260

protein homooligomerization

25453086

HgeneFUS

GO:1905168

positive regulation of double-strand break repair via homologous recombination

10567410

TgenePYCARD

GO:0002218

activation of innate immune response

21575908

TgenePYCARD

GO:0033209

tumor necrosis factor-mediated signaling pathway

12656673

TgenePYCARD

GO:0043065

positive regulation of apoptotic process

12646168

TgenePYCARD

GO:0043124

negative regulation of I-kappaB kinase/NF-kappaB signaling

12486103

TgenePYCARD

GO:0043280

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

15030775

TgenePYCARD

GO:0050718

positive regulation of interleukin-1 beta secretion

15030775

TgenePYCARD

GO:0051091

positive regulation of DNA-binding transcription factor activity

19494289

TgenePYCARD

GO:0051092

positive regulation of NF-kappaB transcription factor activity

12646168|12656673

TgenePYCARD

GO:0051260

protein homooligomerization

24531343

TgenePYCARD

GO:0051607

defense response to virus

21575908

TgenePYCARD

GO:0071222

cellular response to lipopolysaccharide

12486103

TgenePYCARD

GO:0071347

cellular response to interleukin-1

12486103

TgenePYCARD

GO:0071356

cellular response to tumor necrosis factor

12486103

TgenePYCARD

GO:0071901

negative regulation of protein serine/threonine kinase activity

12486103

TgenePYCARD

GO:0090200

positive regulation of release of cytochrome c from mitochondria

14730312

TgenePYCARD

GO:2001056

positive regulation of cysteine-type endopeptidase activity

19158676

TgenePYCARD

GO:2001238

positive regulation of extrinsic apoptotic signaling pathway

16964285

TgenePYCARD

GO:2001242

regulation of intrinsic apoptotic signaling pathway

14730312


check buttonFusion gene breakpoints across FUS (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 PYCARD (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
ChimerDB4COADTCGA-F4-6809-01AFUSchr16

31193743

+PYCARDchr16

31213524

-
ChimerDB4COADTCGA-F4-6809-01AFUSchr16

31193743

+PYCARDchr16

31213524

-


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Fusion Gene ORF analysis for FUS-PYCARD

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-shiftENST00000254108ENST00000247470FUSchr16

31193743

+PYCARDchr16

31213524

-
5CDS-intronENST00000254108ENST00000350605FUSchr16

31193743

+PYCARDchr16

31213524

-
Frame-shiftENST00000380244ENST00000247470FUSchr16

31193743

+PYCARDchr16

31213524

-
5CDS-intronENST00000380244ENST00000350605FUSchr16

31193743

+PYCARDchr16

31213524

-
Frame-shiftENST00000568685ENST00000247470FUSchr16

31193743

+PYCARDchr16

31213524

-
5CDS-intronENST00000568685ENST00000350605FUSchr16

31193743

+PYCARDchr16

31213524

-
intron-3CDSENST00000474990ENST00000247470FUSchr16

31193743

+PYCARDchr16

31213524

-
intron-intronENST00000474990ENST00000350605FUSchr16

31193743

+PYCARDchr16

31213524

-

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 FUS-PYCARD


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.

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 FUS-PYCARD


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

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

P35637

.
FUNCTION: DNA/RNA-binding protein that plays a role in various cellular processes such as transcription regulation, RNA splicing, RNA transport, DNA repair and damage response (PubMed:27731383). Binds to nascent pre-mRNAs and acts as a molecular mediator between RNA polymerase II and U1 small nuclear ribonucleoprotein thereby coupling transcription and splicing (PubMed:26124092). Binds also its own pre-mRNA and autoregulates its expression; this autoregulation mechanism is mediated by non-sense-mediated decay (PubMed:24204307). Plays a role in DNA repair mechanisms by promoting D-loop formation and homologous recombination during DNA double-strand break repair (PubMed:10567410). In neuronal cells, plays crucial roles in dendritic spine formation and stability, RNA transport, mRNA stability and synaptic homeostasis (By similarity). {ECO:0000250|UniProtKB:P56959, ECO:0000269|PubMed:10567410, ECO:0000269|PubMed:24204307, ECO:0000269|PubMed:26124092, ECO:0000269|PubMed:27731383}.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

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 FUS-PYCARD


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 FUS-PYCARD


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 FUS-PYCARD


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 FUS-PYCARD


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneFUSC1842675AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)5UNIPROT
HgeneFUSC3468114Juvenile amyotrophic lateral sclerosis5ORPHANET
HgeneFUSC0002736Amyotrophic Lateral Sclerosis2CTD_human;ORPHANET
HgeneFUSC0206634Liposarcoma, Myxoid2CTD_human;ORPHANET
HgeneFUSC0393554Amyotrophic Lateral Sclerosis With Dementia1CTD_human
HgeneFUSC0497327Dementia1GENOMICS_ENGLAND
HgeneFUSC0543859Amyotrophic Lateral Sclerosis, Guam Form1CTD_human
HgeneFUSC3539195TREMOR, HEREDITARY ESSENTIAL, 41CTD_human;UNIPROT
HgeneFUSC3888102Frontotemporal Dementia With Motor Neuron Disease1ORPHANET
TgenePYCARDC0022658Kidney Diseases2CTD_human
TgenePYCARDC0001418Adenocarcinoma1CTD_human
TgenePYCARDC0001925Albuminuria1CTD_human
TgenePYCARDC0006663Calcinosis1CTD_human
TgenePYCARDC0007131Non-Small Cell Lung Carcinoma1CTD_human
TgenePYCARDC0007137Squamous cell carcinoma1CTD_human
TgenePYCARDC0009402Colorectal Carcinoma1CTD_human
TgenePYCARDC0009404Colorectal Neoplasms1CTD_human
TgenePYCARDC0018824Heart valve disease1CTD_human
TgenePYCARDC0023893Liver Cirrhosis, Experimental1CTD_human
TgenePYCARDC0024121Lung Neoplasms1CTD_human
TgenePYCARDC0024623Malignant neoplasm of stomach1CTD_human
TgenePYCARDC0038356Stomach Neoplasms1CTD_human
TgenePYCARDC0043094Weight Gain1CTD_human
TgenePYCARDC0205641Adenocarcinoma, Basal Cell1CTD_human
TgenePYCARDC0205642Adenocarcinoma, Oxyphilic1CTD_human
TgenePYCARDC0205643Carcinoma, Cribriform1CTD_human
TgenePYCARDC0205644Carcinoma, Granular Cell1CTD_human
TgenePYCARDC0205645Adenocarcinoma, Tubular1CTD_human
TgenePYCARDC0206704Carcinoma, Large Cell1CTD_human
TgenePYCARDC0242379Malignant neoplasm of lung1CTD_human
TgenePYCARDC0262584Carcinoma, Small Cell1CTD_human
TgenePYCARDC0263628Tumoral calcinosis1CTD_human
TgenePYCARDC0345967Malignant mesothelioma1CTD_human
TgenePYCARDC0521174Microcalcification1CTD_human
TgenePYCARDC0598608Hyperhomocysteinemia1CTD_human
TgenePYCARDC1708349Hereditary Diffuse Gastric Cancer1CTD_human
TgenePYCARDC2239176Liver carcinoma1CTD_human