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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:RAD50-BCLAF1

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: RAD50-BCLAF1
FusionPDB ID: 71721
FusionGDB2.0 ID: 71721
HgeneTgene
Gene symbol

RAD50

BCLAF1

Gene ID

10111

9774

Gene nameRAD50 double strand break repair proteinBCL2 associated transcription factor 1
SynonymsNBSLD|RAD502|hRad50BTF|bK211L9.1
Cytomap

5q31.1

6q23.3

Type of geneprotein-codingprotein-coding
DescriptionDNA repair protein RAD50RAD50 homolog, double strand break repair proteinbcl-2-associated transcription factor 1BCLAF1 and THRAP3 family member 1
Modification date2020032020200315
UniProtAcc

RINT1

Q9NYF8

Ensembl transtripts involved in fusion geneENST idsENST00000265335, ENST00000378823, 
ENST00000487596, 
ENST00000392348, 
ENST00000529917, ENST00000031135, 
ENST00000353331, ENST00000527536, 
ENST00000527759, ENST00000530767, 
ENST00000531224, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score9 X 7 X 7=4418 X 6 X 2=96
# samples 108
** MAII scorelog2(10/441*10)=-2.1407786557828
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/96*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: RAD50 [Title/Abstract] AND BCLAF1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)RAD50(131895059)-BCLAF1(136582615), # samples:1
Anticipated loss of major functional domain due to fusion event.RAD50-BCLAF1 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
RAD50-BCLAF1 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
RAD50-BCLAF1 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
RAD50-BCLAF1 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame 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
HgeneRAD50

GO:0000019

regulation of mitotic recombination

8756642

HgeneRAD50

GO:0006281

DNA repair

9705271

HgeneRAD50

GO:0006310

DNA recombination

9705271

HgeneRAD50

GO:0006974

cellular response to DNA damage stimulus

17500065

HgeneRAD50

GO:0007004

telomere maintenance via telomerase

9705271

HgeneRAD50

GO:0031954

positive regulation of protein autophosphorylation

15790808

HgeneRAD50

GO:0033674

positive regulation of kinase activity

15790808

HgeneRAD50

GO:1904354

negative regulation of telomere capping

17694070

TgeneBCLAF1

GO:0043065

positive regulation of apoptotic process

10330179

TgeneBCLAF1

GO:0045892

negative regulation of transcription, DNA-templated

10330179


check buttonFusion gene breakpoints across RAD50 (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 BCLAF1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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
ChimerDB4STADTCGA-EQ-8122RAD50chr5

131895059

+BCLAF1chr6

136582615

-


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000265335RAD50chr5131895059+ENST00000353331BCLAF1chr6136582615-5066600360818152
ENST00000265335RAD50chr5131895059+ENST00000531224BCLAF1chr6136582615-5066600360818152
ENST00000265335RAD50chr5131895059+ENST00000527536BCLAF1chr6136582615-3343600360818152
ENST00000265335RAD50chr5131895059+ENST00000530767BCLAF1chr6136582615-2578600360818152
ENST00000265335RAD50chr5131895059+ENST00000527759BCLAF1chr6136582615-2238600360818152
ENST00000265335RAD50chr5131895059+ENST00000031135BCLAF1chr6136582615-1449600360818152

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
ENST00000265335ENST00000353331RAD50chr5131895059+BCLAF1chr6136582615-0.0083367320.9916632
ENST00000265335ENST00000531224RAD50chr5131895059+BCLAF1chr6136582615-0.0083367320.9916632
ENST00000265335ENST00000527536RAD50chr5131895059+BCLAF1chr6136582615-0.0031082670.9968918
ENST00000265335ENST00000530767RAD50chr5131895059+BCLAF1chr6136582615-0.0068130760.99318695
ENST00000265335ENST00000527759RAD50chr5131895059+BCLAF1chr6136582615-0.0077018370.9922982
ENST00000265335ENST00000031135RAD50chr5131895059+BCLAF1chr6136582615-0.0090215210.9909785

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>71721_71721_1_RAD50-BCLAF1_RAD50_chr5_131895059_ENST00000265335_BCLAF1_chr6_136582615_ENST00000031135_length(amino acids)=152AA_BP=80
MVRLETFANMSRIEKMSILGVRSFGIEDKDKQIITFFSPLTILVGPNGAGKTTIIECLKYICTGDFPPGTKGNTFVHDPKHDDRDDGVDY

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

>71721_71721_2_RAD50-BCLAF1_RAD50_chr5_131895059_ENST00000265335_BCLAF1_chr6_136582615_ENST00000353331_length(amino acids)=152AA_BP=80
MVRLETFANMSRIEKMSILGVRSFGIEDKDKQIITFFSPLTILVGPNGAGKTTIIECLKYICTGDFPPGTKGNTFVHDPKHDDRDDGVDY

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

>71721_71721_3_RAD50-BCLAF1_RAD50_chr5_131895059_ENST00000265335_BCLAF1_chr6_136582615_ENST00000527536_length(amino acids)=152AA_BP=80
MVRLETFANMSRIEKMSILGVRSFGIEDKDKQIITFFSPLTILVGPNGAGKTTIIECLKYICTGDFPPGTKGNTFVHDPKHDDRDDGVDY

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

>71721_71721_4_RAD50-BCLAF1_RAD50_chr5_131895059_ENST00000265335_BCLAF1_chr6_136582615_ENST00000527759_length(amino acids)=152AA_BP=80
MVRLETFANMSRIEKMSILGVRSFGIEDKDKQIITFFSPLTILVGPNGAGKTTIIECLKYICTGDFPPGTKGNTFVHDPKHDDRDDGVDY

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

>71721_71721_5_RAD50-BCLAF1_RAD50_chr5_131895059_ENST00000265335_BCLAF1_chr6_136582615_ENST00000530767_length(amino acids)=152AA_BP=80
MVRLETFANMSRIEKMSILGVRSFGIEDKDKQIITFFSPLTILVGPNGAGKTTIIECLKYICTGDFPPGTKGNTFVHDPKHDDRDDGVDY

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

>71721_71721_6_RAD50-BCLAF1_RAD50_chr5_131895059_ENST00000265335_BCLAF1_chr6_136582615_ENST00000531224_length(amino acids)=152AA_BP=80
MVRLETFANMSRIEKMSILGVRSFGIEDKDKQIITFFSPLTILVGPNGAGKTTIIECLKYICTGDFPPGTKGNTFVHDPKHDDRDDGVDY

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

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Fusion Protein Functional Features


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/chr5:131895059/chr6:136582615)
- 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
RAD50

RINT1

BCLAF1

Q9NYF8

792FUNCTION: Death-promoting transcriptional repressor. May be involved in cyclin-D1/CCND1 mRNA stability through the SNARP complex which associates with both the 3'end of the CCND1 gene and its mRNA. {ECO:0000269|PubMed:18794151}.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneRAD50chr5:131895059chr6:136582615ENST00000265335+22536_4371.01313.0Nucleotide bindingATP
TgeneBCLAF1chr5:131895059chr6:136582615ENST000005307671013749_763675.0748.0Compositional biasNote=Poly-Ser

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneRAD50chr5:131895059chr6:136582615ENST00000265335+225228_35971.01313.0Coiled coilOntology_term=ECO:0000255
HgeneRAD50chr5:131895059chr6:136582615ENST00000265335+225401_59871.01313.0Coiled coilOntology_term=ECO:0000255
HgeneRAD50chr5:131895059chr6:136582615ENST00000265335+225635_67371.01313.0Coiled coilOntology_term=ECO:0000255
HgeneRAD50chr5:131895059chr6:136582615ENST00000265335+225706_73471.01313.0Coiled coilOntology_term=ECO:0000255
HgeneRAD50chr5:131895059chr6:136582615ENST00000265335+225789_107971.01313.0Coiled coilOntology_term=ECO:0000255
HgeneRAD50chr5:131895059chr6:136582615ENST00000378823+225228_35901174.0Coiled coilOntology_term=ECO:0000255
HgeneRAD50chr5:131895059chr6:136582615ENST00000378823+225401_59801174.0Coiled coilOntology_term=ECO:0000255
HgeneRAD50chr5:131895059chr6:136582615ENST00000378823+225635_67301174.0Coiled coilOntology_term=ECO:0000255
HgeneRAD50chr5:131895059chr6:136582615ENST00000378823+225706_73401174.0Coiled coilOntology_term=ECO:0000255
HgeneRAD50chr5:131895059chr6:136582615ENST00000378823+225789_107901174.0Coiled coilOntology_term=ECO:0000255
HgeneRAD50chr5:131895059chr6:136582615ENST00000265335+2251201_123871.01313.0Compositional biasNote=Ala/Asp-rich (DA-box)
HgeneRAD50chr5:131895059chr6:136582615ENST00000378823+2251201_123801174.0Compositional biasNote=Ala/Asp-rich (DA-box)
HgeneRAD50chr5:131895059chr6:136582615ENST00000265335+225635_73471.01313.0DomainZinc-hook
HgeneRAD50chr5:131895059chr6:136582615ENST00000378823+225635_73401174.0DomainZinc-hook
HgeneRAD50chr5:131895059chr6:136582615ENST00000378823+22536_4301174.0Nucleotide bindingATP
TgeneBCLAF1chr5:131895059chr6:136582615ENST00000353331912141_148797.0870.0Compositional biasNote=Poly-Ser
TgeneBCLAF1chr5:131895059chr6:136582615ENST00000353331912749_763797.0870.0Compositional biasNote=Poly-Ser
TgeneBCLAF1chr5:131895059chr6:136582615ENST00000392348710141_148797.0870.0Compositional biasNote=Poly-Ser
TgeneBCLAF1chr5:131895059chr6:136582615ENST00000392348710749_763797.0870.0Compositional biasNote=Poly-Ser
TgeneBCLAF1chr5:131895059chr6:136582615ENST000005277591013141_148846.0919.0Compositional biasNote=Poly-Ser
TgeneBCLAF1chr5:131895059chr6:136582615ENST000005277591013749_763846.0919.0Compositional biasNote=Poly-Ser
TgeneBCLAF1chr5:131895059chr6:136582615ENST000005307671013141_148675.0748.0Compositional biasNote=Poly-Ser
TgeneBCLAF1chr5:131895059chr6:136582615ENST000005312241013141_148848.0921.0Compositional biasNote=Poly-Ser
TgeneBCLAF1chr5:131895059chr6:136582615ENST000005312241013749_763848.0921.0Compositional biasNote=Poly-Ser


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
RAD50
BCLAF1


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to RAD50-BCLAF1


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to RAD50-BCLAF1


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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