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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:RAD51B-UVRAG

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: RAD51B-UVRAG
FusionPDB ID: 71761
FusionGDB2.0 ID: 71761
HgeneTgene
Gene symbol

RAD51B

UVRAG

Gene ID

5890

7405

Gene nameRAD51 paralog BUV radiation resistance associated
SynonymsR51H2|RAD51L1|REC2DHTX|VPS38|p63
Cytomap

14q24.1

11q13.5

Type of geneprotein-codingprotein-coding
DescriptionDNA repair protein RAD51 homolog 2RAD51 homolog BRecA-like proteinrecombination repair proteinUV radiation resistance-associated gene proteinbeclin 1 binding proteindisrupted in heterotaxy
Modification date2020031320200313
UniProtAcc

O15315

.
Ensembl transtripts involved in fusion geneENST idsENST00000469165, ENST00000390683, 
ENST00000471583, ENST00000487270, 
ENST00000487861, ENST00000488612, 
ENST00000356136, ENST00000528420, 
ENST00000531818, ENST00000532130, 
ENST00000533454, ENST00000539288, 
ENST00000525872, ENST00000538870, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score22 X 15 X 11=363028 X 21 X 11=6468
# samples 2236
** MAII scorelog2(22/3630*10)=-4.04439411935845
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(36/6468*10)=-4.16725086714399
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: RAD51B [Title/Abstract] AND UVRAG [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)UVRAG(75827059)-RAD51B(69061202), # samples:3
RAD51B(68934967)-UVRAG(75851755), # samples:2
Anticipated loss of major functional domain due to fusion event.RAD51B-UVRAG 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.
RAD51B-UVRAG 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.
RAD51B-UVRAG 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.
RAD51B-UVRAG 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.
RAD51B-UVRAG seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
RAD51B-UVRAG seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
RAD51B-UVRAG seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
RAD51B-UVRAG seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor 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
TgeneUVRAG

GO:0071900

regulation of protein serine/threonine kinase activity

22542840

TgeneUVRAG

GO:0097352

autophagosome maturation

28306502

TgeneUVRAG

GO:0097680

double-strand break repair via classical nonhomologous end joining

22542840


check buttonFusion gene breakpoints across RAD51B (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 UVRAG (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
ChimerDB4BRCATCGA-AR-A24Q-01ARAD51Bchr14

68934967

-UVRAGchr11

75851755

+
ChimerDB4BRCATCGA-AR-A24Q-01ARAD51Bchr14

68934967

+UVRAGchr11

75851755

+


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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)
ENST00000487861RAD51Bchr1468934967+ENST00000531818UVRAGchr1175851755+30541113291186385
ENST00000471583RAD51Bchr1468934967+ENST00000531818UVRAGchr1175851755+3025108401157385
ENST00000487270RAD51Bchr1468934967+ENST00000531818UVRAGchr1175851755+3025108401157385
ENST00000488612RAD51Bchr1468934967+ENST00000531818UVRAGchr1175851755+3004106301136378
ENST00000390683RAD51Bchr1468934967+ENST00000531818UVRAGchr1175851755+2977103601109369

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
ENST00000487861ENST00000531818RAD51Bchr1468934967+UVRAGchr1175851755+0.0005284040.9994716
ENST00000471583ENST00000531818RAD51Bchr1468934967+UVRAGchr1175851755+0.0005246180.9994754
ENST00000487270ENST00000531818RAD51Bchr1468934967+UVRAGchr1175851755+0.0005246180.9994754
ENST00000488612ENST00000531818RAD51Bchr1468934967+UVRAGchr1175851755+0.0005757910.9994242
ENST00000390683ENST00000531818RAD51Bchr1468934967+UVRAGchr1175851755+0.0005370780.9994629

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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

>71761_71761_1_RAD51B-UVRAG_RAD51B_chr14_68934967_ENST00000390683_UVRAG_chr11_75851755_ENST00000531818_length(amino acids)=369AA_BP=279
MGSKKLKRVGLSQELCDRLSRHQILTCQDFLCLSPLELMKVTGLSYRGVHELLCMVSRACAPKMQTAYGIKAQRSADFSPAFLSTTLSAL
DEALHGGVACGSLTEITGPPGCGKTQFCIMMSILATLPTNMGGLEGAVVYIDTESAFSAERLVEIAESRFPRYFNTEEKLLLTSSKVHLY
RELTCDEVLQRIESLEEEIISKGIKLVILDSVASVVRKEFDAQLQGNLKERNKFLAREASSLKYLAEEFSIPVILTNQITTHLSGALASQ
ADLVSPADDLSLSEGTSGSSCVIAALGNTWSHSVNTRLILQYLDSERRQILIAKSPLAPFTSFVYTIKEEGLVLQVTDITPPVQSLFLRD

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

>71761_71761_2_RAD51B-UVRAG_RAD51B_chr14_68934967_ENST00000471583_UVRAG_chr11_75851755_ENST00000531818_length(amino acids)=385AA_BP=295
LCKGWGNLKVGCCRPGMGSKKLKRVGLSQELCDRLSRHQILTCQDFLCLSPLELMKVTGLSYRGVHELLCMVSRACAPKMQTAYGIKAQR
SADFSPAFLSTTLSALDEALHGGVACGSLTEITGPPGCGKTQFCIMMSILATLPTNMGGLEGAVVYIDTESAFSAERLVEIAESRFPRYF
NTEEKLLLTSSKVHLYRELTCDEVLQRIESLEEEIISKGIKLVILDSVASVVRKEFDAQLQGNLKERNKFLAREASSLKYLAEEFSIPVI
LTNQITTHLSGALASQADLVSPADDLSLSEGTSGSSCVIAALGNTWSHSVNTRLILQYLDSERRQILIAKSPLAPFTSFVYTIKEEGLVL

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

>71761_71761_3_RAD51B-UVRAG_RAD51B_chr14_68934967_ENST00000487270_UVRAG_chr11_75851755_ENST00000531818_length(amino acids)=385AA_BP=295
LCKGWGNLKVGCCRPGMGSKKLKRVGLSQELCDRLSRHQILTCQDFLCLSPLELMKVTGLSYRGVHELLCMVSRACAPKMQTAYGIKAQR
SADFSPAFLSTTLSALDEALHGGVACGSLTEITGPPGCGKTQFCIMMSILATLPTNMGGLEGAVVYIDTESAFSAERLVEIAESRFPRYF
NTEEKLLLTSSKVHLYRELTCDEVLQRIESLEEEIISKGIKLVILDSVASVVRKEFDAQLQGNLKERNKFLAREASSLKYLAEEFSIPVI
LTNQITTHLSGALASQADLVSPADDLSLSEGTSGSSCVIAALGNTWSHSVNTRLILQYLDSERRQILIAKSPLAPFTSFVYTIKEEGLVL

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

>71761_71761_4_RAD51B-UVRAG_RAD51B_chr14_68934967_ENST00000487861_UVRAG_chr11_75851755_ENST00000531818_length(amino acids)=385AA_BP=295
MCKGWGNLKVGCCRPGMGSKKLKRVGLSQELCDRLSRHQILTCQDFLCLSPLELMKVTGLSYRGVHELLCMVSRACAPKMQTAYGIKAQR
SADFSPAFLSTTLSALDEALHGGVACGSLTEITGPPGCGKTQFCIMMSILATLPTNMGGLEGAVVYIDTESAFSAERLVEIAESRFPRYF
NTEEKLLLTSSKVHLYRELTCDEVLQRIESLEEEIISKGIKLVILDSVASVVRKEFDAQLQGNLKERNKFLAREASSLKYLAEEFSIPVI
LTNQITTHLSGALASQADLVSPADDLSLSEGTSGSSCVIAALGNTWSHSVNTRLILQYLDSERRQILIAKSPLAPFTSFVYTIKEEGLVL

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

>71761_71761_5_RAD51B-UVRAG_RAD51B_chr14_68934967_ENST00000488612_UVRAG_chr11_75851755_ENST00000531818_length(amino acids)=378AA_BP=288
LKVGCCRPGMGSKKLKRVGLSQELCDRLSRHQILTCQDFLCLSPLELMKVTGLSYRGVHELLCMVSRACAPKMQTAYGIKAQRSADFSPA
FLSTTLSALDEALHGGVACGSLTEITGPPGCGKTQFCIMMSILATLPTNMGGLEGAVVYIDTESAFSAERLVEIAESRFPRYFNTEEKLL
LTSSKVHLYRELTCDEVLQRIESLEEEIISKGIKLVILDSVASVVRKEFDAQLQGNLKERNKFLAREASSLKYLAEEFSIPVILTNQITT
HLSGALASQADLVSPADDLSLSEGTSGSSCVIAALGNTWSHSVNTRLILQYLDSERRQILIAKSPLAPFTSFVYTIKEEGLVLQVTDITP

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

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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/chr14:75827059/chr11:69061202)
- 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
RAD51B

O15315

.
FUNCTION: Involved in the homologous recombination repair (HRR) pathway of double-stranded DNA breaks arising during DNA replication or induced by DNA-damaging agents. May promote the assembly of presynaptic RAD51 nucleoprotein filaments. Binds single-stranded DNA and double-stranded DNA and has DNA-dependent ATPase activity. Part of the RAD21 paralog protein complex BCDX2 which acts in the BRCA1-BRCA2-dependent HR pathway. Upon DNA damage, BCDX2 acts downstream of BRCA2 recruitment and upstream of RAD51 recruitment. BCDX2 binds predominantly to the intersection of the four duplex arms of the Holliday junction and to junction of replication forks. The BCDX2 complex was originally reported to bind single-stranded DNA, single-stranded gaps in duplex DNA and specifically to nicks in duplex DNA. The BCDX2 subcomplex RAD51B:RAD51C exhibits single-stranded DNA-dependent ATPase activity suggesting an involvement in early stages of the HR pathway. {ECO:0000269|PubMed:11751635, ECO:0000269|PubMed:11751636, ECO:0000269|PubMed:11842113, ECO:0000269|PubMed:12441335, ECO:0000269|PubMed:23108668, ECO:0000269|PubMed:23149936}.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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneRAD51Bchr14:68934967chr11:75851755ENST00000390683+910108_115345.3333333333333367.0Nucleotide bindingATP
HgeneRAD51Bchr14:68934967chr11:75851755ENST00000471583+1011108_115345.3333333333333351.0Nucleotide bindingATP
HgeneRAD51Bchr14:68934967chr11:75851755ENST00000487270+1011108_115345.3333333333333385.0Nucleotide bindingATP
HgeneRAD51Bchr14:68934967chr11:75851755ENST00000488612+1012108_115345.3333333333333495.6666666666667Nucleotide bindingATP

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneUVRAGchr14:68934967chr11:75851755ENST000003561361315224_305465.6666666666667700.0Coiled coilOntology_term=ECO:0000255
TgeneUVRAGchr14:68934967chr11:75851755ENST00000356136131523_149465.6666666666667700.0DomainC2


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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
RAD51BRAD51, RAD51C, RAD51D, XRCC2, SWSAP1, FAM9B, DKKL1, ARL4C, MUC20, ADAMTS4, HELQ, HNRNPL, SPDL1, BRCA1, TPT1, ABL1, MEOX2, RPAIN, ANAPC5, BAGE2, C15orf39, PRPF6, C5orf34, N4BP2L2, BANP, ANKHD1-EIF4EBP3, KLRC2, DSCC1, SATB2, ZNHIT6, PMS1, NUF2, APAF1, PRKACB, MAPRE2, CD300LB, PRKACG, TBC1D2B, MTR,


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
RAD51Ball structure
UVRAG


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 RAD51B-UVRAG


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 RAD51B-UVRAG


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
HgeneRAD51BC0006142Malignant neoplasm of breast1CTD_human
HgeneRAD51BC0013146Drug abuse1CTD_human
HgeneRAD51BC0013170Drug habituation1CTD_human
HgeneRAD51BC0013222Drug Use Disorders1CTD_human
HgeneRAD51BC0029231Organic Mental Disorders, Substance-Induced1CTD_human
HgeneRAD51BC0038580Substance Dependence1CTD_human
HgeneRAD51BC0038586Substance Use Disorders1CTD_human
HgeneRAD51BC0236969Substance-Related Disorders1CTD_human
HgeneRAD51BC0238033Carcinoma of Male Breast1CTD_human
HgeneRAD51BC0242788Breast Neoplasms, Male1CTD_human
HgeneRAD51BC0678222Breast Carcinoma1CTD_human
HgeneRAD51BC0740858Substance abuse problem1CTD_human
HgeneRAD51BC1257931Mammary Neoplasms, Human1CTD_human
HgeneRAD51BC1458155Mammary Neoplasms1CTD_human
HgeneRAD51BC1510472Drug Dependence1CTD_human
HgeneRAD51BC4316881Prescription Drug Abuse1CTD_human
HgeneRAD51BC4704874Mammary Carcinoma, Human1CTD_human