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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:RMDN3-RAD51 (FusionGDB2 ID:74246)

Fusion Gene Summary for RMDN3-RAD51

check button Fusion gene summary
Fusion gene informationFusion gene name: RMDN3-RAD51
Fusion gene ID: 74246
HgeneTgene
Gene symbol

RMDN3

RAD51

Gene ID

55177

5888

Gene nameregulator of microtubule dynamics 3RAD51 recombinase
SynonymsFAM82A2|FAM82C|RMD-3|RMD3|ptpip51BRCC5|FANCR|HRAD51|HsRad51|HsT16930|MRMV2|RAD51A|RECA
Cytomap

15q15.1

15q15.1

Type of geneprotein-codingprotein-coding
Descriptionregulator of microtubule dynamics protein 3TCPTP-interacting protein 51cerebral protein 10family with sequence similarity 82, member A2family with sequence similarity 82, member Cmicrotubule-associated proteinprotein tyrosine phosphatase-interactingDNA repair protein RAD51 homolog 1BRCA1/BRCA2-containing complex, subunit 5RAD51 homolog ARecA, E. coli, homolog ofRecA-like proteinrecombination protein A
Modification date2020031320200322
UniProtAcc

Q96TC7

O15315

Ensembl transtripts involved in fusion geneENST00000260385, ENST00000338376, 
ENST00000558560, 
ENST00000267868, 
ENST00000382643, ENST00000423169, 
ENST00000530766, ENST00000532743, 
ENST00000557850, 
Fusion gene scores* DoF score5 X 5 X 3=757 X 7 X 5=245
# samples 57
** MAII scorelog2(5/75*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/245*10)=-1.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: RMDN3 [Title/Abstract] AND RAD51 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointRMDN3(41039077)-RAD51(41024354), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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
TgeneRAD51

GO:0000724

double-strand break repair via homologous recombination

16428451

TgeneRAD51

GO:0006268

DNA unwinding involved in DNA replication

7988572

TgeneRAD51

GO:0006974

cellular response to DNA damage stimulus

23509288|25585578

TgeneRAD51

GO:0010569

regulation of double-strand break repair via homologous recombination

23754376

TgeneRAD51

GO:0031297

replication fork processing

25585578

TgeneRAD51

GO:0051106

positive regulation of DNA ligation

8929543

TgeneRAD51

GO:0071479

cellular response to ionizing radiation

23509288|23754376

TgeneRAD51

GO:0072757

cellular response to camptothecin

23509288


check buttonFusion gene breakpoints across RMDN3 (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 RAD51 (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
ChiTaRS5.0N/ABM972210RMDN3chr15

41039077

-RAD51chr15

41024354

-


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Fusion Gene ORF analysis for RMDN3-RAD51

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
intron-intronENST00000260385ENST00000267868RMDN3chr15

41039077

-RAD51chr15

41024354

-
intron-intronENST00000260385ENST00000382643RMDN3chr15

41039077

-RAD51chr15

41024354

-
intron-intronENST00000260385ENST00000423169RMDN3chr15

41039077

-RAD51chr15

41024354

-
intron-intronENST00000260385ENST00000530766RMDN3chr15

41039077

-RAD51chr15

41024354

-
intron-intronENST00000260385ENST00000532743RMDN3chr15

41039077

-RAD51chr15

41024354

-
intron-intronENST00000260385ENST00000557850RMDN3chr15

41039077

-RAD51chr15

41024354

-
intron-intronENST00000338376ENST00000267868RMDN3chr15

41039077

-RAD51chr15

41024354

-
intron-intronENST00000338376ENST00000382643RMDN3chr15

41039077

-RAD51chr15

41024354

-
intron-intronENST00000338376ENST00000423169RMDN3chr15

41039077

-RAD51chr15

41024354

-
intron-intronENST00000338376ENST00000530766RMDN3chr15

41039077

-RAD51chr15

41024354

-
intron-intronENST00000338376ENST00000532743RMDN3chr15

41039077

-RAD51chr15

41024354

-
intron-intronENST00000338376ENST00000557850RMDN3chr15

41039077

-RAD51chr15

41024354

-
intron-intronENST00000558560ENST00000267868RMDN3chr15

41039077

-RAD51chr15

41024354

-
intron-intronENST00000558560ENST00000382643RMDN3chr15

41039077

-RAD51chr15

41024354

-
intron-intronENST00000558560ENST00000423169RMDN3chr15

41039077

-RAD51chr15

41024354

-
intron-intronENST00000558560ENST00000530766RMDN3chr15

41039077

-RAD51chr15

41024354

-
intron-intronENST00000558560ENST00000532743RMDN3chr15

41039077

-RAD51chr15

41024354

-
intron-intronENST00000558560ENST00000557850RMDN3chr15

41039077

-RAD51chr15

41024354

-

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 RMDN3-RAD51


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 RMDN3-RAD51


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/:41039077/:41024354)
- 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
RMDN3

Q96TC7

RAD51

O15315

FUNCTION: Involved in cellular calcium homeostasis regulation. May participate in differentiation and apoptosis of keratinocytes. Overexpression induces apoptosis. {ECO:0000269|PubMed:16820967, ECO:0000269|PubMed:22131369}.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}.

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 RMDN3-RAD51


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 RMDN3-RAD51


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 RMDN3-RAD51


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 RMDN3-RAD51


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