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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:MRC2-RND2 (FusionGDB2 ID:54505)

Fusion Gene Summary for MRC2-RND2

check button Fusion gene summary
Fusion gene informationFusion gene name: MRC2-RND2
Fusion gene ID: 54505
HgeneTgene
Gene symbol

MRC2

RND2

Gene ID

9902

8153

Gene namemannose receptor C type 2Rho family GTPase 2
SynonymsCD280|CLEC13E|ENDO180|UPARAPARHN|RHO7|RhoN
Cytomap

17q23.2

17q21.31

Type of geneprotein-codingprotein-coding
DescriptionC-type mannose receptor 2C-type lectin domain family 13 member EUPAR-associated proteinendocytic receptor (macrophage mannose receptor family)endocytic receptor 180macrophage mannose receptor 2urokinase-type plasminogen activator receptor-associatedrho-related GTP-binding protein RhoNCTD-3199J23.4GTP-binding protein Rho7ras homolog gene family, member Nrho-related GTP-binding protein Rho7
Modification date2020031320200313
UniProtAcc

Q9UBG0

.
Ensembl transtripts involved in fusion geneENST00000303375, ENST00000446119, 
ENST00000580916, 
ENST00000587250, 
ENST00000544533, 
Fusion gene scores* DoF score10 X 9 X 5=4502 X 3 X 2=12
# samples 123
** MAII scorelog2(12/450*10)=-1.90689059560852
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/12*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: MRC2 [Title/Abstract] AND RND2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointMRC2(60705281)-RND2(41177977), # samples:3
Anticipated loss of major functional domain due to fusion event.MRC2-RND2 seems lost the major protein functional domain in Hgene 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
HgeneMRC2

GO:0030574

collagen catabolic process

12972549


check buttonFusion gene breakpoints across MRC2 (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 RND2 (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
ChimerDB4GBMTCGA-27-2524-01AMRC2chr17

60705281

+RND2chr17

41177977

+
ChimerDB4GBMTCGA-27-2524MRC2chr17

60705281

+RND2chr17

41177976

+
ChimerDB4GBMTCGA-27-2524-01AMRC2chr17

60705281

+RND2chr17

41177977

+
ChimerDB4GBMTCGA-27-2524-01AMRC2chr17

60705281

-RND2chr17

41177977

+


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Fusion Gene ORF analysis for MRC2-RND2

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-shiftENST00000303375ENST00000587250MRC2chr17

60705281

+RND2chr17

41177977

+
Frame-shiftENST00000303375ENST00000544533MRC2chr17

60705281

+RND2chr17

41177977

+
intron-3CDSENST00000446119ENST00000587250MRC2chr17

60705281

+RND2chr17

41177977

+
intron-3CDSENST00000446119ENST00000544533MRC2chr17

60705281

+RND2chr17

41177977

+
intron-3CDSENST00000580916ENST00000587250MRC2chr17

60705281

+RND2chr17

41177977

+
intron-3CDSENST00000580916ENST00000544533MRC2chr17

60705281

+RND2chr17

41177977

+
Frame-shiftENST00000303375ENST00000587250MRC2chr17

60705281

+RND2chr17

41177976

+
Frame-shiftENST00000303375ENST00000544533MRC2chr17

60705281

+RND2chr17

41177976

+
intron-3CDSENST00000446119ENST00000587250MRC2chr17

60705281

+RND2chr17

41177976

+
intron-3CDSENST00000446119ENST00000544533MRC2chr17

60705281

+RND2chr17

41177976

+
intron-3CDSENST00000580916ENST00000587250MRC2chr17

60705281

+RND2chr17

41177976

+
intron-3CDSENST00000580916ENST00000544533MRC2chr17

60705281

+RND2chr17

41177976

+

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 MRC2-RND2


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 MRC2-RND2


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
MRC2

Q9UBG0

.
FUNCTION: May play a role as endocytotic lectin receptor displaying calcium-dependent lectin activity. Internalizes glycosylated ligands from the extracellular space for release in an endosomal compartment via clathrin-mediated endocytosis. May be involved in plasminogen activation system controlling the extracellular level of PLAUR/PLAU, and thus may regulate protease activity at the cell surface. May contribute to cellular uptake, remodeling and degradation of extracellular collagen matrices. May play a role during cancer progression as well as in other chronic tissue destructive diseases acting on collagen turnover. May participate in remodeling of extracellular matrix cooperating with the matrix metalloproteinases (MMPs). {ECO:0000269|PubMed:10683150, ECO:0000269|PubMed:12972549}.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 MRC2-RND2


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 MRC2-RND2


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 MRC2-RND2


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 MRC2-RND2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneMRC2C0007097Carcinoma1CTD_human
HgeneMRC2C0024667Animal Mammary Neoplasms1CTD_human
HgeneMRC2C0024668Mammary Neoplasms, Experimental1CTD_human
HgeneMRC2C0205696Anaplastic carcinoma1CTD_human
HgeneMRC2C0205697Carcinoma, Spindle-Cell1CTD_human
HgeneMRC2C0205698Undifferentiated carcinoma1CTD_human
HgeneMRC2C0205699Carcinomatosis1CTD_human
HgeneMRC2C1257925Mammary Carcinoma, Animal1CTD_human