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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:HMCN1-RNF2 (FusionGDB2 ID:36783)

Fusion Gene Summary for HMCN1-RNF2

check button Fusion gene summary
Fusion gene informationFusion gene name: HMCN1-RNF2
Fusion gene ID: 36783
HgeneTgene
Gene symbol

HMCN1

RNF2

Gene ID

83872

6045

Gene namehemicentin 1ring finger protein 2
SynonymsARMD1|FBLN6|FIBL-6|FIBL6BAP-1|BAP1|DING|HIPI3|RING1B|RING2
Cytomap

1q25.3-q31.1

1q25.3

Type of geneprotein-codingprotein-coding
Descriptionhemicentin-1LOC100507250/HMCN1 fusionfibulin-6E3 ubiquitin-protein ligase RING2HIP2-interacting protein 3RING finger protein 1BRING finger protein BAP-1RING-type E3 ubiquitin transferase RING2huntingtin-interacting protein 2-interacting protein 3protein DinG
Modification date2020031320200313
UniProtAcc

Q96RW7

Q9NWF9

Ensembl transtripts involved in fusion geneENST00000271588, ENST00000367492, 
ENST00000485744, 
ENST00000367509, 
ENST00000367510, 
Fusion gene scores* DoF score7 X 6 X 4=1684 X 2 X 2=16
# samples 75
** MAII scorelog2(7/168*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/16*10)=1.64385618977472
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: HMCN1 [Title/Abstract] AND RNF2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointHMCN1(185704179)-RNF2(185056684), # samples:1
HMCN1(185704179)-RNF2(185060711), # samples:1
Anticipated loss of major functional domain due to fusion event.HMCN1-RNF2 seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor 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
TgeneRNF2

GO:0035518

histone H2A monoubiquitination

16943429


check buttonFusion gene breakpoints across HMCN1 (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 RNF2 (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
ChimerDB4BRCATCGA-AR-A256-01AHMCN1chr1

185704179

-RNF2chr1

185060711

+
ChimerDB4LUSCTCGA-56-6546-01AHMCN1chr1

185704179

+RNF2chr1

185056684

+


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Fusion Gene ORF analysis for HMCN1-RNF2

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
5CDS-5UTRENST00000271588ENST00000367509HMCN1chr1

185704179

+RNF2chr1

185056684

+
5CDS-5UTRENST00000271588ENST00000367510HMCN1chr1

185704179

+RNF2chr1

185056684

+
5CDS-5UTRENST00000367492ENST00000367509HMCN1chr1

185704179

+RNF2chr1

185056684

+
5CDS-5UTRENST00000367492ENST00000367510HMCN1chr1

185704179

+RNF2chr1

185056684

+
Frame-shiftENST00000271588ENST00000367509HMCN1chr1

185704179

-RNF2chr1

185060711

+
Frame-shiftENST00000271588ENST00000367510HMCN1chr1

185704179

-RNF2chr1

185060711

+
Frame-shiftENST00000367492ENST00000367509HMCN1chr1

185704179

-RNF2chr1

185060711

+
Frame-shiftENST00000367492ENST00000367510HMCN1chr1

185704179

-RNF2chr1

185060711

+
intron-3CDSENST00000485744ENST00000367509HMCN1chr1

185704179

-RNF2chr1

185060711

+
intron-3CDSENST00000485744ENST00000367510HMCN1chr1

185704179

-RNF2chr1

185060711

+
intron-5UTRENST00000485744ENST00000367509HMCN1chr1

185704179

+RNF2chr1

185056684

+
intron-5UTRENST00000485744ENST00000367510HMCN1chr1

185704179

+RNF2chr1

185056684

+

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 HMCN1-RNF2


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)
HMCN1chr1185704179+RNF2chr1185056683+1.73E-070.9999999
HMCN1chr1185704179+RNF2chr1185056683+1.73E-070.9999999

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.
genomic feature of top 1%

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Fusion Protein Features for HMCN1-RNF2


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/:185704179/:185056684)
- 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
HMCN1

Q96RW7

RNF2

Q9NWF9

FUNCTION: Promotes cleavage furrow maturation during cytokinesis in preimplantation embryos. May play a role in the architecture of adhesive and flexible epithelial cell junctions. May play a role during myocardial remodeling by imparting an effect on cardiac fibroblast migration. {ECO:0000250|UniProtKB:D3YXG0}.FUNCTION: Isoform 1 acts as an E3 ubiquitin ligase, which accepts ubiquitin from specific E2 ubiquitin-conjugating enzymes, and then transfers it to substrates promoting their degradation by the proteasome. Promotes degradation of TRAF3, TLR4 and TLR9. Contributes to the regulation of antiviral responses. Down-regulates activation of NF-kappa-B, IRF3 activation and IFNB production. Isoform 3 inhibits TNF and IL-1 mediated activation of NF-kappa-B. Promotes TNF and RIP mediated apoptosis. {ECO:0000269|PubMed:15107846, ECO:0000269|PubMed:19893624}.

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 HMCN1-RNF2


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 HMCN1-RNF2


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 HMCN1-RNF2


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 HMCN1-RNF2


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