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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:RYR2-AIDA (FusionGDB2 ID:78801)

Fusion Gene Summary for RYR2-AIDA

check button Fusion gene summary
Fusion gene informationFusion gene name: RYR2-AIDA
Fusion gene ID: 78801
HgeneTgene
Gene symbol

RYR2

AIDA

Gene ID

6262

64853

Gene nameryanodine receptor 2axin interactor, dorsalization associated
SynonymsARVC2|ARVD2|RYR-2|RyR|VTSIPC1orf80
Cytomap

1q43

1q41

Type of geneprotein-codingprotein-coding
Descriptionryanodine receptor 2cardiac muscle ryanodine receptor-calcium release channelcardiac-type ryanodine receptorislet-type ryanodine receptorkidney-type ryanodine receptorryanodine receptor 2 (cardiac)type 2 ryanodine receptoraxin interactor, dorsalization-associated proteinaxin interaction partner and dorsalization antagonist
Modification date2020031520200327
UniProtAcc.

Q96BJ3

Ensembl transtripts involved in fusion geneENST00000360064, ENST00000366574, 
ENST00000542537, ENST00000609119, 
ENST00000340020, ENST00000355727, 
ENST00000474863, ENST00000541237, 
Fusion gene scores* DoF score10 X 11 X 5=5509 X 9 X 2=162
# samples 119
** MAII scorelog2(11/550*10)=-2.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/162*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: RYR2 [Title/Abstract] AND AIDA [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointRYR2(237973316)-AIDA(222842552), # 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
HgeneRYR2

GO:0005513

detection of calcium ion

10830164

HgeneRYR2

GO:0006816

calcium ion transport

17921453

HgeneRYR2

GO:0031000

response to caffeine

17921453

HgeneRYR2

GO:0035584

calcium-mediated signaling using intracellular calcium source

17921453

HgeneRYR2

GO:0051209

release of sequestered calcium ion into cytosol

12443530|17921453

HgeneRYR2

GO:0051284

positive regulation of sequestering of calcium ion

12443530|12919952

HgeneRYR2

GO:0051775

response to redox state

19226252

HgeneRYR2

GO:0060402

calcium ion transport into cytosol

17921453

HgeneRYR2

GO:0071313

cellular response to caffeine

12919952

HgeneRYR2

GO:0072599

establishment of protein localization to endoplasmic reticulum

12443530

HgeneRYR2

GO:1901896

positive regulation of calcium-transporting ATPase activity

12443530

TgeneAIDA

GO:0043508

negative regulation of JUN kinase activity

17681137


check buttonFusion gene breakpoints across RYR2 (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 AIDA (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/AEC562655RYR2chr1

237973316

-AIDAchr1

222842552

+


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Fusion Gene ORF analysis for RYR2-AIDA

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-3UTRENST00000360064ENST00000340020RYR2chr1

237973316

-AIDAchr1

222842552

+
intron-3UTRENST00000360064ENST00000355727RYR2chr1

237973316

-AIDAchr1

222842552

+
intron-3UTRENST00000366574ENST00000340020RYR2chr1

237973316

-AIDAchr1

222842552

+
intron-3UTRENST00000366574ENST00000355727RYR2chr1

237973316

-AIDAchr1

222842552

+
intron-3UTRENST00000542537ENST00000340020RYR2chr1

237973316

-AIDAchr1

222842552

+
intron-3UTRENST00000542537ENST00000355727RYR2chr1

237973316

-AIDAchr1

222842552

+
intron-3UTRENST00000609119ENST00000340020RYR2chr1

237973316

-AIDAchr1

222842552

+
intron-3UTRENST00000609119ENST00000355727RYR2chr1

237973316

-AIDAchr1

222842552

+
intron-5UTRENST00000360064ENST00000474863RYR2chr1

237973316

-AIDAchr1

222842552

+
intron-5UTRENST00000366574ENST00000474863RYR2chr1

237973316

-AIDAchr1

222842552

+
intron-5UTRENST00000542537ENST00000474863RYR2chr1

237973316

-AIDAchr1

222842552

+
intron-5UTRENST00000609119ENST00000474863RYR2chr1

237973316

-AIDAchr1

222842552

+
intron-intronENST00000360064ENST00000541237RYR2chr1

237973316

-AIDAchr1

222842552

+
intron-intronENST00000366574ENST00000541237RYR2chr1

237973316

-AIDAchr1

222842552

+
intron-intronENST00000542537ENST00000541237RYR2chr1

237973316

-AIDAchr1

222842552

+
intron-intronENST00000609119ENST00000541237RYR2chr1

237973316

-AIDAchr1

222842552

+

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 RYR2-AIDA


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 RYR2-AIDA


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/:237973316/:222842552)
- 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
.AIDA

Q96BJ3

FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.FUNCTION: Acts as a ventralizing factor during embryogenesis. Inhibits axin-mediated JNK activation by binding axin and disrupting axin homodimerization. This in turn antagonizes a Wnt/beta-catenin-independent dorsalization pathway activated by AXIN/JNK-signaling (By similarity). {ECO:0000250}.

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 RYR2-AIDA


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 RYR2-AIDA


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 RYR2-AIDA


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 RYR2-AIDA


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