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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:ATP2A2-BTBD9 (FusionGDB2 ID:7828)

Fusion Gene Summary for ATP2A2-BTBD9

check button Fusion gene summary
Fusion gene informationFusion gene name: ATP2A2-BTBD9
Fusion gene ID: 7828
HgeneTgene
Gene symbol

ATP2A2

BTBD9

Gene ID

488

114781

Gene nameATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2BTB domain containing 9
SynonymsATP2B|DAR|DD|SERCA2dJ322I12.1
Cytomap

12q24.11

6p21.2

Type of geneprotein-codingprotein-coding
Descriptionsarcoplasmic/endoplasmic reticulum calcium ATPase 2ATPase Ca++ transporting cardiac muscle slow twitch 2ATPase, Ca++ dependent, slow-twitch, cardiac muscle-2SR Ca(2+)-ATPase 2calcium pump 2calcium-transporting ATPase sarcoplasmic reticulum type, slowBTB/POZ domain-containing protein 9BTB (POZ) domain containing 9
Modification date2020031320200313
UniProtAcc

P16615

Q96Q07

Ensembl transtripts involved in fusion geneENST00000308664, ENST00000395494, 
ENST00000539276, ENST00000550248, 
ENST00000552636, 
ENST00000314100, 
ENST00000403056, ENST00000408958, 
ENST00000419706, ENST00000481247, 
Fusion gene scores* DoF score17 X 22 X 11=411418 X 18 X 7=2268
# samples 2720
** MAII scorelog2(27/4114*10)=-3.9295104814741
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(20/2268*10)=-3.5033487351675
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ATP2A2 [Title/Abstract] AND BTBD9 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointATP2A2(110739960)-BTBD9(38452592), # 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
HgeneATP2A2

GO:0032469

endoplasmic reticulum calcium ion homeostasis

16402920

HgeneATP2A2

GO:0032470

positive regulation of endoplasmic reticulum calcium ion concentration

16402920

HgeneATP2A2

GO:0070588

calcium ion transmembrane transport

16402920

HgeneATP2A2

GO:1903515

calcium ion transport from cytosol to endoplasmic reticulum

16402920


check buttonFusion gene breakpoints across ATP2A2 (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 BTBD9 (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/AT19626ATP2A2chr12

110739960

-BTBD9chr6

38452592

-


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Fusion Gene ORF analysis for ATP2A2-BTBD9

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-intronENST00000308664ENST00000314100ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000308664ENST00000403056ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000308664ENST00000408958ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000308664ENST00000419706ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000308664ENST00000481247ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000395494ENST00000314100ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000395494ENST00000403056ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000395494ENST00000408958ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000395494ENST00000419706ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000395494ENST00000481247ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000539276ENST00000314100ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000539276ENST00000403056ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000539276ENST00000408958ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000539276ENST00000419706ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000539276ENST00000481247ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000550248ENST00000314100ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000550248ENST00000403056ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000550248ENST00000408958ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000550248ENST00000419706ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000550248ENST00000481247ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000552636ENST00000314100ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000552636ENST00000403056ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000552636ENST00000408958ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000552636ENST00000419706ATP2A2chr12

110739960

-BTBD9chr6

38452592

-
intron-intronENST00000552636ENST00000481247ATP2A2chr12

110739960

-BTBD9chr6

38452592

-

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 ATP2A2-BTBD9


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 ATP2A2-BTBD9


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/:110739960/:38452592)
- 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
ATP2A2

P16615

BTBD9

Q96Q07

FUNCTION: This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol to the sarcoplasmic reticulum lumen (PubMed:16402920). Involved in autophagy in response to starvation. Upon interaction with VMP1 and activation, controls ER-isolation membrane contacts for autophagosome formation (PubMed:28890335). Also modulates ER contacts with lipid droplets, mitochondria and endosomes (PubMed:28890335). {ECO:0000269|PubMed:16402920, ECO:0000269|PubMed:28890335}.; FUNCTION: [Isoform 2]: Involved in the regulation of the contraction/relaxation cycle. Acts as a regulator of TNFSF11-mediated Ca(2+) signaling pathways via its interaction with TMEM64 which is critical for the TNFSF11-induced CREB1 activation and mitochondrial ROS generation necessary for proper osteoclast generation. Association between TMEM64 and SERCA2 in the ER leads to cytosolic Ca(2+) spiking for activation of NFATC1 and production of mitochondrial ROS, thereby triggering Ca(2+) signaling cascades that promote osteoclast differentiation and activation. {ECO:0000250|UniProtKB:O55143}.

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 ATP2A2-BTBD9


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 ATP2A2-BTBD9


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 ATP2A2-BTBD9


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 ATP2A2-BTBD9


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