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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:ATP1B2-SLC37A3

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ATP1B2-SLC37A3
FusionPDB ID: 7813
FusionGDB2.0 ID: 7813
HgeneTgene
Gene symbol

ATP1B2

SLC37A3

Gene ID

482

84255

Gene nameATPase Na+/K+ transporting subunit beta 2solute carrier family 37 member 3
SynonymsAMOG-
Cytomap

17p13.1

7q34

Type of geneprotein-codingprotein-coding
Descriptionsodium/potassium-transporting ATPase subunit beta-2ATPase, Na+/K+ transporting, beta 2 polypeptideNa, K-ATPase beta-2 polypeptideadhesion molecule in gliaadhesion molecule on gliasodium pump subunit beta-2sodium-potassium ATPase subunit beta 2 (non-sugar phosphate exchanger 3solute carrier family 37 (glycerol-3-phosphate transporter), member 3
Modification date2020031320200313
UniProtAcc

P14415

.
Ensembl transtripts involved in fusion geneENST idsENST00000250111, ENST00000429996, 
ENST00000461089, ENST00000326232, 
ENST00000447932, ENST00000340308, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score4 X 4 X 3=486 X 5 X 4=120
# samples 46
** MAII scorelog2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/120*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: ATP1B2 [Title/Abstract] AND SLC37A3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ATP1B2(7554948)-SLC37A3(140037149), # samples:2
Anticipated loss of major functional domain due to fusion event.ATP1B2-SLC37A3 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
ATP1B2-SLC37A3 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
ATP1B2-SLC37A3 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
ATP1B2-SLC37A3 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
ATP1B2-SLC37A3 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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
HgeneATP1B2

GO:0006883

cellular sodium ion homeostasis

10636900|19542013

HgeneATP1B2

GO:0030007

cellular potassium ion homeostasis

10636900|19542013

HgeneATP1B2

GO:0032781

positive regulation of ATPase activity

10636900

HgeneATP1B2

GO:0036376

sodium ion export across plasma membrane

10636900|19542013

HgeneATP1B2

GO:0050821

protein stabilization

10636900

HgeneATP1B2

GO:0086009

membrane repolarization

19542013

HgeneATP1B2

GO:1901018

positive regulation of potassium ion transmembrane transporter activity

10636900

HgeneATP1B2

GO:1903278

positive regulation of sodium ion export across plasma membrane

10636900

HgeneATP1B2

GO:1903288

positive regulation of potassium ion import

10636900

HgeneATP1B2

GO:1990573

potassium ion import across plasma membrane

10636900|19542013

TgeneSLC37A3

GO:0015760

glucose-6-phosphate transport

21949678

TgeneSLC37A3

GO:0035435

phosphate ion transmembrane transport

21949678


check buttonFusion gene breakpoints across ATP1B2 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across SLC37A3 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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
ChimerDB4SARCTCGA-DX-A8BM-01AATP1B2chr17

7554948

-SLC37A3chr7

140037149

-
ChimerDB4SARCTCGA-DX-A8BM-01AATP1B2chr17

7554948

+SLC37A3chr7

140037149

-


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000250111ATP1B2chr177554948+ENST00000340308SLC37A3chr7140037149-2338519290826178

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
ENST00000250111ENST00000340308ATP1B2chr177554948+SLC37A3chr7140037149-0.177590240.82240975

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>7813_7813_1_ATP1B2-SLC37A3_ATP1B2_chr17_7554948_ENST00000250111_SLC37A3_chr7_140037149_ENST00000340308_length(amino acids)=178AA_BP=76
MPAPPSLPVLLGVWRASARGAPASPQPPAPRPDSPRATKMVIQKEKKSCGQVVEEWKEFVWNPRTHQFMGRTGTSWVFSVSDPGQARMDV

--------------------------------------------------------------

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Fusion Protein Functional Features


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/chr17:7554948/chr7:140037149)
- 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
ATP1B2

P14415

.
FUNCTION: This is the non-catalytic component of the active enzyme, which catalyzes the hydrolysis of ATP coupled with the exchange of Na(+) and K(+) ions across the plasma membrane. The exact function of the beta-2 subunit is not known.; FUNCTION: Mediates cell adhesion of neurons and astrocytes, and promotes neurite outgrowth. {ECO:0000250}.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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneATP1B2chr17:7554948chr7:140037149ENST00000250111+171_3937.333333333333336291.0Topological domainCytoplasmic
TgeneSLC37A3chr17:7554948chr7:140037149ENST000003262321215452_472442.0495.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST00000340308912357_377341.3333333333333444.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST00000340308912386_406341.3333333333333444.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST00000340308912428_448341.3333333333333444.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST00000340308912452_472341.3333333333333444.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST000004479321114428_448426.0479.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST000004479321114452_472426.0479.0TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneATP1B2chr17:7554948chr7:140037149ENST00000250111+17193_29037.333333333333336291.0RegionNote=immunoglobulin-like
HgeneATP1B2chr17:7554948chr7:140037149ENST00000250111+1768_29037.333333333333336291.0Topological domainExtracellular
HgeneATP1B2chr17:7554948chr7:140037149ENST00000250111+1740_6737.333333333333336291.0TransmembraneHelical%3B Signal-anchor for type II membrane protein
TgeneSLC37A3chr17:7554948chr7:140037149ENST000003262321215113_133442.0495.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST000003262321215147_167442.0495.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST00000326232121516_36442.0495.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST000003262321215177_197442.0495.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST000003262321215209_229442.0495.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST000003262321215297_317442.0495.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST000003262321215333_353442.0495.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST000003262321215357_377442.0495.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST000003262321215386_406442.0495.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST000003262321215428_448442.0495.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST00000326232121581_101442.0495.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST00000340308912113_133341.3333333333333444.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST00000340308912147_167341.3333333333333444.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST0000034030891216_36341.3333333333333444.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST00000340308912177_197341.3333333333333444.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST00000340308912209_229341.3333333333333444.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST00000340308912297_317341.3333333333333444.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST00000340308912333_353341.3333333333333444.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST0000034030891281_101341.3333333333333444.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST000004479321114113_133426.0479.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST000004479321114147_167426.0479.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST00000447932111416_36426.0479.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST000004479321114177_197426.0479.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST000004479321114209_229426.0479.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST000004479321114297_317426.0479.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST000004479321114333_353426.0479.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST000004479321114357_377426.0479.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST000004479321114386_406426.0479.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST00000447932111481_101426.0479.0TransmembraneHelical


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
ATP1B2
SLC37A3


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to ATP1B2-SLC37A3


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to ATP1B2-SLC37A3


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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