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Center for Computational Systems Medicine
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Fusion Gene and Fusion Protein Summary

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Fusion Amino Acid Sequences (multiple BPs and multiple gene isoforms)

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Fusion Protein Breakpoint Sequences - (for the Screening of the FusionNeoAntigens)

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Potential FusionNeoAntigens in HLA I - (netMHCpan v4.1 + deepHLApan v1.1)

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Potential FusionNeoAntigens in HLA II - (netMHCIIpan v4.1)

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Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D - (Glide)

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Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

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Potential target of CAR-T therapy development

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Information on the samples that have these potential fusion neoantigens

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Fusion Protein Targeting Drugs - (Manual Curation)

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Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:ATP1B2-SLC37A3

Fusion Gene and 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

Main function of 5'-partner protein: 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}.
.
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
Fusion gene context

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

Fusion neoantigen context

PubMed: ATP1B2 [Title/Abstract] AND SLC37A3 [Title/Abstract] AND neoantigen [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 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 buttonRetention analysis results 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, are available here.

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 Amino Acid Sequences


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

check button Predicted full-length fusion amino acid sequences. For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among all the predicted ones.

Get the fusion protein sequences from here.

Fusion protein sequence information is available in the fasta format.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

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Fusion Protein Breakpoint Sequences for ATP1B2-SLC37A3

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ATP1B2chr177554948SLC37A3chr714003714951976RTHQFMGRTGTSWVFSVSDPGQARMD

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Potential FusionNeoAntigen Information of ATP1B2-SLC37A3 in HLA I

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.
ATP1B2-SLC37A3_7554948_140037149.msa

check button Potential FusionNeoAntigen Information
* We used NetMHCpan v4.1 (%rank<0.5) and deepHLApan v1.1 (immunogenic score>0.5)
Fusion geneHchrHbpTgeneTchrTbpHLA IFusionNeoAntigen peptideBinding scoreImmunogenic scoreNeoantigen start (at BP 13)Neoantigen end (at BP 13)
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-B27:05GRTGTSWVF0.99920.8523615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-B27:02GRTGTSWVF0.99920.6295615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-B27:04GRTGTSWVF0.99880.8395615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-B27:07GRTGTSWVF0.99160.6534615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-B38:01GRTGTSWVF0.56150.9675615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-B38:02GRTGTSWVF0.55740.9682615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-B15:18GRTGTSWVF0.30160.9103615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-B27:02MGRTGTSWVF0.99530.6011515
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-B27:02FMGRTGTSWVF0.99350.7257415
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-B27:14GRTGTSWVF0.99890.8457615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-C07:95GRTGTSWVF0.99410.8257615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-B27:03GRTGTSWVF0.99010.8662615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-C07:05GRTGTSWVF0.97820.965615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-C07:27GRTGTSWVF0.96190.9674615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-C07:19GRTGTSWVF0.80960.8792615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-C07:46GRTGTSWVF0.80730.9421615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-C07:10GRTGTSWVF0.78910.9748615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-C07:80GRTGTSWVF0.78860.9668615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-C07:67GRTGTSWVF0.78860.9668615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-B39:12GRTGTSWVF0.70960.921615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-C12:16GRTGTSWVF0.01020.9853615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-B27:08GRTGTSWVF0.9990.8099615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-B27:10GRTGTSWVF0.99870.9043615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-B27:06GRTGTSWVF0.99540.8793615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-C07:01GRTGTSWVF0.99480.8298615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-B27:09GRTGTSWVF0.98740.8317615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-C07:17GRTGTSWVF0.9580.9753615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-C07:02GRTGTSWVF0.78860.9668615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-C07:22GRTGTSWVF0.75910.827615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-C06:08GRTGTSWVF0.67440.9968615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-B39:31GRTGTSWVF0.67080.9178615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-B38:05GRTGTSWVF0.56150.9675615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-C06:17GRTGTSWVF0.00450.9969615
ATP1B2-SLC37A3chr177554948chr7140037149519HLA-C06:02GRTGTSWVF0.00450.9969615

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Potential FusionNeoAntigen Information of ATP1B2-SLC37A3 in HLA II

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.
ATP1B2-SLC37A3_7554948_140037149.msa

check button Potential FusionNeoAntigen Information
* We used NetMHCIIpan v4.1 (%rank<0.5).
Fusion geneHchrHbpTgeneTchrTbpHLA IIFusionNeoAntigen peptideNeoantigen start (at BP 13)Neoantigen end (at BP 13)
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0401GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0403GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0407GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0419GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0431GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0433GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0434GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0435GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0438GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0439GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0441GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0446GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0447GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0449GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0450GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0451GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0452GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0459GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0460GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0461GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0463GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0464GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0469GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0471GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0472GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0474GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0474TGTSWVFSVSDPGQA823
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0475GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0476GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0485GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0902GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0902TGTSWVFSVSDPGQA823
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0902TSWVFSVSDPGQARM1025
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0907GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB1-0908GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB3-0217GTSWVFSVSDPGQAR924
ATP1B2-SLC37A3chr177554948chr7140037149519DRB5-0112GTSWVFSVSDPGQAR924

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Fusion breakpoint peptide structures of ATP1B2-SLC37A3

check button3D structures of the fusion breakpoint peptide of 14AA sequence that have potential fusion neoantigens
* The minimum length of the amino acid sequence in RoseTTAFold is 14AA. Here, we predicted the 14AA fusion protein breakpoint sequence not the fusion neoantigen peptide, which is shorter than 14 AA.
File nameBPseqHgeneTgeneHchrHbpTchrTbpAAlen
3099GRTGTSWVFSVSDPATP1B2SLC37A3chr177554948chr7140037149519

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ATP1B2-SLC37A3

check buttonVirtual screening between 25 HLAs (from PDB) and FusionNeoAntigens
* We used Glide to predict the interaction between HLAs and neoantigens.
HLA allelePDB IDFile nameBPseqDocking scoreGlide score
HLA-B14:023BVN3099GRTGTSWVFSVSDP-6.60553-6.71893
HLA-B14:023BVN3099GRTGTSWVFSVSDP-3.25382-4.28912
HLA-B52:013W393099GRTGTSWVFSVSDP-5.90011-6.01351
HLA-B52:013W393099GRTGTSWVFSVSDP-5.4415-6.4768
HLA-B18:014JQV3099GRTGTSWVFSVSDP-2.23313-2.34653
HLA-A11:014UQ23099GRTGTSWVFSVSDP-6.31705-6.43045
HLA-A11:014UQ23099GRTGTSWVFSVSDP-4.25402-5.28932
HLA-A24:025HGA3099GRTGTSWVFSVSDP-7.95591-8.06931
HLA-A24:025HGA3099GRTGTSWVFSVSDP-6.24522-7.28052
HLA-B27:056PYJ3099GRTGTSWVFSVSDP-3.83335-4.86865
HLA-B44:053DX83099GRTGTSWVFSVSDP-6.2025-6.3159
HLA-B44:053DX83099GRTGTSWVFSVSDP-5.27651-6.31181
HLA-A02:016TDR3099GRTGTSWVFSVSDP-6.48102-6.59442

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Vaccine Design for the FusionNeoAntigens of ATP1B2-SLC37A3

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-Is.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptide sequenceFusionNeoAntigen RNA sequence
ATP1B2-SLC37A3chr177554948chr7140037149415FMGRTGTSWVFTTATGGGCCGCACCGGGACCAGCTGGGTATTTA
ATP1B2-SLC37A3chr177554948chr7140037149515MGRTGTSWVFTGGGCCGCACCGGGACCAGCTGGGTATTTA
ATP1B2-SLC37A3chr177554948chr7140037149615GRTGTSWVFGCCGCACCGGGACCAGCTGGGTATTTA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
ATP1B2-SLC37A3chr177554948chr71400371491025TSWVFSVSDPGQARMCCAGCTGGGTATTTAGTGTCTCTGATCCGGGACAAGCTAGGATGG
ATP1B2-SLC37A3chr177554948chr7140037149823TGTSWVFSVSDPGQACCGGGACCAGCTGGGTATTTAGTGTCTCTGATCCGGGACAAGCTA
ATP1B2-SLC37A3chr177554948chr7140037149924GTSWVFSVSDPGQARGGACCAGCTGGGTATTTAGTGTCTCTGATCCGGGACAAGCTAGGA

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Information of the samples that have these potential fusion neoantigens of ATP1B2-SLC37A3

check button These samples were reported as having these fusion breakpoints. For individual breakpoints, we checked the open reading frames considering multiple gene isoforms and chose the in-frame fusion genes only. Then, we made fusion protein sequences and predicted the fusion neoantigens. These fusion-positive samples may have these potential fusion neoantigens.
Cancer typeFusion geneHchrHbpHenstTchrTbpTenstSample
SARCATP1B2-SLC37A3chr177554948ENST00000250111chr7140037149ENST00000340308TCGA-DX-A8BM-01A

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Potential target of CAR-T therapy development for ATP1B2-SLC37A3

check button Predicted 3D structure. We used RoseTTAFold.

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, to provide the retention of the transmembrane domain, we only show the protein feature retention information of those transmembrane features


* Minus value of BPloci means that the break point is located before the CDS.
- In-frame and retained 'Transmembrane'.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneSLC37A3chr17:7554948chr7:140037149ENST000003262321215452_4720495.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST00000340308912357_3770444.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST00000340308912386_4060444.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST00000340308912428_4480444.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST00000340308912452_4720444.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST000004479321114428_4480479.0TransmembraneHelical
TgeneSLC37A3chr17:7554948chr7:140037149ENST000004479321114452_4720479.0TransmembraneHelical

check button Subcellular localization prediction of the transmembrane domain retained fusion proteins
* We used DeepLoc 1.0. The order of the X-axis of the barplot is as follows: Entry_ID, Localization, Type, Nucleus, Cytoplasm, Extracellular, Mitochondrion, Cell_membrane, Endoplasmic_reticulum, Plastid, Golgi.apparatus, Lysosome.Vacuole, Peroxisome. Y-axis is the output score of DeepLoc. Clicking the image will open a new tab with a large image.
HgeneHchrHbpHenstTgeneTchrTbpTenstDeepLoc result

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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