FusionNeoAntigen Logo

Home

Download

Statistics

Examples

Help

Contact

Terms of Use

Center for Computational Systems Medicine
leaf

Fusion Gene and Fusion Protein Summary

leaf

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

leaf

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

leaf

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

leaf

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

leaf

Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

leaf

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

leaf

Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

leaf

Potential target of CAR-T therapy development

leaf

Information on the samples that have these potential fusion neoantigens

leaf

Fusion Protein Targeting Drugs - (Manual Curation)

leaf

Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:ATP1A1-SLC12A1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ATP1A1-SLC12A1
FusionPDB ID: 7790
FusionGDB2.0 ID: 7790
HgeneTgene
Gene symbol

ATP1A1

SLC12A1

Gene ID

480

6557

Gene nameATPase Na+/K+ transporting subunit alpha 4solute carrier family 12 member 1
SynonymsATP1A1|ATP1AL2BSC1|NKCC2
Cytomap

1q23.2

15q21.1

Type of geneprotein-codingprotein-coding
Descriptionsodium/potassium-transporting ATPase subunit alpha-4ATPase, Na+/K+ transporting, alpha 4 polypeptideATPase, Na+/K+ transporting, alpha polypeptide-like 2Na(+)/K(+) ATPase alpha-4 subunitNa+/K+ ATPase 4Na+/K+ ATPase, alpha-D polypeptideNa,K-ATPase susolute carrier family 12 member 1NKCC2A variant ANa-K-2Cl cotransporterbumetanide-sensitive sodium-(potassium)-chloride cotransporter 2kidney-specific Na-K-Cl symportersolute carrier family 12 (sodium/potassium/chloride transporter), member 1solute
Modification date2020031320200313
UniProtAcc

Q5TC04

Main function of 5'-partner protein:
.
Ensembl transtripts involved in fusion geneENST idsENST00000295598, ENST00000369496, 
ENST00000537345, ENST00000491156, 
ENST00000559723, ENST00000330289, 
ENST00000380993, ENST00000396577, 
ENST00000558405, ENST00000561031, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score16 X 18 X 7=20166 X 7 X 5=210
# samples 237
** MAII scorelog2(23/2016*10)=-3.13178987255554
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/210*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ATP1A1 [Title/Abstract] AND SLC12A1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ATP1A1 [Title/Abstract] AND SLC12A1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ATP1A1(116933513)-SLC12A1(48513118), # samples:1
Anticipated loss of major functional domain due to fusion event.ATP1A1-SLC12A1 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.
ATP1A1-SLC12A1 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.
* 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
HgeneATP1A1

GO:0030317

flagellated sperm motility

12112599

HgeneATP1A1

GO:0030641

regulation of cellular pH

12112599



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/chr1:116933513/chr15:48513118)
- 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 ATP1A1 (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 SLC12A1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


Top

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)
ENST00000295598ATP1A1chr1116933513+ENST00000380993SLC12A1chr1548513118+5523158423743311364
ENST00000295598ATP1A1chr1116933513+ENST00000396577SLC12A1chr1548513118+5525158423743311364
ENST00000295598ATP1A1chr1116933513+ENST00000330289SLC12A1chr1548513118+261015842372324695
ENST00000295598ATP1A1chr1116933513+ENST00000558405SLC12A1chr1548513118+4444158423743311364
ENST00000295598ATP1A1chr1116933513+ENST00000561031SLC12A1chr1548513118+176715842371685482
ENST00000537345ATP1A1chr1116933513+ENST00000380993SLC12A1chr1548513118+5634169531844421374
ENST00000537345ATP1A1chr1116933513+ENST00000396577SLC12A1chr1548513118+5636169531844421374
ENST00000537345ATP1A1chr1116933513+ENST00000330289SLC12A1chr1548513118+272116953182435705
ENST00000537345ATP1A1chr1116933513+ENST00000558405SLC12A1chr1548513118+4555169531844421374
ENST00000537345ATP1A1chr1116933513+ENST00000561031SLC12A1chr1548513118+187816953181796492
ENST00000369496ATP1A1chr1116933513+ENST00000380993SLC12A1chr1548513118+5443150416342511362
ENST00000369496ATP1A1chr1116933513+ENST00000396577SLC12A1chr1548513118+5445150416342511362
ENST00000369496ATP1A1chr1116933513+ENST00000330289SLC12A1chr1548513118+253015041632244693
ENST00000369496ATP1A1chr1116933513+ENST00000558405SLC12A1chr1548513118+4364150416342511362
ENST00000369496ATP1A1chr1116933513+ENST00000561031SLC12A1chr1548513118+168715041631605480

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
ENST00000295598ENST00000380993ATP1A1chr1116933513+SLC12A1chr1548513118+0.000433490.9995665
ENST00000295598ENST00000396577ATP1A1chr1116933513+SLC12A1chr1548513118+0.0004266440.9995734
ENST00000295598ENST00000330289ATP1A1chr1116933513+SLC12A1chr1548513118+0.0030724590.99692756
ENST00000295598ENST00000558405ATP1A1chr1116933513+SLC12A1chr1548513118+0.0008168060.99918324
ENST00000295598ENST00000561031ATP1A1chr1116933513+SLC12A1chr1548513118+0.0023079560.9976921
ENST00000537345ENST00000380993ATP1A1chr1116933513+SLC12A1chr1548513118+0.000403970.99959606
ENST00000537345ENST00000396577ATP1A1chr1116933513+SLC12A1chr1548513118+0.0003960940.9996039
ENST00000537345ENST00000330289ATP1A1chr1116933513+SLC12A1chr1548513118+0.001790550.9982095
ENST00000537345ENST00000558405ATP1A1chr1116933513+SLC12A1chr1548513118+0.0006811390.99931884
ENST00000537345ENST00000561031ATP1A1chr1116933513+SLC12A1chr1548513118+0.0019316760.9980684
ENST00000369496ENST00000380993ATP1A1chr1116933513+SLC12A1chr1548513118+0.0003462930.9996537
ENST00000369496ENST00000396577ATP1A1chr1116933513+SLC12A1chr1548513118+0.0003342780.99966574
ENST00000369496ENST00000330289ATP1A1chr1116933513+SLC12A1chr1548513118+0.0020726490.9979273
ENST00000369496ENST00000558405ATP1A1chr1116933513+SLC12A1chr1548513118+0.0005986870.99940133
ENST00000369496ENST00000561031ATP1A1chr1116933513+SLC12A1chr1548513118+0.0019992050.9980008

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

Top

Fusion Protein Breakpoint Sequences for ATP1A1-SLC12A1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ATP1A1chr1116933513SLC12A1chr15485131181504447VFQANQENLPILKVRCMLNIWGVMLF
ATP1A1chr1116933513SLC12A1chr15485131181584449VFQANQENLPILKVRCMLNIWGVMLF
ATP1A1chr1116933513SLC12A1chr15485131181695459VFQANQENLPILKVRCMLNIWGVMLF

Top

Potential FusionNeoAntigen Information of ATP1A1-SLC12A1 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.
ATP1A1-SLC12A1_116933513_48513118.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)
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B08:01ILKVRCML0.99930.50881018
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B45:01QENLPILKV0.99950.9325514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B57:01KVRCMLNIW0.9990.95921221
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B50:02QENLPILKV0.9990.5968514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B13:01QENLPILKV0.98430.926514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B44:03QENLPILKV0.9780.9605514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B08:01LPILKVRCM0.97540.7693817
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B35:01LPILKVRCM0.96360.6979817
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B08:09LPILKVRCM0.96050.6785817
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B35:03LPILKVRCM0.93020.742817
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B47:01QENLPILKV0.92770.513514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B41:01QENLPILKV0.68410.9622514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B35:02LPILKVRCM0.64740.8005817
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B35:04LPILKVRCM0.64740.8005817
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B50:01QENLPILKV0.55280.6519514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B39:13QENLPILKV0.25930.8952514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B52:01QENLPILKV0.23660.8145514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B40:06QENLPILKV0.9990.6466514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B42:02LPILKVRCM0.98280.7904817
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B42:01LPILKVRCM0.97290.7827817
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B35:12LPILKVRCM0.64740.8005817
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B39:08QENLPILKV0.57770.9006514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B39:10LPILKVRCM0.36590.7511817
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B51:07QENLPILKV0.19690.6872514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B08:18ILKVRCML0.99930.50881018
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B57:10KVRCMLNIW0.9990.95921221
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B58:06KVRCMLNIW0.99680.68741221
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B40:04QENLPILKV0.99130.6947514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-A32:01KVRCMLNIW0.99070.97961221
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B44:26QENLPILKV0.9780.9605514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B44:07QENLPILKV0.9780.9605514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B44:13QENLPILKV0.9780.9605514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B08:18LPILKVRCM0.97540.7693817
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B35:77LPILKVRCM0.96360.6979817
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B35:23LPILKVRCM0.95850.6677817
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B35:24LPILKVRCM0.9010.6683817
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B35:11LPILKVRCM0.84180.7497817
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B41:03QENLPILKV0.81340.72514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B18:11QENLPILKV0.76840.836514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B08:12LPILKVRCM0.73950.8555817
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B18:03QENLPILKV0.71750.8148514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B35:09LPILKVRCM0.64740.8005817
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B50:04QENLPILKV0.55280.6519514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B50:05QENLPILKV0.55280.6519514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B67:01LPILKVRCM0.45940.6314817
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B39:02QENLPILKV0.2710.8909514
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B18:07LPILKVRCM0.11350.6408817
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B35:43LPILKVRCM0.00540.5829817
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B15:08LPILKVRCM0.0050.5846817
ATP1A1-SLC12A1chr1116933513chr15485131181584HLA-B15:11LPILKVRCM0.00480.5912817

Top

Potential FusionNeoAntigen Information of ATP1A1-SLC12A1 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.

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)

Top

Fusion breakpoint peptide structures of ATP1A1-SLC12A1

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
1985ENLPILKVRCMLNIATP1A1SLC12A1chr1116933513chr15485131181584

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ATP1A1-SLC12A1

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-B14:023BVN1985ENLPILKVRCMLNI-7.9962-8.1096
HLA-B14:023BVN1985ENLPILKVRCMLNI-5.70842-6.74372
HLA-B52:013W391985ENLPILKVRCMLNI-6.83737-6.95077
HLA-B52:013W391985ENLPILKVRCMLNI-4.4836-5.5189
HLA-A11:014UQ21985ENLPILKVRCMLNI-10.0067-10.1201
HLA-A11:014UQ21985ENLPILKVRCMLNI-9.03915-10.0745
HLA-A24:025HGA1985ENLPILKVRCMLNI-6.56204-6.67544
HLA-A24:025HGA1985ENLPILKVRCMLNI-5.42271-6.45801
HLA-B44:053DX81985ENLPILKVRCMLNI-7.85648-8.89178
HLA-B44:053DX81985ENLPILKVRCMLNI-5.3978-5.5112
HLA-A02:016TDR1985ENLPILKVRCMLNI-3.37154-4.40684

Top

Vaccine Design for the FusionNeoAntigens of ATP1A1-SLC12A1

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
ATP1A1-SLC12A1chr1116933513chr15485131181018ILKVRCMLATTCTTAAGGTAAGATGCATGCTG
ATP1A1-SLC12A1chr1116933513chr15485131181221KVRCMLNIWAAGGTAAGATGCATGCTGAACATCTGG
ATP1A1-SLC12A1chr1116933513chr1548513118514QENLPILKVCAGGAAAACCTACCTATTCTTAAGGTA
ATP1A1-SLC12A1chr1116933513chr1548513118817LPILKVRCMCTACCTATTCTTAAGGTAAGATGCATG

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

Top

Information of the samples that have these potential fusion neoantigens of ATP1A1-SLC12A1

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
Non-CancerATP1A1-SLC12A1chr1116933513ENST00000295598chr1548513118ENST00000330289TCGA-CZ-5469-11A

Top

Potential target of CAR-T therapy development for ATP1A1-SLC12A1

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
HgeneATP1A1chr1:116933513chr15:48513118ENST00000295598+1023132_1524441024.0TransmembraneHelical
HgeneATP1A1chr1:116933513chr15:48513118ENST00000295598+1023289_3084441024.0TransmembraneHelical
HgeneATP1A1chr1:116933513chr15:48513118ENST00000295598+1023321_3384441024.0TransmembraneHelical
HgeneATP1A1chr1:116933513chr15:48513118ENST00000295598+102388_1084441024.0TransmembraneHelical
HgeneATP1A1chr1:116933513chr15:48513118ENST00000369496+1023132_152413993.0TransmembraneHelical
HgeneATP1A1chr1:116933513chr15:48513118ENST00000369496+1023289_308413993.0TransmembraneHelical
HgeneATP1A1chr1:116933513chr15:48513118ENST00000369496+1023321_338413993.0TransmembraneHelical
HgeneATP1A1chr1:116933513chr15:48513118ENST00000369496+102388_108413993.0TransmembraneHelical
HgeneATP1A1chr1:116933513chr15:48513118ENST00000537345+1023132_1524441024.0TransmembraneHelical
HgeneATP1A1chr1:116933513chr15:48513118ENST00000537345+1023289_3084441024.0TransmembraneHelical
HgeneATP1A1chr1:116933513chr15:48513118ENST00000537345+1023321_3384441024.0TransmembraneHelical
HgeneATP1A1chr1:116933513chr15:48513118ENST00000537345+102388_1084441024.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000380993227202_22201100.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000380993227260_28001100.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000380993227303_32301100.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000380993227328_34801100.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000380993227380_40001100.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000380993227418_43801100.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000380993227485_50501100.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000380993227551_57101100.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000380993227572_59201100.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000380993227610_63001100.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000380993227793_81301100.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000558405126202_22201100.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000558405126260_28001100.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000558405126303_32301100.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000558405126328_34801100.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000558405126380_40001100.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000558405126418_43801100.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000558405126485_50501100.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000558405126551_57101100.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000558405126572_59201100.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000558405126610_63001100.0TransmembraneHelical
TgeneSLC12A1chr1:116933513chr15:48513118ENST00000558405126793_81301100.0TransmembraneHelical

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

Top

Related Drugs to ATP1A1-SLC12A1

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

Top

Related Diseases to ATP1A1-SLC12A1

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