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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:SPIDR-ANK1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SPIDR-ANK1
FusionPDB ID: 85780
FusionGDB2.0 ID: 85780
HgeneTgene
Gene symbol

SPIDR

ANK1

Gene ID

23514

286

Gene namescaffold protein involved in DNA repairankyrin 1
SynonymsKIAA0146ANK|SPH1|SPH2
Cytomap

8q11.21

8p11.21

Type of geneprotein-codingprotein-coding
DescriptionDNA repair-scaffolding proteinscaffolding protein involved in DNA repairankyrin-1ANK-1ankyrin 1, erythrocyticankyrin-Rerythrocyte ankyrin
Modification date2020032020200313
UniProtAcc

Q14159

Main function of 5'-partner protein: FUNCTION: Plays a role in DNA double-strand break (DBS) repair via homologous recombination (HR). Serves as a scaffolding protein that helps to promote the recruitment of DNA-processing enzymes like the helicase BLM and recombinase RAD51 to site of DNA damage, and hence contributes to maintain genomic integrity. {ECO:0000269|PubMed:23509288, ECO:0000269|PubMed:23754376}.

P16157

Main function of 5'-partner protein: FUNCTION: Attaches integral membrane proteins to cytoskeletal elements; binds to the erythrocyte membrane protein band 4.2, to Na-K ATPase, to the lymphocyte membrane protein GP85, and to the cytoskeletal proteins fodrin, tubulin, vimentin and desmin. Erythrocyte ankyrins also link spectrin (beta chain) to the cytoplasmic domain of the erythrocytes anion exchange protein; they retain most or all of these binding functions. {ECO:0000269|PubMed:12456646}.; FUNCTION: [Isoform Mu17]: Together with obscurin in skeletal muscle may provide a molecular link between the sarcoplasmic reticulum and myofibrils. {ECO:0000269|PubMed:12527750}.
Ensembl transtripts involved in fusion geneENST idsENST00000521214, ENST00000297423, 
ENST00000517693, ENST00000518074, 
ENST00000541342, ENST00000518060, 
ENST00000265709, ENST00000289734, 
ENST00000347528, ENST00000352337, 
ENST00000379758, ENST00000396942, 
ENST00000396945, ENST00000314214, 
ENST00000457297, ENST00000521407, 
ENST00000522231, ENST00000522543, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score24 X 12 X 15=432015 X 9 X 9=1215
# samples 2718
** MAII scorelog2(27/4320*10)=-4
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(18/1215*10)=-2.75488750216347
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: SPIDR [Title/Abstract] AND ANK1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: SPIDR [Title/Abstract] AND ANK1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SPIDR(48614577)-ANK1(41615655), # samples:1
Anticipated loss of major functional domain due to fusion event.SPIDR-ANK1 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.
SPIDR-ANK1 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.
SPIDR-ANK1 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.
SPIDR-ANK1 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
HgeneSPIDR

GO:0006974

cellular response to DNA damage stimulus

23509288

HgeneSPIDR

GO:0010569

regulation of double-strand break repair via homologous recombination

23754376

HgeneSPIDR

GO:0031334

positive regulation of protein complex assembly

23509288

HgeneSPIDR

GO:0070202

regulation of establishment of protein localization to chromosome

23509288

HgeneSPIDR

GO:0071479

cellular response to ionizing radiation

23509288|23754376

HgeneSPIDR

GO:0072711

cellular response to hydroxyurea

23509288

HgeneSPIDR

GO:0072757

cellular response to camptothecin

23509288

TgeneANK1

GO:0006888

ER to Golgi vesicle-mediated transport

18768923



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/chr8:48614577/chr8:41615655)
- 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 SPIDR (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 ANK1 (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)
ENST00000297423SPIDRchr848614577+ENST00000347528ANK1chr841615655-1048723615179792642
ENST00000297423SPIDRchr848614577+ENST00000289734ANK1chr841615655-1054723615179762641
ENST00000297423SPIDRchr848614577+ENST00000379758ANK1chr841615655-1034023615178382595
ENST00000297423SPIDRchr848614577+ENST00000396942ANK1chr841615655-1061623615180512666
ENST00000297423SPIDRchr848614577+ENST00000396945ANK1chr841615655-1025623615177542567
ENST00000297423SPIDRchr848614577+ENST00000352337ANK1chr841615655-1047523615179102619
ENST00000297423SPIDRchr848614577+ENST00000265709ANK1chr841615655-833223615179282625
ENST00000518074SPIDRchr848614577+ENST00000347528ANK1chr841615655-10094196817175862471
ENST00000518074SPIDRchr848614577+ENST00000289734ANK1chr841615655-10154196817175832470
ENST00000518074SPIDRchr848614577+ENST00000379758ANK1chr841615655-9947196817174452424
ENST00000518074SPIDRchr848614577+ENST00000396942ANK1chr841615655-10223196817176582495
ENST00000518074SPIDRchr848614577+ENST00000396945ANK1chr841615655-9863196817173612396
ENST00000518074SPIDRchr848614577+ENST00000352337ANK1chr841615655-10082196817175172448
ENST00000518074SPIDRchr848614577+ENST00000265709ANK1chr841615655-7939196817175352454
ENST00000541342SPIDRchr848614577+ENST00000347528ANK1chr841615655-10039191314675312461
ENST00000541342SPIDRchr848614577+ENST00000289734ANK1chr841615655-10099191314675282460
ENST00000541342SPIDRchr848614577+ENST00000379758ANK1chr841615655-9892191314673902414
ENST00000541342SPIDRchr848614577+ENST00000396942ANK1chr841615655-10168191314676032485
ENST00000541342SPIDRchr848614577+ENST00000396945ANK1chr841615655-9808191314673062386
ENST00000541342SPIDRchr848614577+ENST00000352337ANK1chr841615655-10027191314674622438
ENST00000541342SPIDRchr848614577+ENST00000265709ANK1chr841615655-7884191314674802444
ENST00000517693SPIDRchr848614577+ENST00000347528ANK1chr841615655-874261617562342019
ENST00000517693SPIDRchr848614577+ENST00000289734ANK1chr841615655-880261617562312018
ENST00000517693SPIDRchr848614577+ENST00000379758ANK1chr841615655-859561617560931972
ENST00000517693SPIDRchr848614577+ENST00000396942ANK1chr841615655-887161617563062043
ENST00000517693SPIDRchr848614577+ENST00000396945ANK1chr841615655-851161617560091944
ENST00000517693SPIDRchr848614577+ENST00000352337ANK1chr841615655-873061617561651996
ENST00000517693SPIDRchr848614577+ENST00000265709ANK1chr841615655-658761617561832002

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
ENST00000297423ENST00000347528SPIDRchr848614577+ANK1chr841615655-0.0025671610.9974329
ENST00000297423ENST00000289734SPIDRchr848614577+ANK1chr841615655-0.0024904980.9975095
ENST00000297423ENST00000379758SPIDRchr848614577+ANK1chr841615655-0.0018802910.99811965
ENST00000297423ENST00000396942SPIDRchr848614577+ANK1chr841615655-0.0029901240.9970099
ENST00000297423ENST00000396945SPIDRchr848614577+ANK1chr841615655-0.0028241130.99717593
ENST00000297423ENST00000352337SPIDRchr848614577+ANK1chr841615655-0.0029700350.9970299
ENST00000297423ENST00000265709SPIDRchr848614577+ANK1chr841615655-0.0037889730.99621105
ENST00000518074ENST00000347528SPIDRchr848614577+ANK1chr841615655-0.0019931110.9980069
ENST00000518074ENST00000289734SPIDRchr848614577+ANK1chr841615655-0.0019288390.99807113
ENST00000518074ENST00000379758SPIDRchr848614577+ANK1chr841615655-0.0014022490.9985978
ENST00000518074ENST00000396942SPIDRchr848614577+ANK1chr841615655-0.0023229880.997677
ENST00000518074ENST00000396945SPIDRchr848614577+ANK1chr841615655-0.002164430.9978356
ENST00000518074ENST00000352337SPIDRchr848614577+ANK1chr841615655-0.00230310.99769694
ENST00000518074ENST00000265709SPIDRchr848614577+ANK1chr841615655-0.0029330830.9970669
ENST00000541342ENST00000347528SPIDRchr848614577+ANK1chr841615655-0.0019045280.99809545
ENST00000541342ENST00000289734SPIDRchr848614577+ANK1chr841615655-0.0018451470.9981548
ENST00000541342ENST00000379758SPIDRchr848614577+ANK1chr841615655-0.0013374620.9986626
ENST00000541342ENST00000396942SPIDRchr848614577+ANK1chr841615655-0.00222220.99777776
ENST00000541342ENST00000396945SPIDRchr848614577+ANK1chr841615655-0.0020678740.9979321
ENST00000541342ENST00000352337SPIDRchr848614577+ANK1chr841615655-0.002202980.997797
ENST00000541342ENST00000265709SPIDRchr848614577+ANK1chr841615655-0.0027954610.9972045
ENST00000517693ENST00000347528SPIDRchr848614577+ANK1chr841615655-0.0027208590.9972792
ENST00000517693ENST00000289734SPIDRchr848614577+ANK1chr841615655-0.0026168370.9973832
ENST00000517693ENST00000379758SPIDRchr848614577+ANK1chr841615655-0.002058750.9979412
ENST00000517693ENST00000396942SPIDRchr848614577+ANK1chr841615655-0.0031221770.9968778
ENST00000517693ENST00000396945SPIDRchr848614577+ANK1chr841615655-0.0029866160.99701333
ENST00000517693ENST00000352337SPIDRchr848614577+ANK1chr841615655-0.0031063040.99689364
ENST00000517693ENST00000265709SPIDRchr848614577+ANK1chr841615655-0.0047020910.99529797

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 SPIDR-ANK1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
SPIDRchr848614577ANK1chr8416156551913588RCSFYATVIYQKPQADAATSFLRAAR
SPIDRchr848614577ANK1chr8416156551968598RCSFYATVIYQKPQADAATSFLRAAR
SPIDRchr848614577ANK1chr8416156552361769RCSFYATVIYQKPQADAATSFLRAAR
SPIDRchr848614577ANK1chr841615655616146RCSFYATVIYQKPQADAATSFLRAAR

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Potential FusionNeoAntigen Information of SPIDR-ANK1 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.
SPIDR-ANK1_48614577_41615655.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)
SPIDR-ANK1chr848614577chr8416156552361HLA-B08:09VIYQKPQA0.98640.5443715
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:01PQADAATSF0.99480.90541221
SPIDR-ANK1chr848614577chr8416156552361HLA-B39:06YQKPQADAA0.90760.9277918
SPIDR-ANK1chr848614577chr8416156552361HLA-B50:01YQKPQADAA0.71620.8395918
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:03PQADAATSF0.69480.91441221
SPIDR-ANK1chr848614577chr8416156552361HLA-B08:09YQKPQADAA0.55330.7796918
SPIDR-ANK1chr848614577chr8416156552361HLA-B13:01PQADAATSF0.04850.9761221
SPIDR-ANK1chr848614577chr8416156552361HLA-B35:01KPQADAATSF0.94740.72451121
SPIDR-ANK1chr848614577chr8416156552361HLA-B35:08KPQADAATSF0.94720.62631121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:01KPQADAATSF0.94040.69841121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:03KPQADAATSF0.93760.69161121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:25KPQADAATSF0.90520.80051121
SPIDR-ANK1chr848614577chr8416156552361HLA-B35:05KPQADAATSF0.90160.54011121
SPIDR-ANK1chr848614577chr8416156552361HLA-B81:01KPQADAATSF0.49850.52511121
SPIDR-ANK1chr848614577chr8416156552361HLA-B13:01KPQADAATSF0.24890.87091121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:01QKPQADAATSF0.99890.73351021
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:03QKPQADAATSF0.99750.79771021
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:25QKPQADAATSF0.99570.82891021
SPIDR-ANK1chr848614577chr8416156552361HLA-B13:01QKPQADAATSF0.85350.94791021
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:04YQKPQADAA0.94060.9047918
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:05PQADAATSF0.65920.89931221
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:05KPQADAATSF0.91980.73111121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:07KPQADAATSF0.88320.56231121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:04KPQADAATSF0.86580.78661121
SPIDR-ANK1chr848614577chr8416156552361HLA-B42:02KPQADAATSF0.70430.57791121
SPIDR-ANK1chr848614577chr8416156552361HLA-B42:01KPQADAATSF0.62160.56931121
SPIDR-ANK1chr848614577chr8416156552361HLA-C05:09KPQADAATSFL0.99850.9521122
SPIDR-ANK1chr848614577chr8416156552361HLA-B07:12KPQADAATSFL0.99150.55431122
SPIDR-ANK1chr848614577chr8416156552361HLA-C08:15KPQADAATSFL0.98420.97531122
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:05QKPQADAATSF0.98220.79881021
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:34PQADAATSF0.99480.90541221
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:125PQADAATSF0.99480.90541221
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:33PQADAATSF0.99480.90541221
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:27PQADAATSF0.99470.89441221
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:24PQADAATSF0.98820.96261221
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:50PQADAATSF0.97920.89991221
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:53PQADAATSF0.95070.89971221
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:12PQADAATSF0.90220.84311221
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:73YQKPQADAA0.87390.9816918
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:54PQADAATSF0.82330.89671221
SPIDR-ANK1chr848614577chr8416156552361HLA-B50:05YQKPQADAA0.71620.8395918
SPIDR-ANK1chr848614577chr8416156552361HLA-B50:04YQKPQADAA0.71620.8395918
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:20PQADAATSF0.6640.91161221
SPIDR-ANK1chr848614577chr8416156552361HLA-B35:28PQADAATSF0.6230.91631221
SPIDR-ANK1chr848614577chr8416156552361HLA-B48:02PQADAATSF0.48350.90791221
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:68KPQADAATSF0.97860.50891121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:54KPQADAATSF0.97680.6521121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:24KPQADAATSF0.96490.84281121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:08KPQADAATSF0.94970.6361121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:53KPQADAATSF0.94850.66351121
SPIDR-ANK1chr848614577chr8416156552361HLA-B35:77KPQADAATSF0.94740.72451121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:11KPQADAATSF0.94380.66621121
SPIDR-ANK1chr848614577chr8416156552361HLA-B35:43KPQADAATSF0.9430.64421121
SPIDR-ANK1chr848614577chr8416156552361HLA-B35:11KPQADAATSF0.94170.7641121
SPIDR-ANK1chr848614577chr8416156552361HLA-B35:23KPQADAATSF0.94110.73851121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:33KPQADAATSF0.94040.69841121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:125KPQADAATSF0.94040.69841121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:34KPQADAATSF0.94040.69841121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:135KPQADAATSF0.93870.73271121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:27KPQADAATSF0.93710.69751121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:12KPQADAATSF0.9320.71671121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:20KPQADAATSF0.92530.76921121
SPIDR-ANK1chr848614577chr8416156552361HLA-B48:02KPQADAATSF0.92410.76561121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:50KPQADAATSF0.92110.7481121
SPIDR-ANK1chr848614577chr8416156552361HLA-B35:30KPQADAATSF0.91380.63841121
SPIDR-ANK1chr848614577chr8416156552361HLA-B35:17KPQADAATSF0.91380.63841121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:39KPQADAATSF0.90010.74351121
SPIDR-ANK1chr848614577chr8416156552361HLA-B35:28KPQADAATSF0.90010.77911121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:35KPQADAATSF0.87720.70121121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:73KPQADAATSF0.87540.74071121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:30KPQADAATSF0.81930.72961121
SPIDR-ANK1chr848614577chr8416156552361HLA-B67:01KPQADAATSF0.63190.7681121
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:54QKPQADAATSF0.99940.71031021
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:135QKPQADAATSF0.9990.73721021
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:33QKPQADAATSF0.99890.73351021
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:125QKPQADAATSF0.99890.73351021
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:34QKPQADAATSF0.99890.73351021
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:27QKPQADAATSF0.99890.73851021
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:53QKPQADAATSF0.99890.72011021
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:50QKPQADAATSF0.99870.77571021
SPIDR-ANK1chr848614577chr8416156552361HLA-C05:01KPQADAATSFL0.99850.9521122
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:24QKPQADAATSF0.99830.85721021
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:12QKPQADAATSF0.99690.78071021
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:73QKPQADAATSF0.99670.86721021
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:30QKPQADAATSF0.99610.84121021
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:39QKPQADAATSF0.99560.81091021
SPIDR-ANK1chr848614577chr8416156552361HLA-C08:02KPQADAATSFL0.98420.97531122
SPIDR-ANK1chr848614577chr8416156552361HLA-B15:20QKPQADAATSF0.9810.80391021
SPIDR-ANK1chr848614577chr8416156552361HLA-B35:28QKPQADAATSF0.98020.80651021
SPIDR-ANK1chr848614577chr8416156552361HLA-B48:02QKPQADAATSF0.97910.8011021

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Potential FusionNeoAntigen Information of SPIDR-ANK1 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.
SPIDR-ANK1_48614577_41615655.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)
SPIDR-ANK1chr848614577chr8416156552361DRB1-0804ATVIYQKPQADAATS520
SPIDR-ANK1chr848614577chr8416156552361DRB1-1415ATVIYQKPQADAATS520

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Fusion breakpoint peptide structures of SPIDR-ANK1

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
9725TVIYQKPQADAATSSPIDRANK1chr848614577chr8416156552361

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of SPIDR-ANK1

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-B14:023BVN9725TVIYQKPQADAATS-7.9962-8.1096
HLA-B14:023BVN9725TVIYQKPQADAATS-5.70842-6.74372
HLA-B52:013W399725TVIYQKPQADAATS-6.83737-6.95077
HLA-B52:013W399725TVIYQKPQADAATS-4.4836-5.5189
HLA-A11:014UQ29725TVIYQKPQADAATS-10.0067-10.1201
HLA-A11:014UQ29725TVIYQKPQADAATS-9.03915-10.0745
HLA-A24:025HGA9725TVIYQKPQADAATS-6.56204-6.67544
HLA-A24:025HGA9725TVIYQKPQADAATS-5.42271-6.45801
HLA-B44:053DX89725TVIYQKPQADAATS-7.85648-8.89178
HLA-B44:053DX89725TVIYQKPQADAATS-5.3978-5.5112
HLA-A02:016TDR9725TVIYQKPQADAATS-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of SPIDR-ANK1

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
SPIDR-ANK1chr848614577chr8416156551021QKPQADAATSFAAACCACAGGCCGATGCTGCTACCAGCTTTCTG
SPIDR-ANK1chr848614577chr8416156551121KPQADAATSFCCACAGGCCGATGCTGCTACCAGCTTTCTG
SPIDR-ANK1chr848614577chr8416156551122KPQADAATSFLCCACAGGCCGATGCTGCTACCAGCTTTCTGAGA
SPIDR-ANK1chr848614577chr8416156551221PQADAATSFCAGGCCGATGCTGCTACCAGCTTTCTG
SPIDR-ANK1chr848614577chr841615655715VIYQKPQAATTTACCAAAAACCACAGGCCGAT
SPIDR-ANK1chr848614577chr841615655918YQKPQADAACAAAAACCACAGGCCGATGCTGCTACC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
SPIDR-ANK1chr848614577chr841615655520ATVIYQKPQADAATSACGGTGATTTACCAAAAACCACAGGCCGATGCTGCTACCAGCTTT

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Information of the samples that have these potential fusion neoantigens of SPIDR-ANK1

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
COADSPIDR-ANK1chr848614577ENST00000297423chr841615655ENST00000265709TCGA-CM-6172-01A

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Potential target of CAR-T therapy development for SPIDR-ANK1

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

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 SPIDR-ANK1

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 SPIDR-ANK1

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