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:AXIN1-MYO19

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: AXIN1-MYO19
FusionPDB ID: 8563
FusionGDB2.0 ID: 8563
HgeneTgene
Gene symbol

AXIN1

MYO19

Gene ID

8312

80179

Gene nameaxin 1myosin XIX
SynonymsAXIN|PPP1R49MYOHD1
Cytomap

16p13.3

17q12

Type of geneprotein-codingprotein-coding
Descriptionaxin-1axis inhibition protein 1axis inhibitor 1fused, mouse, homolog ofprotein phosphatase 1, regulatory subunit 49unconventional myosin-XIXmyosin head domain containing 1myosin head domain-containing protein 1
Modification date2020032220200313
UniProtAcc

O15169

Main function of 5'-partner protein: FUNCTION: Component of the beta-catenin destruction complex required for regulating CTNNB1 levels through phosphorylation and ubiquitination, and modulating Wnt-signaling (PubMed:12192039, PubMed:27098453). Controls dorsoventral patterning via two opposing effects; down-regulates CTNNB1 to inhibit the Wnt signaling pathway and ventralize embryos, but also dorsalizes embryos by activating a Wnt-independent JNK signaling pathway (PubMed:12192039). In Wnt signaling, probably facilitates the phosphorylation of CTNNB1 and APC by GSK3B (PubMed:12192039). Likely to function as a tumor suppressor. Enhances TGF-beta signaling by recruiting the RNF111 E3 ubiquitin ligase and promoting the degradation of inhibitory SMAD7 (PubMed:16601693). Also component of the AXIN1-HIPK2-TP53 complex which controls cell growth, apoptosis and development (PubMed:17210684). Facilitates the phosphorylation of TP53 by HIPK2 upon ultraviolet irradiation (PubMed:17210684). {ECO:0000269|PubMed:12192039, ECO:0000269|PubMed:16601693, ECO:0000269|PubMed:17210684, ECO:0000269|PubMed:27098453}.

Q96H55

Main function of 5'-partner protein: FUNCTION: Actin-based motor molecule with ATPase activity that localizes to the mitochondrion outer membrane (PubMed:19932026, PubMed:23568824, PubMed:25447992). Motor protein that moves towards the plus-end of actin filaments (By similarity). Required for mitochondrial inheritance during mitosis (PubMed:25447992). May be involved in mitochondrial transport or positioning (PubMed:23568824). {ECO:0000250|UniProtKB:Q5SV80, ECO:0000269|PubMed:19932026, ECO:0000269|PubMed:25447992, ECO:0000305|PubMed:23568824}.
Ensembl transtripts involved in fusion geneENST idsENST00000262320, ENST00000354866, 
ENST00000481769, 
ENST00000544606, 
ENST00000586007, ENST00000590081, 
ENST00000268852, ENST00000431794, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score16 X 10 X 9=14408 X 9 X 5=360
# samples 2310
** MAII scorelog2(23/1440*10)=-2.6463630453853
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(10/360*10)=-1.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: AXIN1 [Title/Abstract] AND MYO19 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: AXIN1 [Title/Abstract] AND MYO19 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)AXIN1(354304)-MYO19(34867294), # samples:1
Anticipated loss of major functional domain due to fusion event.AXIN1-MYO19 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.
AXIN1-MYO19 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.
AXIN1-MYO19 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.
AXIN1-MYO19 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
HgeneAXIN1

GO:0001934

positive regulation of protein phosphorylation

9601641

HgeneAXIN1

GO:0032147

activation of protein kinase activity

9601641

HgeneAXIN1

GO:0034622

cellular protein-containing complex assembly

16601693

HgeneAXIN1

GO:0045732

positive regulation of protein catabolic process

9601641

HgeneAXIN1

GO:0090090

negative regulation of canonical Wnt signaling pathway

10644691

TgeneMYO19

GO:0034642

mitochondrion migration along actin filament

19932026



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/chr16:354304/chr17:34867294)
- 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 AXIN1 (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 MYO19 (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)
ENST00000262320AXIN1chr16354304-ENST00000431794MYO19chr1734867294-426316262136441207
ENST00000262320AXIN1chr16354304-ENST00000268852MYO19chr1734867294-354116262130441007
ENST00000354866AXIN1chr16354304-ENST00000431794MYO19chr1734867294-405314161534341139
ENST00000354866AXIN1chr16354304-ENST00000268852MYO19chr1734867294-33311416152834939

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
ENST00000262320ENST00000431794AXIN1chr16354304-MYO19chr1734867294-0.0061666860.9938333
ENST00000262320ENST00000268852AXIN1chr16354304-MYO19chr1734867294-0.0075602930.99243975
ENST00000354866ENST00000431794AXIN1chr16354304-MYO19chr1734867294-0.0045536490.99544626
ENST00000354866ENST00000268852AXIN1chr16354304-MYO19chr1734867294-0.0068186790.9931813

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 AXIN1-MYO19

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
AXIN1chr16354304MYO19chr17348672941416467EEKLEERLKRVRMVLAGLLHLGNIQF
AXIN1chr16354304MYO19chr17348672941626535EEKLEERLKRVRMVLAGLLHLGNIQF

Top

Potential FusionNeoAntigen Information of AXIN1-MYO19 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.
AXIN1-MYO19_354304_34867294.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)
AXIN1-MYO19chr16354304chr17348672941626HLA-B27:04VRMVLAGLL0.99950.67681019
AXIN1-MYO19chr16354304chr17348672941626HLA-B27:05VRMVLAGLL0.99880.71111019
AXIN1-MYO19chr16354304chr17348672941626HLA-B07:02RVRMVLAGL0.99360.5606918
AXIN1-MYO19chr16354304chr17348672941626HLA-A30:08RVRMVLAGL0.99030.8826918
AXIN1-MYO19chr16354304chr17348672941626HLA-B14:02ERLKRVRMV0.98850.8409514
AXIN1-MYO19chr16354304chr17348672941626HLA-B14:01ERLKRVRMV0.98850.8409514
AXIN1-MYO19chr16354304chr17348672941626HLA-A02:21MVLAGLLHL0.98330.58431221
AXIN1-MYO19chr16354304chr17348672941626HLA-A02:17MVLAGLLHL0.97920.68811221
AXIN1-MYO19chr16354304chr17348672941626HLA-A02:11MVLAGLLHL0.97890.50081221
AXIN1-MYO19chr16354304chr17348672941626HLA-A02:04MVLAGLLHL0.97850.7811221
AXIN1-MYO19chr16354304chr17348672941626HLA-A02:60MVLAGLLHL0.97770.5081221
AXIN1-MYO19chr16354304chr17348672941626HLA-A30:08RLKRVRMVL0.93840.7026615
AXIN1-MYO19chr16354304chr17348672941626HLA-B08:09ERLKRVRMV0.91740.7453514
AXIN1-MYO19chr16354304chr17348672941626HLA-B27:05KRVRMVLAGL0.99990.5682818
AXIN1-MYO19chr16354304chr17348672941626HLA-B27:04KRVRMVLAGL0.99980.5969818
AXIN1-MYO19chr16354304chr17348672941626HLA-B14:02ERLKRVRMVL0.96750.7781515
AXIN1-MYO19chr16354304chr17348672941626HLA-B14:01ERLKRVRMVL0.96750.7781515
AXIN1-MYO19chr16354304chr17348672941626HLA-B27:07VRMVLAGLLHL10.56261021
AXIN1-MYO19chr16354304chr17348672941626HLA-C03:07MVLAGLLHL0.99780.9861221
AXIN1-MYO19chr16354304chr17348672941626HLA-A02:05MVLAGLLHL0.98430.52521221
AXIN1-MYO19chr16354304chr17348672941626HLA-B07:04RVRMVLAGL0.97940.543918
AXIN1-MYO19chr16354304chr17348672941626HLA-A02:07MVLAGLLHL0.97840.5041221
AXIN1-MYO19chr16354304chr17348672941626HLA-B15:04RLKRVRMVL0.75790.8782615
AXIN1-MYO19chr16354304chr17348672941626HLA-B15:07RLKRVRMVL0.6940.741615
AXIN1-MYO19chr16354304chr17348672941626HLA-B27:03KRVRMVLAGL0.99660.6172818
AXIN1-MYO19chr16354304chr17348672941626HLA-B39:12ERLKRVRMVL0.94820.9052515
AXIN1-MYO19chr16354304chr17348672941626HLA-B27:06VRMVLAGLL0.99960.67311019
AXIN1-MYO19chr16354304chr17348672941626HLA-B27:10VRMVLAGLL0.99940.84121019
AXIN1-MYO19chr16354304chr17348672941626HLA-B27:08VRMVLAGLL0.9990.53951019
AXIN1-MYO19chr16354304chr17348672941626HLA-B27:09VRMVLAGLL0.99830.68771019
AXIN1-MYO19chr16354304chr17348672941626HLA-B07:22RVRMVLAGL0.99360.5606918
AXIN1-MYO19chr16354304chr17348672941626HLA-A30:01RVRMVLAGL0.99110.9315918
AXIN1-MYO19chr16354304chr17348672941626HLA-A02:14MVLAGLLHL0.98390.58121221
AXIN1-MYO19chr16354304chr17348672941626HLA-A02:06MVLAGLLHL0.98330.58431221
AXIN1-MYO19chr16354304chr17348672941626HLA-A69:01MVLAGLLHL0.96340.6421221
AXIN1-MYO19chr16354304chr17348672941626HLA-A30:01RLKRVRMVL0.9480.8316615
AXIN1-MYO19chr16354304chr17348672941626HLA-A32:01RLKRVRMVL0.82430.9197615
AXIN1-MYO19chr16354304chr17348672941626HLA-C06:08ERLKRVRMV0.7060.984514
AXIN1-MYO19chr16354304chr17348672941626HLA-C17:01MVLAGLLHL0.5990.98141221
AXIN1-MYO19chr16354304chr17348672941626HLA-B15:73RLKRVRMVL0.57270.8734615
AXIN1-MYO19chr16354304chr17348672941626HLA-B15:30RLKRVRMVL0.43140.8401615
AXIN1-MYO19chr16354304chr17348672941626HLA-C06:17ERLKRVRMV0.13040.9916514
AXIN1-MYO19chr16354304chr17348672941626HLA-C06:02ERLKRVRMV0.13040.9916514
AXIN1-MYO19chr16354304chr17348672941626HLA-C06:17VRMVLAGLL0.05820.99171019
AXIN1-MYO19chr16354304chr17348672941626HLA-C06:02VRMVLAGLL0.05820.99171019
AXIN1-MYO19chr16354304chr17348672941626HLA-B27:10KRVRMVLAGL0.99980.7675818
AXIN1-MYO19chr16354304chr17348672941626HLA-B27:06KRVRMVLAGL0.99970.6254818
AXIN1-MYO19chr16354304chr17348672941626HLA-B27:09KRVRMVLAGL0.99960.5248818
AXIN1-MYO19chr16354304chr17348672941626HLA-B27:09VRMVLAGLLHL10.63251021
AXIN1-MYO19chr16354304chr17348672941626HLA-B27:08VRMVLAGLLHL10.52541021
AXIN1-MYO19chr16354304chr17348672941626HLA-B27:06VRMVLAGLLHL10.70341021

Top

Potential FusionNeoAntigen Information of AXIN1-MYO19 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 AXIN1-MYO19

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
8013RLKRVRMVLAGLLHAXIN1MYO19chr16354304chr17348672941626

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of AXIN1-MYO19

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-B14:023BVN8013RLKRVRMVLAGLLH-7.15543-7.26883
HLA-B14:023BVN8013RLKRVRMVLAGLLH-4.77435-5.80965
HLA-B52:013W398013RLKRVRMVLAGLLH-6.80875-6.92215
HLA-B52:013W398013RLKRVRMVLAGLLH-4.20386-5.23916
HLA-A11:014UQ28013RLKRVRMVLAGLLH-7.5194-8.5547
HLA-A11:014UQ28013RLKRVRMVLAGLLH-6.9601-7.0735
HLA-A24:025HGA8013RLKRVRMVLAGLLH-7.52403-7.63743
HLA-A24:025HGA8013RLKRVRMVLAGLLH-5.82433-6.85963
HLA-B27:056PYJ8013RLKRVRMVLAGLLH-3.28285-4.31815
HLA-B44:053DX88013RLKRVRMVLAGLLH-5.91172-6.94702
HLA-B44:053DX88013RLKRVRMVLAGLLH-4.24346-4.35686

Top

Vaccine Design for the FusionNeoAntigens of AXIN1-MYO19

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
AXIN1-MYO19chr16354304chr17348672941019VRMVLAGLLGTGCGCATGGTCCTAGCTGGACTGCTG
AXIN1-MYO19chr16354304chr17348672941021VRMVLAGLLHLGTGCGCATGGTCCTAGCTGGACTGCTGCACCTT
AXIN1-MYO19chr16354304chr17348672941221MVLAGLLHLATGGTCCTAGCTGGACTGCTGCACCTT
AXIN1-MYO19chr16354304chr1734867294514ERLKRVRMVGAGCGGCTGAAGCGCGTGCGCATGGTC
AXIN1-MYO19chr16354304chr1734867294515ERLKRVRMVLGAGCGGCTGAAGCGCGTGCGCATGGTCCTA
AXIN1-MYO19chr16354304chr1734867294615RLKRVRMVLCGGCTGAAGCGCGTGCGCATGGTCCTA
AXIN1-MYO19chr16354304chr1734867294818KRVRMVLAGLAAGCGCGTGCGCATGGTCCTAGCTGGACTG
AXIN1-MYO19chr16354304chr1734867294918RVRMVLAGLCGCGTGCGCATGGTCCTAGCTGGACTG

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 AXIN1-MYO19

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
STADAXIN1-MYO19chr16354304ENST00000262320chr1734867294ENST00000268852TCGA-BR-8296-01A

Top

Potential target of CAR-T therapy development for AXIN1-MYO19

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

Top

Related Drugs to AXIN1-MYO19

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

Top

Related Diseases to AXIN1-MYO19

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