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:MEIS2-GALK2

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: MEIS2-GALK2
FusionPDB ID: 52897
FusionGDB2.0 ID: 52897
HgeneTgene
Gene symbol

MEIS2

GALK2

Gene ID

4212

2585

Gene nameMeis homeobox 2galactokinase 2
SynonymsCPCMR|HsT18361|MRG1GK2
Cytomap

15q14

15q21.1-q21.2

Type of geneprotein-codingprotein-coding
Descriptionhomeobox protein Meis2Meis homolog 2Meis1, myeloid ecotropic viral integration site 1 homolog 2Meis1-related gene 1TALE homeobox protein Meis2meis1-related protein 1N-acetylgalactosamine kinasegalNAc kinase
Modification date2020031320200313
UniProtAcc

O14770

Main function of 5'-partner protein: FUNCTION: Involved in transcriptional regulation. Binds to HOX or PBX proteins to form dimers, or to a DNA-bound dimer of PBX and HOX proteins and thought to have a role in stabilization of the homeoprotein-DNA complex. Isoform 3 is required for the activity of a PDX1:PBX1b:MEIS2b complex in pancreatic acinar cells involved in the transcriptional activation of the ELA1 enhancer; the complex binds to the enhancer B element and cooperates with the transcription factor 1 complex (PTF1) bound to the enhancer A element; MEIS2 is not involved in complex DNA-binding. Probably in complex with PBX1, is involved in transcriptional regulation by KLF4. Isoform 3 and isoform 4 can bind to a EPHA8 promoter sequence containing the DNA motif 5'-CGGTCA-3'; in cooperation with a PBX protein (such as PBX2) is proposed to be involved in the transcriptional activation of EPHA8 in the developing midbrain. May be involved in regulation of myeloid differentiation. Can bind to the DNA sequence 5'-TGACAG-3'in the activator ACT sequence of the D(1A) dopamine receptor (DRD1) promoter and activate DRD1 transcription; isoform 5 cannot activate DRD1 transcription. {ECO:0000269|PubMed:10764806, ECO:0000269|PubMed:11279116, ECO:0000269|PubMed:21746878}.

Q01415

Main function of 5'-partner protein: FUNCTION: Acts on GalNAc. Also acts as a galactokinase when galactose is present at high concentrations. May be involved in a salvage pathway for the reutilization of free GalNAc derived from the degradation of complex carbohydrates. {ECO:0000269|PubMed:16006554}.
Ensembl transtripts involved in fusion geneENST idsENST00000219869, ENST00000338564, 
ENST00000340545, ENST00000382766, 
ENST00000397620, ENST00000397624, 
ENST00000424352, ENST00000444725, 
ENST00000557796, ENST00000559085, 
ENST00000559561, ENST00000561208, 
ENST00000559408, 
ENST00000543495, 
ENST00000544523, ENST00000559454, 
ENST00000561014, ENST00000327171, 
ENST00000396509, ENST00000560031, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score25 X 16 X 6=24009 X 8 X 5=360
# samples 2710
** MAII scorelog2(27/2400*10)=-3.15200309344505
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: MEIS2 [Title/Abstract] AND GALK2 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: MEIS2 [Title/Abstract] AND GALK2 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MEIS2(37375972)-GALK2(49611801), # samples:1
Anticipated loss of major functional domain due to fusion event.MEIS2-GALK2 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.
MEIS2-GALK2 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.
MEIS2-GALK2 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.
MEIS2-GALK2 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.
MEIS2-GALK2 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
MEIS2-GALK2 seems lost the major protein functional domain in Hgene partner, which is a transcription factor due to the frame-shifted ORF.
MEIS2-GALK2 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene 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
HgeneMEIS2

GO:0045931

positive regulation of mitotic cell cycle

26512644

HgeneMEIS2

GO:0045944

positive regulation of transcription by RNA polymerase II

10764806

HgeneMEIS2

GO:0110024

positive regulation of cardiac muscle myoblast proliferation

26512644



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/chr15:37375972/chr15:49611801)
- 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 MEIS2 (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 GALK2 (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)
ENST00000561208MEIS2chr1537375972-ENST00000327171GALK2chr1549611801+322911734041582392
ENST00000561208MEIS2chr1537375972-ENST00000560031GALK2chr1549611801+194211734041582392
ENST00000561208MEIS2chr1537375972-ENST00000396509GALK2chr1549611801+193811734041582392
ENST00000382766MEIS2chr1537375972-ENST00000327171GALK2chr1549611801+3847179110222200392
ENST00000382766MEIS2chr1537375972-ENST00000560031GALK2chr1549611801+2560179110222200392
ENST00000382766MEIS2chr1537375972-ENST00000396509GALK2chr1549611801+2556179110222200392
ENST00000557796MEIS2chr1537375972-ENST00000327171GALK2chr1549611801+320411483971557386
ENST00000557796MEIS2chr1537375972-ENST00000560031GALK2chr1549611801+191711483971557386
ENST00000557796MEIS2chr1537375972-ENST00000396509GALK2chr1549611801+191311483971557386
ENST00000397620MEIS2chr1537375972-ENST00000327171GALK2chr1549611801+327112157251624299
ENST00000397620MEIS2chr1537375972-ENST00000560031GALK2chr1549611801+198412157251624299
ENST00000397620MEIS2chr1537375972-ENST00000396509GALK2chr1549611801+198012157251624299
ENST00000559561MEIS2chr1537375972-ENST00000327171GALK2chr1549611801+306510092401418392
ENST00000559561MEIS2chr1537375972-ENST00000560031GALK2chr1549611801+177810092401418392
ENST00000559561MEIS2chr1537375972-ENST00000396509GALK2chr1549611801+177410092401418392

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
ENST00000561208ENST00000327171MEIS2chr1537375972-GALK2chr1549611801+0.0019340070.998066
ENST00000561208ENST00000560031MEIS2chr1537375972-GALK2chr1549611801+0.0052611220.9947389
ENST00000561208ENST00000396509MEIS2chr1537375972-GALK2chr1549611801+0.005335780.9946642
ENST00000382766ENST00000327171MEIS2chr1537375972-GALK2chr1549611801+0.0021330780.9978669
ENST00000382766ENST00000560031MEIS2chr1537375972-GALK2chr1549611801+0.0064795090.99352044
ENST00000382766ENST00000396509MEIS2chr1537375972-GALK2chr1549611801+0.0065598480.9934402
ENST00000557796ENST00000327171MEIS2chr1537375972-GALK2chr1549611801+0.0012308990.9987691
ENST00000557796ENST00000560031MEIS2chr1537375972-GALK2chr1549611801+0.0071951710.9928048
ENST00000557796ENST00000396509MEIS2chr1537375972-GALK2chr1549611801+0.0073271780.99267274
ENST00000397620ENST00000327171MEIS2chr1537375972-GALK2chr1549611801+0.0004424240.99955755
ENST00000397620ENST00000560031MEIS2chr1537375972-GALK2chr1549611801+0.0035319350.99646807
ENST00000397620ENST00000396509MEIS2chr1537375972-GALK2chr1549611801+0.0036071940.9963928
ENST00000559561ENST00000327171MEIS2chr1537375972-GALK2chr1549611801+0.0019333190.9980667
ENST00000559561ENST00000560031MEIS2chr1537375972-GALK2chr1549611801+0.0067871870.9932128
ENST00000559561ENST00000396509MEIS2chr1537375972-GALK2chr1549611801+0.0068900430.99310994

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 MEIS2-GALK2

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
MEIS2chr1537375972GALK2chr15496118011009256GHASQSGDNSSEQVLIFKLYQRAKHV
MEIS2chr1537375972GALK2chr15496118011148250GHASQSGDNSSEQVLIFKLYQRAKHV
MEIS2chr1537375972GALK2chr15496118011173256GHASQSGDNSSEQVLIFKLYQRAKHV
MEIS2chr1537375972GALK2chr15496118011215163GHASQSGDNSSEQVLIFKLYQRAKHV
MEIS2chr1537375972GALK2chr15496118011791256GHASQSGDNSSEQVLIFKLYQRAKHV

Top

Potential FusionNeoAntigen Information of MEIS2-GALK2 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.
MEIS2-GALK2_37375972_49611801.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)
MEIS2-GALK2chr1537375972chr15496118011791HLA-B44:03SEQVLIFKL0.9990.7681019
MEIS2-GALK2chr1537375972chr15496118011791HLA-B13:01SEQVLIFKL0.99760.63381019
MEIS2-GALK2chr1537375972chr15496118011791HLA-B15:17NSSEQVLIF0.99080.6828817
MEIS2-GALK2chr1537375972chr15496118011791HLA-B45:01SEQVLIFKL0.97980.5791019
MEIS2-GALK2chr1537375972chr15496118011791HLA-B18:01SEQVLIFKL0.97430.6161019
MEIS2-GALK2chr1537375972chr15496118011791HLA-B35:01NSSEQVLIF0.96890.7319817
MEIS2-GALK2chr1537375972chr15496118011791HLA-B44:03EQVLIFKLY0.96130.75081120
MEIS2-GALK2chr1537375972chr15496118011791HLA-B15:02EQVLIFKLY0.95870.69351120
MEIS2-GALK2chr1537375972chr15496118011791HLA-B57:03NSSEQVLIF0.86370.7762817
MEIS2-GALK2chr1537375972chr15496118011791HLA-B41:01SEQVLIFKL0.53270.68031019
MEIS2-GALK2chr1537375972chr15496118011791HLA-B39:13SEQVLIFKL0.44150.65751019
MEIS2-GALK2chr1537375972chr15496118011791HLA-B44:03SEQVLIFKLY0.99980.74271020
MEIS2-GALK2chr1537375972chr15496118011791HLA-B18:01SEQVLIFKLY0.98440.55061020
MEIS2-GALK2chr1537375972chr15496118011791HLA-C05:09SGDNSSEQV0.99980.9564514
MEIS2-GALK2chr1537375972chr15496118011791HLA-C08:15SGDNSSEQV0.99930.9793514
MEIS2-GALK2chr1537375972chr15496118011791HLA-B15:21NSSEQVLIF0.98920.758817
MEIS2-GALK2chr1537375972chr15496118011791HLA-C15:04NSSEQVLIF0.98780.8366817
MEIS2-GALK2chr1537375972chr15496118011791HLA-B15:21EQVLIFKLY0.95250.58931120
MEIS2-GALK2chr1537375972chr15496118011791HLA-C03:14NSSEQVLIF0.90450.9583817
MEIS2-GALK2chr1537375972chr15496118011791HLA-C12:12NSSEQVLIF0.73440.8045817
MEIS2-GALK2chr1537375972chr15496118011791HLA-B39:08SEQVLIFKL0.58610.61051019
MEIS2-GALK2chr1537375972chr15496118011791HLA-C12:04NSSEQVLIF0.5420.9847817
MEIS2-GALK2chr1537375972chr15496118011791HLA-C06:03NSSEQVLIF0.53750.9827817
MEIS2-GALK2chr1537375972chr15496118011791HLA-B39:08GDNSSEQVL0.40340.8917615
MEIS2-GALK2chr1537375972chr15496118011791HLA-C08:15SGDNSSEQVL0.99980.9746515
MEIS2-GALK2chr1537375972chr15496118011791HLA-C04:03SGDNSSEQV0.99980.9334514
MEIS2-GALK2chr1537375972chr15496118011791HLA-C05:01SGDNSSEQV0.99980.9564514
MEIS2-GALK2chr1537375972chr15496118011791HLA-C08:02SGDNSSEQV0.99930.9793514
MEIS2-GALK2chr1537375972chr15496118011791HLA-B44:13SEQVLIFKL0.9990.7681019
MEIS2-GALK2chr1537375972chr15496118011791HLA-B44:07SEQVLIFKL0.9990.7681019
MEIS2-GALK2chr1537375972chr15496118011791HLA-B44:26SEQVLIFKL0.9990.7681019
MEIS2-GALK2chr1537375972chr15496118011791HLA-C03:02NSSEQVLIF0.99840.907817
MEIS2-GALK2chr1537375972chr15496118011791HLA-C15:09NSSEQVLIF0.98780.8366817
MEIS2-GALK2chr1537375972chr15496118011791HLA-B15:27EQVLIFKLY0.98620.51171120
MEIS2-GALK2chr1537375972chr15496118011791HLA-B35:11NSSEQVLIF0.98310.7579817
MEIS2-GALK2chr1537375972chr15496118011791HLA-B15:50EQVLIFKLY0.98060.58611120
MEIS2-GALK2chr1537375972chr15496118011791HLA-B57:02NSSEQVLIF0.97870.6087817
MEIS2-GALK2chr1537375972chr15496118011791HLA-B18:08SEQVLIFKL0.97860.50451019
MEIS2-GALK2chr1537375972chr15496118011791HLA-B18:05SEQVLIFKL0.97430.6161019
MEIS2-GALK2chr1537375972chr15496118011791HLA-B18:06SEQVLIFKL0.97250.61381019
MEIS2-GALK2chr1537375972chr15496118011791HLA-B18:04EQVLIFKLY0.97040.50391120
MEIS2-GALK2chr1537375972chr15496118011791HLA-B35:23NSSEQVLIF0.970.7253817
MEIS2-GALK2chr1537375972chr15496118011791HLA-B35:77NSSEQVLIF0.96890.7319817
MEIS2-GALK2chr1537375972chr15496118011791HLA-B44:26EQVLIFKLY0.96130.75081120
MEIS2-GALK2chr1537375972chr15496118011791HLA-B44:13EQVLIFKLY0.96130.75081120
MEIS2-GALK2chr1537375972chr15496118011791HLA-B44:07EQVLIFKLY0.96130.75081120
MEIS2-GALK2chr1537375972chr15496118011791HLA-B15:20EQVLIFKLY0.95070.54531120
MEIS2-GALK2chr1537375972chr15496118011791HLA-B35:20EQVLIFKLY0.94080.58281120
MEIS2-GALK2chr1537375972chr15496118011791HLA-B15:24EQVLIFKLY0.93750.53381120
MEIS2-GALK2chr1537375972chr15496118011791HLA-B35:28EQVLIFKLY0.92790.55681120
MEIS2-GALK2chr1537375972chr15496118011791HLA-B18:03SEQVLIFKL0.92370.60711019
MEIS2-GALK2chr1537375972chr15496118011791HLA-B18:11SEQVLIFKL0.90290.51811019
MEIS2-GALK2chr1537375972chr15496118011791HLA-B35:43NSSEQVLIF0.88660.6076817
MEIS2-GALK2chr1537375972chr15496118011791HLA-C16:04NSSEQVLIF0.87480.9491817
MEIS2-GALK2chr1537375972chr15496118011791HLA-B35:24NSSEQVLIF0.85210.7467817
MEIS2-GALK2chr1537375972chr15496118011791HLA-C12:02NSSEQVLIF0.83540.9267817
MEIS2-GALK2chr1537375972chr15496118011791HLA-C12:03NSSEQVLIF0.76670.9491817
MEIS2-GALK2chr1537375972chr15496118011791HLA-C16:01NSSEQVLIF0.71070.9472817
MEIS2-GALK2chr1537375972chr15496118011791HLA-B48:02EQVLIFKLY0.55960.52421120
MEIS2-GALK2chr1537375972chr15496118011791HLA-C16:02NSSEQVLIF0.52430.977817
MEIS2-GALK2chr1537375972chr15496118011791HLA-B39:31SEQVLIFKL0.47460.66051019
MEIS2-GALK2chr1537375972chr15496118011791HLA-B39:02SEQVLIFKL0.45580.66621019
MEIS2-GALK2chr1537375972chr15496118011791HLA-C02:10NSSEQVLIF0.26320.9321817
MEIS2-GALK2chr1537375972chr15496118011791HLA-C02:02NSSEQVLIF0.26320.9321817
MEIS2-GALK2chr1537375972chr15496118011791HLA-B44:07SEQVLIFKLY0.99980.74271020
MEIS2-GALK2chr1537375972chr15496118011791HLA-B44:26SEQVLIFKLY0.99980.74271020
MEIS2-GALK2chr1537375972chr15496118011791HLA-B44:13SEQVLIFKLY0.99980.74271020
MEIS2-GALK2chr1537375972chr15496118011791HLA-C08:02SGDNSSEQVL0.99980.9746515
MEIS2-GALK2chr1537375972chr15496118011791HLA-B18:06SEQVLIFKLY0.98440.54441020
MEIS2-GALK2chr1537375972chr15496118011791HLA-B18:05SEQVLIFKLY0.98440.55061020
MEIS2-GALK2chr1537375972chr15496118011791HLA-B18:03SEQVLIFKLY0.97550.53921020

Top

Potential FusionNeoAntigen Information of MEIS2-GALK2 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.
MEIS2-GALK2_37375972_49611801.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)
MEIS2-GALK2chr1537375972chr15496118011791DRB1-1204SEQVLIFKLYQRAKH1025
MEIS2-GALK2chr1537375972chr15496118011791DRB1-1209SEQVLIFKLYQRAKH1025
MEIS2-GALK2chr1537375972chr15496118011791DRB5-0106SEQVLIFKLYQRAKH1025
MEIS2-GALK2chr1537375972chr15496118011791DRB5-0202SEQVLIFKLYQRAKH1025
MEIS2-GALK2chr1537375972chr15496118011791DRB5-0202SSEQVLIFKLYQRAK924
MEIS2-GALK2chr1537375972chr15496118011791DRB5-0204SEQVLIFKLYQRAKH1025

Top

Fusion breakpoint peptide structures of MEIS2-GALK2

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
2714GDNSSEQVLIFKLYMEIS2GALK2chr1537375972chr15496118011791

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of MEIS2-GALK2

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-B14:023BVN2714GDNSSEQVLIFKLY-7.15543-7.26883
HLA-B14:023BVN2714GDNSSEQVLIFKLY-4.77435-5.80965
HLA-B52:013W392714GDNSSEQVLIFKLY-6.80875-6.92215
HLA-B52:013W392714GDNSSEQVLIFKLY-4.20386-5.23916
HLA-A11:014UQ22714GDNSSEQVLIFKLY-7.5194-8.5547
HLA-A11:014UQ22714GDNSSEQVLIFKLY-6.9601-7.0735
HLA-A24:025HGA2714GDNSSEQVLIFKLY-7.52403-7.63743
HLA-A24:025HGA2714GDNSSEQVLIFKLY-5.82433-6.85963
HLA-B27:056PYJ2714GDNSSEQVLIFKLY-3.28285-4.31815
HLA-B44:053DX82714GDNSSEQVLIFKLY-5.91172-6.94702
HLA-B44:053DX82714GDNSSEQVLIFKLY-4.24346-4.35686

Top

Vaccine Design for the FusionNeoAntigens of MEIS2-GALK2

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
MEIS2-GALK2chr1537375972chr15496118011019SEQVLIFKLGTGAGCAAGTGCTCATCTTCAAACTCT
MEIS2-GALK2chr1537375972chr15496118011020SEQVLIFKLYGTGAGCAAGTGCTCATCTTCAAACTCTATC
MEIS2-GALK2chr1537375972chr15496118011120EQVLIFKLYAGCAAGTGCTCATCTTCAAACTCTATC
MEIS2-GALK2chr1537375972chr1549611801514SGDNSSEQVGCGGAGACAACAGCAGTGAGCAAGTGC
MEIS2-GALK2chr1537375972chr1549611801515SGDNSSEQVLGCGGAGACAACAGCAGTGAGCAAGTGCTCA
MEIS2-GALK2chr1537375972chr1549611801615GDNSSEQVLGAGACAACAGCAGTGAGCAAGTGCTCA
MEIS2-GALK2chr1537375972chr1549611801817NSSEQVLIFACAGCAGTGAGCAAGTGCTCATCTTCA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
MEIS2-GALK2chr1537375972chr15496118011025SEQVLIFKLYQRAKHGTGAGCAAGTGCTCATCTTCAAACTCTATCAGCGGGCAAAGCATG
MEIS2-GALK2chr1537375972chr1549611801924SSEQVLIFKLYQRAKGCAGTGAGCAAGTGCTCATCTTCAAACTCTATCAGCGGGCAAAGC

Top

Information of the samples that have these potential fusion neoantigens of MEIS2-GALK2

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
KIRCMEIS2-GALK2chr1537375972ENST00000382766chr1549611801ENST00000327171TCGA-BP-4165-01A

Top

Potential target of CAR-T therapy development for MEIS2-GALK2

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 MEIS2-GALK2

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

Top

Related Diseases to MEIS2-GALK2

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