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:MTCH2-FHIT

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: MTCH2-FHIT
FusionPDB ID: 55562
FusionGDB2.0 ID: 55562
HgeneTgene
Gene symbol

MTCH2

FHIT

Gene ID

23788

2272

Gene namemitochondrial carrier 2fragile histidine triad diadenosine triphosphatase
SynonymsHSPC032|MIMP|SLC25A50AP3Aase|FRA3B
Cytomap

11p11.2

3p14.2

Type of geneprotein-codingprotein-coding
Descriptionmitochondrial carrier homolog 22310034D24Rikmet-induced mitochondrial proteinsolute carrier family 25, member 50bis(5'-adenosyl)-triphosphataseAP3A hydrolasediadenosine 5',5'''-P1,P3-triphosphate hydrolasedinucleosidetriphosphatase
Modification date2020031320200313
UniProtAcc

Q9Y6C9

Main function of 5'-partner protein: FUNCTION: The substrate transported is not yet known. Induces mitochondrial depolarization.

P49789

Main function of 5'-partner protein: FUNCTION: Possesses dinucleoside triphosphate hydrolase activity (PubMed:12574506, PubMed:15182206, PubMed:8794732, PubMed:9323207, PubMed:9576908, PubMed:9543008). Cleaves P(1)-P(3)-bis(5'-adenosyl) triphosphate (Ap3A) to yield AMP and ADP (PubMed:12574506, PubMed:15182206, PubMed:8794732, PubMed:9323207, PubMed:9576908, PubMed:9543008). Can also hydrolyze P(1)-P(4)-bis(5'-adenosyl) tetraphosphate (Ap4A), but has extremely low activity with ATP (PubMed:8794732). Exhibits adenylylsulfatase activity, hydrolyzing adenosine 5'-phosphosulfate to yield AMP and sulfate (PubMed:18694747). Exhibits adenosine 5'-monophosphoramidase activity, hydrolyzing purine nucleotide phosphoramidates with a single phosphate group such as adenosine 5'monophosphoramidate (AMP-NH2) to yield AMP and NH2 (PubMed:18694747). Exhibits adenylylsulfate-ammonia adenylyltransferase, catalyzing the ammonolysis of adenosine 5'-phosphosulfate resulting in the formation of adenosine 5'-phosphoramidate (PubMed:26181368). Also catalyzes the ammonolysis of adenosine 5-phosphorofluoridate and diadenosine triphosphate (PubMed:26181368). Modulates transcriptional activation by CTNNB1 and thereby contributes to regulate the expression of genes essential for cell proliferation and survival, such as CCND1 and BIRC5 (PubMed:18077326). Plays a role in the induction of apoptosis via SRC and AKT1 signaling pathways (PubMed:16407838). Inhibits MDM2-mediated proteasomal degradation of p53/TP53 and thereby plays a role in p53/TP53-mediated apoptosis (PubMed:15313915). Induction of apoptosis depends on the ability of FHIT to bind P(1)-P(3)-bis(5'-adenosyl) triphosphate or related compounds, but does not require its catalytic activity, it may in part come from the mitochondrial form, which sensitizes the low-affinity Ca(2+) transporters, enhancing mitochondrial calcium uptake (PubMed:12574506, PubMed:19622739). Functions as tumor suppressor (By similarity). {ECO:0000250|UniProtKB:O89106, ECO:0000269|PubMed:12574506, ECO:0000269|PubMed:15313915, ECO:0000269|PubMed:16407838, ECO:0000269|PubMed:18077326, ECO:0000269|PubMed:18694747, ECO:0000269|PubMed:19622739, ECO:0000269|PubMed:26181368, ECO:0000269|PubMed:8794732, ECO:0000269|PubMed:9323207, ECO:0000269|PubMed:9543008}.
Ensembl transtripts involved in fusion geneENST idsENST00000302503, ENST00000542981, 
ENST00000534074, 
ENST00000341848, 
ENST00000466788, ENST00000468189, 
ENST00000476844, ENST00000492590, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score8 X 7 X 4=22427 X 20 X 11=5940
# samples 932
** MAII scorelog2(9/224*10)=-1.31550182572793
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(32/5940*10)=-4.21431912080077
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: MTCH2 [Title/Abstract] AND FHIT [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: MTCH2 [Title/Abstract] AND FHIT [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MTCH2(47660251)-FHIT(59738047), # samples:3
Anticipated loss of major functional domain due to fusion event.MTCH2-FHIT 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.
MTCH2-FHIT 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
TgeneFHIT

GO:0006163

purine nucleotide metabolic process

9323207



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/chr11:47660251/chr3:59738047)
- 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 MTCH2 (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 FHIT (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)
ENST00000302503MTCH2chr1147660251-ENST00000476844FHITchr359738047-79743729532167
ENST00000302503MTCH2chr1147660251-ENST00000492590FHITchr359738047-80843729532167

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
ENST00000302503ENST00000476844MTCH2chr1147660251-FHITchr359738047-0.0292829870.97071695
ENST00000302503ENST00000492590MTCH2chr1147660251-FHITchr359738047-0.0373738260.9626262

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 MTCH2-FHIT

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
MTCH2chr1147660251FHITchr359738047437136GVLGTVVHGKVLQLQKHDKEDFPASW

Top

Potential FusionNeoAntigen Information of MTCH2-FHIT 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.
MTCH2-FHIT_47660251_59738047.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)
MTCH2-FHITchr1147660251chr359738047437HLA-B39:24VHGKVLQL0.99970.5398614
MTCH2-FHITchr1147660251chr359738047437HLA-B39:01VHGKVLQL0.99960.8803614
MTCH2-FHITchr1147660251chr359738047437HLA-B38:02VHGKVLQL0.9990.9545614
MTCH2-FHITchr1147660251chr359738047437HLA-B38:01VHGKVLQL0.99890.9521614
MTCH2-FHITchr1147660251chr359738047437HLA-B14:02VHGKVLQL0.99860.8028614
MTCH2-FHITchr1147660251chr359738047437HLA-B14:01VHGKVLQL0.99860.8028614
MTCH2-FHITchr1147660251chr359738047437HLA-B15:17VVHGKVLQL0.97340.8363514
MTCH2-FHITchr1147660251chr359738047437HLA-B08:01VVHGKVLQL0.94550.7668514
MTCH2-FHITchr1147660251chr359738047437HLA-B15:16VVHGKVLQL0.93530.7881514
MTCH2-FHITchr1147660251chr359738047437HLA-B14:01VVHGKVLQL0.90190.8113514
MTCH2-FHITchr1147660251chr359738047437HLA-B14:02VVHGKVLQL0.90190.8113514
MTCH2-FHITchr1147660251chr359738047437HLA-B08:09VVHGKVLQL0.87940.8474514
MTCH2-FHITchr1147660251chr359738047437HLA-A30:08VVHGKVLQL0.86370.7249514
MTCH2-FHITchr1147660251chr359738047437HLA-A02:17VVHGKVLQL0.84030.5639514
MTCH2-FHITchr1147660251chr359738047437HLA-A02:38VVHGKVLQL0.83980.5849514
MTCH2-FHITchr1147660251chr359738047437HLA-A02:13VVHGKVLQL0.76410.583514
MTCH2-FHITchr1147660251chr359738047437HLA-B52:01VVHGKVLQL0.68690.8517514
MTCH2-FHITchr1147660251chr359738047437HLA-A32:13VVHGKVLQL0.60170.9423514
MTCH2-FHITchr1147660251chr359738047437HLA-B81:01VVHGKVLQL0.40080.5844514
MTCH2-FHITchr1147660251chr359738047437HLA-B48:01VVHGKVLQL0.36430.5968514
MTCH2-FHITchr1147660251chr359738047437HLA-B13:02VVHGKVLQL0.10340.714514
MTCH2-FHITchr1147660251chr359738047437HLA-B13:01VVHGKVLQL0.05840.9715514
MTCH2-FHITchr1147660251chr359738047437HLA-B39:09VHGKVLQL0.99970.7696614
MTCH2-FHITchr1147660251chr359738047437HLA-B39:12VHGKVLQL0.99950.8846614
MTCH2-FHITchr1147660251chr359738047437HLA-B39:05VHGKVLQL0.99850.8652614
MTCH2-FHITchr1147660251chr359738047437HLA-B14:03VHGKVLQL0.94580.7766614
MTCH2-FHITchr1147660251chr359738047437HLA-C15:04VVHGKVLQL0.99920.9158514
MTCH2-FHITchr1147660251chr359738047437HLA-C15:06VVHGKVLQL0.99890.9164514
MTCH2-FHITchr1147660251chr359738047437HLA-C03:07VVHGKVLQL0.99870.9398514
MTCH2-FHITchr1147660251chr359738047437HLA-C03:19VVHGKVLQL0.99860.979514
MTCH2-FHITchr1147660251chr359738047437HLA-C03:08VVHGKVLQL0.99850.8275514
MTCH2-FHITchr1147660251chr359738047437HLA-C06:03VVHGKVLQL0.99730.9743514
MTCH2-FHITchr1147660251chr359738047437HLA-C12:04VVHGKVLQL0.99690.9688514
MTCH2-FHITchr1147660251chr359738047437HLA-C12:12VVHGKVLQL0.99640.9101514
MTCH2-FHITchr1147660251chr359738047437HLA-C04:06VVHGKVLQL0.98180.9396514
MTCH2-FHITchr1147660251chr359738047437HLA-C12:16VVHGKVLQL0.96940.9342514
MTCH2-FHITchr1147660251chr359738047437HLA-B42:02VVHGKVLQL0.96690.7701514
MTCH2-FHITchr1147660251chr359738047437HLA-C04:14VVHGKVLQL0.96170.971514
MTCH2-FHITchr1147660251chr359738047437HLA-C08:04VVHGKVLQL0.9490.9449514
MTCH2-FHITchr1147660251chr359738047437HLA-C08:13VVHGKVLQL0.9490.9449514
MTCH2-FHITchr1147660251chr359738047437HLA-B42:01VVHGKVLQL0.9390.7617514
MTCH2-FHITchr1147660251chr359738047437HLA-C02:06VVHGKVLQL0.92560.9377514
MTCH2-FHITchr1147660251chr359738047437HLA-B15:04VVHGKVLQL0.91460.8699514
MTCH2-FHITchr1147660251chr359738047437HLA-C07:10VVHGKVLQL0.82970.9595514
MTCH2-FHITchr1147660251chr359738047437HLA-B14:03VVHGKVLQL0.79690.8035514
MTCH2-FHITchr1147660251chr359738047437HLA-C07:67VVHGKVLQL0.78930.9334514
MTCH2-FHITchr1147660251chr359738047437HLA-C07:80VVHGKVLQL0.78930.9334514
MTCH2-FHITchr1147660251chr359738047437HLA-C07:05VVHGKVLQL0.78180.9387514
MTCH2-FHITchr1147660251chr359738047437HLA-C07:13VVHGKVLQL0.77440.9232514
MTCH2-FHITchr1147660251chr359738047437HLA-C07:29VVHGKVLQL0.77250.875514
MTCH2-FHITchr1147660251chr359738047437HLA-C07:19VVHGKVLQL0.76320.7054514
MTCH2-FHITchr1147660251chr359738047437HLA-C03:14VVHGKVLQL0.70870.9716514
MTCH2-FHITchr1147660251chr359738047437HLA-C07:46VVHGKVLQL0.7070.8973514
MTCH2-FHITchr1147660251chr359738047437HLA-C07:27VVHGKVLQL0.70560.9176514
MTCH2-FHITchr1147660251chr359738047437HLA-C01:17VVHGKVLQL0.63150.9536514
MTCH2-FHITchr1147660251chr359738047437HLA-C07:95VVHGKVLQL0.6070.5587514
MTCH2-FHITchr1147660251chr359738047437HLA-C08:03VVHGKVLQL0.54810.984514
MTCH2-FHITchr1147660251chr359738047437HLA-C01:30VVHGKVLQL0.50720.951514
MTCH2-FHITchr1147660251chr359738047437HLA-B38:05VHGKVLQL0.99890.9521614
MTCH2-FHITchr1147660251chr359738047437HLA-B15:09VHGKVLQL0.9960.7776614
MTCH2-FHITchr1147660251chr359738047437HLA-C15:09VVHGKVLQL0.99920.9158514
MTCH2-FHITchr1147660251chr359738047437HLA-C15:05VVHGKVLQL0.99860.9446514
MTCH2-FHITchr1147660251chr359738047437HLA-C15:02VVHGKVLQL0.99840.911514
MTCH2-FHITchr1147660251chr359738047437HLA-C03:04VVHGKVLQL0.99820.9735514
MTCH2-FHITchr1147660251chr359738047437HLA-C03:03VVHGKVLQL0.99820.9735514
MTCH2-FHITchr1147660251chr359738047437HLA-C12:03VVHGKVLQL0.99710.9481514
MTCH2-FHITchr1147660251chr359738047437HLA-C03:17VVHGKVLQL0.9960.9418514
MTCH2-FHITchr1147660251chr359738047437HLA-C03:67VVHGKVLQL0.99590.9604514
MTCH2-FHITchr1147660251chr359738047437HLA-C06:02VVHGKVLQL0.99540.969514
MTCH2-FHITchr1147660251chr359738047437HLA-C06:17VVHGKVLQL0.99540.969514
MTCH2-FHITchr1147660251chr359738047437HLA-C03:05VVHGKVLQL0.99480.862514
MTCH2-FHITchr1147660251chr359738047437HLA-C16:04VVHGKVLQL0.99440.9519514
MTCH2-FHITchr1147660251chr359738047437HLA-C03:02VVHGKVLQL0.99290.9573514
MTCH2-FHITchr1147660251chr359738047437HLA-A30:01HGKVLQLQK0.98760.7774716
MTCH2-FHITchr1147660251chr359738047437HLA-C04:04VVHGKVLQL0.97550.9424514
MTCH2-FHITchr1147660251chr359738047437HLA-C16:02VVHGKVLQL0.97260.9749514
MTCH2-FHITchr1147660251chr359738047437HLA-C06:06VVHGKVLQL0.97020.9755514
MTCH2-FHITchr1147660251chr359738047437HLA-C12:02VVHGKVLQL0.96880.9498514
MTCH2-FHITchr1147660251chr359738047437HLA-C16:01VVHGKVLQL0.95240.9619514
MTCH2-FHITchr1147660251chr359738047437HLA-C03:06VVHGKVLQL0.94760.9792514
MTCH2-FHITchr1147660251chr359738047437HLA-B08:18VVHGKVLQL0.94550.7668514
MTCH2-FHITchr1147660251chr359738047437HLA-C07:04VVHGKVLQL0.93250.9517514
MTCH2-FHITchr1147660251chr359738047437HLA-C02:10VVHGKVLQL0.90080.9537514
MTCH2-FHITchr1147660251chr359738047437HLA-C02:02VVHGKVLQL0.90080.9537514
MTCH2-FHITchr1147660251chr359738047437HLA-A32:01VVHGKVLQL0.89480.9446514
MTCH2-FHITchr1147660251chr359738047437HLA-B07:13VVHGKVLQL0.8940.8271514
MTCH2-FHITchr1147660251chr359738047437HLA-C07:22VVHGKVLQL0.88870.6374514
MTCH2-FHITchr1147660251chr359738047437HLA-A30:01VVHGKVLQL0.86210.8481514
MTCH2-FHITchr1147660251chr359738047437HLA-C07:17VVHGKVLQL0.83590.9308514
MTCH2-FHITchr1147660251chr359738047437HLA-B15:73VVHGKVLQL0.83360.9037514
MTCH2-FHITchr1147660251chr359738047437HLA-C06:08VVHGKVLQL0.81380.9745514
MTCH2-FHITchr1147660251chr359738047437HLA-C07:02VVHGKVLQL0.78930.9334514
MTCH2-FHITchr1147660251chr359738047437HLA-B08:12VVHGKVLQL0.78890.8476514
MTCH2-FHITchr1147660251chr359738047437HLA-B15:30VVHGKVLQL0.77210.8774514
MTCH2-FHITchr1147660251chr359738047437HLA-C18:01VVHGKVLQL0.75270.9585514
MTCH2-FHITchr1147660251chr359738047437HLA-C07:01VVHGKVLQL0.67150.5637514
MTCH2-FHITchr1147660251chr359738047437HLA-C01:02VVHGKVLQL0.59410.9523514
MTCH2-FHITchr1147660251chr359738047437HLA-C08:01VVHGKVLQL0.54810.984514
MTCH2-FHITchr1147660251chr359738047437HLA-C01:03VVHGKVLQL0.42660.9521514
MTCH2-FHITchr1147660251chr359738047437HLA-C17:01VVHGKVLQL0.2350.9391514

Top

Potential FusionNeoAntigen Information of MTCH2-FHIT 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.
MTCH2-FHIT_47660251_59738047.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)
MTCH2-FHITchr1147660251chr359738047437DRB4-0101GKVLQLQKHDKEDFP823
MTCH2-FHITchr1147660251chr359738047437DRB4-0101HGKVLQLQKHDKEDF722
MTCH2-FHITchr1147660251chr359738047437DRB4-0101VHGKVLQLQKHDKED621
MTCH2-FHITchr1147660251chr359738047437DRB4-0101KVLQLQKHDKEDFPA924
MTCH2-FHITchr1147660251chr359738047437DRB4-0103GKVLQLQKHDKEDFP823
MTCH2-FHITchr1147660251chr359738047437DRB4-0103HGKVLQLQKHDKEDF722
MTCH2-FHITchr1147660251chr359738047437DRB4-0103VHGKVLQLQKHDKED621
MTCH2-FHITchr1147660251chr359738047437DRB4-0103KVLQLQKHDKEDFPA924
MTCH2-FHITchr1147660251chr359738047437DRB4-0104GKVLQLQKHDKEDFP823
MTCH2-FHITchr1147660251chr359738047437DRB4-0104HGKVLQLQKHDKEDF722
MTCH2-FHITchr1147660251chr359738047437DRB4-0104VHGKVLQLQKHDKED621
MTCH2-FHITchr1147660251chr359738047437DRB4-0104KVLQLQKHDKEDFPA924
MTCH2-FHITchr1147660251chr359738047437DRB4-0106GKVLQLQKHDKEDFP823
MTCH2-FHITchr1147660251chr359738047437DRB4-0106HGKVLQLQKHDKEDF722
MTCH2-FHITchr1147660251chr359738047437DRB4-0106VHGKVLQLQKHDKED621
MTCH2-FHITchr1147660251chr359738047437DRB4-0106KVLQLQKHDKEDFPA924
MTCH2-FHITchr1147660251chr359738047437DRB4-0107GKVLQLQKHDKEDFP823
MTCH2-FHITchr1147660251chr359738047437DRB4-0107HGKVLQLQKHDKEDF722
MTCH2-FHITchr1147660251chr359738047437DRB4-0107VHGKVLQLQKHDKED621
MTCH2-FHITchr1147660251chr359738047437DRB4-0107KVLQLQKHDKEDFPA924
MTCH2-FHITchr1147660251chr359738047437DRB4-0108GKVLQLQKHDKEDFP823
MTCH2-FHITchr1147660251chr359738047437DRB4-0108HGKVLQLQKHDKEDF722
MTCH2-FHITchr1147660251chr359738047437DRB4-0108VHGKVLQLQKHDKED621
MTCH2-FHITchr1147660251chr359738047437DRB4-0108KVLQLQKHDKEDFPA924

Top

Fusion breakpoint peptide structures of MTCH2-FHIT

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
9974VHGKVLQLQKHDKEMTCH2FHITchr1147660251chr359738047437

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of MTCH2-FHIT

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-B14:023BVN9974VHGKVLQLQKHDKE-7.9962-8.1096
HLA-B14:023BVN9974VHGKVLQLQKHDKE-5.70842-6.74372
HLA-B52:013W399974VHGKVLQLQKHDKE-6.83737-6.95077
HLA-B52:013W399974VHGKVLQLQKHDKE-4.4836-5.5189
HLA-A11:014UQ29974VHGKVLQLQKHDKE-10.0067-10.1201
HLA-A11:014UQ29974VHGKVLQLQKHDKE-9.03915-10.0745
HLA-A24:025HGA9974VHGKVLQLQKHDKE-6.56204-6.67544
HLA-A24:025HGA9974VHGKVLQLQKHDKE-5.42271-6.45801
HLA-B44:053DX89974VHGKVLQLQKHDKE-7.85648-8.89178
HLA-B44:053DX89974VHGKVLQLQKHDKE-5.3978-5.5112
HLA-A02:016TDR9974VHGKVLQLQKHDKE-3.37154-4.40684

Top

Vaccine Design for the FusionNeoAntigens of MTCH2-FHIT

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
MTCH2-FHITchr1147660251chr359738047514VVHGKVLQLGTGGTCCATGGTAAAGTTTTACAGCTC
MTCH2-FHITchr1147660251chr359738047614VHGKVLQLGTCCATGGTAAAGTTTTACAGCTC
MTCH2-FHITchr1147660251chr359738047716HGKVLQLQKCATGGTAAAGTTTTACAGCTCCAGAAA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
MTCH2-FHITchr1147660251chr359738047621VHGKVLQLQKHDKEDGTCCATGGTAAAGTTTTACAGCTCCAGAAACATGACAAGGAGGAC
MTCH2-FHITchr1147660251chr359738047722HGKVLQLQKHDKEDFCATGGTAAAGTTTTACAGCTCCAGAAACATGACAAGGAGGACTTT
MTCH2-FHITchr1147660251chr359738047823GKVLQLQKHDKEDFPGGTAAAGTTTTACAGCTCCAGAAACATGACAAGGAGGACTTTCCT
MTCH2-FHITchr1147660251chr359738047924KVLQLQKHDKEDFPAAAAGTTTTACAGCTCCAGAAACATGACAAGGAGGACTTTCCTGCC

Top

Information of the samples that have these potential fusion neoantigens of MTCH2-FHIT

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
OVMTCH2-FHITchr1147660251ENST00000302503chr359738047ENST00000476844TCGA-23-2077-01A

Top

Potential target of CAR-T therapy development for MTCH2-FHIT

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
HgeneMTCH2chr11:47660251chr3:59738047ENST00000302503-3138_2893304.0TransmembraneHelical

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 MTCH2-FHIT

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

Top

Related Diseases to MTCH2-FHIT

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
TgeneFHITC0024121Lung Neoplasms2CTD_human
TgeneFHITC0025500Mesothelioma2CTD_human
TgeneFHITC0242379Malignant neoplasm of lung2CTD_human
TgeneFHITC0007097Carcinoma1CTD_human
TgeneFHITC0007131Non-Small Cell Lung Carcinoma1CTD_human
TgeneFHITC0013146Drug abuse1CTD_human
TgeneFHITC0013170Drug habituation1CTD_human
TgeneFHITC0013222Drug Use Disorders1CTD_human
TgeneFHITC0023903Liver neoplasms1CTD_human
TgeneFHITC0024623Malignant neoplasm of stomach1CTD_human
TgeneFHITC0029231Organic Mental Disorders, Substance-Induced1CTD_human
TgeneFHITC0033578Prostatic Neoplasms1CTD_human
TgeneFHITC0038356Stomach Neoplasms1CTD_human
TgeneFHITC0038580Substance Dependence1CTD_human
TgeneFHITC0038586Substance Use Disorders1CTD_human
TgeneFHITC0042076Urologic Neoplasms1CTD_human
TgeneFHITC0205696Anaplastic carcinoma1CTD_human
TgeneFHITC0205697Carcinoma, Spindle-Cell1CTD_human
TgeneFHITC0205698Undifferentiated carcinoma1CTD_human
TgeneFHITC0205699Carcinomatosis1CTD_human
TgeneFHITC0236733Amphetamine-Related Disorders1CTD_human
TgeneFHITC0236804Amphetamine Addiction1CTD_human
TgeneFHITC0236807Amphetamine Abuse1CTD_human
TgeneFHITC0236969Substance-Related Disorders1CTD_human
TgeneFHITC0345904Malignant neoplasm of liver1CTD_human
TgeneFHITC0376358Malignant neoplasm of prostate1CTD_human
TgeneFHITC0740858Substance abuse problem1CTD_human
TgeneFHITC0751571Cancer of Urinary Tract1CTD_human
TgeneFHITC1510472Drug Dependence1CTD_human
TgeneFHITC1708349Hereditary Diffuse Gastric Cancer1CTD_human
TgeneFHITC4316881Prescription Drug Abuse1CTD_human