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:BRI3BP-MARS

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: BRI3BP-MARS
FusionPDB ID: 10264
FusionGDB2.0 ID: 10264
HgeneTgene
Gene symbol

BRI3BP

MARS

Gene ID

140707

84174

Gene nameBRI3 binding proteinSrc like adaptor 2
SynonymsBNAS1|HCCR-1|HCCR-2|HCCRBP-1|HCCRBP-3|KG19C20orf156|MARS|SLAP-2|SLAP2
Cytomap

12q24.31

20q11.23

Type of geneprotein-codingprotein-coding
DescriptionBRI3-binding proteinI3-binding proteincervical cancer 1 proto-oncogene-binding protein KG19cervical cancer oncogene binding proteinsrc-like-adapter 2Src-like adapter protein-2modulator of antigen receptor signaling
Modification date2020031320200313
UniProtAcc

Q8WY22

Main function of 5'-partner protein: FUNCTION: Involved in tumorigenesis and may function by stabilizing p53/TP53. {ECO:0000269|PubMed:17943721}.

P56192

Main function of 5'-partner protein: FUNCTION: Catalyzes the specific attachment of an amino acid to its cognate tRNA in a 2 step reaction: the amino acid (AA) is first activated by ATP to form AA-AMP and then transferred to the acceptor end of the tRNA (PubMed:11714285). Plays a role in the synthesis of ribosomal RNA in the nucleolus (PubMed:10791971). {ECO:0000269|PubMed:10791971, ECO:0000269|PubMed:11714285}.
Ensembl transtripts involved in fusion geneENST idsENST00000341446, ENST00000447721, 
ENST00000262027, ENST00000315473, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score10 X 4 X 6=24016 X 19 X 8=2432
# samples 1023
** MAII scorelog2(10/240*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(23/2432*10)=-3.40243746249921
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: BRI3BP [Title/Abstract] AND MARS [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: BRI3BP [Title/Abstract] AND MARS [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)BRI3BP(125478549)-MARS(57905480), # samples:1
BRI3BP(125478549)-MARS(57905481), # samples:1
Anticipated loss of major functional domain due to fusion event.BRI3BP-MARS 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.
BRI3BP-MARS 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.
BRI3BP-MARS 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.
BRI3BP-MARS 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
TgeneMARS

GO:0000122

negative regulation of transcription by RNA polymerase II

11696592

TgeneMARS

GO:0050849

negative regulation of calcium-mediated signaling

11696592



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/chr12:125478549/chr12:57905480)
- 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 BRI3BP (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 MARS (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)
ENST00000341446BRI3BPchr12125478549+ENST00000262027MARSchr1257905480+1707304911638515
ENST00000341446BRI3BPchr12125478549+ENST00000315473MARSchr1257905480+1689304911545484
ENST00000341446BRI3BPchr12125478549+ENST00000262027MARSchr1257905481+1707304911638515
ENST00000341446BRI3BPchr12125478549+ENST00000315473MARSchr1257905481+1689304911545484

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
ENST00000341446ENST00000262027BRI3BPchr12125478549+MARSchr1257905480+0.0045477050.99545234
ENST00000341446ENST00000315473BRI3BPchr12125478549+MARSchr1257905480+0.0060538850.99394614
ENST00000341446ENST00000262027BRI3BPchr12125478549+MARSchr1257905481+0.0045477050.99545234
ENST00000341446ENST00000315473BRI3BPchr12125478549+MARSchr1257905481+0.0060538850.99394614

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 BRI3BP-MARS

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
BRI3BPchr12125478549MARSchr125790548030471SLFGEDNVRAAQKLEKRLEEWLGRTL
BRI3BPchr12125478549MARSchr125790548130471SLFGEDNVRAAQKLEKRLEEWLGRTL

Top

Potential FusionNeoAntigen Information of BRI3BP-MARS 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.
BRI3BP-MARS_125478549_57905480.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)
BRI3BP-MARSchr12125478549chr1257905480304HLA-B27:05VRAAQKLEK0.99850.664716
BRI3BP-MARSchr12125478549chr1257905480304HLA-B27:14VRAAQKLEK0.99590.5908716
BRI3BP-MARSchr12125478549chr1257905480304HLA-B44:10GEDNVRAAQKL0.99930.55314
BRI3BP-MARSchr12125478549chr1257905480304HLA-B44:08AQKLEKRLEEW0.99510.91631021
BRI3BP-MARSchr12125478549chr1257905480304HLA-B39:08GEDNVRAAQKL0.99140.9195314
BRI3BP-MARSchr12125478549chr1257905480304HLA-B27:10VRAAQKLEK0.99790.7857716
BRI3BP-MARSchr12125478549chr1257905480304HLA-B40:04GEDNVRAAQKL0.99990.7657314
BRI3BP-MARSchr12125478549chr1257905480304HLA-B15:24AQKLEKRLEEW0.99950.97621021
BRI3BP-MARSchr12125478549chr1257905480304HLA-B41:03GEDNVRAAQKL0.96560.7608314

Top

Potential FusionNeoAntigen Information of BRI3BP-MARS 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.
BRI3BP-MARS_125478549_57905480.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)
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1102EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1103EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1116EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1134EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1136EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1142EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1148EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1157EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1159EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1163EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1165EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1176EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1185EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1186EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1301EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1308EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1315EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1316EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1317EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1319EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1319GEDNVRAAQKLEKRL318
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1320EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1322EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1324EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1327EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1327GEDNVRAAQKLEKRL318
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1335EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1344EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1351EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1352EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1353EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1353GEDNVRAAQKLEKRL318
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1357EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1359EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1361EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1364EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1368EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1369EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1370EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1371EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1371GEDNVRAAQKLEKRL318
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1371FGEDNVRAAQKLEKR217
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1372EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1376EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1376GEDNVRAAQKLEKRL318
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1378EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1379EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1380EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1383EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1384EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1387EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1391EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1392EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1398EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1406EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1412EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1412GEDNVRAAQKLEKRL318
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1417EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1420EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1421EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1429EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1433EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1483EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1484EDNVRAAQKLEKRLE419
BRI3BP-MARSchr12125478549chr1257905480304DRB1-1495EDNVRAAQKLEKRLE419

Top

Fusion breakpoint peptide structures of BRI3BP-MARS

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
6450NVRAAQKLEKRLEEBRI3BPMARSchr12125478549chr1257905480304

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of BRI3BP-MARS

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-B14:023BVN6450NVRAAQKLEKRLEE-7.9962-8.1096
HLA-B14:023BVN6450NVRAAQKLEKRLEE-5.70842-6.74372
HLA-B52:013W396450NVRAAQKLEKRLEE-6.83737-6.95077
HLA-B52:013W396450NVRAAQKLEKRLEE-4.4836-5.5189
HLA-A11:014UQ26450NVRAAQKLEKRLEE-10.0067-10.1201
HLA-A11:014UQ26450NVRAAQKLEKRLEE-9.03915-10.0745
HLA-A24:025HGA6450NVRAAQKLEKRLEE-6.56204-6.67544
HLA-A24:025HGA6450NVRAAQKLEKRLEE-5.42271-6.45801
HLA-B44:053DX86450NVRAAQKLEKRLEE-7.85648-8.89178
HLA-B44:053DX86450NVRAAQKLEKRLEE-5.3978-5.5112
HLA-A02:016TDR6450NVRAAQKLEKRLEE-3.37154-4.40684

Top

Vaccine Design for the FusionNeoAntigens of BRI3BP-MARS

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
BRI3BP-MARSchr12125478549chr12579054801021AQKLEKRLEEWGCTCAGAAGCTGGAGAAGCGACTGGAGGAGTGG
BRI3BP-MARSchr12125478549chr1257905480314GEDNVRAAQKLGGCGAGGACAACGTGCGCGCCGCTCAGAAGCTG
BRI3BP-MARSchr12125478549chr1257905480716VRAAQKLEKGTGCGCGCCGCTCAGAAGCTGGAGAAG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
BRI3BP-MARSchr12125478549chr1257905480217FGEDNVRAAQKLEKRTTCGGCGAGGACAACGTGCGCGCCGCTCAGAAGCTGGAGAAGCGA
BRI3BP-MARSchr12125478549chr1257905480318GEDNVRAAQKLEKRLGGCGAGGACAACGTGCGCGCCGCTCAGAAGCTGGAGAAGCGACTG
BRI3BP-MARSchr12125478549chr1257905480419EDNVRAAQKLEKRLEGAGGACAACGTGCGCGCCGCTCAGAAGCTGGAGAAGCGACTGGAG

Top

Information of the samples that have these potential fusion neoantigens of BRI3BP-MARS

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
READBRI3BP-MARSchr12125478549ENST00000341446chr1257905480ENST00000262027TCGA-AG-4015

Top

Potential target of CAR-T therapy development for BRI3BP-MARS

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
HgeneBRI3BPchr12:125478549chr12:57905480ENST00000341446+1313_3371252.0TransmembraneHelical
HgeneBRI3BPchr12:125478549chr12:57905481ENST00000341446+1313_3371252.0TransmembraneHelical

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 BRI3BP-MARS

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

Top

Related Diseases to BRI3BP-MARS

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