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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:BMPR2-MARCH4

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: BMPR2-MARCH4
FusionPDB ID: 9934
FusionGDB2.0 ID: 9934
HgeneTgene
Gene symbol

BMPR2

MARCH4

Gene ID

659

57574

Gene namebone morphogenetic protein receptor type 2membrane associated ring-CH-type finger 4
SynonymsBMPR-II|BMPR3|BMR2|BRK-3|POVD1|PPH1|T-ALKMARCH-IV|MARCH4|RNF174
Cytomap

2q33.1-q33.2

2q35

Type of geneprotein-codingprotein-coding
Descriptionbone morphogenetic protein receptor type-2BMP type II receptorBMP type-2 receptorbone morphogenetic protein receptor type IIbone morphogenetic protein receptor, type II (serine/threonine kinase)type II activin receptor-like kinasetype II receptor foE3 ubiquitin-protein ligase MARCH4RING finger protein 174RING-type E3 ubiquitin transferase MARCH4membrane associated ring finger 4membrane-associated RING finger protein 4membrane-associated RING-CH protein IVmembrane-associated ring finger (C3HC4)
Modification date2020031320200313
UniProtAcc

Q13873

Main function of 5'-partner protein: FUNCTION: On ligand binding, forms a receptor complex consisting of two type II and two type I transmembrane serine/threonine kinases. Type II receptors phosphorylate and activate type I receptors which autophosphorylate, then bind and activate SMAD transcriptional regulators. Binds to BMP7, BMP2 and, less efficiently, BMP4. Binding is weak but enhanced by the presence of type I receptors for BMPs. Mediates induction of adipogenesis by GDF6. {ECO:0000250|UniProtKB:O35607}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000374574, ENST00000374580, 
ENST00000479069, 
ENST00000273067, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score20 X 12 X 9=21604 X 3 X 4=48
# samples 214
** MAII scorelog2(21/2160*10)=-3.36257007938471
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: BMPR2 [Title/Abstract] AND MARCH4 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: BMPR2 [Title/Abstract] AND MARCH4 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)BMPR2(203407170)-MARCH4(217124402), # samples:4
Anticipated loss of major functional domain due to fusion event.BMPR2-MARCH4 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.
BMPR2-MARCH4 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
HgeneBMPR2

GO:0007178

transmembrane receptor protein serine/threonine kinase signaling pathway

12045205

HgeneBMPR2

GO:0010634

positive regulation of epithelial cell migration

12819188

HgeneBMPR2

GO:0030308

negative regulation of cell growth

12819188

HgeneBMPR2

GO:0030509

BMP signaling pathway

18436533



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/chr2:203407170/chr2:217124402)
- 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 BMPR2 (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 MARCH4 (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)
ENST00000374580BMPR2chr2203407170+ENST00000273067MARCH4chr2217124402-376719525242032502
ENST00000374574BMPR2chr2203407170+ENST00000273067MARCH4chr2217124402-32691454261534502

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
ENST00000374580ENST00000273067BMPR2chr2203407170+MARCH4chr2217124402-0.0042614020.9957386
ENST00000374574ENST00000273067BMPR2chr2203407170+MARCH4chr2217124402-0.0036413340.9963587

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 BMPR2-MARCH4

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
BMPR2chr2203407170MARCH4chr22171244021454476RPKFPEAWKENSLVSSSMKDPRCTAS
BMPR2chr2203407170MARCH4chr22171244021952476RPKFPEAWKENSLVSSSMKDPRCTAS

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Potential FusionNeoAntigen Information of BMPR2-MARCH4 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.
BMPR2-MARCH4_203407170_217124402.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)
BMPR2-MARCH4chr2203407170chr22171244021454HLA-B45:01KENSLVSSS0.93150.6802817
BMPR2-MARCH4chr2203407170chr22171244021454HLA-B41:01KENSLVSSS0.22250.8325817
BMPR2-MARCH4chr2203407170chr22171244021454HLA-B47:01KENSLVSSSM0.99120.616818
BMPR2-MARCH4chr2203407170chr22171244021454HLA-B51:07EAWKENSLV0.99460.6477514
BMPR2-MARCH4chr2203407170chr22171244021454HLA-B40:06KENSLVSSS0.93260.5493817
BMPR2-MARCH4chr2203407170chr22171244021454HLA-A68:02EAWKENSLV0.99790.5591514
BMPR2-MARCH4chr2203407170chr22171244021454HLA-A69:01EAWKENSLV0.99480.702514
BMPR2-MARCH4chr2203407170chr22171244021454HLA-B15:53KENSLVSSSM0.97840.9213818
BMPR2-MARCH4chr2203407170chr22171244021454HLA-B41:03KENSLVSSSM0.79980.5899818

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Potential FusionNeoAntigen Information of BMPR2-MARCH4 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)

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Fusion breakpoint peptide structures of BMPR2-MARCH4

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
725AWKENSLVSSSMKDBMPR2MARCH4chr2203407170chr22171244021454

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of BMPR2-MARCH4

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-B14:023BVN725AWKENSLVSSSMKD-7.9962-8.1096
HLA-B14:023BVN725AWKENSLVSSSMKD-5.70842-6.74372
HLA-B52:013W39725AWKENSLVSSSMKD-6.83737-6.95077
HLA-B52:013W39725AWKENSLVSSSMKD-4.4836-5.5189
HLA-A11:014UQ2725AWKENSLVSSSMKD-10.0067-10.1201
HLA-A11:014UQ2725AWKENSLVSSSMKD-9.03915-10.0745
HLA-A24:025HGA725AWKENSLVSSSMKD-6.56204-6.67544
HLA-A24:025HGA725AWKENSLVSSSMKD-5.42271-6.45801
HLA-B44:053DX8725AWKENSLVSSSMKD-7.85648-8.89178
HLA-B44:053DX8725AWKENSLVSSSMKD-5.3978-5.5112
HLA-A02:016TDR725AWKENSLVSSSMKD-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of BMPR2-MARCH4

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
BMPR2-MARCH4chr2203407170chr2217124402514EAWKENSLVGAAGCCTGGAAAGAAAATAGCCTGGTC
BMPR2-MARCH4chr2203407170chr2217124402817KENSLVSSSAAAGAAAATAGCCTGGTCTCATCATCC
BMPR2-MARCH4chr2203407170chr2217124402818KENSLVSSSMAAAGAAAATAGCCTGGTCTCATCATCCATG

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

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Information of the samples that have these potential fusion neoantigens of BMPR2-MARCH4

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
PRADBMPR2-MARCH4chr2203407170ENST00000374574chr2217124402ENST00000273067TCGA-HC-8258-01A

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Potential target of CAR-T therapy development for BMPR2-MARCH4

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
HgeneBMPR2chr2:203407170chr2:217124402ENST00000374580+1013151_1714711039.0TransmembraneHelical

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

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Related Drugs to BMPR2-MARCH4

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 BMPR2-MARCH4

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