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:BDP1-FAM172A

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: BDP1-FAM172A
FusionPDB ID: 9566
FusionGDB2.0 ID: 9566
HgeneTgene
Gene symbol

BDP1

FAM172A

Gene ID

55814

83989

Gene nameB double prime 1, subunit of RNA polymerase III transcription initiation factor IIIBfamily with sequence similarity 172 member A
SynonymsDFNB112|HSA238520|TAF3B1|TFC5|TFIIIB''|TFIIIB150|TFIIIB90|TFNRC5orf21|Toupee
Cytomap

5q13.2

5q15

Type of geneprotein-codingprotein-coding
Descriptiontranscription factor TFIIIB component B'' homologRNA polymerase III transcription initiation factor B''TATA box binding protein (TBP)-associated factor, RNA polymerase III, GTF3B subunit 1transcription factor IIIB 150transcription factor-like nuclear cotranscriptional regulator FAM172Aprotein FAM172A
Modification date2020031320200313
UniProtAcc

A6H8Y1

Main function of 5'-partner protein: FUNCTION: General activator of RNA polymerase III transcription. Requires for transcription from all three types of polymerase III promoters. Requires for transcription of genes with internal promoter elements and with promoter elements upstream of the initiation site. {ECO:0000269|PubMed:11040218}.

Q8WUF8

Main function of 5'-partner protein: FUNCTION: Plays a role in the regulation of alternative splicing, by interacting with AGO2 and CHD7. Seems to be required for stabilizing protein-protein interactions at the chromatin-spliceosome interface. May have hydrolase activity. {ECO:0000250|UniProtKB:Q3TNH5}.
Ensembl transtripts involved in fusion geneENST idsENST00000358731, ENST00000380675, 
ENST00000504768, ENST00000395965, 
ENST00000505869, ENST00000509163, 
ENST00000509739, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score8 X 8 X 5=32011 X 14 X 6=924
# samples 923
** MAII scorelog2(9/320*10)=-1.83007499855769
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(23/924*10)=-2.00625899047168
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: BDP1 [Title/Abstract] AND FAM172A [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: BDP1 [Title/Abstract] AND FAM172A [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)BDP1(70828254)-FAM172A(93217394), # samples:1
Anticipated loss of major functional domain due to fusion event.BDP1-FAM172A 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.
BDP1-FAM172A 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.
BDP1-FAM172A 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.
BDP1-FAM172A 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


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/chr5:70828254/chr5:93217394)
- 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 BDP1 (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 FAM172A (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)
ENST00000358731BDP1chr570828254-ENST00000395965FAM172Achr593217394-9757615526368382191
ENST00000358731BDP1chr570828254-ENST00000505869FAM172Achr593217394-7135615526368382191
ENST00000358731BDP1chr570828254-ENST00000509739FAM172Achr593217394-6943615526368382191
ENST00000358731BDP1chr570828254-ENST00000509163FAM172Achr593217394-6897615526368382191
ENST00000380675BDP1chr570828254-ENST00000395965FAM172Achr593217394-9757615526368382191
ENST00000380675BDP1chr570828254-ENST00000505869FAM172Achr593217394-7135615526368382191
ENST00000380675BDP1chr570828254-ENST00000509739FAM172Achr593217394-6943615526368382191
ENST00000380675BDP1chr570828254-ENST00000509163FAM172Achr593217394-6897615526368382191

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
ENST00000358731ENST00000395965BDP1chr570828254-FAM172Achr593217394-0.0006183580.99938166
ENST00000358731ENST00000505869BDP1chr570828254-FAM172Achr593217394-0.0019525060.9980475
ENST00000358731ENST00000509739BDP1chr570828254-FAM172Achr593217394-0.0021370270.997863
ENST00000358731ENST00000509163BDP1chr570828254-FAM172Achr593217394-0.0022182380.9977818
ENST00000380675ENST00000395965BDP1chr570828254-FAM172Achr593217394-0.0006183580.99938166
ENST00000380675ENST00000505869BDP1chr570828254-FAM172Achr593217394-0.0019525060.9980475
ENST00000380675ENST00000509739BDP1chr570828254-FAM172Achr593217394-0.0021370270.997863
ENST00000380675ENST00000509163BDP1chr570828254-FAM172Achr593217394-0.0022182380.9977818

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 BDP1-FAM172A

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
BDP1chr570828254FAM172Achr59321739461551958NTDVTTEEMKQEENLSVPFEGYGVIV

Top

Potential FusionNeoAntigen Information of BDP1-FAM172A 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.
BDP1-FAM172A_70828254_93217394.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)
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:01EENLSVPF0.99850.88171119
BDP1-FAM172Achr570828254chr5932173946155HLA-B44:03EENLSVPF0.9980.93111119
BDP1-FAM172Achr570828254chr5932173946155HLA-B39:06MKQEENLSV0.99880.7644817
BDP1-FAM172Achr570828254chr5932173946155HLA-B39:01MKQEENLSV0.99810.9131817
BDP1-FAM172Achr570828254chr5932173946155HLA-B44:03EEMKQEENL0.99260.9649615
BDP1-FAM172Achr570828254chr5932173946155HLA-B44:03QEENLSVPF0.99210.96811019
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:01QEENLSVPF0.98840.87181019
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:01EEMKQEENL0.94340.7486615
BDP1-FAM172Achr570828254chr5932173946155HLA-B15:01KQEENLSVPF0.99960.7748919
BDP1-FAM172Achr570828254chr5932173946155HLA-B13:01KQEENLSVPF0.86660.9029919
BDP1-FAM172Achr570828254chr5932173946155HLA-B44:03EENLSVPFEGY0.99930.97191122
BDP1-FAM172Achr570828254chr5932173946155HLA-B39:05MKQEENLSV0.99680.9004817
BDP1-FAM172Achr570828254chr5932173946155HLA-B39:08QEENLSVPF0.5120.91791019
BDP1-FAM172Achr570828254chr5932173946155HLA-B15:05KQEENLSVPF0.88270.8596919
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:07EENLSVPF0.99870.83771119
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:05EENLSVPF0.99850.88171119
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:04EENLSVPF0.99850.8971119
BDP1-FAM172Achr570828254chr5932173946155HLA-B44:13EENLSVPF0.9980.93111119
BDP1-FAM172Achr570828254chr5932173946155HLA-B44:26EENLSVPF0.9980.93111119
BDP1-FAM172Achr570828254chr5932173946155HLA-B44:07EENLSVPF0.9980.93111119
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:08EENLSVPF0.9980.77921119
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:06EENLSVPF0.99790.88861119
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:03EENLSVPF0.99780.87241119
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:11EENLSVPF0.99280.85191119
BDP1-FAM172Achr570828254chr5932173946155HLA-B40:04EEMKQEENL0.99850.6639615
BDP1-FAM172Achr570828254chr5932173946155HLA-B44:26EEMKQEENL0.99260.9649615
BDP1-FAM172Achr570828254chr5932173946155HLA-B44:07EEMKQEENL0.99260.9649615
BDP1-FAM172Achr570828254chr5932173946155HLA-B44:13EEMKQEENL0.99260.9649615
BDP1-FAM172Achr570828254chr5932173946155HLA-B44:07QEENLSVPF0.99210.96811019
BDP1-FAM172Achr570828254chr5932173946155HLA-B44:13QEENLSVPF0.99210.96811019
BDP1-FAM172Achr570828254chr5932173946155HLA-B44:26QEENLSVPF0.99210.96811019
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:04QEENLSVPF0.98960.88421019
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:05QEENLSVPF0.98840.87181019
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:08QEENLSVPF0.9880.80711019
BDP1-FAM172Achr570828254chr5932173946155HLA-B40:04QEENLSVPF0.98490.66231019
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:06QEENLSVPF0.98120.87371019
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:03QEENLSVPF0.97720.85981019
BDP1-FAM172Achr570828254chr5932173946155HLA-B15:09MKQEENLSV0.97280.7097817
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:11QEENLSVPF0.96560.89511019
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:05EEMKQEENL0.94340.7486615
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:08EEMKQEENL0.93270.6756615
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:06EEMKQEENL0.92990.7614615
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:03EEMKQEENL0.92550.7298615
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:11EEMKQEENL0.92350.7104615
BDP1-FAM172Achr570828254chr5932173946155HLA-B41:03EEMKQEENL0.72230.5911615
BDP1-FAM172Achr570828254chr5932173946155HLA-B41:03QEENLSVPF0.42850.76521019
BDP1-FAM172Achr570828254chr5932173946155HLA-B15:135KQEENLSVPF0.99960.7676919
BDP1-FAM172Achr570828254chr5932173946155HLA-B15:34KQEENLSVPF0.99960.7748919
BDP1-FAM172Achr570828254chr5932173946155HLA-B15:125KQEENLSVPF0.99960.7748919
BDP1-FAM172Achr570828254chr5932173946155HLA-B15:33KQEENLSVPF0.99960.7748919
BDP1-FAM172Achr570828254chr5932173946155HLA-B15:50KQEENLSVPF0.99950.764919
BDP1-FAM172Achr570828254chr5932173946155HLA-B15:53KQEENLSVPF0.99760.7199919
BDP1-FAM172Achr570828254chr5932173946155HLA-B15:54KQEENLSVPF0.99390.6998919
BDP1-FAM172Achr570828254chr5932173946155HLA-B15:73KQEENLSVPF0.98960.7424919
BDP1-FAM172Achr570828254chr5932173946155HLA-B15:30KQEENLSVPF0.9820.7178919
BDP1-FAM172Achr570828254chr5932173946155HLA-B15:20KQEENLSVPF0.88010.9225919
BDP1-FAM172Achr570828254chr5932173946155HLA-B35:28KQEENLSVPF0.86980.9423919
BDP1-FAM172Achr570828254chr5932173946155HLA-B44:07EENLSVPFEGY0.99930.97191122
BDP1-FAM172Achr570828254chr5932173946155HLA-B44:13EENLSVPFEGY0.99930.97191122
BDP1-FAM172Achr570828254chr5932173946155HLA-B44:26EENLSVPFEGY0.99930.97191122
BDP1-FAM172Achr570828254chr5932173946155HLA-B18:11EENLSVPFEGY0.9760.86561122

Top

Potential FusionNeoAntigen Information of BDP1-FAM172A 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.
BDP1-FAM172A_70828254_93217394.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)
BDP1-FAM172Achr570828254chr5932173946155DRB1-1525TEEMKQEENLSVPFE520

Top

Fusion breakpoint peptide structures of BDP1-FAM172A

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
1686EEMKQEENLSVPFEBDP1FAM172Achr570828254chr5932173946155

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of BDP1-FAM172A

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-B14:023BVN1686EEMKQEENLSVPFE-7.15543-7.26883
HLA-B14:023BVN1686EEMKQEENLSVPFE-4.77435-5.80965
HLA-B52:013W391686EEMKQEENLSVPFE-6.80875-6.92215
HLA-B52:013W391686EEMKQEENLSVPFE-4.20386-5.23916
HLA-A11:014UQ21686EEMKQEENLSVPFE-7.5194-8.5547
HLA-A11:014UQ21686EEMKQEENLSVPFE-6.9601-7.0735
HLA-A24:025HGA1686EEMKQEENLSVPFE-7.52403-7.63743
HLA-A24:025HGA1686EEMKQEENLSVPFE-5.82433-6.85963
HLA-B27:056PYJ1686EEMKQEENLSVPFE-3.28285-4.31815
HLA-B44:053DX81686EEMKQEENLSVPFE-5.91172-6.94702
HLA-B44:053DX81686EEMKQEENLSVPFE-4.24346-4.35686

Top

Vaccine Design for the FusionNeoAntigens of BDP1-FAM172A

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
BDP1-FAM172Achr570828254chr5932173941019QEENLSVPFGTACCGTTTGAAGGATATGGAGTAATA
BDP1-FAM172Achr570828254chr5932173941119EENLSVPFCCGTTTGAAGGATATGGAGTAATA
BDP1-FAM172Achr570828254chr5932173941122EENLSVPFEGYCCGTTTGAAGGATATGGAGTAATAGTACTAAAT
BDP1-FAM172Achr570828254chr593217394615EEMKQEENLGAAAATTTGAGTGTACCGTTTGAAGGA
BDP1-FAM172Achr570828254chr593217394817MKQEENLSVTTGAGTGTACCGTTTGAAGGATATGGA
BDP1-FAM172Achr570828254chr593217394919KQEENLSVPFAGTGTACCGTTTGAAGGATATGGAGTAATA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
BDP1-FAM172Achr570828254chr593217394520TEEMKQEENLSVPFEGAAGAAAATTTGAGTGTACCGTTTGAAGGATATGGAGTAATAGTA

Top

Information of the samples that have these potential fusion neoantigens of BDP1-FAM172A

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
LIHCBDP1-FAM172Achr570828254ENST00000358731chr593217394ENST00000395965TCGA-DD-AADB-01A

Top

Potential target of CAR-T therapy development for BDP1-FAM172A

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 BDP1-FAM172A

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

Top

Related Diseases to BDP1-FAM172A

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