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:BRD1-TTLL8

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: BRD1-TTLL8
FusionPDB ID: 10172
FusionGDB2.0 ID: 10172
HgeneTgene
Gene symbol

BRD1

TTLL8

Gene ID

23774

164714

Gene namebromodomain containing 1tubulin tyrosine ligase like 8
SynonymsBRL|BRPF1|BRPF2-
Cytomap

22q13.33

22q13.33

Type of geneprotein-codingprotein-coding
Descriptionbromodomain-containing protein 1BR140-like proteinbromodomain and PHD finger-containing protein 2protein monoglycylase TTLL8tubulin tyrosine ligase-like family, member 8tubulin--tyrosine ligase-like protein 8
Modification date2020032720200313
UniProtAcc

O95696

Main function of 5'-partner protein: FUNCTION: Scaffold subunit of various histone acetyltransferase (HAT) complexes, such as the MOZ/MORF and HBO1 complexes, that acts as a regulator of hematopoiesis (PubMed:16387653, PubMed:21753189, PubMed:21880731). Plays a key role in HBO1 complex by directing KAT7/HBO1 specificity towards histone H3 'Lys-14' acetylation (H3K14ac), thereby promoting erythroid differentiation (PubMed:21753189). {ECO:0000269|PubMed:16387653, ECO:0000269|PubMed:21753189, ECO:0000269|PubMed:21880731}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000216267, ENST00000404034, 
ENST00000404760, ENST00000457780, 
ENST00000542442, ENST00000342989, 
ENST00000459821, 
ENST00000477219, 
ENST00000266182, ENST00000440475, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score7 X 7 X 6=2941 X 1 X 1=1
# samples 81
** MAII scorelog2(8/294*10)=-1.877744249949
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Fusion gene context

PubMed: BRD1 [Title/Abstract] AND TTLL8 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: BRD1 [Title/Abstract] AND TTLL8 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)BRD1(50216599)-TTLL8(50472891), # samples:1
Anticipated loss of major functional domain due to fusion event.BRD1-TTLL8 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.
BRD1-TTLL8 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.
BRD1-TTLL8 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.
BRD1-TTLL8 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.
BRD1-TTLL8 seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
BRD1-TTLL8 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
BRD1-TTLL8 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
BRD1-TTLL8 seems lost the major protein functional domain in Tgene partner, which is a essential 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
HgeneBRD1

GO:0043966

histone H3 acetylation

16387653



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/chr22:50216599/chr22:50472891)
- 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 BRD1 (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 TTLL8 (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)
ENST00000216267BRD1chr2250216599-ENST00000266182TTLL8chr2250472891-3438185418063437543
ENST00000404034BRD1chr2250216599-ENST00000440475TTLL8chr2250472891-312415521311864577
ENST00000404760BRD1chr2250216599-ENST00000440475TTLL8chr2250472891-29691397301709559
ENST00000457780BRD1chr2250216599-ENST00000266182TTLL8chr2250472891-2967138313352966543
ENST00000542442BRD1chr2250216599-ENST00000266182TTLL8chr2250472891-19353513031934543

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
ENST00000216267ENST00000266182BRD1chr2250216599-TTLL8chr2250472891-0.1008338850.89916605
ENST00000404034ENST00000440475BRD1chr2250216599-TTLL8chr2250472891-0.0118436370.98815644
ENST00000404760ENST00000440475BRD1chr2250216599-TTLL8chr2250472891-0.0148658630.9851341
ENST00000457780ENST00000266182BRD1chr2250216599-TTLL8chr2250472891-0.145560790.8544392
ENST00000542442ENST00000266182BRD1chr2250216599-TTLL8chr2250472891-0.151281280.84871876

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 BRD1-TTLL8

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
BRD1chr2250216599TTLL8chr2250472891138316PADRVRSLYSPAECQALLNRITSVNP
BRD1chr2250216599TTLL8chr2250472891185416PADRVRSLYSPAECQALLNRITSVNP
BRD1chr2250216599TTLL8chr225047289135116PADRVRSLYSPAECQALLNRITSVNP

Top

Potential FusionNeoAntigen Information of BRD1-TTLL8 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.
BRD1-TTLL8_50216599_50472891.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)
BRD1-TTLL8chr2250216599chr22504728911854HLA-B35:03SPAECQAL0.69940.757917
BRD1-TTLL8chr2250216599chr22504728911854HLA-B35:02SPAECQAL0.47740.8791917
BRD1-TTLL8chr2250216599chr22504728911854HLA-B35:04SPAECQAL0.47740.8791917
BRD1-TTLL8chr2250216599chr22504728911854HLA-B35:03SPAECQALL0.95860.7538918
BRD1-TTLL8chr2250216599chr22504728911854HLA-B35:08SPAECQALL0.93190.5566918
BRD1-TTLL8chr2250216599chr22504728911854HLA-B35:04SPAECQALL0.82530.8461918
BRD1-TTLL8chr2250216599chr22504728911854HLA-B35:02SPAECQALL0.82530.8461918
BRD1-TTLL8chr2250216599chr22504728911854HLA-B35:03YSPAECQALL0.84310.8099818
BRD1-TTLL8chr2250216599chr22504728911854HLA-B35:04YSPAECQALL0.68730.8862818
BRD1-TTLL8chr2250216599chr22504728911854HLA-B35:02YSPAECQALL0.68730.8862818
BRD1-TTLL8chr2250216599chr22504728911854HLA-B39:10SPAECQAL0.47980.7677917
BRD1-TTLL8chr2250216599chr22504728911854HLA-B35:12SPAECQAL0.47740.8791917
BRD1-TTLL8chr2250216599chr22504728911854HLA-C03:08YSPAECQAL0.99480.7404817
BRD1-TTLL8chr2250216599chr22504728911854HLA-C01:17YSPAECQAL0.8790.8424817
BRD1-TTLL8chr2250216599chr22504728911854HLA-C08:03YSPAECQAL0.86010.9416817
BRD1-TTLL8chr2250216599chr22504728911854HLA-B35:12SPAECQALL0.82530.8461918
BRD1-TTLL8chr2250216599chr22504728911854HLA-B39:10SPAECQALL0.70510.7392918
BRD1-TTLL8chr2250216599chr22504728911854HLA-C01:30YSPAECQAL0.56370.874817
BRD1-TTLL8chr2250216599chr22504728911854HLA-C01:17YSPAECQALL0.97190.8064818
BRD1-TTLL8chr2250216599chr22504728911854HLA-C01:30YSPAECQALL0.86530.8488818
BRD1-TTLL8chr2250216599chr22504728911854HLA-B35:12YSPAECQALL0.68730.8862818
BRD1-TTLL8chr2250216599chr22504728911854HLA-B35:09SPAECQAL0.47740.8791917
BRD1-TTLL8chr2250216599chr22504728911854HLA-B67:01SPAECQAL0.44350.6552917
BRD1-TTLL8chr2250216599chr22504728911854HLA-C03:03YSPAECQAL0.99820.9715817
BRD1-TTLL8chr2250216599chr22504728911854HLA-C03:04YSPAECQAL0.99820.9715817
BRD1-TTLL8chr2250216599chr22504728911854HLA-C03:17YSPAECQAL0.99460.9275817
BRD1-TTLL8chr2250216599chr22504728911854HLA-B35:13SPAECQALL0.9440.7501918
BRD1-TTLL8chr2250216599chr22504728911854HLA-C03:06YSPAECQAL0.91050.972817
BRD1-TTLL8chr2250216599chr22504728911854HLA-C08:01YSPAECQAL0.86010.9416817
BRD1-TTLL8chr2250216599chr22504728911854HLA-C01:02YSPAECQAL0.85390.8378817
BRD1-TTLL8chr2250216599chr22504728911854HLA-B35:09SPAECQALL0.82530.8461918
BRD1-TTLL8chr2250216599chr22504728911854HLA-C01:03YSPAECQAL0.77770.7661817
BRD1-TTLL8chr2250216599chr22504728911854HLA-B67:01SPAECQALL0.69720.6114918
BRD1-TTLL8chr2250216599chr22504728911854HLA-C01:03YSPAECQALL0.98840.741818
BRD1-TTLL8chr2250216599chr22504728911854HLA-C01:02YSPAECQALL0.98080.7992818
BRD1-TTLL8chr2250216599chr22504728911854HLA-C14:02LYSPAECQAL0.97470.881717
BRD1-TTLL8chr2250216599chr22504728911854HLA-C14:03LYSPAECQAL0.97470.881717
BRD1-TTLL8chr2250216599chr22504728911854HLA-B35:09YSPAECQALL0.68730.8862818

Top

Potential FusionNeoAntigen Information of BRD1-TTLL8 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)

Top

Fusion breakpoint peptide structures of BRD1-TTLL8

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
8817SLYSPAECQALLNRBRD1TTLL8chr2250216599chr22504728911854

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of BRD1-TTLL8

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-B14:023BVN8817SLYSPAECQALLNR-6.75571-7.27981
HLA-B14:023BVN8817SLYSPAECQALLNR-4.33758-5.78358
HLA-B52:013W398817SLYSPAECQALLNR-5.55407-6.07817
HLA-B52:013W398817SLYSPAECQALLNR-4.85332-6.29932
HLA-B18:014JQV8817SLYSPAECQALLNR-3.58782-5.03382
HLA-B18:014JQV8817SLYSPAECQALLNR-2.61875-3.14285
HLA-A11:014UQ28817SLYSPAECQALLNR-9.45593-9.98003
HLA-A11:014UQ28817SLYSPAECQALLNR-7.56411-9.01011
HLA-A24:025HGA8817SLYSPAECQALLNR-8.80176-9.32586
HLA-A24:025HGA8817SLYSPAECQALLNR-5.17364-6.61964
HLA-B27:056PYJ8817SLYSPAECQALLNR-3.60482-4.12892
HLA-B27:056PYJ8817SLYSPAECQALLNR-3.57445-5.02045
HLA-B27:036PZ58817SLYSPAECQALLNR-3.43431-4.88031
HLA-B27:036PZ58817SLYSPAECQALLNR10000.510000
HLA-B44:053DX88817SLYSPAECQALLNR-7.53677-8.06087
HLA-B44:053DX88817SLYSPAECQALLNR-3.2142-4.6602
HLA-A02:016TDR8817SLYSPAECQALLNR-3.55142-4.07552

Top

Vaccine Design for the FusionNeoAntigens of BRD1-TTLL8

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
BRD1-TTLL8chr2250216599chr2250472891717LYSPAECQALTTATATTCCCCCGCAGAGTGCCAGGCTCTG
BRD1-TTLL8chr2250216599chr2250472891817YSPAECQALTATTCCCCCGCAGAGTGCCAGGCTCTG
BRD1-TTLL8chr2250216599chr2250472891818YSPAECQALLTATTCCCCCGCAGAGTGCCAGGCTCTGCTG
BRD1-TTLL8chr2250216599chr2250472891917SPAECQALTCCCCCGCAGAGTGCCAGGCTCTG
BRD1-TTLL8chr2250216599chr2250472891918SPAECQALLTCCCCCGCAGAGTGCCAGGCTCTGCTG

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

Top

Information of the samples that have these potential fusion neoantigens of BRD1-TTLL8

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
BRCABRD1-TTLL8chr2250216599ENST00000216267chr2250472891ENST00000266182TCGA-AN-A0FJ-01A

Top

Potential target of CAR-T therapy development for BRD1-TTLL8

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 BRD1-TTLL8

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

Top

Related Diseases to BRD1-TTLL8

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