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:NRBF2-EYA2

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: NRBF2-EYA2
FusionPDB ID: 60197
FusionGDB2.0 ID: 60197
HgeneTgene
Gene symbol

NRBF2

EYA2

Gene ID

29982

2139

Gene namenuclear receptor binding factor 2EYA transcriptional coactivator and phosphatase 2
SynonymsCOPR|COPR1|COPR2|NRBF-2EAB1
Cytomap

10q21.3

20q13.12

Type of geneprotein-codingprotein-coding
Descriptionnuclear receptor-binding factor 2comodulator of PPAR and RXR 1comodulator of PPAR and RXR 2eyes absent homolog 2
Modification date2020031320200313
UniProtAcc

Q96F24

Main function of 5'-partner protein: FUNCTION: May modulate transcriptional activation by target nuclear receptors. Can act as transcriptional activator (in vitro). {ECO:0000269|PubMed:15610520}.; FUNCTION: Involved in starvation-induced autophagy probably by its association with PI3K complex I (PI3KC3-C1). However, effects has been described variably. Involved in the induction of starvation-induced autophagy (PubMed:24785657). Stabilzes PI3KC3-C1 assembly and enhances ATG14-linked lipid kinase activity of PIK3C3 (By similarity). Proposed to negatively regulate basal and starvation-induced autophagy and to inhibit PIK3C3 activity by modulating interactions in PI3KC3-C1 (PubMed:25086043). May be involved in autophagosome biogenesis (PubMed:25086043). May play a role in neural progenitor cell survival during differentiation (By similarity). {ECO:0000250|UniProtKB:Q8VCQ3, ECO:0000269|PubMed:24785657, ECO:0000269|PubMed:25086043}.

O00167

Main function of 5'-partner protein: FUNCTION: Functions both as protein phosphatase and as transcriptional coactivator for SIX1, and probably also for SIX2, SIX4 and SIX5 (PubMed:12500905, PubMed:23435380). Tyrosine phosphatase that dephosphorylates 'Tyr-142' of histone H2AX (H2AXY142ph) and promotes efficient DNA repair via the recruitment of DNA repair complexes containing MDC1. 'Tyr-142' phosphorylation of histone H2AX plays a central role in DNA repair and acts as a mark that distinguishes between apoptotic and repair responses to genotoxic stress (PubMed:19351884). Its function as histone phosphatase may contribute to its function in transcription regulation during organogenesis. Plays an important role in hypaxial muscle development together with SIX1 and DACH2; in this it is functionally redundant with EYA1 (PubMed:12500905). {ECO:0000269|PubMed:12500905, ECO:0000269|PubMed:19351884, ECO:0000269|PubMed:21706047, ECO:0000269|PubMed:23435380}.
Ensembl transtripts involved in fusion geneENST idsENST00000277746, ENST00000435510, 
ENST00000317304, ENST00000497428, 
ENST00000327619, ENST00000357410, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score9 X 6 X 5=27015 X 15 X 10=2250
# samples 1030
** MAII scorelog2(10/270*10)=-1.43295940727611
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(30/2250*10)=-2.90689059560852
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: NRBF2 [Title/Abstract] AND EYA2 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: NRBF2 [Title/Abstract] AND EYA2 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)NRBF2(64893260)-EYA2(45771698), # samples:1
Anticipated loss of major functional domain due to fusion event.NRBF2-EYA2 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.
NRBF2-EYA2 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.
NRBF2-EYA2 seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor 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
TgeneEYA2

GO:0016576

histone dephosphorylation

19351884



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/chr10:64893260/chr20:45771698)
- 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 NRBF2 (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 EYA2 (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)
ENST00000277746NRBF2chr1064893260+ENST00000357410EYA2chr2045771698+141421164702212
ENST00000277746NRBF2chr1064893260+ENST00000327619EYA2chr2045771698+165121164939291

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
ENST00000277746ENST00000357410NRBF2chr1064893260+EYA2chr2045771698+0.0023512370.9976488
ENST00000277746ENST00000327619NRBF2chr1064893260+EYA2chr2045771698+0.0015926620.9984073

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 NRBF2-EYA2

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
NRBF2chr1064893260EYA2chr204577169821149PGSMEVMEGPLNLDTTTSVRIGLMME

Top

Potential FusionNeoAntigen Information of NRBF2-EYA2 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.
NRBF2-EYA2_64893260_45771698.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)
NRBF2-EYA2chr1064893260chr2045771698211HLA-C05:09NLDTTTSV10.98151119
NRBF2-EYA2chr1064893260chr2045771698211HLA-C08:15NLDTTTSV0.99950.97891119
NRBF2-EYA2chr1064893260chr2045771698211HLA-C04:03NLDTTTSV10.92241119
NRBF2-EYA2chr1064893260chr2045771698211HLA-C05:01NLDTTTSV10.98151119
NRBF2-EYA2chr1064893260chr2045771698211HLA-C08:02NLDTTTSV0.99950.97891119

Top

Potential FusionNeoAntigen Information of NRBF2-EYA2 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.
NRBF2-EYA2_64893260_45771698.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)
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0310EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0310MEGPLNLDTTTSVRI621
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0315EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0326EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0326MEGPLNLDTTTSVRI621
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0338EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0338MEGPLNLDTTTSVRI621
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0342EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0342MEGPLNLDTTTSVRI621
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0422EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0422MEGPLNLDTTTSVRI621
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0701EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0701GPLNLDTTTSVRIGL823
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0701PLNLDTTTSVRIGLM924
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0703EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0703GPLNLDTTTSVRIGL823
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0703PLNLDTTTSVRIGLM924
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0705EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0705GPLNLDTTTSVRIGL823
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0705PLNLDTTTSVRIGLM924
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0707EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0707GPLNLDTTTSVRIGL823
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0707PLNLDTTTSVRIGLM924
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0708EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0708GPLNLDTTTSVRIGL823
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0708PLNLDTTTSVRIGLM924
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0709GPLNLDTTTSVRIGL823
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0709EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0712EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0712GPLNLDTTTSVRIGL823
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0712PLNLDTTTSVRIGLM924
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0713EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0713GPLNLDTTTSVRIGL823
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0713PLNLDTTTSVRIGLM924
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0714EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0714GPLNLDTTTSVRIGL823
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0714PLNLDTTTSVRIGLM924
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0715EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0715GPLNLDTTTSVRIGL823
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0715PLNLDTTTSVRIGLM924
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0716EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0716GPLNLDTTTSVRIGL823
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0716PLNLDTTTSVRIGLM924
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0717EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0717GPLNLDTTTSVRIGL823
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0717PLNLDTTTSVRIGLM924
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0719EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0719GPLNLDTTTSVRIGL823
NRBF2-EYA2chr1064893260chr2045771698211DRB1-0719PLNLDTTTSVRIGLM924
NRBF2-EYA2chr1064893260chr2045771698211DRB1-1476EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB1-1476MEGPLNLDTTTSVRI621
NRBF2-EYA2chr1064893260chr2045771698211DRB1-1476VMEGPLNLDTTTSVR520
NRBF2-EYA2chr1064893260chr2045771698211DRB1-1479EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB1-1479MEGPLNLDTTTSVRI621
NRBF2-EYA2chr1064893260chr2045771698211DRB1-1479VMEGPLNLDTTTSVR520
NRBF2-EYA2chr1064893260chr2045771698211DRB1-1525EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0101EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0101MEGPLNLDTTTSVRI621
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0101VMEGPLNLDTTTSVR520
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0104EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0104MEGPLNLDTTTSVRI621
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0104VMEGPLNLDTTTSVR520
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0105EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0105MEGPLNLDTTTSVRI621
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0105VMEGPLNLDTTTSVR520
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0108EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0108MEGPLNLDTTTSVRI621
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0108VMEGPLNLDTTTSVR520
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0109EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0109MEGPLNLDTTTSVRI621
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0111EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0111MEGPLNLDTTTSVRI621
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0111VMEGPLNLDTTTSVR520
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0112EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0112MEGPLNLDTTTSVRI621
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0112VMEGPLNLDTTTSVR520
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0113EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0113MEGPLNLDTTTSVRI621
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0113VMEGPLNLDTTTSVR520
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0114EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0114MEGPLNLDTTTSVRI621
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0114VMEGPLNLDTTTSVR520
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0204EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0301EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0301MEGPLNLDTTTSVRI621
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0303EGPLNLDTTTSVRIG722
NRBF2-EYA2chr1064893260chr2045771698211DRB3-0303MEGPLNLDTTTSVRI621

Top

Fusion breakpoint peptide structures of NRBF2-EYA2

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
5883MEGPLNLDTTTSVRNRBF2EYA2chr1064893260chr2045771698211

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of NRBF2-EYA2

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-B14:023BVN5883MEGPLNLDTTTSVR-7.15543-7.26883
HLA-B14:023BVN5883MEGPLNLDTTTSVR-4.77435-5.80965
HLA-B52:013W395883MEGPLNLDTTTSVR-6.80875-6.92215
HLA-B52:013W395883MEGPLNLDTTTSVR-4.20386-5.23916
HLA-A11:014UQ25883MEGPLNLDTTTSVR-7.5194-8.5547
HLA-A11:014UQ25883MEGPLNLDTTTSVR-6.9601-7.0735
HLA-A24:025HGA5883MEGPLNLDTTTSVR-7.52403-7.63743
HLA-A24:025HGA5883MEGPLNLDTTTSVR-5.82433-6.85963
HLA-B27:056PYJ5883MEGPLNLDTTTSVR-3.28285-4.31815
HLA-B44:053DX85883MEGPLNLDTTTSVR-5.91172-6.94702
HLA-B44:053DX85883MEGPLNLDTTTSVR-4.24346-4.35686

Top

Vaccine Design for the FusionNeoAntigens of NRBF2-EYA2

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
NRBF2-EYA2chr1064893260chr20457716981119NLDTTTSVAACCTGGACACCACGACGTCCGTG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
NRBF2-EYA2chr1064893260chr2045771698520VMEGPLNLDTTTSVRGTAATGGAAGGACCCCTCAACCTGGACACCACGACGTCCGTGCGC
NRBF2-EYA2chr1064893260chr2045771698621MEGPLNLDTTTSVRIATGGAAGGACCCCTCAACCTGGACACCACGACGTCCGTGCGCATT
NRBF2-EYA2chr1064893260chr2045771698722EGPLNLDTTTSVRIGGAAGGACCCCTCAACCTGGACACCACGACGTCCGTGCGCATTGGC
NRBF2-EYA2chr1064893260chr2045771698823GPLNLDTTTSVRIGLGGACCCCTCAACCTGGACACCACGACGTCCGTGCGCATTGGCCTT
NRBF2-EYA2chr1064893260chr2045771698924PLNLDTTTSVRIGLMCCCCTCAACCTGGACACCACGACGTCCGTGCGCATTGGCCTTATG

Top

Information of the samples that have these potential fusion neoantigens of NRBF2-EYA2

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
OVNRBF2-EYA2chr1064893260ENST00000277746chr2045771698ENST00000327619TCGA-24-1842-01A

Top

Potential target of CAR-T therapy development for NRBF2-EYA2

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 NRBF2-EYA2

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

Top

Related Diseases to NRBF2-EYA2

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