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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:SFPQ-FAM134B

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SFPQ-FAM134B
FusionPDB ID: 81132
FusionGDB2.0 ID: 81132
HgeneTgene
Gene symbol

SFPQ

FAM134B

Gene ID

654780

54463

Gene namesplicing factor proline/glutamine-richreticulophagy regulator 1
SynonymsSFPQFAM134B|JK-1|JK1
Cytomap

16q24.1

5p15.1

Type of genencRNAprotein-coding
Description-reticulophagy regulator 1family with sequence similarity 134 member Bprotein FAM134Breticulophagy receptor 1reticulophagy receptor FAM134B
Modification date2020030320200313
UniProtAcc

P23246

Main function of 5'-partner protein: FUNCTION: DNA- and RNA binding protein, involved in several nuclear processes. Essential pre-mRNA splicing factor required early in spliceosome formation and for splicing catalytic step II, probably as a heteromer with NONO. Binds to pre-mRNA in spliceosome C complex, and specifically binds to intronic polypyrimidine tracts. Involved in regulation of signal-induced alternative splicing. During splicing of PTPRC/CD45, a phosphorylated form is sequestered by THRAP3 from the pre-mRNA in resting T-cells; T-cell activation and subsequent reduced phosphorylation is proposed to lead to release from THRAP3 allowing binding to pre-mRNA splicing regulatotry elements which represses exon inclusion. Interacts with U5 snRNA, probably by binding to a purine-rich sequence located on the 3' side of U5 snRNA stem 1b. May be involved in a pre-mRNA coupled splicing and polyadenylation process as component of a snRNP-free complex with SNRPA/U1A. The SFPQ-NONO heteromer associated with MATR3 may play a role in nuclear retention of defective RNAs. SFPQ may be involved in homologous DNA pairing; in vitro, promotes the invasion of ssDNA between a duplex DNA and produces a D-loop formation. The SFPQ-NONO heteromer may be involved in DNA unwinding by modulating the function of topoisomerase I/TOP1; in vitro, stimulates dissociation of TOP1 from DNA after cleavage and enhances its jumping between separate DNA helices. The SFPQ-NONO heteromer binds DNA (PubMed:25765647). The SFPQ-NONO heteromer may be involved in DNA non-homologous end joining (NHEJ) required for double-strand break repair and V(D)J recombination and may stabilize paired DNA ends; in vitro, the complex strongly stimulates DNA end joining, binds directly to the DNA substrates and cooperates with the Ku70/G22P1-Ku80/XRCC5 (Ku) dimer to establish a functional preligation complex. SFPQ is involved in transcriptional regulation. Functions as transcriptional activator (PubMed:25765647). Transcriptional repression is mediated by an interaction of SFPQ with SIN3A and subsequent recruitment of histone deacetylases (HDACs). The SFPQ-NONO-NR5A1 complex binds to the CYP17 promoter and regulates basal and cAMP-dependent transcriptional activity. SFPQ isoform Long binds to the DNA binding domains (DBD) of nuclear hormone receptors, like RXRA and probably THRA, and acts as transcriptional corepressor in absence of hormone ligands. Binds the DNA sequence 5'-CTGAGTC-3' in the insulin-like growth factor response element (IGFRE) and inhibits IGF-I-stimulated transcriptional activity. Regulates the circadian clock by repressing the transcriptional activator activity of the CLOCK-ARNTL/BMAL1 heterodimer. Required for the transcriptional repression of circadian target genes, such as PER1, mediated by the large PER complex through histone deacetylation (By similarity). Required for the assembly of nuclear speckles (PubMed:25765647). Plays a role in the regulation of DNA virus-mediated innate immune response by assembling into the HDP-RNP complex, a complex that serves as a platform for IRF3 phosphorylation and subsequent innate immune response activation through the cGAS-STING pathway (PubMed:28712728). {ECO:0000250|UniProtKB:Q8VIJ6, ECO:0000269|PubMed:10847580, ECO:0000269|PubMed:10858305, ECO:0000269|PubMed:10931916, ECO:0000269|PubMed:11259580, ECO:0000269|PubMed:11525732, ECO:0000269|PubMed:11897684, ECO:0000269|PubMed:15590677, ECO:0000269|PubMed:20932480, ECO:0000269|PubMed:25765647, ECO:0000269|PubMed:28712728, ECO:0000269|PubMed:8045264, ECO:0000269|PubMed:8449401}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000357214, ENST00000468598, 
ENST00000399793, ENST00000509048, 
ENST00000306320, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score14 X 16 X 8=17929 X 6 X 6=324
# samples 1910
** MAII scorelog2(19/1792*10)=-3.23749931372666
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(10/324*10)=-1.6959938131099
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: SFPQ [Title/Abstract] AND FAM134B [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: SFPQ [Title/Abstract] AND FAM134B [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SFPQ(35654603)-FAM134B(16572211), # samples:1
Anticipated loss of major functional domain due to fusion event.SFPQ-FAM134B 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.
SFPQ-FAM134B 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.
SFPQ-FAM134B 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.
SFPQ-FAM134B 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/chr1:35654603/chr5:16572211)
- 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 SFPQ (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 FAM134B (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)
ENST00000357214SFPQchr135654603-ENST00000306320FAM134Bchr516572211-46571796872969960

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
ENST00000357214ENST00000306320SFPQchr135654603-FAM134Bchr516572211-0.0004615480.9995384

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 SFPQ-FAM134B

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
SFPQchr135654603FAM134Bchr5165722111796569HNQEMQKRKEMQLRFLALTPWRVYHL

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Potential FusionNeoAntigen Information of SFPQ-FAM134B 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.
SFPQ-FAM134B_35654603_16572211.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)
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B08:01MQLRFLAL0.99910.90211018
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B14:02MQLRFLAL0.99870.76161018
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B14:01MQLRFLAL0.99870.76161018
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B08:09MQLRFLAL0.99850.78681018
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B08:09EMQLRFLA0.99830.7411917
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B52:01MQLRFLAL0.81730.8961018
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:02KRKEMQLRF0.99980.6426615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:05KRKEMQLRF0.99980.9094615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:04KRKEMQLRF0.99970.7646615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B08:01EMQLRFLAL0.99860.85918
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:02LRFLALTPW0.99810.53761221
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B45:01KEMQLRFLA0.99770.7118817
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B08:09EMQLRFLAL0.99710.7698918
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:04LRFLALTPW0.99490.70611221
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B14:01EMQLRFLAL0.99470.5616918
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B14:02EMQLRFLAL0.99470.5616918
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B41:01KEMQLRFLA0.78830.8534817
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:05QKRKEMQLRF0.99960.6848515
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:04QKRKEMQLRF0.99940.6199515
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:02KRKEMQLRFL0.99940.5772616
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:05KRKEMQLRFL0.99940.8926616
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:04KRKEMQLRFL0.99930.7109616
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B39:13KEMQLRFLAL0.91840.841818
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B73:01LRFLALTP0.99870.93271220
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B14:03MQLRFLAL0.95190.79121018
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:14KRKEMQLRF0.99970.7816615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B42:02EMQLRFLAL0.99910.8408918
SFPQ-FAM134Bchr135654603chr5165722111796HLA-C07:95KRKEMQLRF0.99590.7969615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:03KRKEMQLRF0.99350.9215615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-C07:05KRKEMQLRF0.99310.965615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-C07:27KRKEMQLRF0.97880.9689615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-C07:29KRKEMQLRF0.9530.9614615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-C07:19KRKEMQLRF0.93670.8245615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-C07:67KRKEMQLRF0.90710.9712615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-C07:80KRKEMQLRF0.90710.9712615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-C07:13KRKEMQLRF0.89050.9556615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-C07:46KRKEMQLRF0.87290.9408615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-C07:10KRKEMQLRF0.86840.9679615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B14:03EMQLRFLAL0.81730.7363918
SFPQ-FAM134Bchr135654603chr5165722111796HLA-C12:16KRKEMQLRF0.07440.9756615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:03QKRKEMQLRF0.98950.7006515
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:03KRKEMQLRFL0.98520.9078616
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B40:06RKEMQLRFLA0.86660.6706717
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B08:18MQLRFLAL0.99910.90211018
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B08:12MQLRFLAL0.99820.94651018
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B41:03KEMQLRFL0.97910.5376816
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:08KRKEMQLRF0.99970.8022615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:10KRKEMQLRF0.99970.8957615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:06KRKEMQLRF0.99920.7417615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B08:18EMQLRFLAL0.99860.85918
SFPQ-FAM134Bchr135654603chr5165722111796HLA-C07:01KRKEMQLRF0.99790.7557615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:09KRKEMQLRF0.99660.8853615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B40:04KEMQLRFLA0.97670.5073817
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B08:12EMQLRFLAL0.96770.9032918
SFPQ-FAM134Bchr135654603chr5165722111796HLA-C07:17KRKEMQLRF0.93050.9742615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-C07:02KRKEMQLRF0.90710.9712615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-C06:08KRKEMQLRF0.87860.9744615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-C07:22KRKEMQLRF0.83230.7907615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-C06:06KRKEMQLRF0.15250.9925615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B15:68KRKEMQLRF0.14080.6678615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B15:54KRKEMQLRF0.10890.8991615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-C06:17KRKEMQLRF0.08830.9954615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-C06:02KRKEMQLRF0.08830.9954615
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:10QKRKEMQLRF0.99940.7357515
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:10KRKEMQLRFL0.99930.8783616
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:08KRKEMQLRFL0.99920.7413616
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:06KRKEMQLRFL0.99820.6999616
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B40:04KEMQLRFLAL0.99750.557818
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B27:09KRKEMQLRFL0.99580.8618616
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B39:02KEMQLRFLAL0.93180.8498818
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B41:03KEMQLRFLAL0.89090.709818
SFPQ-FAM134Bchr135654603chr5165722111796HLA-B15:24MQKRKEMQLRF0.99990.852415

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Potential FusionNeoAntigen Information of SFPQ-FAM134B 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.
SFPQ-FAM134B_35654603_16572211.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)
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0101MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0101QLRFLALTPWRVYHL1126
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0101EMQLRFLALTPWRVY924
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0103MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0103QLRFLALTPWRVYHL1126
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0105MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0105QLRFLALTPWRVYHL1126
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0105EMQLRFLALTPWRVY924
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0107MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0107QLRFLALTPWRVYHL1126
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0107EMQLRFLALTPWRVY924
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0109MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0109QLRFLALTPWRVYHL1126
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0109EMQLRFLALTPWRVY924
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0111MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0111QLRFLALTPWRVYHL1126
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0111EMQLRFLALTPWRVY924
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0113MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0113QLRFLALTPWRVYHL1126
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0113EMQLRFLALTPWRVY924
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0115MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0115QLRFLALTPWRVYHL1126
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0115EMQLRFLALTPWRVY924
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0117MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0117QLRFLALTPWRVYHL1126
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0117EMQLRFLALTPWRVY924
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0119MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0119QLRFLALTPWRVYHL1126
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0119EMQLRFLALTPWRVY924
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0121MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0121QLRFLALTPWRVYHL1126
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0125MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0125QLRFLALTPWRVYHL1126
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0125EMQLRFLALTPWRVY924
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0127MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0127QLRFLALTPWRVYHL1126
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0127EMQLRFLALTPWRVY924
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0129MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0129QLRFLALTPWRVYHL1126
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0129EMQLRFLALTPWRVY924
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0131MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0131QLRFLALTPWRVYHL1126
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-0131EMQLRFLALTPWRVY924
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1222MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1527MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1534MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1601MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1602MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1602QLRFLALTPWRVYHL1126
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1603MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1604MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1605MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1607MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1608MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1609MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1609QLRFLALTPWRVYHL1126
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1610MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1610QLRFLALTPWRVYHL1126
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1611MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1611QLRFLALTPWRVYHL1126
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1612MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1612QLRFLALTPWRVYHL1126
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1614MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1616MQLRFLALTPWRVYH1025
SFPQ-FAM134Bchr135654603chr5165722111796DRB1-1616QLRFLALTPWRVYHL1126

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Fusion breakpoint peptide structures of SFPQ-FAM134B

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
4559KRKEMQLRFLALTPSFPQFAM134Bchr135654603chr5165722111796

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of SFPQ-FAM134B

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-B14:023BVN4559KRKEMQLRFLALTP-5.50071-6.53601
HLA-B14:023BVN4559KRKEMQLRFLALTP-5.44997-5.56337
HLA-B52:013W394559KRKEMQLRFLALTP-6.87928-6.99268
HLA-B52:013W394559KRKEMQLRFLALTP-3.95744-4.99274
HLA-A24:025HGA4559KRKEMQLRFLALTP-7.30598-7.41938
HLA-A24:025HGA4559KRKEMQLRFLALTP-5.09366-6.12896
HLA-B44:053DX84559KRKEMQLRFLALTP-5.64505-5.75845
HLA-B44:053DX84559KRKEMQLRFLALTP-4.1878-5.2231
HLA-A02:016TDR4559KRKEMQLRFLALTP-0.0912853-1.12659

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Vaccine Design for the FusionNeoAntigens of SFPQ-FAM134B

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
SFPQ-FAM134Bchr135654603chr5165722111018MQLRFLALGCAATTGAGGTTCCTTGCATTGAC
SFPQ-FAM134Bchr135654603chr5165722111220LRFLALTPGAGGTTCCTTGCATTGACTCCATG
SFPQ-FAM134Bchr135654603chr5165722111221LRFLALTPWGAGGTTCCTTGCATTGACTCCATGGAG
SFPQ-FAM134Bchr135654603chr516572211415MQKRKEMQLRFGCAGAAACGTAAAGAAATGCAATTGAGGTTCCT
SFPQ-FAM134Bchr135654603chr516572211515QKRKEMQLRFGAAACGTAAAGAAATGCAATTGAGGTTCCT
SFPQ-FAM134Bchr135654603chr516572211615KRKEMQLRFACGTAAAGAAATGCAATTGAGGTTCCT
SFPQ-FAM134Bchr135654603chr516572211616KRKEMQLRFLACGTAAAGAAATGCAATTGAGGTTCCTTGC
SFPQ-FAM134Bchr135654603chr516572211717RKEMQLRFLATAAAGAAATGCAATTGAGGTTCCTTGCATT
SFPQ-FAM134Bchr135654603chr516572211816KEMQLRFLAGAAATGCAATTGAGGTTCCTTGC
SFPQ-FAM134Bchr135654603chr516572211817KEMQLRFLAAGAAATGCAATTGAGGTTCCTTGCATT
SFPQ-FAM134Bchr135654603chr516572211818KEMQLRFLALAGAAATGCAATTGAGGTTCCTTGCATTGAC
SFPQ-FAM134Bchr135654603chr516572211917EMQLRFLAAATGCAATTGAGGTTCCTTGCATT
SFPQ-FAM134Bchr135654603chr516572211918EMQLRFLALAATGCAATTGAGGTTCCTTGCATTGAC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
SFPQ-FAM134Bchr135654603chr5165722111025MQLRFLALTPWRVYHGCAATTGAGGTTCCTTGCATTGACTCCATGGAGAGTATATCACCT
SFPQ-FAM134Bchr135654603chr5165722111126QLRFLALTPWRVYHLATTGAGGTTCCTTGCATTGACTCCATGGAGAGTATATCACCTGAT
SFPQ-FAM134Bchr135654603chr516572211924EMQLRFLALTPWRVYAATGCAATTGAGGTTCCTTGCATTGACTCCATGGAGAGTATATCA

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Information of the samples that have these potential fusion neoantigens of SFPQ-FAM134B

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
LGGSFPQ-FAM134Bchr135654603ENST00000357214chr516572211ENST00000306320TCGA-HT-8110

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Potential target of CAR-T therapy development for SFPQ-FAM134B

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
TgeneFAM134Bchr1:35654603chr5:16572211ENST0000030632009119_1390498.0TransmembraneHelical
TgeneFAM134Bchr1:35654603chr5:16572211ENST0000030632009209_2290498.0TransmembraneHelical
TgeneFAM134Bchr1:35654603chr5:16572211ENST0000039979307119_1390357.0TransmembraneHelical
TgeneFAM134Bchr1:35654603chr5:16572211ENST0000039979307209_2290357.0TransmembraneHelical
TgeneFAM134Bchr1:35654603chr5:16572211ENST000003997930760_800357.0TransmembraneHelical
TgeneFAM134Bchr1:35654603chr5:16572211ENST000003997930796_1160357.0TransmembraneHelical

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 SFPQ-FAM134B

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 SFPQ-FAM134B

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
HgeneSFPQC4518356MiT family translocation renal cell carcinoma2ORPHANET
HgeneSFPQC0019693HIV Infections1CTD_human
HgeneSFPQC0037274Dermatologic disorders1CTD_human
HgeneSFPQC0274861Arsenic Poisoning, Inorganic1CTD_human
HgeneSFPQC0274862Nervous System, Organic Arsenic Poisoning1CTD_human
HgeneSFPQC0311375Arsenic Poisoning1CTD_human
HgeneSFPQC0751851Arsenic Encephalopathy1CTD_human
HgeneSFPQC0751852Arsenic Induced Polyneuropathy1CTD_human
HgeneSFPQC4505456HIV Coinfection1CTD_human