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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:HNRNPH1-TRAFD1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: HNRNPH1-TRAFD1
FusionPDB ID: 37203
FusionGDB2.0 ID: 37203
HgeneTgene
Gene symbol

HNRNPH1

TRAFD1

Gene ID

3187

10906

Gene nameheterogeneous nuclear ribonucleoprotein H1TRAF-type zinc finger domain containing 1
SynonymsHNRPH|HNRPH1|hnRNPHFLN29
Cytomap

5q35.3

12q24.13

Type of geneprotein-codingprotein-coding
Descriptionheterogeneous nuclear ribonucleoprotein Hepididymis secretory sperm binding proteinheterogeneous nuclear ribonucleoprotein H1 (H)TRAF-type zinc finger domain-containing protein 1FLN29 gene product
Modification date2020032020200313
UniProtAcc

P31943

Main function of 5'-partner protein: FUNCTION: This protein is a component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complexes which provide the substrate for the processing events that pre-mRNAs undergo before becoming functional, translatable mRNAs in the cytoplasm. Mediates pre-mRNA alternative splicing regulation. Inhibits, together with CUGBP1, insulin receptor (IR) pre-mRNA exon 11 inclusion in myoblast. Binds to the IR RNA. Binds poly(RG). {ECO:0000269|PubMed:11003644, ECO:0000269|PubMed:16946708}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000524180, ENST00000393432, 
ENST00000329433, ENST00000356731, 
ENST00000442819, ENST00000510411, 
ENST00000511300, 
ENST00000257604, 
ENST00000412615, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score21 X 18 X 8=30246 X 8 X 4=192
# samples 218
** MAII scorelog2(21/3024*10)=-3.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/192*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: HNRNPH1 [Title/Abstract] AND TRAFD1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: HNRNPH1 [Title/Abstract] AND TRAFD1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)HNRNPH1(179047892)-TRAFD1(112579892), # samples:1
Anticipated loss of major functional domain due to fusion event.HNRNPH1-TRAFD1 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.
HNRNPH1-TRAFD1 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.
HNRNPH1-TRAFD1 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.
HNRNPH1-TRAFD1 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.
HNRNPH1-TRAFD1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
HNRNPH1-TRAFD1 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
HNRNPH1-TRAFD1 seems lost the major protein functional domain in Tgene partner, which is a transcription 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
HgeneHNRNPH1

GO:0043484

regulation of RNA splicing

16946708



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/chr5:179047892/chr12:112579892)
- 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 HNRNPH1 (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 TRAFD1 (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)
ENST00000442819HNRNPH1chr5179047892-ENST00000412615TRAFD1chr12112579892+24285141171619500
ENST00000442819HNRNPH1chr5179047892-ENST00000257604TRAFD1chr12112579892+24325141171619500
ENST00000356731HNRNPH1chr5179047892-ENST00000412615TRAFD1chr12112579892+3847193315363038500
ENST00000356731HNRNPH1chr5179047892-ENST00000257604TRAFD1chr12112579892+3851193315363038500
ENST00000329433HNRNPH1chr5179047892-ENST00000412615TRAFD1chr12112579892+2346432351537500
ENST00000329433HNRNPH1chr5179047892-ENST00000257604TRAFD1chr12112579892+2350432351537500
ENST00000510411HNRNPH1chr5179047892-ENST00000412615TRAFD1chr12112579892+2347433361538500
ENST00000510411HNRNPH1chr5179047892-ENST00000257604TRAFD1chr12112579892+2351433361538500

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
ENST00000442819ENST00000412615HNRNPH1chr5179047892-TRAFD1chr12112579892+0.0010643270.99893564
ENST00000442819ENST00000257604HNRNPH1chr5179047892-TRAFD1chr12112579892+0.0010334690.9989666
ENST00000356731ENST00000412615HNRNPH1chr5179047892-TRAFD1chr12112579892+0.0014897490.9985102
ENST00000356731ENST00000257604HNRNPH1chr5179047892-TRAFD1chr12112579892+0.0014719850.998528
ENST00000329433ENST00000412615HNRNPH1chr5179047892-TRAFD1chr12112579892+0.0009601380.9990398
ENST00000329433ENST00000257604HNRNPH1chr5179047892-TRAFD1chr12112579892+0.0009370580.99906296
ENST00000510411ENST00000412615HNRNPH1chr5179047892-TRAFD1chr12112579892+0.0009692380.9990308
ENST00000510411ENST00000257604HNRNPH1chr5179047892-TRAFD1chr12112579892+0.0009459180.99905413

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 HNRNPH1-TRAFD1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
HNRNPH1chr5179047892TRAFD1chr121125798921933129GLPFGCSKEEIVQFFSVEEQERQERN
HNRNPH1chr5179047892TRAFD1chr12112579892432129GLPFGCSKEEIVQFFSVEEQERQERN
HNRNPH1chr5179047892TRAFD1chr12112579892433129GLPFGCSKEEIVQFFSVEEQERQERN
HNRNPH1chr5179047892TRAFD1chr12112579892514129GLPFGCSKEEIVQFFSVEEQERQERN

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Potential FusionNeoAntigen Information of HNRNPH1-TRAFD1 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.
HNRNPH1-TRAFD1_179047892_112579892.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)
HNRNPH1-TRAFD1chr5179047892chr12112579892432HLA-B45:01EEIVQFFSV0.99920.9285817
HNRNPH1-TRAFD1chr5179047892chr12112579892432HLA-B50:02EEIVQFFSV0.99510.5787817
HNRNPH1-TRAFD1chr5179047892chr12112579892432HLA-B18:01EEIVQFFSV0.93950.8914817
HNRNPH1-TRAFD1chr5179047892chr12112579892432HLA-A31:02QFFSVEEQER0.94480.5421222
HNRNPH1-TRAFD1chr5179047892chr12112579892432HLA-B40:06EEIVQFFSV0.99870.5445817
HNRNPH1-TRAFD1chr5179047892chr12112579892432HLA-B51:07EEIVQFFSV0.35640.6361817
HNRNPH1-TRAFD1chr5179047892chr12112579892432HLA-B40:04EEIVQFFSV0.99010.7612817
HNRNPH1-TRAFD1chr5179047892chr12112579892432HLA-B18:08EEIVQFFSV0.94780.8844817
HNRNPH1-TRAFD1chr5179047892chr12112579892432HLA-B18:05EEIVQFFSV0.93950.8914817
HNRNPH1-TRAFD1chr5179047892chr12112579892432HLA-B18:06EEIVQFFSV0.9310.9141817
HNRNPH1-TRAFD1chr5179047892chr12112579892432HLA-B18:03EEIVQFFSV0.88130.8825817
HNRNPH1-TRAFD1chr5179047892chr12112579892432HLA-B18:11EEIVQFFSV0.84450.7727817

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Potential FusionNeoAntigen Information of HNRNPH1-TRAFD1 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.
HNRNPH1-TRAFD1_179047892_112579892.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)
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0403KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0405KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0411KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0424KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0427KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0429KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0430KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0439KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0440KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0441KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0442KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0442EEIVQFFSVEEQERQ823
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0445KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0446KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0448KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0449KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0450KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0452KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0453KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0455KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0455EEIVQFFSVEEQERQ823
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0456KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0457KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0458KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0459KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0459EEIVQFFSVEEQERQ823
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0460KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0465KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0465EEIVQFFSVEEQERQ823
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0465SKEEIVQFFSVEEQE621
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0467KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0468KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0471KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0473KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0473EEIVQFFSVEEQERQ823
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0477KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0483KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0484KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0485KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0486KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0488KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0489KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0491KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0810KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-0812KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1410KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1457KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1457SKEEIVQFFSVEEQE621
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1457EEIVQFFSVEEQERQ823
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1501KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1504KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1505KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1506KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1507KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1509KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1512KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1512SKEEIVQFFSVEEQE621
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1512EEIVQFFSVEEQERQ823
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1512CSKEEIVQFFSVEEQ520
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1513KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1516KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1518KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1520KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1521KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1522KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1524KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1528KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1532KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1533KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1535KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1536KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1540KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1541KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1542KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1543KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1545KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1546KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1548KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB1-1549KEEIVQFFSVEEQER722
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB5-0101IVQFFSVEEQERQER1025
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB5-0101EIVQFFSVEEQERQE924
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB5-0102IVQFFSVEEQERQER1025
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB5-0103IVQFFSVEEQERQER1025
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB5-0104IVQFFSVEEQERQER1025
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB5-0104EIVQFFSVEEQERQE924
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB5-0105IVQFFSVEEQERQER1025
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB5-0105EIVQFFSVEEQERQE924
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB5-0108NIVQFFSVEEQERQER1025
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB5-0111IVQFFSVEEQERQER1025
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB5-0111EIVQFFSVEEQERQE924
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB5-0111VQFFSVEEQERQERN1126
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB5-0112IVQFFSVEEQERQER1025
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB5-0113IVQFFSVEEQERQER1025
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB5-0113EIVQFFSVEEQERQE924
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB5-0114IVQFFSVEEQERQER1025
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB5-0114EIVQFFSVEEQERQE924
HNRNPH1-TRAFD1chr5179047892chr12112579892432DRB5-0203IVQFFSVEEQERQER1025

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Fusion breakpoint peptide structures of HNRNPH1-TRAFD1

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
8682SKEEIVQFFSVEEQHNRNPH1TRAFD1chr5179047892chr12112579892432

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of HNRNPH1-TRAFD1

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-B14:023BVN8682SKEEIVQFFSVEEQ-7.15543-7.26883
HLA-B14:023BVN8682SKEEIVQFFSVEEQ-4.77435-5.80965
HLA-B52:013W398682SKEEIVQFFSVEEQ-6.80875-6.92215
HLA-B52:013W398682SKEEIVQFFSVEEQ-4.20386-5.23916
HLA-A11:014UQ28682SKEEIVQFFSVEEQ-7.5194-8.5547
HLA-A11:014UQ28682SKEEIVQFFSVEEQ-6.9601-7.0735
HLA-A24:025HGA8682SKEEIVQFFSVEEQ-7.52403-7.63743
HLA-A24:025HGA8682SKEEIVQFFSVEEQ-5.82433-6.85963
HLA-B27:056PYJ8682SKEEIVQFFSVEEQ-3.28285-4.31815
HLA-B44:053DX88682SKEEIVQFFSVEEQ-5.91172-6.94702
HLA-B44:053DX88682SKEEIVQFFSVEEQ-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of HNRNPH1-TRAFD1

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
HNRNPH1-TRAFD1chr5179047892chr121125798921222QFFSVEEQERCAGTTGAAGAACAAGAGAGGCAGGAAAGGA
HNRNPH1-TRAFD1chr5179047892chr12112579892817EEIVQFFSVTTCAGTTCTTCTCAGTTGAAGAACAAG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
HNRNPH1-TRAFD1chr5179047892chr121125798921025IVQFFSVEEQERQERTCTTCTCAGTTGAAGAACAAGAGAGGCAGGAAAGGAATAGAGGCC
HNRNPH1-TRAFD1chr5179047892chr121125798921126VQFFSVEEQERQERNTCTCAGTTGAAGAACAAGAGAGGCAGGAAAGGAATAGAGGCCAAC
HNRNPH1-TRAFD1chr5179047892chr12112579892520CSKEEIVQFFSVEEQAAGAAATTGTTCAGTTCTTCTCAGTTGAAGAACAAGAGAGGCAGG
HNRNPH1-TRAFD1chr5179047892chr12112579892621SKEEIVQFFSVEEQEAAATTGTTCAGTTCTTCTCAGTTGAAGAACAAGAGAGGCAGGAAA
HNRNPH1-TRAFD1chr5179047892chr12112579892722KEEIVQFFSVEEQERTTGTTCAGTTCTTCTCAGTTGAAGAACAAGAGAGGCAGGAAAGGA
HNRNPH1-TRAFD1chr5179047892chr12112579892823EEIVQFFSVEEQERQTTCAGTTCTTCTCAGTTGAAGAACAAGAGAGGCAGGAAAGGAATA
HNRNPH1-TRAFD1chr5179047892chr12112579892924EIVQFFSVEEQERQEAGTTCTTCTCAGTTGAAGAACAAGAGAGGCAGGAAAGGAATAGAG

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Information of the samples that have these potential fusion neoantigens of HNRNPH1-TRAFD1

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
OVHNRNPH1-TRAFD1chr5179047892ENST00000329433chr12112579892ENST00000257604TCGA-36-1571

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Potential target of CAR-T therapy development for HNRNPH1-TRAFD1

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

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Related Drugs to HNRNPH1-TRAFD1

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 HNRNPH1-TRAFD1

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