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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:NOS1AP-ASH1L

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: NOS1AP-ASH1L
FusionPDB ID: 59665
FusionGDB2.0 ID: 59665
HgeneTgene
Gene symbol

NOS1AP

ASH1L

Gene ID

9722

55870

Gene namenitric oxide synthase 1 adaptor proteinASH1 like histone lysine methyltransferase
Synonyms6330408P19Rik|CAPONASH1|ASH1L1|KMT2H|MRD52
Cytomap

1q23.3

1q22

Type of geneprotein-codingprotein-coding
Descriptioncarboxyl-terminal PDZ ligand of neuronal nitric oxide synthase proteinC-terminal PDZ domain ligand of neuronal nitric oxide synthase (CAPON)C-terminal PDZ ligand of neuronal nitric oxide synthase proteinligand of neuronal nitric oxide synthase with carhistone-lysine N-methyltransferase ASH1LASH1-like proteinabsent small and homeotic disks protein 1 homologash1 (absent, small, or homeotic)-likelysine N-methyltransferase 2Hprobable histone-lysine N-methyltransferase ASH1L
Modification date2020031320200313
UniProtAcc

O75052

Main function of 5'-partner protein: FUNCTION: Adapter protein involved in neuronal nitric-oxide (NO) synthesis regulation via its association with nNOS/NOS1. The complex formed with NOS1 and synapsins is necessary for specific NO and synapsin functions at a presynaptic level. Mediates an indirect interaction between NOS1 and RASD1 leading to enhance the ability of NOS1 to activate RASD1. Competes with DLG4 for interaction with NOS1, possibly affecting NOS1 activity by regulating the interaction between NOS1 and DLG4 (By similarity). {ECO:0000250}.

Q9NR48

Main function of 5'-partner protein: FUNCTION: Histone methyltransferase specifically trimethylating 'Lys-36' of histone H3 forming H3K36me3 (PubMed:21239497). Also monomethylates 'Lys-9' of histone H3 (H3K9me1) in vitro (By similarity). The physiological significance of the H3K9me1 activity is unclear (By similarity). {ECO:0000250|UniProtKB:Q99MY8, ECO:0000269|PubMed:21239497}.
Ensembl transtripts involved in fusion geneENST idsENST00000361897, ENST00000530878, 
ENST00000454693, ENST00000493151, 
ENST00000548830, ENST00000368346, 
ENST00000392403, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score15 X 9 X 8=108017 X 13 X 7=1547
# samples 1818
** MAII scorelog2(18/1080*10)=-2.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(18/1547*10)=-3.10340438511936
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: NOS1AP [Title/Abstract] AND ASH1L [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: NOS1AP [Title/Abstract] AND ASH1L [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)NOS1AP(162257226)-ASH1L(155452240), # samples:1
Anticipated loss of major functional domain due to fusion event.NOS1AP-ASH1L 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.
NOS1AP-ASH1L 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.
NOS1AP-ASH1L 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.
NOS1AP-ASH1L 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
HgeneNOS1AP

GO:0098974

postsynaptic actin cytoskeleton organization

26869880

TgeneASH1L

GO:0097676

histone H3-K36 dimethylation

26002201



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/chr1:162257226/chr1:155452240)
- 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 NOS1AP (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 ASH1L (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)
ENST00000530878NOS1APchr1162257226+ENST00000368346ASH1Lchr1155452240-1155667422191632980
ENST00000530878NOS1APchr1162257226+ENST00000392403ASH1Lchr1155452240-1075467422191482975
ENST00000361897NOS1APchr1162257226+ENST00000368346ASH1Lchr1155452240-1155467221991612980
ENST00000361897NOS1APchr1162257226+ENST00000392403ASH1Lchr1155452240-1075267221991462975

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
ENST00000530878ENST00000368346NOS1APchr1162257226+ASH1Lchr1155452240-0.0002465750.9997534
ENST00000530878ENST00000392403NOS1APchr1162257226+ASH1Lchr1155452240-0.0002396580.9997603
ENST00000361897ENST00000368346NOS1APchr1162257226+ASH1Lchr1155452240-0.000246010.999754
ENST00000361897ENST00000392403NOS1APchr1162257226+ASH1Lchr1155452240-0.0002392590.9997607

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 NOS1AP-ASH1L

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
NOS1APchr1162257226ASH1Lchr1155452240672151VDGVKVILKKKKKDPSKLYKKADDVA
NOS1APchr1162257226ASH1Lchr1155452240674151VDGVKVILKKKKKDPSKLYKKADDVA

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Potential FusionNeoAntigen Information of NOS1AP-ASH1L 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.
NOS1AP-ASH1L_162257226_155452240.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)
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-B15:03KKKDPSKLY0.09890.77431019
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-B15:03KKKKDPSKLY0.87390.7147919
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-C07:95KKKDPSKLY0.88340.64691019
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-C07:27KKKDPSKLY0.83560.91071019
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-C07:19KKKDPSKLY0.75260.61871019
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-C07:46KKKDPSKLY0.6350.79271019
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-B15:07KKKDPSKLY0.2830.6461019
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-C12:16KKKDPSKLY0.01640.89721019
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-C07:01KKKDPSKLY0.91480.62961019
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-C07:22KKKDPSKLY0.46470.60081019
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-B15:50KKKDPSKLY0.3930.76931019
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-B15:35KKKDPSKLY0.31440.87191019
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-B48:02KKKDPSKLY0.16630.88371019
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-B15:53KKKDPSKLY0.07990.86871019
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-B15:54KKKDPSKLY0.03140.85971019
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-B15:68KKKKDPSKL0.02970.5749918
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-B15:54KKKKDPSKL0.02080.8585918
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-B15:68KKKDPSKLY0.010.56431019
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-B15:54KKKKDPSKLY0.95220.8254919
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-A30:01KKKDPSKLYK0.94830.69991020
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-B15:68KKKKDPSKLY0.89310.5427919
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-B15:54KKKKKDPSKLY0.99410.7983819
NOS1AP-ASH1Lchr1162257226chr1155452240672HLA-B15:68KKKKKDPSKLY0.99120.5247819

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Potential FusionNeoAntigen Information of NOS1AP-ASH1L 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.
NOS1AP-ASH1L_162257226_155452240.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)
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-0828VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1102VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1102GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1102DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1103GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1103DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1103VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1103VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1111GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1111DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1111VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1111VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1116VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1116GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1116DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1121VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1121GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1121DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1125VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1136VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1136GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1136DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1141GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1141DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1141VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1141VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1142VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1148VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1148GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1148DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1155GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1155DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1155VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1155VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1155KVILKKKKKDPSKLY419
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1157VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1159GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1159VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1159DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1159VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1163GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1163DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1163VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1163VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1165VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1165GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1165DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1167VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1168VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1168GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1170VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1170GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1170DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1170VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1176GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1176DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1176VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1176VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1185GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1185DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1185VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1185VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1186VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1186DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1186GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1192VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1192DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1192GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1301VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1301GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1301DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1304GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1304DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1304VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1304VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1308VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1308GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1308DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1309VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1315VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1315DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1315GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1315VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1316VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1316DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1316GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1317VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1317DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1317GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1318VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1319VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1319DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1319GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1319VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1320VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1320GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1320DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1322VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1322GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1322DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1324GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1324DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1324VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1324VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1327VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1327DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1327GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1329VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1329GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1332GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1332DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1332VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1332VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1335VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1335GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1335DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1338GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1338DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1338VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1338VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1343GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1343DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1343VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1348GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1348DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1348VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1348VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1351VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1351GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1351DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1352VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1352GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1352DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1353VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1353DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1353GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1353VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1354GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1354VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1354DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1357VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1357DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1357GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1357VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1359VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1359GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1359DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1361VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1361DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1361GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1363GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1363DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1363VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1363VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1364VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1364GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1364DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1365GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1365DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1365VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1365VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1368VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1368GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1368DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1369VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1369GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1369DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1370VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1370GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1370DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1371VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1371DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1371GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1372VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1372GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1372DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1375GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1375DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1375VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1375VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1375KVILKKKKKDPSKLY419
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1376GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1376VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1376DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1378VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1378GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1378DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1379VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1379GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1379DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1380VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1380GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1380DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1383VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1383GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1383DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1384VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1384GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1384DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1387VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1387GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1387DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1391VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1391GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1391DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1392VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1392GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1392DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1393GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1393DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1393VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1393VKVILKKKKKDPSKL318
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1398VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1398GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1398DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1412VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1416GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1416DGVKVILKKKKKDPS116
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1416VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1478GVKVILKKKKKDPSK217
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1478VDGVKVILKKKKKDP015
NOS1AP-ASH1Lchr1162257226chr1155452240672DRB1-1478DGVKVILKKKKKDPS116

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Fusion breakpoint peptide structures of NOS1AP-ASH1L

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
3792ILKKKKKDPSKLYKNOS1APASH1Lchr1162257226chr1155452240672

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of NOS1AP-ASH1L

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-B14:023BVN3792ILKKKKKDPSKLYK-7.9962-8.1096
HLA-B14:023BVN3792ILKKKKKDPSKLYK-5.70842-6.74372
HLA-B52:013W393792ILKKKKKDPSKLYK-6.83737-6.95077
HLA-B52:013W393792ILKKKKKDPSKLYK-4.4836-5.5189
HLA-A11:014UQ23792ILKKKKKDPSKLYK-10.0067-10.1201
HLA-A11:014UQ23792ILKKKKKDPSKLYK-9.03915-10.0745
HLA-A24:025HGA3792ILKKKKKDPSKLYK-6.56204-6.67544
HLA-A24:025HGA3792ILKKKKKDPSKLYK-5.42271-6.45801
HLA-B44:053DX83792ILKKKKKDPSKLYK-7.85648-8.89178
HLA-B44:053DX83792ILKKKKKDPSKLYK-5.3978-5.5112
HLA-A02:016TDR3792ILKKKKKDPSKLYK-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of NOS1AP-ASH1L

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
NOS1AP-ASH1Lchr1162257226chr11554522401019KKKDPSKLYAAGAAAAAGGACCCTTCAAAGTTGTAC
NOS1AP-ASH1Lchr1162257226chr11554522401020KKKDPSKLYKAAGAAAAAGGACCCTTCAAAGTTGTACAAG
NOS1AP-ASH1Lchr1162257226chr1155452240819KKKKKDPSKLYAAGAAGAAGAAAAAGGACCCTTCAAAGTTGTAC
NOS1AP-ASH1Lchr1162257226chr1155452240918KKKKDPSKLAAGAAGAAAAAGGACCCTTCAAAGTTG
NOS1AP-ASH1Lchr1162257226chr1155452240919KKKKDPSKLYAAGAAGAAAAAGGACCCTTCAAAGTTGTAC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
NOS1AP-ASH1Lchr1162257226chr1155452240015VDGVKVILKKKKKDPGTGGATGGAGTGAAAGTGATTCTGAAGAAGAAGAAAAAGGACCCT
NOS1AP-ASH1Lchr1162257226chr1155452240116DGVKVILKKKKKDPSGATGGAGTGAAAGTGATTCTGAAGAAGAAGAAAAAGGACCCTTCA
NOS1AP-ASH1Lchr1162257226chr1155452240217GVKVILKKKKKDPSKGGAGTGAAAGTGATTCTGAAGAAGAAGAAAAAGGACCCTTCAAAG
NOS1AP-ASH1Lchr1162257226chr1155452240318VKVILKKKKKDPSKLGTGAAAGTGATTCTGAAGAAGAAGAAAAAGGACCCTTCAAAGTTG
NOS1AP-ASH1Lchr1162257226chr1155452240419KVILKKKKKDPSKLYAAAGTGATTCTGAAGAAGAAGAAAAAGGACCCTTCAAAGTTGTAC

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Information of the samples that have these potential fusion neoantigens of NOS1AP-ASH1L

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
LUADNOS1AP-ASH1Lchr1162257226ENST00000361897chr1155452240ENST00000368346TCGA-L9-A444-01A

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Potential target of CAR-T therapy development for NOS1AP-ASH1L

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 NOS1AP-ASH1L

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 NOS1AP-ASH1L

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