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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:ATMIN-CAPN8

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ATMIN-CAPN8
FusionPDB ID: 7663
FusionGDB2.0 ID: 7663
HgeneTgene
Gene symbol

ATMIN

CAPN8

Gene ID

23300

388743

Gene nameATM interactorcalpain 8
SynonymsASCIZ|ZNF822nCL-2
Cytomap

16q23.2

1q41

Type of geneprotein-codingprotein-coding
DescriptionATM interactorATM INteracting proteinATM/ATR-Substrate Chk2-Interacting Zn++-finger proteinATM/ATR-substrate CHEK2-interacting zinc finger proteinATM/ATR-substrate CHK2-interacting zinc finger proteinzinc finger protein 822calpain-8new calpain 2stomach-specific M-type calpain
Modification date2020031520200313
UniProtAcc

O43313

Main function of 5'-partner protein: FUNCTION: Transcription factor. Plays a crucial role in cell survival and RAD51 foci formation in response to methylating DNA damage. Involved in regulating the activity of ATM in the absence of DNA damage. May play a role in stabilizing ATM. Binds to the DYNLL1 promoter and activates its transcription. {ECO:0000269|PubMed:15933716, ECO:0000269|PubMed:17525732, ECO:0000269|PubMed:22167198}.

A6NHC0

Main function of 5'-partner protein: FUNCTION: Calcium-regulated non-lysosomal thiol-protease. Involved in membrane trafficking in the gastric surface mucus cells (pit cells) and may involve the membrane trafficking of mucus cells via interactions with coat protein. Proteolytically cleaves the beta-subunit of coatomer complex (By similarity). {ECO:0000250}.
Ensembl transtripts involved in fusion geneENST idsENST00000299575, ENST00000539819, 
ENST00000564241, ENST00000566488, 
ENST00000366873, ENST00000366872, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 5 X 4=12012 X 2 X 4=96
# samples 612
** MAII scorelog2(6/120*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/96*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Fusion gene context

PubMed: ATMIN [Title/Abstract] AND CAPN8 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ATMIN [Title/Abstract] AND CAPN8 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ATMIN(81069811)-CAPN8(223718212), # samples:1
Anticipated loss of major functional domain due to fusion event.ATMIN-CAPN8 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.
ATMIN-CAPN8 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.
ATMIN-CAPN8 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.
ATMIN-CAPN8 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
HgeneATMIN

GO:0045893

positive regulation of transcription, DNA-templated

22167198



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/chr16:81069811/chr1:223718212)
- 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 ATMIN (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 CAPN8 (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)
ENST00000299575ATMINchr1681069811+ENST00000366872CAPN8chr1223718212-85536024638204

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
ENST00000299575ENST00000366872ATMINchr1681069811+CAPN8chr1223718212-0.0087764030.9912236

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 ATMIN-CAPN8

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ATMINchr1681069811CAPN8chr1223718212360110SPALNMHLVKSHRLQEIYWETDYNHS

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Potential FusionNeoAntigen Information of ATMIN-CAPN8 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.
ATMIN-CAPN8_81069811_223718212.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)
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B27:02HRLQEIYW0.99970.77221119
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B15:18SHRLQEIY0.88640.72121018
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B57:01KSHRLQEIY0.9980.9414918
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B39:01MHLVKSHRL0.9970.7772514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B39:06MHLVKSHRL0.99660.5714514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B58:02KSHRLQEIY0.9960.8625918
ATMIN-CAPN8chr1681069811chr1223718212360HLA-A02:60RLQEIYWET0.99420.61911221
ATMIN-CAPN8chr1681069811chr1223718212360HLA-A02:30RLQEIYWET0.99420.61521221
ATMIN-CAPN8chr1681069811chr1223718212360HLA-A02:24RLQEIYWET0.99420.61521221
ATMIN-CAPN8chr1681069811chr1223718212360HLA-A02:67RLQEIYWET0.99420.61521221
ATMIN-CAPN8chr1681069811chr1223718212360HLA-A02:11RLQEIYWET0.99410.63361221
ATMIN-CAPN8chr1681069811chr1223718212360HLA-A02:22RLQEIYWET0.99380.65561221
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B15:17KSHRLQEIY0.99320.8942918
ATMIN-CAPN8chr1681069811chr1223718212360HLA-A02:21RLQEIYWET0.99260.69871221
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B58:01KSHRLQEIY0.99250.8527918
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B38:02MHLVKSHRL0.99240.9128514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B14:01MHLVKSHRL0.99180.5154514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B14:02MHLVKSHRL0.99180.5154514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B38:01MHLVKSHRL0.99170.8874514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-A02:16RLQEIYWET0.99150.55411221
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B15:16KSHRLQEIY0.98840.8163918
ATMIN-CAPN8chr1681069811chr1223718212360HLA-A02:27RLQEIYWET0.98750.63071221
ATMIN-CAPN8chr1681069811chr1223718212360HLA-A02:13RLQEIYWET0.98210.7021221
ATMIN-CAPN8chr1681069811chr1223718212360HLA-A02:04RLQEIYWET0.98110.80121221
ATMIN-CAPN8chr1681069811chr1223718212360HLA-A02:17RLQEIYWET0.97290.65681221
ATMIN-CAPN8chr1681069811chr1223718212360HLA-A02:29RLQEIYWET0.89430.61241221
ATMIN-CAPN8chr1681069811chr1223718212360HLA-A02:19RLQEIYWET0.89140.51861221
ATMIN-CAPN8chr1681069811chr1223718212360HLA-A02:35RLQEIYWET0.8680.62631221
ATMIN-CAPN8chr1681069811chr1223718212360HLA-A02:20RLQEIYWET0.85870.6231221
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B08:01MHLVKSHRL0.73330.6452514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B15:18MHLVKSHRL0.69820.6267514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B08:09MHLVKSHRL0.62440.7157514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B38:01SHRLQEIYW0.47760.95221019
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B38:02SHRLQEIYW0.4290.94821019
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B57:01KSHRLQEIYW0.99990.9638919
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B58:02KSHRLQEIYW0.99960.9346919
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B58:01KSHRLQEIYW0.99940.8955919
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B57:03KSHRLQEIYW0.99880.9743919
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B39:12MHLVKSHRL0.99640.7923514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-A02:01RLQEIYWET0.99420.61521221
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B39:05MHLVKSHRL0.9910.7541514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-C15:04KSHRLQEIY0.87670.8478918
ATMIN-CAPN8chr1681069811chr1223718212360HLA-C07:13MHLVKSHRL0.7640.846514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-C07:29MHLVKSHRL0.76140.9096514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-C07:27MHLVKSHRL0.75140.9494514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-C07:80MHLVKSHRL0.6960.9129514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-C07:67MHLVKSHRL0.6960.9129514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-C07:46MHLVKSHRL0.62860.7515514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-C07:10MHLVKSHRL0.5720.9426514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B14:03MHLVKSHRL0.23980.6213514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-C12:16MHLVKSHRL0.00420.9675514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B73:01HRLQEIYWET0.99430.81411121
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B57:10KSHRLQEIY0.9980.9414918
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B39:31MHLVKSHRL0.99680.7895514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B39:02MHLVKSHRL0.99640.7593514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B15:135KSHRLQEIY0.99550.8977918
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B57:04KSHRLQEIY0.99540.7189918
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B58:06KSHRLQEIY0.99540.7277918
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B15:35KSHRLQEIY0.99410.8546918
ATMIN-CAPN8chr1681069811chr1223718212360HLA-A02:06RLQEIYWET0.99260.69871221
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B38:05MHLVKSHRL0.99170.8874514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B15:50KSHRLQEIY0.99110.8294918
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B15:09MHLVKSHRL0.93040.6375514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B35:28KSHRLQEIY0.89820.8984918
ATMIN-CAPN8chr1681069811chr1223718212360HLA-C15:09KSHRLQEIY0.87670.8478918
ATMIN-CAPN8chr1681069811chr1223718212360HLA-C07:17MHLVKSHRL0.74060.9587514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B08:18MHLVKSHRL0.73330.6452514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-C06:08VKSHRLQEI0.72160.9896817
ATMIN-CAPN8chr1681069811chr1223718212360HLA-C07:02MHLVKSHRL0.6960.9129514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B08:12MHLVKSHRL0.69250.8166514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B38:05SHRLQEIYW0.47760.95221019
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B39:11MHLVKSHRL0.45580.7633514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-C03:67MHLVKSHRL0.42820.9717514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-C07:04MHLVKSHRL0.42150.8729514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-C06:17VKSHRLQEI0.14760.9902817
ATMIN-CAPN8chr1681069811chr1223718212360HLA-C06:02VKSHRLQEI0.14760.9902817
ATMIN-CAPN8chr1681069811chr1223718212360HLA-C06:06MHLVKSHRL0.05820.986514
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B57:10KSHRLQEIYW0.99990.9638919
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B57:04KSHRLQEIYW0.99970.7979919
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B58:06KSHRLQEIYW0.99920.8679919
ATMIN-CAPN8chr1681069811chr1223718212360HLA-B57:02KSHRLQEIYW0.99560.9336919

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Potential FusionNeoAntigen Information of ATMIN-CAPN8 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.
ATMIN-CAPN8_81069811_223718212.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)
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0701PALNMHLVKSHRLQE116
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0701ALNMHLVKSHRLQEI217
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0701SPALNMHLVKSHRLQ015
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0703PALNMHLVKSHRLQE116
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0703ALNMHLVKSHRLQEI217
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0703SPALNMHLVKSHRLQ015
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0704PALNMHLVKSHRLQE116
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0704ALNMHLVKSHRLQEI217
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0705PALNMHLVKSHRLQE116
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0705ALNMHLVKSHRLQEI217
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0705SPALNMHLVKSHRLQ015
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0706PALNMHLVKSHRLQE116
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0706ALNMHLVKSHRLQEI217
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0706SPALNMHLVKSHRLQ015
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0707PALNMHLVKSHRLQE116
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0707ALNMHLVKSHRLQEI217
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0707SPALNMHLVKSHRLQ015
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0708PALNMHLVKSHRLQE116
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0708ALNMHLVKSHRLQEI217
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0708SPALNMHLVKSHRLQ015
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0709PALNMHLVKSHRLQE116
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0709ALNMHLVKSHRLQEI217
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0709SPALNMHLVKSHRLQ015
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0711PALNMHLVKSHRLQE116
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0711ALNMHLVKSHRLQEI217
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0712PALNMHLVKSHRLQE116
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0712ALNMHLVKSHRLQEI217
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0712SPALNMHLVKSHRLQ015
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0713PALNMHLVKSHRLQE116
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0713ALNMHLVKSHRLQEI217
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0713SPALNMHLVKSHRLQ015
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0714PALNMHLVKSHRLQE116
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0714ALNMHLVKSHRLQEI217
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0714SPALNMHLVKSHRLQ015
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0715PALNMHLVKSHRLQE116
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0715ALNMHLVKSHRLQEI217
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0715SPALNMHLVKSHRLQ015
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0716PALNMHLVKSHRLQE116
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0716ALNMHLVKSHRLQEI217
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0716SPALNMHLVKSHRLQ015
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0717PALNMHLVKSHRLQE116
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0717ALNMHLVKSHRLQEI217
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0717SPALNMHLVKSHRLQ015
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0719PALNMHLVKSHRLQE116
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0719ALNMHLVKSHRLQEI217
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-0719SPALNMHLVKSHRLQ015
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-1358LNMHLVKSHRLQEIY318
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-1381LNMHLVKSHRLQEIY318
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-1510ALNMHLVKSHRLQEI217
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-1510PALNMHLVKSHRLQE116
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-1521ALNMHLVKSHRLQEI217
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-1521PALNMHLVKSHRLQE116
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-1615PALNMHLVKSHRLQE116
ATMIN-CAPN8chr1681069811chr1223718212360DRB1-1615ALNMHLVKSHRLQEI217

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Fusion breakpoint peptide structures of ATMIN-CAPN8

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
3419HLVKSHRLQEIYWEATMINCAPN8chr1681069811chr1223718212360

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ATMIN-CAPN8

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-B14:023BVN3419HLVKSHRLQEIYWE-5.34942-6.38472
HLA-B14:023BVN3419HLVKSHRLQEIYWE-5.0153-5.1287
HLA-B52:013W393419HLVKSHRLQEIYWE-7.47358-7.58698
HLA-B52:013W393419HLVKSHRLQEIYWE-4.5023-5.5376
HLA-A11:014UQ23419HLVKSHRLQEIYWE-7.49832-7.61172
HLA-A24:025HGA3419HLVKSHRLQEIYWE-8.30687-8.42027
HLA-A24:025HGA3419HLVKSHRLQEIYWE-5.37786-6.41316
HLA-B27:056PYJ3419HLVKSHRLQEIYWE-6.81213-7.84743
HLA-B44:053DX83419HLVKSHRLQEIYWE-9.00919-9.12259
HLA-B44:053DX83419HLVKSHRLQEIYWE-3.81824-4.85354

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Vaccine Design for the FusionNeoAntigens of ATMIN-CAPN8

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
ATMIN-CAPN8chr1681069811chr12237182121018SHRLQEIYCGCCTGCAGGAGATCTATTGGGAA
ATMIN-CAPN8chr1681069811chr12237182121019SHRLQEIYWCGCCTGCAGGAGATCTATTGGGAAACT
ATMIN-CAPN8chr1681069811chr12237182121119HRLQEIYWCTGCAGGAGATCTATTGGGAAACT
ATMIN-CAPN8chr1681069811chr12237182121121HRLQEIYWETCTGCAGGAGATCTATTGGGAAACTGATTAT
ATMIN-CAPN8chr1681069811chr12237182121221RLQEIYWETCAGGAGATCTATTGGGAAACTGATTAT
ATMIN-CAPN8chr1681069811chr1223718212514MHLVKSHRLCTAGTCAAGAGCCACCGCCTGCAGGAG
ATMIN-CAPN8chr1681069811chr1223718212817VKSHRLQEIAGCCACCGCCTGCAGGAGATCTATTGG
ATMIN-CAPN8chr1681069811chr1223718212918KSHRLQEIYCACCGCCTGCAGGAGATCTATTGGGAA
ATMIN-CAPN8chr1681069811chr1223718212919KSHRLQEIYWCACCGCCTGCAGGAGATCTATTGGGAAACT

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
ATMIN-CAPN8chr1681069811chr1223718212015SPALNMHLVKSHRLQGCGCTCAACATGCACCTAGTCAAGAGCCACCGCCTGCAGGAGATC
ATMIN-CAPN8chr1681069811chr1223718212116PALNMHLVKSHRLQECTCAACATGCACCTAGTCAAGAGCCACCGCCTGCAGGAGATCTAT
ATMIN-CAPN8chr1681069811chr1223718212217ALNMHLVKSHRLQEIAACATGCACCTAGTCAAGAGCCACCGCCTGCAGGAGATCTATTGG
ATMIN-CAPN8chr1681069811chr1223718212318LNMHLVKSHRLQEIYATGCACCTAGTCAAGAGCCACCGCCTGCAGGAGATCTATTGGGAA

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Information of the samples that have these potential fusion neoantigens of ATMIN-CAPN8

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
Non-CancerATMIN-CAPN8chr1681069811ENST00000299575chr1223718212ENST00000366872131Nd

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Potential target of CAR-T therapy development for ATMIN-CAPN8

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 ATMIN-CAPN8

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 ATMIN-CAPN8

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