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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:CCAR1-BLMH

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CCAR1-BLMH
FusionPDB ID: 13514
FusionGDB2.0 ID: 13514
HgeneTgene
Gene symbol

CCAR1

BLMH

Gene ID

55749

642

Gene namecell division cycle and apoptosis regulator 1bleomycin hydrolase
Synonyms-BH|BMH
Cytomap

10q21.3

17q11.2

Type of geneprotein-codingprotein-coding
Descriptioncell division cycle and apoptosis regulator protein 1cell cycle and apoptosis regulatory protein 1death inducer with SAP domainbleomycin hydrolaseBLM hydrolase
Modification date2020031320200313
UniProtAcc

Q8IX12

Main function of 5'-partner protein: FUNCTION: Associates with components of the Mediator and p160 coactivator complexes that play a role as intermediaries transducing regulatory signals from upstream transcriptional activator proteins to basal transcription machinery at the core promoter. Recruited to endogenous nuclear receptor target genes in response to the appropriate hormone. Also functions as a p53 coactivator. May thus play an important role in transcriptional regulation (By similarity). May be involved in apoptosis signaling in the presence of the reinoid CD437. Apoptosis induction involves sequestration of 14-3-3 protein(s) and mediated altered expression of multiple cell cycle regulatory genes including MYC, CCNB1 and CDKN1A. Plays a role in cell cycle progression and/or cell proliferation (PubMed:12816952). In association with CALCOCO1 enhances GATA1- and MED1-mediated transcriptional activation from the gamma-globin promoter during erythroid differentiation of K562 erythroleukemia cells (PubMed:24245781). Can act as a both a coactivator and corepressor of AR-mediated transcription. Contributes to chromatin looping and AR transcription complex assembly by stabilizing AR-GATA2 association on chromatin and facilitating MED1 and RNA polymerase II recruitment to AR-binding sites. May play an important role in the growth and tumorigenesis of prostate cancer cells (PubMed:23887938). {ECO:0000250|UniProtKB:Q8CH18, ECO:0000269|PubMed:12816952, ECO:0000269|PubMed:23887938, ECO:0000269|PubMed:24245781}.

Q13867

Main function of 5'-partner protein: FUNCTION: The normal physiological role of BLM hydrolase is unknown, but it catalyzes the inactivation of the antitumor drug BLM (a glycopeptide) by hydrolyzing the carboxamide bond of its B-aminoalaninamide moiety thus protecting normal and malignant cells from BLM toxicity. {ECO:0000250}.
Ensembl transtripts involved in fusion geneENST idsENST00000265872, ENST00000535016, 
ENST00000543719, ENST00000483264, 
ENST00000582669, ENST00000261714, 
ENST00000394819, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score13 X 11 X 8=11449 X 10 X 8=720
# samples 1711
** MAII scorelog2(17/1144*10)=-2.75048040064069
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/720*10)=-2.71049338280502
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CCAR1 [Title/Abstract] AND BLMH [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CCAR1 [Title/Abstract] AND BLMH [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CCAR1(70517134)-BLMH(28614965), # samples:1
Anticipated loss of major functional domain due to fusion event.CCAR1-BLMH 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.
CCAR1-BLMH 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.
CCAR1-BLMH 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.
CCAR1-BLMH 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
HgeneCCAR1

GO:0043065

positive regulation of apoptotic process

12816952



check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr10:70517134/chr17:28614965)
- 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 CCAR1 (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 BLMH (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)
ENST00000535016CCAR1chr1070517134+ENST00000261714BLMHchr1728614965-385819941193040973
ENST00000535016CCAR1chr1070517134+ENST00000394819BLMHchr1728614965-322619941193040973
ENST00000265872CCAR1chr1070517134+ENST00000261714BLMHchr1728614965-390320391193085988
ENST00000265872CCAR1chr1070517134+ENST00000394819BLMHchr1728614965-327120391193085988
ENST00000543719CCAR1chr1070517134+ENST00000261714BLMHchr1728614965-385219881133034973
ENST00000543719CCAR1chr1070517134+ENST00000394819BLMHchr1728614965-322019881133034973

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
ENST00000535016ENST00000261714CCAR1chr1070517134+BLMHchr1728614965-0.0005693670.9994306
ENST00000535016ENST00000394819CCAR1chr1070517134+BLMHchr1728614965-0.00088730.99911267
ENST00000265872ENST00000261714CCAR1chr1070517134+BLMHchr1728614965-0.0005620510.999438
ENST00000265872ENST00000394819CCAR1chr1070517134+BLMHchr1728614965-0.0009174850.99908257
ENST00000543719ENST00000261714CCAR1chr1070517134+BLMHchr1728614965-0.000553370.9994466
ENST00000543719ENST00000394819CCAR1chr1070517134+BLMHchr1728614965-0.0008513980.9991486

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 CCAR1-BLMH

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CCAR1chr1070517134BLMHchr17286149651988625PTHWSKLDPKTMKVERCYFFLSAFVD
CCAR1chr1070517134BLMHchr17286149651994625PTHWSKLDPKTMKVERCYFFLSAFVD
CCAR1chr1070517134BLMHchr17286149652039640PTHWSKLDPKTMKVERCYFFLSAFVD

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Potential FusionNeoAntigen Information of CCAR1-BLMH 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.
CCAR1-BLMH_70517134_28614965.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)
CCAR1-BLMHchr1070517134chr17286149652039HLA-B57:01KTMKVERCY0.99480.7687918
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:60KLDPKTMKV0.99470.5761514
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:30KLDPKTMKV0.99430.5828514
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:67KLDPKTMKV0.99430.5828514
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:24KLDPKTMKV0.99430.5828514
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:11KLDPKTMKV0.99410.6105514
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:13KLDPKTMKV0.99190.5856514
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:21KLDPKTMKV0.99190.689514
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:38KLDPKTMKV0.99120.6087514
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:27KLDPKTMKV0.98990.5288514
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:04KLDPKTMKV0.98890.6061514
CCAR1-BLMHchr1070517134chr17286149652039HLA-B15:17KTMKVERCY0.98580.6276918
CCAR1-BLMHchr1070517134chr17286149652039HLA-B58:02KTMKVERCY0.98320.6178918
CCAR1-BLMHchr1070517134chr17286149652039HLA-B58:01KTMKVERCY0.97460.5467918
CCAR1-BLMHchr1070517134chr17286149652039HLA-B57:03KTMKVERCY0.95610.7873918
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:29KLDPKTMKV0.94830.589514
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:20KLDPKTMKV0.91130.5855514
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:35KLDPKTMKV0.85270.6032514
CCAR1-BLMHchr1070517134chr17286149652039HLA-A30:08KLDPKTMKV0.7890.7658514
CCAR1-BLMHchr1070517134chr17286149652039HLA-A32:13KLDPKTMKV0.63070.9419514
CCAR1-BLMHchr1070517134chr17286149652039HLA-A32:13KTMKVERCY0.61940.6803918
CCAR1-BLMHchr1070517134chr17286149652039HLA-B13:01KLDPKTMKV0.14880.9314514
CCAR1-BLMHchr1070517134chr17286149652039HLA-B08:09KLDPKTMKV0.10780.5921514
CCAR1-BLMHchr1070517134chr17286149652039HLA-B52:01KLDPKTMKV0.01210.8723514
CCAR1-BLMHchr1070517134chr17286149652039HLA-B57:01KTMKVERCYF0.99960.8468919
CCAR1-BLMHchr1070517134chr17286149652039HLA-B58:02KTMKVERCYF0.99890.6965919
CCAR1-BLMHchr1070517134chr17286149652039HLA-B58:01KTMKVERCYF0.99670.6546919
CCAR1-BLMHchr1070517134chr17286149652039HLA-B57:03KTMKVERCYF0.99640.8656919
CCAR1-BLMHchr1070517134chr17286149652039HLA-B15:17KTMKVERCYF0.99520.6735919
CCAR1-BLMHchr1070517134chr17286149652039HLA-A32:13KTMKVERCYF0.96470.6933919
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:67SKLDPKTMKV0.60650.531414
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:30SKLDPKTMKV0.60650.531414
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:24SKLDPKTMKV0.60650.531414
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:60SKLDPKTMKV0.59610.519414
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:35SKLDPKTMKV0.52450.5482414
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:11SKLDPKTMKV0.52240.5593414
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:20SKLDPKTMKV0.43980.5321414
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:29SKLDPKTMKV0.41520.5379414
CCAR1-BLMHchr1070517134chr17286149652039HLA-B57:01KTMKVERCYFF0.99990.8864920
CCAR1-BLMHchr1070517134chr17286149652039HLA-B58:02KTMKVERCYFF0.99940.7577920
CCAR1-BLMHchr1070517134chr17286149652039HLA-B57:03KTMKVERCYFF0.99920.9014920
CCAR1-BLMHchr1070517134chr17286149652039HLA-B58:01KTMKVERCYFF0.99720.7141920
CCAR1-BLMHchr1070517134chr17286149652039HLA-A74:11KLDPKTMKVER0.99620.745516
CCAR1-BLMHchr1070517134chr17286149652039HLA-A74:03KLDPKTMKVER0.99620.745516
CCAR1-BLMHchr1070517134chr17286149652039HLA-A74:09KLDPKTMKVER0.99620.745516
CCAR1-BLMHchr1070517134chr17286149652039HLA-A31:02KLDPKTMKVER0.99530.7704516
CCAR1-BLMHchr1070517134chr17286149652039HLA-A31:06KLDPKTMKVER0.99210.6328516
CCAR1-BLMHchr1070517134chr17286149652039HLA-C05:09KLDPKTMKV0.99990.9235514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C04:10KLDPKTMKV0.99980.9202514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C04:07KLDPKTMKV0.99960.9114514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C08:15KLDPKTMKV0.99740.9778514
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:01KLDPKTMKV0.99430.5828514
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:07KLDPKTMKV0.99410.5725514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C01:17KLDPKTMKV0.98570.9088514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C04:06KLDPKTMKV0.96520.9097514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C15:06KLDPKTMKV0.95840.8359514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C01:30KLDPKTMKV0.84940.9553514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C04:14KLDPKTMKV0.83740.905514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C02:06KLDPKTMKV0.6810.9178514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C15:04KTMKVERCY0.56020.7907918
CCAR1-BLMHchr1070517134chr17286149652039HLA-C08:13KLDPKTMKV0.37640.9434514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C08:04KLDPKTMKV0.37640.9434514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C08:03KLDPKTMKV0.2760.9778514
CCAR1-BLMHchr1070517134chr17286149652039HLA-B39:08KLDPKTMKV0.21660.8458514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C07:19KLDPKTMKV0.20350.7736514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C07:05KLDPKTMKV0.20080.9546514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C07:13KLDPKTMKV0.08330.9385514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C07:29KLDPKTMKV0.0620.9506514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C07:27KLDPKTMKV0.03880.962514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C05:09SKLDPKTMKV0.99850.8946414
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:07SKLDPKTMKV0.61040.5134414
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:01SKLDPKTMKV0.60650.531414
CCAR1-BLMHchr1070517134chr17286149652039HLA-A31:01KLDPKTMKVER0.99660.7413516
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:07WSKLDPKTMKV0.87250.5536314
CCAR1-BLMHchr1070517134chr17286149652039HLA-C04:03KLDPKTMKV0.99990.9159514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C05:01KLDPKTMKV0.99990.9235514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C18:01KLDPKTMKV0.99980.9125514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C04:01KLDPKTMKV0.99960.9114514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C01:03KLDPKTMKV0.99840.8827514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C08:02KLDPKTMKV0.99740.9778514
CCAR1-BLMHchr1070517134chr17286149652039HLA-B57:10KTMKVERCY0.99480.7687918
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:03KLDPKTMKV0.99410.6097514
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:14KLDPKTMKV0.9920.5929514
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:06KLDPKTMKV0.99190.689514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C01:02KLDPKTMKV0.98680.9029514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C15:02KLDPKTMKV0.9860.7906514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C15:05KLDPKTMKV0.98110.8552514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C06:06KLDPKTMKV0.9790.9879514
CCAR1-BLMHchr1070517134chr17286149652039HLA-B15:35KTMKVERCY0.94030.7231918
CCAR1-BLMHchr1070517134chr17286149652039HLA-A32:01KTMKVERCY0.92750.7866918
CCAR1-BLMHchr1070517134chr17286149652039HLA-C04:04KLDPKTMKV0.89190.8872514
CCAR1-BLMHchr1070517134chr17286149652039HLA-B15:20KTMKVERCY0.77930.6906918
CCAR1-BLMHchr1070517134chr17286149652039HLA-C17:01KLDPKTMKV0.72170.689514
CCAR1-BLMHchr1070517134chr17286149652039HLA-A32:01KLDPKTMKV0.7040.9642514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C15:09KTMKVERCY0.56020.7907918
CCAR1-BLMHchr1070517134chr17286149652039HLA-C08:01KLDPKTMKV0.2760.9778514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C16:02KTMKVERCY0.0670.973918
CCAR1-BLMHchr1070517134chr17286149652039HLA-C07:04KLDPKTMKV0.04060.9638514
CCAR1-BLMHchr1070517134chr17286149652039HLA-B08:12KLDPKTMKV0.02960.5994514
CCAR1-BLMHchr1070517134chr17286149652039HLA-C07:01KLDPKTMKV0.02530.7037514
CCAR1-BLMHchr1070517134chr17286149652039HLA-B07:13KLDPKTMKV0.01230.7235514
CCAR1-BLMHchr1070517134chr17286149652039HLA-B57:10KTMKVERCYF0.99960.8468919
CCAR1-BLMHchr1070517134chr17286149652039HLA-C05:01SKLDPKTMKV0.99850.8946414
CCAR1-BLMHchr1070517134chr17286149652039HLA-B58:06KTMKVERCYF0.99840.5147919
CCAR1-BLMHchr1070517134chr17286149652039HLA-C04:03SKLDPKTMKV0.99820.8715414
CCAR1-BLMHchr1070517134chr17286149652039HLA-C18:01SKLDPKTMKV0.99430.8583414
CCAR1-BLMHchr1070517134chr17286149652039HLA-A32:01KTMKVERCYF0.99370.848919
CCAR1-BLMHchr1070517134chr17286149652039HLA-B57:02KTMKVERCYF0.99060.692919
CCAR1-BLMHchr1070517134chr17286149652039HLA-C07:04SKLDPKTMKV0.78570.9214414
CCAR1-BLMHchr1070517134chr17286149652039HLA-A02:03SKLDPKTMKV0.74170.5192414
CCAR1-BLMHchr1070517134chr17286149652039HLA-B57:10KTMKVERCYFF0.99990.8864920
CCAR1-BLMHchr1070517134chr17286149652039HLA-B58:06KTMKVERCYFF0.99920.5646920
CCAR1-BLMHchr1070517134chr17286149652039HLA-A32:01KTMKVERCYFF0.99810.8563920
CCAR1-BLMHchr1070517134chr17286149652039HLA-B57:02KTMKVERCYFF0.99670.7599920
CCAR1-BLMHchr1070517134chr17286149652039HLA-A74:01KLDPKTMKVER0.99620.745516

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Potential FusionNeoAntigen Information of CCAR1-BLMH 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.

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)

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Fusion breakpoint peptide structures of CCAR1-BLMH

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
4855LDPKTMKVERCYFFCCAR1BLMHchr1070517134chr17286149652039

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CCAR1-BLMH

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-B14:023BVN4855LDPKTMKVERCYFF-6.01316-6.12656
HLA-B14:023BVN4855LDPKTMKVERCYFF-3.92858-4.96388
HLA-B52:013W394855LDPKTMKVERCYFF-5.92102-6.95632
HLA-B52:013W394855LDPKTMKVERCYFF-4.84472-4.95812
HLA-A24:025HGA4855LDPKTMKVERCYFF-8.26357-9.29887
HLA-A24:025HGA4855LDPKTMKVERCYFF-7.03366-7.14706
HLA-B44:053DX84855LDPKTMKVERCYFF-6.13971-6.25311
HLA-B44:053DX84855LDPKTMKVERCYFF-5.20728-6.24258
HLA-A02:016TDR4855LDPKTMKVERCYFF-5.28864-5.40204

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Vaccine Design for the FusionNeoAntigens of CCAR1-BLMH

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
CCAR1-BLMHchr1070517134chr1728614965314WSKLDPKTMKVTGGTCTAAACTTGATCCAAAGACAATGAAGGTT
CCAR1-BLMHchr1070517134chr1728614965414SKLDPKTMKVTCTAAACTTGATCCAAAGACAATGAAGGTT
CCAR1-BLMHchr1070517134chr1728614965514KLDPKTMKVAAACTTGATCCAAAGACAATGAAGGTT
CCAR1-BLMHchr1070517134chr1728614965516KLDPKTMKVERAAACTTGATCCAAAGACAATGAAGGTTGAACGC
CCAR1-BLMHchr1070517134chr1728614965918KTMKVERCYAAGACAATGAAGGTTGAACGCTGTTAT
CCAR1-BLMHchr1070517134chr1728614965919KTMKVERCYFAAGACAATGAAGGTTGAACGCTGTTATTTC
CCAR1-BLMHchr1070517134chr1728614965920KTMKVERCYFFAAGACAATGAAGGTTGAACGCTGTTATTTCTTC

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

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Information of the samples that have these potential fusion neoantigens of CCAR1-BLMH

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
GBMCCAR1-BLMHchr1070517134ENST00000265872chr1728614965ENST00000261714TCGA-02-2483-01A

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Potential target of CAR-T therapy development for CCAR1-BLMH

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 CCAR1-BLMH

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 CCAR1-BLMH

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