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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:CLASRP-CALR

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CLASRP-CALR
FusionPDB ID: 16950
FusionGDB2.0 ID: 16950
HgeneTgene
Gene symbol

CLASRP

CALR

Gene ID

11129

811

Gene nameCLK4 associating serine/arginine rich proteincalreticulin
SynonymsCLASP|SFRS16|SWAP2CRT|HEL-S-99n|RO|SSA|cC1qR
Cytomap

19q13.32

19p13.13

Type of geneprotein-codingprotein-coding
DescriptionCLK4-associating serine/arginine rich proteinClk4 associating SR-related proteinsplicing factor, arginine/serine-rich 16 (suppressor-of-white-apricot homolog, Drosophila)suppressor of white apricot homolog 2calreticulinCRP55ERp60HACBPSicca syndrome antigen A (autoantigen Ro; calreticulin)calregulinendoplasmic reticulum resident protein 60epididymis secretory sperm binding protein Li 99ngrp60
Modification date2020031320200329
UniProtAcc

Q8N2M8

Main function of 5'-partner protein: FUNCTION: Probably functions as an alternative splicing regulator. May regulate the mRNA splicing of genes such as CLK1. May act by regulating members of the CLK kinase family (By similarity). {ECO:0000250}.

Q96L12

Main function of 5'-partner protein: FUNCTION: During spermatogenesis, may act as a lectin-independent chaperone for specific client proteins such as ADAM3. Required for sperm fertility (By similarity). CALR3 capacity for calcium-binding may be absent or much lower than that of CALR. {ECO:0000250, ECO:0000269|PubMed:21590275}.
Ensembl transtripts involved in fusion geneENST idsENST00000221455, ENST00000391953, 
ENST00000544944, 
ENST00000316448, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score16 X 12 X 9=172824 X 30 X 7=5040
# samples 1738
** MAII scorelog2(17/1728*10)=-3.34549656602577
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(38/5040*10)=-3.72935241005633
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CLASRP [Title/Abstract] AND CALR [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CLASRP [Title/Abstract] AND CALR [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CLASRP(45563700)-CALR(13054559), # samples:1
Anticipated loss of major functional domain due to fusion event.CLASRP-CALR 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.
CLASRP-CALR 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.
CLASRP-CALR 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.
CLASRP-CALR 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
TgeneCALR

GO:0000122

negative regulation of transcription by RNA polymerase II

8107809

TgeneCALR

GO:0006611

protein export from nucleus

11149926

TgeneCALR

GO:0017148

negative regulation of translation

14726956

TgeneCALR

GO:0033144

negative regulation of intracellular steroid hormone receptor signaling pathway

8107809

TgeneCALR

GO:0034504

protein localization to nucleus

15998798

TgeneCALR

GO:0045665

negative regulation of neuron differentiation

8107809

TgeneCALR

GO:0045892

negative regulation of transcription, DNA-templated

8107809

TgeneCALR

GO:0048387

negative regulation of retinoic acid receptor signaling pathway

8107809



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/chr19:45563700/chr19:13054559)
- 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 CLASRP (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 CALR (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)
ENST00000221455CLASRPchr1945563700+ENST00000316448CALRchr1913054559+1577833981000300
ENST00000391953CLASRPchr1945563700+ENST00000316448CALRchr1913054559+138564192808238
ENST00000544944CLASRPchr1945563700+ENST00000316448CALRchr1913054559+217114276921594300

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
ENST00000221455ENST00000316448CLASRPchr1945563700+CALRchr1913054559+0.0005146310.9994854
ENST00000391953ENST00000316448CLASRPchr1945563700+CALRchr1913054559+0.0003025440.99969745
ENST00000544944ENST00000316448CLASRPchr1945563700+CALRchr1913054559+0.0003719940.99962795

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 CLASRP-CALR

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CLASRPchr1945563700CALRchr19130545591427245GDFVSEEEKAMYSEEQRLKEEEEDKK
CLASRPchr1945563700CALRchr1913054559641183GDFVSEEEKAMYSEEQRLKEEEEDKK
CLASRPchr1945563700CALRchr1913054559833245GDFVSEEEKAMYSEEQRLKEEEEDKK

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Potential FusionNeoAntigen Information of CLASRP-CALR 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.
CLASRP-CALR_45563700_13054559.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)
CLASRP-CALRchr1945563700chr1913054559833HLA-A02:22AMYSEEQRL0.9960.5164918
CLASRP-CALRchr1945563700chr1913054559833HLA-A02:27AMYSEEQRL0.99420.5557918
CLASRP-CALRchr1945563700chr1913054559833HLA-A02:67AMYSEEQRL0.99330.5659918
CLASRP-CALRchr1945563700chr1913054559833HLA-A02:30AMYSEEQRL0.99330.5659918
CLASRP-CALRchr1945563700chr1913054559833HLA-A02:24AMYSEEQRL0.99330.5659918
CLASRP-CALRchr1945563700chr1913054559833HLA-A02:11AMYSEEQRL0.99230.5992918
CLASRP-CALRchr1945563700chr1913054559833HLA-A02:13AMYSEEQRL0.9920.5969918
CLASRP-CALRchr1945563700chr1913054559833HLA-A02:38AMYSEEQRL0.98560.6241918
CLASRP-CALRchr1945563700chr1913054559833HLA-A02:21AMYSEEQRL0.98340.7169918
CLASRP-CALRchr1945563700chr1913054559833HLA-A02:35AMYSEEQRL0.94410.5902918
CLASRP-CALRchr1945563700chr1913054559833HLA-A02:29AMYSEEQRL0.81780.5667918
CLASRP-CALRchr1945563700chr1913054559833HLA-A02:20AMYSEEQRL0.81370.5678918
CLASRP-CALRchr1945563700chr1913054559833HLA-B52:01AMYSEEQRL0.3510.9613918
CLASRP-CALRchr1945563700chr1913054559833HLA-B39:13AMYSEEQRL0.18980.9192918
CLASRP-CALRchr1945563700chr1913054559833HLA-B13:01AMYSEEQRL0.1070.949918
CLASRP-CALRchr1945563700chr1913054559833HLA-A02:01AMYSEEQRL0.99330.5659918
CLASRP-CALRchr1945563700chr1913054559833HLA-B15:04AMYSEEQRL0.96030.9374918
CLASRP-CALRchr1945563700chr1913054559833HLA-C14:03MYSEEQRL0.92690.96271018
CLASRP-CALRchr1945563700chr1913054559833HLA-C14:02MYSEEQRL0.92690.96271018
CLASRP-CALRchr1945563700chr1913054559833HLA-A02:03AMYSEEQRL0.99460.6295918
CLASRP-CALRchr1945563700chr1913054559833HLA-A02:14AMYSEEQRL0.98350.5905918
CLASRP-CALRchr1945563700chr1913054559833HLA-A02:06AMYSEEQRL0.98340.7169918
CLASRP-CALRchr1945563700chr1913054559833HLA-B15:73AMYSEEQRL0.9590.8635918
CLASRP-CALRchr1945563700chr1913054559833HLA-B15:30AMYSEEQRL0.90440.8339918
CLASRP-CALRchr1945563700chr1913054559833HLA-B39:02AMYSEEQRL0.30980.9153918

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Potential FusionNeoAntigen Information of CLASRP-CALR 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.
CLASRP-CALR_45563700_13054559.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)
CLASRP-CALRchr1945563700chr1913054559833DRB1-0801KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-0801EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-0805KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-0805EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-0816KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-0816EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-0818KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-0818EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-0826KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-0826EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-0829KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-0829EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-0839KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-0839EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-0840KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-0840EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-0840EEKAMYSEEQRLKEE621
CLASRP-CALRchr1945563700chr1913054559833DRB1-0840AMYSEEQRLKEEEED924
CLASRP-CALRchr1945563700chr1913054559833DRB1-1173KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1173EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1179KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1180KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1187KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1193KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1303KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1303EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1303EEKAMYSEEQRLKEE621
CLASRP-CALRchr1945563700chr1913054559833DRB1-1303AMYSEEQRLKEEEED924
CLASRP-CALRchr1945563700chr1913054559833DRB1-13101KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-13101EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-13101EEKAMYSEEQRLKEE621
CLASRP-CALRchr1945563700chr1913054559833DRB1-13101AMYSEEQRLKEEEED924
CLASRP-CALRchr1945563700chr1913054559833DRB1-1310KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1310EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1310EEKAMYSEEQRLKEE621
CLASRP-CALRchr1945563700chr1913054559833DRB1-1310AMYSEEQRLKEEEED924
CLASRP-CALRchr1945563700chr1913054559833DRB1-1312KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1312EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1312EEKAMYSEEQRLKEE621
CLASRP-CALRchr1945563700chr1913054559833DRB1-1313KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1313EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1321KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1321EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1321EEKAMYSEEQRLKEE621
CLASRP-CALRchr1945563700chr1913054559833DRB1-1330KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1330EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1330EEKAMYSEEQRLKEE621
CLASRP-CALRchr1945563700chr1913054559833DRB1-1333KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1333EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1333EEKAMYSEEQRLKEE621
CLASRP-CALRchr1945563700chr1913054559833DRB1-1333AMYSEEQRLKEEEED924
CLASRP-CALRchr1945563700chr1913054559833DRB1-1337KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1337EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1338KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1338EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1349KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1349EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1349EEKAMYSEEQRLKEE621
CLASRP-CALRchr1945563700chr1913054559833DRB1-1355KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1355EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1360KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1365KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1365EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1366KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1366EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1366EEKAMYSEEQRLKEE621
CLASRP-CALRchr1945563700chr1913054559833DRB1-1366AMYSEEQRLKEEEED924
CLASRP-CALRchr1945563700chr1913054559833DRB1-1388KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1388EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1388EEKAMYSEEQRLKEE621
CLASRP-CALRchr1945563700chr1913054559833DRB1-1388AMYSEEQRLKEEEED924
CLASRP-CALRchr1945563700chr1913054559833DRB1-1390KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1390EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1390EEKAMYSEEQRLKEE621
CLASRP-CALRchr1945563700chr1913054559833DRB1-1390AMYSEEQRLKEEEED924
CLASRP-CALRchr1945563700chr1913054559833DRB1-1395KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1395EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1395EEKAMYSEEQRLKEE621
CLASRP-CALRchr1945563700chr1913054559833DRB1-1395AMYSEEQRLKEEEED924
CLASRP-CALRchr1945563700chr1913054559833DRB1-1413KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1413EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1422KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1422EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1425KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1425EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1453KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1453EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1469KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1469EKAMYSEEQRLKEEE722
CLASRP-CALRchr1945563700chr1913054559833DRB1-1485KAMYSEEQRLKEEEE823
CLASRP-CALRchr1945563700chr1913054559833DRB1-1485EKAMYSEEQRLKEEE722

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Fusion breakpoint peptide structures of CLASRP-CALR

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
1671EEKAMYSEEQRLKECLASRPCALRchr1945563700chr1913054559833

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CLASRP-CALR

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-B14:023BVN1671EEKAMYSEEQRLKE-7.9962-8.1096
HLA-B14:023BVN1671EEKAMYSEEQRLKE-5.70842-6.74372
HLA-B52:013W391671EEKAMYSEEQRLKE-6.83737-6.95077
HLA-B52:013W391671EEKAMYSEEQRLKE-4.4836-5.5189
HLA-A11:014UQ21671EEKAMYSEEQRLKE-10.0067-10.1201
HLA-A11:014UQ21671EEKAMYSEEQRLKE-9.03915-10.0745
HLA-A24:025HGA1671EEKAMYSEEQRLKE-6.56204-6.67544
HLA-A24:025HGA1671EEKAMYSEEQRLKE-5.42271-6.45801
HLA-B44:053DX81671EEKAMYSEEQRLKE-7.85648-8.89178
HLA-B44:053DX81671EEKAMYSEEQRLKE-5.3978-5.5112
HLA-A02:016TDR1671EEKAMYSEEQRLKE-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of CLASRP-CALR

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
CLASRP-CALRchr1945563700chr19130545591018MYSEEQRLATGTACTCGGAGGAGCAGAGGCTT
CLASRP-CALRchr1945563700chr1913054559918AMYSEEQRLGCCATGTACTCGGAGGAGCAGAGGCTT

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
CLASRP-CALRchr1945563700chr1913054559621EEKAMYSEEQRLKEEGAGGAGAAGGCCATGTACTCGGAGGAGCAGAGGCTTAAGGAGGAG
CLASRP-CALRchr1945563700chr1913054559722EKAMYSEEQRLKEEEGAGAAGGCCATGTACTCGGAGGAGCAGAGGCTTAAGGAGGAGGAA
CLASRP-CALRchr1945563700chr1913054559823KAMYSEEQRLKEEEEAAGGCCATGTACTCGGAGGAGCAGAGGCTTAAGGAGGAGGAAGAA
CLASRP-CALRchr1945563700chr1913054559924AMYSEEQRLKEEEEDGCCATGTACTCGGAGGAGCAGAGGCTTAAGGAGGAGGAAGAAGAC

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Information of the samples that have these potential fusion neoantigens of CLASRP-CALR

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
BRCACLASRP-CALRchr1945563700ENST00000221455chr1913054559ENST00000316448TCGA-E2-A154-01A

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Potential target of CAR-T therapy development for CLASRP-CALR

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 CLASRP-CALR

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 CLASRP-CALR

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