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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:CLASP1-ANAPC1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CLASP1-ANAPC1
FusionPDB ID: 16929
FusionGDB2.0 ID: 16929
HgeneTgene
Gene symbol

CLASP1

ANAPC1

Gene ID

23332

64682

Gene namecytoplasmic linker associated protein 1anaphase promoting complex subunit 1
SynonymsMAST1APC1|MCPR|TSG24
Cytomap

2q14.2-q14.3

2q13

Type of geneprotein-codingprotein-coding
DescriptionCLIP-associating protein 1multiple asters 1multiple asters homolog 1protein Orbit homolog 1anaphase-promoting complex subunit 1anaphase-promoting complex 1 (meiotic checkpoint regulator)cyclosome subunit 1mitotic checkpoint regulatortestis-specific gene 24 protein
Modification date2020031320200313
UniProtAcc

Q7Z460

Main function of 5'-partner protein: FUNCTION: Microtubule plus-end tracking protein that promotes the stabilization of dynamic microtubules. Involved in the nucleation of noncentrosomal microtubules originating from the trans-Golgi network (TGN). Required for the polarization of the cytoplasmic microtubule arrays in migrating cells towards the leading edge of the cell. May act at the cell cortex to enhance the frequency of rescue of depolymerizing microtubules by attaching their plus-ends to cortical platforms composed of ERC1 and PHLDB2. This cortical microtubule stabilizing activity is regulated at least in part by phosphatidylinositol 3-kinase signaling. Also performs a similar stabilizing function at the kinetochore which is essential for the bipolar alignment of chromosomes on the mitotic spindle. {ECO:0000269|PubMed:11290329, ECO:0000269|PubMed:12837247, ECO:0000269|PubMed:15631994, ECO:0000269|PubMed:16866869, ECO:0000269|PubMed:16914514, ECO:0000269|PubMed:17543864}.

Q96DE5

Main function of 5'-partner protein: FUNCTION: Component of the anaphase promoting complex/cyclosome (APC/C), a cell cycle-regulated E3 ubiquitin ligase that controls progression through mitosis and the G1 phase of the cell cycle. The APC/C complex acts by mediating ubiquitination and subsequent degradation of target proteins: it mainly mediates the formation of 'Lys-11'-linked polyubiquitin chains and, to a lower extent, the formation of 'Lys-48'- and 'Lys-63'-linked polyubiquitin chains. {ECO:0000269|PubMed:20360068}.
Ensembl transtripts involved in fusion geneENST idsENST00000263710, ENST00000397587, 
ENST00000409078, ENST00000455322, 
ENST00000541377, ENST00000430234, 
ENST00000541859, ENST00000545861, 
ENST00000489177, ENST00000341068, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score8 X 6 X 5=2406 X 6 X 4=144
# samples 86
** MAII scorelog2(8/240*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/144*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CLASP1 [Title/Abstract] AND ANAPC1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CLASP1 [Title/Abstract] AND ANAPC1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CLASP1(122363277)-ANAPC1(112608487), # samples:1
Anticipated loss of major functional domain due to fusion event.CLASP1-ANAPC1 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.
CLASP1-ANAPC1 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
HgeneCLASP1

GO:0051294

establishment of spindle orientation

21822276

HgeneCLASP1

GO:0051301

cell division

21822276

TgeneANAPC1

GO:0070979

protein K11-linked ubiquitination

18485873



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/chr2:122363277/chr2:112608487)
- 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 CLASP1 (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 ANAPC1 (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)
ENST00000409078CLASP1chr2122363277-ENST00000341068ANAPC1chr2112608487-666769647450151513
ENST00000541377CLASP1chr2122363277-ENST00000341068ANAPC1chr2112608487-655658536349041513
ENST00000455322CLASP1chr2122363277-ENST00000341068ANAPC1chr2112608487-655658536349041513
ENST00000397587CLASP1chr2122363277-ENST00000341068ANAPC1chr2112608487-655658536349041513
ENST00000263710CLASP1chr2122363277-ENST00000341068ANAPC1chr2112608487-655658536349041513

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
ENST00000409078ENST00000341068CLASP1chr2122363277-ANAPC1chr2112608487-0.0004890270.999511
ENST00000541377ENST00000341068CLASP1chr2122363277-ANAPC1chr2112608487-0.0004591790.9995408
ENST00000455322ENST00000341068CLASP1chr2122363277-ANAPC1chr2112608487-0.0004591790.9995408
ENST00000397587ENST00000341068CLASP1chr2122363277-ANAPC1chr2112608487-0.0004591790.9995408
ENST00000263710ENST00000341068CLASP1chr2122363277-ANAPC1chr2112608487-0.0004591790.9995408

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 CLASP1-ANAPC1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CLASP1chr2122363277ANAPC1chr211260848758573DGLATSWVNSSNYKVGKVFIPGLPAP
CLASP1chr2122363277ANAPC1chr211260848769673DGLATSWVNSSNYKVGKVFIPGLPAP

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Potential FusionNeoAntigen Information of CLASP1-ANAPC1 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.
CLASP1-ANAPC1_122363277_112608487.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)
CLASP1-ANAPC1chr2122363277chr2112608487585HLA-B52:01SNYKVGKVF0.08990.54981019
CLASP1-ANAPC1chr2122363277chr2112608487585HLA-B15:17SSNYKVGKVF0.98050.7709919
CLASP1-ANAPC1chr2122363277chr2112608487585HLA-C14:02NYKVGKVF0.95590.74791119
CLASP1-ANAPC1chr2122363277chr2112608487585HLA-C14:03NYKVGKVF0.95590.74791119
CLASP1-ANAPC1chr2122363277chr2112608487585HLA-C15:02SSNYKVGKV0.99860.6497918
CLASP1-ANAPC1chr2122363277chr2112608487585HLA-C15:05SSNYKVGKV0.99810.6925918
CLASP1-ANAPC1chr2122363277chr2112608487585HLA-A69:01WVNSSNYKV0.96320.7234615
CLASP1-ANAPC1chr2122363277chr2112608487585HLA-B15:53SNYKVGKVF0.92810.5671019
CLASP1-ANAPC1chr2122363277chr2112608487585HLA-B15:54SNYKVGKVF0.89440.5291019
CLASP1-ANAPC1chr2122363277chr2112608487585HLA-B48:02SNYKVGKVF0.6650.70951019

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Potential FusionNeoAntigen Information of CLASP1-ANAPC1 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.
CLASP1-ANAPC1_122363277_112608487.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)
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0469ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0469LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0701ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0701LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0701GLATSWVNSSNYKVG116
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0703ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0703LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0703GLATSWVNSSNYKVG116
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0704ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0704LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0705ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0705LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0705GLATSWVNSSNYKVG116
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0706ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0706LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0707ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0707LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0707GLATSWVNSSNYKVG116
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0708ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0708LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0708GLATSWVNSSNYKVG116
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0709ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0709LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0711ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0711LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0712ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0712LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0713ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0713LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0713GLATSWVNSSNYKVG116
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0714ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0714LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0714GLATSWVNSSNYKVG116
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0715ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0715LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0715GLATSWVNSSNYKVG116
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0716ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0716LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0716GLATSWVNSSNYKVG116
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0717ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0717LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0717GLATSWVNSSNYKVG116
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0719ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0719LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0719GLATSWVNSSNYKVG116
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0901LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0901ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0903LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0903ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0904LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0904ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0905ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0905LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0907ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0907LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0909LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-0909ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-1468ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-1468LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-1493ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-1493LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-1511ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-1511LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-1515ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-1527ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-1529ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-1534ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-1534LATSWVNSSNYKVGK217
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-1601ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-1602ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-1603ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-1605ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-1607ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-1608ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-1611ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-1612ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-1614ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB1-1616ATSWVNSSNYKVGKV318
CLASP1-ANAPC1chr2122363277chr2112608487585DRB5-0112ATSWVNSSNYKVGKV318

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Fusion breakpoint peptide structures of CLASP1-ANAPC1

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
10562WVNSSNYKVGKVFICLASP1ANAPC1chr2122363277chr2112608487585

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CLASP1-ANAPC1

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-B14:023BVN10562WVNSSNYKVGKVFI-7.4838-7.5956
HLA-B14:023BVN10562WVNSSNYKVGKVFI-3.16066-4.20376
HLA-B52:013W3910562WVNSSNYKVGKVFI-6.93679-7.04859
HLA-B52:013W3910562WVNSSNYKVGKVFI-6.10064-7.14374
HLA-A11:014UQ210562WVNSSNYKVGKVFI-7.21307-7.32487
HLA-A24:025HGA10562WVNSSNYKVGKVFI-6.56769-6.67949
HLA-A24:025HGA10562WVNSSNYKVGKVFI-4.65311-5.69621
HLA-B44:053DX810562WVNSSNYKVGKVFI-6.68002-6.79182
HLA-B44:053DX810562WVNSSNYKVGKVFI-3.22493-4.26803

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Vaccine Design for the FusionNeoAntigens of CLASP1-ANAPC1

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
CLASP1-ANAPC1chr2122363277chr21126084871019SNYKVGKVFAATTACAAGGTGGGAAAGGTTTTTATT
CLASP1-ANAPC1chr2122363277chr21126084871119NYKVGKVFTACAAGGTGGGAAAGGTTTTTATT
CLASP1-ANAPC1chr2122363277chr2112608487615WVNSSNYKVGTGAACTCTAGCAATTACAAGGTGGGA
CLASP1-ANAPC1chr2122363277chr2112608487918SSNYKVGKVAGCAATTACAAGGTGGGAAAGGTTTTT
CLASP1-ANAPC1chr2122363277chr2112608487919SSNYKVGKVFAGCAATTACAAGGTGGGAAAGGTTTTTATT

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
CLASP1-ANAPC1chr2122363277chr2112608487116GLATSWVNSSNYKVGCTTGCTACCTCTTGGGTGAACTCTAGCAATTACAAGGTGGGAAAG
CLASP1-ANAPC1chr2122363277chr2112608487217LATSWVNSSNYKVGKGCTACCTCTTGGGTGAACTCTAGCAATTACAAGGTGGGAAAGGTT
CLASP1-ANAPC1chr2122363277chr2112608487318ATSWVNSSNYKVGKVACCTCTTGGGTGAACTCTAGCAATTACAAGGTGGGAAAGGTTTTT

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Information of the samples that have these potential fusion neoantigens of CLASP1-ANAPC1

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-CancerCLASP1-ANAPC1chr2122363277ENST00000263710chr2112608487ENST00000341068ERR315380

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Potential target of CAR-T therapy development for CLASP1-ANAPC1

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 CLASP1-ANAPC1

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 CLASP1-ANAPC1

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