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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:SMARCC1-MAP4

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SMARCC1-MAP4
FusionPDB ID: 83943
FusionGDB2.0 ID: 83943
HgeneTgene
Gene symbol

SMARCC1

MAP4

Gene ID

6599

4134

Gene nameSWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 1microtubule associated protein 4
SynonymsBAF155|CRACC1|Rsc8|SRG3|SWI3-
Cytomap

3p21.31

3p21.31

Type of geneprotein-codingprotein-coding
DescriptionSWI/SNF complex subunit SMARCC1BRG1-associated factor 155SWI/SNF complex 155 kDa subunitSWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily C member 1chromatin remodeling complex BAF155 subunitmammalian chromatin remodemicrotubule-associated protein 4MAP-4
Modification date2020031320200313
UniProtAcc.

Q9Y4K4

Main function of 5'-partner protein: FUNCTION: May play a role in the response to environmental stress. Appears to act upstream of the JUN N-terminal pathway. {ECO:0000269|PubMed:9038372}.
Ensembl transtripts involved in fusion geneENST idsENST00000254480, ENST00000425518, 
ENST00000441748, ENST00000462206, 
ENST00000264724, ENST00000420772, 
ENST00000434267, ENST00000439356, 
ENST00000360240, ENST00000383737, 
ENST00000395734, ENST00000426837, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score19 X 26 X 11=543419 X 21 X 12=4788
# samples 3735
** MAII scorelog2(37/5434*10)=-3.87641738970566
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(35/4788*10)=-3.77399632511117
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: SMARCC1 [Title/Abstract] AND MAP4 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: SMARCC1 [Title/Abstract] AND MAP4 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SMARCC1(47702784)-MAP4(47919013), # samples:3
SMARCC1(47814307)-MAP4(47899002), # samples:3
MAP4(47896738)-SMARCC1(47628033), # samples:1
Anticipated loss of major functional domain due to fusion event.SMARCC1-MAP4 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.
SMARCC1-MAP4 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.
SMARCC1-MAP4 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.
SMARCC1-MAP4 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.
SMARCC1-MAP4 seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
SMARCC1-MAP4 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
SMARCC1-MAP4 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted 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
HgeneSMARCC1

GO:0006337

nucleosome disassembly

8895581

HgeneSMARCC1

GO:0006338

chromatin remodeling

10078207|11018012|11726552

HgeneSMARCC1

GO:0045893

positive regulation of transcription, DNA-templated

11018012



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/chr3:47702784/chr3:47919013)
- 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 SMARCC1 (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 MAP4 (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)
ENST00000254480SMARCC1chr347702783-ENST00000383737MAP4chr347919013-603324409636921198
ENST00000254480SMARCC1chr347702783-ENST00000395734MAP4chr347919013-594524409638481250
ENST00000254480SMARCC1chr347702783-ENST00000426837MAP4chr347919013-583824409638991267
ENST00000254480SMARCC1chr347702783-ENST00000360240MAP4chr347919013-506424409638991267
ENST00000254480SMARCC1chr347702783-ENST00000383737MAP4chr347969840-692424409645831495
ENST00000254480SMARCC1chr347702783-ENST00000395734MAP4chr347969840-765224409655551819
ENST00000254480SMARCC1chr347702783-ENST00000426837MAP4chr347969840-1092924409689902964
ENST00000254480SMARCC1chr347702783-ENST00000360240MAP4chr347969840-677124409656061836
ENST00000254480SMARCC1chr347702784-ENST00000383737MAP4chr347919013-603324409636921198
ENST00000254480SMARCC1chr347702784-ENST00000395734MAP4chr347919013-594524409638481250
ENST00000254480SMARCC1chr347702784-ENST00000426837MAP4chr347919013-583824409638991267
ENST00000254480SMARCC1chr347702784-ENST00000360240MAP4chr347919013-506424409638991267
ENST00000254480SMARCC1chr347702784-ENST00000383737MAP4chr347969840-692424409645831495
ENST00000254480SMARCC1chr347702784-ENST00000395734MAP4chr347969840-765224409655551819
ENST00000254480SMARCC1chr347702784-ENST00000426837MAP4chr347969840-1092924409689902964
ENST00000254480SMARCC1chr347702784-ENST00000360240MAP4chr347969840-677124409656061836
ENST00000254480SMARCC1chr347702784-ENST00000383737MAP4chr347963368-680124409644601454
ENST00000254480SMARCC1chr347702784-ENST00000395734MAP4chr347963368-752924409654321778
ENST00000254480SMARCC1chr347702784-ENST00000426837MAP4chr347963368-1080624409688672923
ENST00000254480SMARCC1chr347702784-ENST00000360240MAP4chr347963368-664824409654831795

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
ENST00000254480ENST00000383737SMARCC1chr347702783-MAP4chr347919013-0.0007086060.9992914
ENST00000254480ENST00000395734SMARCC1chr347702783-MAP4chr347919013-0.0008286450.9991714
ENST00000254480ENST00000426837SMARCC1chr347702783-MAP4chr347919013-0.0005337990.99946624
ENST00000254480ENST00000360240SMARCC1chr347702783-MAP4chr347919013-0.0004514410.9995485
ENST00000254480ENST00000383737SMARCC1chr347702783-MAP4chr347969840-0.0008007190.99919933
ENST00000254480ENST00000395734SMARCC1chr347702783-MAP4chr347969840-0.0009681980.9990318
ENST00000254480ENST00000426837SMARCC1chr347702783-MAP4chr347969840-0.0004969460.999503
ENST00000254480ENST00000360240SMARCC1chr347702783-MAP4chr347969840-0.0009566720.9990433
ENST00000254480ENST00000383737SMARCC1chr347702784-MAP4chr347919013-0.0007086060.9992914
ENST00000254480ENST00000395734SMARCC1chr347702784-MAP4chr347919013-0.0008286450.9991714
ENST00000254480ENST00000426837SMARCC1chr347702784-MAP4chr347919013-0.0005337990.99946624
ENST00000254480ENST00000360240SMARCC1chr347702784-MAP4chr347919013-0.0004514410.9995485
ENST00000254480ENST00000383737SMARCC1chr347702784-MAP4chr347969840-0.0008007190.99919933
ENST00000254480ENST00000395734SMARCC1chr347702784-MAP4chr347969840-0.0009681980.9990318
ENST00000254480ENST00000426837SMARCC1chr347702784-MAP4chr347969840-0.0004969460.999503
ENST00000254480ENST00000360240SMARCC1chr347702784-MAP4chr347969840-0.0009566720.9990433
ENST00000254480ENST00000383737SMARCC1chr347702784-MAP4chr347963368-0.000251880.9997482
ENST00000254480ENST00000395734SMARCC1chr347702784-MAP4chr347963368-0.00094360.9990564
ENST00000254480ENST00000426837SMARCC1chr347702784-MAP4chr347963368-0.0004900730.99950993
ENST00000254480ENST00000360240SMARCC1chr347702784-MAP4chr347963368-0.0009427460.99905723

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 SMARCC1-MAP4

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
SMARCC1chr347702783MAP4chr3479190132440780SCIAGTGPDEPEKLGIARPEEGRPVV
SMARCC1chr347702783MAP4chr3479698402440781CIAGTGPDEPEKLGSPTEFLEEKMAY
SMARCC1chr347702784MAP4chr3479190132440780SCIAGTGPDEPEKLGIARPEEGRPVV
SMARCC1chr347702784MAP4chr3479633682440781CIAGTGPDEPEKLDPFKMYHDDDLAD
SMARCC1chr347702784MAP4chr3479698402440781CIAGTGPDEPEKLGSPTEFLEEKMAY

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Potential FusionNeoAntigen Information of SMARCC1-MAP4 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.
SMARCC1-MAP4_47702783_47969840.msa
SMARCC1-MAP4_47702784_47963368.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)
SMARCC1-MAP4chr347702783chr3479698402440HLA-A02:22KLGSPTEFL0.98510.5241120
SMARCC1-MAP4chr347702783chr3479698402440HLA-A02:30KLGSPTEFL0.97240.69341120
SMARCC1-MAP4chr347702783chr3479698402440HLA-A02:24KLGSPTEFL0.97240.69341120
SMARCC1-MAP4chr347702783chr3479698402440HLA-A02:67KLGSPTEFL0.97240.69341120
SMARCC1-MAP4chr347702783chr3479698402440HLA-A02:60KLGSPTEFL0.97160.64791120
SMARCC1-MAP4chr347702783chr3479698402440HLA-A02:11KLGSPTEFL0.96980.72511120
SMARCC1-MAP4chr347702783chr3479698402440HLA-A02:27KLGSPTEFL0.96710.60791120
SMARCC1-MAP4chr347702783chr3479698402440HLA-A02:16KLGSPTEFL0.95510.51041120
SMARCC1-MAP4chr347702783chr3479698402440HLA-A02:04KLGSPTEFL0.95090.59691120
SMARCC1-MAP4chr347702783chr3479698402440HLA-A02:13KLGSPTEFL0.94320.72681120
SMARCC1-MAP4chr347702783chr3479698402440HLA-A02:38KLGSPTEFL0.91270.65821120
SMARCC1-MAP4chr347702783chr3479698402440HLA-A02:29KLGSPTEFL0.80510.69511120
SMARCC1-MAP4chr347702783chr3479698402440HLA-A02:20KLGSPTEFL0.79750.70191120
SMARCC1-MAP4chr347702783chr3479698402440HLA-A02:35KLGSPTEFL0.780.72031120
SMARCC1-MAP4chr347702783chr3479698402440HLA-B38:02EKLGSPTEF0.65790.90121019
SMARCC1-MAP4chr347702783chr3479698402440HLA-B15:10EKLGSPTEF0.52970.53481019
SMARCC1-MAP4chr347702783chr3479698402440HLA-B15:18EKLGSPTEF0.2960.69591019
SMARCC1-MAP4chr347702783chr3479698402440HLA-B15:03EKLGSPTEF0.29050.73021019
SMARCC1-MAP4chr347702783chr3479698402440HLA-B15:37EKLGSPTEF0.20560.56841019
SMARCC1-MAP4chr347702783chr3479698402440HLA-B13:01KLGSPTEFL0.02630.90371120
SMARCC1-MAP4chr347702783chr3479698402440HLA-B35:08EPEKLGSPTEF0.99620.8033819
SMARCC1-MAP4chr347702783chr3479698402440HLA-B35:01EPEKLGSPTEF0.99240.8907819
SMARCC1-MAP4chr347702783chr3479698402440HLA-A02:01KLGSPTEFL0.97240.69341120
SMARCC1-MAP4chr347702783chr3479698402440HLA-A02:07KLGSPTEFL0.97160.70531120
SMARCC1-MAP4chr347702783chr3479698402440HLA-A02:03KLGSPTEFL0.97850.73251120
SMARCC1-MAP4chr347702783chr3479698402440HLA-A02:14KLGSPTEFL0.9630.72711120
SMARCC1-MAP4chr347702783chr3479698402440HLA-B48:02EKLGSPTEF0.56920.85481019
SMARCC1-MAP4chr347702783chr3479698402440HLA-B15:09EKLGSPTEF0.25460.55121019
SMARCC1-MAP4chr347702783chr3479698402440HLA-B15:54EKLGSPTEF0.0270.81221019
SMARCC1-MAP4chr347702783chr3479698402440HLA-B35:77EPEKLGSPTEF0.99240.8907819
SMARCC1-MAP4chr347702783chr3479698402440HLA-B35:23EPEKLGSPTEF0.99170.879819
SMARCC1-MAP4chr347702783chr3479698402440HLA-B35:24EPEKLGSPTEF0.95220.8912819
SMARCC1-MAP4chr347702784chr3479633682440HLA-B18:01DEPEKLDPF0.98140.9178716
SMARCC1-MAP4chr347702784chr3479633682440HLA-B15:18EKLDPFKMY0.37380.61921019
SMARCC1-MAP4chr347702784chr3479633682440HLA-B44:03PEKLDPFKMY0.92150.9181919
SMARCC1-MAP4chr347702784chr3479633682440HLA-B18:07DEPEKLDPF0.98680.8592716
SMARCC1-MAP4chr347702784chr3479633682440HLA-B18:06DEPEKLDPF0.98370.9179716
SMARCC1-MAP4chr347702784chr3479633682440HLA-B18:05DEPEKLDPF0.98140.9178716
SMARCC1-MAP4chr347702784chr3479633682440HLA-B18:08DEPEKLDPF0.97380.8653716
SMARCC1-MAP4chr347702784chr3479633682440HLA-B18:03DEPEKLDPF0.9690.9129716
SMARCC1-MAP4chr347702784chr3479633682440HLA-B18:04EKLDPFKMY0.62780.93791019
SMARCC1-MAP4chr347702784chr3479633682440HLA-B18:11DEPEKLDPF0.59090.8856716
SMARCC1-MAP4chr347702784chr3479633682440HLA-B18:06EKLDPFKMY0.43870.93261019
SMARCC1-MAP4chr347702784chr3479633682440HLA-B18:03EKLDPFKMY0.39060.91961019
SMARCC1-MAP4chr347702784chr3479633682440HLA-B44:13PEKLDPFKMY0.92150.9181919
SMARCC1-MAP4chr347702784chr3479633682440HLA-B44:26PEKLDPFKMY0.92150.9181919
SMARCC1-MAP4chr347702784chr3479633682440HLA-B44:07PEKLDPFKMY0.92150.9181919
SMARCC1-MAP4chr347702784chr3479633682440HLA-B35:24EPEKLDPFKMY0.99420.8754819

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Potential FusionNeoAntigen Information of SMARCC1-MAP4 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.
SMARCC1-MAP4_47702784_47963368.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)
SMARCC1-MAP4chr347702784chr3479633682440DRB1-1502KLDPFKMYHDDDLAD1126
SMARCC1-MAP4chr347702784chr3479633682440DRB1-1508KLDPFKMYHDDDLAD1126
SMARCC1-MAP4chr347702784chr3479633682440DRB1-1511KLDPFKMYHDDDLAD1126
SMARCC1-MAP4chr347702784chr3479633682440DRB1-1514KLDPFKMYHDDDLAD1126
SMARCC1-MAP4chr347702784chr3479633682440DRB1-1519KLDPFKMYHDDDLAD1126
SMARCC1-MAP4chr347702784chr3479633682440DRB1-1526KLDPFKMYHDDDLAD1126
SMARCC1-MAP4chr347702784chr3479633682440DRB1-1529KLDPFKMYHDDDLAD1126
SMARCC1-MAP4chr347702784chr3479633682440DRB1-1530KLDPFKMYHDDDLAD1126
SMARCC1-MAP4chr347702784chr3479633682440DRB1-1531KLDPFKMYHDDDLAD1126
SMARCC1-MAP4chr347702784chr3479633682440DRB1-1538KLDPFKMYHDDDLAD1126
SMARCC1-MAP4chr347702784chr3479633682440DRB1-1539KLDPFKMYHDDDLAD1126
SMARCC1-MAP4chr347702784chr3479633682440DRB1-1544KLDPFKMYHDDDLAD1126
SMARCC1-MAP4chr347702784chr3479633682440DRB1-1547KLDPFKMYHDDDLAD1126

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Fusion breakpoint peptide structures of SMARCC1-MAP4

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
6534PDEPEKLDPFKMYHSMARCC1MAP4chr347702784chr3479633682440
File nameBPseqHgeneTgeneHchrHbpTchrTbpAAlen
6535PDEPEKLGSPTEFLSMARCC1MAP4chr347702783chr3479698402440

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of SMARCC1-MAP4

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-B14:023BVN6534PDEPEKLDPFKMYH-7.15543-7.26883
HLA-B14:023BVN6534PDEPEKLDPFKMYH-4.77435-5.80965
HLA-B52:013W396534PDEPEKLDPFKMYH-6.80875-6.92215
HLA-B52:013W396534PDEPEKLDPFKMYH-4.20386-5.23916
HLA-A11:014UQ26534PDEPEKLDPFKMYH-7.5194-8.5547
HLA-A11:014UQ26534PDEPEKLDPFKMYH-6.9601-7.0735
HLA-A24:025HGA6534PDEPEKLDPFKMYH-7.52403-7.63743
HLA-A24:025HGA6534PDEPEKLDPFKMYH-5.82433-6.85963
HLA-B27:056PYJ6534PDEPEKLDPFKMYH-3.28285-4.31815
HLA-B44:053DX86534PDEPEKLDPFKMYH-5.91172-6.94702
HLA-B44:053DX86534PDEPEKLDPFKMYH-4.24346-4.35686
HLA-B14:023BVN6535PDEPEKLGSPTEFL-7.15543-7.26883
HLA-B14:023BVN6535PDEPEKLGSPTEFL-4.77435-5.80965
HLA-B52:013W396535PDEPEKLGSPTEFL-6.80875-6.92215
HLA-B52:013W396535PDEPEKLGSPTEFL-4.20386-5.23916
HLA-A11:014UQ26535PDEPEKLGSPTEFL-7.5194-8.5547
HLA-A11:014UQ26535PDEPEKLGSPTEFL-6.9601-7.0735
HLA-A24:025HGA6535PDEPEKLGSPTEFL-7.52403-7.63743
HLA-A24:025HGA6535PDEPEKLGSPTEFL-5.82433-6.85963
HLA-B27:056PYJ6535PDEPEKLGSPTEFL-3.28285-4.31815
HLA-B44:053DX86535PDEPEKLGSPTEFL-5.91172-6.94702
HLA-B44:053DX86535PDEPEKLGSPTEFL-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of SMARCC1-MAP4

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
SMARCC1-MAP4chr347702783chr3479698401019EKLGSPTEFAGAAGCTTGGGTCTCCAACTGAATTCC
SMARCC1-MAP4chr347702783chr3479698401120KLGSPTEFLAGCTTGGGTCTCCAACTGAATTCCTTG
SMARCC1-MAP4chr347702783chr347969840819EPEKLGSPTEFAGCCAGAGAAGCTTGGGTCTCCAACTGAATTCC
SMARCC1-MAP4chr347702784chr3479633681019EKLDPFKMYAGAAGCTTGATCCCTTTAAGATGTACC
SMARCC1-MAP4chr347702784chr347963368716DEPEKLDPFATGAGCCAGAGAAGCTTGATCCCTTTA
SMARCC1-MAP4chr347702784chr347963368819EPEKLDPFKMYAGCCAGAGAAGCTTGATCCCTTTAAGATGTACC
SMARCC1-MAP4chr347702784chr347963368919PEKLDPFKMYCAGAGAAGCTTGATCCCTTTAAGATGTACC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
SMARCC1-MAP4chr347702784chr3479633681126KLDPFKMYHDDDLADAGCTTGATCCCTTTAAGATGTACCATGATGATGACCTGGCAGATT

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Information of the samples that have these potential fusion neoantigens of SMARCC1-MAP4

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
UCSSMARCC1-MAP4chr347702783ENST00000254480chr347969840ENST00000360240TCGA-N6-A4VG
UCSSMARCC1-MAP4chr347702784ENST00000254480chr347963368ENST00000360240TCGA-N6-A4VG

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Potential target of CAR-T therapy development for SMARCC1-MAP4

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 SMARCC1-MAP4

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 SMARCC1-MAP4

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