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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:TYK2-CIB3

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: TYK2-CIB3
FusionPDB ID: 95650
FusionGDB2.0 ID: 95650
HgeneTgene
Gene symbol

TYK2

CIB3

Gene ID

7297

117286

Gene nametyrosine kinase 2calcium and integrin binding family member 3
SynonymsIMD35|JTK1KIP3
Cytomap

19p13.2

19p13.11

Type of geneprotein-codingprotein-coding
Descriptionnon-receptor tyrosine-protein kinase TYK2calcium and integrin-binding family member 3DNA-dependent protein kinase catalytic subunit-interacting protein 3
Modification date2020032920200313
UniProtAcc.

Q96Q77

Main function of 5'-partner protein:
Ensembl transtripts involved in fusion geneENST idsENST00000264818, ENST00000525621, 
ENST00000529370, ENST00000524462, 
ENST00000529422, 
ENST00000541493, 
ENST00000269878, ENST00000379859, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score13 X 11 X 8=11446 X 5 X 5=150
# samples 159
** MAII scorelog2(15/1144*10)=-2.93105264628251
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/150*10)=-0.736965594166206
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: TYK2 [Title/Abstract] AND CIB3 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: TYK2 [Title/Abstract] AND CIB3 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)TYK2(10488890)-CIB3(16275724), # samples:2
Anticipated loss of major functional domain due to fusion event.TYK2-CIB3 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.
TYK2-CIB3 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.
TYK2-CIB3 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.
TYK2-CIB3 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.
TYK2-CIB3 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
TYK2-CIB3 seems lost the major protein functional domain in Hgene partner, which is a kinase due to the frame-shifted ORF.
TYK2-CIB3 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


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/chr19:10488890/chr19:16275724)
- 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 TYK2 (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 CIB3 (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)
ENST00000525621TYK2chr1910488890-ENST00000269878CIB3chr1916275724-990675482892136
ENST00000525621TYK2chr1910488890-ENST00000379859CIB3chr1916275724-943675482892136
ENST00000529370TYK2chr1910488890-ENST00000269878CIB3chr1916275724-839524331741136
ENST00000529370TYK2chr1910488890-ENST00000379859CIB3chr1916275724-792524331741136

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
ENST00000525621ENST00000269878TYK2chr1910488890-CIB3chr1916275724-0.0148777660.9851222
ENST00000525621ENST00000379859TYK2chr1910488890-CIB3chr1916275724-0.0128038990.9871961
ENST00000529370ENST00000269878TYK2chr1910488890-CIB3chr1916275724-0.0100228060.9899771
ENST00000529370ENST00000379859TYK2chr1910488890-CIB3chr1916275724-0.009546280.9904537

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 TYK2-CIB3

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
TYK2chr1910488890CIB3chr191627572452464TAEEVCIHIAHKVDFNNDDYICAWDL
TYK2chr1910488890CIB3chr191627572467564TAEEVCIHIAHKVDFNNDDYICAWDL

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Potential FusionNeoAntigen Information of TYK2-CIB3 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.
TYK2-CIB3_10488890_16275724.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)
TYK2-CIB3chr1910488890chr1916275724675HLA-B39:01IHIAHKVDF0.90730.6004615
TYK2-CIB3chr1910488890chr1916275724675HLA-B38:01IHIAHKVDF0.87670.7625615
TYK2-CIB3chr1910488890chr1916275724675HLA-B38:02IHIAHKVDF0.85780.795615
TYK2-CIB3chr1910488890chr1916275724675HLA-B39:12IHIAHKVDF0.9320.6139615
TYK2-CIB3chr1910488890chr1916275724675HLA-B39:05IHIAHKVDF0.81080.5856615
TYK2-CIB3chr1910488890chr1916275724675HLA-C07:29IHIAHKVDF0.71980.8101615
TYK2-CIB3chr1910488890chr1916275724675HLA-C07:13IHIAHKVDF0.65670.7262615
TYK2-CIB3chr1910488890chr1916275724675HLA-C07:67IHIAHKVDF0.60570.7895615
TYK2-CIB3chr1910488890chr1916275724675HLA-C07:80IHIAHKVDF0.60570.7895615
TYK2-CIB3chr1910488890chr1916275724675HLA-C07:10IHIAHKVDF0.5460.8345615
TYK2-CIB3chr1910488890chr1916275724675HLA-C07:46IHIAHKVDF0.52450.6086615
TYK2-CIB3chr1910488890chr1916275724675HLA-B39:31IHIAHKVDF0.90650.6052615
TYK2-CIB3chr1910488890chr1916275724675HLA-B38:05IHIAHKVDF0.87670.7625615
TYK2-CIB3chr1910488890chr1916275724675HLA-C07:17IHIAHKVDF0.66020.9254615
TYK2-CIB3chr1910488890chr1916275724675HLA-C07:02IHIAHKVDF0.60570.7895615

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Potential FusionNeoAntigen Information of TYK2-CIB3 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.
TYK2-CIB3_10488890_16275724.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)
TYK2-CIB3chr1910488890chr1916275724675DRB1-1113EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1113EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1117EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1134EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1152EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1331EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1343EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1344EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1354EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1377EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1377EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1401EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1401EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1404EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1404EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1405EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1407EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1408EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1411EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1411EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1416EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1417EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1418EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1423EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1426EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1426EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1428EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1428EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1428AEEVCIHIAHKVDFN116
TYK2-CIB3chr1910488890chr1916275724675DRB1-1431EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1431EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1432EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1432EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1433EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1434EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1435EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1435EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1438EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1438EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1439EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1443EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1445EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1450EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1450EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1454EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1454EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1455EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1455EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1456EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1458EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1458EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1459EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1460EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1460EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1461EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1461EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1462EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1462EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1464EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1464EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1465EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1465EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1468EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1470EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1470EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1471EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1471EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1472EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1472EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1475EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1475EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1481EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1482EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1482EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1486EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1486EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1487EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1487EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1488EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1488EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1490EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1490EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1491EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1495EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1495EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1496EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1497EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1497EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1499EVCIHIAHKVDFNND318
TYK2-CIB3chr1910488890chr1916275724675DRB1-1499EEVCIHIAHKVDFNN217
TYK2-CIB3chr1910488890chr1916275724675DRB1-1510AEEVCIHIAHKVDFN116

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Fusion breakpoint peptide structures of TYK2-CIB3

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
3711IHIAHKVDFNNDDYTYK2CIB3chr1910488890chr1916275724675

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of TYK2-CIB3

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-B14:023BVN3711IHIAHKVDFNNDDY-7.9962-8.1096
HLA-B14:023BVN3711IHIAHKVDFNNDDY-5.70842-6.74372
HLA-B52:013W393711IHIAHKVDFNNDDY-6.83737-6.95077
HLA-B52:013W393711IHIAHKVDFNNDDY-4.4836-5.5189
HLA-A11:014UQ23711IHIAHKVDFNNDDY-10.0067-10.1201
HLA-A11:014UQ23711IHIAHKVDFNNDDY-9.03915-10.0745
HLA-A24:025HGA3711IHIAHKVDFNNDDY-6.56204-6.67544
HLA-A24:025HGA3711IHIAHKVDFNNDDY-5.42271-6.45801
HLA-B44:053DX83711IHIAHKVDFNNDDY-7.85648-8.89178
HLA-B44:053DX83711IHIAHKVDFNNDDY-5.3978-5.5112
HLA-A02:016TDR3711IHIAHKVDFNNDDY-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of TYK2-CIB3

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
TYK2-CIB3chr1910488890chr1916275724615IHIAHKVDFTCCACATTGCACATAAAGTTGATTTTA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
TYK2-CIB3chr1910488890chr1916275724116AEEVCIHIAHKVDFNCTGAGGAAGTCTGCATCCACATTGCACATAAAGTTGATTTTAACA
TYK2-CIB3chr1910488890chr1916275724217EEVCIHIAHKVDFNNAGGAAGTCTGCATCCACATTGCACATAAAGTTGATTTTAACAACG
TYK2-CIB3chr1910488890chr1916275724318EVCIHIAHKVDFNNDAAGTCTGCATCCACATTGCACATAAAGTTGATTTTAACAACGACG

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Information of the samples that have these potential fusion neoantigens of TYK2-CIB3

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
SARCTYK2-CIB3chr1910488890ENST00000525621chr1916275724ENST00000269878TCGA-DX-A3LY-01B

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Potential target of CAR-T therapy development for TYK2-CIB3

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 TYK2-CIB3

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 TYK2-CIB3

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