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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:CYLD-HAGH

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CYLD-HAGH
FusionPDB ID: 20992
FusionGDB2.0 ID: 20992
HgeneTgene
Gene symbol

CYLD

HAGH

Gene ID

1540

3029

Gene nameCYLD lysine 63 deubiquitinasehydroxyacylglutathione hydrolase
SynonymsBRSS|CDMT|CYLD1|CYLDI|EAC|MFT|MFT1|SBS|TEM|USPL2GLO2|GLX2|GLXII|HAGH1
Cytomap

16q12.1

16p13.3

Type of geneprotein-codingprotein-coding
Descriptionubiquitin carboxyl-terminal hydrolase CYLDcylindromatosis (turban tumor syndrome)deubiquitinating enzyme CYLDprobable ubiquitin carboxyl-terminal hydrolase CYLDubiquitin specific peptidase like 2ubiquitin thioesterase CYLDubiquitin thiolesterase CYLhydroxyacylglutathione hydrolase, mitochondrialglyoxalase IIhydroxyacylglutathione hydroxylase
Modification date2020032920200313
UniProtAcc

Q9NQC7

Main function of 5'-partner protein: FUNCTION: Deubiquitinase that specifically cleaves 'Lys-63'- and linear 'Met-1'-linked polyubiquitin chains and is involved in NF-kappa-B activation and TNF-alpha-induced necroptosis (PubMed:18636086, PubMed:26670046, PubMed:27458237, PubMed:26997266, PubMed:27591049, PubMed:29291351, PubMed:18313383). Plays an important role in the regulation of pathways leading to NF-kappa-B activation (PubMed:12917689, PubMed:12917691). Contributes to the regulation of cell survival, proliferation and differentiation via its effects on NF-kappa-B activation (PubMed:12917690). Negative regulator of Wnt signaling (PubMed:20227366). Inhibits HDAC6 and thereby promotes acetylation of alpha-tubulin and stabilization of microtubules (PubMed:19893491). Plays a role in the regulation of microtubule dynamics, and thereby contributes to the regulation of cell proliferation, cell polarization, cell migration, and angiogenesis (PubMed:18222923, PubMed:20194890). Required for normal cell cycle progress and normal cytokinesis (PubMed:17495026, PubMed:19893491). Inhibits nuclear translocation of NF-kappa-B (PubMed:18636086). Plays a role in the regulation of inflammation and the innate immune response, via its effects on NF-kappa-B activation (PubMed:18636086). Dispensable for the maturation of intrathymic natural killer cells, but required for the continued survival of immature natural killer cells (By similarity). Negatively regulates TNFRSF11A signaling and osteoclastogenesis (By similarity). Involved in the regulation of ciliogenesis, allowing ciliary basal bodies to migrate and dock to the plasma membrane; this process does not depend on NF-kappa-B activation (By similarity). Ability to remove linear ('Met-1'-linked) polyubiquitin chains regulates innate immunity and TNF-alpha-induced necroptosis: recruited to the LUBAC complex via interaction with SPATA2 and restricts linear polyubiquitin formation on target proteins (PubMed:26997266, PubMed:26670046, PubMed:27458237, PubMed:27591049). Regulates innate immunity by restricting linear polyubiquitin formation on RIPK2 in response to NOD2 stimulation (PubMed:26997266). Involved in TNF-alpha-induced necroptosis by removing linear ('Met-1'-linked) polyubiquitin chains from RIPK1, thereby regulating the kinase activity of RIPK1 (By similarity). Removes 'Lys-63' linked polyubiquitin chain of MAP3K7, which inhibits phosphorylation and blocks downstream activation of the JNK-p38 kinase cascades (PubMed:29291351). {ECO:0000250|UniProtKB:Q80TQ2, ECO:0000269|PubMed:12917689, ECO:0000269|PubMed:12917690, ECO:0000269|PubMed:12917691, ECO:0000269|PubMed:17495026, ECO:0000269|PubMed:18222923, ECO:0000269|PubMed:18313383, ECO:0000269|PubMed:18636086, ECO:0000269|PubMed:19893491, ECO:0000269|PubMed:20194890, ECO:0000269|PubMed:20227366, ECO:0000269|PubMed:26670046, ECO:0000269|PubMed:26997266, ECO:0000269|PubMed:27458237, ECO:0000269|PubMed:27591049, ECO:0000269|PubMed:29291351}.

Q6PII5

Main function of 5'-partner protein: FUNCTION: Hydrolase acting on ester bonds. {ECO:0000305}.
Ensembl transtripts involved in fusion geneENST idsENST00000311559, ENST00000398568, 
ENST00000427738, ENST00000540145, 
ENST00000564326, ENST00000566206, 
ENST00000568704, ENST00000569418, 
ENST00000566709, ENST00000567398, 
ENST00000397353, ENST00000397356, 
ENST00000455446, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 4 X 4=964 X 2 X 4=32
# samples 64
** MAII scorelog2(6/96*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/32*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Fusion gene context

PubMed: CYLD [Title/Abstract] AND HAGH [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CYLD [Title/Abstract] AND HAGH [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CYLD(50788335)-HAGH(1859834), # samples:1
Anticipated loss of major functional domain due to fusion event.CYLD-HAGH 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.
CYLD-HAGH 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.
CYLD-HAGH 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.
CYLD-HAGH 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.
CYLD-HAGH seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
CYLD-HAGH seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
CYLD-HAGH seems lost the major protein functional domain in Tgene partner, which is a cell metabolism 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
HgeneCYLD

GO:0010803

regulation of tumor necrosis factor-mediated signaling pathway

26997266|27458237|27591049

HgeneCYLD

GO:0016579

protein deubiquitination

29291351

HgeneCYLD

GO:0032088

negative regulation of NF-kappaB transcription factor activity

18313383

HgeneCYLD

GO:0045087

innate immune response

26997266

HgeneCYLD

GO:0046329

negative regulation of JNK cascade

29291351

HgeneCYLD

GO:0050727

regulation of inflammatory response

27591049

HgeneCYLD

GO:0060544

regulation of necroptotic process

27458237

HgeneCYLD

GO:0070536

protein K63-linked deubiquitination

18313383|18636086|26997266|27458237|27591049|29291351

HgeneCYLD

GO:1901223

negative regulation of NIK/NF-kappaB signaling

18313383

HgeneCYLD

GO:1903753

negative regulation of p38MAPK cascade

29291351

HgeneCYLD

GO:1990108

protein linear deubiquitination

26997266|27458237|27591049

TgeneHAGH

GO:0006750

glutathione biosynthetic process

8550579



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/chr16:50788335/chr16:1859834)
- 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 CYLD (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 HAGH (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)
ENST00000569418CYLDchr1650788335+ENST00000455446HAGHchr161859834-178211912781300340
ENST00000540145CYLDchr1650788335+ENST00000455446HAGHchr161859834-191913284151437340
ENST00000311559CYLDchr1650788335+ENST00000455446HAGHchr161859834-189513043911413340
ENST00000564326CYLDchr1650788335+ENST00000455446HAGHchr161859834-169811071941216340
ENST00000566206CYLDchr1650788335+ENST00000455446HAGHchr161859834-175411632501272340
ENST00000398568CYLDchr1650788335+ENST00000455446HAGHchr161859834-180412133001322340
ENST00000427738CYLDchr1650788335+ENST00000455446HAGHchr161859834-170911182051227340
ENST00000568704CYLDchr1650788335+ENST00000455446HAGHchr161859834-165410631501172340

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
ENST00000569418ENST00000455446CYLDchr1650788335+HAGHchr161859834-0.0003564860.99964356
ENST00000540145ENST00000455446CYLDchr1650788335+HAGHchr161859834-0.0002150280.999785
ENST00000311559ENST00000455446CYLDchr1650788335+HAGHchr161859834-0.0002126410.9997874
ENST00000564326ENST00000455446CYLDchr1650788335+HAGHchr161859834-0.0004034010.99959666
ENST00000566206ENST00000455446CYLDchr1650788335+HAGHchr161859834-0.0003622950.9996377
ENST00000398568ENST00000455446CYLDchr1650788335+HAGHchr161859834-0.0003427770.9996573
ENST00000427738ENST00000455446CYLDchr1650788335+HAGHchr161859834-0.0003570530.99964297
ENST00000568704ENST00000455446CYLDchr1650788335+HAGHchr161859834-0.0003790310.9996209

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 CYLD-HAGH

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CYLDchr1650788335HAGHchr1618598341063304ESTILLHINDIIPGEVQHRGAHSAIH
CYLDchr1650788335HAGHchr1618598341107304ESTILLHINDIIPGEVQHRGAHSAIH
CYLDchr1650788335HAGHchr1618598341118304ESTILLHINDIIPGEVQHRGAHSAIH
CYLDchr1650788335HAGHchr1618598341163304ESTILLHINDIIPGEVQHRGAHSAIH
CYLDchr1650788335HAGHchr1618598341191304ESTILLHINDIIPGEVQHRGAHSAIH
CYLDchr1650788335HAGHchr1618598341213304ESTILLHINDIIPGEVQHRGAHSAIH
CYLDchr1650788335HAGHchr1618598341304304ESTILLHINDIIPGEVQHRGAHSAIH
CYLDchr1650788335HAGHchr1618598341328304ESTILLHINDIIPGEVQHRGAHSAIH

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Potential FusionNeoAntigen Information of CYLD-HAGH 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.
CYLD-HAGH_50788335_1859834.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)
CYLD-HAGHchr1650788335chr1618598341304HLA-A26:14DIIPGEVQH0.99450.7212918
CYLD-HAGHchr1650788335chr1618598341304HLA-A26:15DIIPGEVQH0.99450.7212918
CYLD-HAGHchr1650788335chr1618598341304HLA-A66:01DIIPGEVQH0.98770.7041918
CYLD-HAGHchr1650788335chr1618598341304HLA-A26:03DIIPGEVQH0.97930.7098918
CYLD-HAGHchr1650788335chr1618598341304HLA-A68:03IIPGEVQHR0.89750.61161019
CYLD-HAGHchr1650788335chr1618598341304HLA-A68:05IIPGEVQHR0.88320.63981019
CYLD-HAGHchr1650788335chr1618598341304HLA-A26:03IIPGEVQHR0.60230.77251019
CYLD-HAGHchr1650788335chr1618598341304HLA-A66:01DIIPGEVQHR0.99780.8921919
CYLD-HAGHchr1650788335chr1618598341304HLA-A26:03DIIPGEVQHR0.9960.892919
CYLD-HAGHchr1650788335chr1618598341304HLA-A68:24DIIPGEVQHR0.9890.8171919
CYLD-HAGHchr1650788335chr1618598341304HLA-A02:22HINDIIPGEV0.98850.7362616
CYLD-HAGHchr1650788335chr1618598341304HLA-A68:03DIIPGEVQHR0.98780.813919
CYLD-HAGHchr1650788335chr1618598341304HLA-A02:21HINDIIPGEV0.96640.9035616
CYLD-HAGHchr1650788335chr1618598341304HLA-A68:06DIIPGEVQHR0.96460.841919
CYLD-HAGHchr1650788335chr1618598341304HLA-A68:05DIIPGEVQHR0.96430.8101919
CYLD-HAGHchr1650788335chr1618598341304HLA-A02:20HINDIIPGEV0.95530.8643616
CYLD-HAGHchr1650788335chr1618598341304HLA-A02:11HINDIIPGEV0.94630.8641616
CYLD-HAGHchr1650788335chr1618598341304HLA-A02:35HINDIIPGEV0.94470.8816616
CYLD-HAGHchr1650788335chr1618598341304HLA-A33:01DIIPGEVQHR0.9320.8293919
CYLD-HAGHchr1650788335chr1618598341304HLA-A33:05DIIPGEVQHR0.9320.8293919
CYLD-HAGHchr1650788335chr1618598341304HLA-A34:01DIIPGEVQHR0.89860.7644919
CYLD-HAGHchr1650788335chr1618598341304HLA-A34:05DIIPGEVQHR0.89860.7644919
CYLD-HAGHchr1650788335chr1618598341304HLA-A68:08DIIPGEVQHR0.84750.8464919
CYLD-HAGHchr1650788335chr1618598341304HLA-A66:03DIIPGEVQHR0.78560.6062919
CYLD-HAGHchr1650788335chr1618598341304HLA-A26:01DIIPGEVQH0.99450.7212918
CYLD-HAGHchr1650788335chr1618598341304HLA-A02:05HINDIIPGEV0.99130.5151616
CYLD-HAGHchr1650788335chr1618598341304HLA-A68:01DIIPGEVQHR0.9890.8171919
CYLD-HAGHchr1650788335chr1618598341304HLA-A33:03DIIPGEVQHR0.81720.7544919
CYLD-HAGHchr1650788335chr1618598341304HLA-A02:03HINDIIPGEV0.98680.828616
CYLD-HAGHchr1650788335chr1618598341304HLA-A68:02HINDIIPGEV0.98540.7985616
CYLD-HAGHchr1650788335chr1618598341304HLA-A02:06HINDIIPGEV0.96640.9035616
CYLD-HAGHchr1650788335chr1618598341304HLA-A69:01HINDIIPGEV0.95920.9653616
CYLD-HAGHchr1650788335chr1618598341304HLA-A66:02DIIPGEVQHR0.86470.6277919

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Potential FusionNeoAntigen Information of CYLD-HAGH 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.
CYLD-HAGH_50788335_1859834.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)
CYLD-HAGHchr1650788335chr1618598341304DRB1-0303INDIIPGEVQHRGAH722
CYLD-HAGHchr1650788335chr1618598341304DRB1-0303HINDIIPGEVQHRGA621
CYLD-HAGHchr1650788335chr1618598341304DRB3-0201TILLHINDIIPGEVQ217
CYLD-HAGHchr1650788335chr1618598341304DRB3-0201STILLHINDIIPGEV116
CYLD-HAGHchr1650788335chr1618598341304DRB3-0204TILLHINDIIPGEVQ217
CYLD-HAGHchr1650788335chr1618598341304DRB3-0204STILLHINDIIPGEV116
CYLD-HAGHchr1650788335chr1618598341304DRB3-0205TILLHINDIIPGEVQ217
CYLD-HAGHchr1650788335chr1618598341304DRB3-0214TILLHINDIIPGEVQ217
CYLD-HAGHchr1650788335chr1618598341304DRB3-0217TILLHINDIIPGEVQ217
CYLD-HAGHchr1650788335chr1618598341304DRB3-0224TILLHINDIIPGEVQ217
CYLD-HAGHchr1650788335chr1618598341304DRB3-0224STILLHINDIIPGEV116
CYLD-HAGHchr1650788335chr1618598341304DRB5-0106INDIIPGEVQHRGAH722
CYLD-HAGHchr1650788335chr1618598341304DRB5-0106HINDIIPGEVQHRGA621

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Fusion breakpoint peptide structures of CYLD-HAGH

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
3369HINDIIPGEVQHRGCYLDHAGHchr1650788335chr1618598341304

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CYLD-HAGH

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-B14:023BVN3369HINDIIPGEVQHRG-7.9962-8.1096
HLA-B14:023BVN3369HINDIIPGEVQHRG-5.70842-6.74372
HLA-B52:013W393369HINDIIPGEVQHRG-6.83737-6.95077
HLA-B52:013W393369HINDIIPGEVQHRG-4.4836-5.5189
HLA-A11:014UQ23369HINDIIPGEVQHRG-10.0067-10.1201
HLA-A11:014UQ23369HINDIIPGEVQHRG-9.03915-10.0745
HLA-A24:025HGA3369HINDIIPGEVQHRG-6.56204-6.67544
HLA-A24:025HGA3369HINDIIPGEVQHRG-5.42271-6.45801
HLA-B44:053DX83369HINDIIPGEVQHRG-7.85648-8.89178
HLA-B44:053DX83369HINDIIPGEVQHRG-5.3978-5.5112
HLA-A02:016TDR3369HINDIIPGEVQHRG-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of CYLD-HAGH

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
CYLD-HAGHchr1650788335chr1618598341019IIPGEVQHRTCATCCCAGGAGAAGTACAGCATCGGG
CYLD-HAGHchr1650788335chr161859834616HINDIIPGEVACATCAATGATATCATCCCAGGAGAAGTAC
CYLD-HAGHchr1650788335chr161859834918DIIPGEVQHATATCATCCCAGGAGAAGTACAGCATC
CYLD-HAGHchr1650788335chr161859834919DIIPGEVQHRATATCATCCCAGGAGAAGTACAGCATCGGG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
CYLD-HAGHchr1650788335chr161859834116STILLHINDIIPGEVGTACAATTCTATTGCACATCAATGATATCATCCCAGGAGAAGTAC
CYLD-HAGHchr1650788335chr161859834217TILLHINDIIPGEVQCAATTCTATTGCACATCAATGATATCATCCCAGGAGAAGTACAGC
CYLD-HAGHchr1650788335chr161859834621HINDIIPGEVQHRGAACATCAATGATATCATCCCAGGAGAAGTACAGCATCGGGGAGCCC
CYLD-HAGHchr1650788335chr161859834722INDIIPGEVQHRGAHTCAATGATATCATCCCAGGAGAAGTACAGCATCGGGGAGCCCACA

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Information of the samples that have these potential fusion neoantigens of CYLD-HAGH

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
GBMCYLD-HAGHchr1650788335ENST00000311559chr161859834ENST00000455446TCGA-14-0736-02A

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Potential target of CAR-T therapy development for CYLD-HAGH

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 CYLD-HAGH

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 CYLD-HAGH

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