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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:ETHE1-UPK3A

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ETHE1-UPK3A
FusionPDB ID: 27653
FusionGDB2.0 ID: 27653
HgeneTgene
Gene symbol

ETHE1

UPK3A

Gene ID

23474

7380

Gene nameETHE1 persulfide dioxygenaseuroplakin 3A
SynonymsHSCO|YF13H12UP3A|UPIII|UPIIIA|UPK3
Cytomap

19q13.31

22q13.31

Type of geneprotein-codingprotein-coding
Descriptionpersulfide dioxygenase ETHE1, mitochondrialethylmalonic encephalopathy 1hepatoma subtracted clone one proteinprotein ETHE1, mitochondrialsulfur dioxygenase ETHE1uroplakin-3auroplakin 3uroplakin III
Modification date2020031320200313
UniProtAcc

O95571

Main function of 5'-partner protein: FUNCTION: Sulfur dioxygenase that plays an essential role in hydrogen sulfide catabolism in the mitochondrial matrix. Hydrogen sulfide (H(2)S) is first oxidized by SQRDL, giving rise to cysteine persulfide residues. ETHE1 consumes molecular oxygen to catalyze the oxidation of the persulfide, once it has been transferred to a thiophilic acceptor, such as glutathione (R-SSH). Plays an important role in metabolic homeostasis in mitochondria by metabolizing hydrogen sulfide and preventing the accumulation of supraphysiological H(2)S levels that have toxic effects, due to the inhibition of cytochrome c oxidase. First described as a protein that can shuttle between the nucleus and the cytoplasm and suppress p53-induced apoptosis by sequestering the transcription factor RELA/NFKB3 in the cytoplasm and preventing its accumulation in the nucleus (PubMed:12398897). {ECO:0000269|PubMed:12398897, ECO:0000269|PubMed:14732903, ECO:0000269|PubMed:19136963, ECO:0000269|PubMed:23144459}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000292147, ENST00000600651, 
ENST00000216211, ENST00000396082, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score10 X 7 X 8=5603 X 2 X 3=18
# samples 113
** MAII scorelog2(11/560*10)=-2.34792330342031
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Fusion gene context

PubMed: ETHE1 [Title/Abstract] AND UPK3A [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ETHE1 [Title/Abstract] AND UPK3A [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ETHE1(44030667)-UPK3A(45691441), # samples:3
Anticipated loss of major functional domain due to fusion event.ETHE1-UPK3A seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
ETHE1-UPK3A seems lost the major protein functional domain in Hgene 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
HgeneETHE1

GO:0006749

glutathione metabolic process

23144459

HgeneETHE1

GO:0070813

hydrogen sulfide metabolic process

23144459

TgeneUPK3A

GO:0030855

epithelial cell differentiation

10514386



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/chr19:44030667/chr22:45691441)
- 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 ETHE1 (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 UPK3A (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)
ENST00000292147ETHE1chr1944030667-ENST00000216211UPK3Achr2245691441+60829367396109
ENST00000600651ETHE1chr1944030667-ENST00000216211UPK3Achr2245691441+56525024353109

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
ENST00000292147ENST00000216211ETHE1chr1944030667-UPK3Achr2245691441+0.212518980.78748095
ENST00000600651ENST00000216211ETHE1chr1944030667-UPK3Achr2245691441+0.25198420.74801576

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 ETHE1-UPK3A

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ETHE1chr1944030667UPK3Achr224569144125075QLIKELGLRLLYAGTWGVLMGKRLTT
ETHE1chr1944030667UPK3Achr224569144129375QLIKELGLRLLYAGTWGVLMGKRLTT

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Potential FusionNeoAntigen Information of ETHE1-UPK3A 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.
ETHE1-UPK3A_44030667_45691441.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)
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:22LLYAGTWGV0.9980.8331918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-B27:02LRLLYAGTW0.99780.6693716
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:27LLYAGTWGV0.99720.8578918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:11LLYAGTWGV0.99720.8062918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:13LLYAGTWGV0.99710.8996918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:30LLYAGTWGV0.9970.7905918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:24LLYAGTWGV0.9970.7905918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:60LLYAGTWGV0.9970.8006918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:67LLYAGTWGV0.9970.7905918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:21LLYAGTWGV0.99660.8467918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:16LLYAGTWGV0.99620.7791918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:38LLYAGTWGV0.99430.7614918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:19LLYAGTWGV0.9930.8024918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:29LLYAGTWGV0.99290.7943918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:35LLYAGTWGV0.9920.8024918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:04LLYAGTWGV0.98920.9503918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:20LLYAGTWGV0.98820.8918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:17LLYAGTWGV0.97470.9515918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A24:23LYAGTWGVL0.95860.591019
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A24:10LYAGTWGVL0.93540.55611019
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:22RLLYAGTWGV0.99690.7533818
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:11RLLYAGTWGV0.99660.7167818
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:13RLLYAGTWGV0.99640.8254818
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:60RLLYAGTWGV0.99640.7043818
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:67RLLYAGTWGV0.99620.6928818
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:24RLLYAGTWGV0.99620.6928818
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:30RLLYAGTWGV0.99620.6928818
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:27RLLYAGTWGV0.99610.7858818
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:16RLLYAGTWGV0.99560.643818
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:04RLLYAGTWGV0.99320.9036818
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:19RLLYAGTWGV0.98830.7124818
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:29RLLYAGTWGV0.97820.699818
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:35RLLYAGTWGV0.97120.7162818
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:04LLYAGTWGVL0.97080.9271919
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:20RLLYAGTWGV0.95550.703818
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A03:12AGTWGVLMGK0.95430.61141222
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A03:25AGTWGVLMGK0.9520.58441222
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A74:09AGTWGVLMGK0.660.70931222
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A74:11AGTWGVLMGK0.660.70931222
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A74:03AGTWGVLMGK0.660.70931222
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:02LLYAGTWGV0.99810.8474918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:05LLYAGTWGV0.99790.888918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:07LLYAGTWGV0.9970.7982918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:01LLYAGTWGV0.9970.7905918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C03:08YAGTWGVLM0.9950.9631120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C03:19YAGTWGVLM0.99430.99761120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C03:07YAGTWGVLM0.99380.99241120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C15:06YAGTWGVLM0.9870.98221120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C04:06YAGTWGVLM0.97660.99341120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C08:13YAGTWGVLM0.95450.99631120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C08:04YAGTWGVLM0.95450.99631120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C03:14YAGTWGVLM0.83980.99441120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C08:03YAGTWGVLM0.80180.99841120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C06:03YAGTWGVLM0.68690.99891120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C12:04YAGTWGVLM0.66880.99871120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C12:12YAGTWGVLM0.63080.98481120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C02:06YAGTWGVLM0.3520.99241120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:01RLLYAGTWGV0.99620.6928818
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A03:01AGTWGVLMGK0.9520.58441222
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:03LLYAGTWGV0.99870.8918918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:14LLYAGTWGV0.99670.8276918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:06LLYAGTWGV0.99660.8467918
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C03:04YAGTWGVLM0.99640.99651120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C03:03YAGTWGVLM0.99640.99651120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C03:02YAGTWGVLM0.99340.98951120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C03:05YAGTWGVLM0.99240.96861120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C03:17YAGTWGVLM0.99120.98791120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A24:03LYAGTWGVL0.95860.591019
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C03:06YAGTWGVLM0.93360.99641120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C16:04YAGTWGVLM0.92760.99551120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-B35:13YAGTWGVLM0.8950.96741120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C16:01YAGTWGVLM0.85870.99051120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C12:02YAGTWGVLM0.82650.99251120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C08:01YAGTWGVLM0.80180.99841120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C16:02YAGTWGVLM0.74310.99571120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C12:03YAGTWGVLM0.68970.99621120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C02:10YAGTWGVLM0.26810.99361120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C02:02YAGTWGVLM0.26810.99361120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C14:02LYAGTWGVL0.13480.99021019
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C14:03LYAGTWGVL0.13480.99021019
ETHE1-UPK3Achr1944030667chr2245691441293HLA-C17:01YAGTWGVLM0.11460.98491120
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A02:03RLLYAGTWGV0.99710.7864818
ETHE1-UPK3Achr1944030667chr2245691441293HLA-A74:01AGTWGVLMGK0.660.70931222

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Potential FusionNeoAntigen Information of ETHE1-UPK3A 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.
ETHE1-UPK3A_44030667_45691441.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)
ETHE1-UPK3Achr1944030667chr2245691441293DRB1-0101YAGTWGVLMGKRLTT1126
ETHE1-UPK3Achr1944030667chr2245691441293DRB1-0105YAGTWGVLMGKRLTT1126
ETHE1-UPK3Achr1944030667chr2245691441293DRB1-0107YAGTWGVLMGKRLTT1126
ETHE1-UPK3Achr1944030667chr2245691441293DRB1-0109YAGTWGVLMGKRLTT1126
ETHE1-UPK3Achr1944030667chr2245691441293DRB1-0111YAGTWGVLMGKRLTT1126
ETHE1-UPK3Achr1944030667chr2245691441293DRB1-0115YAGTWGVLMGKRLTT1126
ETHE1-UPK3Achr1944030667chr2245691441293DRB1-0119YAGTWGVLMGKRLTT1126
ETHE1-UPK3Achr1944030667chr2245691441293DRB1-0125YAGTWGVLMGKRLTT1126
ETHE1-UPK3Achr1944030667chr2245691441293DRB1-0127YAGTWGVLMGKRLTT1126
ETHE1-UPK3Achr1944030667chr2245691441293DRB1-0129YAGTWGVLMGKRLTT1126
ETHE1-UPK3Achr1944030667chr2245691441293DRB1-0131YAGTWGVLMGKRLTT1126

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Fusion breakpoint peptide structures of ETHE1-UPK3A

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
2955GLRLLYAGTWGVLMETHE1UPK3Achr1944030667chr2245691441293

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ETHE1-UPK3A

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-B14:023BVN2955GLRLLYAGTWGVLM-7.9962-8.1096
HLA-B14:023BVN2955GLRLLYAGTWGVLM-5.70842-6.74372
HLA-B52:013W392955GLRLLYAGTWGVLM-6.83737-6.95077
HLA-B52:013W392955GLRLLYAGTWGVLM-4.4836-5.5189
HLA-A11:014UQ22955GLRLLYAGTWGVLM-10.0067-10.1201
HLA-A11:014UQ22955GLRLLYAGTWGVLM-9.03915-10.0745
HLA-A24:025HGA2955GLRLLYAGTWGVLM-6.56204-6.67544
HLA-A24:025HGA2955GLRLLYAGTWGVLM-5.42271-6.45801
HLA-B44:053DX82955GLRLLYAGTWGVLM-7.85648-8.89178
HLA-B44:053DX82955GLRLLYAGTWGVLM-5.3978-5.5112
HLA-A02:016TDR2955GLRLLYAGTWGVLM-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of ETHE1-UPK3A

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
ETHE1-UPK3Achr1944030667chr22456914411019LYAGTWGVLTCTATGCTGGGACATGGGGAGTTCTGA
ETHE1-UPK3Achr1944030667chr22456914411120YAGTWGVLMATGCTGGGACATGGGGAGTTCTGATGG
ETHE1-UPK3Achr1944030667chr22456914411222AGTWGVLMGKCTGGGACATGGGGAGTTCTGATGGGGAAAC
ETHE1-UPK3Achr1944030667chr2245691441716LRLLYAGTWTGCGGCTGCTCTATGCTGGGACATGGG
ETHE1-UPK3Achr1944030667chr2245691441818RLLYAGTWGVGGCTGCTCTATGCTGGGACATGGGGAGTTC
ETHE1-UPK3Achr1944030667chr2245691441918LLYAGTWGVTGCTCTATGCTGGGACATGGGGAGTTC
ETHE1-UPK3Achr1944030667chr2245691441919LLYAGTWGVLTGCTCTATGCTGGGACATGGGGAGTTCTGA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
ETHE1-UPK3Achr1944030667chr22456914411126YAGTWGVLMGKRLTTATGCTGGGACATGGGGAGTTCTGATGGGGAAACGACTCACGACTC

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Information of the samples that have these potential fusion neoantigens of ETHE1-UPK3A

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
OVETHE1-UPK3Achr1944030667ENST00000292147chr2245691441ENST00000216211TCGA-13-1405-01A

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Potential target of CAR-T therapy development for ETHE1-UPK3A

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
TgeneUPK3Achr19:44030667chr22:45691441ENST0000039608224208_2350167.0TransmembraneHelical

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 ETHE1-UPK3A

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 ETHE1-UPK3A

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