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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:MAEA-ATP6V0C

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: MAEA-ATP6V0C
FusionPDB ID: 50699
FusionGDB2.0 ID: 50699
HgeneTgene
Gene symbol

MAEA

ATP6V0C

Gene ID

10296

527

Gene namemacrophage erythroblast attacher, E3 ubiquitin ligaseATPase H+ transporting V0 subunit c
SynonymsEMLP|EMP|GID9|HLC-10|P44EMLP|PIG5ATP6C|ATP6L|ATPL|VATL|VPPC|Vma3
Cytomap

4p16.3

16p13.3

Type of geneprotein-codingprotein-coding
DescriptionE3 ubiquitin-protein transferase MAEAGID complex subunit 9, FYV10 homologcell proliferation-inducing gene 5 proteinerythroblast macrophage proteinhuman lung cancer oncogene 10 proteinlung cancer-related protein 10macrophage erythroblast attacherV-type proton ATPase 16 kDa proteolipid subunitATPase, H+ transporting, lysosomal 16kDa, V0 subunit cH(+)-transporting two-sector ATPase, 16 kDa subunitV-ATPase 16 kDa proteolipid subunitvacuolar ATP synthase 16 kDa proteolipid subunitvacuolar H+ ATP
Modification date2020031420200313
UniProtAcc

Q7L5Y9

Main function of 5'-partner protein: FUNCTION: Core component of the CTLH E3 ubiquitin-protein ligase complex that selectively accepts ubiquitin from UBE2H and mediates ubiquitination and subsequent proteasomal degradation of the transcription factor HBP1. MAEA and RMND5A are both required for catalytic activity of the CTLH E3 ubiquitin-protein ligase complex (PubMed:29911972). MAEA is required for normal cell proliferation (PubMed:29911972). The CTLH E3 ubiquitin-protein ligase complex is not required for the degradation of enzymes involved in gluconeogenesis, such as FBP1 (PubMed:29911972). Plays a role in erythroblast enucleation during erythrocyte maturation and in the development of mature macrophages (By similarity). Mediates the attachment of erythroid cell to mature macrophages; this MAEA-mediated contact inhibits erythroid cell apoptosis (PubMed:9763581). Participates in erythroblastic island formation, which is the functional unit of definitive erythropoiesis. Associates with F-actin to regulate actin distribution in erythroblasts and macrophages (By similarity). May contribute to nuclear architecture and cells division events (Probable). {ECO:0000250|UniProtKB:Q4VC33, ECO:0000269|PubMed:29911972, ECO:0000269|PubMed:9763581, ECO:0000305|PubMed:16510120}.

P27449

Main function of 5'-partner protein: FUNCTION: Proton-conducting pore forming subunit of the membrane integral V0 complex of vacuolar ATPase. V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells.
Ensembl transtripts involved in fusion geneENST idsENST00000264750, ENST00000303400, 
ENST00000452175, ENST00000505177, 
ENST00000514708, ENST00000505839, 
ENST00000510794, ENST00000512289, 
ENST00000564973, ENST00000565223, 
ENST00000330398, ENST00000568562, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score7 X 7 X 5=2458 X 8 X 3=192
# samples 119
** MAII scorelog2(11/245*10)=-1.15527822547791
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/192*10)=-1.09310940439148
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: MAEA [Title/Abstract] AND ATP6V0C [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: MAEA [Title/Abstract] AND ATP6V0C [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MAEA(1283770)-ATP6V0C(2569219), # samples:1
Anticipated loss of major functional domain due to fusion event.MAEA-ATP6V0C 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.
MAEA-ATP6V0C 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.
MAEA-ATP6V0C seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
MAEA-ATP6V0C seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
MAEA-ATP6V0C seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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
HgeneMAEA

GO:0007155

cell adhesion

9763581

HgeneMAEA

GO:0033033

negative regulation of myeloid cell apoptotic process

9763581



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/chr4:1283770/chr16:2569219)
- 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 MAEA (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 ATP6V0C (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)
ENST00000303400MAEAchr41283770+ENST00000568562ATP6V0Cchr162569219+45513244454137
ENST00000505177MAEAchr41283770+ENST00000568562ATP6V0Cchr162569219+419968418137
ENST00000264750MAEAchr41283770+ENST00000568562ATP6V0Cchr162569219+415924414137
ENST00000452175MAEAchr41283770+ENST00000568562ATP6V0Cchr162569219+412891411137
ENST00000514708MAEAchr41283770+ENST00000568562ATP6V0Cchr162569219+411880410137

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
ENST00000303400ENST00000568562MAEAchr41283770+ATP6V0Cchr162569219+0.242037550.75796247
ENST00000505177ENST00000568562MAEAchr41283770+ATP6V0Cchr162569219+0.259750660.7402493
ENST00000264750ENST00000568562MAEAchr41283770+ATP6V0Cchr162569219+0.2572170.742783
ENST00000452175ENST00000568562MAEAchr41283770+ATP6V0Cchr162569219+0.223892230.77610785
ENST00000514708ENST00000568562MAEAchr41283770+ATP6V0Cchr162569219+0.223467380.77653265

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 MAEA-ATP6V0C

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
MAEAchr41283770ATP6V0Cchr16256921913227SVVHDPEGPGVPDPQALGAAYGTAKS
MAEAchr41283770ATP6V0Cchr1625692198827SVVHDPEGPGVPDPQALGAAYGTAKS
MAEAchr41283770ATP6V0Cchr1625692198927SVVHDPEGPGVPDPQALGAAYGTAKS
MAEAchr41283770ATP6V0Cchr1625692199227SVVHDPEGPGVPDPQALGAAYGTAKS
MAEAchr41283770ATP6V0Cchr1625692199627SVVHDPEGPGVPDPQALGAAYGTAKS

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Potential FusionNeoAntigen Information of MAEA-ATP6V0C 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.
MAEA-ATP6V0C_1283770_2569219.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)
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:01DPQALGAAY0.96650.78171221
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:08DPQALGAAY0.95690.65291221
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B56:01VPDPQALGA0.93620.57611019
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:02VPDPQALGA0.69760.92781019
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:04VPDPQALGA0.69760.92781019
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:05DPQALGAAY0.65310.51651221
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B07:02GPGVPDPQAL0.99380.7279717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B07:05GPGVPDPQAL0.99380.7313717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B56:01VPDPQALGAA0.94920.6241020
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B81:01GPGVPDPQAL0.71360.8392717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B82:01GPGVPDPQAL0.55730.838717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:03GPGVPDPQAL0.54030.8844717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:04GPGVPDPQAL0.33270.9693717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:02GPGVPDPQAL0.33270.9693717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:01VPDPQALGAAY0.99020.54731021
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:08VPDPQALGAAY0.96840.54351021
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B15:02VPDPQALGAAY0.91040.7391021
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:04VPDPQALGAAY0.42830.82081021
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:02VPDPQALGAAY0.42830.82081021
MAEA-ATP6V0Cchr41283770chr16256921992HLA-C01:17GVPDPQAL0.99250.9583917
MAEA-ATP6V0Cchr41283770chr16256921992HLA-C01:30GVPDPQAL0.96920.9711917
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B15:31DPQALGAAY0.96920.78261221
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B54:01VPDPQALGA0.96740.76261019
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B78:01VPDPQALGA0.80770.69941019
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B56:04VPDPQALGA0.70250.72631019
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:12VPDPQALGA0.69760.92781019
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B39:10VPDPQALGA0.1290.93691019
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B07:12GPGVPDPQAL0.98850.7741717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B54:01VPDPQALGAA0.98180.79241020
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B07:04GPGVPDPQAL0.90270.7506717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B56:04GPGVPDPQAL0.59390.7462717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B42:01GPGVPDPQAL0.50590.7758717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B39:10GPGVPDPQAL0.42980.9679717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:12GPGVPDPQAL0.33270.9693717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B15:31VPDPQALGAAY0.98680.54911021
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:12VPDPQALGAAY0.42830.82081021
MAEA-ATP6V0Cchr41283770chr16256921992HLA-C01:02GVPDPQAL0.99230.9585917
MAEA-ATP6V0Cchr41283770chr16256921992HLA-C01:03GVPDPQAL0.99010.9664917
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:24DPQALGAAY0.97880.79351221
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:23DPQALGAAY0.96690.79971221
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:77DPQALGAAY0.96650.78171221
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:20DPQALGAAY0.95630.83011221
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B55:02VPDPQALGA0.87240.57781019
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:11DPQALGAAY0.85710.83341221
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B18:04DPQALGAAY0.8010.84731221
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B78:02VPDPQALGA0.77310.81821019
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B59:01VPDPQALGA0.73010.64031019
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B56:02VPDPQALGA0.70250.72631019
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:09VPDPQALGA0.69760.92781019
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:17DPQALGAAY0.67870.64021221
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:30DPQALGAAY0.67870.64021221
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B53:02DPQALGAAY0.63450.53411221
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B18:07DPQALGAAY0.5420.78611221
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B18:03DPQALGAAY0.53220.81451221
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B18:08DPQALGAAY0.48030.87051221
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B67:01VPDPQALGA0.3030.92111019
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B15:08DPQALGAAY0.26090.67631221
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B15:11DPQALGAAY0.25630.68121221
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:43DPQALGAAY0.19820.68631221
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B07:22GPGVPDPQAL0.99380.7279717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B55:02VPDPQALGAA0.94220.64751020
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B07:26GPGVPDPQAL0.78480.6083717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B56:02GPGVPDPQAL0.59390.7462717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B82:02GPGVPDPQAL0.55730.838717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B55:04GPGVPDPQAL0.51340.7243717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:13GPGVPDPQAL0.49150.8902717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:22GPGVPDPQAL0.46340.743717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B67:01GPGVPDPQAL0.40010.9761717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:09GPGVPDPQAL0.33270.9693717
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:77VPDPQALGAAY0.99020.54731021
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:20VPDPQALGAAY0.98970.60411021
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:23VPDPQALGAAY0.98860.55251021
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:24VPDPQALGAAY0.97680.62351021
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B15:08VPDPQALGAAY0.92490.581021
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B15:11VPDPQALGAAY0.92260.5961021
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:11VPDPQALGAAY0.91950.66511021
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:43VPDPQALGAAY0.9180.58771021
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B18:07VPDPQALGAAY0.52840.6371021
MAEA-ATP6V0Cchr41283770chr16256921992HLA-B35:09VPDPQALGAAY0.42830.82081021

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Potential FusionNeoAntigen Information of MAEA-ATP6V0C 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.

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)

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Fusion breakpoint peptide structures of MAEA-ATP6V0C

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
1747EGPGVPDPQALGAAMAEAATP6V0Cchr41283770chr16256921992

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of MAEA-ATP6V0C

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-B14:023BVN1747EGPGVPDPQALGAA-7.42139-7.53479
HLA-B14:023BVN1747EGPGVPDPQALGAA-4.88283-5.91813
HLA-B52:013W391747EGPGVPDPQALGAA-7.29998-7.41338
HLA-B52:013W391747EGPGVPDPQALGAA-5.08875-6.12405
HLA-A11:014UQ21747EGPGVPDPQALGAA-5.89811-6.93341
HLA-A24:025HGA1747EGPGVPDPQALGAA-5.76292-6.79822
HLA-A24:025HGA1747EGPGVPDPQALGAA-5.64621-5.75961
HLA-B27:056PYJ1747EGPGVPDPQALGAA-6.68895-7.72425
HLA-B27:056PYJ1747EGPGVPDPQALGAA-2.75311-2.86651
HLA-B44:053DX81747EGPGVPDPQALGAA-6.52728-6.64068
HLA-B44:053DX81747EGPGVPDPQALGAA-4.41635-5.45165

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Vaccine Design for the FusionNeoAntigens of MAEA-ATP6V0C

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
MAEA-ATP6V0Cchr41283770chr1625692191019VPDPQALGAACCCTCAAGCCCTGGGCGCTGCCTATG
MAEA-ATP6V0Cchr41283770chr1625692191020VPDPQALGAAACCCTCAAGCCCTGGGCGCTGCCTATGGCA
MAEA-ATP6V0Cchr41283770chr1625692191021VPDPQALGAAYACCCTCAAGCCCTGGGCGCTGCCTATGGCACAG
MAEA-ATP6V0Cchr41283770chr1625692191221DPQALGAAYAAGCCCTGGGCGCTGCCTATGGCACAG
MAEA-ATP6V0Cchr41283770chr162569219717GPGVPDPQALGAGTACCCGACCCTCAAGCCCTGGGCGCTG
MAEA-ATP6V0Cchr41283770chr162569219917GVPDPQALCCGACCCTCAAGCCCTGGGCGCTG

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

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Information of the samples that have these potential fusion neoantigens of MAEA-ATP6V0C

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-CancerMAEA-ATP6V0Cchr41283770ENST00000264750chr162569219ENST00000568562ERR315486

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Potential target of CAR-T therapy development for MAEA-ATP6V0C

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
TgeneATP6V0Cchr4:1283770chr16:2569219ENST0000033039803132_1520156.0TransmembraneHelical
TgeneATP6V0Cchr4:1283770chr16:2569219ENST000003303980356_760156.0TransmembraneHelical
TgeneATP6V0Cchr4:1283770chr16:2569219ENST000003303980393_1140156.0TransmembraneHelical

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 MAEA-ATP6V0C

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 MAEA-ATP6V0C

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