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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:LGMN-DGCR8

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: LGMN-DGCR8
FusionPDB ID: 44573
FusionGDB2.0 ID: 44573
HgeneTgene
Gene symbol

LGMN

DGCR8

Gene ID

5641

54487

Gene namelegumainDGCR8 microprocessor complex subunit
SynonymsAEP|LGMN1|PRSC1C22orf12|DGCRK6|Gy1|pasha
Cytomap

14q32.12

22q11.21

Type of geneprotein-codingprotein-coding
Descriptionlegumainasparaginyl endopeptidasecysteine protease 1protease, cysteine 1protease, cysteine, 1 (legumain)microprocessor complex subunit DGCR8DiGeorge syndrome critical region 8DiGeorge syndrome critical region gene 8
Modification date2020031320200320
UniProtAcc

Q99538

Main function of 5'-partner protein: FUNCTION: Has a strict specificity for hydrolysis of asparaginyl bonds. Can also cleave aspartyl bonds slowly, especially under acidic conditions. Required for normal lysosomal protein degradation in renal proximal tubules. Required for normal degradation of internalized EGFR. Plays a role in the regulation of cell proliferation via its role in EGFR degradation (By similarity). May be involved in the processing of proteins for MHC class II antigen presentation in the lysosomal/endosomal system. {ECO:0000250, ECO:0000269|PubMed:23776206}.

Q8WYQ5

Main function of 5'-partner protein: FUNCTION: Component of the microprocessor complex that acts as a RNA- and heme-binding protein that is involved in the initial step of microRNA (miRNA) biogenesis. Component of the microprocessor complex that is required to process primary miRNA transcripts (pri-miRNAs) to release precursor miRNA (pre-miRNA) in the nucleus. Within the microprocessor complex, DGCR8 function as a molecular anchor necessary for the recognition of pri-miRNA at dsRNA-ssRNA junction and directs DROSHA to cleave 11 bp away form the junction to release hairpin-shaped pre-miRNAs that are subsequently cut by the cytoplasmic DICER to generate mature miRNAs (PubMed:26027739, PubMed:26748718). The heme-bound DGCR8 dimer binds pri-miRNAs as a cooperative trimer (of dimers) and is active in triggering pri-miRNA cleavage, whereas the heme-free DGCR8 monomer binds pri-miRNAs as a dimer and is much less active. Both double-stranded and single-stranded regions of a pri-miRNA are required for its binding (PubMed:15531877, PubMed:15574589, PubMed:15589161, PubMed:16751099, PubMed:16906129, PubMed:16963499, PubMed:17159994). Specifically recognizes and binds N6-methyladenosine (m6A)-containing pri-miRNAs, a modification required for pri-miRNAs processing (PubMed:25799998). Involved in the silencing of embryonic stem cell self-renewal (By similarity). {ECO:0000250|UniProtKB:Q9EQM6, ECO:0000269|PubMed:15531877, ECO:0000269|PubMed:15574589, ECO:0000269|PubMed:15589161, ECO:0000269|PubMed:16751099, ECO:0000269|PubMed:16906129, ECO:0000269|PubMed:16963499, ECO:0000269|PubMed:17159994, ECO:0000269|PubMed:25799998, ECO:0000269|PubMed:26027739, ECO:0000269|PubMed:26748718}.
Ensembl transtripts involved in fusion geneENST idsENST00000334869, ENST00000555699, 
ENST00000557434, ENST00000393218, 
ENST00000557034, 
ENST00000351989, 
ENST00000383024, ENST00000407755, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 6 X 3=1089 X 8 X 6=432
# samples 69
** MAII scorelog2(6/108*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/432*10)=-2.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: LGMN [Title/Abstract] AND DGCR8 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: LGMN [Title/Abstract] AND DGCR8 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)LGMN(93180168)-DGCR8(20077499), # samples:1
Anticipated loss of major functional domain due to fusion event.LGMN-DGCR8 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.
LGMN-DGCR8 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.
LGMN-DGCR8 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.
LGMN-DGCR8 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.
LGMN-DGCR8 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
LGMN-DGCR8 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
LGMN-DGCR8 seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
LGMN-DGCR8 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
HgeneLGMN

GO:0010447

response to acidic pH

18374643

HgeneLGMN

GO:0035729

cellular response to hepatocyte growth factor stimulus

21237226

HgeneLGMN

GO:0071277

cellular response to calcium ion

21237226

HgeneLGMN

GO:0090026

positive regulation of monocyte chemotaxis

18377911

HgeneLGMN

GO:0097202

activation of cysteine-type endopeptidase activity

9821970|18374643

HgeneLGMN

GO:0097264

self proteolysis

9821970|18374643

HgeneLGMN

GO:1904646

cellular response to amyloid-beta

25326800

HgeneLGMN

GO:2001028

positive regulation of endothelial cell chemotaxis

18377911

TgeneDGCR8

GO:0031053

primary miRNA processing

15531877|15574589|24449907|24910438



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/chr14:93180168/chr22:20077499)
- 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 LGMN (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 DGCR8 (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)
ENST00000393218LGMNchr1493180168-ENST00000351989DGCR8chr2220077499+39438813382179613
ENST00000393218LGMNchr1493180168-ENST00000383024DGCR8chr2220077499+38488813382080580
ENST00000393218LGMNchr1493180168-ENST00000407755DGCR8chr2220077499+38458813382080580

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
ENST00000393218ENST00000351989LGMNchr1493180168-DGCR8chr2220077499+0.0019046410.99809533
ENST00000393218ENST00000383024LGMNchr1493180168-DGCR8chr2220077499+0.0020467080.9979533
ENST00000393218ENST00000407755LGMNchr1493180168-DGCR8chr2220077499+0.0020597750.99794024

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 LGMN-DGCR8

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
LGMNchr1493180168DGCR8chr2220077499881181TIHYMYKHKMYRKKHDPPLSSIPCLH

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Potential FusionNeoAntigen Information of LGMN-DGCR8 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.
LGMN-DGCR8_93180168_20077499.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)
LGMN-DGCR8chr1493180168chr2220077499881HLA-B27:04YRKKHDPPL0.98510.77731019
LGMN-DGCR8chr1493180168chr2220077499881HLA-B39:06YRKKHDPPL0.98320.74961019
LGMN-DGCR8chr1493180168chr2220077499881HLA-B14:02YRKKHDPPL0.97910.78921019
LGMN-DGCR8chr1493180168chr2220077499881HLA-B14:01YRKKHDPPL0.97910.78921019
LGMN-DGCR8chr1493180168chr2220077499881HLA-B39:01YRKKHDPPL0.96520.81561019
LGMN-DGCR8chr1493180168chr2220077499881HLA-B08:09YRKKHDPPL0.83480.55351019
LGMN-DGCR8chr1493180168chr2220077499881HLA-B15:10YRKKHDPPL0.69260.61771019
LGMN-DGCR8chr1493180168chr2220077499881HLA-B15:37YRKKHDPPL0.33240.70571019
LGMN-DGCR8chr1493180168chr2220077499881HLA-B38:01KKHDPPLSSI0.92130.86191222
LGMN-DGCR8chr1493180168chr2220077499881HLA-B38:02KKHDPPLSSI0.90860.84861222
LGMN-DGCR8chr1493180168chr2220077499881HLA-B38:02RKKHDPPLSSI0.91550.91741122
LGMN-DGCR8chr1493180168chr2220077499881HLA-B38:01RKKHDPPLSSI0.90130.92781122
LGMN-DGCR8chr1493180168chr2220077499881HLA-C07:05YRKKHDPPL0.97880.93921019
LGMN-DGCR8chr1493180168chr2220077499881HLA-B39:09YRKKHDPPL0.97570.56991019
LGMN-DGCR8chr1493180168chr2220077499881HLA-C07:95YRKKHDPPL0.9690.64351019
LGMN-DGCR8chr1493180168chr2220077499881HLA-C07:27YRKKHDPPL0.96840.93821019
LGMN-DGCR8chr1493180168chr2220077499881HLA-B39:12YRKKHDPPL0.95440.82591019
LGMN-DGCR8chr1493180168chr2220077499881HLA-C07:13YRKKHDPPL0.94920.85541019
LGMN-DGCR8chr1493180168chr2220077499881HLA-C07:29YRKKHDPPL0.93960.87961019
LGMN-DGCR8chr1493180168chr2220077499881HLA-B39:05YRKKHDPPL0.89680.79121019
LGMN-DGCR8chr1493180168chr2220077499881HLA-C07:46YRKKHDPPL0.87790.84971019
LGMN-DGCR8chr1493180168chr2220077499881HLA-C07:67YRKKHDPPL0.81280.91531019
LGMN-DGCR8chr1493180168chr2220077499881HLA-C07:80YRKKHDPPL0.81280.91531019
LGMN-DGCR8chr1493180168chr2220077499881HLA-C07:19YRKKHDPPL0.78930.71531019
LGMN-DGCR8chr1493180168chr2220077499881HLA-C07:10YRKKHDPPL0.78730.93511019
LGMN-DGCR8chr1493180168chr2220077499881HLA-B14:03YRKKHDPPL0.32240.78421019
LGMN-DGCR8chr1493180168chr2220077499881HLA-C12:16YRKKHDPPL0.07850.93251019
LGMN-DGCR8chr1493180168chr2220077499881HLA-B39:05KKHDPPLSSI0.87510.71721222
LGMN-DGCR8chr1493180168chr2220077499881HLA-B73:01YRKKHDPPLSS0.9980.70921021
LGMN-DGCR8chr1493180168chr2220077499881HLA-B39:05RKKHDPPLSSI0.89120.80131122
LGMN-DGCR8chr1493180168chr2220077499881HLA-B27:06YRKKHDPPL0.99010.76121019
LGMN-DGCR8chr1493180168chr2220077499881HLA-B27:10YRKKHDPPL0.98470.89661019
LGMN-DGCR8chr1493180168chr2220077499881HLA-B27:09YRKKHDPPL0.98030.86771019
LGMN-DGCR8chr1493180168chr2220077499881HLA-B27:08YRKKHDPPL0.97810.81461019
LGMN-DGCR8chr1493180168chr2220077499881HLA-C07:01YRKKHDPPL0.97670.64861019
LGMN-DGCR8chr1493180168chr2220077499881HLA-B39:31YRKKHDPPL0.96610.81671019
LGMN-DGCR8chr1493180168chr2220077499881HLA-C07:17YRKKHDPPL0.88510.93461019
LGMN-DGCR8chr1493180168chr2220077499881HLA-C07:04YRKKHDPPL0.82880.89451019
LGMN-DGCR8chr1493180168chr2220077499881HLA-C07:02YRKKHDPPL0.81280.91531019
LGMN-DGCR8chr1493180168chr2220077499881HLA-C06:08YRKKHDPPL0.77140.98641019
LGMN-DGCR8chr1493180168chr2220077499881HLA-C07:22YRKKHDPPL0.74060.64221019
LGMN-DGCR8chr1493180168chr2220077499881HLA-B15:09YRKKHDPPL0.54260.7671019
LGMN-DGCR8chr1493180168chr2220077499881HLA-C03:67YRKKHDPPL0.37850.98011019
LGMN-DGCR8chr1493180168chr2220077499881HLA-C06:06YRKKHDPPL0.20940.97921019
LGMN-DGCR8chr1493180168chr2220077499881HLA-C06:17YRKKHDPPL0.18780.98771019
LGMN-DGCR8chr1493180168chr2220077499881HLA-C06:02YRKKHDPPL0.18780.98771019
LGMN-DGCR8chr1493180168chr2220077499881HLA-C18:01KKHDPPLSSI0.99240.75941222
LGMN-DGCR8chr1493180168chr2220077499881HLA-B38:05KKHDPPLSSI0.92130.86191222
LGMN-DGCR8chr1493180168chr2220077499881HLA-B39:11KKHDPPLSSI0.81540.52921222
LGMN-DGCR8chr1493180168chr2220077499881HLA-B39:11RKKHDPPLSSI0.98320.68071122
LGMN-DGCR8chr1493180168chr2220077499881HLA-B38:05RKKHDPPLSSI0.90130.92781122

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Potential FusionNeoAntigen Information of LGMN-DGCR8 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.
LGMN-DGCR8_93180168_20077499.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)
LGMN-DGCR8chr1493180168chr2220077499881DRB1-1111TIHYMYKHKMYRKKH015
LGMN-DGCR8chr1493180168chr2220077499881DRB1-1114TIHYMYKHKMYRKKH015
LGMN-DGCR8chr1493180168chr2220077499881DRB1-1120TIHYMYKHKMYRKKH015
LGMN-DGCR8chr1493180168chr2220077499881DRB1-1168TIHYMYKHKMYRKKH015
LGMN-DGCR8chr1493180168chr2220077499881DRB1-1186TIHYMYKHKMYRKKH015
LGMN-DGCR8chr1493180168chr2220077499881DRB1-1186IHYMYKHKMYRKKHD116
LGMN-DGCR8chr1493180168chr2220077499881DRB1-1302TIHYMYKHKMYRKKH015
LGMN-DGCR8chr1493180168chr2220077499881DRB1-1316TIHYMYKHKMYRKKH015
LGMN-DGCR8chr1493180168chr2220077499881DRB1-1316IHYMYKHKMYRKKHD116
LGMN-DGCR8chr1493180168chr2220077499881DRB1-1323TIHYMYKHKMYRKKH015
LGMN-DGCR8chr1493180168chr2220077499881DRB1-1329TIHYMYKHKMYRKKH015
LGMN-DGCR8chr1493180168chr2220077499881DRB1-1334TIHYMYKHKMYRKKH015
LGMN-DGCR8chr1493180168chr2220077499881DRB1-1336TIHYMYKHKMYRKKH015
LGMN-DGCR8chr1493180168chr2220077499881DRB1-1339TIHYMYKHKMYRKKH015
LGMN-DGCR8chr1493180168chr2220077499881DRB1-1341TIHYMYKHKMYRKKH015
LGMN-DGCR8chr1493180168chr2220077499881DRB1-1363TIHYMYKHKMYRKKH015
LGMN-DGCR8chr1493180168chr2220077499881DRB1-1373TIHYMYKHKMYRKKH015
LGMN-DGCR8chr1493180168chr2220077499881DRB1-1374TIHYMYKHKMYRKKH015
LGMN-DGCR8chr1493180168chr2220077499881DRB1-1396TIHYMYKHKMYRKKH015
LGMN-DGCR8chr1493180168chr2220077499881DRB1-1397TIHYMYKHKMYRKKH015
LGMN-DGCR8chr1493180168chr2220077499881DRB1-1399TIHYMYKHKMYRKKH015

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Fusion breakpoint peptide structures of LGMN-DGCR8

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
4270KHKMYRKKHDPPLSLGMNDGCR8chr1493180168chr2220077499881

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of LGMN-DGCR8

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-B14:023BVN4270KHKMYRKKHDPPLS-7.15543-7.26883
HLA-B14:023BVN4270KHKMYRKKHDPPLS-4.77435-5.80965
HLA-B52:013W394270KHKMYRKKHDPPLS-6.80875-6.92215
HLA-B52:013W394270KHKMYRKKHDPPLS-4.20386-5.23916
HLA-A11:014UQ24270KHKMYRKKHDPPLS-7.5194-8.5547
HLA-A11:014UQ24270KHKMYRKKHDPPLS-6.9601-7.0735
HLA-A24:025HGA4270KHKMYRKKHDPPLS-7.52403-7.63743
HLA-A24:025HGA4270KHKMYRKKHDPPLS-5.82433-6.85963
HLA-B27:056PYJ4270KHKMYRKKHDPPLS-3.28285-4.31815
HLA-B44:053DX84270KHKMYRKKHDPPLS-5.91172-6.94702
HLA-B44:053DX84270KHKMYRKKHDPPLS-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of LGMN-DGCR8

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
LGMN-DGCR8chr1493180168chr22200774991019YRKKHDPPLTACCGAAAGAAACACGACCCTCCTCTG
LGMN-DGCR8chr1493180168chr22200774991021YRKKHDPPLSSTACCGAAAGAAACACGACCCTCCTCTGAGTAGC
LGMN-DGCR8chr1493180168chr22200774991122RKKHDPPLSSICGAAAGAAACACGACCCTCCTCTGAGTAGCATC
LGMN-DGCR8chr1493180168chr22200774991222KKHDPPLSSIAAGAAACACGACCCTCCTCTGAGTAGCATC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
LGMN-DGCR8chr1493180168chr2220077499015TIHYMYKHKMYRKKHACCATCCATTACATGTACAAACACAAAATGTACCGAAAGAAACAC
LGMN-DGCR8chr1493180168chr2220077499116IHYMYKHKMYRKKHDATCCATTACATGTACAAACACAAAATGTACCGAAAGAAACACGAC

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Information of the samples that have these potential fusion neoantigens of LGMN-DGCR8

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
STADLGMN-DGCR8chr1493180168ENST00000393218chr2220077499ENST00000351989TCGA-D7-6820-01A

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Potential target of CAR-T therapy development for LGMN-DGCR8

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 LGMN-DGCR8

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 LGMN-DGCR8

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