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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:LANCL2-SEPT14

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: LANCL2-SEPT14
FusionPDB ID: 44028
FusionGDB2.0 ID: 44028
HgeneTgene
Gene symbol

LANCL2

SEPT14

Gene ID

55915

346288

Gene nameLanC like 2septin 14
SynonymsGPR69B|TASPSEPT14
Cytomap

7p11.2

7p11.2

Type of geneprotein-codingprotein-coding
DescriptionlanC-like protein 2G protein-coupled receptor 69BLanC (bacterial lantibiotic synthetase component C)-like 2LanC lantibiotic synthetase component C-like 2testis-specific adriamycin sensitivity proteinseptin-14
Modification date2020031320200313
UniProtAcc

Q9NS86

Main function of 5'-partner protein: FUNCTION: Necessary for abscisic acid (ABA) binding on the cell membrane and activation of the ABA signaling pathway in granulocytes. {ECO:0000269|PubMed:19667068}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000254770, ENST00000486376, 
ENST00000388975, ENST00000477628, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score9 X 5 X 5=2256 X 5 X 5=150
# samples 1013
** MAII scorelog2(10/225*10)=-1.16992500144231
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(13/150*10)=-0.206450877467426
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: LANCL2 [Title/Abstract] AND SEPT14 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: LANCL2 [Title/Abstract] AND SEPT14 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)LANCL2(55479782)-SEPT14(55886916), # samples:7
Anticipated loss of major functional domain due to fusion event.LANCL2-SEPT14 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.
LANCL2-SEPT14 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.
LANCL2-SEPT14 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.
LANCL2-SEPT14 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.
* 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
HgeneLANCL2

GO:0009789

positive regulation of abscisic acid-activated signaling pathway

19667068

HgeneLANCL2

GO:0045892

negative regulation of transcription, DNA-templated

12566319



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/chr7:55479782/chr7:55886916)
- 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 LANCL2 (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 SEPT14 (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)
ENST00000254770LANCL2chr755479782+ENST00000388975SEPT14chr755886916-453415865452164539
ENST00000254770LANCL2chr755433922+ENST00000388975SEPT14chr755914330-43967825452026493

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
ENST00000254770ENST00000388975LANCL2chr755479782+SEPT14chr755886916-0.000182050.999818
ENST00000254770ENST00000388975LANCL2chr755433922+SEPT14chr755914330-0.0001149570.9998851

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 LANCL2-SEPT14

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
LANCL2chr755433922SEPT14chr75591433078278TTDEPGLPFHQDGKQKENNIRCLTTI
LANCL2chr755479782SEPT14chr7558869161586347APGVIHMLMQAYKGLLPFAVVGSTDE

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Potential FusionNeoAntigen Information of LANCL2-SEPT14 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.
LANCL2-SEPT14_55479782_55886916.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)
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:02QAYKGLLPF0.9990.958918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:25QAYKGLLPF0.9990.9518918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:01QAYKGLLPF0.99860.9107918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:03QAYKGLLPF0.9970.8613918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B35:08QAYKGLLPF0.9940.9197918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:17QAYKGLLPF0.99340.9602918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B35:05QAYKGLLPF0.99280.7298918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:16QAYKGLLPF0.99130.9207918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B35:01QAYKGLLPF0.9910.9188918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B58:02QAYKGLLPF0.96520.9682918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B57:03QAYKGLLPF0.95490.9919918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B58:01QAYKGLLPF0.95170.973918
LANCL2-SEPT14chr755479782chr7558869161586HLA-A32:13QAYKGLLPF0.88120.948918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B52:01QAYKGLLPF0.67780.9847918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:01MQAYKGLLPF0.99980.9559818
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:25MQAYKGLLPF0.99560.9569818
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:03MQAYKGLLPF0.99310.8967818
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:21QAYKGLLPF0.99890.916918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:07QAYKGLLPF0.99870.7228918
LANCL2-SEPT14chr755479782chr7558869161586HLA-C03:08QAYKGLLPF0.9940.9076918
LANCL2-SEPT14chr755479782chr7558869161586HLA-C03:19QAYKGLLPF0.99340.987918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:05QAYKGLLPF0.99220.9207918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:31QAYKGLLPF0.99080.933918
LANCL2-SEPT14chr755479782chr7558869161586HLA-C12:12QAYKGLLPF0.98730.918918
LANCL2-SEPT14chr755479782chr7558869161586HLA-C15:04QAYKGLLPF0.98680.9285918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:04QAYKGLLPF0.98370.9441918
LANCL2-SEPT14chr755479782chr7558869161586HLA-C03:07QAYKGLLPF0.95910.9832918
LANCL2-SEPT14chr755479782chr7558869161586HLA-C03:14QAYKGLLPF0.9190.9777918
LANCL2-SEPT14chr755479782chr7558869161586HLA-C12:04QAYKGLLPF0.91360.9929918
LANCL2-SEPT14chr755479782chr7558869161586HLA-C06:03QAYKGLLPF0.90280.993918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:07MQAYKGLLPF0.99940.8148818
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:04MQAYKGLLPF0.99910.9711818
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:05MQAYKGLLPF0.95320.9406818
LANCL2-SEPT14chr755479782chr7558869161586HLA-C14:02AYKGLLPF0.91970.97641018
LANCL2-SEPT14chr755479782chr7558869161586HLA-C14:03AYKGLLPF0.91970.97641018
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:39QAYKGLLPF0.9990.8969918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:08QAYKGLLPF0.99880.8534918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B35:11QAYKGLLPF0.99880.9217918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:27QAYKGLLPF0.99870.9219918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:11QAYKGLLPF0.99870.8654918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:135QAYKGLLPF0.99860.9204918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:125QAYKGLLPF0.99860.9107918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:33QAYKGLLPF0.99860.9107918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:34QAYKGLLPF0.99860.9107918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:35QAYKGLLPF0.99850.9053918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B35:43QAYKGLLPF0.99850.8593918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:24QAYKGLLPF0.99790.9538918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:50QAYKGLLPF0.9970.92918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:54QAYKGLLPF0.99640.8827918
LANCL2-SEPT14chr755479782chr7558869161586HLA-C03:02QAYKGLLPF0.99640.9647918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:13QAYKGLLPF0.99580.8603918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B35:17QAYKGLLPF0.99450.8741918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B35:30QAYKGLLPF0.99450.8741918
LANCL2-SEPT14chr755479782chr7558869161586HLA-C03:04QAYKGLLPF0.99420.9859918
LANCL2-SEPT14chr755479782chr7558869161586HLA-C03:03QAYKGLLPF0.99420.9859918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:20QAYKGLLPF0.99260.9506918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B35:28QAYKGLLPF0.99170.9543918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B58:06QAYKGLLPF0.99160.9327918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B35:77QAYKGLLPF0.9910.9188918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B35:23QAYKGLLPF0.99080.9302918
LANCL2-SEPT14chr755479782chr7558869161586HLA-C12:02QAYKGLLPF0.98960.9663918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B35:20QAYKGLLPF0.98950.9583918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:12QAYKGLLPF0.98940.8948918
LANCL2-SEPT14chr755479782chr7558869161586HLA-C16:04QAYKGLLPF0.98820.9782918
LANCL2-SEPT14chr755479782chr7558869161586HLA-C03:17QAYKGLLPF0.98730.9645918
LANCL2-SEPT14chr755479782chr7558869161586HLA-C15:09QAYKGLLPF0.98680.9285918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B48:02QAYKGLLPF0.98510.9454918
LANCL2-SEPT14chr755479782chr7558869161586HLA-C03:05QAYKGLLPF0.98460.8915918
LANCL2-SEPT14chr755479782chr7558869161586HLA-C12:03QAYKGLLPF0.98340.98918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B57:02QAYKGLLPF0.97880.945918
LANCL2-SEPT14chr755479782chr7558869161586HLA-A32:01QAYKGLLPF0.96690.9423918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B35:24QAYKGLLPF0.95830.8942918
LANCL2-SEPT14chr755479782chr7558869161586HLA-C16:01QAYKGLLPF0.95820.9703918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B35:13QAYKGLLPF0.92390.934918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B53:02QAYKGLLPF0.89120.5525918
LANCL2-SEPT14chr755479782chr7558869161586HLA-C16:02QAYKGLLPF0.74110.9895918
LANCL2-SEPT14chr755479782chr7558869161586HLA-A25:01QAYKGLLPF0.6290.9024918
LANCL2-SEPT14chr755479782chr7558869161586HLA-C02:02QAYKGLLPF0.60570.9744918
LANCL2-SEPT14chr755479782chr7558869161586HLA-C02:10QAYKGLLPF0.60570.9744918
LANCL2-SEPT14chr755479782chr7558869161586HLA-A30:01AYKGLLPFA0.5860.96211019
LANCL2-SEPT14chr755479782chr7558869161586HLA-B18:07QAYKGLLPF0.43640.7979918
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:50MQAYKGLLPF0.99980.9632818
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:34MQAYKGLLPF0.99980.9559818
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:125MQAYKGLLPF0.99980.9559818
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:33MQAYKGLLPF0.99980.9559818
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:27MQAYKGLLPF0.99980.9685818
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:135MQAYKGLLPF0.99980.9598818
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:53MQAYKGLLPF0.99980.9513818
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:24MQAYKGLLPF0.99970.9603818
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:35MQAYKGLLPF0.99930.9567818
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:12MQAYKGLLPF0.9990.8958818
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:68MQAYKGLLPF0.9990.737818
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:54MQAYKGLLPF0.99880.9394818
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:39MQAYKGLLPF0.9960.9262818
LANCL2-SEPT14chr755479782chr7558869161586HLA-B15:20MQAYKGLLPF0.95390.9617818
LANCL2-SEPT14chr755479782chr7558869161586HLA-B35:28MQAYKGLLPF0.95280.9643818
LANCL2-SEPT14chr755479782chr7558869161586HLA-B48:02MQAYKGLLPF0.92260.9555818

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Potential FusionNeoAntigen Information of LANCL2-SEPT14 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.
LANCL2-SEPT14_55433922_55914330.msa
LANCL2-SEPT14_55479782_55886916.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)
LANCL2-SEPT14chr755433922chr755914330782DRB1-0305GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-0305PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755433922chr755914330782DRB1-0305EPGLPFHQDGKQKEN318
LANCL2-SEPT14chr755433922chr755914330782DRB1-0305LPFHQDGKQKENNIR621
LANCL2-SEPT14chr755433922chr755914330782DRB1-0340GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-0340PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755433922chr755914330782DRB1-0340EPGLPFHQDGKQKEN318
LANCL2-SEPT14chr755433922chr755914330782DRB1-0340LPFHQDGKQKENNIR621
LANCL2-SEPT14chr755433922chr755914330782DRB1-0466GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-0466PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755433922chr755914330782DRB1-0466EPGLPFHQDGKQKEN318
LANCL2-SEPT14chr755433922chr755914330782DRB1-0840GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-0840PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755433922chr755914330782DRB1-0840EPGLPFHQDGKQKEN318
LANCL2-SEPT14chr755433922chr755914330782DRB1-0840LPFHQDGKQKENNIR621
LANCL2-SEPT14chr755433922chr755914330782DRB1-1153GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-1153PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755433922chr755914330782DRB1-1153EPGLPFHQDGKQKEN318
LANCL2-SEPT14chr755433922chr755914330782DRB1-1179GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-1179PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755433922chr755914330782DRB1-1179EPGLPFHQDGKQKEN318
LANCL2-SEPT14chr755433922chr755914330782DRB1-1303GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-1303PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755433922chr755914330782DRB1-1303EPGLPFHQDGKQKEN318
LANCL2-SEPT14chr755433922chr755914330782DRB1-1303LPFHQDGKQKENNIR621
LANCL2-SEPT14chr755433922chr755914330782DRB1-1303DEPGLPFHQDGKQKE217
LANCL2-SEPT14chr755433922chr755914330782DRB1-13101GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-13101PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755433922chr755914330782DRB1-13101EPGLPFHQDGKQKEN318
LANCL2-SEPT14chr755433922chr755914330782DRB1-13101LPFHQDGKQKENNIR621
LANCL2-SEPT14chr755433922chr755914330782DRB1-1310GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-1310PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755433922chr755914330782DRB1-1310EPGLPFHQDGKQKEN318
LANCL2-SEPT14chr755433922chr755914330782DRB1-1310LPFHQDGKQKENNIR621
LANCL2-SEPT14chr755433922chr755914330782DRB1-1312GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-1333GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-1333PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755433922chr755914330782DRB1-1333EPGLPFHQDGKQKEN318
LANCL2-SEPT14chr755433922chr755914330782DRB1-1333LPFHQDGKQKENNIR621
LANCL2-SEPT14chr755433922chr755914330782DRB1-1333DEPGLPFHQDGKQKE217
LANCL2-SEPT14chr755433922chr755914330782DRB1-1337GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-1337PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755433922chr755914330782DRB1-1338GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-1338PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755433922chr755914330782DRB1-1338EPGLPFHQDGKQKEN318
LANCL2-SEPT14chr755433922chr755914330782DRB1-1338LPFHQDGKQKENNIR621
LANCL2-SEPT14chr755433922chr755914330782DRB1-1365GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-1365PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755433922chr755914330782DRB1-1365EPGLPFHQDGKQKEN318
LANCL2-SEPT14chr755433922chr755914330782DRB1-1365LPFHQDGKQKENNIR621
LANCL2-SEPT14chr755433922chr755914330782DRB1-1366GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-1366PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755433922chr755914330782DRB1-1366EPGLPFHQDGKQKEN318
LANCL2-SEPT14chr755433922chr755914330782DRB1-1366LPFHQDGKQKENNIR621
LANCL2-SEPT14chr755433922chr755914330782DRB1-1388GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-1388PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755433922chr755914330782DRB1-1388EPGLPFHQDGKQKEN318
LANCL2-SEPT14chr755433922chr755914330782DRB1-1388LPFHQDGKQKENNIR621
LANCL2-SEPT14chr755433922chr755914330782DRB1-1388DEPGLPFHQDGKQKE217
LANCL2-SEPT14chr755433922chr755914330782DRB1-1390GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-1390PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755433922chr755914330782DRB1-1390EPGLPFHQDGKQKEN318
LANCL2-SEPT14chr755433922chr755914330782DRB1-1390LPFHQDGKQKENNIR621
LANCL2-SEPT14chr755433922chr755914330782DRB1-1390DEPGLPFHQDGKQKE217
LANCL2-SEPT14chr755433922chr755914330782DRB1-1395GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-1395PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755433922chr755914330782DRB1-1395EPGLPFHQDGKQKEN318
LANCL2-SEPT14chr755433922chr755914330782DRB1-1395LPFHQDGKQKENNIR621
LANCL2-SEPT14chr755433922chr755914330782DRB1-1395DEPGLPFHQDGKQKE217
LANCL2-SEPT14chr755433922chr755914330782DRB1-1409GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-1409PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755433922chr755914330782DRB1-1413GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-1413PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755433922chr755914330782DRB1-1419GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-1419PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755433922chr755914330782DRB1-1469GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB1-1469PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755433922chr755914330782DRB3-0114GLPFHQDGKQKENNI520
LANCL2-SEPT14chr755433922chr755914330782DRB3-0114PGLPFHQDGKQKENN419
LANCL2-SEPT14chr755479782chr7558869161586DRB1-0117MQAYKGLLPFAVVGS823
LANCL2-SEPT14chr755479782chr7558869161586DRB1-0129MQAYKGLLPFAVVGS823
LANCL2-SEPT14chr755479782chr7558869161586DRB1-0437YKGLLPFAVVGSTDE1126
LANCL2-SEPT14chr755479782chr7558869161586DRB1-0442YKGLLPFAVVGSTDE1126
LANCL2-SEPT14chr755479782chr7558869161586DRB1-0453YKGLLPFAVVGSTDE1126
LANCL2-SEPT14chr755479782chr7558869161586DRB1-0455YKGLLPFAVVGSTDE1126
LANCL2-SEPT14chr755479782chr7558869161586DRB1-0458YKGLLPFAVVGSTDE1126
LANCL2-SEPT14chr755479782chr7558869161586DRB1-0465YKGLLPFAVVGSTDE1126
LANCL2-SEPT14chr755479782chr7558869161586DRB1-0473YKGLLPFAVVGSTDE1126

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Fusion breakpoint peptide structures of LANCL2-SEPT14

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
5956MLMQAYKGLLPFAVLANCL2SEPT14chr755479782chr7558869161586

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of LANCL2-SEPT14

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-B14:023BVN5956MLMQAYKGLLPFAV-7.75776-7.86956
HLA-B14:023BVN5956MLMQAYKGLLPFAV-4.52646-5.56956
HLA-B52:013W395956MLMQAYKGLLPFAV-7.1873-7.2991
HLA-B52:013W395956MLMQAYKGLLPFAV-2.81174-3.85484
HLA-A11:014UQ25956MLMQAYKGLLPFAV-5.13576-5.24756
HLA-A24:025HGA5956MLMQAYKGLLPFAV-8.42076-8.53256
HLA-A24:025HGA5956MLMQAYKGLLPFAV-7.10496-8.14806
HLA-B27:056PYJ5956MLMQAYKGLLPFAV-9.28296-9.39476
HLA-B44:053DX85956MLMQAYKGLLPFAV-6.88262-6.99442
HLA-B44:053DX85956MLMQAYKGLLPFAV-5.46822-6.51132

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Vaccine Design for the FusionNeoAntigens of LANCL2-SEPT14

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
LANCL2-SEPT14chr755479782chr7558869161018AYKGLLPFGCGTACAAGGGGCTGTTACCCTTT
LANCL2-SEPT14chr755479782chr7558869161019AYKGLLPFAGCGTACAAGGGGCTGTTACCCTTTGCT
LANCL2-SEPT14chr755479782chr755886916818MQAYKGLLPFATGCAGGCGTACAAGGGGCTGTTACCCTTT
LANCL2-SEPT14chr755479782chr755886916918QAYKGLLPFCAGGCGTACAAGGGGCTGTTACCCTTT

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
LANCL2-SEPT14chr755433922chr755914330217DEPGLPFHQDGKQKEGAGCCCGGCCTCCCTTTTCATCAGGACGGGAAGCAAAAAGAAAAT
LANCL2-SEPT14chr755433922chr755914330318EPGLPFHQDGKQKENCCCGGCCTCCCTTTTCATCAGGACGGGAAGCAAAAAGAAAATAAT
LANCL2-SEPT14chr755433922chr755914330419PGLPFHQDGKQKENNGGCCTCCCTTTTCATCAGGACGGGAAGCAAAAAGAAAATAATATT
LANCL2-SEPT14chr755433922chr755914330520GLPFHQDGKQKENNICTCCCTTTTCATCAGGACGGGAAGCAAAAAGAAAATAATATTCGT
LANCL2-SEPT14chr755433922chr755914330621LPFHQDGKQKENNIRCCTTTTCATCAGGACGGGAAGCAAAAAGAAAATAATATTCGTTGT
LANCL2-SEPT14chr755479782chr7558869161126YKGLLPFAVVGSTDETACAAGGGGCTGTTACCCTTTGCTGTGGTAGGGAGTACAGATGAA
LANCL2-SEPT14chr755479782chr755886916823MQAYKGLLPFAVVGSATGCAGGCGTACAAGGGGCTGTTACCCTTTGCTGTGGTAGGGAGT

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Information of the samples that have these potential fusion neoantigens of LANCL2-SEPT14

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
GBMLANCL2-SEPT14chr755479782ENST00000254770chr755886916ENST00000388975TCGA-06-0211-01A

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Potential target of CAR-T therapy development for LANCL2-SEPT14

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 LANCL2-SEPT14

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 LANCL2-SEPT14

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