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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:CRISPLD2-JAK1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CRISPLD2-JAK1
FusionPDB ID: 19475
FusionGDB2.0 ID: 19475
HgeneTgene
Gene symbol

CRISPLD2

JAK1

Gene ID

83716

3716

Gene namecysteine rich secretory protein LCCL domain containing 2Janus kinase 1
SynonymsCRISP11|LCRISP2|LGL1JAK1A|JAK1B|JTK3
Cytomap

16q24.1

1p31.3

Type of geneprotein-codingprotein-coding
Descriptioncysteine-rich secretory protein LCCL domain-containing 2CRISP-11LCCL domain-containing cysteine-rich secretory protein 2cysteine-rich secretory protein 11late gestation lung 1testis secretory sperm-binding protein Li 207atrypsin inhibitortyrosine-protein kinase JAK1
Modification date2020031320200327
UniProtAcc

Q9H0B8

Main function of 5'-partner protein: FUNCTION: Promotes matrix assembly. {ECO:0000250}.

P23458

Main function of 5'-partner protein: FUNCTION: Tyrosine kinase of the non-receptor type, involved in the IFN-alpha/beta/gamma signal pathway (PubMed:7615558). Kinase partner for the interleukin (IL)-2 receptor (PubMed:11909529) as well as interleukin (IL)-10 receptor (PubMed:12133952). {ECO:0000269|PubMed:11909529, ECO:0000269|PubMed:7615558}.
Ensembl transtripts involved in fusion geneENST idsENST00000262424, ENST00000567845, 
ENST00000564567, ENST00000566431, 
ENST00000569090, 
ENST00000465376, 
ENST00000342505, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score5 X 3 X 4=6019 X 18 X 6=2052
# samples 519
** MAII scorelog2(5/60*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(19/2052*10)=-3.43295940727611
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CRISPLD2 [Title/Abstract] AND JAK1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CRISPLD2 [Title/Abstract] AND JAK1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CRISPLD2(84922969)-JAK1(65339206), # samples:1
Anticipated loss of major functional domain due to fusion event.CRISPLD2-JAK1 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.
CRISPLD2-JAK1 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.
CRISPLD2-JAK1 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.
CRISPLD2-JAK1 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
TgeneJAK1

GO:0038110

interleukin-2-mediated signaling pathway

11909529

TgeneJAK1

GO:0046677

response to antibiotic

16280321



check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr16:84922969/chr1:65339206)
- 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 CRISPLD2 (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 JAK1 (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)
ENST00000262424CRISPLD2chr1684922969+ENST00000342505JAK1chr165339206-6132166313447981554
ENST00000567845CRISPLD2chr1684922969+ENST00000342505JAK1chr165339206-6122165312747881553

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
ENST00000262424ENST00000342505CRISPLD2chr1684922969+JAK1chr165339206-0.0003458120.9996542
ENST00000567845ENST00000342505CRISPLD2chr1684922969+JAK1chr165339206-0.0003380910.9996619

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 CRISPLD2-JAK1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CRISPLD2chr1684922969JAK1chr1653392061653508TYVGSLRNGVQSERFYFTNWHGTNDN
CRISPLD2chr1684922969JAK1chr1653392061663509TYVGSLRNGVQSERFYFTNWHGTNDN

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Potential FusionNeoAntigen Information of CRISPLD2-JAK1 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.
CRISPLD2-JAK1_84922969_65339206.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)
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B15:03VQSERFYF0.99250.8123917
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B44:03SERFYFTNW0.99930.95321120
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B18:01SERFYFTNW0.93770.93921120
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-A32:13GVQSERFYF0.89230.9729817
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B27:04LRNGVQSERF0.99970.6865515
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B57:01QSERFYFTNW0.99950.98661020
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-A31:02SLRNGVQSER0.91260.6419414
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B15:01SLRNGVQSERF10.9382415
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B15:25SLRNGVQSERF0.99650.955415
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B27:03LRNGVQSERF0.99630.6529515
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B15:07SLRNGVQSERF0.99990.8147415
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B44:26SERFYFTNW0.99930.95321120
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B44:13SERFYFTNW0.99930.95321120
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B44:07SERFYFTNW0.99930.95321120
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B27:10LRNGVQSER0.99240.6553514
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-A32:01GVQSERFYF0.97810.9635817
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B18:08SERFYFTNW0.95460.85111120
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B18:05SERFYFTNW0.93770.93921120
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B18:03SERFYFTNW0.87020.93491120
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B27:08LRNGVQSERF0.99980.5301515
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B27:06LRNGVQSERF0.99950.7451515
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B57:10QSERFYFTNW0.99950.98661020
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B27:09LRNGVQSERF0.99920.6409515
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B57:04QSERFYFTNW0.99760.91371020
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-C07:22LRNGVQSERF0.99670.7925515
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B15:135SLRNGVQSERF10.9447415
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B15:33SLRNGVQSERF10.9382415
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B15:34SLRNGVQSERF10.9382415
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B15:27SLRNGVQSERF10.9362415
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B15:125SLRNGVQSERF10.9382415
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B15:50SLRNGVQSERF0.99990.9479415
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B15:35SLRNGVQSERF0.99990.9296415
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B15:24SLRNGVQSERF0.99990.9679415
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B15:12SLRNGVQSERF0.99950.9342415
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B15:24VQSERFYFTNW0.99940.8524920
CRISPLD2-JAK1chr1684922969chr1653392061663HLA-B15:39SLRNGVQSERF0.99680.9009415

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Potential FusionNeoAntigen Information of CRISPLD2-JAK1 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 CRISPLD2-JAK1

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
8049RNGVQSERFYFTNWCRISPLD2JAK1chr1684922969chr1653392061663

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CRISPLD2-JAK1

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-B14:023BVN8049RNGVQSERFYFTNW-7.15543-7.26883
HLA-B14:023BVN8049RNGVQSERFYFTNW-4.77435-5.80965
HLA-B52:013W398049RNGVQSERFYFTNW-6.80875-6.92215
HLA-B52:013W398049RNGVQSERFYFTNW-4.20386-5.23916
HLA-A11:014UQ28049RNGVQSERFYFTNW-7.5194-8.5547
HLA-A11:014UQ28049RNGVQSERFYFTNW-6.9601-7.0735
HLA-A24:025HGA8049RNGVQSERFYFTNW-7.52403-7.63743
HLA-A24:025HGA8049RNGVQSERFYFTNW-5.82433-6.85963
HLA-B27:056PYJ8049RNGVQSERFYFTNW-3.28285-4.31815
HLA-B44:053DX88049RNGVQSERFYFTNW-5.91172-6.94702
HLA-B44:053DX88049RNGVQSERFYFTNW-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of CRISPLD2-JAK1

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
CRISPLD2-JAK1chr1684922969chr1653392061020QSERFYFTNWGTCTGAAAGGTTCTATTTCACCAATTGGCA
CRISPLD2-JAK1chr1684922969chr1653392061120SERFYFTNWTGAAAGGTTCTATTTCACCAATTGGCA
CRISPLD2-JAK1chr1684922969chr165339206414SLRNGVQSERGCTCAGGAATGGAGTTCAGTCTGAAAGGTT
CRISPLD2-JAK1chr1684922969chr165339206415SLRNGVQSERFGCTCAGGAATGGAGTTCAGTCTGAAAGGTTCTA
CRISPLD2-JAK1chr1684922969chr165339206514LRNGVQSERCAGGAATGGAGTTCAGTCTGAAAGGTT
CRISPLD2-JAK1chr1684922969chr165339206515LRNGVQSERFCAGGAATGGAGTTCAGTCTGAAAGGTTCTA
CRISPLD2-JAK1chr1684922969chr165339206817GVQSERFYFAGTTCAGTCTGAAAGGTTCTATTTCAC
CRISPLD2-JAK1chr1684922969chr165339206917VQSERFYFTCAGTCTGAAAGGTTCTATTTCAC
CRISPLD2-JAK1chr1684922969chr165339206920VQSERFYFTNWTCAGTCTGAAAGGTTCTATTTCACCAATTGGCA

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 CRISPLD2-JAK1

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
STADCRISPLD2-JAK1chr1684922969ENST00000262424chr165339206ENST00000342505TCGA-CD-5798-01A

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Potential target of CAR-T therapy development for CRISPLD2-JAK1

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 CRISPLD2-JAK1

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 CRISPLD2-JAK1

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