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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:SPINT2-GRIP1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SPINT2-GRIP1
FusionPDB ID: 85845
FusionGDB2.0 ID: 85845
HgeneTgene
Gene symbol

SPINT2

GRIP1

Gene ID

10653

85329

Gene nameserine peptidase inhibitor, Kunitz type 2galectin 12
SynonymsDIAR3|HAI-2|HAI2|Kop|PBGAL12|GRIP1
Cytomap

19q13.2

11q12.3

Type of geneprotein-codingprotein-coding
Descriptionkunitz-type protease inhibitor 2hepatocyte growth factor activator inhibitor type 2serine protease inhibitor, Kunitz type, 2testicular tissue protein Li 183galectin-12galectin-related inhibitor of proliferationlectin, galactoside-binding, soluble, 12testicular secretory protein Li 26
Modification date2020031520200313
UniProtAcc.

Q9Y3R0

Main function of 5'-partner protein: FUNCTION: May play a role as a localized scaffold for the assembly of a multiprotein signaling complex and as mediator of the trafficking of its binding partners at specific subcellular location in neurons (PubMed:10197531). Through complex formation with NSG1, GRIA2 and STX12 controls the intracellular fate of AMPAR and the endosomal sorting of the GRIA2 subunit toward recycling and membrane targeting (By similarity). {ECO:0000250|UniProtKB:P97879, ECO:0000269|PubMed:10197531}.
Ensembl transtripts involved in fusion geneENST idsENST00000301244, ENST00000454580, 
ENST00000587090, 
ENST00000542021, 
ENST00000286445, ENST00000359742, 
ENST00000398016, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score16 X 8 X 9=115225 X 17 X 10=4250
# samples 2127
** MAII scorelog2(21/1152*10)=-2.45567948377619
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(27/4250*10)=-3.9764315288616
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: SPINT2 [Title/Abstract] AND GRIP1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: SPINT2 [Title/Abstract] AND GRIP1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SPINT2(38781215)-GRIP1(66935730), # samples:2
Anticipated loss of major functional domain due to fusion event.SPINT2-GRIP1 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.
SPINT2-GRIP1 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
HgeneSPINT2

GO:0022408

negative regulation of cell-cell adhesion

19592578

HgeneSPINT2

GO:2000146

negative regulation of cell motility

19592578

TgeneGRIP1

GO:0097193

intrinsic apoptotic signaling pathway

11435439



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/chr19:38781215/chr12:66935730)
- 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 SPINT2 (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 GRIP1 (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)
ENST00000301244SPINT2chr1938781215+ENST00000398016GRIP1chr1266935730-5710102741141211236
ENST00000301244SPINT2chr1938781215+ENST00000359742GRIP1chr1266935730-5866102741142771288
ENST00000301244SPINT2chr1938781215+ENST00000286445GRIP1chr1266935730-5821102741142321273
ENST00000587090SPINT2chr1938781215+ENST00000398016GRIP1chr1266935730-53176346337281221
ENST00000587090SPINT2chr1938781215+ENST00000359742GRIP1chr1266935730-54736346338841273
ENST00000587090SPINT2chr1938781215+ENST00000286445GRIP1chr1266935730-54286346338391258
ENST00000454580SPINT2chr1938781215+ENST00000398016GRIP1chr1266935730-542173829338321179
ENST00000454580SPINT2chr1938781215+ENST00000359742GRIP1chr1266935730-557773829339881231
ENST00000454580SPINT2chr1938781215+ENST00000286445GRIP1chr1266935730-553273829339431216

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
ENST00000301244ENST00000398016SPINT2chr1938781215+GRIP1chr1266935730-0.000952970.999047
ENST00000301244ENST00000359742SPINT2chr1938781215+GRIP1chr1266935730-0.0005797740.9994203
ENST00000301244ENST00000286445SPINT2chr1938781215+GRIP1chr1266935730-0.0007728760.99922717
ENST00000587090ENST00000398016SPINT2chr1938781215+GRIP1chr1266935730-0.0005441960.99945575
ENST00000587090ENST00000359742SPINT2chr1938781215+GRIP1chr1266935730-0.0003301420.9996699
ENST00000587090ENST00000286445SPINT2chr1938781215+GRIP1chr1266935730-0.0004379970.99956197
ENST00000454580ENST00000398016SPINT2chr1938781215+GRIP1chr1266935730-0.0008204010.99917954
ENST00000454580ENST00000359742SPINT2chr1938781215+GRIP1chr1266935730-0.0005031980.9994968
ENST00000454580ENST00000286445SPINT2chr1938781215+GRIP1chr1266935730-0.0006666850.9993333

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 SPINT2-GRIP1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
SPINT2chr1938781215GRIP1chr12669357301027205RQQENPPLPLGSKEEFKGSTVVELMK
SPINT2chr1938781215GRIP1chr1266935730634190RQQENPPLPLGSKEEFKGSTVVELMK
SPINT2chr1938781215GRIP1chr1266935730738148RQQENPPLPLGSKEEFKGSTVVELMK

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Potential FusionNeoAntigen Information of SPINT2-GRIP1 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.
SPINT2-GRIP1_38781215_66935730.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)
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B35:01LPLGSKEEF0.99770.9567716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B45:01KEEFKGSTV0.99680.86041221
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B50:02KEEFKGSTV0.9960.74741221
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B35:05LPLGSKEEF0.99540.8204716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B35:08LPLGSKEEF0.99380.9572716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B53:01LPLGSKEEF0.98220.5796716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B35:03LPLGSKEEF0.98120.9635716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B35:04LPLGSKEEF0.77150.9877716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B35:02LPLGSKEEF0.77150.9877716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B41:01KEEFKGSTV0.49510.94531221
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B50:01KEEFKGSTV0.45220.79261221
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B39:13KEEFKGSTV0.34990.90311221
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B82:01LPLGSKEEF0.0820.5775716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B41:01KEEFKGSTVV0.91480.94871222
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B50:01KEEFKGSTVV0.8990.80711222
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B39:13KEEFKGSTVV0.81750.94031222
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B50:01SKEEFKGSTVV0.99530.81791122
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B41:01SKEEFKGSTVV0.98840.94991122
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B40:06KEEFKGSTV0.99960.67821221
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B15:31LPLGSKEEF0.99750.9514716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B42:02LPLGSKEEF0.8280.9562716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B07:12LPLGSKEEF0.79440.6755716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B35:12LPLGSKEEF0.77150.9877716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B42:01LPLGSKEEF0.72290.954716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B39:08KEEFKGSTV0.57320.93391221
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B51:08LPLGSKEEF0.52150.5649716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B39:10LPLGSKEEF0.30220.9876716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B40:06KEEFKGSTVV0.99910.69011222
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B40:06SKEEFKGSTVV0.99060.73061122
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B40:04KEEFKGSTV0.99790.79541221
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B35:23LPLGSKEEF0.99790.9621716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B35:77LPLGSKEEF0.99770.9567716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B35:20LPLGSKEEF0.99680.9672716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B35:17LPLGSKEEF0.99570.9179716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B35:30LPLGSKEEF0.99570.9179716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B35:24LPLGSKEEF0.99240.9597716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B35:11LPLGSKEEF0.98560.9581716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B07:09LPLGSKEEF0.9850.5276716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B35:13LPLGSKEEF0.97330.9648716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B53:02LPLGSKEEF0.9540.6236716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B15:13LPLGSKEEF0.92780.9068716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B35:22LPLGSKEEF0.88260.5364716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B55:04LPLGSKEEF0.79680.5027716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B35:09LPLGSKEEF0.77150.9877716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B18:04LPLGSKEEF0.75490.9656716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B51:06LPLGSKEEF0.68370.5951716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B41:03KEEFKGSTV0.68010.68931221
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B50:05KEEFKGSTV0.45220.79261221
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B50:04KEEFKGSTV0.45220.79261221
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B18:07LPLGSKEEF0.43020.9497716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B07:26LPLGSKEEF0.41720.6056716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B67:01LPLGSKEEF0.41570.8005716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B39:02KEEFKGSTV0.28690.90641221
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B35:43LPLGSKEEF0.22470.9352716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B15:08LPLGSKEEF0.21360.9339716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B15:11LPLGSKEEF0.20320.9177716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B82:02LPLGSKEEF0.0820.5775716
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B40:04KEEFKGSTVV0.9950.8171222
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B50:04KEEFKGSTVV0.8990.80711222
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B50:05KEEFKGSTVV0.8990.80711222
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B41:03KEEFKGSTVV0.86060.72051222
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B50:05SKEEFKGSTVV0.99530.81791122
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B50:04SKEEFKGSTVV0.99530.81791122
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B40:04SKEEFKGSTVV0.89370.83491122
SPINT2-GRIP1chr1938781215chr12669357301027HLA-B40:36SKEEFKGSTVV0.80750.52711122

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Potential FusionNeoAntigen Information of SPINT2-GRIP1 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.
SPINT2-GRIP1_38781215_66935730.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)
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0469SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0701SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0703SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0704SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0705SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0706SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0707SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0708SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0709SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0711SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0712SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0713SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0714SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0715SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0716SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0717SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0719SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0901SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0901GSKEEFKGSTVVELM1025
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0902SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0903SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0904SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0904GSKEEFKGSTVVELM1025
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0905SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0905GSKEEFKGSTVVELM1025
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0907SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0907GSKEEFKGSTVVELM1025
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0908SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0909SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-0909GSKEEFKGSTVVELM1025
SPINT2-GRIP1chr1938781215chr12669357301027DRB1-1493SKEEFKGSTVVELMK1126
SPINT2-GRIP1chr1938781215chr12669357301027DRB5-0112SKEEFKGSTVVELMK1126

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Fusion breakpoint peptide structures of SPINT2-GRIP1

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
6780PLPLGSKEEFKGSTSPINT2GRIP1chr1938781215chr12669357301027

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of SPINT2-GRIP1

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-B14:023BVN6780PLPLGSKEEFKGST-7.9962-8.1096
HLA-B14:023BVN6780PLPLGSKEEFKGST-5.70842-6.74372
HLA-B52:013W396780PLPLGSKEEFKGST-6.83737-6.95077
HLA-B52:013W396780PLPLGSKEEFKGST-4.4836-5.5189
HLA-A11:014UQ26780PLPLGSKEEFKGST-10.0067-10.1201
HLA-A11:014UQ26780PLPLGSKEEFKGST-9.03915-10.0745
HLA-A24:025HGA6780PLPLGSKEEFKGST-6.56204-6.67544
HLA-A24:025HGA6780PLPLGSKEEFKGST-5.42271-6.45801
HLA-B44:053DX86780PLPLGSKEEFKGST-7.85648-8.89178
HLA-B44:053DX86780PLPLGSKEEFKGST-5.3978-5.5112
HLA-A02:016TDR6780PLPLGSKEEFKGST-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of SPINT2-GRIP1

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
SPINT2-GRIP1chr1938781215chr12669357301122SKEEFKGSTVVCAAAGGAGGAATTCAAGGGCTCCACAGTCGTCG
SPINT2-GRIP1chr1938781215chr12669357301221KEEFKGSTVAGGAGGAATTCAAGGGCTCCACAGTCG
SPINT2-GRIP1chr1938781215chr12669357301222KEEFKGSTVVAGGAGGAATTCAAGGGCTCCACAGTCGTCG
SPINT2-GRIP1chr1938781215chr1266935730716LPLGSKEEFTGCCCCTTGGCTCAAAGGAGGAATTCA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
SPINT2-GRIP1chr1938781215chr12669357301025GSKEEFKGSTVVELMGCTCAAAGGAGGAATTCAAGGGCTCCACAGTCGTCGAGCTGATGA
SPINT2-GRIP1chr1938781215chr12669357301126SKEEFKGSTVVELMKCAAAGGAGGAATTCAAGGGCTCCACAGTCGTCGAGCTGATGAAGA

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Information of the samples that have these potential fusion neoantigens of SPINT2-GRIP1

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
BLCASPINT2-GRIP1chr1938781215ENST00000301244chr1266935730ENST00000286445TCGA-FD-A6TG-01A

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Potential target of CAR-T therapy development for SPINT2-GRIP1

check button Predicted 3D structure. We used RoseTTAFold.
474_SPINT2-GRIP1_t000_.e2e.pdb


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
SPINT2chr1938781215ENST00000301244GRIP1chr1266935730ENST00000286445
SPINT2chr1938781215ENST00000301244GRIP1chr1266935730ENST00000359742
SPINT2chr1938781215ENST00000301244GRIP1chr1266935730ENST00000398016
SPINT2chr1938781215ENST00000454580GRIP1chr1266935730ENST00000286445
SPINT2chr1938781215ENST00000454580GRIP1chr1266935730ENST00000359742
SPINT2chr1938781215ENST00000454580GRIP1chr1266935730ENST00000398016
SPINT2chr1938781215ENST00000587090GRIP1chr1266935730ENST00000286445
SPINT2chr1938781215ENST00000587090GRIP1chr1266935730ENST00000359742
SPINT2chr1938781215ENST00000587090GRIP1chr1266935730ENST00000398016

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Related Drugs to SPINT2-GRIP1

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 SPINT2-GRIP1

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
TgeneGRIP1C0265233Cryptophthalmos syndrome3GENOMICS_ENGLAND;ORPHANET
TgeneGRIP1C4551480FRASER SYNDROME 13GENOMICS_ENGLAND
TgeneGRIP1C4540040FRASER SYNDROME 32GENOMICS_ENGLAND
TgeneGRIP1C0015397Disorder of eye1GENOMICS_ENGLAND
TgeneGRIP1C0152423Congenital small ears1GENOMICS_ENGLAND
TgeneGRIP1C0152427Polydactyly1GENOMICS_ENGLAND