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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:GUCY1A2-NLK

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: GUCY1A2-NLK
FusionPDB ID: 35338
FusionGDB2.0 ID: 35338
HgeneTgene
Gene symbol

GUCY1A2

NLK

Gene ID

2977

51701

Gene nameguanylate cyclase 1 soluble subunit alpha 2nemo like kinase
SynonymsGC-SA2|GUC1A2-
Cytomap

11q22.3

17q11.2

Type of geneprotein-codingprotein-coding
Descriptionguanylate cyclase soluble subunit alpha-2GCS-alpha-2guanylate cyclase 1, soluble, alpha 2serine/threonine-protein kinase NLK
Modification date2020031320200313
UniProtAcc

P33402

Main function of 5'-partner protein: FUNCTION: Has guanylyl cyclase on binding to the beta-1 subunit.; FUNCTION: Isoform 2 acts as a negative regulator of guanylyl cyclase activity as it forms non-functional heterodimers with the beta subunits.

Q9UBE8

Main function of 5'-partner protein: FUNCTION: Serine/threonine-protein kinase that regulates a number of transcription factors with key roles in cell fate determination. Positive effector of the non-canonical Wnt signaling pathway, acting downstream of WNT5A, MAP3K7/TAK1 and HIPK2. Negative regulator of the canonical Wnt/beta-catenin signaling pathway. Binds to and phosphorylates TCF7L2/TCF4 and LEF1, promoting the dissociation of the TCF7L2/LEF1/beta-catenin complex from DNA, as well as the ubiquitination and subsequent proteolysis of LEF1. Together these effects inhibit the transcriptional activation of canonical Wnt/beta-catenin target genes. Negative regulator of the Notch signaling pathway. Binds to and phosphorylates NOTCH1, thereby preventing the formation of a transcriptionally active ternary complex of NOTCH1, RBPJ/RBPSUH and MAML1. Negative regulator of the MYB family of transcription factors. Phosphorylation of MYB leads to its subsequent proteolysis while phosphorylation of MYBL1 and MYBL2 inhibits their interaction with the coactivator CREBBP. Other transcription factors may also be inhibited by direct phosphorylation of CREBBP itself. Acts downstream of IL6 and MAP3K7/TAK1 to phosphorylate STAT3, which is in turn required for activation of NLK by MAP3K7/TAK1. Upon IL1B stimulus, cooperates with ATF5 to activate the transactivation activity of C/EBP subfamily members. Phosphorylates ATF5 but also stabilizes ATF5 protein levels in a kinase-independent manner (PubMed:25512613). {ECO:0000250|UniProtKB:O54949, ECO:0000269|PubMed:12482967, ECO:0000269|PubMed:14960582, ECO:0000269|PubMed:15004007, ECO:0000269|PubMed:15764709, ECO:0000269|PubMed:20061393, ECO:0000269|PubMed:20118921, ECO:0000269|PubMed:20874444, ECO:0000269|PubMed:21454679, ECO:0000269|PubMed:25512613}.
Ensembl transtripts involved in fusion geneENST idsENST00000282249, ENST00000347596, 
ENST00000526355, 
ENST00000582037, 
ENST00000583517, ENST00000407008, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score3 X 3 X 2=1810 X 10 X 5=500
# samples 315
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(15/500*10)=-1.73696559416621
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: GUCY1A2 [Title/Abstract] AND NLK [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: GUCY1A2 [Title/Abstract] AND NLK [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)GUCY1A2(106647165)-NLK(26512205), # samples:1
Anticipated loss of major functional domain due to fusion event.GUCY1A2-NLK 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.
GUCY1A2-NLK 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.
GUCY1A2-NLK 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.
GUCY1A2-NLK 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
TgeneNLK

GO:0050821

protein stabilization

25512613



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/chr11:106647165/chr17:26512205)
- 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 GUCY1A2 (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 NLK (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)
ENST00000526355GUCY1A2chr11106647165-ENST00000407008NLKchr1726512205+448523054692739756
ENST00000282249GUCY1A2chr11106647165-ENST00000407008NLKchr1726512205+440622263902660756
ENST00000347596GUCY1A2chr11106647165-ENST00000407008NLKchr1726512205+41751995962429777

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
ENST00000526355ENST00000407008GUCY1A2chr11106647165-NLKchr1726512205+0.0005957150.9994043
ENST00000282249ENST00000407008GUCY1A2chr11106647165-NLKchr1726512205+0.0005329280.9994671
ENST00000347596ENST00000407008GUCY1A2chr11106647165-NLKchr1726512205+0.0003799820.99961996

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 GUCY1A2-NLK

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
GUCY1A2chr11106647165NLKchr1726512205199552RSPPGPLEPSPAAAAAAAAPAPTPAA
GUCY1A2chr11106647165NLKchr1726512205222652RSPPGPLEPSPAAAAAAAAPAPTPAA
GUCY1A2chr11106647165NLKchr1726512205230552RSPPGPLEPSPAAAAAAAAPAPTPAA

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Potential FusionNeoAntigen Information of GUCY1A2-NLK 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.
GUCY1A2-NLK_106647165_26512205.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)
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B50:01LEPSPAAA0.97310.9169614
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B56:01SPAAAAAA0.9640.8216917
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B55:01SPAAAAAA0.95590.5672917
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B07:05SPAAAAAAA0.99730.7043918
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B07:02SPAAAAAAA0.99710.7347918
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B56:01EPSPAAAAA0.98180.6437716
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B50:02LEPSPAAAA0.95880.8135615
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B56:01SPAAAAAAA0.93280.8591918
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B45:01LEPSPAAAA0.92840.975615
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B55:01SPAAAAAAA0.89080.6561918
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B35:02EPSPAAAAA0.66430.9435716
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B35:04EPSPAAAAA0.66430.9435716
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B50:01LEPSPAAAA0.47110.9471615
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B41:01LEPSPAAAA0.38280.98615
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B82:01EPSPAAAAA0.27790.5119716
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B82:01SPAAAAAAA0.12560.8906918
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B56:01GPLEPSPAAA0.95320.938414
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B55:01GPLEPSPAAA0.93860.8495414
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B50:02LEPSPAAAAA0.93220.8511616
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B56:01SPAAAAAAAA0.93070.8947919
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B55:01SPAAAAAAAA0.91090.7344919
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B50:01LEPSPAAAAA0.79850.9602616
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B56:01LEPSPAAAAA0.78070.811616
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B55:01LEPSPAAAAA0.70620.6383616
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B55:01GPLEPSPAAAA0.99660.9073415
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B56:01GPLEPSPAAAA0.99440.9594415
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B40:06LEPSPAAAA0.99170.8001615
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B54:01SPAAAAAAA0.98780.9481918
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B54:01EPSPAAAAA0.98310.8895716
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B56:04EPSPAAAAA0.92690.6558716
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B07:12SPAAAAAAA0.89710.8021918
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B56:04SPAAAAAAA0.83670.8607918
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B07:04SPAAAAAAA0.81710.7036918
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B35:12EPSPAAAAA0.66430.9435716
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B39:10SPAAAAAAA0.49590.9695918
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B78:01EPSPAAAAA0.47250.9298716
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B39:10EPSPAAAAA0.40470.9728716
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B78:01SPAAAAAAA0.29690.9288918
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B54:01SPAAAAAAAA0.98830.9566919
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B54:01GPLEPSPAAA0.98330.9708414
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B54:01LEPSPAAAAA0.91770.9631616
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B54:01GPLEPSPAAAA0.99920.9814415
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B50:05LEPSPAAA0.97310.9169614
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B50:04LEPSPAAA0.97310.9169614
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B56:05SPAAAAAA0.96260.7986917
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B55:02SPAAAAAA0.94830.8444917
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B07:22SPAAAAAAA0.99710.7347918
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B07:09SPAAAAAAA0.99660.732918
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B55:02SPAAAAAAA0.96870.8823918
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B55:02EPSPAAAAA0.94340.7987716
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B56:02EPSPAAAAA0.92690.6558716
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B55:04SPAAAAAAA0.90420.815918
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B56:02SPAAAAAAA0.83670.8607918
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B56:05EPSPAAAAA0.82370.8688716
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B56:05SPAAAAAAA0.68550.833918
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B35:09EPSPAAAAA0.66430.9435716
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B67:01SPAAAAAAA0.62050.9822918
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B67:01EPSPAAAAA0.60690.9696716
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B07:26SPAAAAAAA0.55450.6036918
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B50:04LEPSPAAAA0.47110.9471615
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B50:05LEPSPAAAA0.47110.9471615
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B78:02EPSPAAAAA0.34920.9467716
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B82:02EPSPAAAAA0.27790.5119716
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B78:02SPAAAAAAA0.21960.9395918
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B82:02SPAAAAAAA0.12560.8906918
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B55:02SPAAAAAAAA0.96150.9072919
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B55:02GPLEPSPAAA0.94050.9388414
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B50:04LEPSPAAAAA0.79850.9602616
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B50:05LEPSPAAAAA0.79850.9602616
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B56:05GPLEPSPAAA0.78080.911414
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B55:02LEPSPAAAAA0.75060.9226616
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B56:05LEPSPAAAAA0.61160.9256616
GUCY1A2-NLKchr11106647165chr17265122052226HLA-B55:02GPLEPSPAAAA0.99740.9634415

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Potential FusionNeoAntigen Information of GUCY1A2-NLK 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.
GUCY1A2-NLK_106647165_26512205.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)
GUCY1A2-NLKchr11106647165chr17265122052226DRB1-0444PGPLEPSPAAAAAAA318
GUCY1A2-NLKchr11106647165chr17265122052226DRB1-0478PGPLEPSPAAAAAAA318
GUCY1A2-NLKchr11106647165chr17265122052226DRB1-0902PGPLEPSPAAAAAAA318
GUCY1A2-NLKchr11106647165chr17265122052226DRB1-0906PGPLEPSPAAAAAAA318
GUCY1A2-NLKchr11106647165chr17265122052226DRB1-1367PGPLEPSPAAAAAAA318
GUCY1A2-NLKchr11106647165chr17265122052226DRB3-0201PGPLEPSPAAAAAAA318
GUCY1A2-NLKchr11106647165chr17265122052226DRB3-0201PPGPLEPSPAAAAAA217
GUCY1A2-NLKchr11106647165chr17265122052226DRB3-0204PGPLEPSPAAAAAAA318
GUCY1A2-NLKchr11106647165chr17265122052226DRB3-0214PGPLEPSPAAAAAAA318
GUCY1A2-NLKchr11106647165chr17265122052226DRB3-0217PGPLEPSPAAAAAAA318
GUCY1A2-NLKchr11106647165chr17265122052226DRB3-0224PGPLEPSPAAAAAAA318
GUCY1A2-NLKchr11106647165chr17265122052226DRB3-0224PPGPLEPSPAAAAAA217

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Fusion breakpoint peptide structures of GUCY1A2-NLK

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
4920LEPSPAAAAAAAAPGUCY1A2NLKchr11106647165chr17265122052226

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of GUCY1A2-NLK

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-B14:023BVN4920LEPSPAAAAAAAAP-6.80686-6.92026
HLA-B14:023BVN4920LEPSPAAAAAAAAP-5.01234-6.04764
HLA-B52:013W394920LEPSPAAAAAAAAP-6.71251-6.82591
HLA-B52:013W394920LEPSPAAAAAAAAP-4.13165-5.16695
HLA-A11:014UQ24920LEPSPAAAAAAAAP-4.31699-4.43039
HLA-A11:014UQ24920LEPSPAAAAAAAAP-4.19959-5.23489
HLA-A24:025HGA4920LEPSPAAAAAAAAP-7.74913-7.86253
HLA-A24:025HGA4920LEPSPAAAAAAAAP-5.75888-6.79418
HLA-B27:036PZ54920LEPSPAAAAAAAAP1000110000
HLA-B44:053DX84920LEPSPAAAAAAAAP-4.89721-5.01061
HLA-B44:053DX84920LEPSPAAAAAAAAP-3.74482-4.78012
HLA-A02:016TDR4920LEPSPAAAAAAAAP-5.01451-6.04981

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Vaccine Design for the FusionNeoAntigens of GUCY1A2-NLK

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
GUCY1A2-NLKchr11106647165chr1726512205414GPLEPSPAAACTGACACCTGATGGAAGACCGATTCAGCCA
GUCY1A2-NLKchr11106647165chr1726512205415GPLEPSPAAAACTGACACCTGATGGAAGACCGATTCAGCCATCT
GUCY1A2-NLKchr11106647165chr1726512205614LEPSPAAACCTGATGGAAGACCGATTCAGCCA
GUCY1A2-NLKchr11106647165chr1726512205615LEPSPAAAACCTGATGGAAGACCGATTCAGCCATCT
GUCY1A2-NLKchr11106647165chr1726512205616LEPSPAAAAACCTGATGGAAGACCGATTCAGCCATCTCTT
GUCY1A2-NLKchr11106647165chr1726512205716EPSPAAAAAGATGGAAGACCGATTCAGCCATCTCTT
GUCY1A2-NLKchr11106647165chr1726512205917SPAAAAAAAGACCGATTCAGCCATCTCTTCCT
GUCY1A2-NLKchr11106647165chr1726512205918SPAAAAAAAAGACCGATTCAGCCATCTCTTCCTGTA
GUCY1A2-NLKchr11106647165chr1726512205919SPAAAAAAAAAGACCGATTCAGCCATCTCTTCCTGTACTC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
GUCY1A2-NLKchr11106647165chr1726512205217PPGPLEPSPAAAAAAGAGGTGCTGACACCTGATGGAAGACCGATTCAGCCATCTCTTCCT
GUCY1A2-NLKchr11106647165chr1726512205318PGPLEPSPAAAAAAAGTGCTGACACCTGATGGAAGACCGATTCAGCCATCTCTTCCTGTA

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Information of the samples that have these potential fusion neoantigens of GUCY1A2-NLK

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
BLCAGUCY1A2-NLKchr11106647165ENST00000282249chr1726512205ENST00000407008TCGA-2F-A9KO-01A

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Potential target of CAR-T therapy development for GUCY1A2-NLK

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 GUCY1A2-NLK

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 GUCY1A2-NLK

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