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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:SEC23B-CNGB3

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SEC23B-CNGB3
FusionPDB ID: 80053
FusionGDB2.0 ID: 80053
HgeneTgene
Gene symbol

SEC23B

CNGB3

Gene ID

10483

54714

Gene nameSEC23 homolog B, COPII coat complex componentcyclic nucleotide gated channel subunit beta 3
SynonymsCDA-II|CDAII|CDAN2|CWS7|HEMPAS|hSec23BACHM1
Cytomap

20p11.23

8q21.3

Type of geneprotein-codingprotein-coding
Descriptionprotein transport protein Sec23BSEC23 homolog B, coat complex II componentSEC23-like protein BSEC23-related protein Btransport protein SEC23Bcyclic nucleotide-gated cation channel beta-3CNG channel beta-3cone photoreceptor cGMP-gated cation channel beta-subunitcyclic nucleotide gated channel beta 3cyclic nucleotide-gated cation channel modulatory subunit
Modification date2020031320200313
UniProtAcc.

Q9NQW8

Main function of 5'-partner protein: FUNCTION: Visual signal transduction is mediated by a G-protein coupled cascade using cGMP as second messenger. This protein can be activated by cGMP which leads to an opening of the cation channel and thereby causing a depolarization of rod photoreceptors. Induced a flickering channel gating, weakened the outward rectification in the presence of extracellular calcium, increased sensitivity for L-cis diltiazem and enhanced the cAMP efficiency of the channel when coexpressed with CNGA3 (By similarity). Essential for the generation of light-evoked electrical responses in the red-, green- and blue sensitive cones. {ECO:0000250, ECO:0000269|PubMed:10888875}.
Ensembl transtripts involved in fusion geneENST idsENST00000262544, ENST00000336714, 
ENST00000377465, ENST00000377475, 
ENST00000494645, 
ENST00000519777, 
ENST00000320005, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score12 X 12 X 9=12963 X 3 X 3=27
# samples 153
** MAII scorelog2(15/1296*10)=-3.11103131238874
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Fusion gene context

PubMed: SEC23B [Title/Abstract] AND CNGB3 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: SEC23B [Title/Abstract] AND CNGB3 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SEC23B(18516386)-CNGB3(87751964), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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
TgeneCNGB3

GO:0006812

cation transport

24164424



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/chr20:18516386/chr8:87751964)
- 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 SEC23B (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 CNGB3 (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)
ENST00000262544SEC23Bchr2018516386-ENST00000320005CNGB3chr887751964-6064189449041941234
ENST00000336714SEC23Bchr2018516386-ENST00000320005CNGB3chr887751964-6006183643241361234
ENST00000377475SEC23Bchr2018516386-ENST00000320005CNGB3chr887751964-6000183042641301234
ENST00000377465SEC23Bchr2018516386-ENST00000320005CNGB3chr887751964-5824165425039541234

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
ENST00000262544ENST00000320005SEC23Bchr2018516386-CNGB3chr887751964-0.0003061370.9996939
ENST00000336714ENST00000320005SEC23Bchr2018516386-CNGB3chr887751964-0.0002860260.99971396
ENST00000377475ENST00000320005SEC23Bchr2018516386-CNGB3chr887751964-0.0002945910.9997054
ENST00000377465ENST00000320005SEC23Bchr2018516386-CNGB3chr887751964-0.0002326840.99976736

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 SEC23B-CNGB3

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
SEC23Bchr2018516386CNGB3chr8877519641654468TSTLGIYFEVVNQEENKGEEKSLKTK
SEC23Bchr2018516386CNGB3chr8877519641830468TSTLGIYFEVVNQEENKGEEKSLKTK
SEC23Bchr2018516386CNGB3chr8877519641836468TSTLGIYFEVVNQEENKGEEKSLKTK
SEC23Bchr2018516386CNGB3chr8877519641894468TSTLGIYFEVVNQEENKGEEKSLKTK

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Potential FusionNeoAntigen Information of SEC23B-CNGB3 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.
SEC23B-CNGB3_18516386_87751964.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)
SEC23B-CNGB3chr2018516386chr8877519641894HLA-B41:03QEENKGEEKSL0.98790.67651223

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Potential FusionNeoAntigen Information of SEC23B-CNGB3 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.
SEC23B-CNGB3_18516386_87751964.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)
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0403TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0405LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0405TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0405GIYFEVVNQEENKGE419
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0405STLGIYFEVVNQEEN116
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0407LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0407TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0409TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0409LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0409GIYFEVVNQEENKGE419
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0409STLGIYFEVVNQEEN116
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0411TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0417LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0417TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0417GIYFEVVNQEENKGE419
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0417STLGIYFEVVNQEEN116
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0422TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0424LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0424TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0424GIYFEVVNQEENKGE419
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0424STLGIYFEVVNQEEN116
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0427TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0429LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0429TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0429GIYFEVVNQEENKGE419
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0429STLGIYFEVVNQEEN116
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0430LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0430TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0430GIYFEVVNQEENKGE419
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0430STLGIYFEVVNQEEN116
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0439TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0441TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0443LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0445LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0445TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0445GIYFEVVNQEENKGE419
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0445STLGIYFEVVNQEEN116
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0446TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0448LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0448TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0448GIYFEVVNQEENKGE419
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0448STLGIYFEVVNQEEN116
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0449TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0450TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0451TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0452TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0457LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0457TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0457GIYFEVVNQEENKGE419
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0457STLGIYFEVVNQEEN116
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0459TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0459LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0460TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0462TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0462LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0462STLGIYFEVVNQEEN116
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0467TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0467STLGIYFEVVNQEEN116
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0469LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0469TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0471TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0477LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0477TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0477GIYFEVVNQEENKGE419
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0477STLGIYFEVVNQEEN116
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0480TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0480LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0480GIYFEVVNQEENKGE419
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0482LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0482TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0483LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0483TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0483GIYFEVVNQEENKGE419
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0483STLGIYFEVVNQEEN116
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0484LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0484TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0484GIYFEVVNQEENKGE419
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0484STLGIYFEVVNQEEN116
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0485TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0486LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0486TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0486GIYFEVVNQEENKGE419
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0487TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0487LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0487GIYFEVVNQEENKGE419
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0487STLGIYFEVVNQEEN116
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0488TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0489LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0489TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0489GIYFEVVNQEENKGE419
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0489STLGIYFEVVNQEEN116
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0491TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0832GIYFEVVNQEENKGE419
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0832LGIYFEVVNQEENKG318
SEC23B-CNGB3chr2018516386chr8877519641894DRB1-0832TLGIYFEVVNQEENK217
SEC23B-CNGB3chr2018516386chr8877519641894DRB4-0101YFEVVNQEENKGEEK621
SEC23B-CNGB3chr2018516386chr8877519641894DRB4-0103YFEVVNQEENKGEEK621
SEC23B-CNGB3chr2018516386chr8877519641894DRB4-0106YFEVVNQEENKGEEK621
SEC23B-CNGB3chr2018516386chr8877519641894DRB4-0107YFEVVNQEENKGEEK621
SEC23B-CNGB3chr2018516386chr8877519641894DRB4-0108YFEVVNQEENKGEEK621

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Fusion breakpoint peptide structures of SEC23B-CNGB3

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
10624YFEVVNQEENKGEESEC23BCNGB3chr2018516386chr8877519641894

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of SEC23B-CNGB3

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-B14:023BVN10624YFEVVNQEENKGEE-7.15543-7.26883
HLA-B14:023BVN10624YFEVVNQEENKGEE-4.77435-5.80965
HLA-B52:013W3910624YFEVVNQEENKGEE-6.80875-6.92215
HLA-B52:013W3910624YFEVVNQEENKGEE-4.20386-5.23916
HLA-A11:014UQ210624YFEVVNQEENKGEE-7.5194-8.5547
HLA-A11:014UQ210624YFEVVNQEENKGEE-6.9601-7.0735
HLA-A24:025HGA10624YFEVVNQEENKGEE-7.52403-7.63743
HLA-A24:025HGA10624YFEVVNQEENKGEE-5.82433-6.85963
HLA-B27:056PYJ10624YFEVVNQEENKGEE-3.28285-4.31815
HLA-B44:053DX810624YFEVVNQEENKGEE-5.91172-6.94702
HLA-B44:053DX810624YFEVVNQEENKGEE-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of SEC23B-CNGB3

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
SEC23B-CNGB3chr2018516386chr8877519641223QEENKGEEKSLCAGGAAGAAAACAAAGGTGAAGAGAAATCTCTC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
SEC23B-CNGB3chr2018516386chr887751964116STLGIYFEVVNQEENTCTACACTTGGCATCTATTTTGAAGTTGTCAATCAGGAAGAAAAC
SEC23B-CNGB3chr2018516386chr887751964217TLGIYFEVVNQEENKACACTTGGCATCTATTTTGAAGTTGTCAATCAGGAAGAAAACAAA
SEC23B-CNGB3chr2018516386chr887751964318LGIYFEVVNQEENKGCTTGGCATCTATTTTGAAGTTGTCAATCAGGAAGAAAACAAAGGT
SEC23B-CNGB3chr2018516386chr887751964419GIYFEVVNQEENKGEGGCATCTATTTTGAAGTTGTCAATCAGGAAGAAAACAAAGGTGAA
SEC23B-CNGB3chr2018516386chr887751964621YFEVVNQEENKGEEKTATTTTGAAGTTGTCAATCAGGAAGAAAACAAAGGTGAAGAGAAA

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Information of the samples that have these potential fusion neoantigens of SEC23B-CNGB3

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
LUSCSEC23B-CNGB3chr2018516386ENST00000262544chr887751964ENST00000320005TCGA-37-A5EL-01A

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Potential target of CAR-T therapy development for SEC23B-CNGB3

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
TgeneCNGB3chr20:18516386chr8:87751964ENST00000320005018217_2370810.0TransmembraneHelical%3B Name%3DH1
TgeneCNGB3chr20:18516386chr8:87751964ENST00000320005018251_2710810.0TransmembraneHelical%3B Name%3DH2
TgeneCNGB3chr20:18516386chr8:87751964ENST00000320005018303_3230810.0TransmembraneHelical%3B Name%3DH3
TgeneCNGB3chr20:18516386chr8:87751964ENST00000320005018360_3800810.0TransmembraneHelical%3B Name%3DH4
TgeneCNGB3chr20:18516386chr8:87751964ENST00000320005018418_4380810.0TransmembraneHelical%3B Name%3DH5
TgeneCNGB3chr20:18516386chr8:87751964ENST00000320005018505_5250810.0TransmembraneHelical%3B Name%3DH6

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 SEC23B-CNGB3

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 SEC23B-CNGB3

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