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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:GSE1-CDH13

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: GSE1-CDH13
FusionPDB ID: 34999
FusionGDB2.0 ID: 42038
HgeneTgene
Gene symbol

GSE1

CDH13

Gene ID

23199

1012

Gene nameGse1 coiled-coil proteincadherin 13
SynonymsCRHSP24|KIAA0182CDHH|P105
Cytomap

16q24.1

16q23.3

Type of geneprotein-codingprotein-coding
Descriptiongenetic suppressor element 1CTC-786C10.1Gse1 coiled-coil protein homologcadherin-13H-cadherin (heart)T-cadT-cadherincadherin 13, H-cadherin (heart)heart cadherin
Modification date2020032720200315
UniProtAcc

Q14687

P55290

Ensembl transtripts involved in fusion geneENST idsENST00000253458, ENST00000393243, 
ENST00000405402, ENST00000471070, 
ENST00000569454, ENST00000428848, 
ENST00000431540, ENST00000446376, 
ENST00000565636, ENST00000567445, 
ENST00000268613, ENST00000566620, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score23 X 18 X 8=331215 X 16 X 5=1200
# samples 2316
** MAII scorelog2(23/3312*10)=-3.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(16/1200*10)=-2.90689059560852
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: GSE1 [Title/Abstract] AND CDH13 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)GSE1(85647004)-CDH13(83520082), # samples:2
Anticipated loss of major functional domain due to fusion event.GSE1-CDH13 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.
GSE1-CDH13 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.
GSE1-CDH13 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.
GSE1-CDH13 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
TgeneCDH13

GO:0002040

sprouting angiogenesis

16873731

TgeneCDH13

GO:0007156

homophilic cell adhesion via plasma membrane adhesion molecules

10601632

TgeneCDH13

GO:0007162

negative regulation of cell adhesion

14729458

TgeneCDH13

GO:0008285

negative regulation of cell proliferation

10737605

TgeneCDH13

GO:0016339

calcium-dependent cell-cell adhesion via plasma membrane cell adhesion molecules

10601632

TgeneCDH13

GO:0030032

lamellipodium assembly

15703273

TgeneCDH13

GO:0030335

positive regulation of cell migration

14729458

TgeneCDH13

GO:0043542

endothelial cell migration

14729458

TgeneCDH13

GO:0043616

keratinocyte proliferation

15816843

TgeneCDH13

GO:0050850

positive regulation of calcium-mediated signaling

16013438

TgeneCDH13

GO:0050927

positive regulation of positive chemotaxis

16013438

TgeneCDH13

GO:0055096

low-density lipoprotein particle mediated signaling

16013438


check buttonFusion gene breakpoints across GSE1 (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 CDH13 (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 Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4STADTCGA-BR-8590-01AGSE1chr16

85647004

+CDH13chr16

83520082

+


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Fusion ORF Analysis


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)
ENST00000253458GSE1chr1685647004+ENST00000566620CDH13chr1683520082+31131831611543460
ENST00000253458GSE1chr1685647004+ENST00000268613CDH13chr1683520082+18901831611543460
ENST00000393243GSE1chr1685647004+ENST00000566620CDH13chr1683520082+297747251407460
ENST00000393243GSE1chr1685647004+ENST00000268613CDH13chr1683520082+175447251407460

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
ENST00000253458ENST00000566620GSE1chr1685647004+CDH13chr1683520082+0.0004934350.9995066
ENST00000253458ENST00000268613GSE1chr1685647004+CDH13chr1683520082+0.0009784230.99902153
ENST00000393243ENST00000566620GSE1chr1685647004+CDH13chr1683520082+0.0004095160.99959046
ENST00000393243ENST00000268613GSE1chr1685647004+CDH13chr1683520082+0.0007381250.9992619

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>34999_34999_1_GSE1-CDH13_GSE1_chr16_85647004_ENST00000253458_CDH13_chr16_83520082_ENST00000268613_length(amino acids)=460AA_BP=7
MRGPGMKGTTVMRMTAFDADDPATDNALLRYNIRQQTPDKPSPNMFYIDPEKGDIVTVVSPALLDRETLENPKYELIIEAQDMAGLDVGL
TGTATATIMIDDKNDHSPKFTKKEFQATVEEGAVGVIVNLTVEDKDDPTTGAWRAAYTIINGNPGQSFEIHTNPQTNEGMLSVVKPLDYE
ISAFHTLLIKVENEDPLVPDVSYGPSSTATVHITVLDVNEGPVFYPDPMMVTRQEDLSVGSVLLTVNATDPDSLQHQTIRYSVYKDPAGW
LNINPINGTVDTTAVLDRESPFVDNSVYTALFLAIDSGNPPATGTGTLLITLEDVNDNAPFIYPTVAEVCDDAKNLSVVILGASDKDLHP
NTDPFKFEIHKQAVPDKVWKISKINNTHALVSLLQNLNKANYNLPIMVTDSGKPPMTNITDLRVQVCSCRNSKVDCNAAGALRFSLPSVL

--------------------------------------------------------------

>34999_34999_2_GSE1-CDH13_GSE1_chr16_85647004_ENST00000253458_CDH13_chr16_83520082_ENST00000566620_length(amino acids)=460AA_BP=7
MRGPGMKGTTVMRMTAFDADDPATDNALLRYNIRQQTPDKPSPNMFYIDPEKGDIVTVVSPALLDRETLENPKYELIIEAQDMAGLDVGL
TGTATATIMIDDKNDHSPKFTKKEFQATVEEGAVGVIVNLTVEDKDDPTTGAWRAAYTIINGNPGQSFEIHTNPQTNEGMLSVVKPLDYE
ISAFHTLLIKVENEDPLVPDVSYGPSSTATVHITVLDVNEGPVFYPDPMMVTRQEDLSVGSVLLTVNATDPDSLQHQTIRYSVYKDPAGW
LNINPINGTVDTTAVLDRESPFVDNSVYTALFLAIDSGNPPATGTGTLLITLEDVNDNAPFIYPTVAEVCDDAKNLSVVILGASDKDLHP
NTDPFKFEIHKQAVPDKVWKISKINNTHALVSLLQNLNKANYNLPIMVTDSGKPPMTNITDLRVQVCSCRNSKVDCNAAGALRFSLPSVL

--------------------------------------------------------------

>34999_34999_3_GSE1-CDH13_GSE1_chr16_85647004_ENST00000393243_CDH13_chr16_83520082_ENST00000268613_length(amino acids)=460AA_BP=7
MRGPGMKGTTVMRMTAFDADDPATDNALLRYNIRQQTPDKPSPNMFYIDPEKGDIVTVVSPALLDRETLENPKYELIIEAQDMAGLDVGL
TGTATATIMIDDKNDHSPKFTKKEFQATVEEGAVGVIVNLTVEDKDDPTTGAWRAAYTIINGNPGQSFEIHTNPQTNEGMLSVVKPLDYE
ISAFHTLLIKVENEDPLVPDVSYGPSSTATVHITVLDVNEGPVFYPDPMMVTRQEDLSVGSVLLTVNATDPDSLQHQTIRYSVYKDPAGW
LNINPINGTVDTTAVLDRESPFVDNSVYTALFLAIDSGNPPATGTGTLLITLEDVNDNAPFIYPTVAEVCDDAKNLSVVILGASDKDLHP
NTDPFKFEIHKQAVPDKVWKISKINNTHALVSLLQNLNKANYNLPIMVTDSGKPPMTNITDLRVQVCSCRNSKVDCNAAGALRFSLPSVL

--------------------------------------------------------------

>34999_34999_4_GSE1-CDH13_GSE1_chr16_85647004_ENST00000393243_CDH13_chr16_83520082_ENST00000566620_length(amino acids)=460AA_BP=7
MRGPGMKGTTVMRMTAFDADDPATDNALLRYNIRQQTPDKPSPNMFYIDPEKGDIVTVVSPALLDRETLENPKYELIIEAQDMAGLDVGL
TGTATATIMIDDKNDHSPKFTKKEFQATVEEGAVGVIVNLTVEDKDDPTTGAWRAAYTIINGNPGQSFEIHTNPQTNEGMLSVVKPLDYE
ISAFHTLLIKVENEDPLVPDVSYGPSSTATVHITVLDVNEGPVFYPDPMMVTRQEDLSVGSVLLTVNATDPDSLQHQTIRYSVYKDPAGW
LNINPINGTVDTTAVLDRESPFVDNSVYTALFLAIDSGNPPATGTGTLLITLEDVNDNAPFIYPTVAEVCDDAKNLSVVILGASDKDLHP
NTDPFKFEIHKQAVPDKVWKISKINNTHALVSLLQNLNKANYNLPIMVTDSGKPPMTNITDLRVQVCSCRNSKVDCNAAGALRFSLPSVL

--------------------------------------------------------------

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Fusion Protein Functional Features


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/chr16:85647004/chr16:83520082)
- 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 buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
GSE1

Q14687

CDH13

P55290

FUNCTION: Cadherins are calcium-dependent cell adhesion proteins. They preferentially interact with themselves in a homophilic manner in connecting cells; cadherins may thus contribute to the sorting of heterogeneous cell types. May act as a negative regulator of neural cell growth. {ECO:0000269|PubMed:10737605}.

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, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page

* Minus value of BPloci means that the break pointn is located before the CDS.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneCDH13chr16:85647004chr16:83520082ENST00000268613615364_477307.3333333333333761.0DomainCadherin 3
TgeneCDH13chr16:85647004chr16:83520082ENST00000268613615478_585307.3333333333333761.0DomainCadherin 4
TgeneCDH13chr16:85647004chr16:83520082ENST00000268613615584_694307.3333333333333761.0DomainCadherin 5
TgeneCDH13chr16:85647004chr16:83520082ENST0000043154005139_2450191.0DomainCadherin 1
TgeneCDH13chr16:85647004chr16:83520082ENST0000043154005246_3630191.0DomainCadherin 2
TgeneCDH13chr16:85647004chr16:83520082ENST0000043154005364_4770191.0DomainCadherin 3
TgeneCDH13chr16:85647004chr16:83520082ENST0000043154005478_5850191.0DomainCadherin 4
TgeneCDH13chr16:85647004chr16:83520082ENST0000043154005584_6940191.0DomainCadherin 5
TgeneCDH13chr16:85647004chr16:83520082ENST0000044637605139_2450.0176.0DomainCadherin 1
TgeneCDH13chr16:85647004chr16:83520082ENST0000044637605246_3630.0176.0DomainCadherin 2
TgeneCDH13chr16:85647004chr16:83520082ENST0000044637605364_4770.0176.0DomainCadherin 3
TgeneCDH13chr16:85647004chr16:83520082ENST0000044637605478_5850.0176.0DomainCadherin 4
TgeneCDH13chr16:85647004chr16:83520082ENST0000044637605584_6940.0176.0DomainCadherin 5
TgeneCDH13chr16:85647004chr16:83520082ENST0000056563606139_2450171.33333333333334DomainCadherin 1
TgeneCDH13chr16:85647004chr16:83520082ENST0000056563606246_3630171.33333333333334DomainCadherin 2
TgeneCDH13chr16:85647004chr16:83520082ENST0000056563606364_4770171.33333333333334DomainCadherin 3
TgeneCDH13chr16:85647004chr16:83520082ENST0000056563606478_5850171.33333333333334DomainCadherin 4
TgeneCDH13chr16:85647004chr16:83520082ENST0000056563606584_6940171.33333333333334DomainCadherin 5
TgeneCDH13chr16:85647004chr16:83520082ENST00000566620514364_477260.3333333333333714.0DomainCadherin 3
TgeneCDH13chr16:85647004chr16:83520082ENST00000566620514478_585260.3333333333333714.0DomainCadherin 4
TgeneCDH13chr16:85647004chr16:83520082ENST00000566620514584_694260.3333333333333714.0DomainCadherin 5

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneGSE1chr16:85647004chr16:83520082ENST00000253458+1161127_12012.33333333333333351218.0Coiled coilOntology_term=ECO:0000255
HgeneGSE1chr16:85647004chr16:83520082ENST00000253458+116321_4032.33333333333333351218.0Coiled coilOntology_term=ECO:0000255
HgeneGSE1chr16:85647004chr16:83520082ENST00000393243+1151127_12012.33333333333333351145.0Coiled coilOntology_term=ECO:0000255
HgeneGSE1chr16:85647004chr16:83520082ENST00000393243+115321_4032.33333333333333351145.0Coiled coilOntology_term=ECO:0000255
HgeneGSE1chr16:85647004chr16:83520082ENST00000405402+1151127_120101114.0Coiled coilOntology_term=ECO:0000255
HgeneGSE1chr16:85647004chr16:83520082ENST00000405402+115321_40301114.0Coiled coilOntology_term=ECO:0000255
HgeneGSE1chr16:85647004chr16:83520082ENST00000253458+1161102_11072.33333333333333351218.0Compositional biasNote=Poly-Glu
HgeneGSE1chr16:85647004chr16:83520082ENST00000253458+116532_7222.33333333333333351218.0Compositional biasNote=Pro-rich
HgeneGSE1chr16:85647004chr16:83520082ENST00000253458+116745_7482.33333333333333351218.0Compositional biasNote=Poly-Arg
HgeneGSE1chr16:85647004chr16:83520082ENST00000393243+1151102_11072.33333333333333351145.0Compositional biasNote=Poly-Glu
HgeneGSE1chr16:85647004chr16:83520082ENST00000393243+115532_7222.33333333333333351145.0Compositional biasNote=Pro-rich
HgeneGSE1chr16:85647004chr16:83520082ENST00000393243+115745_7482.33333333333333351145.0Compositional biasNote=Poly-Arg
HgeneGSE1chr16:85647004chr16:83520082ENST00000405402+1151102_110701114.0Compositional biasNote=Poly-Glu
HgeneGSE1chr16:85647004chr16:83520082ENST00000405402+115532_72201114.0Compositional biasNote=Pro-rich
HgeneGSE1chr16:85647004chr16:83520082ENST00000405402+115745_74801114.0Compositional biasNote=Poly-Arg
TgeneCDH13chr16:85647004chr16:83520082ENST00000268613615139_245307.3333333333333761.0DomainCadherin 1
TgeneCDH13chr16:85647004chr16:83520082ENST00000268613615246_363307.3333333333333761.0DomainCadherin 2
TgeneCDH13chr16:85647004chr16:83520082ENST00000566620514139_245260.3333333333333714.0DomainCadherin 1
TgeneCDH13chr16:85647004chr16:83520082ENST00000566620514246_363260.3333333333333714.0DomainCadherin 2


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Fusion Protein-Protein Interaction


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
GSE1
CDH13


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to GSE1-CDH13


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 GSE1-CDH13


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