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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:ETNK1-TSPAN13

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ETNK1-TSPAN13
FusionPDB ID: 27666
FusionGDB2.0 ID: 27666
HgeneTgene
Gene symbol

ETNK1

TSPAN13

Gene ID

55500

27075

Gene nameethanolamine kinase 1tetraspanin 13
SynonymsEKI|EKI 1|EKI1|Nbla10396NET-6|NET6|TM4SF13
Cytomap

12p12.1

7p21.1

Type of geneprotein-codingprotein-coding
Descriptionethanolamine kinase 1putative protein product of Nbla10396tetraspanin-13tetraspan NET-6transmembrane 4 superfamily member 13transmembrane 4 superfamily member tetraspan NET-6tspan-13
Modification date2020031320200313
UniProtAcc

Q9HBU6

.
Ensembl transtripts involved in fusion geneENST idsENST00000266517, ENST00000335148, 
ENST00000466195, ENST00000262067, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score11 X 7 X 7=5397 X 6 X 6=252
# samples 149
** MAII scorelog2(14/539*10)=-1.94485844580754
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/252*10)=-1.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: ETNK1 [Title/Abstract] AND TSPAN13 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ETNK1(22778520)-TSPAN13(16815836), # samples:1
Anticipated loss of major functional domain due to fusion event.ETNK1-TSPAN13 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.
ETNK1-TSPAN13 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
HgeneETNK1

GO:0006646

phosphatidylethanolamine biosynthetic process

11044454


check buttonFusion gene breakpoints across ETNK1 (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 TSPAN13 (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-B7-5818-01AETNK1chr12

22778520

+TSPAN13chr7

16815836

+


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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)
ENST00000266517ETNK1chr1222778520+ENST00000262067TSPAN13chr716815836+2109512891063324
ENST00000335148ETNK1chr1222778520+ENST00000262067TSPAN13chr716815836+204344623997324

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
ENST00000266517ENST00000262067ETNK1chr1222778520+TSPAN13chr716815836+0.0113123560.98868763
ENST00000335148ENST00000262067ETNK1chr1222778520+TSPAN13chr716815836+0.0092309320.9907691

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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

>27666_27666_1_ETNK1-TSPAN13_ETNK1_chr12_22778520_ENST00000266517_TSPAN13_chr7_16815836_ENST00000262067_length(amino acids)=324AA_BP=137
MLCGRPRSSSDNRNFLRERAGLSSAAVQTRIGNSAASRRSPAARPPVPAPPALPRGRPGTEGSTSLSAPAVLVVAVAVVVVVVSAVAWAM
ANYIHVPPGSPEVPKLNVTVQDQEEHRCREGALSLLQHLRPHWDPQEVTLQLVSLLLIGIAAWGIGFGLISSLRVVGVVIAVGIFLFLIA
LVGLIGAVKHHQVLLFFYMIILLLVFIVQFSVSCACLALNQEQQGQLLEVGWNNTASARNDIQRNLNCCGFRSVNPNDTCLASCVKSDHS

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

>27666_27666_2_ETNK1-TSPAN13_ETNK1_chr12_22778520_ENST00000335148_TSPAN13_chr7_16815836_ENST00000262067_length(amino acids)=324AA_BP=137
MLCGRPRSSSDNRNFLRERAGLSSAAVQTRIGNSAASRRSPAARPPVPAPPALPRGRPGTEGSTSLSAPAVLVVAVAVVVVVVSAVAWAM
ANYIHVPPGSPEVPKLNVTVQDQEEHRCREGALSLLQHLRPHWDPQEVTLQLVSLLLIGIAAWGIGFGLISSLRVVGVVIAVGIFLFLIA
LVGLIGAVKHHQVLLFFYMIILLLVFIVQFSVSCACLALNQEQQGQLLEVGWNNTASARNDIQRNLNCCGFRSVNPNDTCLASCVKSDHS

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

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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/chr12:22778520/chr7:16815836)
- 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
ETNK1

Q9HBU6

.
FUNCTION: Highly specific for ethanolamine phosphorylation. May be a rate-controlling step in phosphatidylethanolamine biosynthesis. {ECO:0000269|PubMed:11044454}.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

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
HgeneETNK1chr12:22778520chr7:16815836ENST00000266517+1873_83141.0453.0Compositional biasNote=Poly-Val
HgeneETNK1chr12:22778520chr7:16815836ENST00000335148+1373_83141.0259.0Compositional biasNote=Poly-Val
TgeneTSPAN13chr12:22778520chr7:16815836ENST0000026206706189_20421.0205.0Topological domainCytoplasmic
TgeneTSPAN13chr12:22778520chr7:16815836ENST000002620670641_4421.0205.0Topological domainExtracellular
TgeneTSPAN13chr12:22778520chr7:16815836ENST000002620670666_7221.0205.0Topological domainCytoplasmic
TgeneTSPAN13chr12:22778520chr7:16815836ENST000002620670694_16721.0205.0Topological domainExtracellular
TgeneTSPAN13chr12:22778520chr7:16815836ENST0000026206706168_18821.0205.0TransmembraneHelical
TgeneTSPAN13chr12:22778520chr7:16815836ENST000002620670620_4021.0205.0TransmembraneHelical
TgeneTSPAN13chr12:22778520chr7:16815836ENST000002620670645_6521.0205.0TransmembraneHelical
TgeneTSPAN13chr12:22778520chr7:16815836ENST000002620670673_9321.0205.0TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneTSPAN13chr12:22778520chr7:16815836ENST00000262067061_1921.0205.0Topological domainCytoplasmic


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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
ETNK1
TSPAN13


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 ETNK1-TSPAN13


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 ETNK1-TSPAN13


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