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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 39746

FusionGeneSummary for TSEN2_SYN2

check button Fusion gene summary
Fusion gene informationFusion gene name: TSEN2_SYN2
Fusion gene ID: 39746
HgeneTgene
Gene symbol

TSEN2

SYN2

Gene ID

80746

6854

Gene nametRNA splicing endonuclease subunit 2synapsin II
SynonymsPCH2B|SEN2|SEN2LSYNII
Cytomap

3p25.2

3p25.2

Type of geneprotein-codingprotein-coding
DescriptiontRNA-splicing endonuclease subunit Sen2TSEN2 tRNA splicing endonuclease subunithsSen2tRNA-intron endonuclease Sen2synapsin-2
Modification date2018052320180523
UniProtAcc

Q8NCE0

Ensembl transtripts involved in fusion geneENST00000314571, ENST00000383797, 
ENST00000454502, ENST00000402228, 
ENST00000444864, ENST00000284995, 
ENST00000415684, ENST00000475595, 
ENST00000432424, 
Fusion gene scores* DoF score5 X 6 X 3=903 X 5 X 2=30
# samples 74
** MAII scorelog2(7/90*10)=-0.362570079384708
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/30*10)=0.415037499278844
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: TSEN2 [Title/Abstract] AND SYN2 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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
HgeneTSEN2

GO:0006388

tRNA splicing, via endonucleolytic cleavage and ligation

17495927


check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
TCGARVBLCATCGA-XF-AAMY-01ATSEN2chr3

12538053

+SYN2chr3

12224812

+
TCGALDBLCATCGA-DK-AA75-01ATSEN2chr3

12546730

+SYN2chr3

12182151

+
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
5CDS-3UTRENST00000314571ENST00000432424TSEN2chr3

12538053

+SYN2chr3

12224812

+
5CDS-3UTRENST00000383797ENST00000432424TSEN2chr3

12538053

+SYN2chr3

12224812

+
5CDS-3UTRENST00000454502ENST00000432424TSEN2chr3

12538053

+SYN2chr3

12224812

+
5CDS-3UTRENST00000402228ENST00000432424TSEN2chr3

12538053

+SYN2chr3

12224812

+
5CDS-3UTRENST00000444864ENST00000432424TSEN2chr3

12538053

+SYN2chr3

12224812

+
5CDS-3UTRENST00000284995ENST00000432424TSEN2chr3

12538053

+SYN2chr3

12224812

+
5CDS-3UTRENST00000415684ENST00000432424TSEN2chr3

12538053

+SYN2chr3

12224812

+
intron-3UTRENST00000475595ENST00000432424TSEN2chr3

12538053

+SYN2chr3

12224812

+
intron-3UTRENST00000314571ENST00000432424TSEN2chr3

12546730

+SYN2chr3

12182151

+
5CDS-3UTRENST00000383797ENST00000432424TSEN2chr3

12546730

+SYN2chr3

12182151

+
5CDS-3UTRENST00000454502ENST00000432424TSEN2chr3

12546730

+SYN2chr3

12182151

+
5CDS-3UTRENST00000402228ENST00000432424TSEN2chr3

12546730

+SYN2chr3

12182151

+
intron-3UTRENST00000444864ENST00000432424TSEN2chr3

12546730

+SYN2chr3

12182151

+
5CDS-3UTRENST00000284995ENST00000432424TSEN2chr3

12546730

+SYN2chr3

12182151

+
intron-3UTRENST00000415684ENST00000432424TSEN2chr3

12546730

+SYN2chr3

12182151

+
intron-3UTRENST00000475595ENST00000432424TSEN2chr3

12546730

+SYN2chr3

12182151

+

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FusionProtFeatures for TSEN2_SYN2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
TSEN2

Q8NCE0

SYN2

Constitutes one of the two catalytic subunit of thetRNA-splicing endonuclease complex, a complex responsible foridentification and cleavage of the splice sites in pre-tRNA. Itcleaves pre-tRNA at the 5'- and 3'-splice sites to release theintron. The products are an intron and two tRNA half-moleculesbearing 2',3'-cyclic phosphate and 5'-OH termini. There are noconserved sequences at the splice sites, but the intron isinvariably located at the same site in the gene, placing thesplice sites an invariant distance from the constant structuralfeatures of the tRNA body. Isoform 1 probably carries the activesite for 5'-splice site cleavage. The tRNA splicing endonucleaseis also involved in mRNA processing via its association with pre-mRNA 3'-end processing factors, establishing a link between pre-tRNA splicing and pre-mRNA 3'-end formation, suggesting that theendonuclease subunits function in multiple RNA-processing events.Isoform 2 is responsible for processing a yet unknown RNAsubstrate. The complex containing isoform 2 is not able to cleavepre-tRNAs properly, although it retains endonucleolytic activity.{ECO:0000269|PubMed:15109492}. Lectin that binds to various sugars: galactose > mannose= fucose > N-acetylglucosamine > N-acetylgalactosamine(PubMed:10224141). Acts as a chemoattractant, probably involved inthe regulation of cell migration (PubMed:28301481).{ECO:0000269|PubMed:10224141, ECO:0000269|PubMed:28301481}.

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.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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FusionGeneSequence for TSEN2_SYN2


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for TSEN2_SYN2


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 (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors
TSEN2TSEN34, TSEN54, TSEN15, CLP1, POLD1, POLD3, PRPF39, TBC1D2, TBC1D4, TRIP10, USP8, RTBDN, CLPB, PRELP, TUBB2B, ZNRF1, RAP1B, SORT1, VPS18, BAG6, GREB1L, TMED8, SFSWAP, XPC, TRIM25SYN2SYN2, SYN1, YWHAZ, YWHAE, SYN3, NOS1AP, PSMC3, IQCB1, GNB2L1, ARMC1, HAX1, DGUOK, DNAAF2, POLL


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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RelatedDrugs for TSEN2_SYN2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for TSEN2_SYN2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneTSEN2C0011168Deglutition Disorders1CTD_human
HgeneTSEN2C0025958Microcephaly1CTD_human
HgeneTSEN2C0026650Movement Disorders1CTD_human
HgeneTSEN2C0042790Vision Disorders1CTD_human
HgeneTSEN2C0043094Weight Gain1CTD_human
HgeneTSEN2C2676466Pontocerebellar Hypoplasia Type 2B1CTD_human;UNIPROT
HgeneTSEN2C3714756Intellectual Disability1CTD_human
TgeneSYN2C0005586Bipolar Disorder2PSYGENET
TgeneSYN2C0020429Hyperalgesia1CTD_human
TgeneSYN2C0036572Seizures1CTD_human