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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: 12265

FusionGeneSummary for EXOC3_TRIP13

check button Fusion gene summary
Fusion gene informationFusion gene name: EXOC3_TRIP13
Fusion gene ID: 12265
HgeneTgene
Gene symbol

EXOC3

TRIP13

Gene ID

11336

9319

Gene nameexocyst complex component 3thyroid hormone receptor interactor 13
SynonymsSEC6|SEC6L1|Sec6p16E1BP|MVA3
Cytomap

5p15.33

5p15.33

Type of geneprotein-codingprotein-coding
Descriptionexocyst complex component 3SEC6-like 1Sec 6 homologexocyst complex component Sec6pachytene checkpoint protein 2 homolog16E1-BPHPV16 E1 protein binding proteinSH3TC1/TRIP13 fusionTR-interacting protein 13TRIP-13human papillomavirus type 16 E1 protein-binding proteinthyroid receptor-interacting protein 13
Modification date2018052320180523
UniProtAcc

O60645

Q15645

Ensembl transtripts involved in fusion geneENST00000512944, ENST00000510441, 
ENST00000315013, 
ENST00000166345, 
ENST00000510412, 
Fusion gene scores* DoF score2 X 2 X 2=81 X 1 X 1=1
# samples 21
** MAII scorelog2(2/8*10)=1.32192809488736log2(1/1*10)=3.32192809488736
Context

PubMed: EXOC3 [Title/Abstract] AND TRIP13 [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

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
TCGALDSKCMTCGA-FR-A8YE-06AEXOC3chr5

447867

+TRIP13chr5

894902

+
* 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
Frame-shiftENST00000512944ENST00000166345EXOC3chr5

447867

+TRIP13chr5

894902

+
5CDS-intronENST00000512944ENST00000510412EXOC3chr5

447867

+TRIP13chr5

894902

+
intron-3CDSENST00000510441ENST00000166345EXOC3chr5

447867

+TRIP13chr5

894902

+
intron-intronENST00000510441ENST00000510412EXOC3chr5

447867

+TRIP13chr5

894902

+
Frame-shiftENST00000315013ENST00000166345EXOC3chr5

447867

+TRIP13chr5

894902

+
5CDS-intronENST00000315013ENST00000510412EXOC3chr5

447867

+TRIP13chr5

894902

+

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FusionProtFeatures for EXOC3_TRIP13


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
EXOC3

O60645

TRIP13

Q15645

Component of the exocyst complex involved in the dockingof exocytic vesicles with fusion sites on the plasma membrane. Plays a key role in chromosome recombination andchromosome structure development during meiosis. Required at earlysteps in meiotic recombination that leads to non-crossoverspathways. Also needed for efficient completion of homologoussynapsis by influencing crossover distribution along thechromosomes affecting both crossovers and non-crossovers pathways.Also required for development of higher-order chromosomestructures and is needed for synaptonemal-complex formation. Inmales, required for efficient synapsis of the sex chromosomes andfor sex body formation. Promotes early steps of the DNA double-strand breaks (DSBs) repair process upstream of the assembly ofRAD51 complexes. Required for depletion of HORMAD1 and HORMAD2from synapsed chromosomes (By similarity). Plays a role in mitoticspindle assembly checkpoint (SAC) activation (PubMed:28553959).{ECO:0000250|UniProtKB:Q3UA06, ECO:0000269|PubMed:28553959}.

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 EXOC3_TRIP13


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 EXOC3_TRIP13


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
EXOC3EXOC5, EXOC4, DLG3, GRIN2B, MYO5A, APP, EXOC2, EXOC8, EXOC6, MLH1, EGFR, BUB3, PRPF19, KIAA0907, CCDC8, VAMP2, BSG, DTNBP1, EXOC1, EXOC7, METAP1, TRMT2A, NTRK1, TMEM17, MKNK2, KIF2A, SNW1, CDH1, PTPRA, PTPRH, GCC2, TRIP11, SCLT1, EXOC6B, KIZ, KLC2, IL1R2, IFT20, KIF3A, CCDC136, PIBF1, PKD2, KXD1, KLC1, RGPD2, MACROD1, RGPD5, SDC2, TMED1, RALB, TRIM32, TULP3, TRIM25TRIP13C11orf54, GPRIN2, LASP1, COMT, PPP2CA, TEX37, ASB13, TRIP13, MAD2L1BP, CYB5R2, STAMBPL1, HDHD3, GPSM1, CARD14, ZNF655, NME4, TLDC1, LNX1, RBPMS, DTX2, PLSCR4, SELENBP1, PARK2, GLYCTK, ADAM15, DDAH2, LOXL4, SEC24A, SMUG1, SIGLEC5, PLAC8, PBLD, NIF3L1, GALT, SEMA4G, PLSCR3, CPSF3L, WDYHV1, KRTAP3-2, PLK3, ARL11, CRMP1, USP32, MEPCE, CLN3, FBXW8, MYC, FBXO25, CUL3, CD99, UBA1, RAB9A, ALYREF, TTC37, ECT2, MDC1, MPPED2, CRYBA2, STAMBP, PARP11, RHOXF2, MAD2L2, LRRC61, MMS19, FBXO6, AASDHPPT, HIST1H2AB, S100A4, SGTA, ZC3HC1, DCP1A, MVP, BUB1B, MAD2L1, MAD1L1, ARSA, CCBL1, QARS, SCP2, TPT1, DPYSL4, DIP2A, TNRC6A, AMDHD2, PCMTD2, PELI1, SPRYD7, TINAGL1, FNDC3B, ZNF34, LRR1, M1AP, C4orf33, MGAT5B, METTL15, MORN3, KRTAP12-2, KRTAP12-1, KRTAP26-1, CCDC8, MSH2, TARDBP, TTC4, NTRK1, UBE2I, NCSTN, ELMSAN1, ARMC6, CDC20, SNW1, CDC5L, DPPA4, POU5F1, MTG1, METTL8, PUSL1, ADAT3, CRYZ, PI4K2B, AARSD1, PTPN1, TRIM25, TES


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 EXOC3_TRIP13


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 EXOC3_TRIP13


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource