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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: 39570

FusionGeneSummary for TRIOBP_PES1

check button Fusion gene summary
Fusion gene informationFusion gene name: TRIOBP_PES1
Fusion gene ID: 39570
HgeneTgene
Gene symbol

TRIOBP

PES1

Gene ID

11078

23481

Gene nameTRIO and F-actin binding proteinpescadillo ribosomal biogenesis factor 1
SynonymsDFNB28|HRIHFB2122|TAP68|TARA|dJ37E16.4NOP7|PES
Cytomap

22q13.1

22q12.2

Type of geneprotein-codingprotein-coding
DescriptionTRIO and F-actin-binding proteinprotein Taratara-like proteintrio-associated repeat on actinpescadillo homologpescadillo homolog 1, containing BRCT domain
Modification date2018052020180523
UniProtAcc

Q9H2D6

O00541

Ensembl transtripts involved in fusion geneENST00000406386, ENST00000407319, 
ENST00000403663, 
ENST00000354694, 
ENST00000402281, ENST00000405677, 
ENST00000402284, ENST00000335214, 
ENST00000492986, 
Fusion gene scores* DoF score6 X 6 X 5=1804 X 4 X 3=48
# samples 64
** MAII scorelog2(6/180*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: TRIOBP [Title/Abstract] AND PES1 [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
HgeneTRIOBP

GO:1900026

positive regulation of substrate adhesion-dependent cell spreading

11148140


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
TCGARVUCSTCGA-N9-A4PZ-01ATRIOBPchr22

38161824

+PES1chr22

30988385

-
* 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-intronENST00000406386ENST00000354694TRIOBPchr22

38161824

+PES1chr22

30988385

-
5CDS-5UTRENST00000406386ENST00000402281TRIOBPchr22

38161824

+PES1chr22

30988385

-
5CDS-5UTRENST00000406386ENST00000405677TRIOBPchr22

38161824

+PES1chr22

30988385

-
5CDS-intronENST00000406386ENST00000402284TRIOBPchr22

38161824

+PES1chr22

30988385

-
5CDS-intronENST00000406386ENST00000335214TRIOBPchr22

38161824

+PES1chr22

30988385

-
5CDS-intronENST00000406386ENST00000492986TRIOBPchr22

38161824

+PES1chr22

30988385

-
intron-intronENST00000407319ENST00000354694TRIOBPchr22

38161824

+PES1chr22

30988385

-
intron-5UTRENST00000407319ENST00000402281TRIOBPchr22

38161824

+PES1chr22

30988385

-
intron-5UTRENST00000407319ENST00000405677TRIOBPchr22

38161824

+PES1chr22

30988385

-
intron-intronENST00000407319ENST00000402284TRIOBPchr22

38161824

+PES1chr22

30988385

-
intron-intronENST00000407319ENST00000335214TRIOBPchr22

38161824

+PES1chr22

30988385

-
intron-intronENST00000407319ENST00000492986TRIOBPchr22

38161824

+PES1chr22

30988385

-
5CDS-intronENST00000403663ENST00000354694TRIOBPchr22

38161824

+PES1chr22

30988385

-
5CDS-5UTRENST00000403663ENST00000402281TRIOBPchr22

38161824

+PES1chr22

30988385

-
5CDS-5UTRENST00000403663ENST00000405677TRIOBPchr22

38161824

+PES1chr22

30988385

-
5CDS-intronENST00000403663ENST00000402284TRIOBPchr22

38161824

+PES1chr22

30988385

-
5CDS-intronENST00000403663ENST00000335214TRIOBPchr22

38161824

+PES1chr22

30988385

-
5CDS-intronENST00000403663ENST00000492986TRIOBPchr22

38161824

+PES1chr22

30988385

-

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FusionProtFeatures for TRIOBP_PES1


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

Q9H2D6

PES1

O00541

Component of the PeBoW complex, which is required formaturation of 28S and 5.8S ribosomal RNAs and formation of the 60Sribosome. {ECO:0000255|HAMAP-Rule:MF_03028,ECO:0000269|PubMed:16738141, ECO:0000269|PubMed:17189298,ECO:0000269|PubMed:17353269}.

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 TRIOBP_PES1


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 TRIOBP_PES1


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
TRIOBPVIM, HECTD3, ELAVL1, PLK1, POLR1C, GTF2H1, IKBKG, FYTTD1, C17orf59, RAI14, FBXW11, CAPZA2, KIF2A, MYH9, MYO1C, POLR2F, PPP1CB, SORT1, IQGAP1, SYNCRIP, ANLN, L1TD1, TMEM132A, HAUS2, MYO18A, BAG6, VTN, JPH4, CORO6, VAPB, PACSIN1, VAPA, NDEL1PES1ARRB1, ARRB2, MYC, SIRT7, CUL3, CAND1, WDR12, BOP1, NAP1L1, NOC4L, NAP1L4, PES1, HDAC11, ARL2, LZTFL1, BLMH, MOV10, NXF1, CUL7, OBSL1, RNF2, MAGEA10, NIFK, PRR11, CASQ2, BRIX1, CEBPZ, FBL, FTSJ3, GNL1, GNL3, GTPBP4, KRR1, NHP2L1, NIP7, NOC2L, NOP2, NSA2, DDX24, DDX27, DHX15, EBNA1BP2, GNL3L, KIAA0020, MRTO4, NOC3L, NOP56, ORC2, RBM28, RPL18A, RPL31, RPL38, RPL4, RPL7A, RPL8, SUPT16H, PWP1, RPF2, RPL23, RPL27, RPL27A, RPL7, UBA52, UTP14A, NTRK1, SCARNA22, APP, IFI16, TP53, FOXL2, FOXM1, MYBBP1A, G3BP1, RRP12, RRBP1, DKC1, C1orf35, PRPF40A, TOP1, ZC3HAV1, KIF2A, TCEB3, PDIA3, SART1, MYH9, BUB3, DDX18, RPL7L1, RRS1, RRP1B, POP1, IGKC, CDC14B, BRD2, PFKFB3, NAF1, CWC22, UBTF, TRIM26, TNRC18, SETD1A, AFF4, CXXC1, MLLT3, CENPB, KLHL23, PNN, CSNK2A1, NVL, PPIL4, INPP5K, RNPS1, C18orf25, CCDC91, WDR55, SRRM2, AP3B1, KBTBD7, RPL36, NCL


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 TRIOBP_PES1


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 TRIOBP_PES1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneTRIOBPC1853276Deafness, Autosomal Recessive 281CTD_human;UNIPROT