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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: 14584

FusionGeneSummary for GGA1_TRIOBP

check button Fusion gene summary
Fusion gene informationFusion gene name: GGA1_TRIOBP
Fusion gene ID: 14584
HgeneTgene
Gene symbol

GGA1

TRIOBP

Gene ID

26088

11078

Gene namegolgi associated, gamma adaptin ear containing, ARF binding protein 1TRIO and F-actin binding protein
Synonyms-DFNB28|HRIHFB2122|TAP68|TARA|dJ37E16.4
Cytomap

22q13.1

22q13.1

Type of geneprotein-codingprotein-coding
DescriptionADP-ribosylation factor-binding protein GGA1ADP-ribosylation factor binding protein 1gamma-adaptin related protein 1golgi-localized, gamma ear-containing, ARF-binding protein 1TRIO and F-actin-binding proteinprotein Taratara-like proteintrio-associated repeat on actin
Modification date2018052220180520
UniProtAcc

Q9UJY5

Q9H2D6

Ensembl transtripts involved in fusion geneENST00000414350, ENST00000343632, 
ENST00000381756, ENST00000405147, 
ENST00000325180, ENST00000337437, 
ENST00000406772, ENST00000488672, 
ENST00000406386, ENST00000407319, 
ENST00000403663, 
Fusion gene scores* DoF score2 X 1 X 2=48 X 9 X 5=360
# samples 211
** MAII scorelog2(2/4*10)=2.32192809488736log2(11/360*10)=-1.71049338280502
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: GGA1 [Title/Abstract] AND TRIOBP [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
TgeneTRIOBP

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
TCGALDBRCATCGA-B6-A0IJ-01AGGA1chr22

38004910

+TRIOBPchr22

38161677

+
* 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-shiftENST00000414350ENST00000406386GGA1chr22

38004910

+TRIOBPchr22

38161677

+
5CDS-intronENST00000414350ENST00000407319GGA1chr22

38004910

+TRIOBPchr22

38161677

+
5CDS-intronENST00000414350ENST00000403663GGA1chr22

38004910

+TRIOBPchr22

38161677

+
Frame-shiftENST00000343632ENST00000406386GGA1chr22

38004910

+TRIOBPchr22

38161677

+
5CDS-intronENST00000343632ENST00000407319GGA1chr22

38004910

+TRIOBPchr22

38161677

+
5CDS-intronENST00000343632ENST00000403663GGA1chr22

38004910

+TRIOBPchr22

38161677

+
Frame-shiftENST00000381756ENST00000406386GGA1chr22

38004910

+TRIOBPchr22

38161677

+
5CDS-intronENST00000381756ENST00000407319GGA1chr22

38004910

+TRIOBPchr22

38161677

+
5CDS-intronENST00000381756ENST00000403663GGA1chr22

38004910

+TRIOBPchr22

38161677

+
Frame-shiftENST00000405147ENST00000406386GGA1chr22

38004910

+TRIOBPchr22

38161677

+
5CDS-intronENST00000405147ENST00000407319GGA1chr22

38004910

+TRIOBPchr22

38161677

+
5CDS-intronENST00000405147ENST00000403663GGA1chr22

38004910

+TRIOBPchr22

38161677

+
Frame-shiftENST00000325180ENST00000406386GGA1chr22

38004910

+TRIOBPchr22

38161677

+
5CDS-intronENST00000325180ENST00000407319GGA1chr22

38004910

+TRIOBPchr22

38161677

+
5CDS-intronENST00000325180ENST00000403663GGA1chr22

38004910

+TRIOBPchr22

38161677

+
Frame-shiftENST00000337437ENST00000406386GGA1chr22

38004910

+TRIOBPchr22

38161677

+
5CDS-intronENST00000337437ENST00000407319GGA1chr22

38004910

+TRIOBPchr22

38161677

+
5CDS-intronENST00000337437ENST00000403663GGA1chr22

38004910

+TRIOBPchr22

38161677

+
intron-3CDSENST00000406772ENST00000406386GGA1chr22

38004910

+TRIOBPchr22

38161677

+
intron-intronENST00000406772ENST00000407319GGA1chr22

38004910

+TRIOBPchr22

38161677

+
intron-intronENST00000406772ENST00000403663GGA1chr22

38004910

+TRIOBPchr22

38161677

+
intron-3CDSENST00000488672ENST00000406386GGA1chr22

38004910

+TRIOBPchr22

38161677

+
intron-intronENST00000488672ENST00000407319GGA1chr22

38004910

+TRIOBPchr22

38161677

+
intron-intronENST00000488672ENST00000403663GGA1chr22

38004910

+TRIOBPchr22

38161677

+

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FusionProtFeatures for GGA1_TRIOBP


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
GGA1

Q9UJY5

TRIOBP

Q9H2D6


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 GGA1_TRIOBP


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 GGA1_TRIOBP


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
GGA1ARF3, NECAP2, ARF1, M6PR, CLTC, SYNRG, RABEP1, RABGEF1, BACE2, SORL1, SORT1, VPS18, UBC, RNF11, TSG101, BACE1, CCDC91, IGF2R, CSNK2A1, CDKN2A, APP, STAB1, GGA1, CLINT1, GGA2, GGA3, LRP3, VCP, MON2, SMAD3, MAP1A, BAG3, F8, CDKL3, ARF5, ARF6, DTNB, C1orf216, TOLLIP, DHX15, EIF4EBP1, AKT2, DNM2, FLNB, STAM, GIPC1, LIX1L, RABEPK, TMEM17, AP1G1, CEP72, CLCN3, E2F5, TFDP1, CEP44, RABGAP1, CCDC53, C17orf70, DTNBP1, LRP10, MAP1S, RABGAP1L, TMEM9B, EXOC4, SLC38A7, CENPH, SNAP47, ECHDC1, TRIM25TRIOBPVIM, 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, NDEL1


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 GGA1_TRIOBP


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 GGA1_TRIOBP


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneTRIOBPC1853276Deafness, Autosomal Recessive 281CTD_human;UNIPROT