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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: 2848

FusionGeneSummary for ARRDC2_FBXO32

check button Fusion gene summary
Fusion gene informationFusion gene name: ARRDC2_FBXO32
Fusion gene ID: 2848
HgeneTgene
Gene symbol

ARRDC2

FBXO32

Gene ID

27106

114907

Gene namearrestin domain containing 2F-box protein 32
SynonymsCLONE24945|PP2703Fbx32|MAFbx
Cytomap

19p13.11

8q24.13

Type of geneprotein-codingprotein-coding
Descriptionarrestin domain-containing protein 2F-box only protein 32atrogin 1muscle atrophy F-box protein
Modification date2018051920180519
UniProtAcc

Q8TBH0

Q969P5

Ensembl transtripts involved in fusion geneENST00000379656, ENST00000222250, 
ENST00000608009, 
ENST00000517956, 
ENST00000443022, 
Fusion gene scores* DoF score2 X 2 X 2=83 X 3 X 2=18
# samples 23
** MAII scorelog2(2/8*10)=1.32192809488736log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: ARRDC2 [Title/Abstract] AND FBXO32 [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
TgeneFBXO32

GO:0016567

protein ubiquitination

26753747


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
ChiTaRS3.1AI083499ARRDC2chr19

18120621

+FBXO32chr8

124553354

-
* 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-5UTRENST00000379656ENST00000517956ARRDC2chr19

18120621

+FBXO32chr8

124553354

-
5CDS-5UTRENST00000379656ENST00000443022ARRDC2chr19

18120621

+FBXO32chr8

124553354

-
5CDS-5UTRENST00000222250ENST00000517956ARRDC2chr19

18120621

+FBXO32chr8

124553354

-
5CDS-5UTRENST00000222250ENST00000443022ARRDC2chr19

18120621

+FBXO32chr8

124553354

-
3UTR-5UTRENST00000608009ENST00000517956ARRDC2chr19

18120621

+FBXO32chr8

124553354

-
3UTR-5UTRENST00000608009ENST00000443022ARRDC2chr19

18120621

+FBXO32chr8

124553354

-

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FusionProtFeatures for ARRDC2_FBXO32


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ARRDC2

Q8TBH0

FBXO32

Q969P5

Substrate recognition component of a SCF (SKP1-CUL1-F-box protein) E3 ubiquitin-protein ligase complex which mediatesthe ubiquitination and subsequent proteasomal degradation oftarget proteins. Probably recognizes and binds to phosphorylatedtarget proteins during skeletal muscle atrophy. Recognizes TERF1.{ECO:0000269|PubMed:15531760}.

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 ARRDC2_FBXO32


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 ARRDC2_FBXO32


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


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 ARRDC2_FBXO32


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 ARRDC2_FBXO32


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneFBXO32C0026846Muscular Atrophy1CTD_human