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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: 2948

FusionGeneSummary for ASCC3_WASF1

check button Fusion gene summary
Fusion gene informationFusion gene name: ASCC3_WASF1
Fusion gene ID: 2948
HgeneTgene
Gene symbol

ASCC3

WASF1

Gene ID

10973

8936

Gene nameactivating signal cointegrator 1 complex subunit 3WAS protein family member 1
SynonymsASC1p200|HELIC1|RNAHSCAR1|WAVE|WAVE1
Cytomap

6q16.3

6q21

Type of geneprotein-codingprotein-coding
Descriptionactivating signal cointegrator 1 complex subunit 3ASC-1 complex subunit P200RNA helicase familyhelicase, ATP binding 1trip4 complex subunit p200wiskott-Aldrich syndrome protein family member 1WASP family protein member 1homology of dictyostelium scar 1protein WAVE-1verprolin homology domain-containing protein 1
Modification date2018052320180522
UniProtAcc

Q8N3C0

Q92558

Ensembl transtripts involved in fusion geneENST00000369162, ENST00000522650, 
ENST00000369143, 
ENST00000392587, 
ENST00000392586, ENST00000392588, 
ENST00000392589, ENST00000359451, 
Fusion gene scores* DoF score8 X 7 X 7=3928 X 7 X 3=168
# samples 88
** MAII scorelog2(8/392*10)=-2.29278174922785
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/168*10)=-1.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ASCC3 [Title/Abstract] AND WASF1 [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
HgeneASCC3

GO:0006307

DNA dealkylation involved in DNA repair

22055184

HgeneASCC3

GO:0032508

DNA duplex unwinding

22055184


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
TCGARVSARCTCGA-HB-A3YV-01AASCC3chr6

101315784

-WASF1chr6

110448832

-
* 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-5UTRENST00000369162ENST00000392587ASCC3chr6

101315784

-WASF1chr6

110448832

-
5CDS-5UTRENST00000369162ENST00000392586ASCC3chr6

101315784

-WASF1chr6

110448832

-
5CDS-5UTRENST00000369162ENST00000392588ASCC3chr6

101315784

-WASF1chr6

110448832

-
5CDS-5UTRENST00000369162ENST00000392589ASCC3chr6

101315784

-WASF1chr6

110448832

-
5CDS-5UTRENST00000369162ENST00000359451ASCC3chr6

101315784

-WASF1chr6

110448832

-
5CDS-5UTRENST00000522650ENST00000392587ASCC3chr6

101315784

-WASF1chr6

110448832

-
5CDS-5UTRENST00000522650ENST00000392586ASCC3chr6

101315784

-WASF1chr6

110448832

-
5CDS-5UTRENST00000522650ENST00000392588ASCC3chr6

101315784

-WASF1chr6

110448832

-
5CDS-5UTRENST00000522650ENST00000392589ASCC3chr6

101315784

-WASF1chr6

110448832

-
5CDS-5UTRENST00000522650ENST00000359451ASCC3chr6

101315784

-WASF1chr6

110448832

-
5CDS-5UTRENST00000369143ENST00000392587ASCC3chr6

101315784

-WASF1chr6

110448832

-
5CDS-5UTRENST00000369143ENST00000392586ASCC3chr6

101315784

-WASF1chr6

110448832

-
5CDS-5UTRENST00000369143ENST00000392588ASCC3chr6

101315784

-WASF1chr6

110448832

-
5CDS-5UTRENST00000369143ENST00000392589ASCC3chr6

101315784

-WASF1chr6

110448832

-
5CDS-5UTRENST00000369143ENST00000359451ASCC3chr6

101315784

-WASF1chr6

110448832

-

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FusionProtFeatures for ASCC3_WASF1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ASCC3

Q8N3C0

WASF1

Q92558

3'-5' DNA helicase involved in repair of alkylated DNA.Promotes DNA unwinding to generate single-stranded substrateneeded for ALKBH3, enabling ALKBH3 to process alkylated N3-methylcytosine (3mC) within double-stranded regions. Enhances NF-kappa-B, SRF and AP1 transactivation.{ECO:0000269|PubMed:22055184}. Downstream effector molecule involved in thetransmission of signals from tyrosine kinase receptors and smallGTPases to the actin cytoskeleton. Promotes formation of actinfilaments. Part of the WAVE complex that regulates lamellipodiaformation. The WAVE complex regulates actin filamentreorganization via its interaction with the Arp2/3 complex (Bysimilarity). As component of the WAVE1 complex, required for BDNF-NTRK2 endocytic trafficking and signaling from early endosomes (Bysimilarity). {ECO:0000250|UniProtKB:Q8R5H6,ECO:0000269|PubMed:9889097}.

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 ASCC3_WASF1


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 ASCC3_WASF1


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
ASCC3EIF3F, OTUD6B, G3BP1, G3BP2, SIRT7, CAND1, NOTCH1, SKIL, SOX2, HECW2, LGR4, ENO1, MOV10, NXF1, CCDC8, ALKBH3, RPS2, ASCC1, THBS3, ASCC2, NTRK1, IFI16, CC2D2A, CEP170, CEP128, CDK1, IQGAP1, HCCS, ZNF263, UBCWASF1DNMBP, PFN1, BAIAP2, RYK, SORBS2, ABL1, PTPN12, ZC3H15, TXNDC9, PRKACA, PRKAR2A, TRIP10, IFT20, ZNF511, UBXN11, NCK2, ATP6V1C2, FNBP1L, ABI1, CYFIP1, CYFIP2, NCKAP1, WASL, NTRK1, RAC1, MED20, TCF4, ACTR3, MAPKAPK2, ZNF746, PTPRE, ABI2, TIMM50, AMZ1, CCDC53, CBLC, NHSL2, CGB2, NYAP2, CDH23, NXN, AIPL1, TRIM25


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 ASCC3_WASF1


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 ASCC3_WASF1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneASCC3C3714756Intellectual Disability1CTD_human