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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: 9225

FusionGeneSummary for DAAM2_CCDC80

check button Fusion gene summary
Fusion gene informationFusion gene name: DAAM2_CCDC80
Fusion gene ID: 9225
HgeneTgene
Gene symbol

DAAM2

CCDC80

Gene ID

23500

151887

Gene namedishevelled associated activator of morphogenesis 2coiled-coil domain containing 80
SynonymsdJ90A20A.1DRO1|SSG1|URB|okuribin
Cytomap

6p21.2

3q13.2

Type of geneprotein-codingprotein-coding
Descriptiondisheveled-associated activator of morphogenesis 2coiled-coil domain-containing protein 80down-regulated by oncogenes protein 1nuclear envelope protein okuribinsteroid sensitive gene 1up-regulated in BRS-3 deficient mouse homolog
Modification date2018051920180519
UniProtAcc

Q86T65

Q76M96

Ensembl transtripts involved in fusion geneENST00000274867, ENST00000398904, 
ENST00000538976, ENST00000405961, 
ENST00000494405, 
ENST00000206423, 
ENST00000439685, ENST00000475181, 
Fusion gene scores* DoF score1 X 1 X 1=14 X 5 X 2=40
# samples 26
** MAII scorelog2(2/1*10)=4.32192809488736log2(6/40*10)=0.584962500721156
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: DAAM2 [Title/Abstract] AND CCDC80 [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
ChiTaRS3.1AX747160DAAM2chr6

39847030

+CCDC80chr3

112328854

-
ChiTaRS3.1AK091749DAAM2chr6

39847030

+CCDC80chr3

112328854

-
* 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-shiftENST00000274867ENST00000206423DAAM2chr6

39847030

+CCDC80chr3

112328854

-
Frame-shiftENST00000274867ENST00000439685DAAM2chr6

39847030

+CCDC80chr3

112328854

-
5CDS-intronENST00000274867ENST00000475181DAAM2chr6

39847030

+CCDC80chr3

112328854

-
Frame-shiftENST00000398904ENST00000206423DAAM2chr6

39847030

+CCDC80chr3

112328854

-
Frame-shiftENST00000398904ENST00000439685DAAM2chr6

39847030

+CCDC80chr3

112328854

-
5CDS-intronENST00000398904ENST00000475181DAAM2chr6

39847030

+CCDC80chr3

112328854

-
Frame-shiftENST00000538976ENST00000206423DAAM2chr6

39847030

+CCDC80chr3

112328854

-
Frame-shiftENST00000538976ENST00000439685DAAM2chr6

39847030

+CCDC80chr3

112328854

-
5CDS-intronENST00000538976ENST00000475181DAAM2chr6

39847030

+CCDC80chr3

112328854

-
intron-3CDSENST00000405961ENST00000206423DAAM2chr6

39847030

+CCDC80chr3

112328854

-
intron-3CDSENST00000405961ENST00000439685DAAM2chr6

39847030

+CCDC80chr3

112328854

-
intron-intronENST00000405961ENST00000475181DAAM2chr6

39847030

+CCDC80chr3

112328854

-
intron-3CDSENST00000494405ENST00000206423DAAM2chr6

39847030

+CCDC80chr3

112328854

-
intron-3CDSENST00000494405ENST00000439685DAAM2chr6

39847030

+CCDC80chr3

112328854

-
intron-intronENST00000494405ENST00000475181DAAM2chr6

39847030

+CCDC80chr3

112328854

-

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FusionProtFeatures for DAAM2_CCDC80


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
DAAM2

Q86T65

CCDC80

Q76M96

Key regulator of the Wnt signaling pathway, which isrequired for various processes during development, such as dorsalpatterning, determination of left/right symmetry or myelination inthe central nervous system. Acts downstream of Wnt ligands andupstream of beta-catenin (CTNNB1). Required for canonical Wntsignaling pathway during patterning in the dorsal spinal cord bypromoting the aggregation of Disheveled (Dvl) complexes, therebyclustering and formation of Wnt receptor signalosomes andpotentiating Wnt activity. During dorsal patterning of the spinalcord, inhibits oligodendrocytes differentiation via interactionwith PIP5K1A. Also regulates non-canonical Wnt signaling pathway.Acts downstream of PITX2 in the developing gut and is required forleft/right asymmetry within dorsal mesentery: affects mesenchymalcondensation by lengthening cadherin-based junctions through WNT5Aand non-canonical Wnt signaling, inducing polarized condensationin the left dorsal mesentery necessary to initiate gut rotation.Together with DAAM1, required for myocardial maturation andsarcomere assembly. {ECO:0000250|UniProtKB:Q80U19}. Promotes cell adhesion and matrix assembly.{ECO:0000250}.

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 DAAM2_CCDC80


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 DAAM2_CCDC80


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 DAAM2_CCDC80


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 DAAM2_CCDC80


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneDAAM2C0036341Schizophrenia1PSYGENET
TgeneCCDC80C0011615Dermatitis, Atopic1CTD_human
TgeneCCDC80C4277682Chemical and Drug Induced Liver Injury1CTD_human