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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: 8620

FusionGeneSummary for CSN2_CSN1S1

check button Fusion gene summary
Fusion gene informationFusion gene name: CSN2_CSN1S1
Fusion gene ID: 8620
HgeneTgene
Gene symbol

CSN2

CSN1S1

Gene ID

9318

1446

Gene nameCOP9 signalosome subunit 2casein alpha s1
SynonymsALIEN|CSN2|SGN2|TRIP15CASA|CSN1
Cytomap

15q21.1

4q13.3

Type of geneprotein-codingprotein-coding
DescriptionCOP9 signalosome complex subunit 2COP9 constitutive photomorphogenic homolog subunit 2JAB1-containing signalosome subunit 2TR-interacting protein 15TRIP-15alien homologsignalosome subunit 2thyroid receptor-interacting protein 15alpha-S1-caseincasein, alpha
Modification date2018052320180523
UniProtAcc

P05814

P47710

Ensembl transtripts involved in fusion geneENST00000353151, ENST00000444405, 
ENST00000246891, ENST00000507763, 
ENST00000507772, ENST00000505782, 
Fusion gene scores* DoF score2 X 2 X 1=42 X 2 X 2=8
# samples 12
** MAII scorelog2(1/4*10)=1.32192809488736log2(2/8*10)=1.32192809488736
Context

PubMed: CSN2 [Title/Abstract] AND CSN1S1 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotationTissue-specifically expressed gene involved fusion gene, inframe and retained their domain.
* 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
HgeneCSN2

GO:0000338

protein deneddylation

19141280


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-AO-A1KO-01ACSN2chr4

70822992

-CSN1S1chr4

70801644

+
* 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
In-frameENST00000353151ENST00000444405CSN2chr4

70822992

-CSN1S1chr4

70801644

+
In-frameENST00000353151ENST00000246891CSN2chr4

70822992

-CSN1S1chr4

70801644

+
In-frameENST00000353151ENST00000507763CSN2chr4

70822992

-CSN1S1chr4

70801644

+
In-frameENST00000353151ENST00000507772CSN2chr4

70822992

-CSN1S1chr4

70801644

+
In-frameENST00000353151ENST00000505782CSN2chr4

70822992

-CSN1S1chr4

70801644

+

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FusionProtFeatures for CSN2_CSN1S1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CSN2

P05814

CSN1S1

P47710

Important role in determination of the surfaceproperties of the casein micelles. Important role in the capacity of milk to transportcalcium phosphate. Casoxin D acts as opioid antagonist and has vasorelaxingactivity mediated by bradykinin B1 receptors.

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 CSN2_CSN1S1


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 CSN2_CSN1S1


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
CSN2CDC42, GRB2, NFYC, RAC1, TOLLIP, PLK1, ARRB1, ARRB2, CUL1, CUL4B, COPS7A, CSNK2A1, CDK1, HTRA2, NEK2, AURKA, CSNK2B, FHL2, NEK9, CORO2A, PPP3CCCSN1S1TOLLIP, COPS5, CSNK2A1, CSNK2B, CUL1, CUL4A, COPS7A, PLK1, PARK7, PRSS2, PDE10A, B4GALNT4, LTBP1, EMILIN3, KLHL15, HSPA5, TIMP3, ERF, BCOR, CDKN2AIP, FAM120A, ETV3


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 CSN2_CSN1S1


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 CSN2_CSN1S1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCSN2C0024667Animal Mammary Neoplasms2CTD_human
HgeneCSN2C0024668Mammary Neoplasms, Experimental2CTD_human