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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: 8106

FusionGeneSummary for COPS8_RIN3

check button Fusion gene summary
Fusion gene informationFusion gene name: COPS8_RIN3
Fusion gene ID: 8106
HgeneTgene
Gene symbol

COPS8

RIN3

Gene ID

10920

79890

Gene nameCOP9 signalosome subunit 8Ras and Rab interactor 3
SynonymsCOP9|CSN8|SGN8-
Cytomap

2q37.3

14q32.12

Type of geneprotein-codingprotein-coding
DescriptionCOP9 signalosome complex subunit 8COP9 constitutive photomorphogenic homolog subunit 8COP9 homologJAB1-containing signalosome subunit 8hCOP9signalosome subunit 8ras and Rab interactor 3RAB5 interacting protein 3ras interaction/interference protein 3
Modification date2018052320180522
UniProtAcc

Q99627

Q8TB24

Ensembl transtripts involved in fusion geneENST00000354371, ENST00000392008, 
ENST00000409334, ENST00000409629, 
ENST00000216487, ENST00000418924, 
ENST00000557762, 
Fusion gene scores* DoF score2 X 2 X 2=87 X 8 X 5=280
# samples 210
** MAII scorelog2(2/8*10)=1.32192809488736log2(10/280*10)=-1.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: COPS8 [Title/Abstract] AND RIN3 [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
HgeneCOPS8

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
TCGALDHNSCTCGA-T2-A6X0-01ACOPS8chr2

238007681

+RIN3chr14

93151332

+
* 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
3UTR-3CDSENST00000354371ENST00000216487COPS8chr2

238007681

+RIN3chr14

93151332

+
3UTR-3UTRENST00000354371ENST00000418924COPS8chr2

238007681

+RIN3chr14

93151332

+
3UTR-intronENST00000354371ENST00000557762COPS8chr2

238007681

+RIN3chr14

93151332

+
intron-3CDSENST00000392008ENST00000216487COPS8chr2

238007681

+RIN3chr14

93151332

+
intron-3UTRENST00000392008ENST00000418924COPS8chr2

238007681

+RIN3chr14

93151332

+
intron-intronENST00000392008ENST00000557762COPS8chr2

238007681

+RIN3chr14

93151332

+
intron-3CDSENST00000409334ENST00000216487COPS8chr2

238007681

+RIN3chr14

93151332

+
intron-3UTRENST00000409334ENST00000418924COPS8chr2

238007681

+RIN3chr14

93151332

+
intron-intronENST00000409334ENST00000557762COPS8chr2

238007681

+RIN3chr14

93151332

+
intron-3CDSENST00000409629ENST00000216487COPS8chr2

238007681

+RIN3chr14

93151332

+
intron-3UTRENST00000409629ENST00000418924COPS8chr2

238007681

+RIN3chr14

93151332

+
intron-intronENST00000409629ENST00000557762COPS8chr2

238007681

+RIN3chr14

93151332

+

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FusionProtFeatures for COPS8_RIN3


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
COPS8

Q99627

RIN3

Q8TB24

Component of the COP9 signalosome complex (CSN), acomplex involved in various cellular and developmental processes.The CSN complex is an essential regulator of the ubiquitin (Ubl)conjugation pathway by mediating the deneddylation of the cullinsubunits of SCF-type E3 ligase complexes, leading to decrease theUbl ligase activity of SCF-type complexes such as SCF, CSA orDDB2. The complex is also involved in phosphorylation of p53/TP53,c-jun/JUN, IkappaBalpha/NFKBIA, ITPK1 and IRF8/ICSBP, possibly viaits association with CK2 and PKD kinases. CSN-dependentphosphorylation of TP53 and JUN promotes and protects degradationby the Ubl system, respectively. {ECO:0000269|PubMed:11285227,ECO:0000269|PubMed:11337588, ECO:0000269|PubMed:12628923,ECO:0000269|PubMed:12732143, ECO:0000269|PubMed:9535219}. Ras effector protein that functions as a guaninenucleotide exchange (GEF) for RAB5B and RAB31, by exchanging boundGDP for free GTP. Required for normal RAB31 function.{ECO:0000269|PubMed:12972505, ECO:0000269|PubMed:21586568}.

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 COPS8_RIN3


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 COPS8_RIN3


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
COPS8GPS1, COPS2, COPS3, COPS4, COPS5, COPS6, COPS8, COPS7A, COPS7B, CUL1, MAPRE1, RAE1, DDB1, CUL4A, RFWD2, CTNNB1, DDB2, ERCC8, VPRBP, CUL3, CUL4B, CUL5, CUL2, DCUN1D1, NEDD8, GFER, LRR1, DDA1, PINK1, DDIT3, IRF5, FBXW4, FBXO6, SRRT, VIM, WDR77, USHBP1, ADCYAP1, AMBRA1, KRAS, CENPA, MYEOV2, DUSP13, APPBP2, BTBD1, DCAF4, DCAF11, FEM1B, DTL, CRBN, RNF138, BTBD2, BMX, SLC9A3R2, USH1C, PRPF31, DLD, HSD17B10, DCAF4L2RIN3RAB5B, RAB5A, BIN1, RABAC1, RGS2, TNFAIP1, MYC, ASB8, DOK3, FAM127C, MPEG1, PLB1, SPATA12, SPRY4, TM4SF19, TSSK3, ASB3, CRK, CRKL, CSRP3, CYP2C8, CYP46A1, EPS8L2, EZH2, FAM46A, GATA1, GRAP2, ID2, KCTD17, LCK, MT2A, POLR3F, PSMD9, SUV39H1, SYMPK, TGM1, TSC1, ZBTB24, ZNF639, ZNF655, ZNF71


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 COPS8_RIN3


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 COPS8_RIN3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneRIN3C0029401Osteitis Deformans1CTD_human