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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:C9orf3-COPS7A (FusionGDB2 ID:12171)

Fusion Gene Summary for C9orf3-COPS7A

check button Fusion gene summary
Fusion gene informationFusion gene name: C9orf3-COPS7A
Fusion gene ID: 12171
HgeneTgene
Gene symbol

C9orf3

COPS7A

Gene ID

84909

50813

Gene nameaminopeptidase O (putative)COP9 signalosome subunit 7A
SynonymsAP-O|APO|C90RF3|C9orf3|ONPEPCSN7|CSN7A|SGN7a
Cytomap

9q22.32

12p13.31

Type of geneprotein-codingprotein-coding
Descriptionaminopeptidase OCOP9 signalosome complex subunit 7aCOP9 complex subunit 7aCOP9 constitutive photomorphogenic homolog subunit 7AJAB1-containing signalosome subunit 7adermal papilla-derived protein 10
Modification date2020031320200313
UniProtAcc.

Q9UBW8

Ensembl transtripts involved in fusion geneENST00000277198, ENST00000297979, 
ENST00000375315, ENST00000395357, 
ENST00000425634, ENST00000433691, 
ENST00000473778, 
ENST00000543155, 
ENST00000542150, ENST00000229251, 
ENST00000539735, ENST00000538410, 
ENST00000534947, ENST00000534877, 
Fusion gene scores* DoF score17 X 15 X 11=28053 X 3 X 1=9
# samples 213
** MAII scorelog2(21/2805*10)=-3.73953953783003
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/9*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: C9orf3 [Title/Abstract] AND COPS7A [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointC9orf3(97795471)-COPS7A(6837092), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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
TgeneCOPS7A

GO:0000338

protein deneddylation

19141280


check buttonFusion gene breakpoints across C9orf3 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across COPS7A (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS5.0N/AAA210971C9orf3chr9

97795471

-COPS7Achr12

6837092

+


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Fusion Gene ORF analysis for C9orf3-COPS7A

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
intron-3CDSENST00000277198ENST00000543155C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000277198ENST00000542150C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000277198ENST00000229251C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000277198ENST00000539735C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000277198ENST00000538410C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000277198ENST00000534947C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000277198ENST00000534877C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-3CDSENST00000297979ENST00000543155C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000297979ENST00000542150C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000297979ENST00000229251C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000297979ENST00000539735C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000297979ENST00000538410C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000297979ENST00000534947C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000297979ENST00000534877C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-3CDSENST00000375315ENST00000543155C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000375315ENST00000542150C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000375315ENST00000229251C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000375315ENST00000539735C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000375315ENST00000538410C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000375315ENST00000534947C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000375315ENST00000534877C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-3CDSENST00000395357ENST00000543155C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000395357ENST00000542150C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000395357ENST00000229251C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000395357ENST00000539735C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000395357ENST00000538410C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000395357ENST00000534947C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000395357ENST00000534877C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-3CDSENST00000425634ENST00000543155C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000425634ENST00000542150C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000425634ENST00000229251C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000425634ENST00000539735C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000425634ENST00000538410C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000425634ENST00000534947C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000425634ENST00000534877C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-3CDSENST00000433691ENST00000543155C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000433691ENST00000542150C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000433691ENST00000229251C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000433691ENST00000539735C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000433691ENST00000538410C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000433691ENST00000534947C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000433691ENST00000534877C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-3CDSENST00000473778ENST00000543155C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000473778ENST00000542150C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000473778ENST00000229251C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000473778ENST00000539735C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000473778ENST00000538410C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000473778ENST00000534947C9orf3chr9

97795471

-COPS7Achr12

6837092

+
intron-intronENST00000473778ENST00000534877C9orf3chr9

97795471

-COPS7Achr12

6837092

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for C9orf3-COPS7A


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for C9orf3-COPS7A


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.COPS7A

Q9UBW8

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Component of the COP9 signalosome complex (CSN), a complex 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 cullin subunits of SCF-type E3 ligase complexes, leading to decrease the Ubl ligase activity of SCF-type complexes such as SCF, CSA or DDB2. The complex is also involved in phosphorylation of p53/TP53, JUN, I-kappa-B-alpha/NFKBIA, ITPK1 and IRF8/ICSBP, possibly via its association with CK2 and PKD kinases. CSN-dependent phosphorylation of TP53 and JUN promotes and protects degradation by the Ubl system, respectively. {ECO:0000269|PubMed:11285227, ECO:0000269|PubMed:11337588, ECO:0000269|PubMed:12628923, ECO:0000269|PubMed:12732143, ECO:0000269|PubMed:9535219}.

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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Fusion Gene Sequence for C9orf3-COPS7A


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for C9orf3-COPS7A


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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Related Drugs for C9orf3-COPS7A


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for C9orf3-COPS7A


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneCOPS7AC0024623Malignant neoplasm of stomach1CTD_human
TgeneCOPS7AC0038356Stomach Neoplasms1CTD_human
TgeneCOPS7AC0235874Disease Exacerbation1CTD_human
TgeneCOPS7AC1708349Hereditary Diffuse Gastric Cancer1CTD_human