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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:COG5-FOXP1 (FusionGDB2 ID:18022)

Fusion Gene Summary for COG5-FOXP1

check button Fusion gene summary
Fusion gene informationFusion gene name: COG5-FOXP1
Fusion gene ID: 18022
HgeneTgene
Gene symbol

COG5

FOXP1

Gene ID

10466

27086

Gene namecomponent of oligomeric golgi complex 5forkhead box P1
SynonymsCDG2I|GOLTC1|GTC9012CC4|HSPC215|MFH|QRF1|hFKH1B
Cytomap

7q22.3

3p13

Type of geneprotein-codingprotein-coding
Descriptionconserved oligomeric Golgi complex subunit 513S golgi transport complex 1 90 kDa subunitCOG complex subunit 5conserved oligomeric Golgi complex protein 5forkhead box protein P1fork head-related protein like Bglutamine-rich factor 1mac-1-regulated forkhead
Modification date2020031320200329
UniProtAcc

Q9UP83

Q9H334

Ensembl transtripts involved in fusion geneENST00000297135, ENST00000347053, 
ENST00000393603, ENST00000475638, 
ENST00000318779, ENST00000318789, 
ENST00000475937, ENST00000493089, 
ENST00000468577, ENST00000472382, 
ENST00000484350, ENST00000491238, 
ENST00000498215, 
Fusion gene scores* DoF score18 X 12 X 10=216047 X 26 X 20=24440
# samples 1952
** MAII scorelog2(19/2160*10)=-3.50695998871988
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(52/24440*10)=-5.55458885167764
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: COG5 [Title/Abstract] AND FOXP1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCOG5(107188556)-FOXP1(71542706), # samples:3
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
HgeneCOG5

GO:0048219

inter-Golgi cisterna vesicle-mediated transport

9792665

TgeneFOXP1

GO:0002903

negative regulation of B cell apoptotic process

25267198

TgeneFOXP1

GO:0010629

negative regulation of gene expression

30111844

TgeneFOXP1

GO:0030316

osteoclast differentiation

18799727

TgeneFOXP1

GO:0032496

response to lipopolysaccharide

18799727

TgeneFOXP1

GO:0032680

regulation of tumor necrosis factor production

18799727

TgeneFOXP1

GO:0035926

chemokine (C-C motif) ligand 2 secretion

18799727

TgeneFOXP1

GO:0036035

osteoclast development

18799727

TgeneFOXP1

GO:0042116

macrophage activation

18799727

TgeneFOXP1

GO:0042117

monocyte activation

18799727

TgeneFOXP1

GO:0045655

regulation of monocyte differentiation

15286807

TgeneFOXP1

GO:0045892

negative regulation of transcription, DNA-templated

20950788

TgeneFOXP1

GO:0050706

regulation of interleukin-1 beta secretion

18799727

TgeneFOXP1

GO:0050727

regulation of inflammatory response

18799727

TgeneFOXP1

GO:0060766

negative regulation of androgen receptor signaling pathway

18640093

TgeneFOXP1

GO:1900424

regulation of defense response to bacterium

18799727

TgeneFOXP1

GO:1901256

regulation of macrophage colony-stimulating factor production

18799727

TgeneFOXP1

GO:2001182

regulation of interleukin-12 secretion

18799727


check buttonFusion gene breakpoints across COG5 (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 FOXP1 (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
ChimerDB4BLCATCGA-ZF-AA5H-01ACOG5chr7

107188556

-FOXP1chr3

71542706

-
ChimerDB4BLCATCGA-ZF-AA5HCOG5chr7

107188556

-FOXP1chr3

71542706

-


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Fusion Gene ORF analysis for COG5-FOXP1

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-5UTRENST00000297135ENST00000318779COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-5UTRENST00000297135ENST00000318789COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-5UTRENST00000297135ENST00000475937COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-5UTRENST00000297135ENST00000493089COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-5UTRENST00000347053ENST00000318779COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-5UTRENST00000347053ENST00000318789COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-5UTRENST00000347053ENST00000475937COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-5UTRENST00000347053ENST00000493089COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-5UTRENST00000393603ENST00000318779COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-5UTRENST00000393603ENST00000318789COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-5UTRENST00000393603ENST00000475937COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-5UTRENST00000393603ENST00000493089COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-intronENST00000297135ENST00000468577COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-intronENST00000297135ENST00000472382COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-intronENST00000297135ENST00000484350COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-intronENST00000297135ENST00000491238COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-intronENST00000297135ENST00000498215COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-intronENST00000347053ENST00000468577COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-intronENST00000347053ENST00000472382COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-intronENST00000347053ENST00000484350COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-intronENST00000347053ENST00000491238COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-intronENST00000347053ENST00000498215COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-intronENST00000393603ENST00000468577COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-intronENST00000393603ENST00000472382COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-intronENST00000393603ENST00000484350COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-intronENST00000393603ENST00000491238COG5chr7

107188556

-FOXP1chr3

71542706

-
5CDS-intronENST00000393603ENST00000498215COG5chr7

107188556

-FOXP1chr3

71542706

-
5UTR-5UTRENST00000475638ENST00000318779COG5chr7

107188556

-FOXP1chr3

71542706

-
5UTR-5UTRENST00000475638ENST00000318789COG5chr7

107188556

-FOXP1chr3

71542706

-
5UTR-5UTRENST00000475638ENST00000475937COG5chr7

107188556

-FOXP1chr3

71542706

-
5UTR-5UTRENST00000475638ENST00000493089COG5chr7

107188556

-FOXP1chr3

71542706

-
5UTR-intronENST00000475638ENST00000468577COG5chr7

107188556

-FOXP1chr3

71542706

-
5UTR-intronENST00000475638ENST00000472382COG5chr7

107188556

-FOXP1chr3

71542706

-
5UTR-intronENST00000475638ENST00000484350COG5chr7

107188556

-FOXP1chr3

71542706

-
5UTR-intronENST00000475638ENST00000491238COG5chr7

107188556

-FOXP1chr3

71542706

-
5UTR-intronENST00000475638ENST00000498215COG5chr7

107188556

-FOXP1chr3

71542706

-

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 COG5-FOXP1


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 COG5-FOXP1


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:107188556/:71542706)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
COG5

Q9UP83

FOXP1

Q9H334

FUNCTION: Required for normal Golgi function. {ECO:0000250}.FUNCTION: Transcriptional repressor (PubMed:18347093, PubMed:26647308). Can act with CTBP1 to synergistically repress transcription but CTPBP1 is not essential (By similarity). Plays an important role in the specification and differentiation of lung epithelium. Acts cooperatively with FOXP4 to regulate lung secretory epithelial cell fate and regeneration by restricting the goblet cell lineage program; the function may involve regulation of AGR2. Essential transcriptional regulator of B-cell development. Involved in regulation of cardiac muscle cell proliferation. Involved in the columnar organization of spinal motor neurons. Promotes the formation of the lateral motor neuron column (LMC) and the preganglionic motor column (PGC) and is required for respective appropriate motor axon projections. The segment-appropriate generation of spinal chord motor columns requires cooperation with other Hox proteins. Can regulate PITX3 promoter activity; may promote midbrain identity in embryonic stem cell-derived dopamine neurons by regulating PITX3. Negatively regulates the differentiation of T follicular helper cells T(FH)s. Involved in maintenance of hair follicle stem cell quiescence; the function probably involves regulation of FGF18 (By similarity). Represses transcription of various pro-apoptotic genes and cooperates with NF-kappa B-signaling in promoting B-cell expansion by inhibition of caspase-dependent apoptosis (PubMed:25267198). Binds to CSF1R promoter elements and is involved in regulation of monocyte differentiation and macrophage functions; repression of CSF1R in monocytes seems to involve NCOR2 as corepressor (PubMed:15286807, PubMed:18799727, PubMed:18347093). Involved in endothelial cell proliferation, tube formation and migration indicative for a role in angiogenesis; the role in neovascularization seems to implicate suppression of SEMA5B (PubMed:24023716). Can negatively regulate androgen receptor signaling (PubMed:18640093). Acts as a transcriptional activator of the FBXL7 promoter; this activity is regulated by AURKA (PubMed:28218735). {ECO:0000250|UniProtKB:P58462, ECO:0000269|PubMed:15286807, ECO:0000269|PubMed:18640093, ECO:0000269|PubMed:18799727, ECO:0000269|PubMed:24023716, ECO:0000269|PubMed:25267198, ECO:0000269|PubMed:26647308, ECO:0000269|PubMed:28218735, ECO:0000305|PubMed:18347093, ECO:0000305|PubMed:24023716}.; FUNCTION: [Isoform 8]: Involved in transcriptional regulation in embryonic stem cells (ESCs). Stimulates expression of transcription factors that are required for pluripotency and decreases expression of differentiation-associated genes. Has distinct DNA-binding specifities as compared to the canonical form and preferentially binds DNA with the sequence 5'-CGATACAA-3' (or closely related sequences) (PubMed:21924763). Promotes ESC self-renewal and pluripotency (By similarity). {ECO:0000250|UniProtKB:P58462, ECO:0000269|PubMed:21924763}.

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 COG5-FOXP1


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 COG5-FOXP1


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 COG5-FOXP1


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 COG5-FOXP1


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