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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:CCL21-GEMIN5 (FusionGDB2 ID:14040)

Fusion Gene Summary for CCL21-GEMIN5

check button Fusion gene summary
Fusion gene informationFusion gene name: CCL21-GEMIN5
Fusion gene ID: 14040
HgeneTgene
Gene symbol

CCL21

GEMIN5

Gene ID

6366

25929

Gene nameC-C motif chemokine ligand 21gem nuclear organelle associated protein 5
Synonyms6Ckine|CKb9|ECL|SCYA21|SLC|TCA4GEMIN-5
Cytomap

9p13.3

5q33.2

Type of geneprotein-codingprotein-coding
DescriptionC-C motif chemokine 21Efficient Chemoattractant for Lymphocytesbeta chemokine exodus-2chemokine (C-C motif) ligand 21secondary lymphoid tissue chemokinesmall inducible cytokine subfamily A (Cys-Cys), member 21gem-associated protein 5
Modification date2020031320200322
UniProtAcc

O00585

Q8TEQ6

Ensembl transtripts involved in fusion geneENST00000259607, ENST00000378792, 
ENST00000285873, 
Fusion gene scores* DoF score1 X 1 X 1=11 X 1 X 1=1
# samples 11
** MAII scorelog2(1/1*10)=3.32192809488736log2(1/1*10)=3.32192809488736
Context

PubMed: CCL21 [Title/Abstract] AND GEMIN5 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCCL21(34709139)-GEMIN5(154267910), # 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
HgeneCCL21

GO:0001768

establishment of T cell polarity

12729902

HgeneCCL21

GO:0001954

positive regulation of cell-matrix adhesion

15569314|18308860

HgeneCCL21

GO:0002407

dendritic cell chemotaxis

15778365

HgeneCCL21

GO:0007186

G protein-coupled receptor signaling pathway

18308860

HgeneCCL21

GO:0030838

positive regulation of actin filament polymerization

11242036

HgeneCCL21

GO:0031274

positive regulation of pseudopodium assembly

11242036

HgeneCCL21

GO:0031529

ruffle organization

15569314

HgeneCCL21

GO:0033630

positive regulation of cell adhesion mediated by integrin

15569314

HgeneCCL21

GO:0034695

response to prostaglandin E

14592837

HgeneCCL21

GO:0035759

mesangial cell-matrix adhesion

15569314

HgeneCCL21

GO:0043123

positive regulation of I-kappaB kinase/NF-kappaB signaling

15059845

HgeneCCL21

GO:0043552

positive regulation of phosphatidylinositol 3-kinase activity

15059845|15778365

HgeneCCL21

GO:0045860

positive regulation of protein kinase activity

15059845

HgeneCCL21

GO:0046330

positive regulation of JNK cascade

15778365

HgeneCCL21

GO:0051209

release of sequestered calcium ion into cytosol

14592837

HgeneCCL21

GO:0051491

positive regulation of filopodium assembly

15569314

HgeneCCL21

GO:0051897

positive regulation of protein kinase B signaling

15059845|15778365

HgeneCCL21

GO:0060326

cell chemotaxis

18308860

HgeneCCL21

GO:0070374

positive regulation of ERK1 and ERK2 cascade

12729902|15778365

HgeneCCL21

GO:0090023

positive regulation of neutrophil chemotaxis

21051556

HgeneCCL21

GO:0090630

activation of GTPase activity

15778365

HgeneCCL21

GO:1903237

negative regulation of leukocyte tethering or rolling

18308860

HgeneCCL21

GO:2000147

positive regulation of cell motility

15778365

HgeneCCL21

GO:2000406

positive regulation of T cell migration

23620790

HgeneCCL21

GO:2000529

positive regulation of myeloid dendritic cell chemotaxis

14592837

HgeneCCL21

GO:2000669

negative regulation of dendritic cell apoptotic process

15059845

TgeneGEMIN5

GO:0000387

spliceosomal snRNP assembly

18984161


check buttonFusion gene breakpoints across CCL21 (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 GEMIN5 (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/AAI749414CCL21chr9

34709139

+GEMIN5chr5

154267910

-


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Fusion Gene ORF analysis for CCL21-GEMIN5

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-3CDSENST00000259607ENST00000285873CCL21chr9

34709139

+GEMIN5chr5

154267910

-
intron-3CDSENST00000378792ENST00000285873CCL21chr9

34709139

+GEMIN5chr5

154267910

-

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 CCL21-GEMIN5


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 CCL21-GEMIN5


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/:34709139/:154267910)
- 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
CCL21

O00585

GEMIN5

Q8TEQ6

FUNCTION: Inhibits hemopoiesis and stimulates chemotaxis. Chemotactic in vitro for thymocytes and activated T-cells, but not for B-cells, macrophages, or neutrophils. Shows preferential activity towards naive T-cells. May play a role in mediating homing of lymphocytes to secondary lymphoid organs. Binds to atypical chemokine receptor ACKR4 and mediates the recruitment of beta-arrestin (ARRB1/2) to ACKR4.FUNCTION: Required for the assembly of the SMN complex that plays a catalyst role in the assembly of small nuclear ribonucleoproteins (snRNPs), the building blocks of the spliceosome (PubMed:16857593, PubMed:18984161, PubMed:20513430). Thereby, plays an important role in the splicing of cellular pre-mRNAs. Most spliceosomal snRNPs contain a common set of Sm proteins SNRPB, SNRPD1, SNRPD2, SNRPD3, SNRPE, SNRPF and SNRPG that assemble in a heptameric protein ring on the Sm site of the small nuclear RNA to form the core snRNP. In the cytosol, the Sm proteins SNRPD1, SNRPD2, SNRPE, SNRPF and SNRPG are trapped in an inactive 6S pICln-Sm complex by the chaperone CLNS1A that controls the assembly of the core snRNP (PubMed:18984161). Dissociation by the SMN complex of CLNS1A from the trapped Sm proteins and their transfer to an SMN-Sm complex triggers the assembly of core snRNPs and their transport to the nucleus (PubMed:18984161). GEMIN5 acts as the snRNA-binding protein of the SMN complex (PubMed:11714716, PubMed:16857593, PubMed:19377484, PubMed:19750007, PubMed:20513430, PubMed:27834343, PubMed:27881600, PubMed:27881601). Binds to the 7-methylguanosine cap of RNA molecules (PubMed:19750007, PubMed:27834343, PubMed:27881600, PubMed:27881601, Ref.25). Binds to the 3'-UTR of SMN1 mRNA and regulates its translation; does not affect mRNA stability (PubMed:25911097). May play a role in the regulation of protein synthesis via its interaction with ribosomes (PubMed:27507887). {ECO:0000269|PubMed:11714716, ECO:0000269|PubMed:16857593, ECO:0000269|PubMed:18984161, ECO:0000269|PubMed:19377484, ECO:0000269|PubMed:19750007, ECO:0000269|PubMed:20513430, ECO:0000269|PubMed:25911097, ECO:0000269|PubMed:27507887, ECO:0000269|PubMed:27834343, ECO:0000269|PubMed:27881600, ECO:0000269|PubMed:27881601, ECO:0000269|Ref.25}.

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 CCL21-GEMIN5


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 CCL21-GEMIN5


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 CCL21-GEMIN5


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 CCL21-GEMIN5


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