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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:ANXA5-CCNA2 (FusionGDB2 ID:5175)

Fusion Gene Summary for ANXA5-CCNA2

check button Fusion gene summary
Fusion gene informationFusion gene name: ANXA5-CCNA2
Fusion gene ID: 5175
HgeneTgene
Gene symbol

ANXA5

CCNA2

Gene ID

308

890

Gene nameannexin A5cyclin A2
SynonymsANX5|ENX2|HEL-S-7|PP4|RPRGL3CCN1|CCNA
Cytomap

4q27

4q27

Type of geneprotein-codingprotein-coding
Descriptionannexin A5CBP-IPAP-IVAC-alphaanchorin CIIannexin Vannexin-5calphobindin Iendonexin IIepididymis secretory protein Li 7lipocortin Vplacental anticoagulant protein 4placental anticoagulant protein Ithromboplastin inhibitorvascular anticoagulancyclin-A2cyclin-A
Modification date2020031320200313
UniProtAcc

P08758

P20248

Ensembl transtripts involved in fusion geneENST00000296511, ENST00000501272, 
ENST00000515017, ENST00000509016, 
ENST00000274026, 
Fusion gene scores* DoF score7 X 8 X 4=2246 X 2 X 2=24
# samples 86
** MAII scorelog2(8/224*10)=-1.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/24*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: ANXA5 [Title/Abstract] AND CCNA2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointANXA5(122602825)-CCNA2(122742246), # 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
TgeneCCNA2

GO:0000086

G2/M transition of mitotic cell cycle

1312467

TgeneCCNA2

GO:0016572

histone phosphorylation

11746698

TgeneCCNA2

GO:0044843

cell cycle G1/S phase transition

1312467


check buttonFusion gene breakpoints across ANXA5 (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 CCNA2 (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
ChimerDB4STADTCGA-VQ-A8DZANXA5chr4

122602825

-CCNA2chr4

122742246

-


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Fusion Gene ORF analysis for ANXA5-CCNA2

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
Frame-shiftENST00000296511ENST00000274026ANXA5chr4

122602825

-CCNA2chr4

122742246

-
Frame-shiftENST00000501272ENST00000274026ANXA5chr4

122602825

-CCNA2chr4

122742246

-
intron-3CDSENST00000515017ENST00000274026ANXA5chr4

122602825

-CCNA2chr4

122742246

-
5UTR-3CDSENST00000509016ENST00000274026ANXA5chr4

122602825

-CCNA2chr4

122742246

-

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 ANXA5-CCNA2


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 ANXA5-CCNA2


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
ANXA5

P08758

CCNA2

P20248

FUNCTION: This protein is an anticoagulant protein that acts as an indirect inhibitor of the thromboplastin-specific complex, which is involved in the blood coagulation cascade.FUNCTION: Cyclin which controls both the G1/S and the G2/M transition phases of the cell cycle. Functions through the formation of specific serine/threonine protein kinase holoenzyme complexes with the cyclin-dependent protein kinases CDK1 or CDK2. The cyclin subunit confers the substrate specificity of these complexes and differentially interacts with and activates CDK1 and CDK2 throughout the cell cycle. {ECO:0000269|PubMed:1312467}.

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 ANXA5-CCNA2


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 ANXA5-CCNA2


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 ANXA5-CCNA2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneANXA5P08758DB09130CopperSmall moleculeApproved|Investigational
HgeneANXA5P08758DB09130CopperSmall moleculeApproved|Investigational
HgeneANXA5P08758DB09130CopperSmall moleculeApproved|Investigational
HgeneANXA5P08758DB09130CopperSmall moleculeApproved|Investigational
HgeneANXA5P08758DB00591Fluocinolone acetonideInducerSmall moleculeApproved|Investigational|Vet_approved
HgeneANXA5P08758DB00591Fluocinolone acetonideInducerSmall moleculeApproved|Investigational|Vet_approved
HgeneANXA5P08758DB00591Fluocinolone acetonideInducerSmall moleculeApproved|Investigational|Vet_approved
HgeneANXA5P08758DB00591Fluocinolone acetonideInducerSmall moleculeApproved|Investigational|Vet_approved

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Related Diseases for ANXA5-CCNA2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneANXA5C0007137Squamous cell carcinoma1CTD_human
HgeneANXA5C0019202Hepatolenticular Degeneration1CTD_human
HgeneANXA5C0023467Leukemia, Myelocytic, Acute1CTD_human
HgeneANXA5C0023893Liver Cirrhosis, Experimental1CTD_human
HgeneANXA5C0024623Malignant neoplasm of stomach1CTD_human
HgeneANXA5C0026640Mouth Neoplasms1CTD_human
HgeneANXA5C0026998Acute Myeloid Leukemia, M11CTD_human
HgeneANXA5C0032914Pre-Eclampsia1CTD_human
HgeneANXA5C0038356Stomach Neoplasms1CTD_human
HgeneANXA5C0043094Weight Gain1CTD_human
HgeneANXA5C0152013Adenocarcinoma of lung (disorder)1CTD_human
HgeneANXA5C0153381Malignant neoplasm of mouth1CTD_human
HgeneANXA5C1527352Hepatic Form of Wilson Disease1CTD_human
HgeneANXA5C1708349Hereditary Diffuse Gastric Cancer1CTD_human
HgeneANXA5C1879321Acute Myeloid Leukemia (AML-M2)1CTD_human
TgeneCCNA2C0020796Profound Mental Retardation1CTD_human
TgeneCCNA2C0023893Liver Cirrhosis, Experimental1CTD_human
TgeneCCNA2C0025363Mental Retardation, Psychosocial1CTD_human
TgeneCCNA2C0036341Schizophrenia1PSYGENET
TgeneCCNA2C0917816Mental deficiency1CTD_human
TgeneCCNA2C1168401Squamous cell carcinoma of the head and neck1CTD_human
TgeneCCNA2C3714756Intellectual Disability1CTD_human