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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:CCND3-GUCA1B (FusionGDB2 ID:14159)

Fusion Gene Summary for CCND3-GUCA1B

check button Fusion gene summary
Fusion gene informationFusion gene name: CCND3-GUCA1B
Fusion gene ID: 14159
HgeneTgene
Gene symbol

CCND3

GUCA1B

Gene ID

896

2979

Gene namecyclin D3guanylate cyclase activator 1B
Synonyms-GCAP 2|GCAP2|GUCA2|RP48
Cytomap

6p21.1

6p21.1

Type of geneprotein-codingprotein-coding
DescriptionG1/S-specific cyclin-D3D3-type cyclinguanylyl cyclase-activating protein 2guanylate cyclase activator 1B (retina)guanylate cyclase-activating protein, photoreceptor 2
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000511642, ENST00000415497, 
ENST00000372988, ENST00000510503, 
ENST00000511686, ENST00000372991, 
ENST00000372987, ENST00000414200, 
ENST00000230361, 
Fusion gene scores* DoF score17 X 5 X 11=9352 X 1 X 2=4
# samples 214
** MAII scorelog2(21/935*10)=-2.15457703710888
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/4*10)=3.32192809488736
Context

PubMed: CCND3 [Title/Abstract] AND GUCA1B [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCCND3(42016239)-GUCA1B(42156469), # 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
HgeneCCND3

GO:0001934

positive regulation of protein phosphorylation

8114739

HgeneCCND3

GO:0045737

positive regulation of cyclin-dependent protein serine/threonine kinase activity

8114739


check buttonFusion gene breakpoints across CCND3 (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 GUCA1B (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
ChimerDB4BRCATCGA-AR-A1AI-01ACCND3chr6

42016239

-GUCA1Bchr6

42156469

-
ChimerDB4BRCATCGA-AR-A1AICCND3chr6

42016238

-GUCA1Bchr6

42156469

-
ChimerDB4BRCATCGA-AR-A1AI-01ACCND3chr6

42016239

-GUCA1Bchr6

42156469

-
ChimerDB4BRCATCGA-AR-A1AI-01ACCND3chr6

42016239

-GUCA1Bchr6

42156469

-


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Fusion Gene ORF analysis for CCND3-GUCA1B

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-3CDSENST00000511642ENST00000230361CCND3chr6

42016239

-GUCA1Bchr6

42156469

-
5UTR-3CDSENST00000415497ENST00000230361CCND3chr6

42016239

-GUCA1Bchr6

42156469

-
5UTR-3CDSENST00000372988ENST00000230361CCND3chr6

42016239

-GUCA1Bchr6

42156469

-
5UTR-3CDSENST00000510503ENST00000230361CCND3chr6

42016239

-GUCA1Bchr6

42156469

-
5UTR-3CDSENST00000511686ENST00000230361CCND3chr6

42016239

-GUCA1Bchr6

42156469

-
intron-3CDSENST00000372991ENST00000230361CCND3chr6

42016239

-GUCA1Bchr6

42156469

-
intron-3CDSENST00000372987ENST00000230361CCND3chr6

42016239

-GUCA1Bchr6

42156469

-
intron-3CDSENST00000414200ENST00000230361CCND3chr6

42016239

-GUCA1Bchr6

42156469

-
intron-3CDSENST00000511642ENST00000230361CCND3chr6

42016238

-GUCA1Bchr6

42156469

-
5UTR-3CDSENST00000415497ENST00000230361CCND3chr6

42016238

-GUCA1Bchr6

42156469

-
5UTR-3CDSENST00000372988ENST00000230361CCND3chr6

42016238

-GUCA1Bchr6

42156469

-
5UTR-3CDSENST00000510503ENST00000230361CCND3chr6

42016238

-GUCA1Bchr6

42156469

-
5UTR-3CDSENST00000511686ENST00000230361CCND3chr6

42016238

-GUCA1Bchr6

42156469

-
intron-3CDSENST00000372991ENST00000230361CCND3chr6

42016238

-GUCA1Bchr6

42156469

-
intron-3CDSENST00000372987ENST00000230361CCND3chr6

42016238

-GUCA1Bchr6

42156469

-
intron-3CDSENST00000414200ENST00000230361CCND3chr6

42016238

-GUCA1Bchr6

42156469

-

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 CCND3-GUCA1B


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 CCND3-GUCA1B


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
..
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: 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.

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 CCND3-GUCA1B


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 CCND3-GUCA1B


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 CCND3-GUCA1B


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 CCND3-GUCA1B


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCCND3C1961099Precursor T-Cell Lymphoblastic Leukemia-Lymphoma1CTD_human
TgeneGUCA1BC0035334Retinitis Pigmentosa2CTD_human;GENOMICS_ENGLAND
TgeneGUCA1BC3151190RETINITIS PIGMENTOSA 482CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneGUCA1BC0015397Disorder of eye1GENOMICS_ENGLAND