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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:CNPY2-ABCD3 (FusionGDB2 ID:17813)

Fusion Gene Summary for CNPY2-ABCD3

check button Fusion gene summary
Fusion gene informationFusion gene name: CNPY2-ABCD3
Fusion gene ID: 17813
HgeneTgene
Gene symbol

CNPY2

ABCD3

Gene ID

10330

5825

Gene namecanopy FGF signaling regulator 2ATP binding cassette subfamily D member 3
SynonymsHP10390|MSAP|TMEM4|ZSIG9ABC43|CBAS5|PMP70|PXMP1|ZWS2
Cytomap

12q13.3

1p21.3

Type of geneprotein-codingprotein-coding
Descriptionprotein canopy homolog 2MIR-interacting saposin-like proteinputative secreted protein Zsig9transmembrane protein 4ATP-binding cassette sub-family D member 370 kDa peroxisomal membrane proteinATP-binding cassette, sub-family D (ALD), member 3Peroxisomal membrane protein-1 (70kD)dJ824O18.1 (ATP-binding cassette, sub-family D (ALD), member 3 (PMP70, PXMP1))peroxiso
Modification date2020031320200313
UniProtAcc

Q9Y2B0

P28288

Ensembl transtripts involved in fusion geneENST00000273308, ENST00000551720, 
ENST00000484213, ENST00000315713, 
ENST00000370214, ENST00000394233, 
ENST00000454898, ENST00000536817, 
Fusion gene scores* DoF score13 X 8 X 7=72810 X 6 X 6=360
# samples 1410
** MAII scorelog2(14/728*10)=-2.37851162325373
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(10/360*10)=-1.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CNPY2 [Title/Abstract] AND ABCD3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCNPY2(56708634)-ABCD3(94964157), # samples:1
Anticipated loss of major functional domain due to fusion event.CNPY2-ABCD3 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
CNPY2-ABCD3 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
CNPY2-ABCD3 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
* 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
TgeneABCD3

GO:0007031

peroxisome organization

9425230


check buttonFusion gene breakpoints across CNPY2 (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 ABCD3 (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-HQ-A2OECNPY2chr12

56708634

-ABCD3chr1

94964157

+


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Fusion Gene ORF analysis for CNPY2-ABCD3

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-3UTRENST00000273308ENST00000484213CNPY2chr12

56708634

-ABCD3chr1

94964157

+
5CDS-intronENST00000273308ENST00000315713CNPY2chr12

56708634

-ABCD3chr1

94964157

+
5UTR-3CDSENST00000551720ENST00000370214CNPY2chr12

56708634

-ABCD3chr1

94964157

+
5UTR-3CDSENST00000551720ENST00000394233CNPY2chr12

56708634

-ABCD3chr1

94964157

+
5UTR-3CDSENST00000551720ENST00000454898CNPY2chr12

56708634

-ABCD3chr1

94964157

+
5UTR-3CDSENST00000551720ENST00000536817CNPY2chr12

56708634

-ABCD3chr1

94964157

+
5UTR-3UTRENST00000551720ENST00000484213CNPY2chr12

56708634

-ABCD3chr1

94964157

+
5UTR-intronENST00000551720ENST00000315713CNPY2chr12

56708634

-ABCD3chr1

94964157

+
Frame-shiftENST00000273308ENST00000370214CNPY2chr12

56708634

-ABCD3chr1

94964157

+
Frame-shiftENST00000273308ENST00000394233CNPY2chr12

56708634

-ABCD3chr1

94964157

+
Frame-shiftENST00000273308ENST00000454898CNPY2chr12

56708634

-ABCD3chr1

94964157

+
Frame-shiftENST00000273308ENST00000536817CNPY2chr12

56708634

-ABCD3chr1

94964157

+

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 CNPY2-ABCD3


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)
CNPY2chr1256708634-ABCD3chr194964157+7.03E-060.99999297
CNPY2chr1256708634-ABCD3chr194964157+7.03E-060.99999297

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.
genomic feature of top 1%

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Fusion Protein Features for CNPY2-ABCD3


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/:56708634/:94964157)
- 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
CNPY2

Q9Y2B0

ABCD3

P28288

FUNCTION: Positive regulator of neurite outgrowth by stabilizing myosin regulatory light chain (MRLC). It prevents MIR-mediated MRLC ubiquitination and its subsequent proteasomal degradation.FUNCTION: Probable transporter involved in the transport of branched-chain fatty acids and C27 bile acids into the peroxisome; the latter function is a crucial step in bile acid biosynthesis (PubMed:25168382). The nucleotide-binding fold acts as an ATP-binding subunit with ATPase activity (PubMed:11248239). {ECO:0000269|PubMed:11248239, ECO:0000269|PubMed:25168382}.

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 CNPY2-ABCD3


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 CNPY2-ABCD3


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 CNPY2-ABCD3


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 CNPY2-ABCD3


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