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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 7743

FusionGeneSummary for CNPY2_CNPY2

check button Fusion gene summary
Fusion gene informationFusion gene name: CNPY2_CNPY2
Fusion gene ID: 7743
HgeneTgene
Gene symbol

CNPY2

CNPY2

Gene ID

10330

10330

Gene namecanopy FGF signaling regulator 2canopy FGF signaling regulator 2
SynonymsHP10390|MSAP|TMEM4|ZSIG9HP10390|MSAP|TMEM4|ZSIG9
Cytomap

12q13.3

12q13.3

Type of geneprotein-codingprotein-coding
Descriptionprotein canopy homolog 2MIR-interacting saposin-like proteinputative secreted protein Zsig9transmembrane protein 4protein canopy homolog 2MIR-interacting saposin-like proteinputative secreted protein Zsig9transmembrane protein 4
Modification date2018052320180523
UniProtAcc

Q9Y2B0

Q9Y2B0

Ensembl transtripts involved in fusion geneENST00000273308, ENST00000551720, 
ENST00000273308, ENST00000551720, 
Fusion gene scores* DoF score2 X 3 X 1=62 X 3 X 1=6
# samples 93
** MAII scorelog2(9/6*10)=3.90689059560852log2(3/6*10)=2.32192809488736
Context

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

Functional or gene categories assigned by FusionGDB annotation
* 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

check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS3.1AL831869CNPY2chr12

56704354

-CNPY2chr12

56704256

+
ChiTaRS3.1BE826144CNPY2chr12

56705195

+CNPY2chr12

56705155

-
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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-3UTRENST00000273308ENST00000273308CNPY2chr12

56704354

-CNPY2chr12

56704256

+
intron-intronENST00000273308ENST00000551720CNPY2chr12

56704354

-CNPY2chr12

56704256

+
intron-3UTRENST00000551720ENST00000273308CNPY2chr12

56704354

-CNPY2chr12

56704256

+
intron-intronENST00000551720ENST00000551720CNPY2chr12

56704354

-CNPY2chr12

56704256

+
intron-3CDSENST00000273308ENST00000273308CNPY2chr12

56705195

+CNPY2chr12

56705155

-
intron-5UTRENST00000273308ENST00000551720CNPY2chr12

56705195

+CNPY2chr12

56705155

-
intron-3CDSENST00000551720ENST00000273308CNPY2chr12

56705195

+CNPY2chr12

56705155

-
intron-5UTRENST00000551720ENST00000551720CNPY2chr12

56705195

+CNPY2chr12

56705155

-

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FusionProtFeatures for CNPY2_CNPY2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CNPY2

Q9Y2B0

CNPY2

Q9Y2B0

Positive regulator of neurite outgrowth by stabilizingmyosin regulatory light chain (MRLC). It prevents MIR-mediatedMRLC ubiquitination and its subsequent proteasomal degradation. Positive regulator of neurite outgrowth by stabilizingmyosin regulatory light chain (MRLC). It prevents MIR-mediatedMRLC ubiquitination and its subsequent proteasomal degradation.

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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FusionGeneSequence for CNPY2_CNPY2


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for CNPY2_CNPY2


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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RelatedDrugs for CNPY2_CNPY2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for CNPY2_CNPY2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCNPY2C0038356Stomach Neoplasms1CTD_human
TgeneCNPY2C0038356Stomach Neoplasms1CTD_human