FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

FusionGeneSummary

leaf

FusionProtFeature

leaf

FusionGeneSequence

leaf

FusionGenePPI

leaf

RelatedDrugs

leaf

RelatedDiseases

Fusion gene ID: 7678

FusionGeneSummary for CNN2_WAC

check button Fusion gene summary
Fusion gene informationFusion gene name: CNN2_WAC
Fusion gene ID: 7678
HgeneTgene
Gene symbol

CNN2

WAC

Gene ID

1265

51322

Gene namecalponin 2WW domain containing adaptor with coiled-coil
Synonyms-BM-016|DESSH|PRO1741|Wwp4
Cytomap

19p13.3

10p12.1|10p12.1-p11.2

Type of geneprotein-codingprotein-coding
Descriptioncalponin-2calponin H2, smooth muscleneutral calponinWW domain-containing adapter protein with coiled-coil
Modification date2018052220180519
UniProtAcc

Q99439

Q9BTA9

Ensembl transtripts involved in fusion geneENST00000263097, ENST00000606983, 
ENST00000348419, ENST00000565096, 
ENST00000562958, 
ENST00000375664, 
ENST00000375646, ENST00000347934, 
ENST00000354911, ENST00000428935, 
ENST00000532233, 
Fusion gene scores* DoF score8 X 8 X 5=3209 X 11 X 3=297
# samples 813
** MAII scorelog2(8/320*10)=-2
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(13/297*10)=-1.19195130777231
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CNN2 [Title/Abstract] AND WAC [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
HgeneCNN2

GO:0032970

regulation of actin filament-based process

16236705

HgeneCNN2

GO:0071260

cellular response to mechanical stimulus

16236705


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
ChiTaRS3.1BQ004560CNN2chr19

1038780

-WACchr10

28907931

-
* 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
3UTR-intronENST00000263097ENST00000375664CNN2chr19

1038780

-WACchr10

28907931

-
3UTR-intronENST00000263097ENST00000375646CNN2chr19

1038780

-WACchr10

28907931

-
3UTR-intronENST00000263097ENST00000347934CNN2chr19

1038780

-WACchr10

28907931

-
3UTR-intronENST00000263097ENST00000354911CNN2chr19

1038780

-WACchr10

28907931

-
3UTR-intronENST00000263097ENST00000428935CNN2chr19

1038780

-WACchr10

28907931

-
3UTR-intronENST00000263097ENST00000532233CNN2chr19

1038780

-WACchr10

28907931

-
3UTR-intronENST00000606983ENST00000375664CNN2chr19

1038780

-WACchr10

28907931

-
3UTR-intronENST00000606983ENST00000375646CNN2chr19

1038780

-WACchr10

28907931

-
3UTR-intronENST00000606983ENST00000347934CNN2chr19

1038780

-WACchr10

28907931

-
3UTR-intronENST00000606983ENST00000354911CNN2chr19

1038780

-WACchr10

28907931

-
3UTR-intronENST00000606983ENST00000428935CNN2chr19

1038780

-WACchr10

28907931

-
3UTR-intronENST00000606983ENST00000532233CNN2chr19

1038780

-WACchr10

28907931

-
3UTR-intronENST00000348419ENST00000375664CNN2chr19

1038780

-WACchr10

28907931

-
3UTR-intronENST00000348419ENST00000375646CNN2chr19

1038780

-WACchr10

28907931

-
3UTR-intronENST00000348419ENST00000347934CNN2chr19

1038780

-WACchr10

28907931

-
3UTR-intronENST00000348419ENST00000354911CNN2chr19

1038780

-WACchr10

28907931

-
3UTR-intronENST00000348419ENST00000428935CNN2chr19

1038780

-WACchr10

28907931

-
3UTR-intronENST00000348419ENST00000532233CNN2chr19

1038780

-WACchr10

28907931

-
intron-intronENST00000565096ENST00000375664CNN2chr19

1038780

-WACchr10

28907931

-
intron-intronENST00000565096ENST00000375646CNN2chr19

1038780

-WACchr10

28907931

-
intron-intronENST00000565096ENST00000347934CNN2chr19

1038780

-WACchr10

28907931

-
intron-intronENST00000565096ENST00000354911CNN2chr19

1038780

-WACchr10

28907931

-
intron-intronENST00000565096ENST00000428935CNN2chr19

1038780

-WACchr10

28907931

-
intron-intronENST00000565096ENST00000532233CNN2chr19

1038780

-WACchr10

28907931

-
intron-intronENST00000562958ENST00000375664CNN2chr19

1038780

-WACchr10

28907931

-
intron-intronENST00000562958ENST00000375646CNN2chr19

1038780

-WACchr10

28907931

-
intron-intronENST00000562958ENST00000347934CNN2chr19

1038780

-WACchr10

28907931

-
intron-intronENST00000562958ENST00000354911CNN2chr19

1038780

-WACchr10

28907931

-
intron-intronENST00000562958ENST00000428935CNN2chr19

1038780

-WACchr10

28907931

-
intron-intronENST00000562958ENST00000532233CNN2chr19

1038780

-WACchr10

28907931

-

Top

FusionProtFeatures for CNN2_WAC


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CNN2

Q99439

WAC

Q9BTA9

Thin filament-associated protein that is implicated inthe regulation and modulation of smooth muscle contraction. It iscapable of binding to actin, calmodulin, troponin C andtropomyosin. The interaction of calponin with actin inhibits theactomyosin Mg-ATPase activity.

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


Top

FusionGeneSequence for CNN2_WAC


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).

Top

FusionGenePPI for CNN2_WAC


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


Top

RelatedDrugs for CNN2_WAC


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

Top

RelatedDiseases for CNN2_WAC


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCNN2C0007134Renal Cell Carcinoma1CTD_human