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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: 7668

FusionGeneSummary for CNN1_DYNLRB1

check button Fusion gene summary
Fusion gene informationFusion gene name: CNN1_DYNLRB1
Fusion gene ID: 7668
HgeneTgene
Gene symbol

CNN1

DYNLRB1

Gene ID

1264

83658

Gene namecalponin 1dynein light chain roadblock-type 1
SynonymsHEL-S-14|SMCC|Sm-CalpBITH|BLP|DNCL2A|DNLC2A|ROBLD1
Cytomap

19p13.2

20q11.22

Type of geneprotein-codingprotein-coding
Descriptioncalponin-1basic calponincalponin 1, basic, smooth musclecalponin H1, smooth musclecalponins, basicepididymis secretory protein Li 14dynein light chain roadblock-type 1ROBL/LC7-like 1bithoraxoid-like proteindynein, cytoplasmic, light polypeptide 2Adynein-associated protein Km23roadblock domain-containing protein 1
Modification date2018051920180523
UniProtAcc

P51911

Q9NP97

Ensembl transtripts involved in fusion geneENST00000252456, ENST00000592923, 
ENST00000535659, ENST00000588468, 
ENST00000544952, 
ENST00000357156, 
ENST00000480759, ENST00000417166, 
ENST00000300469, ENST00000374846, 
Fusion gene scores* DoF score6 X 4 X 3=726 X 5 X 4=120
# samples 66
** MAII scorelog2(6/72*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/120*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CNN1 [Title/Abstract] AND DYNLRB1 [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
ChiTaRS3.1BG107757CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
* 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-3UTRENST00000252456ENST00000357156CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
3UTR-3UTRENST00000252456ENST00000480759CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
3UTR-intronENST00000252456ENST00000417166CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
3UTR-intronENST00000252456ENST00000300469CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
3UTR-3UTRENST00000252456ENST00000374846CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
3UTR-3UTRENST00000592923ENST00000357156CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
3UTR-3UTRENST00000592923ENST00000480759CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
3UTR-intronENST00000592923ENST00000417166CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
3UTR-intronENST00000592923ENST00000300469CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
3UTR-3UTRENST00000592923ENST00000374846CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
intron-3UTRENST00000535659ENST00000357156CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
intron-3UTRENST00000535659ENST00000480759CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
intron-intronENST00000535659ENST00000417166CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
intron-intronENST00000535659ENST00000300469CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
intron-3UTRENST00000535659ENST00000374846CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
intron-3UTRENST00000588468ENST00000357156CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
intron-3UTRENST00000588468ENST00000480759CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
intron-intronENST00000588468ENST00000417166CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
intron-intronENST00000588468ENST00000300469CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
intron-3UTRENST00000588468ENST00000374846CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
intron-3UTRENST00000544952ENST00000357156CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
intron-3UTRENST00000544952ENST00000480759CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
intron-intronENST00000544952ENST00000417166CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
intron-intronENST00000544952ENST00000300469CNN1chr19

11660852

+DYNLRB1chr20

33128625

+
intron-3UTRENST00000544952ENST00000374846CNN1chr19

11660852

+DYNLRB1chr20

33128625

+

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FusionProtFeatures for CNN1_DYNLRB1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CNN1

P51911

DYNLRB1

Q9NP97

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 (By similarity). {ECO:0000250}. Acts as one of several non-catalytic accessorycomponents of the cytoplasmic dynein 1 complex that are thought tobe involved in linking dynein to cargos and to adapter proteinsthat regulate dynein function. Cytoplasmic dynein 1 acts as amotor for the intracellular retrograde motility of vesicles andorganelles along microtubules.

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 CNN1_DYNLRB1


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 CNN1_DYNLRB1


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 CNN1_DYNLRB1


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 CNN1_DYNLRB1


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