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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: 27765

FusionGeneSummary for PLXNC1_CCDC41

check button Fusion gene summary
Fusion gene informationFusion gene name: PLXNC1_CCDC41
Fusion gene ID: 27765
HgeneTgene
Gene symbol

PLXNC1

CCDC41

Gene ID

10154

51134

Gene nameplexin C1centrosomal protein 83
SynonymsCD232|PLXN-C1|VESPRCCDC41|NPHP18|NY-REN-58
Cytomap

12q22

12q22

Type of geneprotein-codingprotein-coding
Descriptionplexin-C1plexin (semaphorin receptor)receptor for viral semaphorin proteinreceptor for virally-encoded semaphorinvirus-encoded semaphorin protein receptorcentrosomal protein of 83 kDaNY-REN-58 antigencoiled-coil domain-containing protein 41renal carcinoma antigen NY-REN-58
Modification date2018052320180519
UniProtAcc

O60486

Ensembl transtripts involved in fusion geneENST00000258526, ENST00000547057, 
ENST00000551495, ENST00000545312, 
ENST00000397809, ENST00000339839, 
ENST00000397807, ENST00000547575, 
ENST00000549352, 
Fusion gene scores* DoF score5 X 5 X 4=1001 X 1 X 1=1
# samples 61
** MAII scorelog2(6/100*10)=-0.736965594166206
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: PLXNC1 [Title/Abstract] AND CCDC41 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotationTumor suppressor gene involved fusion gene, in-frame but not retained their domain.
* 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
TCGARVSARCTCGA-DX-A2IZ-01APLXNC1chr12

94659001

+CCDC41chr12

94706793

-
* 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
In-frameENST00000258526ENST00000397809PLXNC1chr12

94659001

+CCDC41chr12

94706793

-
In-frameENST00000258526ENST00000339839PLXNC1chr12

94659001

+CCDC41chr12

94706793

-
5CDS-intronENST00000258526ENST00000397807PLXNC1chr12

94659001

+CCDC41chr12

94706793

-
5CDS-intronENST00000258526ENST00000547575PLXNC1chr12

94659001

+CCDC41chr12

94706793

-
5CDS-intronENST00000258526ENST00000549352PLXNC1chr12

94659001

+CCDC41chr12

94706793

-
In-frameENST00000547057ENST00000397809PLXNC1chr12

94659001

+CCDC41chr12

94706793

-
In-frameENST00000547057ENST00000339839PLXNC1chr12

94659001

+CCDC41chr12

94706793

-
5CDS-intronENST00000547057ENST00000397807PLXNC1chr12

94659001

+CCDC41chr12

94706793

-
5CDS-intronENST00000547057ENST00000547575PLXNC1chr12

94659001

+CCDC41chr12

94706793

-
5CDS-intronENST00000547057ENST00000549352PLXNC1chr12

94659001

+CCDC41chr12

94706793

-
intron-3CDSENST00000551495ENST00000397809PLXNC1chr12

94659001

+CCDC41chr12

94706793

-
intron-3CDSENST00000551495ENST00000339839PLXNC1chr12

94659001

+CCDC41chr12

94706793

-
intron-intronENST00000551495ENST00000397807PLXNC1chr12

94659001

+CCDC41chr12

94706793

-
intron-intronENST00000551495ENST00000547575PLXNC1chr12

94659001

+CCDC41chr12

94706793

-
intron-intronENST00000551495ENST00000549352PLXNC1chr12

94659001

+CCDC41chr12

94706793

-
5UTR-3CDSENST00000545312ENST00000397809PLXNC1chr12

94659001

+CCDC41chr12

94706793

-
5UTR-3CDSENST00000545312ENST00000339839PLXNC1chr12

94659001

+CCDC41chr12

94706793

-
5UTR-intronENST00000545312ENST00000397807PLXNC1chr12

94659001

+CCDC41chr12

94706793

-
5UTR-intronENST00000545312ENST00000547575PLXNC1chr12

94659001

+CCDC41chr12

94706793

-
5UTR-intronENST00000545312ENST00000549352PLXNC1chr12

94659001

+CCDC41chr12

94706793

-

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FusionProtFeatures for PLXNC1_CCDC41


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
PLXNC1

O60486

CCDC41

Receptor for SEMA7A, for smallpox semaphorin A39R,vaccinia virus semaphorin A39R and for herpesvirus Sema protein.Binding of semaphorins triggers cellular responses leading to therearrangement of the cytoskeleton and to secretion of IL6 and IL8(By similarity). {ECO:0000250, ECO:0000269|PubMed:20727575}. Lectin that binds to various sugars: galactose > mannose= fucose > N-acetylglucosamine > N-acetylgalactosamine(PubMed:10224141). Acts as a chemoattractant, probably involved inthe regulation of cell migration (PubMed:28301481).{ECO:0000269|PubMed:10224141, ECO:0000269|PubMed:28301481}.

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
HgenePLXNC1chr12:94659001chr12:94706793ENST00000258526+213135_45211991569DomainSema
HgenePLXNC1chr12:94659001chr12:94706793ENST00000258526+213135_94411991569Topological domainExtracellular
HgenePLXNC1chr12:94659001chr12:94706793ENST00000258526+2131945_96511991569TransmembraneHelical
TgeneCCDC41chr12:94659001chr12:94706793ENST00000397807-01440_634-211569Coiled coilOntology_term=ECO:0000255
TgeneCCDC41chr12:94659001chr12:94706793ENST00000397807-014665_698-211569Coiled coilOntology_term=ECO:0000255

- In-frame and not-retained protein feature among the 13 regional features.
>
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgenePLXNC1chr12:94659001chr12:94706793ENST00000258526+2131966_156811991569Topological domainCytoplasmic


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FusionGeneSequence for PLXNC1_CCDC41


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 PLXNC1_CCDC41


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
PLXNC1CCDC41


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 PLXNC1_CCDC41


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 PLXNC1_CCDC41


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePLXNC1C0014175Endometriosis1CTD_human