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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: 13617

FusionGeneSummary for FMNL3_CPNE8

check button Fusion gene summary
Fusion gene informationFusion gene name: FMNL3_CPNE8
Fusion gene ID: 13617
HgeneTgene
Gene symbol

FMNL3

CPNE8

Gene ID

91010

144402

Gene nameformin like 3copine 8
SynonymsFHOD3|FRL2|WBP-3|WBP3-
Cytomap

12q13.12

12q12

Type of geneprotein-codingprotein-coding
Descriptionformin-like protein 3WW domain binding protein 3formin homology 2 domain-containing protein 3copine-8copine VIII
Modification date2018051920180523
UniProtAcc

Q8IVF7

Q86YQ8

Ensembl transtripts involved in fusion geneENST00000335154, ENST00000550488, 
ENST00000352151, ENST00000293590, 
ENST00000550668, 
ENST00000331366, 
ENST00000538596, ENST00000546603, 
ENST00000360449, 
Fusion gene scores* DoF score6 X 5 X 4=1204 X 3 X 4=48
# samples 64
** MAII scorelog2(6/120*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: FMNL3 [Title/Abstract] AND CPNE8 [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
TCGARVSKCMTCGA-GN-A264-06AFMNL3chr12

50100838

-CPNE8chr12

39071356

-
* 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
Frame-shiftENST00000335154ENST00000331366FMNL3chr12

50100838

-CPNE8chr12

39071356

-
Frame-shiftENST00000335154ENST00000538596FMNL3chr12

50100838

-CPNE8chr12

39071356

-
5CDS-5UTRENST00000335154ENST00000546603FMNL3chr12

50100838

-CPNE8chr12

39071356

-
5CDS-5UTRENST00000335154ENST00000360449FMNL3chr12

50100838

-CPNE8chr12

39071356

-
Frame-shiftENST00000550488ENST00000331366FMNL3chr12

50100838

-CPNE8chr12

39071356

-
Frame-shiftENST00000550488ENST00000538596FMNL3chr12

50100838

-CPNE8chr12

39071356

-
5CDS-5UTRENST00000550488ENST00000546603FMNL3chr12

50100838

-CPNE8chr12

39071356

-
5CDS-5UTRENST00000550488ENST00000360449FMNL3chr12

50100838

-CPNE8chr12

39071356

-
Frame-shiftENST00000352151ENST00000331366FMNL3chr12

50100838

-CPNE8chr12

39071356

-
Frame-shiftENST00000352151ENST00000538596FMNL3chr12

50100838

-CPNE8chr12

39071356

-
5CDS-5UTRENST00000352151ENST00000546603FMNL3chr12

50100838

-CPNE8chr12

39071356

-
5CDS-5UTRENST00000352151ENST00000360449FMNL3chr12

50100838

-CPNE8chr12

39071356

-
Frame-shiftENST00000293590ENST00000331366FMNL3chr12

50100838

-CPNE8chr12

39071356

-
Frame-shiftENST00000293590ENST00000538596FMNL3chr12

50100838

-CPNE8chr12

39071356

-
5CDS-5UTRENST00000293590ENST00000546603FMNL3chr12

50100838

-CPNE8chr12

39071356

-
5CDS-5UTRENST00000293590ENST00000360449FMNL3chr12

50100838

-CPNE8chr12

39071356

-
intron-3CDSENST00000550668ENST00000331366FMNL3chr12

50100838

-CPNE8chr12

39071356

-
intron-3CDSENST00000550668ENST00000538596FMNL3chr12

50100838

-CPNE8chr12

39071356

-
intron-5UTRENST00000550668ENST00000546603FMNL3chr12

50100838

-CPNE8chr12

39071356

-
intron-5UTRENST00000550668ENST00000360449FMNL3chr12

50100838

-CPNE8chr12

39071356

-

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FusionProtFeatures for FMNL3_CPNE8


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FMNL3

Q8IVF7

CPNE8

Q86YQ8

Plays a role in the regulation of cell morphology andcytoskeletal organization. Required in the control of cell shapeand migration. Required for developmental angiogenesis (Bysimilarity). In this process, required for microtubulereorganization and for efficient endothelial cell elongation. Inquiescent endothelial cells, triggers rearrangement of the actincytoskeleton, but does not alter microtubule alignement.{ECO:0000250|UniProtKB:Q6NXC0, ECO:0000269|PubMed:21834987,ECO:0000269|PubMed:22275430}. Probable calcium-dependent phospholipid-binding proteinthat may play a role in calcium-mediated intracellular processes.{ECO:0000250|UniProtKB:Q99829}.

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 FMNL3_CPNE8


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 FMNL3_CPNE8


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
FMNL3PRPF40A, APP, MMS19, FAM96B, CIAO1, NTRK1CPNE8ELAVL1, ARRB1, CYSRT1, LAMTOR2, SHMT2, MOV10, NXF1, CCDC8, CSPP1, SLC25A41, TMEM185A, EIF3I, NDUFS1, TMEM17, CTDSPL2, MCM2


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 FMNL3_CPNE8


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 FMNL3_CPNE8


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