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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: 32016

FusionGeneSummary for RPP14_FLNB

check button Fusion gene summary
Fusion gene informationFusion gene name: RPP14_FLNB
Fusion gene ID: 32016
HgeneTgene
Gene symbol

RPP14

FLNB

Gene ID

11102

2317

Gene nameribonuclease P/MRP subunit p14filamin B
SynonymsP14ABP-278|ABP-280|AOI|FH1|FLN-B|FLN1L|LRS1|SCT|TABP|TAP
Cytomap

3p14.3

3p14.3

Type of geneprotein-codingprotein-coding
Descriptionribonuclease P protein subunit p14ribonuclease P/MRP 14kDa subunitfilamin-BABP-280 homologLarsen syndrome 1 (autosomal dominant)actin binding protein 278actin-binding-like proteinbeta-filaminfilamin B, betafilamin homolog 1filamin-3thyroid autoantigen
Modification date2018052220180522
UniProtAcc

O95059

O75369

Ensembl transtripts involved in fusion geneENST00000445193, ENST00000477305, 
ENST00000295959, ENST00000466547, 
ENST00000528153, 
ENST00000490882, 
ENST00000429972, ENST00000295956, 
ENST00000358537, ENST00000357272, 
ENST00000348383, ENST00000493452, 
ENST00000419752, ENST00000484981, 
Fusion gene scores* DoF score4 X 3 X 3=367 X 11 X 5=385
# samples 513
** MAII scorelog2(5/36*10)=0.473931188332412
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(13/385*10)=-1.56634682255381
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: RPP14 [Title/Abstract] AND FLNB [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
HgeneRPP14

GO:0001682

tRNA 5'-leader removal

16723659


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
TCGARVSTADTCGA-VQ-A8PH-01ARPP14chr3

58296318

+FLNBchr3

58154167

+
* 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-shiftENST00000445193ENST00000490882RPP14chr3

58296318

+FLNBchr3

58154167

+
Frame-shiftENST00000445193ENST00000429972RPP14chr3

58296318

+FLNBchr3

58154167

+
Frame-shiftENST00000445193ENST00000295956RPP14chr3

58296318

+FLNBchr3

58154167

+
Frame-shiftENST00000445193ENST00000358537RPP14chr3

58296318

+FLNBchr3

58154167

+
5CDS-3UTRENST00000445193ENST00000357272RPP14chr3

58296318

+FLNBchr3

58154167

+
5CDS-3UTRENST00000445193ENST00000348383RPP14chr3

58296318

+FLNBchr3

58154167

+
5CDS-3UTRENST00000445193ENST00000493452RPP14chr3

58296318

+FLNBchr3

58154167

+
5CDS-3UTRENST00000445193ENST00000419752RPP14chr3

58296318

+FLNBchr3

58154167

+
5CDS-3UTRENST00000445193ENST00000484981RPP14chr3

58296318

+FLNBchr3

58154167

+
3UTR-3CDSENST00000477305ENST00000490882RPP14chr3

58296318

+FLNBchr3

58154167

+
3UTR-3CDSENST00000477305ENST00000429972RPP14chr3

58296318

+FLNBchr3

58154167

+
3UTR-3CDSENST00000477305ENST00000295956RPP14chr3

58296318

+FLNBchr3

58154167

+
3UTR-3CDSENST00000477305ENST00000358537RPP14chr3

58296318

+FLNBchr3

58154167

+
3UTR-3UTRENST00000477305ENST00000357272RPP14chr3

58296318

+FLNBchr3

58154167

+
3UTR-3UTRENST00000477305ENST00000348383RPP14chr3

58296318

+FLNBchr3

58154167

+
3UTR-3UTRENST00000477305ENST00000493452RPP14chr3

58296318

+FLNBchr3

58154167

+
3UTR-3UTRENST00000477305ENST00000419752RPP14chr3

58296318

+FLNBchr3

58154167

+
3UTR-3UTRENST00000477305ENST00000484981RPP14chr3

58296318

+FLNBchr3

58154167

+
Frame-shiftENST00000295959ENST00000490882RPP14chr3

58296318

+FLNBchr3

58154167

+
Frame-shiftENST00000295959ENST00000429972RPP14chr3

58296318

+FLNBchr3

58154167

+
Frame-shiftENST00000295959ENST00000295956RPP14chr3

58296318

+FLNBchr3

58154167

+
Frame-shiftENST00000295959ENST00000358537RPP14chr3

58296318

+FLNBchr3

58154167

+
5CDS-3UTRENST00000295959ENST00000357272RPP14chr3

58296318

+FLNBchr3

58154167

+
5CDS-3UTRENST00000295959ENST00000348383RPP14chr3

58296318

+FLNBchr3

58154167

+
5CDS-3UTRENST00000295959ENST00000493452RPP14chr3

58296318

+FLNBchr3

58154167

+
5CDS-3UTRENST00000295959ENST00000419752RPP14chr3

58296318

+FLNBchr3

58154167

+
5CDS-3UTRENST00000295959ENST00000484981RPP14chr3

58296318

+FLNBchr3

58154167

+
Frame-shiftENST00000466547ENST00000490882RPP14chr3

58296318

+FLNBchr3

58154167

+
Frame-shiftENST00000466547ENST00000429972RPP14chr3

58296318

+FLNBchr3

58154167

+
Frame-shiftENST00000466547ENST00000295956RPP14chr3

58296318

+FLNBchr3

58154167

+
Frame-shiftENST00000466547ENST00000358537RPP14chr3

58296318

+FLNBchr3

58154167

+
5CDS-3UTRENST00000466547ENST00000357272RPP14chr3

58296318

+FLNBchr3

58154167

+
5CDS-3UTRENST00000466547ENST00000348383RPP14chr3

58296318

+FLNBchr3

58154167

+
5CDS-3UTRENST00000466547ENST00000493452RPP14chr3

58296318

+FLNBchr3

58154167

+
5CDS-3UTRENST00000466547ENST00000419752RPP14chr3

58296318

+FLNBchr3

58154167

+
5CDS-3UTRENST00000466547ENST00000484981RPP14chr3

58296318

+FLNBchr3

58154167

+
intron-3CDSENST00000528153ENST00000490882RPP14chr3

58296318

+FLNBchr3

58154167

+
intron-3CDSENST00000528153ENST00000429972RPP14chr3

58296318

+FLNBchr3

58154167

+
intron-3CDSENST00000528153ENST00000295956RPP14chr3

58296318

+FLNBchr3

58154167

+
intron-3CDSENST00000528153ENST00000358537RPP14chr3

58296318

+FLNBchr3

58154167

+
intron-3UTRENST00000528153ENST00000357272RPP14chr3

58296318

+FLNBchr3

58154167

+
intron-3UTRENST00000528153ENST00000348383RPP14chr3

58296318

+FLNBchr3

58154167

+
intron-3UTRENST00000528153ENST00000493452RPP14chr3

58296318

+FLNBchr3

58154167

+
intron-3UTRENST00000528153ENST00000419752RPP14chr3

58296318

+FLNBchr3

58154167

+
intron-3UTRENST00000528153ENST00000484981RPP14chr3

58296318

+FLNBchr3

58154167

+

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FusionProtFeatures for RPP14_FLNB


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
RPP14

O95059

FLNB

O75369

Part of ribonuclease P, a protein complex that generatesmature tRNA molecules by cleaving their 5'-ends.

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 RPP14_FLNB


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 RPP14_FLNB


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
RPP14POP5, RPP30, RPP40, IGSF21, DOCK7, A2M, MSH2, WIZ, KMT2B, PSME1, ATP5B, CAPZB, PKM, NOVA1, ELAVL1, POP4, RPP25, C3orf17, C18orf21, RPP21FLNBNPHP1, PSEN1, PSEN2, FLNA, ITGB1, ITGB3, ITGB6, FBLIM1, TSHR, GP1BA, OTUD1, G3BP1, PLEKHO1, RAD21, SIRT7, ISG15, ASB2, RAC1, MAP3K1, MAPK8, CDK2, HNRNPA0, VCP, ZC3H4, NUP210, HNRNPM, CSTB, SEPT9, ESR1, MDC1, FMNL1, VCAM1, FN1, SMURF2, MLH1, ITGA4, NPM1, DCTN2, DCTN3, TXNL1, UBR4, FLNC, LEO1, MAD1L1, PSMD12, PSMD3, SQSTM1, TRIM55, CUL7, OBSL1, CCDC8, SUZ12, RNF2, SIRT6, ABCE1, HSPB1, AP1G1, BASP1, EIF4EBP1, AHNAK, AP1B1, ARFIP1, DCPS, MAP4, NUP50, SEPT6, TARDBP, GGA1, NMD3, RSU1, SEC13, TLDC1, UFD1L, VBP1, MAP2K4, PTEN, MED4, CAPZA2, DBN1, MYH9, PPP1CB, RALA, IQGAP1, SYNPO, ITGB3BP, LIMA1, ANLN, MYO19, MYO18A, MCM2, MCM5, CDC73, TSC22D2, CDH1, HSPB7, ARRB2, TRIM25, BRCA1, TES


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 RPP14_FLNB


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 RPP14_FLNB


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneFLNBC0175778Larsen syndrome2UNIPROT
TgeneFLNBC0036341Schizophrenia1PSYGENET
TgeneFLNBC0265283Atelosteogenesis, type 11CTD_human;ORPHANET;UNIPROT
TgeneFLNBC0432201Boomerang dysplasia1CTD_human;ORPHANET;UNIPROT
TgeneFLNBC1848934SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME1CTD_human;ORPHANET
TgeneFLNBC2931648Larsen syndrome, dominant type1CTD_human;ORPHANET
TgeneFLNBC3668942Atelosteogenesis Type 31CTD_human;ORPHANET;UNIPROT