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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: 12871

FusionGeneSummary for FAM83F_FST

check button Fusion gene summary
Fusion gene informationFusion gene name: FAM83F_FST
Fusion gene ID: 12871
HgeneTgene
Gene symbol

FAM83F

FST

Gene ID

113828

10468

Gene namefamily with sequence similarity 83 member Ffollistatin
Synonyms-FS
Cytomap

22q13.1

5q11.2

Type of geneprotein-codingprotein-coding
Descriptionprotein FAM83Ffollistatinactivin-binding proteinfollistatin isoform FST317
Modification date2018051920180519
UniProtAcc

Q8NEG4

P19883

Ensembl transtripts involved in fusion geneENST00000333407, ENST00000488874, 
ENST00000473717, 
ENST00000256759, 
ENST00000396947, 
Fusion gene scores* DoF score2 X 2 X 2=83 X 3 X 2=18
# samples 23
** MAII scorelog2(2/8*10)=1.32192809488736log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: FAM83F [Title/Abstract] AND FST [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
TgeneFST

GO:0000122

negative regulation of transcription by RNA polymerase II

12702211

TgeneFST

GO:0002244

hematopoietic progenitor cell differentiation

15451575

TgeneFST

GO:0032926

negative regulation of activin receptor signaling pathway

11948405|12697670

TgeneFST

GO:0051798

positive regulation of hair follicle development

12514121


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
TCGALDLUSCTCGA-51-4081-01AFAM83Fchr22

40422050

+FSTchr5

52782785

+
* 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
intron-3UTRENST00000333407ENST00000256759FAM83Fchr22

40422050

+FSTchr5

52782785

+
intron-3UTRENST00000333407ENST00000396947FAM83Fchr22

40422050

+FSTchr5

52782785

+
intron-3UTRENST00000488874ENST00000256759FAM83Fchr22

40422050

+FSTchr5

52782785

+
intron-3UTRENST00000488874ENST00000396947FAM83Fchr22

40422050

+FSTchr5

52782785

+
intron-3UTRENST00000473717ENST00000256759FAM83Fchr22

40422050

+FSTchr5

52782785

+
intron-3UTRENST00000473717ENST00000396947FAM83Fchr22

40422050

+FSTchr5

52782785

+

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FusionProtFeatures for FAM83F_FST


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FAM83F

Q8NEG4

FST

P19883

Binds directly to activin and functions as an activinantagonist. Specific inhibitor of the biosynthesis and secretionof pituitary follicle stimulating hormone (FSH).

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 FAM83F_FST


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 FAM83F_FST


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
FAM83FMME, ELAVL1FSTTXN, INHBE, MEST, TK1, C8orf33, INHBA, BMPR1A, BMPR2


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 FAM83F_FST


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 FAM83F_FST


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneFSTC2239176Liver carcinoma2CTD_human
TgeneFSTC0000786Spontaneous abortion1CTD_human
TgeneFSTC0023903Liver neoplasms1CTD_human
TgeneFSTC0038356Stomach Neoplasms1CTD_human
TgeneFSTC0162557Liver Failure, Acute1CTD_human
TgeneFSTC1458155Mammary Neoplasms1CTD_human