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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: 28848

FusionGeneSummary for PROSER1_TCOF1

check button Fusion gene summary
Fusion gene informationFusion gene name: PROSER1_TCOF1
Fusion gene ID: 28848
HgeneTgene
Gene symbol

PROSER1

TCOF1

Gene ID

80209

6949

Gene nameproline and serine rich 1treacle ribosome biogenesis factor 1
SynonymsC13orf23MFD1|TCS|TCS1|treacle
Cytomap

13q13.3

5q32-q33.1

Type of geneprotein-codingprotein-coding
Descriptionproline and serine-rich protein 1treacle proteinTreacher Collins syndrome proteinTreacher Collins-Franceschetti syndrome 1nucleolar trafficking phosphoprotein
Modification date2018051920180522
UniProtAcc

Q86XN7

Q13428

Ensembl transtripts involved in fusion geneENST00000352251, ENST00000350125, 
ENST00000484434, 
ENST00000451292, 
ENST00000377797, ENST00000445265, 
ENST00000323668, ENST00000439160, 
ENST00000394269, ENST00000504761, 
ENST00000513346, ENST00000506063, 
Fusion gene scores* DoF score3 X 3 X 2=189 X 8 X 8=576
# samples 310
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(10/576*10)=-2.52606881166759
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PROSER1 [Title/Abstract] AND TCOF1 [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
ChiTaRS3.1BF799173PROSER1chr13

39587108

+TCOF1chr5

149756048

+
* 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-3CDSENST00000352251ENST00000451292PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000352251ENST00000377797PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000352251ENST00000445265PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000352251ENST00000323668PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000352251ENST00000439160PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000352251ENST00000394269PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000352251ENST00000504761PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000352251ENST00000513346PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-intronENST00000352251ENST00000506063PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000350125ENST00000451292PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000350125ENST00000377797PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000350125ENST00000445265PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000350125ENST00000323668PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000350125ENST00000439160PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000350125ENST00000394269PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000350125ENST00000504761PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000350125ENST00000513346PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-intronENST00000350125ENST00000506063PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000484434ENST00000451292PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000484434ENST00000377797PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000484434ENST00000445265PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000484434ENST00000323668PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000484434ENST00000439160PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000484434ENST00000394269PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000484434ENST00000504761PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-3CDSENST00000484434ENST00000513346PROSER1chr13

39587108

+TCOF1chr5

149756048

+
intron-intronENST00000484434ENST00000506063PROSER1chr13

39587108

+TCOF1chr5

149756048

+

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FusionProtFeatures for PROSER1_TCOF1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
PROSER1

Q86XN7

TCOF1

Q13428

Nucleolar protein that acts as a regulator of RNApolymerase I by connecting RNA polymerase I with enzymesresponsible for ribosomal processing and modification(PubMed:12777385, PubMed:26399832). Required for neural crestspecification: following monoubiquitination by the BCR(KBTBD8)complex, associates with NOLC1 and acts as a platform to connectRNA polymerase I with enzymes responsible for ribosomal processingand modification, leading to remodel the translational program ofdifferentiating cells in favor of neural crest specification(PubMed:26399832). {ECO:0000269|PubMed:12777385,ECO:0000269|PubMed:26399832}.

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 PROSER1_TCOF1


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 PROSER1_TCOF1


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 PROSER1_TCOF1


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 PROSER1_TCOF1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneTCOF1C0242387Mandibulofacial Dysostosis2CTD_human;ORPHANET;UNIPROT
TgeneTCOF1C0376634Craniofacial Abnormalities1CTD_human