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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:TCOF1-DSP (FusionGDB2 ID:89233)

Fusion Gene Summary for TCOF1-DSP

check button Fusion gene summary
Fusion gene informationFusion gene name: TCOF1-DSP
Fusion gene ID: 89233
HgeneTgene
Gene symbol

TCOF1

DSP

Gene ID

6949

1834

Gene nametreacle ribosome biogenesis factor 1dentin sialophosphoprotein
SynonymsMFD1|TCS|TCS1|treacleDFNA39|DGI1|DMP3|DPP|DSP
Cytomap

5q32-q33.1

4q22.1

Type of geneprotein-codingprotein-coding
Descriptiontreacle proteinTreacher Collins syndrome proteinTreacher Collins-Franceschetti syndrome 1nucleolar trafficking phosphoproteindentin sialophosphoproteindeafness, autosomal dominant 39dentin phosphophoryndentin phosphoproteindentin phosphoryndentin sialoprotein
Modification date2020031320200313
UniProtAcc.

P15924

Ensembl transtripts involved in fusion geneENST00000451292, ENST00000377797, 
ENST00000445265, ENST00000323668, 
ENST00000439160, ENST00000394269, 
ENST00000504761, ENST00000513346, 
ENST00000506063, 
ENST00000379802, 
ENST00000418664, 
Fusion gene scores* DoF score20 X 12 X 3=72022 X 19 X 10=4180
# samples 2126
** MAII scorelog2(21/720*10)=-1.77760757866355
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(26/4180*10)=-4.00691941393979
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: TCOF1 [Title/Abstract] AND DSP [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointTCOF1(149776157)-DSP(7581583), # samples:1
Anticipated loss of major functional domain due to fusion event.TCOF1-DSP seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor due to the frame-shifted ORF.
* 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 buttonFusion gene breakpoints across TCOF1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across DSP (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS5.0N/ABE165642TCOF1chr5

149776157

+DSPchr6

7581583

+


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Fusion Gene ORF analysis for TCOF1-DSP

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-shiftENST00000451292ENST00000379802TCOF1chr5

149776157

+DSPchr6

7581583

+
5CDS-intronENST00000451292ENST00000418664TCOF1chr5

149776157

+DSPchr6

7581583

+
Frame-shiftENST00000377797ENST00000379802TCOF1chr5

149776157

+DSPchr6

7581583

+
5CDS-intronENST00000377797ENST00000418664TCOF1chr5

149776157

+DSPchr6

7581583

+
Frame-shiftENST00000445265ENST00000379802TCOF1chr5

149776157

+DSPchr6

7581583

+
5CDS-intronENST00000445265ENST00000418664TCOF1chr5

149776157

+DSPchr6

7581583

+
Frame-shiftENST00000323668ENST00000379802TCOF1chr5

149776157

+DSPchr6

7581583

+
5CDS-intronENST00000323668ENST00000418664TCOF1chr5

149776157

+DSPchr6

7581583

+
Frame-shiftENST00000439160ENST00000379802TCOF1chr5

149776157

+DSPchr6

7581583

+
5CDS-intronENST00000439160ENST00000418664TCOF1chr5

149776157

+DSPchr6

7581583

+
intron-3CDSENST00000394269ENST00000379802TCOF1chr5

149776157

+DSPchr6

7581583

+
intron-intronENST00000394269ENST00000418664TCOF1chr5

149776157

+DSPchr6

7581583

+
Frame-shiftENST00000504761ENST00000379802TCOF1chr5

149776157

+DSPchr6

7581583

+
5CDS-intronENST00000504761ENST00000418664TCOF1chr5

149776157

+DSPchr6

7581583

+
Frame-shiftENST00000513346ENST00000379802TCOF1chr5

149776157

+DSPchr6

7581583

+
5CDS-intronENST00000513346ENST00000418664TCOF1chr5

149776157

+DSPchr6

7581583

+
intron-3CDSENST00000506063ENST00000379802TCOF1chr5

149776157

+DSPchr6

7581583

+
intron-intronENST00000506063ENST00000418664TCOF1chr5

149776157

+DSPchr6

7581583

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for TCOF1-DSP


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for TCOF1-DSP


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

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

P15924

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Major high molecular weight protein of desmosomes. Involved in the organization of the desmosomal cadherin-plakoglobin complexes into discrete plasma membrane domains and in the anchoring of intermediate filaments to the desmosomes.

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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Fusion Gene Sequence for TCOF1-DSP


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for TCOF1-DSP


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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Related Drugs for TCOF1-DSP


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneDSPP15924DB01593ZincSmall moleculeApproved|Investigational
TgeneDSPP15924DB14487Zinc acetateSmall moleculeApproved|Investigational

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Related Diseases for TCOF1-DSP


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneTCOF1C0265241Franceschetti-Klein syndrome7CLINGEN
HgeneTCOF1C0242387Mandibulofacial Dysostosis5CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneTCOF1C0152423Congenital small ears1GENOMICS_ENGLAND
HgeneTCOF1C0376634Craniofacial Abnormalities1CTD_human
TgeneDSPC1843896Arrhythmogenic Right Ventricular Dysplasia, Familial, 88CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneDSPC1854063Cardiomyopathy dilated with Woolly hair and keratoderma7CTD_human;GENOMICS_ENGLAND;ORPHANET
TgeneDSPC1864826Epidermolysis bullosa, lethal acantholytic7CTD_human;GENOMICS_ENGLAND;ORPHANET
TgeneDSPC1843292Skin Fragility-Woolly Hair Syndrome6CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneDSPC4014393CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS6CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneDSPC1852127KERATOSIS PALMOPLANTARIS STRIATA II5CTD_human;GENOMICS_ENGLAND
TgeneDSPC0024117Chronic Obstructive Airway Disease1CTD_human
TgeneDSPC0034069Pulmonary Fibrosis1CTD_human
TgeneDSPC0085298Sudden Cardiac Death1CTD_human
TgeneDSPC0085786Hamman-Rich syndrome1ORPHANET
TgeneDSPC1527303Chronic Airflow Obstruction1CTD_human
TgeneDSPC1720824Sudden Cardiac Arrest1CTD_human
TgeneDSPC1800706Idiopathic Pulmonary Fibrosis1CTD_human;ORPHANET
TgeneDSPC3809719Severe dermatitis, multiple allergies, metabolic wasting syndrome1ORPHANET
TgeneDSPC4707237Striate palmoplantar keratoderma1ORPHANET
TgeneDSPC4721507Alveolitis, Fibrosing1CTD_human
TgeneDSPC4721508Hamman-Rich Disease1CTD_human
TgeneDSPC4721509Usual Interstitial Pneumonia1CTD_human
TgeneDSPC4721952Familial Idiopathic Pulmonary Fibrosis1CTD_human