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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:TMCC1-DDX5 (FusionGDB2 ID:90731)

Fusion Gene Summary for TMCC1-DDX5

check button Fusion gene summary
Fusion gene informationFusion gene name: TMCC1-DDX5
Fusion gene ID: 90731
HgeneTgene
Gene symbol

TMCC1

DDX5

Gene ID

23023

1655

Gene nametransmembrane and coiled-coil domain family 1DEAD-box helicase 5
Synonyms-G17P1|HLR1|HUMP68|p68
Cytomap

3q22.1

17q23.3

Type of geneprotein-codingprotein-coding
Descriptiontransmembrane and coiled-coil domains protein 1probable ATP-dependent RNA helicase DDX5ATP-dependent RNA helicase DDX5DEAD (Asp-Glu-Ala-Asp) box helicase 5DEAD (Asp-Glu-Ala-Asp) box polypeptide 5DEAD box protein 5DEAD box-5DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 5 (RNA helicase, 68kD)RNA h
Modification date2020031320200313
UniProtAcc.

Q5T1V6

Ensembl transtripts involved in fusion geneENST00000432054, ENST00000393238, 
ENST00000426664, ENST00000329333, 
ENST00000515024, 
ENST00000225792, 
ENST00000450599, ENST00000578804, 
ENST00000580026, 
Fusion gene scores* DoF score15 X 14 X 5=105020 X 12 X 8=1920
# samples 1719
** MAII scorelog2(17/1050*10)=-2.62678267641578
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(19/1920*10)=-3.33703498727757
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: TMCC1 [Title/Abstract] AND DDX5 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointTMCC1(129392259)-DDX5(62500180), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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
HgeneTMCC1

GO:0016197

endosomal transport

30220460

HgeneTMCC1

GO:0090148

membrane fission

30220460

HgeneTMCC1

GO:0097750

endosome membrane tubulation

30220460

TgeneDDX5

GO:0000122

negative regulation of transcription by RNA polymerase II

15298701

TgeneDDX5

GO:0000381

regulation of alternative mRNA splicing, via spliceosome

21343338

TgeneDDX5

GO:0000956

nuclear-transcribed mRNA catabolic process

23788676


check buttonFusion gene breakpoints across TMCC1 (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 DDX5 (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/ABG955538TMCC1chr3

129392259

+DDX5chr17

62500180

-


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Fusion Gene ORF analysis for TMCC1-DDX5

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-3CDSENST00000432054ENST00000225792TMCC1chr3

129392259

+DDX5chr17

62500180

-
intron-intronENST00000432054ENST00000450599TMCC1chr3

129392259

+DDX5chr17

62500180

-
intron-intronENST00000432054ENST00000578804TMCC1chr3

129392259

+DDX5chr17

62500180

-
intron-intronENST00000432054ENST00000580026TMCC1chr3

129392259

+DDX5chr17

62500180

-
intron-3CDSENST00000393238ENST00000225792TMCC1chr3

129392259

+DDX5chr17

62500180

-
intron-intronENST00000393238ENST00000450599TMCC1chr3

129392259

+DDX5chr17

62500180

-
intron-intronENST00000393238ENST00000578804TMCC1chr3

129392259

+DDX5chr17

62500180

-
intron-intronENST00000393238ENST00000580026TMCC1chr3

129392259

+DDX5chr17

62500180

-
intron-3CDSENST00000426664ENST00000225792TMCC1chr3

129392259

+DDX5chr17

62500180

-
intron-intronENST00000426664ENST00000450599TMCC1chr3

129392259

+DDX5chr17

62500180

-
intron-intronENST00000426664ENST00000578804TMCC1chr3

129392259

+DDX5chr17

62500180

-
intron-intronENST00000426664ENST00000580026TMCC1chr3

129392259

+DDX5chr17

62500180

-
intron-3CDSENST00000329333ENST00000225792TMCC1chr3

129392259

+DDX5chr17

62500180

-
intron-intronENST00000329333ENST00000450599TMCC1chr3

129392259

+DDX5chr17

62500180

-
intron-intronENST00000329333ENST00000578804TMCC1chr3

129392259

+DDX5chr17

62500180

-
intron-intronENST00000329333ENST00000580026TMCC1chr3

129392259

+DDX5chr17

62500180

-
intron-3CDSENST00000515024ENST00000225792TMCC1chr3

129392259

+DDX5chr17

62500180

-
intron-intronENST00000515024ENST00000450599TMCC1chr3

129392259

+DDX5chr17

62500180

-
intron-intronENST00000515024ENST00000578804TMCC1chr3

129392259

+DDX5chr17

62500180

-
intron-intronENST00000515024ENST00000580026TMCC1chr3

129392259

+DDX5chr17

62500180

-

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 TMCC1-DDX5


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 TMCC1-DDX5


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
.DDX5

Q5T1V6

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.

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 TMCC1-DDX5


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 TMCC1-DDX5


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 TMCC1-DDX5


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

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Related Diseases for TMCC1-DDX5


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneDDX5C0014175Endometriosis1CTD_human
TgeneDDX5C0269102Endometrioma1CTD_human