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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:TRIM32-DDX21

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: TRIM32-DDX21
FusionPDB ID: 94068
FusionGDB2.0 ID: 94068
HgeneTgene
Gene symbol

TRIM32

DDX21

Gene ID

22954

54606

Gene nametripartite motif containing 32DEAD-box helicase 56
SynonymsBBS11|HT2A|LGMD2H|LGMDR8|TATIPDDX21|DDX26|NOH61
Cytomap

9q33.1

7p13

Type of geneprotein-codingprotein-coding
DescriptionE3 ubiquitin-protein ligase TRIM3272 kDa Tat-interacting proteinRING-type E3 ubiquitin transferase TRIM32TAT-interactive protein, 72-KDtripartite motif-containing protein 32zinc-finger protein HT2Aprobable ATP-dependent RNA helicase DDX5661-kd nucleolar helicaseATP-dependent 61 kDa nucleolar RNA helicaseDEAD (Asp-Glu-Ala-Asp) box helicase 56DEAD (Asp-Glu-Ala-Asp) box polypeptide 56DEAD box protein 21DEAD box protein 56DEAD-box RNA helicasen
Modification date2020032720200313
UniProtAcc.

Q9NR30

Ensembl transtripts involved in fusion geneENST idsENST00000450136, ENST00000373983, 
ENST00000354185, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score2 X 2 X 2=836 X 11 X 14=5544
# samples 337
** MAII scorelog2(3/8*10)=1.90689059560852log2(37/5544*10)=-3.9053300816209
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: TRIM32 [Title/Abstract] AND DDX21 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)TRIM32(119461323)-DDX21(70738619), # samples:1
Anticipated loss of major functional domain due to fusion event.TRIM32-DDX21 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
TRIM32-DDX21 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
TRIM32-DDX21 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
TRIM32-DDX21 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
TRIM32-DDX21 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
TRIM32-DDX21 seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF.
TRIM32-DDX21 seems lost the major protein functional domain in Tgene partner, which is a essential gene 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
HgeneTRIM32

GO:0000209

protein polyubiquitination

18632609

HgeneTRIM32

GO:0016567

protein ubiquitination

16816390

HgeneTRIM32

GO:0030307

positive regulation of cell growth

18632609

HgeneTRIM32

GO:0030335

positive regulation of cell migration

18632609

HgeneTRIM32

GO:0032897

negative regulation of viral transcription

18248090

HgeneTRIM32

GO:0043123

positive regulation of I-kappaB kinase/NF-kappaB signaling

23077300

HgeneTRIM32

GO:0045087

innate immune response

18248090

HgeneTRIM32

GO:0045787

positive regulation of cell cycle

18632609

HgeneTRIM32

GO:0045862

positive regulation of proteolysis

18632609

HgeneTRIM32

GO:0051091

positive regulation of DNA-binding transcription factor activity

23077300

HgeneTRIM32

GO:0051092

positive regulation of NF-kappaB transcription factor activity

23077300

HgeneTRIM32

GO:1902187

negative regulation of viral release from host cell

18248090

HgeneTRIM32

GO:1902230

negative regulation of intrinsic apoptotic signaling pathway in response to DNA damage

18632609


check buttonFusion gene breakpoints across TRIM32 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across DDX21 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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/ACN278368TRIM32chr9

119461323

+DDX21chr10

70738619

+


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000373983TRIM32chr9119461323+ENST00000354185DDX21chr1070738619+4997230855711218

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
ENST00000373983ENST00000354185TRIM32chr9119461323+DDX21chr1070738619+0.0019081440.9980919

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>94068_94068_1_TRIM32-DDX21_TRIM32_chr9_119461323_ENST00000373983_DDX21_chr10_70738619_ENST00000354185_length(amino acids)=218AA_BP=
MNCQGLIGVTDSYDNSLKVYTLDGHCVACHRSQLSKPWGITALPSGQFVVTDVEGGKLWCFTVDRGSGVVKYSCLCSAVRPKFVTCDAEG
TVYFTQGLGLNLENRQNEHHLEGGFSIGSVGPDGQLGRQISHFFSENEDFRCIAGMCVDARGDLIVADSSRKEILHFPKGGGYSVLIREG

--------------------------------------------------------------

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Fusion Protein Functional Features


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr9:119461323/chr10:70738619)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.DDX21

Q9NR30

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: RNA helicase that acts as a sensor of the transcriptional status of both RNA polymerase (Pol) I and II: promotes ribosomal RNA (rRNA) processing and transcription from polymerase II (Pol II) (PubMed:25470060, PubMed:28790157). Binds various RNAs, such as rRNAs, snoRNAs, 7SK and, at lower extent, mRNAs (PubMed:25470060). In the nucleolus, localizes to rDNA locus, where it directly binds rRNAs and snoRNAs, and promotes rRNA transcription, processing and modification. Required for rRNA 2'-O-methylation, possibly by promoting the recruitment of late-acting snoRNAs SNORD56 and SNORD58 with pre-ribosomal complexes (PubMed:25470060, PubMed:25477391). In the nucleoplasm, binds 7SK RNA and is recruited to the promoters of Pol II-transcribed genes: acts by facilitating the release of P-TEFb from inhibitory 7SK snRNP in a manner that is dependent on its helicase activity, thereby promoting transcription of its target genes (PubMed:25470060). Functions as cofactor for JUN-activated transcription: required for phosphorylation of JUN at 'Ser-77' (PubMed:11823437, PubMed:25260534). Can unwind double-stranded RNA (helicase) and can fold or introduce a secondary structure to a single-stranded RNA (foldase) (PubMed:9461305). Together with SIRT7, required to prevent R-loop-associated DNA damage and transcription-associated genomic instability: deacetylation by SIRT7 activates the helicase activity, thereby overcoming R-loop-mediated stalling of RNA polymerases (PubMed:28790157). Involved in rRNA processing (PubMed:14559904, PubMed:18180292). May bind to specific miRNA hairpins (PubMed:28431233). Component of a multi-helicase-TICAM1 complex that acts as a cytoplasmic sensor of viral double-stranded RNA (dsRNA) and plays a role in the activation of a cascade of antiviral responses including the induction of proinflammatory cytokines via the adapter molecule TICAM1 (By similarity). {ECO:0000250|UniProtKB:Q9JIK5, ECO:0000269|PubMed:11823437, ECO:0000269|PubMed:14559904, ECO:0000269|PubMed:18180292, ECO:0000269|PubMed:25260534, ECO:0000269|PubMed:25470060, ECO:0000269|PubMed:25477391, ECO:0000269|PubMed:28431233, ECO:0000269|PubMed:28790157, ECO:0000269|PubMed:9461305}.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneDDX21chr9:119461323chr10:70738619ENST00000354185015217_3960784.0DomainHelicase ATP-binding
TgeneDDX21chr9:119461323chr10:70738619ENST00000354185015429_5730784.0DomainHelicase C-terminal
TgeneDDX21chr9:119461323chr10:70738619ENST00000354185015186_2140784.0MotifQ motif
TgeneDDX21chr9:119461323chr10:70738619ENST00000354185015339_3420784.0MotifDEAD box
TgeneDDX21chr9:119461323chr10:70738619ENST00000354185015230_2370784.0Nucleotide bindingATP
TgeneDDX21chr9:119461323chr10:70738619ENST00000354185015724_7480784.0RegionNote=3 X 5 AA repeats
TgeneDDX21chr9:119461323chr10:70738619ENST00000354185015724_7280784.0RepeatNote=1
TgeneDDX21chr9:119461323chr10:70738619ENST00000354185015734_7380784.0RepeatNote=2
TgeneDDX21chr9:119461323chr10:70738619ENST00000354185015744_7480784.0RepeatNote=3

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneTRIM32chr9:119461323chr10:70738619ENST00000373983+12138_1970654.0Coiled coilOntology_term=ECO:0000255
HgeneTRIM32chr9:119461323chr10:70738619ENST00000450136+12138_1970654.0Coiled coilOntology_term=ECO:0000255
HgeneTRIM32chr9:119461323chr10:70738619ENST00000373983+122_60654.0Compositional biasNote=Poly-Ala
HgeneTRIM32chr9:119461323chr10:70738619ENST00000450136+122_60654.0Compositional biasNote=Poly-Ala
HgeneTRIM32chr9:119461323chr10:70738619ENST00000373983+12358_4010654.0RepeatNote=NHL 1
HgeneTRIM32chr9:119461323chr10:70738619ENST00000373983+12415_4580654.0RepeatNote=NHL 2
HgeneTRIM32chr9:119461323chr10:70738619ENST00000373983+12459_4990654.0RepeatNote=NHL 3
HgeneTRIM32chr9:119461323chr10:70738619ENST00000373983+12562_6050654.0RepeatNote=NHL 4
HgeneTRIM32chr9:119461323chr10:70738619ENST00000373983+12606_6460654.0RepeatNote=NHL 5
HgeneTRIM32chr9:119461323chr10:70738619ENST00000450136+12358_4010654.0RepeatNote=NHL 1
HgeneTRIM32chr9:119461323chr10:70738619ENST00000450136+12415_4580654.0RepeatNote=NHL 2
HgeneTRIM32chr9:119461323chr10:70738619ENST00000450136+12459_4990654.0RepeatNote=NHL 3
HgeneTRIM32chr9:119461323chr10:70738619ENST00000450136+12562_6050654.0RepeatNote=NHL 4
HgeneTRIM32chr9:119461323chr10:70738619ENST00000450136+12606_6460654.0RepeatNote=NHL 5
HgeneTRIM32chr9:119461323chr10:70738619ENST00000373983+12103_1330654.0Zinc fingerB box-type
HgeneTRIM32chr9:119461323chr10:70738619ENST00000373983+1220_650654.0Zinc fingerRING-type
HgeneTRIM32chr9:119461323chr10:70738619ENST00000450136+12103_1330654.0Zinc fingerB box-type
HgeneTRIM32chr9:119461323chr10:70738619ENST00000450136+1220_650654.0Zinc fingerRING-type


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
TRIM32
DDX21


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to TRIM32-DDX21


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to TRIM32-DDX21


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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