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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:DEK-NR1D2

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: DEK-NR1D2
FusionPDB ID: 22179
FusionGDB2.0 ID: 22179
HgeneTgene
Gene symbol

DEK

NR1D2

Gene ID

7913

9975

Gene nameDEK proto-oncogenenuclear receptor subfamily 1 group D member 2
SynonymsD6S231EBD73|EAR-1R|REVERBB|REVERBbeta|RVR
Cytomap

6p22.3

3p24.2

Type of geneprotein-codingprotein-coding
Descriptionprotein DEKDEK oncogene (DNA binding)nuclear receptor subfamily 1 group D member 2V-erbA-related protein 1-relatednuclear receptor Rev-ErbA beta variant 1nuclear receptor Rev-ErbA beta variant 2orphan nuclear hormone receptor BD73rev-erb alpha-related receptorrev-erb-betarev-erba-alph
Modification date2020031320200313
UniProtAcc

P35659

Q14995

Ensembl transtripts involved in fusion geneENST idsENST00000244776, ENST00000397239, 
ENST00000492552, ENST00000312521, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score11 X 13 X 6=8584 X 4 X 4=64
# samples 154
** MAII scorelog2(15/858*10)=-2.51601514700366
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/64*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: DEK [Title/Abstract] AND NR1D2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)DEK(18236682)-NR1D2(24018713), # samples:1
Anticipated loss of major functional domain due to fusion event.DEK-NR1D2 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.
DEK-NR1D2 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.
DEK-NR1D2 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.
DEK-NR1D2 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.
* 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
TgeneNR1D2

GO:0045892

negative regulation of transcription, DNA-templated

17892483|17996965


check buttonFusion gene breakpoints across DEK (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 NR1D2 (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
ChimerDB4Non-Cancer265NDEKchr6

18236682

-NR1D2chr3

24018713

+


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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)
ENST00000397239DEKchr618236682-ENST00000312521NR1D2chr324018713+489114954481509353
ENST00000244776DEKchr618236682-ENST00000312521NR1D2chr324018713+450711111661125319

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
ENST00000397239ENST00000312521DEKchr618236682-NR1D2chr324018713+0.0001682010.9998318
ENST00000244776ENST00000312521DEKchr618236682-NR1D2chr324018713+0.0001044430.9998956

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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

>22179_22179_1_DEK-NR1D2_DEK_chr6_18236682_ENST00000244776_NR1D2_chr3_24018713_ENST00000312521_length(amino acids)=319AA_BP=
MSASAPAAEGEGTPTQPASEKEPEMPGPREESEEEEDEDDEEEEEEEKGKGQKLCEIERIHFFLSKKKTDELRNLHKLLYNRPGTVSSLK
KNVGQFSGFPFEKGSVQYKKKEEMLKKFRNAMLKSICEVLDLERSGVNSELVKRILNFLMHPKPSGKPLPKSKKTCSKGSKKERNSSGMA
RKAKRTKCPEILSDESSSDEDEKKNKEESSDDEDKESEEEPPKKTAKREKPKQKATSKSKKSVKSANVKKADSSTTKKNQNSSKKESESE

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

>22179_22179_2_DEK-NR1D2_DEK_chr6_18236682_ENST00000397239_NR1D2_chr3_24018713_ENST00000312521_length(amino acids)=353AA_BP=
MSASAPAAEGEGTPTQPASEKEPEMPGPREESEEEEDEDDEEEEEEEKEKSLIVEGKREKKKVERLTMQVSSLQREPFTIAQGKGQKLCE
IERIHFFLSKKKTDELRNLHKLLYNRPGTVSSLKKNVGQFSGFPFEKGSVQYKKKEEMLKKFRNAMLKSICEVLDLERSGVNSELVKRIL
NFLMHPKPSGKPLPKSKKTCSKGSKKERNSSGMARKAKRTKCPEILSDESSSDEDEKKNKEESSDDEDKESEEEPPKKTAKREKPKQKAT

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

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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/chr6:18236682/chr3:24018713)
- 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
DEK

P35659

NR1D2

Q14995

FUNCTION: Involved in chromatin organization. {ECO:0000269|PubMed:17524367}.FUNCTION: Transcriptional repressor which coordinates circadian rhythm and metabolic pathways in a heme-dependent manner. Integral component of the complex transcription machinery that governs circadian rhythmicity and forms a critical negative limb of the circadian clock by directly repressing the expression of core clock components ARNTL/BMAL1 and CLOCK. Also regulates genes involved in metabolic functions, including lipid metabolism and the inflammatory response. Acts as a receptor for heme which stimulates its interaction with the NCOR1/HDAC3 corepressor complex, enhancing transcriptional repression. Recognizes two classes of DNA response elements within the promoter of its target genes and can bind to DNA as either monomers or homodimers, depending on the nature of the response element. Binds as a monomer to a response element composed of the consensus half-site motif 5'-[A/G]GGTCA-3' preceded by an A/T-rich 5' sequence (RevRE), or as a homodimer to a direct repeat of the core motif spaced by two nuclegotides (RevDR-2). Acts as a potent competitive repressor of ROR alpha (RORA) function and also negatively regulates the expression of NR1D1. Regulates lipid and energy homeostasis in the skeletal muscle via repression of genes involved in lipid metabolism and myogenesis including: CD36, FABP3, FABP4, UCP3, SCD1 and MSTN. Regulates hepatic lipid metabolism via the repression of APOC3. Represses gene expression at a distance in macrophages by inhibiting the transcription of enhancer-derived RNAs (eRNAs). In addition to its activity as a repressor, can also act as a transcriptional activator. Acts as a transcriptional activator of the sterol regulatory element-binding protein 1 (SREBF1) and the inflammatory mediator interleukin-6 (IL6) in the skeletal muscle (By similarity). Plays a role in the regulation of circadian sleep/wake cycle; essential for maintaining wakefulness during the dark phase or active period (By similarity). Key regulator of skeletal muscle mitochondrial function; negatively regulates the skeletal muscle expression of core clock genes and genes involved in mitochondrial biogenesis, fatty acid beta-oxidation and lipid metabolism (By similarity). May play a role in the circadian control of neutrophilic inflammation in the lung (By similarity). {ECO:0000250|UniProtKB:Q60674, ECO:0000269|PubMed:17892483, ECO:0000269|PubMed:17996965}.

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
HgeneDEKchr6:18236682chr3:24018713ENST00000244776-810228_236315.0342.0Compositional biasNote=Asp/Glu-rich (acidic)
HgeneDEKchr6:18236682chr3:24018713ENST00000244776-810241_254315.0342.0Compositional biasNote=Asp/Glu-rich (acidic)
HgeneDEKchr6:18236682chr3:24018713ENST00000244776-810300_310315.0342.0Compositional biasNote=Asp/Glu-rich (acidic)
HgeneDEKchr6:18236682chr3:24018713ENST00000244776-81030_49315.0342.0Compositional biasNote=Asp/Glu-rich (highly acidic)
HgeneDEKchr6:18236682chr3:24018713ENST00000397239-911228_236349.0376.0Compositional biasNote=Asp/Glu-rich (acidic)
HgeneDEKchr6:18236682chr3:24018713ENST00000397239-911241_254349.0376.0Compositional biasNote=Asp/Glu-rich (acidic)
HgeneDEKchr6:18236682chr3:24018713ENST00000397239-911300_310349.0376.0Compositional biasNote=Asp/Glu-rich (acidic)
HgeneDEKchr6:18236682chr3:24018713ENST00000397239-91130_49349.0376.0Compositional biasNote=Asp/Glu-rich (highly acidic)
HgeneDEKchr6:18236682chr3:24018713ENST00000397239-911337_351349.0376.0DNA binding.
HgeneDEKchr6:18236682chr3:24018713ENST00000244776-810149_183315.0342.0DomainNote=SAP
HgeneDEKchr6:18236682chr3:24018713ENST00000397239-911149_183349.0376.0DomainNote=SAP
HgeneDEKchr6:18236682chr3:24018713ENST00000244776-810205_221315.0342.0MotifNuclear localization signal
HgeneDEKchr6:18236682chr3:24018713ENST00000397239-911205_221349.0376.0MotifNuclear localization signal

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneDEKchr6:18236682chr3:24018713ENST00000244776-810337_351315.0342.0DNA binding.
HgeneDEKchr6:18236682chr3:24018713ENST00000244776-810367_371315.0342.0DNA binding.
HgeneDEKchr6:18236682chr3:24018713ENST00000397239-911367_371349.0376.0DNA binding.
TgeneNR1D2chr6:18236682chr3:24018713ENST000003125216813_20514.3333333333334580.0Compositional biasNote=Poly-Ser
TgeneNR1D2chr6:18236682chr3:24018713ENST000003125216835_39514.3333333333334580.0Compositional biasNote=Poly-Ser
TgeneNR1D2chr6:18236682chr3:24018713ENST0000031252168100_176514.3333333333334580.0DNA bindingNuclear receptor
TgeneNR1D2chr6:18236682chr3:24018713ENST0000031252168369_579514.3333333333334580.0DomainNR LBD
TgeneNR1D2chr6:18236682chr3:24018713ENST00000312521681_60514.3333333333334580.0RegionRequired for phosphorylation by CSNK1E and cytoplasmic localization
TgeneNR1D2chr6:18236682chr3:24018713ENST00000312521681_99514.3333333333334580.0RegionNote=Modulating
TgeneNR1D2chr6:18236682chr3:24018713ENST0000031252168103_123514.3333333333334580.0Zinc fingerNR C4-type
TgeneNR1D2chr6:18236682chr3:24018713ENST0000031252168140_164514.3333333333334580.0Zinc fingerNR C4-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
DEK
NR1D2


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
TgeneNR1D2chr6:18236682chr3:24018713ENST0000031252168397_579514.3333333333334580.0ZNHIT1


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Related Drugs to DEK-NR1D2


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 DEK-NR1D2


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