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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:NCOR2-DHX37

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: NCOR2-DHX37
FusionPDB ID: 57865
FusionGDB2.0 ID: 57865
HgeneTgene
Gene symbol

NCOR2

DHX37

Gene ID

9612

57647

Gene namenuclear receptor corepressor 2DEAH-box helicase 37
SynonymsCTG26|N-CoR2|SMAP270|SMRT|SMRTE|SMRTE-tau|TNRC14|TRAC|TRAC-1|TRAC1DDX37|Dhr1|NEDBAVC
Cytomap

12q24.31

12q24.31

Type of geneprotein-codingprotein-coding
Descriptionnuclear receptor corepressor 2CTG repeat protein 26T3 receptor-associating factorsilencing mediator for retinoid and thyroid hormone receptorsthyroid-, retinoic-acid-receptor-associated corepressorprobable ATP-dependent RNA helicase DHX37DEAD/DEAH box helicase DDX37DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 37DEAH (Asp-Glu-Ala-His) box polypeptide 37DEAH box protein 37
Modification date2020031320200313
UniProtAcc

Q9Y618

Q8IY37

Ensembl transtripts involved in fusion geneENST idsENST00000356219, ENST00000397355, 
ENST00000404621, ENST00000405201, 
ENST00000429285, ENST00000404121, 
ENST00000544745, ENST00000308736, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score35 X 38 X 19=252704 X 6 X 6=144
# samples 518
** MAII scorelog2(51/25270*10)=-5.63078460697328
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/144*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: NCOR2 [Title/Abstract] AND DHX37 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)DHX37(125467056)-NCOR2(124922542), # samples:2
NCOR2(124950719)-DHX37(125450358), # samples:2
NCOR2(124970987)-DHX37(125470811), # samples:2
NCOR2(124846672)-DHX37(125435350), # samples:2
Anticipated loss of major functional domain due to fusion event.DHX37-NCOR2 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.
DHX37-NCOR2 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.
NCOR2-DHX37 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.
NCOR2-DHX37 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.
NCOR2-DHX37 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
NCOR2-DHX37 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
NCOR2-DHX37 seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
NCOR2-DHX37 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
NCOR2-DHX37 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

check buttonFusion gene breakpoints across NCOR2 (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 DHX37 (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
ChimerDB4GBMTCGA-06-0878-01ANCOR2chr12

124950719

-DHX37chr12

125450358

-
ChimerDB4OVTCGA-13-A5FT-01ANCOR2chr12

124970987

-DHX37chr12

125470811

-
ChimerDB4OVTCGA-13-A5FTNCOR2chr12

124970986

-DHX37chr12

125470811

-
ChimerDB4STADTCGA-CG-4449-01ANCOR2chr12

124846672

-DHX37chr12

125435350

-


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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)
ENST00000405201NCOR2chr12124950719-ENST00000308736DHX37chr12125450358-356570612589862
ENST00000405201NCOR2chr12124950719-ENST00000544745DHX37chr12125450358-375770612643880

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
ENST00000405201ENST00000308736NCOR2chr12124950719-DHX37chr12125450358-0.0039874080.99601257
ENST00000405201ENST00000544745NCOR2chr12124950719-DHX37chr12125450358-0.0034110510.99658895

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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

>57865_57865_1_NCOR2-DHX37_NCOR2_chr12_124950719_ENST00000405201_DHX37_chr12_125450358_ENST00000308736_length(amino acids)=862AA_BP=235
MSGSTQPVAQTWRATEPRYPPHSLSYPVQIARTHTDVGLLEYQHHSRDYASHLSPGSIIQPQRRRPSLLSEFQPGNERSQELHLRPESHS
YLPELGKSEMEFIESKRPRLELLPDPLLRPSPLLATGQPAGSEDLTKDRSLTGKLEPVSPPSPPHTDPELELVPPRLSKEELIQNMDRVD
REITMVEQQISKLKKKQQQLEEEAAKPPEPEKPVSPPPIESKHRSLVQIIYDENRVLPQINLDHYSVLPAGEGDEDREAEVDEEEGALDS
DLDLDLGDGGQDGGEQPDASLPLHVLPLYSLLAPEKQAQVFKPPPEGTRLCVVATNVAETSLTIPGIKYVVDCGKVKKRYYDRVTGVSSF
RVTWVSQASADQRAGRAGRTEPGHCYRLYSSAVFGDFEQFPPPEITRRPVEDLILQMKALNVEKVINFPFPTPPSVEALLAAEELLIALG
ALQPPQKAERVKQLQENRLSCPITALGRTMATFPVAPRYAKMLALSRQHGCLPYAITIVASMTVRELFEELDRPAASDEELTRLKSKRAR
VAQMKRTWAGQGASLKLGDLMVLLGAVGACEYASCTPQFCEANGLRYKAMMEIRRLRGQLTTAVNAVCPEAELFVDPKMQPPTESQVTYL
RQIVTAGLGDHLARRVQSEEMLEDKWRNAYKTPLLDDPVFIHPSSVLFKELPEFVVYQEIVETTKMYMKGVSSVEVQWIPALLPSYCQFD
KPLEEPAPTYCPERGRVLCHRASVFYRVGWPLPAIEVDFPEGIDRYKHFARFLLEGQVFRKLASYRSCLLSSPGTMLKTWARLQPRTESL

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>57865_57865_2_NCOR2-DHX37_NCOR2_chr12_124950719_ENST00000405201_DHX37_chr12_125450358_ENST00000544745_length(amino acids)=880AA_BP=235
MSGSTQPVAQTWRATEPRYPPHSLSYPVQIARTHTDVGLLEYQHHSRDYASHLSPGSIIQPQRRRPSLLSEFQPGNERSQELHLRPESHS
YLPELGKSEMEFIESKRPRLELLPDPLLRPSPLLATGQPAGSEDLTKDRSLTGKLEPVSPPSPPHTDPELELVPPRLSKEELIQNMDRVD
REITMVEQQISKLKKKQQQLEEEAAKPPEPEKPVSPPPIESKHRSLVQIIYDENRVLPQINLDHYSVLPAGEGDEDREAEVDEEEGALDS
DLDLDLGDGGQDGGEQPDASLPLHVLPLYSLLAPEKQAQVFKPPPEGTRLCVVATNVAETSLTIPGIKYVVDCGKVKKRYYDRVTGVSSF
RVTWVSQASADQRAGRAGRTEPGHCYRLYSSAVFGDFEQFPPPEITRRPVEDLILQMKALNVEKVINFPFPTPPSVEALLAAEELLIALG
ALQPPQKAERVKQLQENRLSCPITALGRTMATFPVAPRYAKMLALSRQHGCLPYAITIVASMTVRELFEELDRPAASDEELTRLKSKRAR
VAQMKRTWAGQGASLKLGDLMVLLGAVGACEYASCTPQFCEANGLRYKAMMEIRRLRGQLTTAVNAVCPEAELFVDPKMQPPTESQVTYL
RQIVTAGLGDHLARRVQSEEMLEDKWRNAYKTPLLDDPVFIHPSSVLFKELPEFVVYQEIVETTKMYMKGVSSVEVQWIPALLPSYCQFD
KPLEEPAPTYCPERGRVLCHRASVFYRVGWPLPAIEVDFPEGIDRYKHFARFLLEGQVFRKLASYRSCLLSSPGTMLKTWARLQPRTESL

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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/chr12:125467056/chr12:124922542)
- 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
NCOR2

Q9Y618

DHX37

Q8IY37

FUNCTION: Transcriptional corepressor (PubMed:20812024). Mediates the transcriptional repression activity of some nuclear receptors by promoting chromatin condensation, thus preventing access of the basal transcription. Isoform 1 and isoform 4 have different affinities for different nuclear receptors. Involved in the regulation BCL6-dependent of the germinal center (GC) reactions, mainly through the control of the GC B-cells proliferation and survival. Recruited by ZBTB7A to the androgen response elements/ARE on target genes, negatively regulates androgen receptor signaling and androgen-induced cell proliferation (PubMed:20812024). {ECO:0000269|PubMed:18212045, ECO:0000269|PubMed:20812024, ECO:0000269|PubMed:23911289}.FUNCTION: ATP-binding RNA helicase that plays a role in maturation of the small ribosomal subunit in ribosome biogenesis (PubMed:30582406). Required for the release of the U3 snoRNP from pre-ribosomal particles (PubMed:30582406). Plays a role in early testis development (PubMed:31287541, PubMed:31337883). Probably plays also a role in brain development (PubMed:31256877). {ECO:0000269|PubMed:30582406, ECO:0000269|PubMed:31256877, ECO:0000269|PubMed:31287541, ECO:0000269|PubMed:31337883}.

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
HgeneNCOR2chr12:124950719chr12:125450358ENST00000356219-648174_215235.02522.0Coiled coilOntology_term=ECO:0000255

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneNCOR2chr12:124950719chr12:125450358ENST00000356219-648522_561235.02522.0Coiled coilOntology_term=ECO:0000255
HgeneNCOR2chr12:124950719chr12:125450358ENST00000356219-6481384_1389235.02522.0Compositional biasNote=Poly-Pro
HgeneNCOR2chr12:124950719chr12:125450358ENST00000356219-6481839_1843235.02522.0Compositional biasNote=Poly-Gly
HgeneNCOR2chr12:124950719chr12:125450358ENST00000356219-6482476_2479235.02522.0Compositional biasNote=Poly-Pro
HgeneNCOR2chr12:124950719chr12:125450358ENST00000356219-648494_510235.02522.0Compositional biasNote=Poly-Gln
HgeneNCOR2chr12:124950719chr12:125450358ENST00000356219-648682_685235.02522.0Compositional biasNote=Poly-Lys
HgeneNCOR2chr12:124950719chr12:125450358ENST00000356219-648778_820235.02522.0Compositional biasNote=Pro-rich
HgeneNCOR2chr12:124950719chr12:125450358ENST00000356219-648995_1003235.02522.0Compositional biasNote=Poly-Pro
HgeneNCOR2chr12:124950719chr12:125450358ENST00000356219-648427_478235.02522.0DomainSANT 1
HgeneNCOR2chr12:124950719chr12:125450358ENST00000356219-648610_661235.02522.0DomainSANT 2
HgeneNCOR2chr12:124950719chr12:125450358ENST00000356219-6482136_2140235.02522.0MotifNote=CORNR box of ID1
HgeneNCOR2chr12:124950719chr12:125450358ENST00000356219-6482339_2343235.02522.0MotifNote=CORNR box of ID2
TgeneDHX37chr12:124950719chr12:125450358ENST000003087361127262_429530.01158.0DomainHelicase ATP-binding
TgeneDHX37chr12:124950719chr12:125450358ENST000003087361127459_716530.01158.0DomainHelicase C-terminal
TgeneDHX37chr12:124950719chr12:125450358ENST000003087361127372_375530.01158.0MotifNote=DEAH box
TgeneDHX37chr12:124950719chr12:125450358ENST000003087361127275_282530.01158.0Nucleotide bindingATP


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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
NCOR2
DHX37


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
HgeneNCOR2chr12:124950719chr12:125450358ENST00000356219-648254_312235.02522.0SIN3A/B


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Related Drugs to NCOR2-DHX37


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 NCOR2-DHX37


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