UTHEALTH HOME    ABOUT SBMI    A-Z    WEBMAIL    INSIDE THE UNIVERSITY
FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Terms of Use

Center for Computational Systems Medicine level1
leaf

Fusion Gene Summary

leaf

Fusion Gene Sample Information

leaf

Fusion ORF Analysis

leaf

Fusion Amino Acid Sequences

leaf

Fusion Protein Functional Features

leaf

Fusion Protein-Protein Interaction

leaf

Related drugs with this fusion protein

leaf

Related disease with this fusion protein

Fusion Protein:SET-BRD1

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SET-BRD1
FusionPDB ID: 80856
FusionGDB2.0 ID: 80856
HgeneTgene
Gene symbol

SET

BRD1

Gene ID

6418

23774

Gene nameSET nuclear proto-oncogenebromodomain containing 1
Synonyms2PP2A|I2PP2A|IGAAD|IPP2A2|MRD58|PHAPII|TAF-I|TAF-IBETABRL|BRPF1|BRPF2
Cytomap

9q34.11

22q13.33

Type of geneprotein-codingprotein-coding
Descriptionprotein SETHLA-DR-associated protein IISET nuclear oncogeneSET translocation (myeloid leukemia-associated)Template-Activating Factor-I, chromatin remodelling factorchromatin remodelling factorinhibitor of granzyme A-activated DNaseinhibitor-2 of prbromodomain-containing protein 1BR140-like proteinbromodomain and PHD finger-containing protein 2
Modification date2020031320200327
UniProtAcc

Q9BYW2

O95696

Ensembl transtripts involved in fusion geneENST idsENST00000322030, ENST00000372688, 
ENST00000372692, ENST00000409104, 
ENST00000477806, 
ENST00000459821, 
ENST00000457780, ENST00000216267, 
ENST00000342989, ENST00000404034, 
ENST00000404760, ENST00000542442, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score16 X 14 X 3=6726 X 7 X 4=168
# samples 177
** MAII scorelog2(17/672*10)=-1.98292648664106
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/168*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: SET [Title/Abstract] AND BRD1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SET(131451934)-BRD1(50171461), # samples:1
Anticipated loss of major functional domain due to fusion event.SET-BRD1 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.
SET-BRD1 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.
SET-BRD1 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.
SET-BRD1 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.
SET-BRD1 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
SET-BRD1 seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
SET-BRD1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
SET-BRD1 seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF.
SET-BRD1 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
SET-BRD1 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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
HgeneSET

GO:0045892

negative regulation of transcription, DNA-templated

19343227

TgeneBRD1

GO:0043966

histone H3 acetylation

16387653


check buttonFusion gene breakpoints across SET (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 BRD1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


Top

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
ChimerDB4STADTCGA-VQ-A8PESETchr9

131451934

+BRD1chr22

50171461

-


Top

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)
ENST00000322030SETchr9131451934+ENST00000216267BRD1chr2250171461-20934303571142261
ENST00000322030SETchr9131451934+ENST00000404034BRD1chr2250171461-20934303571142261
ENST00000322030SETchr9131451934+ENST00000404760BRD1chr2250171461-20934303571142261
ENST00000322030SETchr9131451934+ENST00000542442BRD1chr2250171461-15584303571142261
ENST00000322030SETchr9131451934+ENST00000342989BRD1chr2250171461-15494303571142261

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
ENST00000322030ENST00000216267SETchr9131451934+BRD1chr2250171461-0.0086620930.9913379
ENST00000322030ENST00000404034SETchr9131451934+BRD1chr2250171461-0.0086620930.9913379
ENST00000322030ENST00000404760SETchr9131451934+BRD1chr2250171461-0.0086620930.9913379
ENST00000322030ENST00000542442SETchr9131451934+BRD1chr2250171461-0.0260948610.9739051
ENST00000322030ENST00000342989SETchr9131451934+BRD1chr2250171461-0.0274742840.9725257

Top

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

>80856_80856_1_SET-BRD1_SET_chr9_131451934_ENST00000322030_BRD1_chr22_50171461_ENST00000216267_length(amino acids)=261AA_BP=24
MSAPAAKVSKKELNSNHDGADETSGLTNGFGGARSEQEPGGGLGRKATPRRRCASESSISSSNSPLCDSSFNAPKCGRGKPALVRRHTLE
DRSELISCIENGNYAKAARIAAEVGQSSMWISTDAAASVLEPLKVVWAKCSGYPSYPALIIDPKMPRVPGHHNGVTIPAPPLDVLKIGEH

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

>80856_80856_2_SET-BRD1_SET_chr9_131451934_ENST00000322030_BRD1_chr22_50171461_ENST00000342989_length(amino acids)=261AA_BP=24
MSAPAAKVSKKELNSNHDGADETSGLTNGFGGARSEQEPGGGLGRKATPRRRCASESSISSSNSPLCDSSFNAPKCGRGKPALVRRHTLE
DRSELISCIENGNYAKAARIAAEVGQSSMWISTDAAASVLEPLKVVWAKCSGYPSYPALIIDPKMPRVPGHHNGVTIPAPPLDVLKIGEH

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

>80856_80856_3_SET-BRD1_SET_chr9_131451934_ENST00000322030_BRD1_chr22_50171461_ENST00000404034_length(amino acids)=261AA_BP=24
MSAPAAKVSKKELNSNHDGADETSGLTNGFGGARSEQEPGGGLGRKATPRRRCASESSISSSNSPLCDSSFNAPKCGRGKPALVRRHTLE
DRSELISCIENGNYAKAARIAAEVGQSSMWISTDAAASVLEPLKVVWAKCSGYPSYPALIIDPKMPRVPGHHNGVTIPAPPLDVLKIGEH

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

>80856_80856_4_SET-BRD1_SET_chr9_131451934_ENST00000322030_BRD1_chr22_50171461_ENST00000404760_length(amino acids)=261AA_BP=24
MSAPAAKVSKKELNSNHDGADETSGLTNGFGGARSEQEPGGGLGRKATPRRRCASESSISSSNSPLCDSSFNAPKCGRGKPALVRRHTLE
DRSELISCIENGNYAKAARIAAEVGQSSMWISTDAAASVLEPLKVVWAKCSGYPSYPALIIDPKMPRVPGHHNGVTIPAPPLDVLKIGEH

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

>80856_80856_5_SET-BRD1_SET_chr9_131451934_ENST00000322030_BRD1_chr22_50171461_ENST00000542442_length(amino acids)=261AA_BP=24
MSAPAAKVSKKELNSNHDGADETSGLTNGFGGARSEQEPGGGLGRKATPRRRCASESSISSSNSPLCDSSFNAPKCGRGKPALVRRHTLE
DRSELISCIENGNYAKAARIAAEVGQSSMWISTDAAASVLEPLKVVWAKCSGYPSYPALIIDPKMPRVPGHHNGVTIPAPPLDVLKIGEH

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

Top

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/chr9:131451934/chr22:50171461)
- 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
SET

Q9BYW2

BRD1

O95696

FUNCTION: Histone methyltransferase that specifically trimethylates 'Lys-36' of histone H3 (H3K36me3) using dimethylated 'Lys-36' (H3K36me2) as substrate (PubMed:16118227, PubMed:19141475, PubMed:21526191, PubMed:21792193, PubMed:23043551, PubMed:27474439). It is capable of trimethylating unmethylated H3K36 (H3K36me0) in vitro (PubMed:19332550). Represents the main enzyme generating H3K36me3, a specific tag for epigenetic transcriptional activation (By similarity). Plays a role in chromatin structure modulation during elongation by coordinating recruitment of the FACT complex and by interacting with hyperphosphorylated POLR2A (PubMed:23325844). Acts as a key regulator of DNA mismatch repair in G1 and early S phase by generating H3K36me3, a mark required to recruit MSH6 subunit of the MutS alpha complex: early recruitment of the MutS alpha complex to chromatin to be replicated allows a quick identification of mismatch DNA to initiate the mismatch repair reaction (PubMed:23622243). Required for DNA double-strand break repair in response to DNA damage: acts by mediating formation of H3K36me3, promoting recruitment of RAD51 and DNA repair via homologous recombination (HR) (PubMed:24843002). Acts as a tumor suppressor (PubMed:24509477). H3K36me3 also plays an essential role in the maintenance of a heterochromatic state, by recruiting DNA methyltransferase DNMT3A (PubMed:27317772). H3K36me3 is also enhanced in intron-containing genes, suggesting that SETD2 recruitment is enhanced by splicing and that splicing is coupled to recruitment of elongating RNA polymerase (PubMed:21792193). Required during angiogenesis (By similarity). Required for endoderm development by promoting embryonic stem cell differentiation toward endoderm: acts by mediating formation of H3K36me3 in distal promoter regions of FGFR3, leading to regulate transcription initiation of FGFR3 (By similarity). In addition to histones, also mediates methylation of other proteins, such as tubulins and STAT1 (PubMed:27518565, PubMed:28753426). Trimethylates 'Lys-40' of alpha-tubulins such as TUBA1B (alpha-TubK40me3); alpha-TubK40me3 is required for normal mitosis and cytokinesis and may be a specific tag in cytoskeletal remodeling (PubMed:27518565). Involved in interferon-alpha-induced antiviral defense by mediating both monomethylation of STAT1 at 'Lys-525' and catalyzing H3K36me3 on promoters of some interferon-stimulated genes (ISGs) to activate gene transcription (PubMed:28753426). {ECO:0000250|UniProtKB:E9Q5F9, ECO:0000269|PubMed:16118227, ECO:0000269|PubMed:19141475, ECO:0000269|PubMed:21526191, ECO:0000269|PubMed:21792193, ECO:0000269|PubMed:23043551, ECO:0000269|PubMed:23325844, ECO:0000269|PubMed:23622243, ECO:0000269|PubMed:24509477, ECO:0000269|PubMed:24843002, ECO:0000269|PubMed:27317772, ECO:0000269|PubMed:27474439, ECO:0000269|PubMed:27518565, ECO:0000269|PubMed:28753426}.; FUNCTION: (Microbial infection) Recruited to the promoters of adenovirus 12 E1A gene in case of infection, possibly leading to regulate its expression. {ECO:0000269|PubMed:11461154}.FUNCTION: Scaffold subunit of various histone acetyltransferase (HAT) complexes, such as the MOZ/MORF and HBO1 complexes, that acts as a regulator of hematopoiesis (PubMed:16387653, PubMed:21753189, PubMed:21880731). Plays a key role in HBO1 complex by directing KAT7/HBO1 specificity towards histone H3 'Lys-14' acetylation (H3K14ac), thereby promoting erythroid differentiation (PubMed:21753189). {ECO:0000269|PubMed:16387653, ECO:0000269|PubMed:21753189, ECO:0000269|PubMed:21880731}.

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
TgeneBRD1chr9:131451934chr22:50171461ENST00000216267612929_1012821.33333333333341059.0DomainPWWP
TgeneBRD1chr9:131451934chr22:50171461ENST00000404034713929_1012821.33333333333341059.0DomainPWWP

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneSETchr9:131451934chr22:50171461ENST00000322030+18239_29024.333333333333332278.0Compositional biasNote=Asp/Glu-rich (highly acidic)
HgeneSETchr9:131451934chr22:50171461ENST00000372688+18239_2900.0267.0Compositional biasNote=Asp/Glu-rich (highly acidic)
HgeneSETchr9:131451934chr22:50171461ENST00000372692+18239_2900291.0Compositional biasNote=Asp/Glu-rich (highly acidic)
HgeneSETchr9:131451934chr22:50171461ENST00000409104+18239_2900269.0Compositional biasNote=Asp/Glu-rich (highly acidic)
HgeneSETchr9:131451934chr22:50171461ENST00000322030+1831_7824.333333333333332278.0RegionNote=Dimerization
HgeneSETchr9:131451934chr22:50171461ENST00000322030+1879_22524.333333333333332278.0RegionNote=Earmuff domain
HgeneSETchr9:131451934chr22:50171461ENST00000372688+1831_780.0267.0RegionNote=Dimerization
HgeneSETchr9:131451934chr22:50171461ENST00000372688+1879_2250.0267.0RegionNote=Earmuff domain
HgeneSETchr9:131451934chr22:50171461ENST00000372692+1831_780291.0RegionNote=Dimerization
HgeneSETchr9:131451934chr22:50171461ENST00000372692+1879_2250291.0RegionNote=Earmuff domain
HgeneSETchr9:131451934chr22:50171461ENST00000409104+1831_780269.0RegionNote=Dimerization
HgeneSETchr9:131451934chr22:50171461ENST00000409104+1879_2250269.0RegionNote=Earmuff domain
TgeneBRD1chr9:131451934chr22:50171461ENST00000216267612579_649821.33333333333341059.0DomainBromo
TgeneBRD1chr9:131451934chr22:50171461ENST00000404034713579_649821.33333333333341059.0DomainBromo
TgeneBRD1chr9:131451934chr22:50171461ENST00000404760713579_649952.33333333333341190.0DomainBromo
TgeneBRD1chr9:131451934chr22:50171461ENST00000404760713929_1012952.33333333333341190.0DomainPWWP
TgeneBRD1chr9:131451934chr22:50171461ENST00000216267612214_264821.33333333333341059.0Zinc fingerPHD-type 1
TgeneBRD1chr9:131451934chr22:50171461ENST00000216267612268_301821.33333333333341059.0Zinc fingerC2HC pre-PHD-type
TgeneBRD1chr9:131451934chr22:50171461ENST00000216267612325_389821.33333333333341059.0Zinc fingerPHD-type 2
TgeneBRD1chr9:131451934chr22:50171461ENST00000404034713214_264821.33333333333341059.0Zinc fingerPHD-type 1
TgeneBRD1chr9:131451934chr22:50171461ENST00000404034713268_301821.33333333333341059.0Zinc fingerC2HC pre-PHD-type
TgeneBRD1chr9:131451934chr22:50171461ENST00000404034713325_389821.33333333333341059.0Zinc fingerPHD-type 2
TgeneBRD1chr9:131451934chr22:50171461ENST00000404760713214_264952.33333333333341190.0Zinc fingerPHD-type 1
TgeneBRD1chr9:131451934chr22:50171461ENST00000404760713268_301952.33333333333341190.0Zinc fingerC2HC pre-PHD-type
TgeneBRD1chr9:131451934chr22:50171461ENST00000404760713325_389952.33333333333341190.0Zinc fingerPHD-type 2


Top

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
SET
BRD1


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
TgeneBRD1chr9:131451934chr22:50171461ENST0000021626761231_80821.33333333333341059.0KAT7/HBO1 and histones
TgeneBRD1chr9:131451934chr22:50171461ENST0000040403471331_80821.33333333333341059.0KAT7/HBO1 and histones
TgeneBRD1chr9:131451934chr22:50171461ENST0000040476071331_80952.33333333333341190.0KAT7/HBO1 and histones


Top

Related Drugs to SET-BRD1


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

Top

Related Diseases to SET-BRD1


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