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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:AFF1-U2SURP

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: AFF1-U2SURP
FusionPDB ID: 2668
FusionGDB2.0 ID: 2668
HgeneTgene
Gene symbol

AFF1

U2SURP

Gene ID

4299

23350

Gene nameAF4/FMR2 family member 1U2 snRNP associated SURP domain containing
SynonymsAF4|MLLT2|PBM1SR140|fSAPa
Cytomap

4q21.3-q22.1

3q23

Type of geneprotein-codingprotein-coding
DescriptionAF4/FMR2 family member 1ALL1-fused gene from chromosome 4 proteinmyeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 2pre-B-cell monocytic leukemia partner 1proto-oncogene AF4U2 snRNP-associated SURP motif-containing protein140 kDa Ser/Arg-rich domain proteinSer/Arg-rich domain protein, 140 kDaU2-associated SR140 proteinU2-associated protein SR140functional spliceosome-associated protein a
Modification date2020031320200313
UniProtAcc

P51825

.
Ensembl transtripts involved in fusion geneENST idsENST00000511996, ENST00000395146, 
ENST00000307808, ENST00000544085, 
ENST00000397933, ENST00000473835, 
ENST00000493598, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score27 X 51 X 13=179019 X 10 X 3=270
# samples 6811
** MAII scorelog2(68/17901*10)=-4.71836162613835
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/270*10)=-1.29545588352617
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: AFF1 [Title/Abstract] AND U2SURP [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)AFF1(87869723)-U2SURP(142751625), # samples:1
Anticipated loss of major functional domain due to fusion event.AFF1-U2SURP 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.
AFF1-U2SURP 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.
AFF1-U2SURP 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.
AFF1-U2SURP 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

check buttonFusion gene breakpoints across AFF1 (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 U2SURP (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-Cancer2397NAFF1chr4

87869723

+U2SURPchr3

142751625

+


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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)
ENST00000395146AFF1chr487869723+ENST00000397933U2SURPchr3142751625+60683132661792508
ENST00000395146AFF1chr487869723+ENST00000473835U2SURPchr3142751625+58893132661792508
ENST00000395146AFF1chr487869723+ENST00000493598U2SURPchr3142751625+21893132661792508

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
ENST00000395146ENST00000397933AFF1chr487869723+U2SURPchr3142751625+9.45E-050.99990547
ENST00000395146ENST00000473835AFF1chr487869723+U2SURPchr3142751625+9.85E-050.99990153
ENST00000395146ENST00000493598AFF1chr487869723+U2SURPchr3142751625+0.0005693280.9994306

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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

>2668_2668_1_AFF1-U2SURP_AFF1_chr4_87869723_ENST00000395146_U2SURP_chr3_142751625_ENST00000397933_length(amino acids)=508AA_BP=15
METMAFTERVNSSGNRQRDKLEEILRGLTPRKNDIGDAMVFCLNNAEAAEEIVDCITESLSILKTPLPKKIARLYLVSDVLYNSSAKVAN
ASYYRKFFETKLCQIFSDLNATYRTIQGHLQSENFKQRVMTCFRAWEDWAIYPEPFLIKLQNIFLGLVNIIEEKETEDVPDDLDGAPIEE
ELDGAPLEDVDGIPIDATPIDDLDGVPIKSLDDDLDGVPLDATEDSKKNEPIFKVAPSKWEAVDESELEAQAVTTSKWELFDQHEESEEE
ENQNQEEESEDEEDTQSSKSEEHHLYSNPIKEEMTESKFSKYSEMSEEKRAKLREIELKVMKFQDELESGKRPKKPGQSFQEQVEHYRDK
LLQREKEKELERERERDKKDKEKLESRSKDKKEKDECTPTRKERKRRHSTSPSPSRSSSGRRVKSPSPKSERSERSERSHKESSRSRSSH

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

>2668_2668_2_AFF1-U2SURP_AFF1_chr4_87869723_ENST00000395146_U2SURP_chr3_142751625_ENST00000473835_length(amino acids)=508AA_BP=15
METMAFTERVNSSGNRQRDKLEEILRGLTPRKNDIGDAMVFCLNNAEAAEEIVDCITESLSILKTPLPKKIARLYLVSDVLYNSSAKVAN
ASYYRKFFETKLCQIFSDLNATYRTIQGHLQSENFKQRVMTCFRAWEDWAIYPEPFLIKLQNIFLGLVNIIEEKETEDVPDDLDGAPIEE
ELDGAPLEDVDGIPIDATPIDDLDGVPIKSLDDDLDGVPLDATEDSKKNEPIFKVAPSKWEAVDESELEAQAVTTSKWELFDQHEESEEE
ENQNQEEESEDEEDTQSSKSEEHHLYSNPIKEEMTESKFSKYSEMSEEKRAKLREIELKVMKFQDELESGKRPKKPGQSFQEQVEHYRDK
LLQREKEKELERERERDKKDKEKLESRSKDKKEKDECTPTRKERKRRHSTSPSPSRSSSGRRVKSPSPKSERSERSERSHKESSRSRSSH

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

>2668_2668_3_AFF1-U2SURP_AFF1_chr4_87869723_ENST00000395146_U2SURP_chr3_142751625_ENST00000493598_length(amino acids)=508AA_BP=15
METMAFTERVNSSGNRQRDKLEEILRGLTPRKNDIGDAMVFCLNNAEAAEEIVDCITESLSILKTPLPKKIARLYLVSDVLYNSSAKVAN
ASYYRKFFETKLCQIFSDLNATYRTIQGHLQSENFKQRVMTCFRAWEDWAIYPEPFLIKLQNIFLGLVNIIEEKETEDVPDDLDGAPIEE
ELDGAPLEDVDGIPIDATPIDDLDGVPIKSLDDDLDGVPLDATEDSKKNEPIFKVAPSKWEAVDESELEAQAVTTSKWELFDQHEESEEE
ENQNQEEESEDEEDTQSSKSEEHHLYSNPIKEEMTESKFSKYSEMSEEKRAKLREIELKVMKFQDELESGKRPKKPGQSFQEQVEHYRDK
LLQREKEKELERERERDKKDKEKLESRSKDKKEKDECTPTRKERKRRHSTSPSPSRSSSGRRVKSPSPKSERSERSERSHKESSRSRSSH

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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/chr4:87869723/chr3:142751625)
- 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
AFF1

P51825

.
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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneU2SURPchr4:87869723chr3:142751625ENST000003979331427192_232127.66666666666667621.0Coiled coilOntology_term=ECO:0000255
TgeneU2SURPchr4:87869723chr3:142751625ENST000003979331427837_915127.66666666666667621.0Coiled coilOntology_term=ECO:0000255
TgeneU2SURPchr4:87869723chr3:142751625ENST000004738351528837_915536.66666666666661030.0Coiled coilOntology_term=ECO:0000255
TgeneU2SURPchr4:87869723chr3:142751625ENST000003979331427357_402127.66666666666667621.0Compositional biasNote=Pro-rich
TgeneU2SURPchr4:87869723chr3:142751625ENST000003979331427689_746127.66666666666667621.0Compositional biasNote=Asp-rich
TgeneU2SURPchr4:87869723chr3:142751625ENST000003979331427762_917127.66666666666667621.0Compositional biasNote=Glu-rich
TgeneU2SURPchr4:87869723chr3:142751625ENST000003979331427922_1001127.66666666666667621.0Compositional biasNote=Arg/Ser-rich
TgeneU2SURPchr4:87869723chr3:142751625ENST000004738351528689_746536.66666666666661030.0Compositional biasNote=Asp-rich
TgeneU2SURPchr4:87869723chr3:142751625ENST000004738351528762_917536.66666666666661030.0Compositional biasNote=Glu-rich
TgeneU2SURPchr4:87869723chr3:142751625ENST000004738351528922_1001536.66666666666661030.0Compositional biasNote=Arg/Ser-rich
TgeneU2SURPchr4:87869723chr3:142751625ENST000003979331427274_355127.66666666666667621.0DomainRRM
TgeneU2SURPchr4:87869723chr3:142751625ENST000003979331427534_679127.66666666666667621.0DomainCID
TgeneU2SURPchr4:87869723chr3:142751625ENST000004738351528534_679536.66666666666661030.0DomainCID
TgeneU2SURPchr4:87869723chr3:142751625ENST000003979331427430_473127.66666666666667621.0RepeatNote=SURP motif

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneAFF1chr4:87869723chr3:142751625ENST00000307808+120483_49201211.0Compositional biasNote=Poly-Ser
HgeneAFF1chr4:87869723chr3:142751625ENST00000307808+120835_84301211.0Compositional biasNote=Poly-Ser
HgeneAFF1chr4:87869723chr3:142751625ENST00000307808+120866_86901211.0Compositional biasNote=Poly-Pro
HgeneAFF1chr4:87869723chr3:142751625ENST00000307808+120871_87401211.0Compositional biasNote=Poly-Ser
HgeneAFF1chr4:87869723chr3:142751625ENST00000395146+221483_49212.6666666666666661219.0Compositional biasNote=Poly-Ser
HgeneAFF1chr4:87869723chr3:142751625ENST00000395146+221835_84312.6666666666666661219.0Compositional biasNote=Poly-Ser
HgeneAFF1chr4:87869723chr3:142751625ENST00000395146+221866_86912.6666666666666661219.0Compositional biasNote=Poly-Pro
HgeneAFF1chr4:87869723chr3:142751625ENST00000395146+221871_87412.6666666666666661219.0Compositional biasNote=Poly-Ser
TgeneU2SURPchr4:87869723chr3:142751625ENST00000397933142792_121127.66666666666667621.0Coiled coilOntology_term=ECO:0000255
TgeneU2SURPchr4:87869723chr3:142751625ENST000004738351528192_232536.66666666666661030.0Coiled coilOntology_term=ECO:0000255
TgeneU2SURPchr4:87869723chr3:142751625ENST00000473835152892_121536.66666666666661030.0Coiled coilOntology_term=ECO:0000255
TgeneU2SURPchr4:87869723chr3:142751625ENST000004738351528357_402536.66666666666661030.0Compositional biasNote=Pro-rich
TgeneU2SURPchr4:87869723chr3:142751625ENST000004738351528274_355536.66666666666661030.0DomainRRM
TgeneU2SURPchr4:87869723chr3:142751625ENST000004738351528430_473536.66666666666661030.0RepeatNote=SURP motif


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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
AFF1MLLT1, CCNT1, NT5E, MLLT3, CDK9, AFF4, KMT2A, AFF1, BRD4, RELA, NPM1, PCSK1, MLLT10, DOT1L, POLR2A, DDX6, HEXIM1, HIST3H3, NSD1, CARM1, SIAH1, SIAH2, SMAD9, tat, MED26, EAF1, ELL2, LARP7, ELL3, HDAC1, MYH7, SLC16A6, ZNF526, Mllt1, Mad2l1bp, Rrbp1, Rcc1, VDR, PIP4K2A, CAMKV, TRIM25, HNRNPL, ESR2, KIAA1429, SASH1, DYRK1A, ARFIP1, MRPL12, KIF20A, CCAR2, FGF12, PLCD3, EPB41L1, EPB41L3,


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
AFF1all structure
U2SURP


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 AFF1-U2SURP


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 AFF1-U2SURP


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