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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:ANXA1-U2SURP

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ANXA1-U2SURP
FusionPDB ID: 5024
FusionGDB2.0 ID: 5024
HgeneTgene
Gene symbol

ANXA1

U2SURP

Gene ID

301

23350

Gene nameannexin A1U2 snRNP associated SURP domain containing
SynonymsANX1|LPC1SR140|fSAPa
Cytomap

9q21.13

3q23

Type of geneprotein-codingprotein-coding
Descriptionannexin A1annexin I (lipocortin I)annexin-1calpactin IIcalpactin-2chromobindin-9epididymis secretory sperm binding proteinphospholipase A2 inhibitory proteinU2 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 date2020032920200313
UniProtAcc

P27216

.
Ensembl transtripts involved in fusion geneENST idsENST00000257497, ENST00000376911, 
ENST00000491192, 
ENST00000397933, 
ENST00000473835, ENST00000493598, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 6 X 3=1089 X 10 X 3=270
# samples 611
** MAII scorelog2(6/108*10)=-0.84799690655495
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: ANXA1 [Title/Abstract] AND U2SURP [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ANXA1(75775236)-U2SURP(142769845), # samples:1
Anticipated loss of major functional domain due to fusion event.ANXA1-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.
ANXA1-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
HgeneANXA1

GO:0002548

monocyte chemotaxis

15187149

HgeneANXA1

GO:0007187

G protein-coupled receptor signaling pathway, coupled to cyclic nucleotide second messenger

25664854

HgeneANXA1

GO:0008360

regulation of cell shape

15187149

HgeneANXA1

GO:0018149

peptide cross-linking

10908733

HgeneANXA1

GO:0030216

keratinocyte differentiation

10908733

HgeneANXA1

GO:0031340

positive regulation of vesicle fusion

2138016

HgeneANXA1

GO:0031532

actin cytoskeleton reorganization

15187149

HgeneANXA1

GO:0032743

positive regulation of interleukin-2 production

17008549

HgeneANXA1

GO:0035924

cellular response to vascular endothelial growth factor stimulus

22773844

HgeneANXA1

GO:0042102

positive regulation of T cell proliferation

17008549

HgeneANXA1

GO:0045627

positive regulation of T-helper 1 cell differentiation

17008549

HgeneANXA1

GO:0045629

negative regulation of T-helper 2 cell differentiation

17008549

HgeneANXA1

GO:0071385

cellular response to glucocorticoid stimulus

2936963

HgeneANXA1

GO:0071621

granulocyte chemotaxis

15187149

HgeneANXA1

GO:0090050

positive regulation of cell migration involved in sprouting angiogenesis

22773844

HgeneANXA1

GO:0090303

positive regulation of wound healing

25664854


check buttonFusion gene breakpoints across ANXA1 (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
ChiTaRS5.0N/ACB132862ANXA1chr9

75775236

+U2SURPchr3

142769845

+


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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)
ENST00000257497ANXA1chr975775236+ENST00000397933U2SURPchr3142769845+5264508611988125
ENST00000257497ANXA1chr975775236+ENST00000473835U2SURPchr3142769845+5085508806420128
ENST00000257497ANXA1chr975775236+ENST00000493598U2SURPchr3142769845+1385508611988125
ENST00000376911ANXA1chr975775236+ENST00000397933U2SURPchr3142769845+5964120815061120128
ENST00000376911ANXA1chr975775236+ENST00000473835U2SURPchr3142769845+5785120815061120128
ENST00000376911ANXA1chr975775236+ENST00000493598U2SURPchr3142769845+2085120815061120128

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
ENST00000257497ENST00000397933ANXA1chr975775236+U2SURPchr3142769845+0.206882010.79311794
ENST00000257497ENST00000473835ANXA1chr975775236+U2SURPchr3142769845+0.107404780.89259523
ENST00000257497ENST00000493598ANXA1chr975775236+U2SURPchr3142769845+0.128723080.8712769
ENST00000376911ENST00000397933ANXA1chr975775236+U2SURPchr3142769845+0.19371220.80628777
ENST00000376911ENST00000473835ANXA1chr975775236+U2SURPchr3142769845+0.098521270.9014787
ENST00000376911ENST00000493598ANXA1chr975775236+U2SURPchr3142769845+0.133972020.866028

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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

>5024_5024_1_ANXA1-U2SURP_ANXA1_chr9_75775236_ENST00000257497_U2SURP_chr3_142769845_ENST00000397933_length(amino acids)=125AA_BP=
MESRSKDKKEKDECTPTRKERKRRHSTSPSPSRSSSGRRVKSPSPKSERSERSERSHKESSRSRSSHKDSPRDVSKKAKRSPSGSRTPKR

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

>5024_5024_2_ANXA1-U2SURP_ANXA1_chr9_75775236_ENST00000257497_U2SURP_chr3_142769845_ENST00000473835_length(amino acids)=128AA_BP=0
MTWTVSSLYEIFLNALIAPILVMGISLVYHCYCEMGWGMYCVASSFPSLSEYTHLFPSCLWSEIPIFLYLSCLFLVLFLTLSLSLVEEVY

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

>5024_5024_3_ANXA1-U2SURP_ANXA1_chr9_75775236_ENST00000257497_U2SURP_chr3_142769845_ENST00000493598_length(amino acids)=125AA_BP=
MESRSKDKKEKDECTPTRKERKRRHSTSPSPSRSSSGRRVKSPSPKSERSERSERSHKESSRSRSSHKDSPRDVSKKAKRSPSGSRTPKR

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

>5024_5024_4_ANXA1-U2SURP_ANXA1_chr9_75775236_ENST00000376911_U2SURP_chr3_142769845_ENST00000397933_length(amino acids)=128AA_BP=0
MTWTVSSLYEIFLNALIAPILVMGISLVYHCYCEMGWGMYCVASSFPSLSEYTHLFPSCLWSEIPIFLYLSCLFLVLFLTLSLSLVEEVY

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

>5024_5024_5_ANXA1-U2SURP_ANXA1_chr9_75775236_ENST00000376911_U2SURP_chr3_142769845_ENST00000473835_length(amino acids)=128AA_BP=0
MTWTVSSLYEIFLNALIAPILVMGISLVYHCYCEMGWGMYCVASSFPSLSEYTHLFPSCLWSEIPIFLYLSCLFLVLFLTLSLSLVEEVY

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

>5024_5024_6_ANXA1-U2SURP_ANXA1_chr9_75775236_ENST00000376911_U2SURP_chr3_142769845_ENST00000493598_length(amino acids)=128AA_BP=0
MTWTVSSLYEIFLNALIAPILVMGISLVYHCYCEMGWGMYCVASSFPSLSEYTHLFPSCLWSEIPIFLYLSCLFLVLFLTLSLSLVEEVY

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

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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/chr9:75775236/chr3:142769845)
- 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
ANXA1

P27216

.
FUNCTION: [Isoform A]: Binds to membranes enriched in phosphatidylserine or phosphatidylglycerol in a calcium-dependent manner (PubMed:27676605, PubMed:30610115). Half-maximal membrane binding requires about 60 uM calcium. Does not bind to membranes that lack phospholipids with an acidic headgroup (PubMed:27676605). {ECO:0000269|PubMed:27676605, ECO:0000269|PubMed:30610115}.; FUNCTION: [Isoform B]: Binds to membranes enriched in phosphatidylserine or phosphatidylglycerol in a calcium-dependent manner, but requires higher calcium levels for membrane binding than isoform A. Half-maximal membrane binding requires about 320 uM calcium. {ECO:0000269|PubMed:27676605}.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
TgeneU2SURPchr9:75775236chr3:142769845ENST00000397933027192_2320621.0Coiled coilOntology_term=ECO:0000255
TgeneU2SURPchr9:75775236chr3:142769845ENST00000397933027837_9150621.0Coiled coilOntology_term=ECO:0000255
TgeneU2SURPchr9:75775236chr3:142769845ENST0000039793302792_1210621.0Coiled coilOntology_term=ECO:0000255
TgeneU2SURPchr9:75775236chr3:142769845ENST00000473835028192_23201030.0Coiled coilOntology_term=ECO:0000255
TgeneU2SURPchr9:75775236chr3:142769845ENST00000473835028837_91501030.0Coiled coilOntology_term=ECO:0000255
TgeneU2SURPchr9:75775236chr3:142769845ENST0000047383502892_12101030.0Coiled coilOntology_term=ECO:0000255
TgeneU2SURPchr9:75775236chr3:142769845ENST00000397933027357_4020621.0Compositional biasNote=Pro-rich
TgeneU2SURPchr9:75775236chr3:142769845ENST00000397933027689_7460621.0Compositional biasNote=Asp-rich
TgeneU2SURPchr9:75775236chr3:142769845ENST00000397933027762_9170621.0Compositional biasNote=Glu-rich
TgeneU2SURPchr9:75775236chr3:142769845ENST00000397933027922_10010621.0Compositional biasNote=Arg/Ser-rich
TgeneU2SURPchr9:75775236chr3:142769845ENST00000473835028357_40201030.0Compositional biasNote=Pro-rich
TgeneU2SURPchr9:75775236chr3:142769845ENST00000473835028689_74601030.0Compositional biasNote=Asp-rich
TgeneU2SURPchr9:75775236chr3:142769845ENST00000473835028762_91701030.0Compositional biasNote=Glu-rich
TgeneU2SURPchr9:75775236chr3:142769845ENST00000473835028922_100101030.0Compositional biasNote=Arg/Ser-rich
TgeneU2SURPchr9:75775236chr3:142769845ENST00000397933027274_3550621.0DomainRRM
TgeneU2SURPchr9:75775236chr3:142769845ENST00000397933027534_6790621.0DomainCID
TgeneU2SURPchr9:75775236chr3:142769845ENST00000473835028274_35501030.0DomainRRM
TgeneU2SURPchr9:75775236chr3:142769845ENST00000473835028534_67901030.0DomainCID
TgeneU2SURPchr9:75775236chr3:142769845ENST00000397933027430_4730621.0RepeatNote=SURP motif
TgeneU2SURPchr9:75775236chr3:142769845ENST00000473835028430_47301030.0RepeatNote=SURP motif

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneANXA1chr9:75775236chr3:142769845ENST00000257497+113114_1850347.0RepeatAnnexin 2
HgeneANXA1chr9:75775236chr3:142769845ENST00000257497+113197_2690347.0RepeatAnnexin 3
HgeneANXA1chr9:75775236chr3:142769845ENST00000257497+113273_3440347.0RepeatAnnexin 4
HgeneANXA1chr9:75775236chr3:142769845ENST00000257497+11342_1130347.0RepeatAnnexin 1
HgeneANXA1chr9:75775236chr3:142769845ENST00000376911+112114_1850347.0RepeatAnnexin 2
HgeneANXA1chr9:75775236chr3:142769845ENST00000376911+112197_2690347.0RepeatAnnexin 3
HgeneANXA1chr9:75775236chr3:142769845ENST00000376911+112273_3440347.0RepeatAnnexin 4
HgeneANXA1chr9:75775236chr3:142769845ENST00000376911+11242_1130347.0RepeatAnnexin 1


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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
ANXA1
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 ANXA1-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 ANXA1-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