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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:FNBP1-RAC2

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: FNBP1-RAC2
FusionPDB ID: 30871
FusionGDB2.0 ID: 30871
HgeneTgene
Gene symbol

FNBP1

RAC2

Gene ID

23048

5880

Gene nameformin binding protein 1Rac family small GTPase 2
SynonymsFBP17EN-7|Gx|HSPC022|p21-Rac2
Cytomap

9q34.11

22q13.1

Type of geneprotein-codingprotein-coding
Descriptionformin-binding protein 1formin-binding protein 17ras-related C3 botulinum toxin substrate 2Ras-related C3 botulinum toxin substrate 3 (rho family, small GTP-binding protein Rac2)ras-related C3 botulinum toxin substrate 2 (rho family, small GTP binding protein Rac2)small G protein
Modification date2020031320200313
UniProtAcc

Q5T0N5

.
Ensembl transtripts involved in fusion geneENST idsENST00000355681, ENST00000420781, 
ENST00000446176, ENST00000443566, 
ENST00000478129, 
ENST00000401529, 
ENST00000249071, ENST00000406508, 
ENST00000405484, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score9 X 12 X 3=3247 X 5 X 6=210
# samples 128
** MAII scorelog2(12/324*10)=-1.43295940727611
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/210*10)=-1.39231742277876
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: FNBP1 [Title/Abstract] AND RAC2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)FNBP1(132805231)-RAC2(37622843), # samples:1
Anticipated loss of major functional domain due to fusion event.FNBP1-RAC2 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.
FNBP1-RAC2 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.
FNBP1-RAC2 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
FNBP1-RAC2 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
TgeneRAC2

GO:0060263

regulation of respiratory burst

16636067


check buttonFusion gene breakpoints across FNBP1 (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 RAC2 (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
ChimerDB4STADTCGA-D7-8574-01AFNBP1chr9

132805231

-RAC2chr22

37622843

-


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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)
ENST00000446176FNBP1chr9132805231-ENST00000405484RAC2chr2237622843-3422115134196
ENST00000420781FNBP1chr9132805231-ENST00000405484RAC2chr2237622843-3742433121104
ENST00000355681FNBP1chr9132805231-ENST00000405484RAC2chr2237622843-3472165634697

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
ENST00000446176ENST00000405484FNBP1chr9132805231-RAC2chr2237622843-0.80204620.1979538
ENST00000420781ENST00000405484FNBP1chr9132805231-RAC2chr2237622843-0.829903660.17009631
ENST00000355681ENST00000405484FNBP1chr9132805231-RAC2chr2237622843-0.776019750.22398026

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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

>30871_30871_1_FNBP1-RAC2_FNBP1_chr9_132805231_ENST00000355681_RAC2_chr22_37622843_ENST00000405484_length(amino acids)=97AA_BP=53
MRAGGGRADSGLSAVAGISGGKGIAGEGDQRAAPAARSAPSRPLHHELGHRALDSVKYLECSALTQRGLKTVFDEAIRAVLCPQPTRQQK

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

>30871_30871_2_FNBP1-RAC2_FNBP1_chr9_132805231_ENST00000420781_RAC2_chr22_37622843_ENST00000405484_length(amino acids)=104AA_BP=0
MASSNTVFRPLWVRAEHSRYFTESRARCPSSWCRGREGALRAAGAALWSPSPAIPLPPEIPATAESPESARPPPARSSSPGVSSAAPPPR

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

>30871_30871_3_FNBP1-RAC2_FNBP1_chr9_132805231_ENST00000446176_RAC2_chr22_37622843_ENST00000405484_length(amino acids)=96AA_BP=53
MRAGGGRADSGLSAVAGISGGKGIAGEGDQRAAPAARSAPSRPLHHELGHRALDSVKYLECSALTQRGLKTVFDEAIRAVLCPQPTRQQK

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

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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/chr9:132805231/chr22:37622843)
- 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
FNBP1

Q5T0N5

.
FUNCTION: Required to coordinate membrane tubulation with reorganization of the actin cytoskeleton during endocytosis. May bind to lipids such as phosphatidylinositol 4,5-bisphosphate and phosphatidylserine and promote membrane invagination and the formation of tubules. Also promotes CDC42-induced actin polymerization by activating the WASL/N-WASP-WASPIP/WIP complex, the predominant form of WASL/N-WASP in cells. Actin polymerization may promote the fission of membrane tubules to form endocytic vesicles. Essential for autophagy of intracellular bacterial pathogens. {ECO:0000269|PubMed:15260990, ECO:0000269|PubMed:16326391, ECO:0000269|PubMed:19342671}.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

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneFNBP1chr9:132805231chr22:37622843ENST00000355681-116398_4908.0593.0Coiled coilOntology_term=ECO:0000250
HgeneFNBP1chr9:132805231chr22:37622843ENST00000355681-11667_2598.0593.0Coiled coilOntology_term=ECO:0000269
HgeneFNBP1chr9:132805231chr22:37622843ENST00000446176-117398_4908.0618.0Coiled coilOntology_term=ECO:0000250
HgeneFNBP1chr9:132805231chr22:37622843ENST00000446176-11767_2598.0618.0Coiled coilOntology_term=ECO:0000269
HgeneFNBP1chr9:132805231chr22:37622843ENST00000355681-116340_3458.0593.0Compositional biasNote=Poly-Pro
HgeneFNBP1chr9:132805231chr22:37622843ENST00000446176-117340_3458.0618.0Compositional biasNote=Poly-Pro
HgeneFNBP1chr9:132805231chr22:37622843ENST00000355681-1161_2648.0593.0DomainF-BAR
HgeneFNBP1chr9:132805231chr22:37622843ENST00000355681-116404_4818.0593.0DomainREM-1
HgeneFNBP1chr9:132805231chr22:37622843ENST00000355681-116550_6118.0593.0DomainSH3
HgeneFNBP1chr9:132805231chr22:37622843ENST00000446176-1171_2648.0618.0DomainF-BAR
HgeneFNBP1chr9:132805231chr22:37622843ENST00000446176-117404_4818.0618.0DomainREM-1
HgeneFNBP1chr9:132805231chr22:37622843ENST00000446176-117550_6118.0618.0DomainSH3
HgeneFNBP1chr9:132805231chr22:37622843ENST00000355681-1161_798.0593.0RegionNote=Required for self-association and induction of membrane tubulation
HgeneFNBP1chr9:132805231chr22:37622843ENST00000355681-116251_6178.0593.0RegionNote=Required for self-association and induction of membrane tubulation
HgeneFNBP1chr9:132805231chr22:37622843ENST00000446176-1171_798.0618.0RegionNote=Required for self-association and induction of membrane tubulation
HgeneFNBP1chr9:132805231chr22:37622843ENST00000446176-117251_6178.0618.0RegionNote=Required for self-association and induction of membrane tubulation
TgeneRAC2chr9:132805231chr22:37622843ENST000002490714732_40149.33333333333334420.6666666666667MotifEffector region
TgeneRAC2chr9:132805231chr22:37622843ENST000002490714710_17149.33333333333334420.6666666666667Nucleotide bindingGTP
TgeneRAC2chr9:132805231chr22:37622843ENST0000024907147115_118149.33333333333334420.6666666666667Nucleotide bindingGTP
TgeneRAC2chr9:132805231chr22:37622843ENST000002490714757_61149.33333333333334420.6666666666667Nucleotide bindingGTP


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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
FNBP1
RAC2


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
HgeneFNBP1chr9:132805231chr22:37622843ENST00000355681-116550_6178.0593.0ARHGAP17%2C DAAM1%2C DIAPH1 and DIAPH2
HgeneFNBP1chr9:132805231chr22:37622843ENST00000446176-117550_6178.0618.0ARHGAP17%2C DAAM1%2C DIAPH1 and DIAPH2
HgeneFNBP1chr9:132805231chr22:37622843ENST00000355681-116535_6178.0593.0DNM1 and DNM3
HgeneFNBP1chr9:132805231chr22:37622843ENST00000446176-117535_6178.0618.0DNM1 and DNM3
HgeneFNBP1chr9:132805231chr22:37622843ENST00000355681-116553_6098.0593.0DNM2 and WASL
HgeneFNBP1chr9:132805231chr22:37622843ENST00000446176-117553_6098.0618.0DNM2 and WASL
HgeneFNBP1chr9:132805231chr22:37622843ENST00000355681-116553_6108.0593.0FASLG
HgeneFNBP1chr9:132805231chr22:37622843ENST00000446176-117553_6108.0618.0FASLG
HgeneFNBP1chr9:132805231chr22:37622843ENST00000355681-1161_3358.0593.0microtubules
HgeneFNBP1chr9:132805231chr22:37622843ENST00000446176-1171_3358.0618.0microtubules
HgeneFNBP1chr9:132805231chr22:37622843ENST00000355681-116495_6178.0593.0PDE6G
HgeneFNBP1chr9:132805231chr22:37622843ENST00000446176-117495_6178.0618.0PDE6G
HgeneFNBP1chr9:132805231chr22:37622843ENST00000355681-116400_5528.0593.0RND2
HgeneFNBP1chr9:132805231chr22:37622843ENST00000446176-117400_5528.0618.0RND2


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Related Drugs to FNBP1-RAC2


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 FNBP1-RAC2


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