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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:UBASH3B-GRIK4

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: UBASH3B-GRIK4
FusionPDB ID: 95950
FusionGDB2.0 ID: 95950
HgeneTgene
Gene symbol

UBASH3B

GRIK4

Gene ID

84959

2900

Gene nameubiquitin associated and SH3 domain containing Bglutamate ionotropic receptor kainate type subunit 4
SynonymsSTS-1|STS1|TULA-2|TULA2|p70EAA1|GRIK|GluK4|KA1
Cytomap

11q24.1

11q23.3

Type of geneprotein-codingprotein-coding
Descriptionubiquitin-associated and SH3 domain-containing protein BCbl-interacting protein Sts-1SH3 domain-containing 70 kDa protein, suppressor of T-cell receptor signaling 1, nm23-phosphorylated unknown substrateT-cell ubiquitin ligand 2cbl-interacting proteinglutamate receptor ionotropic, kainate 4excitatory amino acid receptor 1glutamate receptor KA1glutamate receptor, ionotropic, kainate 4
Modification date2020032720200320
UniProtAcc.

Q16099

Ensembl transtripts involved in fusion geneENST idsENST00000525711, ENST00000284273, 
ENST00000438375, ENST00000527524, 
ENST00000527130, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score7 X 6 X 3=1267 X 11 X 6=462
# samples 810
** MAII scorelog2(8/126*10)=-0.655351828612554
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(10/462*10)=-2.20789285164133
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: UBASH3B [Title/Abstract] AND GRIK4 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)UBASH3B(122526918)-GRIK4(120823564), # samples:3
Anticipated loss of major functional domain due to fusion event.UBASH3B-GRIK4 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.
UBASH3B-GRIK4 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.
UBASH3B-GRIK4 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.
UBASH3B-GRIK4 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.
UBASH3B-GRIK4 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
UBASH3B-GRIK4 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

check buttonFusion gene breakpoints across UBASH3B (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 GRIK4 (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
ChimerDB4SKCMTCGA-FR-A3YO-06AUBASH3Bchr11

122526918

-GRIK4chr11

120823564

+
ChimerDB4SKCMTCGA-FR-A3YO-06AUBASH3Bchr11

122526918

+GRIK4chr11

120823564

+
ChimerDB4SKCMTCGA-FR-A3YO-06AUBASH3Bchr11

122526918

+GRIK4chr11

120827489

+
ChimerDB4SKCMTCGA-FR-A3YO-06AUBASH3Bchr11

122526918

+GRIK4chr11

120831618

+


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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)
ENST00000284273UBASH3Bchr11122526918+ENST00000527524GRIK4chr11120827489+43515363751706443
ENST00000284273UBASH3Bchr11122526918+ENST00000438375GRIK4chr11120827489+27085363751706443
ENST00000284273UBASH3Bchr11122526918+ENST00000527524GRIK4chr11120831618+41775363751532385
ENST00000284273UBASH3Bchr11122526918+ENST00000438375GRIK4chr11120831618+25345363751532385

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
ENST00000284273ENST00000527524UBASH3Bchr11122526918+GRIK4chr11120827489+0.0067529230.99324703
ENST00000284273ENST00000438375UBASH3Bchr11122526918+GRIK4chr11120827489+0.016356960.983643
ENST00000284273ENST00000527524UBASH3Bchr11122526918+GRIK4chr11120831618+0.0042058950.99579406
ENST00000284273ENST00000438375UBASH3Bchr11122526918+GRIK4chr11120831618+0.0121464380.9878535

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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

>95950_95950_1_UBASH3B-GRIK4_UBASH3B_chr11_122526918_ENST00000284273_GRIK4_chr11_120827489_ENST00000438375_length(amino acids)=443AA_BP=49
MAQYGHPSPLGMAAREELYSKVTPRRNRQQRPGTIKHGSALDVLLSMGFPRARALTPYEWYSPHPCAQGRCNLLVNQYSLGNSLWFPVGG
FMQQGSTIAPRALSTRCVSGVWWAFTLIIISSYTANLAAFLTVQRMDVPIESVDDLADQTAIEYGTIHGGSSMTFFQNSRYQTYQRMWNY
MYSKQPSVFVKSTEEGIARVLNSNYAFLLESTMNEYYRQRNCNLTQIGGLLDTKGYGIGMPVGSVFRDEFDLAILQLQENNRLEILKRKW
WEGGKCPKEEDHRAKGLGMENIGGIFVVLICGLIVAIFMAMLEFLWTLRHSEATEVSVCQEMVTELRSIILCQDSIHPRRRRAAVPPPRP

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

>95950_95950_2_UBASH3B-GRIK4_UBASH3B_chr11_122526918_ENST00000284273_GRIK4_chr11_120827489_ENST00000527524_length(amino acids)=443AA_BP=49
MAQYGHPSPLGMAAREELYSKVTPRRNRQQRPGTIKHGSALDVLLSMGFPRARALTPYEWYSPHPCAQGRCNLLVNQYSLGNSLWFPVGG
FMQQGSTIAPRALSTRCVSGVWWAFTLIIISSYTANLAAFLTVQRMDVPIESVDDLADQTAIEYGTIHGGSSMTFFQNSRYQTYQRMWNY
MYSKQPSVFVKSTEEGIARVLNSNYAFLLESTMNEYYRQRNCNLTQIGGLLDTKGYGIGMPVGSVFRDEFDLAILQLQENNRLEILKRKW
WEGGKCPKEEDHRAKGLGMENIGGIFVVLICGLIVAIFMAMLEFLWTLRHSEATEVSVCQEMVTELRSIILCQDSIHPRRRRAAVPPPRP

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

>95950_95950_3_UBASH3B-GRIK4_UBASH3B_chr11_122526918_ENST00000284273_GRIK4_chr11_120831618_ENST00000438375_length(amino acids)=385AA_BP=49
MAQYGHPSPLGMAAREELYSKVTPRRNRQQRPGTIKHGSALDVLLSMGFPRARAWAFTLIIISSYTANLAAFLTVQRMDVPIESVDDLAD
QTAIEYGTIHGGSSMTFFQNSRYQTYQRMWNYMYSKQPSVFVKSTEEGIARVLNSNYAFLLESTMNEYYRQRNCNLTQIGGLLDTKGYGI
GMPVGSVFRDEFDLAILQLQENNRLEILKRKWWEGGKCPKEEDHRAKGLGMENIGGIFVVLICGLIVAIFMAMLEFLWTLRHSEATEVSV
CQEMVTELRSIILCQDSIHPRRRRAAVPPPRPPIPEERRPRGTATLSNGKLCGAGEPDQLAQRLAQEAALVARGCTHIRVCPECRRFQGL

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

>95950_95950_4_UBASH3B-GRIK4_UBASH3B_chr11_122526918_ENST00000284273_GRIK4_chr11_120831618_ENST00000527524_length(amino acids)=385AA_BP=49
MAQYGHPSPLGMAAREELYSKVTPRRNRQQRPGTIKHGSALDVLLSMGFPRARAWAFTLIIISSYTANLAAFLTVQRMDVPIESVDDLAD
QTAIEYGTIHGGSSMTFFQNSRYQTYQRMWNYMYSKQPSVFVKSTEEGIARVLNSNYAFLLESTMNEYYRQRNCNLTQIGGLLDTKGYGI
GMPVGSVFRDEFDLAILQLQENNRLEILKRKWWEGGKCPKEEDHRAKGLGMENIGGIFVVLICGLIVAIFMAMLEFLWTLRHSEATEVSV
CQEMVTELRSIILCQDSIHPRRRRAAVPPPRPPIPEERRPRGTATLSNGKLCGAGEPDQLAQRLAQEAALVARGCTHIRVCPECRRFQGL

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

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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/chr11:122526918/chr11:120823564)
- 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
.GRIK4

Q16099

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.FUNCTION: Receptor for glutamate. L-glutamate acts as an excitatory neurotransmitter at many synapses in the central nervous system. The postsynaptic actions of Glu are mediated by a variety of receptors that are named according to their selective agonists.

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
TgeneGRIK4chr11:122526918chr11:120827489ENST000004383751320862_865566.6666666666666957.0Compositional biasNote=Poly-Arg
TgeneGRIK4chr11:122526918chr11:120827489ENST000005275241421862_865566.6666666666666957.0Compositional biasNote=Poly-Arg
TgeneGRIK4chr11:122526918chr11:120831618ENST000004383751420862_865624.6666666666666957.0Compositional biasNote=Poly-Arg
TgeneGRIK4chr11:122526918chr11:120831618ENST000005275241521862_865624.6666666666666957.0Compositional biasNote=Poly-Arg
TgeneGRIK4chr11:122526918chr11:120827489ENST000004383751320567_623566.6666666666666957.0Topological domainCytoplasmic
TgeneGRIK4chr11:122526918chr11:120827489ENST000004383751320645_804566.6666666666666957.0Topological domainExtracellular
TgeneGRIK4chr11:122526918chr11:120827489ENST000004383751320826_956566.6666666666666957.0Topological domainCytoplasmic
TgeneGRIK4chr11:122526918chr11:120827489ENST000005275241421567_623566.6666666666666957.0Topological domainCytoplasmic
TgeneGRIK4chr11:122526918chr11:120827489ENST000005275241421645_804566.6666666666666957.0Topological domainExtracellular
TgeneGRIK4chr11:122526918chr11:120827489ENST000005275241421826_956566.6666666666666957.0Topological domainCytoplasmic
TgeneGRIK4chr11:122526918chr11:120831618ENST000004383751420645_804624.6666666666666957.0Topological domainExtracellular
TgeneGRIK4chr11:122526918chr11:120831618ENST000004383751420826_956624.6666666666666957.0Topological domainCytoplasmic
TgeneGRIK4chr11:122526918chr11:120831618ENST000005275241521645_804624.6666666666666957.0Topological domainExtracellular
TgeneGRIK4chr11:122526918chr11:120831618ENST000005275241521826_956624.6666666666666957.0Topological domainCytoplasmic
TgeneGRIK4chr11:122526918chr11:120827489ENST000004383751320624_644566.6666666666666957.0TransmembraneHelical
TgeneGRIK4chr11:122526918chr11:120827489ENST000004383751320805_825566.6666666666666957.0TransmembraneHelical
TgeneGRIK4chr11:122526918chr11:120827489ENST000005275241421624_644566.6666666666666957.0TransmembraneHelical
TgeneGRIK4chr11:122526918chr11:120827489ENST000005275241421805_825566.6666666666666957.0TransmembraneHelical
TgeneGRIK4chr11:122526918chr11:120831618ENST000004383751420624_644624.6666666666666957.0TransmembraneHelical
TgeneGRIK4chr11:122526918chr11:120831618ENST000004383751420805_825624.6666666666666957.0TransmembraneHelical
TgeneGRIK4chr11:122526918chr11:120831618ENST000005275241521624_644624.6666666666666957.0TransmembraneHelical
TgeneGRIK4chr11:122526918chr11:120831618ENST000005275241521805_825624.6666666666666957.0TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneUBASH3Bchr11:122526918chr11:120827489ENST00000284273+114254_31953.666666666666664650.0DomainSH3
HgeneUBASH3Bchr11:122526918chr11:120827489ENST00000284273+11427_7653.666666666666664650.0DomainUBA
HgeneUBASH3Bchr11:122526918chr11:120831618ENST00000284273+114254_31953.666666666666664650.0DomainSH3
HgeneUBASH3Bchr11:122526918chr11:120831618ENST00000284273+11427_7653.666666666666664650.0DomainUBA
HgeneUBASH3Bchr11:122526918chr11:120827489ENST00000284273+114380_64953.666666666666664650.0RegionProtein tyrosine phosphatase
HgeneUBASH3Bchr11:122526918chr11:120831618ENST00000284273+114380_64953.666666666666664650.0RegionProtein tyrosine phosphatase
TgeneGRIK4chr11:122526918chr11:120827489ENST00000438375132021_545566.6666666666666957.0Topological domainExtracellular
TgeneGRIK4chr11:122526918chr11:120827489ENST00000527524142121_545566.6666666666666957.0Topological domainExtracellular
TgeneGRIK4chr11:122526918chr11:120831618ENST00000438375142021_545624.6666666666666957.0Topological domainExtracellular
TgeneGRIK4chr11:122526918chr11:120831618ENST000004383751420567_623624.6666666666666957.0Topological domainCytoplasmic
TgeneGRIK4chr11:122526918chr11:120831618ENST00000527524152121_545624.6666666666666957.0Topological domainExtracellular
TgeneGRIK4chr11:122526918chr11:120831618ENST000005275241521567_623624.6666666666666957.0Topological domainCytoplasmic
TgeneGRIK4chr11:122526918chr11:120827489ENST000004383751320546_566566.6666666666666957.0TransmembraneHelical
TgeneGRIK4chr11:122526918chr11:120827489ENST000005275241421546_566566.6666666666666957.0TransmembraneHelical
TgeneGRIK4chr11:122526918chr11:120831618ENST000004383751420546_566624.6666666666666957.0TransmembraneHelical
TgeneGRIK4chr11:122526918chr11:120831618ENST000005275241521546_566624.6666666666666957.0TransmembraneHelical


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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
UBASH3B
GRIK4


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 UBASH3B-GRIK4


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 UBASH3B-GRIK4


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