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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:NCKIPSD-RIMKLB

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: NCKIPSD-RIMKLB
FusionPDB ID: 57650
FusionGDB2.0 ID: 57650
HgeneTgene
Gene symbol

NCKIPSD

RIMKLB

Gene ID

51517

57494

Gene nameNCK interacting protein with SH3 domainribosomal modification protein rimK like family member B
SynonymsAF3P21|DIP|DIP1|ORF1|SPIN90|VIP54|WASLBP|WISHFAM80B|NAAGS|NAAGS-I
Cytomap

3p21.31

12p13.31

Type of geneprotein-codingprotein-coding
DescriptionNCK-interacting protein with SH3 domain54 kDa VacA-interacting protein54 kDa vimentin-interacting protein90 kDa SH3 protein interacting with NckSH3 adapter protein SPIN90SH3 protein interacting with Nck, 90 kDaWASP-interacting SH3-domain proteindiabeta-citrylglutamate synthase BN-acetyl-aspartyl-glutamate synthetase BN-acetyl-aspartylglutamate synthetase BN-acetylaspartyl-glutamate synthetase BNAAG synthetase Bbeta-citryl-glutamate synthase Bfamily with sequence similarity 80, member Briboso
Modification date2020031320200313
UniProtAcc

Q9NZQ3

.
Ensembl transtripts involved in fusion geneENST idsENST00000294129, ENST00000341520, 
ENST00000416649, 
ENST00000299673, 
ENST00000538135, ENST00000357529, 
ENST00000535829, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score4 X 4 X 4=647 X 7 X 5=245
# samples 49
** MAII scorelog2(4/64*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/245*10)=-1.4447848426729
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: NCKIPSD [Title/Abstract] AND RIMKLB [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)NCKIPSD(48719477)-RIMKLB(8904552), # samples:1
Anticipated loss of major functional domain due to fusion event.NCKIPSD-RIMKLB 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.
NCKIPSD-RIMKLB 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.
NCKIPSD-RIMKLB 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.
NCKIPSD-RIMKLB 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 NCKIPSD (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 RIMKLB (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-Cancer135NNCKIPSDchr3

48719477

-RIMKLBchr12

8904552

+


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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)
ENST00000341520NCKIPSDchr348719477-ENST00000535829RIMKLBchr128904552+2068692821446454
ENST00000341520NCKIPSDchr348719477-ENST00000357529RIMKLBchr128904552+4854692821446454
ENST00000416649NCKIPSDchr348719477-ENST00000535829RIMKLBchr128904552+2030654651408447
ENST00000416649NCKIPSDchr348719477-ENST00000357529RIMKLBchr128904552+4816654651408447
ENST00000294129NCKIPSDchr348719477-ENST00000535829RIMKLBchr128904552+20947181081472454
ENST00000294129NCKIPSDchr348719477-ENST00000357529RIMKLBchr128904552+48807181081472454

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
ENST00000341520ENST00000535829NCKIPSDchr348719477-RIMKLBchr128904552+0.0021647320.99783534
ENST00000341520ENST00000357529NCKIPSDchr348719477-RIMKLBchr128904552+0.000248670.99975127
ENST00000416649ENST00000535829NCKIPSDchr348719477-RIMKLBchr128904552+0.0018756770.9981243
ENST00000416649ENST00000357529NCKIPSDchr348719477-RIMKLBchr128904552+0.0002062360.9997938
ENST00000294129ENST00000535829NCKIPSDchr348719477-RIMKLBchr128904552+0.0019648370.99803513
ENST00000294129ENST00000357529NCKIPSDchr348719477-RIMKLBchr128904552+0.0002337660.9997663

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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

>57650_57650_1_NCKIPSD-RIMKLB_NCKIPSD_chr3_48719477_ENST00000294129_RIMKLB_chr12_8904552_ENST00000357529_length(amino acids)=454AA_BP=203
MPGLMYRALYAFRSAEPNALAFAAGETFLVLERSSAHWWLAARARSGETGYVPPAYLRRLQGLEQDVLQAIDRAIEAVHNTAMRDGGKYS
LEQRGVLQKLIHHRKETLSRRGPSASSVAVMTSSTSDHHLDAAAARQPNGVCRAGFERQHSLPSSEHLGADGGLYQIPLPSSQIPPQPRR
AAPTTPPPPVKRRDREALMASGSGGHENFAKMIDEAEVLEFPMVVKNTRGHRGKAVFLARDKHHLADLSHLIRHEAPYLFQKYVKESHGR
DVRVIVVGGRVVGTMLRCSTDGRMQSNCSLGGVGMMCSLSEQGKQLAIQVSNILGMDVCGIDLLMKDDGSFCVCEANANVGFIAFDKACN
LDVAGIIADYAASLLPSGRLTRRMSLLSVVSTASETSEPELGPPASTAVDNMSASSSSVDSDPESTERELLTKLPGGLFNMNQLLANEIK

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

>57650_57650_2_NCKIPSD-RIMKLB_NCKIPSD_chr3_48719477_ENST00000294129_RIMKLB_chr12_8904552_ENST00000535829_length(amino acids)=454AA_BP=203
MPGLMYRALYAFRSAEPNALAFAAGETFLVLERSSAHWWLAARARSGETGYVPPAYLRRLQGLEQDVLQAIDRAIEAVHNTAMRDGGKYS
LEQRGVLQKLIHHRKETLSRRGPSASSVAVMTSSTSDHHLDAAAARQPNGVCRAGFERQHSLPSSEHLGADGGLYQIPLPSSQIPPQPRR
AAPTTPPPPVKRRDREALMASGSGGHENFAKMIDEAEVLEFPMVVKNTRGHRGKAVFLARDKHHLADLSHLIRHEAPYLFQKYVKESHGR
DVRVIVVGGRVVGTMLRCSTDGRMQSNCSLGGVGMMCSLSEQGKQLAIQVSNILGMDVCGIDLLMKDDGSFCVCEANANVGFIAFDKACN
LDVAGIIADYAASLLPSGRLTRRMSLLSVVSTASETSEPELGPPASTAVDNMSASSSSVDSDPESTERELLTKLPGGLFNMNQLLANEIK

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

>57650_57650_3_NCKIPSD-RIMKLB_NCKIPSD_chr3_48719477_ENST00000341520_RIMKLB_chr12_8904552_ENST00000357529_length(amino acids)=454AA_BP=203
MPGLMYRALYAFRSAEPNALAFAAGETFLVLERSSAHWWLAARARSGETGYVPPAYLRRLQGLEQDVLQAIDRAIEAVHNTAMRDGGKYS
LEQRGVLQKLIHHRKETLSRRGPSASSVAVMTSSTSDHHLDAAAARQPNGVCRAGFERQHSLPSSEHLGADGGLYQIPLPSSQIPPQPRR
AAPTTPPPPVKRRDREALMASGSGGHENFAKMIDEAEVLEFPMVVKNTRGHRGKAVFLARDKHHLADLSHLIRHEAPYLFQKYVKESHGR
DVRVIVVGGRVVGTMLRCSTDGRMQSNCSLGGVGMMCSLSEQGKQLAIQVSNILGMDVCGIDLLMKDDGSFCVCEANANVGFIAFDKACN
LDVAGIIADYAASLLPSGRLTRRMSLLSVVSTASETSEPELGPPASTAVDNMSASSSSVDSDPESTERELLTKLPGGLFNMNQLLANEIK

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

>57650_57650_4_NCKIPSD-RIMKLB_NCKIPSD_chr3_48719477_ENST00000341520_RIMKLB_chr12_8904552_ENST00000535829_length(amino acids)=454AA_BP=203
MPGLMYRALYAFRSAEPNALAFAAGETFLVLERSSAHWWLAARARSGETGYVPPAYLRRLQGLEQDVLQAIDRAIEAVHNTAMRDGGKYS
LEQRGVLQKLIHHRKETLSRRGPSASSVAVMTSSTSDHHLDAAAARQPNGVCRAGFERQHSLPSSEHLGADGGLYQIPLPSSQIPPQPRR
AAPTTPPPPVKRRDREALMASGSGGHENFAKMIDEAEVLEFPMVVKNTRGHRGKAVFLARDKHHLADLSHLIRHEAPYLFQKYVKESHGR
DVRVIVVGGRVVGTMLRCSTDGRMQSNCSLGGVGMMCSLSEQGKQLAIQVSNILGMDVCGIDLLMKDDGSFCVCEANANVGFIAFDKACN
LDVAGIIADYAASLLPSGRLTRRMSLLSVVSTASETSEPELGPPASTAVDNMSASSSSVDSDPESTERELLTKLPGGLFNMNQLLANEIK

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

>57650_57650_5_NCKIPSD-RIMKLB_NCKIPSD_chr3_48719477_ENST00000416649_RIMKLB_chr12_8904552_ENST00000357529_length(amino acids)=447AA_BP=196
MPGLMYRALYAFRSAEPNALAFAAGETFLVLERSSAHWWLAARARSGETGYVPPAYLRRLQGLEQDVLQAIDRAIEAVHNTAMRDGGKYS
LEQRGVLQKLIHHRKETLSRRGPSASSVAVMTSSTSDHHLDAAAARQPNGVCRAGFERQHSLPSSEHLGADGGLYQIPPQPRRAAPTTPP
PPVKRRDREALMASGSGGHENFAKMIDEAEVLEFPMVVKNTRGHRGKAVFLARDKHHLADLSHLIRHEAPYLFQKYVKESHGRDVRVIVV
GGRVVGTMLRCSTDGRMQSNCSLGGVGMMCSLSEQGKQLAIQVSNILGMDVCGIDLLMKDDGSFCVCEANANVGFIAFDKACNLDVAGII

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

>57650_57650_6_NCKIPSD-RIMKLB_NCKIPSD_chr3_48719477_ENST00000416649_RIMKLB_chr12_8904552_ENST00000535829_length(amino acids)=447AA_BP=196
MPGLMYRALYAFRSAEPNALAFAAGETFLVLERSSAHWWLAARARSGETGYVPPAYLRRLQGLEQDVLQAIDRAIEAVHNTAMRDGGKYS
LEQRGVLQKLIHHRKETLSRRGPSASSVAVMTSSTSDHHLDAAAARQPNGVCRAGFERQHSLPSSEHLGADGGLYQIPPQPRRAAPTTPP
PPVKRRDREALMASGSGGHENFAKMIDEAEVLEFPMVVKNTRGHRGKAVFLARDKHHLADLSHLIRHEAPYLFQKYVKESHGRDVRVIVV
GGRVVGTMLRCSTDGRMQSNCSLGGVGMMCSLSEQGKQLAIQVSNILGMDVCGIDLLMKDDGSFCVCEANANVGFIAFDKACNLDVAGII

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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/chr3:48719477/chr12:8904552)
- 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
NCKIPSD

Q9NZQ3

.
FUNCTION: Has an important role in stress fiber formation induced by active diaphanous protein homolog 1 (DRF1). Induces microspike formation, in vivo (By similarity). In vitro, stimulates N-WASP-induced ARP2/3 complex activation in the absence of CDC42 (By similarity). May play an important role in the maintenance of sarcomeres and/or in the assembly of myofibrils into sarcomeres. Implicated in regulation of actin polymerization and cell adhesion. Plays a role in angiogenesis. {ECO:0000250, ECO:0000269|PubMed:22419821}.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
HgeneNCKIPSDchr3:48719477chr12:8904552ENST00000294129-4131_58199.33333333333334723.0DomainSH3
HgeneNCKIPSDchr3:48719477chr12:8904552ENST00000341520-4131_58199.33333333333334723.0DomainSH3
HgeneNCKIPSDchr3:48719477chr12:8904552ENST00000416649-4131_58192.33333333333334716.0DomainSH3
HgeneNCKIPSDchr3:48719477chr12:8904552ENST00000294129-413175_192199.33333333333334723.0MotifNuclear localization signal
HgeneNCKIPSDchr3:48719477chr12:8904552ENST00000341520-413175_192199.33333333333334723.0MotifNuclear localization signal
HgeneNCKIPSDchr3:48719477chr12:8904552ENST00000416649-413175_192192.33333333333334716.0MotifNuclear localization signal
TgeneRIMKLBchr3:48719477chr12:8904552ENST0000035752937193_203135.33333333333334387.0Nucleotide bindingATP
TgeneRIMKLBchr3:48719477chr12:8904552ENST0000053582926193_203135.33333333333334387.0Nucleotide bindingATP
TgeneRIMKLBchr3:48719477chr12:8904552ENST0000053813526193_203135.33333333333334387.0Nucleotide bindingATP

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneNCKIPSDchr3:48719477chr12:8904552ENST00000294129-413171_275199.33333333333334723.0Compositional biasNote=Pro-rich
HgeneNCKIPSDchr3:48719477chr12:8904552ENST00000294129-413197_240199.33333333333334723.0Compositional biasNote=Ser/Thr-rich
HgeneNCKIPSDchr3:48719477chr12:8904552ENST00000294129-413442_487199.33333333333334723.0Compositional biasNote=Leu-rich
HgeneNCKIPSDchr3:48719477chr12:8904552ENST00000294129-413534_601199.33333333333334723.0Compositional biasNote=Leu-rich
HgeneNCKIPSDchr3:48719477chr12:8904552ENST00000341520-413171_275199.33333333333334723.0Compositional biasNote=Pro-rich
HgeneNCKIPSDchr3:48719477chr12:8904552ENST00000341520-413197_240199.33333333333334723.0Compositional biasNote=Ser/Thr-rich
HgeneNCKIPSDchr3:48719477chr12:8904552ENST00000341520-413442_487199.33333333333334723.0Compositional biasNote=Leu-rich
HgeneNCKIPSDchr3:48719477chr12:8904552ENST00000341520-413534_601199.33333333333334723.0Compositional biasNote=Leu-rich
HgeneNCKIPSDchr3:48719477chr12:8904552ENST00000416649-413171_275192.33333333333334716.0Compositional biasNote=Pro-rich
HgeneNCKIPSDchr3:48719477chr12:8904552ENST00000416649-413197_240192.33333333333334716.0Compositional biasNote=Ser/Thr-rich
HgeneNCKIPSDchr3:48719477chr12:8904552ENST00000416649-413442_487192.33333333333334716.0Compositional biasNote=Leu-rich
HgeneNCKIPSDchr3:48719477chr12:8904552ENST00000416649-413534_601192.33333333333334716.0Compositional biasNote=Leu-rich
TgeneRIMKLBchr3:48719477chr12:8904552ENST0000035752937119_304135.33333333333334387.0DomainATP-grasp
TgeneRIMKLBchr3:48719477chr12:8904552ENST0000053582926119_304135.33333333333334387.0DomainATP-grasp
TgeneRIMKLBchr3:48719477chr12:8904552ENST0000053813526119_304135.33333333333334387.0DomainATP-grasp


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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
NCKIPSDall structure
RIMKLB


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 NCKIPSD-RIMKLB


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 NCKIPSD-RIMKLB


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