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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:KPNA1-CHRNA9 (FusionGDB2 ID:43356)

Fusion Gene Summary for KPNA1-CHRNA9

check button Fusion gene summary
Fusion gene informationFusion gene name: KPNA1-CHRNA9
Fusion gene ID: 43356
HgeneTgene
Gene symbol

KPNA1

CHRNA9

Gene ID

3836

55584

Gene namekaryopherin subunit alpha 1cholinergic receptor nicotinic alpha 9 subunit
SynonymsIPOA5|NPI-1|RCH2|SRP1HSA243342|NACHRA9
Cytomap

3q21.1

4p14

Type of geneprotein-codingprotein-coding
Descriptionimportin subunit alpha-5RAG cohort protein 2SRP1-betaimportin alpha 5importin subunit alpha-1importin-alpha-S1karyopherin alpha 1 (importin alpha 5)nucleoprotein interactor 1recombination activating gene cohort 2neuronal acetylcholine receptor subunit alpha-9NACHR alpha 9acetylcholine receptor, neuronal nicotinic, alpha-9 subunitcholinergic receptor, nicotinic alpha 9cholinergic receptor, nicotinic, alpha 9 (neuronal)cholinergic receptor, nicotinic, alpha po
Modification date2020031320200313
UniProtAcc

P52294

Q9UGM1

Ensembl transtripts involved in fusion geneENST00000344337, ENST00000466923, 
ENST00000310169, ENST00000502377, 
Fusion gene scores* DoF score19 X 10 X 13=24704 X 4 X 4=64
# samples 265
** MAII scorelog2(26/2470*10)=-3.24792751344359
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/64*10)=-0.356143810225275
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: KPNA1 [Title/Abstract] AND CHRNA9 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointKPNA1(122233604)-CHRNA9(40350899), # samples:3
Anticipated loss of major functional domain due to fusion event.
* 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 KPNA1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across CHRNA9 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

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
ChimerDB4CESCTCGA-LP-A5U2-01AKPNA1chr3

122233604

-CHRNA9chr4

40350899

+
ChimerDB4CESCTCGA-LP-A5U2-01AKPNA1chr3

122233604

-CHRNA9chr4

40355996

+
ChimerDB4CESCTCGA-LP-A5U2KPNA1chr3

122233603

-CHRNA9chr4

40350898

+


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Fusion Gene ORF analysis for KPNA1-CHRNA9

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
5UTR-3CDSENST00000344337ENST00000310169KPNA1chr3

122233604

-CHRNA9chr4

40350899

+
5UTR-3CDSENST00000344337ENST00000310169KPNA1chr3

122233604

-CHRNA9chr4

40355996

+
5UTR-3CDSENST00000344337ENST00000310169KPNA1chr3

122233603

-CHRNA9chr4

40350898

+
5UTR-intronENST00000344337ENST00000502377KPNA1chr3

122233604

-CHRNA9chr4

40350899

+
5UTR-intronENST00000344337ENST00000502377KPNA1chr3

122233604

-CHRNA9chr4

40355996

+
5UTR-intronENST00000344337ENST00000502377KPNA1chr3

122233603

-CHRNA9chr4

40350898

+
intron-3CDSENST00000466923ENST00000310169KPNA1chr3

122233604

-CHRNA9chr4

40350899

+
intron-3CDSENST00000466923ENST00000310169KPNA1chr3

122233604

-CHRNA9chr4

40355996

+
intron-3CDSENST00000466923ENST00000310169KPNA1chr3

122233603

-CHRNA9chr4

40350898

+
intron-intronENST00000466923ENST00000502377KPNA1chr3

122233604

-CHRNA9chr4

40350899

+
intron-intronENST00000466923ENST00000502377KPNA1chr3

122233604

-CHRNA9chr4

40355996

+
intron-intronENST00000466923ENST00000502377KPNA1chr3

122233603

-CHRNA9chr4

40350898

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

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

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Fusion Genomic Features for KPNA1-CHRNA9


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)
KPNA1chr3122233603-CHRNA9chr440350898+2.16E-070.99999976
KPNA1chr3122233603-CHRNA9chr440350898+2.16E-070.99999976
KPNA1chr3122233603-CHRNA9chr440355995+1.66E-081
KPNA1chr3122233603-CHRNA9chr440350898+2.16E-070.99999976
KPNA1chr3122233603-CHRNA9chr440350898+2.16E-070.99999976
KPNA1chr3122233603-CHRNA9chr440355995+1.66E-081

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.
genomic feature of top 1%

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Fusion Protein Features for KPNA1-CHRNA9


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/:122233604/:40350899)
- 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
KPNA1

P52294

CHRNA9

Q9UGM1

FUNCTION: Functions in nuclear protein import as an adapter protein for nuclear receptor KPNB1. Binds specifically and directly to substrates containing either a simple or bipartite NLS motif. Docking of the importin/substrate complex to the nuclear pore complex (NPC) is mediated by KPNB1 through binding to nucleoporin FxFG repeats and the complex is subsequently translocated through the pore by an energy requiring, Ran-dependent mechanism. At the nucleoplasmic side of the NPC, Ran binds to importin-beta and the three components separate and importin-alpha and -beta are re-exported from the nucleus to the cytoplasm where GTP hydrolysis releases Ran from importin. The directionality of nuclear import is thought to be conferred by an asymmetric distribution of the GTP- and GDP-bound forms of Ran between the cytoplasm and nucleus. In vitro, mediates the nuclear import of human cytomegalovirus UL84 by recognizing a non-classical NLS.FUNCTION: Ionotropic receptor with a probable role in the modulation of auditory stimuli. Agonist binding induces a conformation change that leads to the opening of an ion-conducting channel across the plasma membrane (PubMed:11752216, PubMed:25282151). The channel is permeable to a range of divalent cations including calcium, the influx of which may activate a potassium current which hyperpolarizes the cell membrane (PubMed:11752216, PubMed:25282151). In the ear, this may lead to a reduction in basilar membrane motion, altering the activity of auditory nerve fibers and reducing the range of dynamic hearing. This may protect against acoustic trauma. May also regulate keratinocyte adhesion (PubMed:11021840). {ECO:0000269|PubMed:11021840, ECO:0000269|PubMed:11752216, ECO:0000269|PubMed:25282151, ECO:0000305}.

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.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for KPNA1-CHRNA9


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for KPNA1-CHRNA9


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 (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for KPNA1-CHRNA9


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for KPNA1-CHRNA9


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource