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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 19172

FusionGeneSummary for KPNA3_SLC7A1

check button Fusion gene summary
Fusion gene informationFusion gene name: KPNA3_SLC7A1
Fusion gene ID: 19172
HgeneTgene
Gene symbol

KPNA3

SLC7A1

Gene ID

3839

6541

Gene namekaryopherin subunit alpha 3solute carrier family 7 member 1
SynonymsIPOA4|SRP1|SRP1gamma|SRP4|hSRP1ATRC1|CAT-1|ERR|HCAT1|REC1L
Cytomap

13q14.2

13q12.3

Type of geneprotein-codingprotein-coding
Descriptionimportin subunit alpha-4SRP1-gammaimportin alpha 4importin alpha Q2importin alpha-3importin subunit alpha-3karyopherin alpha 3 (importin alpha 4)qip2high affinity cationic amino acid transporter 1CAT1amino acid transporter, cationic 1ecotropic retroviral leukemia receptor homologecotropic retroviral receptorecotropic retrovirus receptor homologsolute carrier family 7 (cationic amino acid transpo
Modification date2018052320180523
UniProtAcc

O00505

P30825

Ensembl transtripts involved in fusion geneENST00000261667, ENST00000380752, 
ENST00000473577, 
Fusion gene scores* DoF score8 X 5 X 7=2802 X 2 X 2=8
# samples 92
** MAII scorelog2(9/280*10)=-1.63742992061529
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: KPNA3 [Title/Abstract] AND SLC7A1 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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 button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
TCGARVHNSCTCGA-D6-6827-01AKPNA3chr13

50285027

-SLC7A1chr13

30107119

-
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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
Frame-shiftENST00000261667ENST00000380752KPNA3chr13

50285027

-SLC7A1chr13

30107119

-
5CDS-intronENST00000261667ENST00000473577KPNA3chr13

50285027

-SLC7A1chr13

30107119

-

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FusionProtFeatures for KPNA3_SLC7A1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
KPNA3

O00505

SLC7A1

P30825

Functions in nuclear protein import as an adapterprotein for nuclear receptor KPNB1. Binds specifically anddirectly to substrates containing either a simple or bipartite NLSmotif. Docking of the importin/substrate complex to the nuclearpore complex (NPC) is mediated by KPNB1 through binding tonucleoporin FxFG repeats and the complex is subsequentlytranslocated through the pore by an energy requiring, Ran-dependent mechanism. At the nucleoplasmic side of the NPC, Ranbinds to importin-beta and the three components separate andimportin-alpha and -beta are re-exported from the nucleus to thecytoplasm where GTP hydrolysis releases Ran from importin. Thedirectionality of nuclear import is thought to be conferred by anasymmetric distribution of the GTP- and GDP-bound forms of Ranbetween the cytoplasm and nucleus. In vitro, mediates the nuclearimport of human cytomegalovirus UL84 by recognizing a non-classical NLS. Recognizes NLSs of influenza A virus nucleoproteinprobably through ARM repeats 7-9. High-affinity, low capacity permease involved in thetransport of the cationic amino acids (arginine, lysine andornithine) in non-hepatic tissues. {ECO:0000269|PubMed:10485994}.

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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FusionGeneSequence for KPNA3_SLC7A1


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for KPNA3_SLC7A1


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
KPNA3HNRNPC, FAM50B, ARRB2, ARRB1, NFKB1, KPNB1, RCC1, USP42, MEPCE, SIRT1, CUL3, COIL, ZNF131, BARD1, TP53BP1, CBX5, NACC1, HDAC1, MYOD1, NFE2L2, EPHA2, ERCC3, GATA6, GTF2H1, MCM4, KPNA6, MCM6, MMS19, HSF1, MVP, FTL, MTA1, DDX21, ZBTB24, TSSC4, NUP50, MAT2B, ZCCHC10, RPRD1A, APOL6, SLC5A11, TEX37, POLDIP3, APEX1, IER2, HSPB1, ACTR1A, CANX, CLGN, COPB1, GNL1, HSP90B1, IPO8, IPO9, KPNA2, NRD1, KPNA4, TMCO1, NTRK1, KIF22, NCBP1, NUP153, NCBP2, C10orf12, KMT2E, UBXN7, RBBP4, FAM204A, CTDSPL2, PPM1D, MECP2, B2M, LMNA, GTF2IRD1, BRCA1SLC7A1ELAVL1, APP, BAG3, FATE1, TMEM17, SLC33A1, UBXN8, RAC3, BCL2L13, METTL7A, MTCH2, DGAT1, ZDHHC21, TMEM120B, TMEM11, STX4, LEMD2, AGPAT3, SLC35B2, TVP23C, MGAT5, AGPAT4, FKRP, FLVCR1, SLC39A1, SLC19A2, YIPF4, TSPAN15, STX12, MBOAT7, ELOVL5, FITM2, MAVS, C9orf91, GNPAT, CYB5R1, NDC1, CKAP4, ACP2, GHITM, SGPP1, PIGW, TMEM223, SYNGR2, KIAA1715, CMTM4, GPR89A, YIPF6, TMEM186, GPRC5C, GOLM1, SLC22A18, PRAF2, ZDHHC9, C19orf52, ELOVL4, NAT14, HS2ST1, PARL, LMNA


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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RelatedDrugs for KPNA3_SLC7A1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneSLC7A1P30825DB00123L-LysineHigh affinity cationic amino acid transporter 1small moleculeapproved|nutraceutical
TgeneSLC7A1P30825DB00125L-ArginineHigh affinity cationic amino acid transporter 1small moleculeapproved|nutraceutical

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RelatedDiseases for KPNA3_SLC7A1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneKPNA3C0036341Schizophrenia3PSYGENET
HgeneKPNA3C0001973Alcoholic Intoxication, Chronic1PSYGENET
HgeneKPNA3C0041696Unipolar Depression1PSYGENET
HgeneKPNA3C1269683Major Depressive Disorder1PSYGENET
TgeneSLC7A1C0023893Liver Cirrhosis, Experimental1CTD_human
TgeneSLC7A1C0033578Prostatic Neoplasms1CTD_human