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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: 22514

FusionGeneSummary for MRPL48_MAGOH

check button Fusion gene summary
Fusion gene informationFusion gene name: MRPL48_MAGOH
Fusion gene ID: 22514
HgeneTgene
Gene symbol

MRPL48

MAGOH

Gene ID

51642

4116

Gene namemitochondrial ribosomal protein L48mago homolog, exon junction complex subunit
SynonymsCGI-118|HSPC290|L48MT|MRP-L48MAGOH1|MAGOHA
Cytomap

11q13.4

1p32.3

Type of geneprotein-codingprotein-coding
Description39S ribosomal protein L48, mitochondrialmitochondrial large ribosomal subunit protein mL48protein mago nashi homologmago homolog, exon junction complex core componentmago-nashi homolog, proliferation-associated
Modification date2018052320180523
UniProtAcc

Q96GC5

P61326

Ensembl transtripts involved in fusion geneENST00000310614, ENST00000535529, 
ENST00000411840, ENST00000398483, 
ENST00000542303, ENST00000314282, 
ENST00000371470, ENST00000371466, 
ENST00000462941, 
Fusion gene scores* DoF score11 X 4 X 8=3521 X 1 X 1=1
# samples 171
** MAII scorelog2(17/352*10)=-1.0500406824996
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: MRPL48 [Title/Abstract] AND MAGOH [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
ChiTaRS3.1BX109950MRPL48chr11

73569262

+MAGOHchr1

53696039

-
* 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
intron-intronENST00000310614ENST00000371470MRPL48chr11

73569262

+MAGOHchr1

53696039

-
intron-intronENST00000310614ENST00000371466MRPL48chr11

73569262

+MAGOHchr1

53696039

-
intron-intronENST00000310614ENST00000462941MRPL48chr11

73569262

+MAGOHchr1

53696039

-
intron-intronENST00000535529ENST00000371470MRPL48chr11

73569262

+MAGOHchr1

53696039

-
intron-intronENST00000535529ENST00000371466MRPL48chr11

73569262

+MAGOHchr1

53696039

-
intron-intronENST00000535529ENST00000462941MRPL48chr11

73569262

+MAGOHchr1

53696039

-
intron-intronENST00000411840ENST00000371470MRPL48chr11

73569262

+MAGOHchr1

53696039

-
intron-intronENST00000411840ENST00000371466MRPL48chr11

73569262

+MAGOHchr1

53696039

-
intron-intronENST00000411840ENST00000462941MRPL48chr11

73569262

+MAGOHchr1

53696039

-
intron-intronENST00000398483ENST00000371470MRPL48chr11

73569262

+MAGOHchr1

53696039

-
intron-intronENST00000398483ENST00000371466MRPL48chr11

73569262

+MAGOHchr1

53696039

-
intron-intronENST00000398483ENST00000462941MRPL48chr11

73569262

+MAGOHchr1

53696039

-
intron-intronENST00000542303ENST00000371470MRPL48chr11

73569262

+MAGOHchr1

53696039

-
intron-intronENST00000542303ENST00000371466MRPL48chr11

73569262

+MAGOHchr1

53696039

-
intron-intronENST00000542303ENST00000462941MRPL48chr11

73569262

+MAGOHchr1

53696039

-
intron-intronENST00000314282ENST00000371470MRPL48chr11

73569262

+MAGOHchr1

53696039

-
intron-intronENST00000314282ENST00000371466MRPL48chr11

73569262

+MAGOHchr1

53696039

-
intron-intronENST00000314282ENST00000462941MRPL48chr11

73569262

+MAGOHchr1

53696039

-

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FusionProtFeatures for MRPL48_MAGOH


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MRPL48

Q96GC5

MAGOH

P61326

Core component of the splicing-dependent multiproteinexon junction complex (EJC) deposited at splice junctions onmRNAs. The EJC is a dynamic structure consisting of core proteinsand several peripheral nuclear and cytoplasmic associated factorsthat join the complex only transiently either during EJC assemblyor during subsequent mRNA metabolism. The EJC marks the positionof the exon-exon junction in the mature mRNA for the geneexpression machinery and the core components remain bound tospliced mRNAs throughout all stages of mRNA metabolism therebyinfluencing downstream processes including nuclear mRNA export,subcellular mRNA localization, translation efficiency andnonsense-mediated mRNA decay (NMD). The MAGOH-RBM8A heterodimerinhibits the ATPase activity of EIF4A3, thereby trapping the ATP-bound EJC core onto spliced mRNA in a stable conformation. TheMAGOH-RBM8A heterodimer interacts with the EJC key regulator PYM1leading to EJC disassembly in the cytoplasm and translationenhancement of EJC-bearing spliced mRNAs by recruiting them to theribosomal 48S preinitiation complex. Involved in the splicingmodulation of BCL2L1/Bcl-X (and probably other apoptotic genes);specifically inhibits formation of proapoptotic isoforms such asBcl-X(S); the function is different from the established EJCassembly. {ECO:0000269|PubMed:12730685,ECO:0000269|PubMed:16209946, ECO:0000269|PubMed:22203037}.

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 MRPL48_MAGOH


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 MRPL48_MAGOH


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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RelatedDrugs for MRPL48_MAGOH


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for MRPL48_MAGOH


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