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Fusion gene ID: 40849 |
FusionGeneSummary for UPF1_EIF3M |
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Fusion gene information | Fusion gene name: UPF1_EIF3M | Fusion gene ID: 40849 | Hgene | Tgene | Gene symbol | UPF1 | EIF3M | Gene ID | 5976 | 10480 |
Gene name | UPF1, RNA helicase and ATPase | eukaryotic translation initiation factor 3 subunit M | |
Synonyms | HUPF1|NORF1|RENT1|pNORF1|smg-2 | B5|GA17|PCID1|TANGO7|hfl-B5 | |
Cytomap | 19p13.11 | 11p13 | |
Type of gene | protein-coding | protein-coding | |
Description | regulator of nonsense transcripts 1ATP-dependent helicase RENT1UPF1 regulator of nonsense transcripts homologdelta helicasenonsense mRNA reducing factor 1smg-2 homolog, nonsense mediated mRNA decay factorup-frameshift mutation 1 homologup-frameshif | eukaryotic translation initiation factor 3 subunit MB5 receptorPCI domain containing 1 (herpesvirus entry mediator)PCI domain-containing protein 1dendritic cell proteinfetal lung protein B5transport and golgi organization 7 homolog | |
Modification date | 20180523 | 20180523 | |
UniProtAcc | Q92900 | Q7L2H7 | |
Ensembl transtripts involved in fusion gene | ENST00000262803, ENST00000599848, ENST00000600310, | ENST00000531120, ENST00000524896, ENST00000532054, | |
Fusion gene scores | * DoF score | 5 X 6 X 4=120 | 7 X 5 X 4=140 |
# samples | 5 | 8 | |
** MAII score | log2(5/120*10)=-1.26303440583379 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(8/140*10)=-0.807354922057604 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: UPF1 [Title/Abstract] AND EIF3M [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) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | UPF1 | GO:0000184 | nuclear-transcribed mRNA catabolic process, nonsense-mediated decay | 17468741 |
Hgene | UPF1 | GO:0006281 | DNA repair | 16488880 |
Hgene | UPF1 | GO:0032201 | telomere maintenance via semi-conservative replication | 21829167 |
Hgene | UPF1 | GO:0071222 | cellular response to lipopolysaccharide | 26255671 |
Hgene | UPF1 | GO:0071347 | cellular response to interleukin-1 | 26255671 |
![]() (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 type | Source | Cancer type | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
TCGA | RV | PRAD | TCGA-EJ-5494-01A | UPF1 | chr19 | 18979038 | + | EIF3M | chr11 | 32611132 | + |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
![]() * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
ORF | Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
3UTR-3CDS | ENST00000262803 | ENST00000531120 | UPF1 | chr19 | 18979038 | + | EIF3M | chr11 | 32611132 | + |
3UTR-3CDS | ENST00000262803 | ENST00000524896 | UPF1 | chr19 | 18979038 | + | EIF3M | chr11 | 32611132 | + |
3UTR-intron | ENST00000262803 | ENST00000532054 | UPF1 | chr19 | 18979038 | + | EIF3M | chr11 | 32611132 | + |
Frame-shift | ENST00000599848 | ENST00000531120 | UPF1 | chr19 | 18979038 | + | EIF3M | chr11 | 32611132 | + |
Frame-shift | ENST00000599848 | ENST00000524896 | UPF1 | chr19 | 18979038 | + | EIF3M | chr11 | 32611132 | + |
5CDS-intron | ENST00000599848 | ENST00000532054 | UPF1 | chr19 | 18979038 | + | EIF3M | chr11 | 32611132 | + |
intron-3CDS | ENST00000600310 | ENST00000531120 | UPF1 | chr19 | 18979038 | + | EIF3M | chr11 | 32611132 | + |
intron-3CDS | ENST00000600310 | ENST00000524896 | UPF1 | chr19 | 18979038 | + | EIF3M | chr11 | 32611132 | + |
intron-intron | ENST00000600310 | ENST00000532054 | UPF1 | chr19 | 18979038 | + | EIF3M | chr11 | 32611132 | + |
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FusionProtFeatures for UPF1_EIF3M |
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Hgene | Tgene |
UPF1 | EIF3M |
RNA-dependent helicase and ATPase required for nonsense-mediated decay (NMD) of mRNAs containing premature stop codons. Isrecruited to mRNAs upon translation termination and undergoes acycle of phosphorylation and dephosphorylation; itsphosphorylation appears to be a key step in NMD. Recruited byrelease factors to stalled ribosomes together with the SMG1Cprotein kinase complex to form the transient SURF (SMG1-UPF1-eRF1-eRF3) complex. In EJC-dependent NMD, the SURF complex associateswith the exon junction complex (EJC) (located 50-55 or morenucleotides downstream from the termination codon) through UPF2and allows the formation of an UPF1-UPF2-UPF3 surveillance complexwhich is believed to activate NMD. Phosphorylated UPF1 isrecognized by EST1B/SMG5, SMG6 and SMG7 which are thought toprovide a link to the mRNA degradation machinery involvingexonucleolytic and endonucleolytic pathways, and to serve asadapters to protein phosphatase 2A (PP2A), thereby triggering UPF1dephosphorylation and allowing the recycling of NMD factors. UPF1can also activate NMD without UPF2 or UPF3, and in the absence ofthe NMD-enhancing downstream EJC indicative for alternative NMDpathways. Plays a role in replication-dependent histone mRNAdegradation at the end of phase S; the function is independent ofUPF2. For the recognition of premature termination codons (PTC)and initiation of NMD a competitive interaction between UPF1 andPABPC1 with the ribosome-bound release factors is proposed. TheATPase activity of UPF1 is required for disassembly of mRNPsundergoing NMD. Essential for embryonic viability.{ECO:0000269|PubMed:11163187, ECO:0000269|PubMed:16086026,ECO:0000269|PubMed:18172165, ECO:0000269|PubMed:21145460,ECO:0000269|PubMed:21419344}. | Component of the eukaryotic translation initiationfactor 3 (eIF-3) complex, which is required for several steps inthe initiation of protein synthesis (PubMed:17403899,PubMed:25849773, PubMed:27462815). The eIF-3 complex associateswith the 40S ribosome and facilitates the recruitment of eIF-1,eIF-1A, eIF-2:GTP:methionyl-tRNAi and eIF-5 to form the 43S pre-initiation complex (43S PIC). The eIF-3 complex stimulates mRNArecruitment to the 43S PIC and scanning of the mRNA for AUGrecognition. The eIF-3 complex is also required for disassemblyand recycling of post-termination ribosomal complexes andsubsequently prevents premature joining of the 40S and 60Sribosomal subunits prior to initiation (PubMed:17403899). The eIF-3 complex specifically targets and initiates translation of asubset of mRNAs involved in cell proliferation, including cellcycling, differentiation and apoptosis, and uses different modesof RNA stem-loop binding to exert either translational activationor repression (PubMed:25849773). {ECO:0000255|HAMAP-Rule:MF_03012,ECO:0000269|PubMed:17403899, ECO:0000269|PubMed:25849773,ECO:0000269|PubMed:27462815}. (Microbial infection) May favor virus entry in case ofinfection with herpes simplex virus 1 (HSV1) or herpes simplexvirus 2 (HSV2). {ECO:0000269|PubMed:15919898}. |
![]() * 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. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
- In-frame and not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
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FusionGeneSequence for UPF1_EIF3M |
![]() (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 UPF1_EIF3M |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
UPF1 | HIRA, UPF2, UPF3B, DCP2, XRN1, EXOSC2, EXOSC4, PARN, EXOSC10, PABPC1, UPF3A, SMG1, DCP1A, ATR, POLD1, SLBP, HDAC5, CSNK2B, NDRG1, SIRT7, TSG101, CUL3, CUL5, CDK2, COPS5, CAND1, RNPS1, HNRNPU, HDLBP, VPS35, TMX1, SMG8, SMG9, RBM8A, RPL11, RPS6, EEF2, GSPT1, RPL7A, RPS3, NCBP1, NCBP2, EIF4A3, MAGOH, ESR1, HBB, SMG5, SMG7, SMG6, ETF1, EDC4, EDC3, ADAR, SNRPN, SNRPB, VCAM1, FN1, YWHAQ, EIF3A, EIF3B, EIF2S1, EIF2S2, ITGA4, FUS, GSPT2, RUVBL1, RUVBL2, PLEKHB2, NADSYN1, ACSS2, ABHD16A, RHOXF2, RPRD2, GNPTG, NDUFB10, DXO, LSM8, PLEKHA5, TARDBP, LIN28A, MOV10, POP1, STAU1, STAU2, DNA2, CDC37, IVNS1ABP, EZH2, SUZ12, RNF2, BMI1, HIST1H1A, TRA2A, RPL6, NIFK, MEMO1, ZC3H3, HNRNPA1, PRR11, ILF2, ABCF3, DIAPH1, HNRNPR, SMARCA4, SYNCRIP, TTC4, UBL7, DDX5, NTRK1, IFI16, FBXW11, EWSR1, CEP170, CEP104, CEP162, CNTRL, NIN, RPGRIP1L, SCLT1, DCTN1, CEP19, STIL, XPO1, CNOT2, OAZ1, SORT1, SAMD1, SNW1, CDC5L, PCGF1, DPPA4, POU5F1, U2AF2, WDR46, ELAVL2, GLTSCR2, DGCR8, APOBEC3D, CDX1, SNRNP70, HIST1H1T, PRDM5, ZCRB1, STRBP, HIST1H1E, ZC3H18, E4F1, H2AFX, NXF2, ZC3HAV1, PPAN, RPF1, NSA2, ZFC3H1, FGF8, ZNF576, RBM3, CYLD, TRIM25, G3BP1, BRCA1, YAP1 | EIF3M | EIF1B, EIF4A2, EIF3A, EIF3F, EIF3H, TADA2A, EIF3B, APP, EIF3C, EIF3E, EIF3D, EIF3I, EIF3K, EIF3L, EIF3G, MMS19, NPM1, EXOSC10, SRPK1, FAM96B, HUWE1, EGFR, EIF3CL, USP34, HSPB1, AHCYL1, COPS4, RPN1, EIF3J, NTRK1, MED4, HERC2, NF2, PTP4A1, PSMD12, EIF4A1, GPBP1L1, UBE2N, CYLD, DLD, TRIM25, G3BP1, BRCA1 |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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RelatedDrugs for UPF1_EIF3M |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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RelatedDiseases for UPF1_EIF3M |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |