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Fusion gene ID: 13223 |
FusionGeneSummary for FBXW7_MGST2 |
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Fusion gene information | Fusion gene name: FBXW7_MGST2 | Fusion gene ID: 13223 | Hgene | Tgene | Gene symbol | FBXW7 | MGST2 | Gene ID | 55294 | 4258 |
Gene name | F-box and WD repeat domain containing 7 | microsomal glutathione S-transferase 2 | |
Synonyms | AGO|CDC4|FBW6|FBW7|FBX30|FBXO30|FBXW6|SEL-10|SEL10|hAgo|hCdc4 | GST2|MGST-II | |
Cytomap | 4q31.3 | 4q31.1 | |
Type of gene | protein-coding | protein-coding | |
Description | F-box/WD repeat-containing protein 7F-box and WD repeat domain containing 7, E3 ubiquitin protein ligaseF-box and WD-40 domain protein 7 (archipelago homolog, Drosophila)F-box protein FBW7F-box protein FBX30F-box protein SEL-10archipelagohomolog of | microsomal glutathione S-transferase 2microsomal GST-2microsomal GST-II | |
Modification date | 20180527 | 20180523 | |
UniProtAcc | Q969H0 | Q99735 | |
Ensembl transtripts involved in fusion gene | ENST00000281708, ENST00000603548, ENST00000604872, ENST00000296555, ENST00000263981, ENST00000393956, ENST00000603841, ENST00000604095, | ENST00000515137, ENST00000265498, ENST00000506797, | |
Fusion gene scores | * DoF score | 9 X 5 X 7=315 | 7 X 4 X 6=168 |
# samples | 10 | 8 | |
** MAII score | log2(10/315*10)=-1.65535182861255 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(8/168*10)=-1.0703893278914 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: FBXW7 [Title/Abstract] AND MGST2 [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 | FBXW7 | GO:0016567 | protein ubiquitination | 12354302|15103331 |
Hgene | FBXW7 | GO:0031146 | SCF-dependent proteasomal ubiquitin-dependent protein catabolic process | 15103331|17434132 |
Hgene | FBXW7 | GO:0031398 | positive regulation of protein ubiquitination | 12628165 |
Hgene | FBXW7 | GO:0045741 | positive regulation of epidermal growth factor-activated receptor activity | 20208556 |
Hgene | FBXW7 | GO:0050821 | protein stabilization | 20208556 |
Hgene | FBXW7 | GO:0051443 | positive regulation of ubiquitin-protein transferase activity | 12628165 |
Hgene | FBXW7 | GO:1901800 | positive regulation of proteasomal protein catabolic process | 23858059 |
Hgene | FBXW7 | GO:1903378 | positive regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway | 23858059 |
Hgene | FBXW7 | GO:2000060 | positive regulation of ubiquitin-dependent protein catabolic process | 20208556 |
Tgene | MGST2 | GO:0006629 | lipid metabolic process | 9278457 |
Tgene | MGST2 | GO:0006750 | glutathione biosynthetic process | 8703034 |
Tgene | MGST2 | GO:0019370 | leukotriene biosynthetic process | 8703034|9092565|23409838 |
Tgene | MGST2 | GO:0046466 | membrane lipid catabolic process | 23409838 |
![]() (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 | LD | BRCA | TCGA-A1-A0SP-01A | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
* 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 |
5CDS-3UTR | ENST00000281708 | ENST00000515137 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
5CDS-intron | ENST00000281708 | ENST00000265498 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
5CDS-intron | ENST00000281708 | ENST00000506797 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
5CDS-3UTR | ENST00000603548 | ENST00000515137 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
5CDS-intron | ENST00000603548 | ENST00000265498 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
5CDS-intron | ENST00000603548 | ENST00000506797 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
intron-3UTR | ENST00000604872 | ENST00000515137 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
intron-intron | ENST00000604872 | ENST00000265498 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
intron-intron | ENST00000604872 | ENST00000506797 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
5CDS-3UTR | ENST00000296555 | ENST00000515137 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
5CDS-intron | ENST00000296555 | ENST00000265498 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
5CDS-intron | ENST00000296555 | ENST00000506797 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
5CDS-3UTR | ENST00000263981 | ENST00000515137 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
5CDS-intron | ENST00000263981 | ENST00000265498 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
5CDS-intron | ENST00000263981 | ENST00000506797 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
5CDS-3UTR | ENST00000393956 | ENST00000515137 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
5CDS-intron | ENST00000393956 | ENST00000265498 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
5CDS-intron | ENST00000393956 | ENST00000506797 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
5CDS-3UTR | ENST00000603841 | ENST00000515137 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
5CDS-intron | ENST00000603841 | ENST00000265498 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
5CDS-intron | ENST00000603841 | ENST00000506797 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
intron-3UTR | ENST00000604095 | ENST00000515137 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
intron-intron | ENST00000604095 | ENST00000265498 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
intron-intron | ENST00000604095 | ENST00000506797 | FBXW7 | chr4 | 153268082 | - | MGST2 | chr4 | 140661366 | + |
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FusionProtFeatures for FBXW7_MGST2 |
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Hgene | Tgene |
FBXW7 | MGST2 |
Substrate recognition component of a SCF (SKP1-CUL1-F-box protein) E3 ubiquitin-protein ligase complex which mediatesthe ubiquitination and subsequent proteasomal degradation oftarget proteins. Recognizes and binds phosphorylatedsites/phosphodegrons within target proteins and thereafter bringthem to the SCF complex for ubiquitination (PubMed:17434132).Identified substrates include cyclin-E (CCNE1 or CCNE2), JUN, MYC,NOTCH1 released notch intracellular domain (NICD), NOTCH2, MCL1,and probably PSEN1 (PubMed:11565034, PubMed:12354302,PubMed:11585921, PubMed:15103331, PubMed:14739463,PubMed:17558397, PubMed:17873522, PubMed:22608923,PubMed:29149593, PubMed:25775507, PubMed:28007894). Acts as anegative regulator of JNK signaling by binding to phosphorylatedJUN and promoting its ubiquitination and subsequent degradation(PubMed:14739463). SCF(FBXW7) complex mediates the ubiquitinationand subsequent degradation of NFE2L1 (By similarity). Involved inbone homeostasis and negative regulation of osteoclastdifferentiation (PubMed:29149593). {ECO:0000250|UniProtKB:Q8VBV4,ECO:0000269|PubMed:11565034, ECO:0000269|PubMed:11585921,ECO:0000269|PubMed:14739463, ECO:0000269|PubMed:15103331,ECO:0000269|PubMed:17434132, ECO:0000269|PubMed:17558397,ECO:0000269|PubMed:17873522, ECO:0000269|PubMed:22608923,ECO:0000269|PubMed:25775507, ECO:0000269|PubMed:28007894,ECO:0000269|PubMed:29149593, ECO:0000305|PubMed:12354302}. | Can catalyze the production of LTC4 from LTA4 andreduced glutathione. Can catalyze the conjugation of 1-chloro-2,4-dinitrobenzene with reduced glutathione. |
![]() * 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 FBXW7_MGST2 |
![]() (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 FBXW7_MGST2 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
FBXW7 | NFKB2, CCNE1, PARK2, SKP1, MMS22L, LINGO1, KIAA1875, SUMF2, ARL6IP1, SHPRH, CUL1, PSEN1, NOTCH1, MTOR, MYB, HIPK2, PPARGC1A, MYC, SREBF1, KLF5, GNB2L1, CCNE2, MYCN, AURKA, DCLRE1C, HIF1A, EIF3E, FBXW7, NFE2L1, PIN1, TP63, RBX1, EBNA1BP2, USP28, TOP2A, PSMA2, REST, GSK3B, RICTOR, GLMN, JAG1, BTG1, CDC34, AURKB, MED12, MED1, MED13, MED13L, MED14, MED23, MED16, MED15, MED4, MED8, MED24, MED20, MED22, MED27, MED10, MED9, MED17, MED11, MED19, MED21, MED28, MED29, MED30, MED31, MED6, CCNC, CCDC6, STOML1, CDK2, HSP90AA1, KLF2, PTEN, NCOA3, CSF3R, UBE2QL1, MAP4K1, EYA1, YAP1, DAB2IP, MCL1, MOV10, NXF1, USP36, SNCA, CRY2, GATA3, CUL7, BUB1B, FANCD2, RAB4B, RAG1, RFWD3, KRAS, MAPK3, ANGPTL4, BCAS3, BEX1, IL24, SCGB3A1, TRIM25, GATA2, NFE2L3, RUNX2, FAM83D, RND3, MYCBP2, FBXO45, HECTD1, CCT3, HSF1, FKBP5, DDX39A, YBX1, SERBP1, RAE1, FMR1, RPL29, SF3A3, TSEN34, BCAS2, RPL10L, CPSF3, NMT1, RBM28, SPRYD3, IPO4, CDK8, DDX17, EP400, NAA10, ARID4B, FAM60A, GTF3C2, MAX, TAF9, RCOR1, HIST1H2AD, HIST1H1E, CREB3L2, MORF4L2, CEBPZ, SIN3A, SSRP1, RIOK1, PPP1CB, ACLY, CSNK1A1L, SMU1, GFPT2, ATG16L2, DPM1, HADHA, TUBBP2, TUBA1C, TMOD3, ACTR2, PRPH, MAP7D1, MAGEF1, AP3D1, CLASP1, SNX8, PSMA4, MYO5A, MAGEC2, ENO1, FGA, RERE, GAK, CPSF1, OSGIN2, SPAG11B, MS4A1, CDH19, HERC2P2, PVRL3, SUPT6H, MPPED1, GAMTP1, SSBP1, TXLNGY, SSH2, CYBB, CYLD, PUF60, CMIP, RSBN1L, C6orf136, EPOR, GRM3, NAPG, TBX4, GGCT, MASTL, DDO, KATNAL1, RSPRY1, MOCS1, NDUFB9, NELFE, NCOR1, TRAT1, EXOSC4, TMEM126B, C8orf44, ACTR5, C5orf64, SOX7, GMDS, MEP1A, PTPRN2, CTDP1, UBAC1, NAT8B, RNPC3, VPS16, MTFMT, ZC3H18, SPRED1, SNRNP70, LETM2, EBF3, SPTBN1, PHF20L1, CINP, EIF4E3, COL1A2, SLC35A1, DIDO1, TNFRSF19, TMEM65, LINC00173, AP2A1, EIF4A3, TUBA1B, ZCCHC3, EFHC1, DNAJC21, MMAA, C5orf51, LRRTM1, LCE1B, COPS6, FAM32A, TBCB, ITGAV, POLR2K, SNRPB2, BARX2, CTIF, DUSP16, OR51V1, COL12A1, CDK18, PTGDS, SLC17A1, COPS3, TRIM58, ZFR, SRBD1, SHROOM4, RALYL, NUDT4P1, GRIK3, DLC1, RBMX, PALM2-AKAP2, CDR2, LPA, SPDL1, H2AFY2, C5orf15, SENP7, ALKBH8, ZNF563, PRPSAP1, SNRPF, TJP2, RERG, B3GALNT2, BRAF, JUN, SOX10, DEPTOR, FOXM1, C1orf86, STAT3, PLK1, CDX2, CTNNB1, SOX9, PA2G4, EGLN2, STYX, FBXW2, PRR36, CREB3L1, TRAF2, TP53, MAGEA1, ARHGDIA, EXT1, TSC22D4, PLK2, NONO, HNRNPK, BLM, DISC1 | MGST2 | MGST2, RELL2 |
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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 FBXW7_MGST2 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Tgene | MGST2 | Q99735 | DB00143 | Glutathione | Microsomal glutathione S-transferase 2 | small molecule | approved|investigational|nutraceutical |
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RelatedDiseases for FBXW7_MGST2 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | FBXW7 | C1961099 | Precursor T-Cell Lymphoblastic Leukemia-Lymphoma | 2 | CTD_human |
Hgene | FBXW7 | C0007117 | Basal cell carcinoma | 1 | CTD_human |
Hgene | FBXW7 | C0010606 | Adenoid Cystic Carcinoma | 1 | CTD_human |
Hgene | FBXW7 | C0014170 | Endometrial Neoplasms | 1 | CTD_human |
Hgene | FBXW7 | C0017638 | Glioma | 1 | CTD_human |
Hgene | FBXW7 | C0279626 | Squamous cell carcinoma of esophagus | 1 | CTD_human |
Hgene | FBXW7 | C0919532 | Genomic Instability | 1 | CTD_human |
Hgene | FBXW7 | C1458155 | Mammary Neoplasms | 1 | CTD_human |