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Translation Factor: METTL3 (NCBI Gene ID:56339) |
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Gene Information | Gene Name: METTL3 | Gene ID: 56339 | Gene Symbol | METTL3 | Gene ID | 56339 |
Gene Name | methyltransferase like 3 | |
Synonyms | IME4|M6A|MT-A70|Spo8|hMETTL3 | |
Cytomap | 14q11.2 | |
Type of Gene | protein-coding | |
Description | N6-adenosine-methyltransferase catalytic subunitN6-adenosine-methyltransferase 70 kDa subunitadoMet-binding subunit of the human mRNA (N6-adenosine)-methyltransferasemRNA (2'-O-methyladenosine-N(6)-)-methyltransferasemRNA m(6)A methyltransferasemethy | |
Modification date | 20200322 | |
UniProtAcc | Q86U44 |
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GO ID | GO term |
GO:0017148 | Negative regulation of translation |
GO:0006417 | Regulation of translation |
GO:0045727 | Positive regulation of translation |
GO:0002181 | Cytoplasmic translation |
GO:0006413 | Translational initiation |
GO:0006412 | Translation |
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Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | METTL3 | GO:0006974 | cellular response to DNA damage stimulus | 28297716 |
Hgene | METTL3 | GO:0009048 | dosage compensation by inactivation of X chromosome | 27602518 |
Hgene | METTL3 | GO:0031053 | primary miRNA processing | 25799998 |
Hgene | METTL3 | GO:0034644 | cellular response to UV | 28297716 |
Hgene | METTL3 | GO:0080009 | mRNA methylation | 24316715|27281194|27373337|27627798|28297716 |
Hgene | METTL3 | GO:1990744 | primary miRNA methylation | 25799998 |
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Gene | Inferred gene age group among (0 - 67.6], (67.6 - 355.7], (355.7 - 733], (733 - 1119.25], >1119.25 |
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Gene | Title | PMID |
METTL3 | New insight into the catalytic -dependent and -independent roles of METTL3 in sustaining aberrant translation in chronic myeloid leukemia | 34561421 |
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![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. For more annotations, please visit our ExonSkipDB. |
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![]() * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
ENST | Exon skip start (DNA) | Exon Skip end (DNA) | ORF |
ENST00000298717 | 21967449 | 21967515 | In-frame |
ENST00000298717 | 21967907 | 21967946 | In-frame |
ENST00000298717 | 21968636 | 21968824 | Frame-shift |
ENST00000298717 | 21969869 | 21970045 | Frame-shift |
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ENST | Exon skip start (DNA) | Exon Skip end (DNA) | Len(transcript seq) | Exon skip start (mRNA) | Exon Skip end (mRNA) | Len(amino acid seq) | Exon skip start (AA) | Exon Skip end (AA) |
ENST00000298717 | 21967449 | 21967515 | 2032 | 1605 | 1670 | 580 | 484 | 506 |
ENST00000298717 | 21967907 | 21967946 | 2032 | 1457 | 1495 | 580 | 435 | 447 |
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UniProtAcc | Exon skip start (AA) | Exon Skip end (AA) | Function feature start (AA) | Function feature end (AA) | Functional feature type | Functional feature desc. |
Q86U44 | 435 | 447 | 2 | 580 | Chain | ID=PRO_0000207630;Note=N6-adenosine-methyltransferase catalytic subunit |
Q86U44 | 484 | 506 | 2 | 580 | Chain | ID=PRO_0000207630;Note=N6-adenosine-methyltransferase catalytic subunit |
Q86U44 | 435 | 447 | 438 | 438 | Binding site | Note=Interaction with METTL14;Ontology_term=ECO:0000244,ECO:0000244,ECO:0000269;evidence=ECO:0000244|PDB:5IL1,ECO:0000244|PDB:5IL2,ECO:0000269|PubMed:27281194;Dbxref=PMID:27281194 |
Q86U44 | 435 | 447 | 441 | 441 | Binding site | Note=Interaction with METTL14;Ontology_term=ECO:0000244,ECO:0000244,ECO:0000269;evidence=ECO:0000244|PDB:5IL1,ECO:0000244|PDB:5IL2,ECO:0000269|PubMed:27281194;Dbxref=PMID:27281194 |
Q86U44 | 484 | 506 | 486 | 505 | Alternative sequence | ID=VSP_007865;Note=In isoform 2. GVKGNPQGFNQGLDCDVIVA->SSSGAQFNRWSTKKNHLISY;Ontology_term=ECO:0000303;evidence=ECO:0000303|Ref.2 |
Q86U44 | 484 | 506 | 506 | 580 | Alternative sequence | ID=VSP_007866;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|Ref.2 |
Q86U44 | 435 | 447 | 436 | 446 | Helix | Ontology_term=ECO:0000244;evidence=ECO:0000244|PDB:5IL2 |
Q86U44 | 484 | 506 | 480 | 489 | Beta strand | Ontology_term=ECO:0000244;evidence=ECO:0000244|PDB:5IL2 |
Q86U44 | 484 | 506 | 498 | 506 | Beta strand | Ontology_term=ECO:0000244;evidence=ECO:0000244|PDB:5IL2 |
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Cancer type | Translation factor | FC | adj.pval |
CHOL | METTL3 | -3.31943495691848 | 0.0390625 |
COAD | METTL3 | -3.54288918740857 | 2.08616256713867e-06 |
LIHC | METTL3 | -1.43381447667708 | 3.17814170396599e-08 |
PRAD | METTL3 | 2.27777667743557 | 5.10126106041513e-07 |
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Cancer type | Gene | miRNA | TargetScan binding score (Context++ score percentile) | Coefficient | Pvalue |
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Cancer type | Gene | methyl group b | methyl group a | DEG pval | avg methyl in b | avg methyl in a | avg exp in b | avg exp in a |
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Cancer type | Gene | methyl group b | methyl group a | DEG pval | avg methyl in b | avg methyl in a | avg exp in b | avg exp in a |
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Cancer type | Gene | Coefficient | Pvalue |
LUSC | METTL3 | 0.103034917 | 0.043100556 |
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Cancer type | Gene group | Translation factor | Correlated gene | Coefficient | Pvalue |
DLBC | TSG | METTL3 | PNN | 0.835703056 | 1.48E-13 |
THYM | Cell metabolism gene | METTL3 | SRP54 | 0.824212781 | 2.03E-31 |
THYM | Cell metabolism gene | METTL3 | AGK | 0.829946228 | 3.33E-32 |
THYM | TF | METTL3 | ZNF280C | 0.805364221 | 5.02E-29 |
THYM | TF | METTL3 | ZBTB1 | 0.864996701 | 9.65E-38 |
THYM | TSG | METTL3 | RINT1 | 0.814663336 | 3.58E-30 |
THYM | TSG | METTL3 | PNN | 0.815251453 | 3.02E-30 |
UCS | Cell metabolism gene | METTL3 | SRP54 | 0.824212781 | 2.03E-31 |
UCS | Cell metabolism gene | METTL3 | AGK | 0.829946228 | 3.33E-32 |
UCS | TF | METTL3 | ZNF280C | 0.805364221 | 5.02E-29 |
UCS | TF | METTL3 | ZBTB1 | 0.864996701 | 9.65E-38 |
UCS | TSG | METTL3 | RINT1 | 0.814663336 | 3.58E-30 |
UCS | TSG | METTL3 | PNN | 0.815251453 | 3.02E-30 |
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![]() Visit iCn3D. |
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![]() * Overlap between up-regulated DEGs (log2FC<-1 and adj.P<0.05) and STRING PPI network (center: Translation factor, node: DEGs, edges: weighted by -log2(adj.P)) |
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![]() * Edge colors based on TCGA cancer types. |
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Cancer type | Translation factor | Interacting protein coding gene | FC | adj.pval |
KICH | METTL3 | RBM15B | -2.89224914085525 | 0.000102996826171875 |
KIRP | METTL3 | RBM15B | -4.15875719217488 | 0.000280400272458792 |
LIHC | METTL3 | ZC3H13 | 2.3058315858446 | 0.000458084191609093 |
KIRC | METTL3 | RBM15 | -1.35007713201106 | 0.000600141235926365 |
COAD | METTL3 | KIAA1429 | -3.39420981646075 | 0.000664144754409791 |
LUAD | METTL3 | METTL14 | -1.43596594596523 | 0.00121089428940613 |
HNSC | METTL3 | RBM15B | -2.90773760599283 | 0.00186235073124408 |
PRAD | METTL3 | RBM15 | -1.09327807917714 | 0.00277499505363991 |
CHOL | METTL3 | RBM15B | -2.36781718450114 | 0.0078125 |
LUAD | METTL3 | WTAP | -1.78616226090853 | 0.00791615044666943 |
LUAD | METTL3 | RBM15 | -1.24579793729144 | 0.0103856608841715 |
KIRC | METTL3 | WTAP | -2.70273660495067 | 0.0143053039058135 |
BLCA | METTL3 | WTAP | -2.90881954846739 | 0.0159721374511719 |
PRAD | METTL3 | ZC3H13 | -1.09839670176628 | 0.0176746638162561 |
STAD | METTL3 | KIAA1429 | -1.61567103280556 | 0.020511694252491 |
ESCA | METTL3 | RBM15B | -2.20401464424729 | 0.0244140625 |
LUAD | METTL3 | CBLL1 | -1.32279721521585 | 0.0345442316474578 |
BRCA | METTL3 | RBM15B | -1.21088084774422 | 0.0367624289903515 |
CHOL | METTL3 | KIAA1429 | -2.83229200442768 | 0.0390625 |
UCEC | METTL3 | WTAP | -3.78629147221377 | 0.046875 |
THCA | METTL3 | ZC3H13 | -7.58640410905415 | 1.49948359448794e-05 |
LUAD | METTL3 | NCBP1 | -2.33130964948431 | 1.81586577755686e-08 |
THCA | METTL3 | KIAA1429 | 1.4688007829704 | 2.5764473552472e-05 |
KIRC | METTL3 | NCBP1 | 1.82316126239442 | 2.95519875508206e-07 |
THCA | METTL3 | METTL14 | -2.3091931665824 | 3.03433720687169e-07 |
KIRC | METTL3 | ZC3H13 | -2.50855351713892 | 5.02527105682381e-05 |
HNSC | METTL3 | RBM15 | 1.40615182569303 | 5.61373060463667e-05 |
THCA | METTL3 | WTAP | -2.89392443867004 | 5.83719995580266e-05 |
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PPI interactors with METTL3 |
METTL14, MOV10, HIST1H2BG, CEP19, ROBO2, SEL1L, WTAP, RBM15B, PPHLN1, MPP1, MYC, ACTR2, SNW1, NSUN2, ARNTL2, SIRT6, LGALS7, OLFM2, SMAD2, SMAD3, HSPA8, KRT1, KRT2, HSPA1A, KRT10, KRT9, TUBB, KRT5, TUBA1C, HSPA9, KRT14, KRT16, ALB, ACTB, ANXA2, HSPA5, TUFM, EEF1A1, ACTC1, UBC, IGHG1, LMNA, HNRNPH1, VIM, DSP, DDX5, IGKV1-5, CASP14, HIST4H4, DCD, PCBP2, ZC3H13, CBLL1, HRNR, C4A, HIST1H2BK, PRDX2, COL14A1, FLG2, C18orf63, LSM4, TXN, PRSS3, C1orf68, BRMS1, HNRNPK, HNRNPU, KIAA1429, METTL3, TRIM28, CCT2, CCT7, CCT3, CCT8, TCP1, CCT6A, CCT5, CCT4, TUBB4B, DNAJA1, HSP90AA1, DNAJA2, HSP90AB1, BAG2, WRNIP1, HSPD1, HNRNPR, NPM1, PTBP1, DDX3Y, CUL2, SYNCRIP, RPL23, MATR3, HNRNPF, KRT72, NONO, MCM3, KRT18, PRAME, DSG1, CDKN2A, IGHG2, FUS, SF3B2, TCEB1, HUWE1, SNRNP200, LTF, SFPQ, EIF4B, HNRNPA3, VCP, RPS14, SNRPD3, RPL24, EWSR1, DSC1, TARDBP, BTN1A1, HNRNPD, PCBP1, RBBP7, PRMT1, PUF60, THRAP3, KHDRBS3, GAPDH, SNRNP70, XRCC6, EEF2, SNRPB, ATP5A1, U2AF2, RPL13, HNRNPM, RPS26, PRKDC, SRSF2, C1QBP, ILF2, TCEB2, KRT6A, UBR5, DDX39A, MSH2, HNRNPCL1, CSTA, ANXA1, DYNLL1, H3F3C, RBM15, TUBB2A, HSPH1, TUBB4A, TUBA4A, DNAJC7, RUVBL2, RUVBL1, CCAR2, BAG5, DDX3X, POLD1, STIP1, BAG6, PSMC5, HSPA4, DDB1, DNAJB4, DNAJB1, PSMC1, HDAC2, KRT84, TMPO, FASN, MSH6, AMBRA1, HSPBP1, TUBAL3, HSPA4L, IMPDH2, PSMC4, PFKP, ARID5B, PSMC3, ARFIP2, PSMC6, HDAC1, TMEM200B, BAG1, PRMT5, PHGDH, HTATSF1, NUDT21, DNAJB6, KCNH1, ACAT1, CAD, LYZ, RPL38, MLF2, TBR1, C1orf167, AFMID, TBC1D10C, CD302, PRPF31, RAPGEF4, DDB2, WDR77, TSEN34, UCKL1, DMBT1, GTF3C4, VPS4A, STUB1, GTF3C5, NFIB, NDUFAB1, RYR1, CDK9, GTF2I, KHSRP, GNL3, SPATA5L1, TBL1XR1, XRN2, AKAP8L, PSMD13, BAG3, ZRANB2, NCBP1, EIF3G, EIF3I, EIF3J, EIF3M, EIF3H, EIF3B, EIF4E, MTDH, ESR1, EIF4A3, ECT2, UCHL1, BRD4, MAPK1, MAPK3, MAPK14, MAPK8, USP5, TERF2IP, WDR5, LMNB2, SNAPC4, SPANXN4, SHARPIN, SPANXN5, PIAS4, NUP210P1, FUBP1, BRD2, |
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Gene | Chr | Position | RefSeq | VarSeq | RefSeeq | VarType | Pathogenic | Disease | VarInfo |
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Gene | Cancer type | Chromosome | Start | End | RefSeeq | MutSeq | Mutation type | AAchange | # samples |
METTL3 | CESC | chr14 | 21967916 | 21967916 | A | G | Silent | 8 | |
METTL3 | BLCA | chr14 | 21967676 | 21967676 | C | T | Missense_Mutation | p.R471H | 4 |
METTL3 | BLCA | chr14 | 21967206 | 21967206 | C | T | Missense_Mutation | 4 | |
METTL3 | ESCA | chr14 | 21969886 | 21969886 | G | A | Missense_Mutation | p.R295C | 3 |
METTL3 | HNSC | chr14 | 21969087 | 21969087 | C | T | Missense_Mutation | p.D362N | 3 |
METTL3 | SKCM | chr14 | 21967278 | 21967278 | G | A | Missense_Mutation | p.R508C | 3 |
METTL3 | PAAD | chr14 | 21971467 | 21971467 | G | A | Missense_Mutation | p.A191V | 3 |
METTL3 | UCEC | chr14 | 21967459 | 21967459 | G | A | Silent | p.I503 | 2 |
METTL3 | LAML | chr14 | 21049123 | 21049123 | T | C | Missense_Mutation | p.Q28R | 2 |
METTL3 | COAD | chr14 | 21971694 | 21971694 | C | A | Silent | p.G115G | 2 |
METTL3 | UCEC | chr14 | 21967927 | 21967927 | C | A | Nonsense_Mutation | p.E442* | 2 |
METTL3 | BLCA | chr14 | 21967254 | 21967254 | C | T | Missense_Mutation | 2 | |
METTL3 | PRAD | chr14 | 21971365 | 21971365 | A | C | Nonstop_Mutation | p.*154E | 2 |
METTL3 | LGG | chr14 | 21971990 | 21971990 | G | A | Silent | p.T45T | 2 |
METTL3 | UCEC | chr14 | 21969242 | 21969242 | G | T | Missense_Mutation | p.S310Y | 2 |
METTL3 | HNSC | chr14 | 21971721 | 21971721 | C | A | Splice_Site | 2 | |
METTL3 | STAD | chr14 | 21966442 | 21966442 | C | A | Missense_Mutation | p.R568M | 2 |
METTL3 | UCEC | chr14 | 21971488 | 21971488 | G | A | Missense_Mutation | p.S184L | 2 |
METTL3 | LGG | chr14 | 21968795 | 21968795 | G | A | Silent | p.D382D | 2 |
METTL3 | STAD | chr14 | 21971372 | 21971372 | G | A | Silent | p.L223L | 2 |
METTL3 | ESCA | chr14 | 21971933 | 21971933 | G | T | Missense_Mutation | p.S64R | 2 |
METTL3 | UCEC | chr14 | 21971601 | 21971601 | G | T | Silent | p.T146 | 2 |
METTL3 | BLCA | chr14 | 21967676 | 21967676 | C | T | Missense_Mutation | 2 | |
METTL3 | BLCA | chr14 | 21967206 | 21967206 | C | G | Missense_Mutation | p.E532Q | 2 |
METTL3 | ESCA | chr14 | 21969886 | 21969886 | G | A | Missense_Mutation | 2 | |
METTL3 | BRCA | chr14 | 21967278 | 21967278 | G | C | Missense_Mutation | p.R508G | 2 |
METTL3 | THYM | chr14 | 21971828 | 21971828 | G | T | Silent | 2 | |
METTL3 | BLCA | chr14 | 21967731 | 21967731 | C | T | Missense_Mutation | p.D453N | 2 |
METTL3 | HNSC | chr14 | 21971333 | 21971333 | C | T | Missense_Mutation | p.E236K | 2 |
METTL3 | BRCA | chr14 | 21968764 | 21968764 | T | C | Missense_Mutation | p.M393V | 2 |
METTL3 | BLCA | chr14 | 21979365 | 21979365 | T | C | Translation_Start_Site | p.M1V | 2 |
METTL3 | SARC | chr14 | 21967642 | 21967642 | G | A | Silent | 2 | |
METTL3 | SKCM | chr14 | 21967496 | 21967496 | G | A | Missense_Mutation | p.P491L | 2 |
METTL3 | UCEC | chr14 | 21966407 | 21966407 | A | C | Missense_Mutation | p.L580V | 2 |
METTL3 | BLCA | chr14 | 21967254 | 21967254 | C | T | Missense_Mutation | p.E516K | 2 |
METTL3 | BLCA | chr14 | 21967685 | 21967685 | C | T | Missense_Mutation | p.R468Q | 2 |
METTL3 | PAAD | chr14 | 21971467 | 21971467 | G | A | Missense_Mutation | 2 | |
METTL3 | UCEC | chr14 | 21967277 | 21967277 | C | T | Missense_Mutation | p.R508H | 2 |
METTL3 | KIRP | chr14 | 21979335 | 21979335 | G | T | Missense_Mutation | 1 | |
METTL3 | SKCM | chr14 | 21970035 | 21970035 | T | C | Missense_Mutation | p.E245G | 1 |
METTL3 | BLCA | chr14 | 21967257 | 21967257 | C | A | Missense_Mutation | 1 | |
METTL3 | COAD | chr14 | 21966439 | 21966439 | T | C | Missense_Mutation | p.Y569C | 1 |
METTL3 | LIHC | chr14 | 21969916 | 21969916 | T | C | Missense_Mutation | 1 | |
METTL3 | BLCA | chr14 | 21969223 | 21969223 | G | C | Missense_Mutation | p.F316L | 1 |
METTL3 | HNSC | chr14 | 21971933 | 21971933 | G | A | Silent | 1 | |
METTL3 | BLCA | chr14 | 21971461 | 21971461 | G | A | Missense_Mutation | 1 | |
METTL3 | BLCA | chr14 | 21969985 | 21969985 | C | T | Missense_Mutation | p.E262K | 1 |
METTL3 | HNSC | chr14 | 21969183 | 21969183 | G | A | Missense_Mutation | p.H330Y | 1 |
METTL3 | PRAD | chr14 | 21971365 | 21971365 | A | C | Missense_Mutation | p.I225R | 1 |
METTL3 | SKCM | chr14 | 21966419 | 21966422 | TAGA | - | Frame_Shift_Del | p.SK575fs | 1 |
METTL3 | BLCA | chr14 | 21969985 | 21969985 | C | T | Missense_Mutation | 1 | |
METTL3 | LIHC | chr14 | 21967194 | 21967194 | G | T | Silent | 1 | |
METTL3 | BLCA | chr14 | 21968750 | 21968750 | G | C | Silent | p.P397P | 1 |
METTL3 | HNSC | chr14 | 21967215 | 21967215 | G | A | Missense_Mutation | 1 | |
METTL3 | BLCA | chr14 | 21967260 | 21967260 | G | T | Missense_Mutation | p.P514T | 1 |
METTL3 | HNSC | chr14 | 21967215 | 21967215 | G | A | Missense_Mutation | p.R529C | 1 |
METTL3 | STAD | chr14 | 21966442 | 21966442 | C | A | Missense_Mutation | 1 | |
METTL3 | BLCA | chr14 | 21967260 | 21967260 | G | T | Missense_Mutation | 1 | |
METTL3 | COAD | chr14 | 21971992 | 21971992 | T | C | Missense_Mutation | p.T45A | 1 |
METTL3 | LIHC | chr14 | 21970017 | 21970017 | T | - | Frame_Shift_Del | p.N251fs | 1 |
METTL3 | BLCA | chr14 | 21968750 | 21968750 | G | C | Silent | 1 | |
METTL3 | BLCA | chr14 | 21967452 | 21967452 | C | T | Missense_Mutation | p.E506K | 1 |
METTL3 | KIRC | chr14 | 21967473 | 21967473 | C | G | Missense_Mutation | p.D499H | 1 |
METTL3 | PRAD | chr14 | 21969230 | 21969230 | C | G | Missense_Mutation | p.C314S | 1 |
METTL3 | LGG | chr14 | 21971545 | 21971545 | C | T | Missense_Mutation | p.G165D | 1 |
METTL3 | BLCA | chr14 | 21967264 | 21967264 | A | C | Missense_Mutation | 1 | |
METTL3 | LUAD | chr14 | 21969067 | 21969067 | G | C | Silent | p.L368L | 1 |
METTL3 | BLCA | chr14 | 21969218 | 21969218 | T | A | Missense_Mutation | p.N318I | 1 |
METTL3 | BLCA | chr14 | 21969223 | 21969223 | G | C | Missense_Mutation | 1 | |
METTL3 | BLCA | chr14 | 21967264 | 21967264 | A | C | Missense_Mutation | p.H512Q | 1 |
METTL3 | KIRC | chr14 | 21966492 | 21966492 | C | T | Silent | p.L551L | 1 |
METTL3 | PRAD | chr14 | 21967909 | 21967909 | C | A | Splice_Site | p.G448W | 1 |
METTL3 | BLCA | chr14 | 21967452 | 21967452 | C | T | Missense_Mutation | 1 | |
METTL3 | LUAD | chr14 | 21967720 | 21967720 | A | C | Missense_Mutation | p.I456M | 1 |
METTL3 | BLCA | chr14 | 21971651 | 21971651 | C | A | Nonsense_Mutation | p.E130* | 1 |
METTL3 | HNSC | chr14 | 21971933 | 21971933 | G | A | Silent | p.S64S | 1 |
METTL3 | KIRC | chr14 | 21967449 | 21967449 | C | G | Splice_Site | . | 1 |
METTL3 | READ | chr14 | 21971454 | 21971454 | G | A | Silent | p.V195V | 1 |
METTL3 | LGG | chr14 | 21971507 | 21971507 | G | A | Missense_Mutation | p.R178W | 1 |
METTL3 | TGCT | chr14 | 21967677 | 21967677 | G | A | Missense_Mutation | 1 | |
METTL3 | BLCA | chr14 | 21969072 | 21969072 | G | A | Nonsense_Mutation | p.R367* | 1 |
METTL3 | LUAD | chr14 | 21971952 | 21971952 | G | A | Missense_Mutation | p.S58F | 1 |
METTL3 | BLCA | chr14 | 21972010 | 21972010 | C | T | Missense_Mutation | p.E39K | 1 |
METTL3 | HNSC | chr14 | 21971906 | 21971906 | A | T | Silent | p.A73A | 1 |
METTL3 | BLCA | chr14 | 21969218 | 21969218 | T | A | Missense_Mutation | 1 | |
METTL3 | KIRC | chr14 | 21967512 | 21967512 | C | T | Missense_Mutation | p.G486S | 1 |
METTL3 | READ | chr14 | 21967202 | 21967202 | A | G | Missense_Mutation | p.L533S | 1 |
METTL3 | LGG | chr14 | 21967506 | 21967506 | T | C | Missense_Mutation | p.K488E | 1 |
METTL3 | GBM | chr14 | 21969222 | 21969222 | G | T | Missense_Mutation | 1 | |
METTL3 | LUAD | chr14 | 21971722 | 21971722 | T | C | Splice_Site | p.P107_splice | 1 |
METTL3 | BLCA | chr14 | 21971844 | 21971844 | G | A | Missense_Mutation | p.P94L | 1 |
METTL3 | BLCA | chr14 | 21971844 | 21971844 | G | A | Missense_Mutation | 1 | |
METTL3 | KIRC | chr14 | 21967647 | 21967647 | C | T | Missense_Mutation | p.E481K | 1 |
METTL3 | SARC | chr14 | 21968716 | 21968716 | G | T | Missense_Mutation | 1 | |
METTL3 | LGG | chr14 | 21971404 | 21971406 | TTC | - | In_Frame_Del | p.KK211del | 1 |
METTL3 | THYM | chr14 | 21971828 | 21971828 | G | T | Silent | p.S99S | 1 |
METTL3 | HNSC | chr14 | 21979310 | 21979310 | C | A | Missense_Mutation | 1 | |
METTL3 | LUSC | chr14 | 21979304 | 21979304 | C | A | Missense_Mutation | p.R21M | 1 |
METTL3 | BLCA | chr14 | 21967728 | 21967728 | C | T | Missense_Mutation | p.E454K | 1 |
METTL3 | KIRP | chr14 | 21967914 | 21967914 | A | C | Missense_Mutation | p.L446R | 1 |
METTL3 | LGG | chr14 | 21971990 | 21971990 | G | A | Silent | 1 | |
METTL3 | UCEC | chr14 | 21971350 | 21971350 | T | C | Missense_Mutation | p.N230S | 1 |
METTL3 | BLCA | chr14 | 21971461 | 21971461 | G | A | Missense_Mutation | p.S193L | 1 |
METTL3 | HNSC | chr14 | 21969087 | 21969087 | C | T | Missense_Mutation | 1 | |
METTL3 | BLCA | chr14 | 21967206 | 21967206 | C | T | Missense_Mutation | p.E532K | 1 |
METTL3 | OV | chr14 | 21041205 | 21041205 | A | G | Missense_Mutation | p.I225T | 1 |
METTL3 | KIRP | chr14 | 21969115 | 21969115 | C | G | Missense_Mutation | p.E352D | 1 |
METTL3 | BLCA | chr14 | 21967728 | 21967728 | C | T | Missense_Mutation | 1 | |
METTL3 | CESC | chr14 | 21971383 | 21971383 | G | A | Missense_Mutation | 1 | |
METTL3 | LGG | chr14 | 21971507 | 21971507 | G | A | Missense_Mutation | 1 | |
METTL3 | HNSC | chr14 | 21971333 | 21971333 | C | T | Missense_Mutation | 1 | |
METTL3 | BLCA | chr14 | 21967731 | 21967731 | C | T | Missense_Mutation | 1 | |
METTL3 | KIRP | chr14 | 21969207 | 21969207 | G | T | Missense_Mutation | 1 | |
METTL3 | BLCA | chr14 | 21967685 | 21967685 | C | T | Missense_Mutation | 1 | |
METTL3 | CESC | chr14 | 21971383 | 21971383 | G | A | Nonsense_Mutation | p.Q148* | 1 |
METTL3 | LGG | chr14 | 21971545 | 21971545 | C | T | Missense_Mutation | 1 | |
METTL3 | BLCA | chr14 | 21971663 | 21971663 | G | A | Nonsense_Mutation | p.Q126* | 1 |
METTL3 | HNSC | chr14 | 21971906 | 21971906 | A | T | Silent | 1 | |
METTL3 | BLCA | chr14 | 21979365 | 21979365 | T | C | Translation_Start_Site | 1 | |
METTL3 | BLCA | chr14 | 21967257 | 21967257 | C | A | Missense_Mutation | p.D515Y | 1 |
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FusionGDB2 ID | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
87720 | LUSC | TCGA-39-5019-01A | DHRS1 | chr14 | 24768163 | - | METTL3 | chr14 | 21970045 | - |
87720 | UCEC | TCGA-AX-A3G7-01A | HSPA8 | chr11 | 122931834 | - | METTL3 | chr14 | 21967183 | - |
87720 | STAD | TCGA-D7-8574-01A | KTN1 | chr14 | 56047072 | + | METTL3 | chr14 | 21972024 | - |
60272 | N/A | CA437449 | METTL3 | chr14 | 21967264 | - | BAP1 | chr3 | 52438507 | + |
94937 | BLCA | TCGA-G2-A3IE-01A | METTL3 | chr14 | 21971316 | - | SALL2 | chr14 | 21990378 | - |
87720 | N/A | BM148718 | NCKAP5 | chr2 | 134276307 | + | METTL3 | chr14 | 21966285 | + |
87720 | OV | TCGA-13-0911 | PLXDC2 | chr10 | 20466338 | + | METTL3 | chr14 | 21967946 | - |
87720 | PRAD | TCGA-KK-A7B2 | SRP54 | chr14 | 35488280 | + | METTL3 | chr14 | 21967946 | - |
87728 | KIRC | TCGA-CJ-5677-01A | STRN3 | chr14 | 31398407 | - | METTL3 | chr14 | 21972024 | - |
87728 | KIRC | TCGA-CJ-5677-01A | STRN3 | chr14 | 31404369 | - | METTL3 | chr14 | 21972024 | - |
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Cancer type | Translation factor | Coefficent | Hazard ratio | Wald test pval | Likelihool ratio pval | Logrank test pval | # samples |
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Cancer type | Translation factor | pval | adj.p |
BLCA | METTL3 | 0.031938741584673 | 0.89 |
LIHC | METTL3 | 0.0324147782186373 | 0.89 |
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Cancer type | Translation factor | pval | adj.p |
LUAD | METTL3 | 0.00564780203591982 | 0.19 |
LUSC | METTL3 | 0.0123471169835721 | 0.4 |
KICH | METTL3 | 0.0384146623907679 | 1 |
LGG | METTL3 | 0.0294374771250239 | 0.91 |
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![]() (DrugBank Version 5.1.8 2021-05-08) |
UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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![]() (DisGeNet 4.0) |
Disease ID | Disease Name | # PubMeds | Disease source |