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Center for Computational Systems Medicine
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Gene Summary

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Translation studies in PubMed

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Exon Skipping Events

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Expression

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Expression Regulation

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Associated Genes

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Protein 3D Structure

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Protein-Protein Interaction

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Mutations

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Prognostic Analysis

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Gender Association

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Age Association

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Related Drugs

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Related Diseases

Translation Factor: EEF2 (NCBI Gene ID:1938)


Gene Summary

check button Gene Summary
Gene InformationGene Name: EEF2
Gene ID: 1938
Gene Symbol

EEF2

Gene ID

1938

Gene Nameeukaryotic translation elongation factor 2
SynonymsEEF-2|EF-2|EF2|SCA26
Cytomap

19p13.3

Type of Geneprotein-coding
Descriptionelongation factor 2epididymis secretory sperm binding proteinpolypeptidyl-tRNA translocase
Modification date20200313
UniProtAcc

P13639


check button Child GO biological process term(s) under GO:0006412
GO IDGO term
GO:0006417Regulation of translation
GO:0008135Translation factor activity, RNA binding
GO:0045727Positive regulation of translation
GO:0006414Translational elongation
GO:0006412Translation


check button Gene ontology of translaction factor with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID


check button Inferred gene age of translation factor.
GeneInferred gene age group among (0 - 67.6], (67.6 - 355.7], (355.7 - 733], (733 - 1119.25], >1119.25
EEF2>1119.25


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Translation Studies in PubMed

check button We searched PubMed using 'EEF2[title] AND translation [title] AND human.'
GeneTitlePMID
EEF2dentification and characterization of a novel evolutionarily conserved lysine-specific methyltransferase targeting eukaryotic translation elongation factor 2 (eEF2)25231979


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Exon Skipping Events

check buttonSkipped exons in TCGA and GTEx based on Ensembl gene isoform structure.
* 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.
all structure

check button Open reading frame (ORF) analsis of exon skipping events 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.
ENSTExon skip start (DNA)Exon Skip end (DNA)ORF
ENST0000030931139772123977345Frame-shift
ENST0000030931139774253977608In-frame
ENST0000030931139778163978170In-frame
ENST0000030931139798053980064Frame-shift
ENST0000030931139813363981450In-frame
ENST0000030931139841333984348Frame-shift

check button Exon skipping position in the amino acid sequence.
ENSTExon 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)
ENST0000030931139774253977608318121572339858689750
ENST0000030931139778163978170318118032156858571689
ENST000003093113981336398145031819871100858299337

check button Potentially (partially) lost protein functional features of UniProt.
UniProtAccExon skip start (AA)Exon Skip end (AA)Function feature start (AA)Function feature end (AA)Functional feature typeFunctional feature desc.
P136396897502858ChainID=PRO_0000091000;Note=Elongation factor 2
P136395716892858ChainID=PRO_0000091000;Note=Elongation factor 2
P136392993372858ChainID=PRO_0000091000;Note=Elongation factor 2
P1363929933717362DomainNote=tr-type G;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU01059
P13639571689586587SiteNote=Cleavage;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:24648518;Dbxref=PMID:24648518
P13639571689605606SiteNote=Cleavage;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:24648518;Dbxref=PMID:24648518
P13639299337325325Modified residueNote=Phosphoserine;Ontology_term=ECO:0000250;evidence=ECO:0000250|UniProtKB:P05197
P13639571689572572Modified residueNote=N6-succinyllysine;Ontology_term=ECO:0000250;evidence=ECO:0000250|UniProtKB:P58252
P13639571689595595Modified residueNote=Phosphoserine%3B by CDK2;Ontology_term=ECO:0000244,ECO:0000269;evidence=ECO:0000244|PubMed:23186163,ECO:0000269|PubMed:23184662;Dbxref=PMID:23186163,PMID:23184662
P13639571689619619Modified residueNote=N6-acetyllysine;Ontology_term=ECO:0000250;evidence=ECO:0000250|UniProtKB:P58252
P13639689750715715Modified residueNote=Diphthamide;Ontology_term=ECO:0000250;evidence=ECO:0000250
P13639299337322322Cross-linkNote=Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in SUMO);Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:24648518;Dbxref=PMID:24648518
P13639571689596596Natural variantID=VAR_070792;Note=In SCA26%3B compromises the mechanics of translocation. P->H;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:23001565;Dbxref=dbSNP:rs587777052,PMID:23001565
P13639571689595595MutagenesisNote=Strongly reduced phosphorylation at Thr-57. S->A;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:23184662;Dbxref=PMID:23184662
P13639571689599599MutagenesisNote=Strongly reduced phosphorylation at Thr-57. H->P;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:23184662;Dbxref=PMID:23184662


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Expression


check buttonGene expression level across TCGA pancancer
all structure

check buttonGene expression level across GTEx pantissue
all structure

check buttonExpression level of gene isoforms across TCGA pancancer
all structure

check buttonExpression level of gene isoforms across GTEx pantissue
all structure

check buttonCancer(tissue) type-specific expression level of Translation factor using z-score distriution
all structure

check buttonDifferential expression between tumor and matched normal (in the cancer types with more than 10 matched samples)
all structure
Cancer typeTranslation factorFCadj.pval
HNSCEEF2-1.908053300693020.000299885096865183
THCAEEF21.355748584961760.000711089919756285
COADEEF21.670251136868660.00197160243988037
STADEEF2-1.878461903444480.00733334058895707
ESCAEEF2-3.45983264174140.0185546875
PRADEEF21.639264798941912.70126293247147e-08


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Expression Regulation


check buttonTranslation factor expression regulation through miRNA binding
Cancer typeGenemiRNATargetScan binding score (Context++ score percentile)CoefficientPvalue


check buttonTranslation factor expression regulation through methylation in the promoter of Translation factor
all structure
Cancer typeGenemethyl group bmethyl group aDEG pvalavg methyl in bavg methyl in aavg exp in bavg exp in a

check buttonTranslation factor expression regulation through methylation in the gene body of Translation factor (positive regulation)
all structure
Cancer typeGenemethyl group bmethyl group aDEG pvalavg methyl in bavg methyl in aavg exp in bavg exp in a

check buttonTranslation factor expression regulation through copy number variation of Translation factor
all structure
Cancer typeGeneCoefficientPvalue
OVEEF2-0.0714386210.045524397
KIRCEEF2-0.050483070.045613842

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Associated Genes


check button Strongly correlated genes belong to cellular important gene groups with EEF2 (coefficient>0.8, pval<0.05, node color based on FC between tumor and matched normal). Significantly associated important genes in the individual cancer types. * Cell metabolism gene: cell metabolism genes from REACTOME (black edge), IUPHAR: drug target genes from IUPHAR (blue edge), Kinase: human kinase genes (brown edge), CGC: cancer gene census genes (orange edge), TSG: tumor suppresor genes (purple edge), Epifactor: epigenetic factors (light blue edge), TF: transcription factors (green)
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Cancer typeGene groupTranslation factorCorrelated geneCoefficientPvalue
LAMLTSGEEF2GNB2L10.8117231628.63E-42
LAMLTSGEEF2GLTSCR20.8418365151.15E-47
TGCTTFEEF2ZNF4900.8072262424.34E-37
UVMCell metabolism geneEEF2IMPDH20.8306097591.59E-21
UVMEpifactorEEF2TRIM280.8014215214.33E-19
UVMEpifactorEEF2FBL0.8074149391.48E-19
UVMIUPHAREEF2TRIM280.8014215214.33E-19
UVMIUPHAREEF2IMPDH20.8306097591.59E-21
UVMKinaseEEF2TRIM280.8014215214.33E-19
UVMTFEEF2ZNF5810.8043244012.58E-19
UVMTSGEEF2GLTSCR20.8249472935.10E-21
UVMTSGEEF2GNB2L10.8570515573.59E-24


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Protein structure


check button Protein 3D structure
Visit iCn3D.


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Protein-Protein Interaction


check button Protein-protein interaction networks
* 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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check buttonOverlap between down-regulated DEGs (log2FC>1 and adj.P<0.05) and STRING PPI network (center: Translation factor, node: DEGs, edges: weighted by -log2(adj.P))
all structure
check button
* Edge colors based on TCGA cancer types.

check button* Overlap between DEGs (log2FC>1 and adj.P<0.05) and STRING PPI network per cancer (center: Translation factor, node: DEGs, node color: log2FC, edges: weighted by -log2(adj.P))
all structure
Cancer typeTranslation factorInteracting protein coding geneFCadj.pval
KIRPEEF2RPL18A-1.516513928088850.00016188295558095
KIRPEEF2RPS16-1.359570436175170.00019507110118866
COADEEF2RPS31.487303751430140.000411599874496461
COADEEF2RPL132.117453144829120.000465095043182374
LIHCEEF2RPL8-4.845882849745580.00110314154326131
THCAEEF2RPL41.387940635413070.00128543522995411
PRADEEF2RPL41.25897758922730.00136912931788367
PRADEEF2RPL18A1.406001757484990.00205137828390396
KICHEEF2RPL191.369011828940890.00250792503356934
KICHEEF2RPLP2-2.799410307210410.00250792503356934
ESCAEEF2RPL151.766294175356440.0048828125
STADEEF2RPL41.505417101290020.00647870777174831
LUADEEF2RPL19-1.313980266157250.00993159558412698
THCAEEF2RPS16-6.163227981565770.0115764821363307
BLCAEEF2RPL4-1.272082912879920.0180816650390625
HNSCEEF2RPS3-4.735058190951350.0273726439852453
STADEEF2RPL13-1.170787228548760.0294188209809363
COADEEF2RPLP21.741016657325820.0334101617336274
KICHEEF2RPL13-5.956180471753940.0366820693016052
COADEEF2RPS91.186120144022350.0381683111190796
LUSCEEF2RPL19-2.146698895166660.044366810398747
KIRCEEF2RPL19-2.734852712766761.33980982873695e-10
BRCAEEF2RPS91.93314775463492.31299392089389e-07
KIRCEEF2RPL13-3.440155711112922.58914497097505e-10
KIRCEEF2RPL4-2.620090405077813.30026076039221e-08
KIRCEEF2RPLP2-1.312941494219463.74941832864519e-08
KIRCEEF2RPL8-1.182524599717735.64962994208288e-07
KIRPEEF2RPL8-1.530036923501196.0301274061203e-05
KIRPEEF2RPLP2-1.337400481333756.0301274061203e-05
KIRCEEF2RPS9-1.326808164409876.53264115309597e-07
KIRCEEF2RPS16-1.661498698893847.8509870430991e-09
KIRCEEF2RPS3-1.295608479263879.05905681935088e-10
KIRCEEF2RPL18A-4.430793049608439.2516163152192e-11


check button Protein-protein interactors with this translation factor (BIOGRID-3.4.160)
PPI interactors with EEF2
TP53, MLLT3, POU5F1, UCHL5, Mapk13, PPP2R1A, PPP2R1B, NOP56, DISC1, PSMA3, NDRG1, HDGF, ARRB2, ISG15, FBXO25, EEF2K, CUL3, CUL4B, CUL5, CDK2, CUL1, COPS5, COPS6, CAND1, GRK5, RAD23A, RPL5, RPS6, RPS3A, RPL7, RPS4X, RPL7A, EEF1A1, RPS16, RPS23, RPL31, RPS24, RPL12, RPL4, RPS15A, RPL10A, RPL14, RPL6, RPL18, RPS7, RPL21, RPL11, RPL23, RPS2, RPS5, RPS19, TARS, MRPS5, HSPD1, HSPA8, EIF4A1, PABPC1, FARSA, RPLP0P6, XRCC6, RPL10L, FLOT2, RRM1, HNRNPA0, EPHA2, ERLIN2, RBM4, HNRNPH1, RHOT2, HNRNPDL, HNRNPL, DDX5, ATP6V1H, NUP62, HNRNPA3, UPF1, SMURF1, CCT2, HSP90AA1, HSP90AB1, FN1, VCAM1, ATF2, MLH1, EEF2KMT, UBL4A, ITGA4, NPM1, SMG1, ADRB2, HNRNPD, MAPK14, HIPK4, CDK18, CDK20, TARDBP, CDKN2A, BZW1, CASP7, CKB, CAPN1, FTO, GSR, PGD, TYMP, EIF4H, GINS2, MAT2A, PAK2, PFAS, RPS6KA1, XPO1, YWHAQ, SHFM1, LGR4, EFM3, HUWE1, FUS, MDM2, RNF2, SIRT6, ARAF, BLK, BUB1B, CASK, CDK13, DAPK1, IRAK1, LIMK2, WEE1, ESR1, HNRNPA1, UNK, EP300, CALR, ABCC3, ABCD3, AHNAK, ARPC2, ATIC, ATP1B3, AURKA, CASP3, CSE1L, DPH1, DPH2, EEF1A2, ENO1, GSPT1, HSD17B10, NDUFV1, NOTCH2, PGK1, TAGLN, TAGLN2, TOMM40, TXN, HCFC1, HSD17B4, IPO4, ISYNA1, OPA1, RDX, TUBB, NTRK1, PTEN, PPME1, Cct3, GAN, CRY1, CRY2, MCM2, SENP3, U2AF2, NFATC2, CDC73, WWP2, ZNF746, CDH1, FBXO9, DEFA1, SLC25A48, CYLD, DLD, DLST, DNM1L, PARK7, SDHA, SOAT1, SOD1, VDAC1, TRIM25, BRCA1, HDAC6, CFTR, CPEB2, ZNF598, KEAP1, EGLN3, ADSS, JUP, PCBP1, PPP6C, COPE, CTNNB1, GALE, IGF1R, KRAS, TGFB1, YAF2, YAP1, UBE2M, PRPF8, EFTUD2, AAR2, PIH1D1, AKTIP, RNF4, TNF, CDC34, HEXIM1, MEPCE, LARP7, PPT1, NBN, SNAI1, AGR2, RECQL4, DCPS, RNF144A, ZFP36L2, MYC, CDC37, NEK2, GRWD1, KRT17, METTL3, METTL14, KIAA1429, USP18, RC3H2, ATG16L1, ACTC1, PHB, FAF1, RBX1, NR2C2, UBQLN2, UBE3C, HDAC2, AGRN, BMH2, BMH1, ATXN3, VRK3, HMOX2, ATP6V1B2, UQCRC2, LRRC59, PDHA1, PHB2, APOE, UQCRC1, NDUFS7, POR, AGPS, PDHB, NDUFS8, BCKDHA, ATP5B, NNT, NDUFS3, P4HA1, EMC8, HADHA, CYC1, CANX, EMC2, ASPH, NDUFA8, ATP6V1A, LONP1, NIPSNAP1, UQCRH, RCN2, TUFM, MGST1, EMC4, PRDX3, OGDH, NCF1, ITFG1, GSK3B, BIRC3, NFX1, BRD7, UBC, SOX2, PARK2, PPIA, ARIH2, PLEKHA4, PINK1, TFCP2, FANCD2, LINC01554, ZC3H18, FYN, GRB2, LCK, RAC1, SH3GL3, SHC1, NME1, ANKRD55, NEK4, DUX4, CIT, ANLN, CHMP4C, KIF14, KIF20A, KIF23, PRC1, PRNP, SUMO2, NDN, BIN1, BRD4, RBM45, CIC, Apc2, RBM39, FBP1, LGALS9, CSPG4, IFI16, CREBBP, INSIG1, USP15, RIN3, DDX58, BAG5, AR, UFL1, DDRGK1, LINC00152, TRIM37, FZR1, WDR5, PAGE4, BGLT3, HSPA1A, DTX3, SPRTN, USP11, BTF3, FBXW7, NLRP7, LHPP, E, nsp1, nsp12, nsp14, nsp15, nsp8, ORF3a, ORF7b, KDM4C, HECTD1, MAP1LC3B, CALCOCO2, SQSTM1, ANTXR1, PER2, MAGEL2,


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Mutations


check button Clinically associated variants from ClinVar.
GeneChrPositionRefSeqVarSeqRefSeeqVarTypePathogenicDiseaseVarInfo
EEF2chr193976253GAsingle_nucleotide_variantBenignnot_providedSO:0001624|3_prime_UTR_variantSO:0001624|3_prime_UTR_variant
EEF2chr193976321TGsingle_nucleotide_variantBenignnot_providedSO:0001624|3_prime_UTR_variantSO:0001624|3_prime_UTR_variant
EEF2chr193976441GAsingle_nucleotide_variantBenignnot_providedSO:0001624|3_prime_UTR_variantSO:0001624|3_prime_UTR_variant
EEF2chr193976549CTsingle_nucleotide_variantBenignnot_specified|not_providedSO:0001624|3_prime_UTR_variantSO:0001624|3_prime_UTR_variant
EEF2chr193976599GAsingle_nucleotide_variantBenignnot_specified|not_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193976633GAsingle_nucleotide_variantBenign/Likely_benignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193976666GAsingle_nucleotide_variantLikely_benignnot_specifiedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193976669CAsingle_nucleotide_variantLikely_benignnot_specifiedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193976669CGsingle_nucleotide_variantBenignnot_specified|not_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193976680ACsingle_nucleotide_variantUncertain_significancenot_providedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193976699GAsingle_nucleotide_variantBenignnot_specifiedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193976705CTsingle_nucleotide_variantBenignnot_specified|not_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193976714GAsingle_nucleotide_variantBenign/Likely_benignnot_specified|not_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193976863CTsingle_nucleotide_variantBenignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193977205GAsingle_nucleotide_variantLikely_benignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193977217GAsingle_nucleotide_variantBenignnot_specified|not_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193977265GAsingle_nucleotide_variantBenignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193977289GAsingle_nucleotide_variantBenignnot_specifiedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193977416TCsingle_nucleotide_variantBenignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193977435CTsingle_nucleotide_variantLikely_benignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193977471GAsingle_nucleotide_variantBenignnot_specified|not_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193977471GCsingle_nucleotide_variantLikely_benignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193977486AGsingle_nucleotide_variantBenignSpinocerebellar_ataxia_type_26|not_specified|not_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193977501TCsingle_nucleotide_variantBenignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193977528GAsingle_nucleotide_variantBenignnot_specifiedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193977540GAsingle_nucleotide_variantBenignnot_specifiedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193977543GAsingle_nucleotide_variantBenignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193977546GAsingle_nucleotide_variantBenignnot_specifiedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193977561GAsingle_nucleotide_variantBenignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193977567GAsingle_nucleotide_variantBenignnot_specifiedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193977586AGsingle_nucleotide_variantUncertain_significancenot_providedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193977762GAsingle_nucleotide_variantLikely_benignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193977807CTsingle_nucleotide_variantBenignnot_specified|not_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193977895GAsingle_nucleotide_variantBenignnot_specifiedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193977905TCsingle_nucleotide_variantnot_providedSpinocerebellar_ataxia_type_26SO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193977953GAsingle_nucleotide_variantUncertain_significancenot_specifiedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193977976GCsingle_nucleotide_variantBenign/Likely_benignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193977988CTsingle_nucleotide_variantLikely_benignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193978015GAsingle_nucleotide_variantLikely_benignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193978097GTsingle_nucleotide_variantPathogenicSpinocerebellar_ataxia_type_26|not_providedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193978100GAsingle_nucleotide_variantUncertain_significancenot_providedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193978114GAsingle_nucleotide_variantBenignnot_specifiedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193978138CGsingle_nucleotide_variantLikely_benignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193978138CTsingle_nucleotide_variantBenignnot_specifiedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193978159CTsingle_nucleotide_variantLikely_benignnot_specifiedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193978176AGsingle_nucleotide_variantLikely_benignnot_specifiedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193979156GCsingle_nucleotide_variantBenignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193979312TCsingle_nucleotide_variantBenignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193979319CAsingle_nucleotide_variantBenignnot_specifiedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193979338TCsingle_nucleotide_variantUncertain_significancenot_providedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193979363CTsingle_nucleotide_variantBenignnot_specified|not_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193979372GTsingle_nucleotide_variantBenignnot_specified|not_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193979402GAsingle_nucleotide_variantLikely_benignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193979408AGsingle_nucleotide_variantBenignSpinocerebellar_ataxia_type_26|not_specified|not_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193979690CCTDuplicationLikely_benignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193979820CTsingle_nucleotide_variantUncertain_significancenot_providedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193979842CTsingle_nucleotide_variantBenignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193979862GAsingle_nucleotide_variantBenignnot_specified|not_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193979869CTsingle_nucleotide_variantBenignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193979932GAsingle_nucleotide_variantLikely_benignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193979941GAsingle_nucleotide_variantBenign/Likely_benignnot_specified|not_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193979965CTsingle_nucleotide_variantBenignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193980061TCsingle_nucleotide_variantLikely_benignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193980072ACsingle_nucleotide_variantBenignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193980367GTsingle_nucleotide_variantBenignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193980535GAsingle_nucleotide_variantBenignnot_specifiedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193980565CTsingle_nucleotide_variantLikely_benignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193980607GTsingle_nucleotide_variantUncertain_significancenot_providedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193980625GAsingle_nucleotide_variantBenignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193980643GAsingle_nucleotide_variantBenignnot_specified|not_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193980682GAsingle_nucleotide_variantBenignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193980689GAsingle_nucleotide_variantUncertain_significancenot_specifiedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193980690GCsingle_nucleotide_variantUncertain_significancenot_providedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193980714GAsingle_nucleotide_variantBenign/Likely_benignnot_specified|not_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193980824AGsingle_nucleotide_variantBenignSpinocerebellar_ataxia_type_26|not_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193980835GAsingle_nucleotide_variantBenignnot_specifiedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193980839CAsingle_nucleotide_variantUncertain_significancenot_providedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193980852GAsingle_nucleotide_variantBenignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193980901GAsingle_nucleotide_variantUncertain_significancenot_providedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193981320CTsingle_nucleotide_variantLikely_benignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193981439CTsingle_nucleotide_variantLikely_benignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193981442AGsingle_nucleotide_variantBenignnot_specified|not_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193981443TAsingle_nucleotide_variantUncertain_significancenot_providedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193981460CTsingle_nucleotide_variantUncertain_significancenot_specifiedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193981526AGsingle_nucleotide_variantBenignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193982005GAsingle_nucleotide_variantLikely_benignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193982031CTsingle_nucleotide_variantLikely_benignnot_specifiedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193982041GAsingle_nucleotide_variantLikely_benignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193982054GCsingle_nucleotide_variantUncertain_significancenot_specifiedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193982235GAsingle_nucleotide_variantLikely_benignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193982248CGsingle_nucleotide_variantUncertain_significancenot_providedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193982289CTsingle_nucleotide_variantLikely_benignnot_providedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193982294GAsingle_nucleotide_variantBenignnot_specifiedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193982323CTsingle_nucleotide_variantUncertain_significancenot_providedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193982324GAsingle_nucleotide_variantBenignnot_specified|not_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193982368AGsingle_nucleotide_variantUncertain_significancenot_providedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193982377CTsingle_nucleotide_variantUncertain_significancenot_providedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193982398CAsingle_nucleotide_variantUncertain_significancenot_providedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193982402GAsingle_nucleotide_variantBenignnot_specifiedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193982408GAsingle_nucleotide_variantBenign/Likely_benignnot_specified|not_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193982785CTsingle_nucleotide_variantBenignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193982826GAsingle_nucleotide_variantBenignnot_specifiedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193982832GAsingle_nucleotide_variantUncertain_significancenot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193982847GAsingle_nucleotide_variantUncertain_significancenot_specifiedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193982850GAsingle_nucleotide_variantBenignnot_specified|not_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193982874GAsingle_nucleotide_variantBenignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193982895GAsingle_nucleotide_variantBenignnot_specifiedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193982931GAsingle_nucleotide_variantBenignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193982967GAsingle_nucleotide_variantBenignnot_specified|not_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193982973GAsingle_nucleotide_variantBenign/Likely_benignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193982984GAsingle_nucleotide_variantUncertain_significancenot_providedSO:0001587|nonsenseSO:0001587|nonsense
EEF2chr193983015GAsingle_nucleotide_variantBenignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193983082GAsingle_nucleotide_variantBenignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193983142GAsingle_nucleotide_variantUncertain_significancenot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193983169CTsingle_nucleotide_variantLikely_benignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193983184AGsingle_nucleotide_variantBenignnot_specified|not_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193983190GAsingle_nucleotide_variantBenignnot_specifiedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193983220GAsingle_nucleotide_variantBenignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193983225CTsingle_nucleotide_variantLikely_benignnot_specifiedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193983226GAsingle_nucleotide_variantBenignnot_specifiedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193983229CTsingle_nucleotide_variantBenignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193983232GAsingle_nucleotide_variantUncertain_significancenot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193983302GAsingle_nucleotide_variantBenignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193983562TCsingle_nucleotide_variantBenignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193983930GAsingle_nucleotide_variantLikely_benignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193984134GAsingle_nucleotide_variantUncertain_significancenot_providedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193984142GAsingle_nucleotide_variantBenignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193984199GAsingle_nucleotide_variantBenignnot_specifiedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193984209GAsingle_nucleotide_variantUncertain_significancenot_providedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193984224GAsingle_nucleotide_variantUncertain_significancenot_providedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193984238GAsingle_nucleotide_variantLikely_benignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193984266TGsingle_nucleotide_variantUncertain_significancenot_providedSO:0001583|missense_variantSO:0001583|missense_variant
EEF2chr193984292GTsingle_nucleotide_variantBenignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193984337CTsingle_nucleotide_variantBenignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
EEF2chr193984351GCsingle_nucleotide_variantUncertain_significancenot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193984356ATsingle_nucleotide_variantLikely_benignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193984412GAsingle_nucleotide_variantBenignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193984453GAsingle_nucleotide_variantBenignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193984489CTsingle_nucleotide_variantLikely_benignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193984540TCsingle_nucleotide_variantBenignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193985148AGsingle_nucleotide_variantBenignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193985242CAsingle_nucleotide_variantLikely_benignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193985250CGsingle_nucleotide_variantBenignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
EEF2chr193985385GCsingle_nucleotide_variantUncertain_significancenot_providedSO:0001623|5_prime_UTR_variantSO:0001623|5_prime_UTR_variant
EEF2chr193985576CTsingle_nucleotide_variantBenignnot_provided


check button nsSNVs with sample frequency (size of circle) from TCGA 33 cancers.
all structure


check button SNVs and Indels
GeneCancer typeChromosomeStartEndRefSeeqMutSeqMutation typeAAchange# samples
EEF2KIRPchr1939799853979985CTMissense_Mutationp.D476N10
EEF2BRCAchr1939823473982347CTMissense_Mutationp.E230K5
EEF2ESCAchr1939806333980633GAMissense_Mutationp.R409W5
EEF2STADchr1939767133976713CTMissense_Mutationp.G806S5
EEF2KIRPchr1939799853979985CTMissense_Mutation4
EEF2PAADchr1939800403980040GCNonsense_Mutationp.Y457*4
EEF2SKCMchr1939824203982420GASilentp.I205I4
EEF2ESCAchr1939820153982015GAMissense_Mutationp.S276L4
EEF2UCECchr1939799383979938CTSilentp.A4914
EEF2COADchr1939819823981982CTMissense_Mutationp.R287H3
EEF2UCECchr1939819833981983GAMissense_Mutationp.R287C3
EEF2UCECchr1939829333982933GAMissense_Mutationp.R162C3
EEF2PAADchr1939819653981965TCMissense_Mutationp.I293V3
EEF2PAADchr1939775293977529CTMissense_Mutationp.R716H3
EEF2BRCAchr1939824203982420GCMissense_Mutationp.I205M3
EEF2PAADchr1939766823976682TAMissense_Mutationp.H816L3
EEF2ESCAchr1939820153982015GAMissense_Mutation3
EEF2UCECchr1939842243984225-CCTTFrame_Shift_Insp.A43fs3
EEF2ESCAchr1939800083980008TCMissense_Mutationp.N468S3
EEF2LUADchr1939820083982008GTSilentp.T278T3
EEF2THYMchr1939775393977539CTMissense_Mutationp.A713T3
EEF2ACCchr1939793533979353CTMissense_Mutationp.E563K3
EEF2COADchr1939774863977486AGSilentp.Y730Y3
EEF2ACCchr1939766623976662CGMissense_Mutationp.D823H3
EEF2ESCAchr1939823353982335CAMissense_Mutationp.A234S3
EEF2ESCAchr1939842163984216TCMissense_Mutationp.I46V3
EEF2PRADchr1939842033984203CGMissense_Mutationp.R50P3
EEF2PAADchr1939819653981965TCMissense_Mutation2
EEF2BLCAchr1939772343977234GASilentp.L788L2
EEF2BRCAchr1939805443980544CTSilentp.K4382
EEF2ESCAchr1939820323982032GASilentp.N270N2
EEF2STADchr1939772283977228CTMissense_Mutationp.V790I2
EEF2UCECchr1939799943979994CTMissense_Mutationp.V473M2
EEF2PAADchr1939800403980040GCNonsense_Mutationp.Y457X2
EEF2BLCAchr1939799713979971CASilentp.V480V2
EEF2COADchr1939823143982314C-Frame_Shift_Delp.E241fs2
EEF2BRCAchr1939831503983150GCMissense_Mutationp.R120G2
EEF2ESCAchr1939842163984216TCMissense_Mutation2
EEF2SARCchr1939809143980914GAMissense_Mutation2
EEF2STADchr1939823693982369GTSilentp.A222A2
EEF2UCECchr1939814383981438TCMissense_Mutationp.I304V2
EEF2STADchr1939779453977945GAMissense_Mutation2
EEF2ESCAchr1939806333980633GAMissense_Mutation2
EEF2UCECchr1939822933982293CTMissense_Mutationp.E248K2
EEF2LUADchr1939794293979429GASilentp.I537I2
EEF2STADchr1939800443980044CTMissense_Mutation2
EEF2UCECchr1939823003982300CTSilentp.G2452
EEF2HNSCchr1939779013977901GASilentp.I661I2
EEF2STADchr1939800443980044CTMissense_Mutationp.R456H2
EEF2BLCAchr1939820473982047GASilentp.Y265Y2
EEF2UCECchr1939828393982839CTMissense_Mutationp.G193D2
EEF2LUADchr1939793993979399CASilentp.A547A2
EEF2STADchr1939779453977945GAMissense_Mutationp.R647C2
EEF2CESCchr1939799653979965CTSilent2
EEF2UCECchr1939766183976618CTSilentp.E8372
EEF2SKCMchr1939800323980032GAMissense_Mutationp.P460L2
EEF2ESCAchr1939823353982335CAMissense_Mutation2
EEF2UCECchr1939767373976737CTMissense_Mutationp.A798T2
EEF2ESCAchr1939820323982032GASilent2
EEF2PAADchr1939800403980040GCNonsense_Mutation2
EEF2STADchr1939820223982022TCMissense_Mutationp.S274G2
EEF2SKCMchr1939779003977900GAMissense_Mutationp.L662F2
EEF2UCECchr1939778783977878AGMissense_Mutationp.V669A2
EEF2KIRPchr1939832913983293TGA-Splice_Site.2
EEF2STADchr1939779443977944CTMissense_Mutationp.R647H2
EEF2SKCMchr1939794263979426GASilentp.I538I2
EEF2CESCchr1939780833978083GAMissense_Mutation2
EEF2UCECchr1939779183977918CTMissense_Mutationp.G656S2
EEF2PAADchr1939775293977529CTMissense_Mutation2
EEF2BRCAchr1939781463978146GAMissense_Mutationp.R580C2
EEF2STADchr1939780143978014CTMissense_Mutationp.A624T2
EEF2SKCMchr1939813853981385GASilentp.I321I2
EEF2BLCAchr1939841333984133CGSplice_Site2
EEF2CESCchr1939842043984204GAMissense_Mutation2
EEF2UCECchr1939799843979984TAMissense_Mutationp.D476V2
EEF2HNSCchr1939793933979393GASilentp.A549A1
EEF2LUADchr1939842593984259GASilentp.G31G1
EEF2SKCMchr1939806613980661GASilentp.S399S1
EEF2ESCAchr1939823273982327GASilentp.F2361
EEF2KIRPchr1939832913983293TGA-Splice_Sitep.T73_splice1
EEF2PRADchr1939841593984159CANonsense_Mutationp.E65*1
EEF2SKCMchr1939824163982416GAMissense_Mutationp.P207S1
EEF2BLCAchr1939799713979971CASilent1
EEF2CESCchr1939779373977937GASilentp.I649I1
EEF2HNSCchr1939819533981954--Frame_Shift_Ins1
EEF2LIHCchr1939806573980657T-Frame_Shift_Delp.M401fs1
EEF2HNSCchr1939778713977871GASilentp.Y671Y1
EEF2LUADchr1939823163982316CAMissense_Mutationp.G240V1
EEF2STADchr1939793723979372GASilent1
EEF2ESCAchr1939823273982327GASilentp.F236F1
EEF2SKCMchr1939829043982904GASilentp.P171P1
EEF2BLCAchr1939779373977937GCMissense_Mutation1
EEF2CESCchr1939779373977937GASilentp.I6491
EEF2HNSCchr1939831513983151GCSilent1
EEF2LIHCchr1939823513982351A-Frame_Shift_Delp.F228fs1
EEF2HNSCchr1939809753980975AGSilentp.A338A1
EEF2LUADchr1939823123982312CAMissense_Mutationp.E241D1
EEF2BLCAchr1939779373977937GCMissense_Mutationp.I649M1
EEF2COADchr1939829673982967GASilentp.R150R1
EEF2ESCAchr1939800083980008TCMissense_Mutation1
EEF2KIRPchr1939832793983279GTMissense_Mutation1
EEF2SARCchr1939774863977486AGSilent1
EEF2STADchr1939822583982260CTT-In_Frame_Delp.259_260del1
EEF2SKCMchr1939841823984182GAMissense_Mutationp.T57I1
EEF2BLCAchr1939794083979408AGSilent1
EEF2CESCchr1939780833978083GAMissense_Mutationp.R601W1
EEF2HNSCchr1939832633983263GAMissense_Mutation1
EEF2LIHCchr1939841953984195C-Frame_Shift_Delp.E53fs1
EEF2HNSCchr1939832593983259CTSilentp.E83E1
EEF2BLCAchr1939832083983208GTSilentp.I100I1
EEF2COADchr1939841343984134GAMissense_Mutationp.T73I1
EEF2ESCAchr1939842813984281AGMissense_Mutation1
EEF2UCECchr1939799383979938CTSilentp.A491A1
EEF2GBMchr1939806653980665ACMissense_Mutationp.I398S1
EEF2LGGchr1939806803980680GTMissense_Mutationp.P393H1
EEF2SARCchr1939828973982897GTMissense_Mutation1
EEF2STADchr1939775753977575GAMissense_Mutationp.R701C1
EEF2SKCMchr1939806623980662GAMissense_Mutationp.S399F1
EEF2BLCAchr1939832083983208GTSilent1
EEF2CESCchr1939842043984204GAMissense_Mutationp.R50W1
EEF2HNSCchr1939832593983259CTSilent1
EEF2LIHCchr1939820023982002G-Frame_Shift_Delp.P280fs1
EEF2DLBCchr1939808523980852GASilentp.D379D1
EEF2BRCAchr1939831843983184AGSilentp.H1081
EEF2GBMchr1939779923977992CTMissense_Mutation1
EEF2LGGchr1939806803980680GTMissense_Mutation1
EEF2SKCMchr1939774713977471GASilentp.T735T1
EEF2STADchr1939822583982260CTT-In_Frame_Delp.259_260KL>T1
EEF2LUADchr1939841423984142GCMissense_Mutationp.I70M1
EEF2SKCMchr1939775643977564GASilentp.V704V1
EEF2BLCAchr1939820473982047GASilent1
EEF2CESCchr1939799653979965CTSilentp.T4821
EEF2HNSCchr1939767133976713CAMissense_Mutation1
EEF2HNSCchr1939793443979344CTMissense_Mutationp.A566T1
EEF2BLCAchr1939799773979977GASilentp.F478F1
EEF2GBMchr1939842843984284GTMissense_Mutation1
EEF2LGGchr1939798903979890CASilent1
EEF2THYMchr1939842233984223CTSilent1
EEF2LUADchr1939831803983181-AFrame_Shift_Insp.L110fs1
EEF2SKCMchr1939775133977513GASilentp.I721I1
EEF2BLCAchr1939799773979977GASilent1
EEF2CESCchr1939843403984340GASilentp.F41
EEF2UCSchr1939793923979393-GGCGCCCGCGATGATGTFrame_Shift_Insp.G550fs1
EEF2HNSCchr1939779013977901GASilent1
EEF2HNSCchr1939819533981954-GFrame_Shift_Insp.L297fs1
EEF2PAADchr1939766823976682TAMissense_Mutation1
EEF2STADchr1939793723979372GASilentp.I556I1
EEF2BLCAchr1939841653984165CTMissense_Mutationp.E63K1
EEF2THYMchr1939772973977297GAMissense_Mutationp.R767W1
EEF2CESCchr1939820203982020GTMissense_Mutation1
EEF2GBMchr1939843253984325GASilent1
EEF2LIHCchr1939832273983227TCMissense_Mutation1
EEF2HNSCchr1939793443979344CTMissense_Mutation1
EEF2LUADchr1939766263976626CAMissense_Mutationp.V835L1
EEF2LUADchr1939766263976627CCAAMissense_Mutationp.V835L1
EEF2SKCMchr1939766543976654GASilentp.F825F1
EEF2BLCAchr1939841653984165CTMissense_Mutation1
EEF2COADchr1939766963976696CTSilentp.Q811Q1
EEF2KIRCchr1939800443980044CAMissense_Mutationp.R456L1
EEF2BLCAchr1939798403979840ATMissense_Mutationp.L524Q1
EEF2CESCchr1939843403984340GASilent1
EEF2GBMchr1939800623980062GTMissense_Mutation1
EEF2LIHCchr1939806693980669ATMissense_Mutation1
EEF2HNSCchr1939793933979393GASilent1
EEF2LUADchr1939766273976627CASilentp.V834V1
EEF2LUSCchr1939778463977846CAMissense_Mutationp.V680L1
EEF2SKCMchr1939780423978042GASilentp.A614A1
EEF2BLCAchr1939798403979840ATMissense_Mutation1
EEF2BLCAchr1939806683980668TCMissense_Mutationp.Y397C1
EEF2ESCAchr1939820323982032GASilentp.N2701
EEF2ESCAchr1939767443976744GTSilentp.G795G1
EEF2PAADchr1939774583977458GTMissense_Mutation1
EEF2THYMchr1939766463976646CTMissense_Mutationp.S828N1
EEF2GBMchr1939806653980665ACMissense_Mutation1
EEF2LIHCchr1939813593981359TGMissense_Mutationp.K330T1
EEF2HNSCchr1939832633983263GAMissense_Mutationp.S82L1
EEF2LUADchr1939841923984192TAMissense_Mutationp.T54S1
EEF2LUSCchr1939800123980013CA-Frame_Shift_Delp.C466fs1
EEF2SKCMchr1939780153978015GASilentp.S623S1
EEF2BLCAchr1939794253979425CTMissense_Mutation1
EEF2COADchr1939779163977916GASilentp.G656G1
EEF2BLCAchr1939841333984133CGSplice_Sitep.T73_splice1
EEF2ESCAchr1939842813984281AGMissense_Mutationp.V24A1
EEF2PCPGchr1939781453978145CTMissense_Mutationp.R580H1
EEF2SKCMchr1939799503979950GASilentp.T487T1
EEF2THYMchr1939842233984223CTSilentp.A43A1
EEF2BLCAchr1939772343977234GASilent1
EEF2CESCchr1939823143982314C-Frame_Shift_Del1
EEF2HNSCchr1939778713977871GASilent1
EEF2LIHCchr1939809173980917GCMissense_Mutationp.L358V1
EEF2HNSCchr1939831513983151GCSilentp.L119L1
EEF2LUADchr1939831683983168CANonsense_Mutationp.E114*1
EEF2SKCMchr1939823043982304AGMissense_Mutationp.L244S1
EEF2BLCAchr1939806683980668TCMissense_Mutation1
EEF2COADchr1939799403979940CTMissense_Mutationp.A491T1
EEF2ESCAchr1939780643978064CAMissense_Mutationp.R607L1
EEF2KIRPchr1939832913983293TGA-Splice_Site1
EEF2UCECchr1939823003982300CTSilentp.G245G1
EEF2HNSCchr1939823473982347CTMissense_Mutation1
EEF2LIHCchr1939822873982287C-Frame_Shift_Delp.A250fs1

check buttonCopy number variation (CNV) of EEF2
* Click on the image to open the original image in a new window.
all structure

check buttonFusion gene breakpoints (product of the structural variants (SVs)) across EEF2
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


check button Fusion genes with this translation factor from FusionGDB2.0.
FusionGDB2 IDDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
103029N/AAA452576AP2S1chr1947341564+EEF2chr193981413+
103029N/AAA706989AUP1chr274754188+EEF2chr193981945+
103029N/AEC561306BCKDHBchr680826093+EEF2chr193977959+
103029N/AEC572773BRINP1chr9121964314+EEF2chr193979858+
103029STADTCGA-CG-5721-01ACCT4chr262104595-EEF2chr193982053-
96529N/AT05979EEF2chr193976484+ABHD6chr358223591+
102890THCATCGA-EM-A1YA-01AEEF2chr193976055-ANKS1Achr634977682+
95236KIRPTCGA-A4-A5Y1-01AEEF2chr193976055-ARFGEF2chr2047615777+
101628STADTCGA-BR-A4PD-01AEEF2chr193976108-B2Mchr1545009809+
97738LUADTCGA-86-A4D0-01AEEF2chr193976055-CBSchr2144476011-
100476OVTCGA-09-2056EEF2chr193977816-CKS1Bchr1154947117+
98105HNSCTCGA-BB-4223-01AEEF2chr193976055-CLCN3chr4170623929+
99855N/ABC068002EEF2chr193979817-CSNK1Dchr1780206799-
102507TGCTTCGA-SB-A6J6-01AEEF2chr193976055-DDX21chr1070723858+
102756STADTCGA-BR-8589-01AEEF2chr193976055-DDX27chr2047849303+
98111SARCTCGA-HB-A3YV-01AEEF2chr193976055-EEA1chr1293229203-
103029N/AAI075687EEF2chr193982344+EEF2chr193977241+
103029N/ABE173877EEF2chr193977925-EEF2chr193982305-
103029N/ABE763496EEF2chr193980915+EEF2chr193976336+
103029N/ABF761203EEF2chr193976742+EEF2chr193980695-
103029N/ABF801948EEF2chr193978117-EEF2chr193979344+
103029N/ABF927334EEF2chr193976340-EEF2chr193984194-
103029N/ABG031663EEF2chr193976181+EEF2chr193976433-
103029N/ABQ347823EEF2chr193976563-EEF2chr193976441+
103029N/ABQ349979EEF2chr193980548+EEF2chr193985461-
103029N/ACD580061EEF2chr193981383-EEF2chr193982967-
103029N/ACN263823EEF2chr193976672+EEF2chr193976591-
103029N/AEC450536EEF2chr193980048+EEF2chr193980523-
94732STADTCGA-BR-8679-01AEEF2chr193976055-EIF2AK2chr237342384-
93482THCATCGA-ET-A3DR-01AEEF2chr193976055-ERBB3chr1256492035+
94051N/AN93529EEF2chr193976177+F10chr13113803434-
96636STADTCGA-BR-8680-01AEEF2chr193976055-FAR1chr1113744912+
101372N/AEC555622EEF2chr193980022+GALNTL6chr4173722742+
25266HNSCTCGA-UF-A7JJEEF2chr193984205-IGHG1chr14106209405-
25266HNSCTCGA-UF-A7JJEEF2chr193984205-IGHG1chr14106237740-
98118SARCTCGA-KD-A5QU-01AEEF2chr193976055-LAMA4chr6112507969-
100140STADTCGA-CG-4301-01AEEF2chr193972316-LIPFchr1090424198+
97185N/AT19923EEF2chr193976585+LNX2chr1328179015-
25266N/AAW499012EEF2chr193982298-LRRC4Bchr1951037650-
100470Non-Cancer235NEEF2chr193985375-MAP2K2chr194090706-
99162N/AAW021402EEF2chr193976057-MEF2C-AS1chr588390023-
98609N/ABG060184EEF2chr193976054-MFHAS1chr88643265-
81580ACCTCGA-OR-A5L8-01AEEF2chr193979830-NRXN2chr1164416337-
98284N/ABQ308618EEF2chr193981364-OSR2chr899961810+
90662UVMTCGA-V4-A9E7-01AEEF2chr193972316-PABPC1chr8101734220-
89496N/ABI495206EEF2chr193976054-PAPSS1chr4108538387-
96331N/AAW874543EEF2chr193976308+PEX14chr110690464-
98134LUADTCGA-86-6851-01AEEF2chr193976055-PLEKHA5chr1219441012+
96928N/ABU958708EEF2chr193976149-PRMT3chr1120530001+
98139ACCTCGA-OR-A5KT-01AEEF2chr193976055-SEC63chr6108214782-
60961GBMTCGA-27-2524-01AEEF2chr193979327-SHDchr194282867+
98682KIRCTCGA-CW-5581-01AEEF2chr193976055-SIAEchr11124543777-
67087N/ADA998089EEF2chr193984161-SLC25A10chr1779679488+
82610PRADTCGA-EJ-A46GEEF2chr193983108-SLC25A23chr196436479-
82610PRADTCGA-EJ-A46G-01AEEF2chr193983108-SLC25A23chr196436475-
101736Non-CancerTCGA-K1-A3PO-11AEEF2chr193982805-SMARCA4chr1911151983+
102816N/ACV392722EEF2chr193980943+SPTBN1chr254687249-
94171N/ABI861553EEF2chr193976054-SUN2chr2239159588-
98474N/AAI905878EEF2chr193980927+TAPBPchr633272807+
99016LUADTCGA-44-5644-01AEEF2chr193976055-THSD4chr1572072881+
94367N/ACV351549EEF2chr193978077-TRRAPchr798602225+
102742DLBCTCGA-GS-A9TT-01AEEF2chr193976055-TYK2chr1910491352-
103029OVTCGA-61-1728GNB2chr7100275038+EEF2chr193978170-
103029N/ABG059476GPC6chr1394011252+EEF2chr193976054+
103029N/AAA523503GRIK1chr2130946173-EEF2chr193976054+
103029Non-CancerTCGA-IN-8462-11AMED25chr1950339202+EEF2chr193976745-
103029LGGTCGA-DH-A66DPAK6chr1540531758+EEF2chr193982056-
103029THYMTCGA-ZB-A965-01APLTPchr2044527399-EEF2chr193985461-
103029STADTCGA-BR-4292RPS5chr1958905962+EEF2chr193980707-
103029PRADTCGA-EJ-7125-01ASPON2chr41201668-EEF2chr193984348-
103029N/ABG230879SUN2chr2239159588+EEF2chr193976054+
103029PRADTCGA-CH-5763-01ATGM4chr344945479+EEF2chr193984348-
103031PRADTCGA-EJ-5511-01AZNF827chr4146682281-EEF2chr193985461-


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Prognostic Analysis


check button Kaplan-Meier plots with logrank tests of overall survival (OS)
all structure
Cancer typeTranslation factorCoefficentHazard ratioWald test pvalLikelihool ratio pvalLogrank test pval# samples
THYMEEF22.615926389044880.9616182944547370.003528522416457810.004962297817059970.0022970543894486121
LGGEEF21.718297244129090.5413338261335610.004672932554192960.005664509236800740.00473431463683783525
LUADEEF20.733569455303711-0.3098329956246650.01291175957774540.01264822988108660.0129797780188127564
LUADEEF20.733569455303711-0.3098329956246650.01291175957774540.01264822988108660.0129797780188127564
PAADEEF21.867972296382690.6248535090664250.01435914602407460.01126397039059140.0142905816478425182
PAADEEF21.867972296382690.6248535090664250.01435914602407460.01126397039059140.0142905816478425182
COADEEF21.688673635446520.5239433896970860.01686787549844750.01529746236599470.0167444072187299315
COADEEF21.688673635446520.5239433896970860.01686787549844750.01529746236599470.0167444072187299315
LIHCEEF20.705089620999105-0.3494303622646370.01822308799907760.01887021470670130.0185886870552413417
LIHCEEF20.705089620999105-0.3494303622646370.01822308799907760.01887021470670130.0185886870552413417
LAMLEEF20.612397908871423-0.4903730298494040.0237053903077990.02386822835783510.0235911972159276160
PCPGEEF20.184290693633243-1.691240911331480.03140700014019260.01559318999254960.0353360200441583185
PCPGEEF20.184290693633243-1.691240911331480.03140700014019260.01559318999254960.0353360200441583185


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Translation factor and Gender


check button Differential gene expression between female and male. (Wilcoxon test, pval<0.05)
all structure
Cancer typeTranslation factorpvaladj.p
TGCTEEF20.0003952825022513960.011
KIRCEEF20.00723614528056920.2
LGGEEF20.04096898703329431

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Translation factor and Age


check button Differential gene expression between young and old age groups (Wilcoxon test, pval<0.05)
all structure
Cancer typeTranslation factorpvaladj.p
LGGEEF20.00209595458317380.067
UCECEEF20.0003404236301897670.011

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Related Drugs


check button Drugs targeting genes involved in this translation factor.
(DrugBank Version 5.1.8 2021-05-08)
UniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
P13639DB03223DiphthamideSmall moleculeExperimental
P13639DB08348N~2~,N~2~-DIMETHYL-N~1~-(6-OXO-5,6-DIHYDROPHENANTHRIDIN-2-YL)GLYCINAMIDESmall moleculeExperimental
P13639DB11823EsketamineInhibitorSmall moleculeApproved|Investigational
P13639DB12688Moxetumomab PasudotoxInactivatorBiotechApproved|Investigational
P13639DB03223Diphthamide
P13639DB08348N~2~,N~2~-DIMETHYL-N~1~-(6-OXO-5,6-DIHYDROPHENANTHRIDIN-2-YL)GLYCINAMIDE
P13639DB11823EsketamineInhibitor
P13639DB12688Moxetumomab PasudotoxInactivator

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Related Diseases


check button Diseases associated with this translation factor.
(DisGeNet 4.0)
Disease IDDisease Name# PubMedsDisease source
C0006142Malignant neoplasm of breast1CTD_human
C0007134Renal Cell Carcinoma1CTD_human
C0029408Degenerative polyarthritis1CTD_human
C0086743Osteoarthrosis Deformans1CTD_human
C0205641Adenocarcinoma, Basal Cell1CTD_human
C0205642Adenocarcinoma, Oxyphilic1CTD_human
C0205643Carcinoma, Cribriform1CTD_human
C0205644Carcinoma, Granular Cell1CTD_human
C0205645Adenocarcinoma, Tubular1CTD_human
C0242379Malignant neoplasm of lung1CTD_human
C0279702Conventional (Clear Cell) Renal Cell Carcinoma1CTD_human
C0678222Breast Carcinoma1CTD_human
C1257931Mammary Neoplasms, Human1CTD_human
C1266042Chromophobe Renal Cell Carcinoma1CTD_human
C1266043Sarcomatoid Renal Cell Carcinoma1CTD_human
C1266044Collecting Duct Carcinoma of the Kidney1CTD_human
C1306837Papillary Renal Cell Carcinoma1CTD_human
C1836395SPINOCEREBELLAR ATAXIA 261CTD_human;ORPHANET;UNIPROT
C4704874Mammary Carcinoma, Human1CTD_human