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Translation Factor: EIF4B (NCBI Gene ID:1975) |
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Gene Summary |
| Gene Information | Gene Name: EIF4B | Gene ID: 1975 | Gene Symbol | EIF4B | Gene ID | 1975 |
| Gene Name | eukaryotic translation initiation factor 4B | |
| Synonyms | EIF-4B|PRO1843 | |
| Cytomap | 12q13.13 | |
| Type of Gene | protein-coding | |
| Description | eukaryotic translation initiation factor 4B | |
| Modification date | 20200313 | |
| UniProtAcc | P23588 | |
Child GO biological process term(s) under GO:0006412 |
| GO ID | GO term |
| GO:0006417 | Regulation of translation |
| GO:0008135 | Translation factor activity, RNA binding |
| GO:0002181 | Cytoplasmic translation |
| GO:0006413 | Translational initiation |
| GO:0006412 | Translation |
Gene ontology of translaction factor with evidence of Inferred from Direct Assay (IDA) from Entrez |
| Partner | Gene | GO ID | GO term | PubMed ID |
Inferred gene age of translation factor. |
| Gene | Inferred gene age group among (0 - 67.6], (67.6 - 355.7], (355.7 - 733], (733 - 1119.25], >1119.25 |
| EIF4B | (733 - 1119.25] |
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We searched PubMed using 'EIF4B[title] AND translation [title] AND human.' |
| Gene | Title | PMID |
| EIF4B | eIF4B phosphorylation at Ser504 links synaptic activity with protein translation in physiology and pathology | 28874824 |
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Skipped 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. |
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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. |
| ENST | Exon skip start (DNA) | Exon Skip end (DNA) | ORF |
| ENST00000262056 | 53413693 | 53413810 | In-frame |
| ENST00000262056 | 53416276 | 53416411 | In-frame |
| ENST00000262056 | 53421565 | 53421703 | In-frame |
| ENST00000262056 | 53431192 | 53431406 | Frame-shift |
| ENST00000262056 | 53433021 | 53433127 | Frame-shift |
| ENST00000262056 | 53433413 | 53433486 | Frame-shift |
Exon skipping position in the amino acid sequence. |
| 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) |
| ENST00000262056 | 53413693 | 53413810 | 4165 | 687 | 803 | 611 | 120 | 159 |
| ENST00000262056 | 53416276 | 53416411 | 4165 | 859 | 993 | 611 | 177 | 222 |
| ENST00000262056 | 53421565 | 53421703 | 4165 | 994 | 1131 | 611 | 222 | 268 |
Potentially (partially) lost protein functional features of UniProt. |
| UniProtAcc | Exon skip start (AA) | Exon Skip end (AA) | Function feature start (AA) | Function feature end (AA) | Functional feature type | Functional feature desc. |
| P23588 | 177 | 222 | 1 | 611 | Chain | ID=PRO_0000081616;Note=Eukaryotic translation initiation factor 4B |
| P23588 | 120 | 159 | 1 | 611 | Chain | ID=PRO_0000081616;Note=Eukaryotic translation initiation factor 4B |
| P23588 | 222 | 268 | 1 | 611 | Chain | ID=PRO_0000081616;Note=Eukaryotic translation initiation factor 4B |
| P23588 | 120 | 159 | 96 | 173 | Domain | Note=RRM;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00176 |
| P23588 | 177 | 222 | 164 | 331 | Compositional bias | Note=Arg-rich |
| P23588 | 222 | 268 | 164 | 331 | Compositional bias | Note=Arg-rich |
| P23588 | 177 | 222 | 169 | 325 | Compositional bias | Note=Asp-rich |
| P23588 | 222 | 268 | 169 | 325 | Compositional bias | Note=Asp-rich |
| P23588 | 177 | 222 | 192 | 192 | Modified residue | Note=Phosphoserine;Ontology_term=ECO:0000244,ECO:0000244;evidence=ECO:0000244|PubMed:20068231,ECO:0000244|PubMed:23186163;Dbxref=PMID:20068231,PMID:23186163 |
| P23588 | 177 | 222 | 207 | 207 | Modified residue | Note=Phosphoserine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:23186163;Dbxref=PMID:23186163 |
| P23588 | 177 | 222 | 219 | 219 | Modified residue | Note=Phosphoserine;Ontology_term=ECO:0000244,ECO:0000244,ECO:0000244;evidence=ECO:0000244|PubMed:18669648,ECO:0000244|PubMed:20068231,ECO:0000244|PubMed:23186163;Dbxref=PMID:18669648,PMID:20068231,PMID:23186163 |
| P23588 | 120 | 159 | 121 | 159 | Alternative sequence | ID=VSP_057351;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039 |
| P23588 | 177 | 222 | 203 | 203 | Natural variant | ID=VAR_064710;Note=Found in a renal cell carcinoma case%3B somatic mutation. P->R;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21248752;Dbxref=PMID:21248752 |
| P23588 | 222 | 268 | 246 | 246 | Sequence conflict | Note=R->C;Ontology_term=ECO:0000305;evidence=ECO:0000305 |
| P23588 | 120 | 159 | 121 | 125 | Beta strand | Ontology_term=ECO:0000244;evidence=ECO:0000244|PDB:1WI8 |
| P23588 | 120 | 159 | 130 | 133 | Turn | Ontology_term=ECO:0000244;evidence=ECO:0000244|PDB:2J76 |
| P23588 | 120 | 159 | 140 | 146 | Beta strand | Ontology_term=ECO:0000244;evidence=ECO:0000244|PDB:1WI8 |
| P23588 | 120 | 159 | 147 | 154 | Helix | Ontology_term=ECO:0000244;evidence=ECO:0000244|PDB:1WI8 |
| P23588 | 120 | 159 | 155 | 157 | Helix | Ontology_term=ECO:0000244;evidence=ECO:0000244|PDB:1WI8 |
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Gene expression level across TCGA pancancer |
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Gene expression level across GTEx pantissue |
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Expression level of gene isoforms across TCGA pancancer |
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Expression level of gene isoforms across GTEx pantissue |
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Cancer(tissue) type-specific expression level of Translation factor using z-score distriution |
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Differential expression between tumor and matched normal (in the cancer types with more than 10 matched samples) |
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| Cancer type | Translation factor | FC | adj.pval |
| BRCA | EIF4B | -2.16032742029696 | 2.35556737304054e-22 |
| KIRC | EIF4B | 1.14997140510474 | 7.59366366705366e-09 |
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Translation factor expression regulation through miRNA binding |
| Cancer type | Gene | miRNA | TargetScan binding score (Context++ score percentile) | Coefficient | Pvalue |
| GBM | EIF4B | hsa-miR-185-5p | 94 | 1 | 0.0166666666666667 |
| UCEC | EIF4B | hsa-miR-185-5p | 94 | -0.344843391902215 | 0.0464108520833579 |
Translation factor expression regulation through methylation in the promoter of Translation factor |
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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 |
Translation factor expression regulation through methylation in the gene body of Translation factor (positive regulation) |
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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 |
| LUSC | EIF4B | 2 | 1 | 0.0488464358388931 | 0.213660170212766 | 0.167375911949686 | 0.100389310731222 | 0.043691412296842 |
| SARC | EIF4B | 2 | 1 | 0.0392624624230068 | 0.224499581151832 | 0.166057435897436 | 0.00809409183848272 | 0.097534989945601 |
Translation factor expression regulation through copy number variation of Translation factor |
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| Cancer type | Gene | Coefficient | Pvalue |
| LIHC | EIF4B | 0.046786327 | 0.018955082 |
| CHOL | EIF4B | 0.044699099 | 0.048740155 |
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Strongly correlated genes belong to cellular important gene groups with EIF4B (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) |
| Cancer type | Gene group | Translation factor | Correlated gene | Coefficient | Pvalue |
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Protein 3D structureVisit iCn3D. |
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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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Overlap 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)) |
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![]() * Edge colors based on TCGA cancer types. |
* 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)) |
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| Cancer type | Translation factor | Interacting protein coding gene | FC | adj.pval |
| KIRC | EIF4B | RPS6 | -3.4556058277803 | 0.0001224322154943 |
| LUAD | EIF4B | EIF4A2 | 1.8359785836448 | 0.000162905479402723 |
| PRAD | EIF4B | RPS6KB1 | 1.25047501981198 | 0.000199084406212897 |
| PRAD | EIF4B | EIF3A | 1.13680328391952 | 0.000363360004697762 |
| BRCA | EIF4B | EIF5 | -1.16704316213885 | 0.00107943958337404 |
| COAD | EIF4B | RPS6KB1 | -1.1133069567678 | 0.00144392251968384 |
| THCA | EIF4B | RPS6 | 1.46346143665389 | 0.00305071956645465 |
| CHOL | EIF4B | PABPC1 | -4.56272528815353 | 0.00390625 |
| KIRP | EIF4B | EIF3G | -2.4178322962129 | 0.00471024587750435 |
| BLCA | EIF4B | EIF3A | -4.45104058307747 | 0.00532913208007812 |
| KICH | EIF4B | EIF4G1 | -1.46656081150743 | 0.00612920522689819 |
| KIRP | EIF4B | RPS6 | -1.15360907834159 | 0.0111397774890065 |
| COAD | EIF4B | RPS6 | 1.03379589520851 | 0.011966735124588 |
| BLCA | EIF4B | RPS6 | -1.76940777579938 | 0.012359619140625 |
| BLCA | EIF4B | PABPC1 | 1.31485302792746 | 0.0180816650390625 |
| HNSC | EIF4B | RPS6KB1 | -1.27996809705029 | 0.0301271170746986 |
| UCEC | EIF4B | EIF3G | -3.35078334696571 | 0.03125 |
| BLCA | EIF4B | EIF3G | -3.07707559649091 | 0.0323410034179688 |
| ESCA | EIF4B | EIF4A1 | -1.24538073199285 | 0.0419921875 |
| BRCA | EIF4B | EIF3G | 1.87948385011271 | 1.9107949115022e-06 |
| KIRP | EIF4B | RPS6KB1 | -1.46465474284348 | 2.00420618057251e-06 |
| LIHC | EIF4B | PABPC1 | -1.72076961362188 | 2.98009622125841e-06 |
| LIHC | EIF4B | EIF5 | -2.12060405382854 | 4.66164898670786e-08 |
| KICH | EIF4B | EIF4E | 1.61675210562671 | 6.55651092529297e-06 |
| BRCA | EIF4B | EIF3A | -1.218215573148 | 7.39403582934137e-06 |
| KICH | EIF4B | EIF4A1 | 1.14485583309571 | 8.16583633422851e-06 |
| PRAD | EIF4B | PABPC1 | -2.10200318363476 | 8.55379952759014e-07 |
Protein-protein interactors with this translation factor (BIOGRID-3.4.160) |
| PPI interactors with EIF4B |
| PABPC1, EIF3B, EIF4B, EIF3A, EIF3F, USP11, USP7, ALK, KBTBD7, AGO3, AGO4, Ccdc15, ELAVL1, ARRB1, ARRB2, TSG101, TERF1, TINF2, ACD, POT1, CUL3, EIF4A1, EIF4G1, RPL29, PHAX, EIF4G2, MYH9, CSTF2, NUP107, NUP153, SLC4A1AP, CCT6B, POLR1C, MAGOH, EIF4A3, SMURF1, YWHAE, CSNK2A1, PAN2, FBXO6, PARK2, Stk11, CTNNA1, CUL4B, NARS, OSBP, SAMHD1, SEC23A, XRCC5, PRMT3, SF1, XPO7, ASB2, ZBTB1, SMAD3, FBXW11, MAEL, CCT6A, CFL1, CTPS1, DDX39A, DOHH, LASP1, GSPT1, HSPB1, IMPDH2, KHSRP, SFN, YWHAQ, YWHAZ, NTRK1, gag, SRPK2, XPO1, HIST1H3E, AHSA1, CDC25B, ERCC6L, Crebbp, Smad3, Pten, Wiz, Naa10, Tmed10, Ttll12, GAN, RHOU, RC3H1, CDH1, EGFR, CYLD, TRIM25, G3BP1, YAP1, OTUD6B, GRHPR, UBE2M, EFTUD2, TNIP2, RNF31, SNAI1, RECQL4, GPC1, KCNJ2, ZFP36L2, METTL3, METTL14, KIAA1429, ALB, ANKRD53, ARPC5, BAZ2A, C14orf166, RTCB, CDON, DDX1, DDX3X, DDX3Y, DENND1C, DLEC1, DSG4, EIF3D, EIF3E, EIF3G, EIF3H, EIF3I, EIF3J, EIF3K, EIF3L, FAM98A, FEZF2, FGF11, HIST1H4A, HNRNPA1, HNRNPD, HNRNPU, HSPA1A, HSPA6, HSPA8, MRPS23, PRMT1, RBM12B, RBMX, RPL14, RPL18, RPL22, RPL23A, RPL24, RPL31, RPL9, RPS10, RPS11, RPS12, RPS13, RPS14, RPS15A, RPS16, RPS17, RPS18, RPS19, RPS20, RPS23, RPS24, RPS25, RPS26, RPS3, RPS3A, RPS4X, RPS5, RPS6, RPS7, RPS8, RPS9, RPSAP58, SRSF3, SLC45A3, SNRPD1, SNRPD3, SNRPN, SRSF9, TMEM232, TNFAIP1, TRAPPC8, USP9Y, USP9X, EIF3C, EIF3M, RC3H2, ATG16L1, GBF1, DCAF15, BICD2, PSMD14, DYRK1A, nsp8ab, SQSTM1, PLEKHA4, PINK1, LINC01554, TRIM6, DOK2, RAB5A, KIAA1211L, GATAD2A, PHACTR1, nsp1, ESR1, LAMTOR5, EIF4A2, CHMP4C, PRNP, FASN, HNRNPH1, INS, Rnf183, BRD4, CIC, Apc2, RBM39, FBP1, CSPG4, IFI16, GRB7, TXNIP, TBK1, IKBKE, PRDM13, TDRD5, PLK4, UFL1, TP53, SERBP1, FZR1, PAGE4, NUDCD2, NAA40, NIF3L1, RANBP10, NCOA5, NLRP7, AGO2, TOLLIP, SLFN11, MAGEL2, |
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Clinically associated variants from ClinVar. |
| Gene | Chr | Position | RefSeq | VarSeq | RefSeeq | VarType | Pathogenic | Disease | VarInfo |
nsSNVs with sample frequency (size of circle) from TCGA 33 cancers. |
SNVs and Indels |
| Gene | Cancer type | Chromosome | Start | End | RefSeeq | MutSeq | Mutation type | AAchange | # samples |
Copy number variation (CNV) of EIF4B * Click on the image to open the original image in a new window. |
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Fusion gene breakpoints (product of the structural variants (SVs)) across EIF4B * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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Fusion genes with this translation factor from FusionGDB2.0. |
| FusionGDB2 ID | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
| 101952 | STAD | TCGA-D7-A4YT | ADAP1 | chr7 | 994031 | - | EIF4B | chr12 | 53427589 | + |
| 101952 | STAD | TCGA-D7-A4YT-01A | ADAP1 | chr7 | 985398 | - | EIF4B | chr12 | 53427590 | + |
| 101952 | STAD | TCGA-D7-A4YT-01A | ADAP1 | chr7 | 994032 | - | EIF4B | chr12 | 53427590 | + |
| 92821 | STAD | TCGA-D7-A4YT | EIF4B | chr12 | 53421972 | + | ADAP1 | chr7 | 975141 | - |
| 25966 | HNSC | TCGA-BA-5152 | EIF4B | chr12 | 53400280 | + | C19orf71 | chr19 | 3543232 | + |
| 82974 | STAD | TCGA-D7-A4YT-01A | EIF4B | chr12 | 53421972 | + | COX19 | chr7 | 975141 | - |
| 85888 | N/A | BF340503 | EIF4B | chr12 | 53435988 | + | FAM53C | chr5 | 137678717 | + |
| 95270 | N/A | BF829819 | EIF4B | chr12 | 53435656 | + | KMT2D | chr12 | 49431501 | - |
| 80172 | N/A | AA736805 | EIF4B | chr12 | 53435937 | + | LHFPL3 | chr7 | 104311984 | - |
| 103326 | ESCA | TCGA-R6-A6L6 | EIF4B | chr12 | 53416411 | + | RNPC3 | chr1 | 104097655 | + |
| 103283 | UCEC | TCGA-EO-A3AY | EIF4B | chr12 | 53431406 | + | RPLP0 | chr12 | 120635265 | - |
| 85320 | N/A | BG213873 | EIF4B | chr12 | 53408728 | + | TNNC1 | chr3 | 52486122 | + |
| 101952 | N/A | BF882453 | FYTTD1 | chr3 | 197481885 | + | EIF4B | chr12 | 53435318 | + |
| 101952 | N/A | BI491355 | MYL1 | chr2 | 211171731 | + | EIF4B | chr12 | 53435993 | - |
| 101952 | N/A | FN093739 | SEMA5A | chr5 | 9496148 | + | EIF4B | chr12 | 53435058 | + |
| 101952 | SKCM | TCGA-EE-A29D-06A | TMTC3 | chr12 | 88570096 | - | EIF4B | chr12 | 53410257 | + |
| 101955 | N/A | AW386153 | ZNF384 | chr12 | 6775904 | - | EIF4B | chr12 | 53433209 | - |
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Kaplan-Meier plots with logrank tests of overall survival (OS) |
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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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Differential gene expression between female and male. (Wilcoxon test, pval<0.05) |
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| Cancer type | Translation factor | pval | adj.p |
| TGCT | EIF4B | 0.0306805619471656 | 0.86 |
| LUAD | EIF4B | 0.0425135570423456 | 1 |
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Differential gene expression between young and old age groups (Wilcoxon test, pval<0.05) |
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| Cancer type | Translation factor | pval | adj.p |
| LUAD | EIF4B | 0.00259391837660188 | 0.086 |
| LGG | EIF4B | 0.0210150298309777 | 0.67 |
| THYM | EIF4B | 0.0383557436267372 | 1 |
| SARC | EIF4B | 0.0427072128644206 | 1 |
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Drugs targeting genes involved in this translation factor. (DrugBank Version 5.1.8 2021-05-08) |
| UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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Diseases associated with this translation factor. (DisGeNet 4.0) |
| Disease ID | Disease Name | # PubMeds | Disease source |
| C0041696 | Unipolar Depression | 1 | PSYGENET |
| C1269683 | Major Depressive Disorder | 1 | PSYGENET |