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Translation Factor: MIF4GD (NCBI Gene ID:57409) |
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Gene Summary |
| Gene Information | Gene Name: MIF4GD | Gene ID: 57409 | Gene Symbol | MIF4GD | Gene ID | 57409 |
| Gene Name | MIF4G domain containing | |
| Synonyms | AD023|MIFD|SLIP1 | |
| Cytomap | 17q25.1 | |
| Type of Gene | protein-coding | |
| Description | MIF4G domain-containing proteinSLBP (stem loop binding protein)-interacting protein 1SLBP-interacting protein 1 | |
| Modification date | 20200313 | |
| UniProtAcc | A9UHW6 | |
Child GO biological process term(s) under GO:0006412 |
| GO ID | GO term |
| GO:0006417 | Regulation of translation |
| GO:0045727 | Positive regulation of translation |
| 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 |
| MIF4GD | (733 - 1119.25] |
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We searched PubMed using 'MIF4GD[title] AND translation [title] AND human.' |
| Gene | Title | PMID |
| MIF4GD | INT6 interacts with MIF4GD/SLIP1 and is necessary for efficient histone mRNA translation | 22532700 |
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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 |
| ENST00000325102 | 73263826 | 73263982 | In-frame |
| ENST00000325102 | 73264163 | 73264273 | 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) |
| ENST00000325102 | 73263826 | 73263982 | 1323 | 318 | 473 | 222 | 64 | 116 |
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. |
| A9UHW6 | 64 | 116 | 1 | 222 | Chain | ID=PRO_0000337089;Note=MIF4G domain-containing protein |
| A9UHW6 | 64 | 116 | 3 | 205 | Domain | Note=MIF4G |
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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 |
| CHOL | MIF4GD | -2.92474154465758 | 0.00390625 |
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Translation factor expression regulation through miRNA binding |
| Cancer type | Gene | miRNA | TargetScan binding score (Context++ score percentile) | Coefficient | Pvalue |
| DLBC | MIF4GD | hsa-miR-1306-5p | 97 | 0.424838112858464 | 0.00315279076167981 |
| UCEC | MIF4GD | hsa-miR-1306-5p | 97 | -0.393430099312452 | 0.0220331895014324 |
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 |
Translation factor expression regulation through copy number variation of Translation factor |
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| Cancer type | Gene | Coefficient | Pvalue |
| LUSC | MIF4GD | 0.101786156 | 0.037249785 |
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Strongly correlated genes belong to cellular important gene groups with MIF4GD (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 type | Gene group | Translation factor | Correlated gene | Coefficient | Pvalue |
| THYM | Cell metabolism gene | MIF4GD | MDH2 | 0.815222611 | 3.04E-30 |
| THYM | IUPHAR | MIF4GD | VRK3 | 0.800537752 | 1.87E-28 |
| THYM | Kinase | MIF4GD | VRK3 | 0.800537752 | 1.87E-28 |
| UCS | Cell metabolism gene | MIF4GD | MDH2 | 0.815222611 | 3.04E-30 |
| UCS | IUPHAR | MIF4GD | VRK3 | 0.800537752 | 1.87E-28 |
| UCS | Kinase | MIF4GD | VRK3 | 0.800537752 | 1.87E-28 |
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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 |
| KIRP | MIF4GD | DDX19B | 2.11618331213695 | 0.000110303983092308 |
| LIHC | MIF4GD | DDX25 | 2.64811993137191 | 0.000341801925418751 |
| PRAD | MIF4GD | ERI2 | 1.56813430634897 | 0.00175864963925712 |
| KIRC | MIF4GD | PAIP1 | -5.71279064132007 | 0.00220467399393826 |
| THCA | MIF4GD | DDX19A | -1.09168230331841 | 0.00232210128712262 |
| CHOL | MIF4GD | ERI2 | -2.35448132349041 | 0.00390625 |
| KIRP | MIF4GD | EIF3G | -2.4178322962129 | 0.00471024587750435 |
| KICH | MIF4GD | EIF4G1 | -1.46656081150743 | 0.00612920522689819 |
| CHOL | MIF4GD | SLBP | -2.47916114694844 | 0.0078125 |
| HNSC | MIF4GD | DDX19A | 1.44814616243363 | 0.0129453654280951 |
| CHOL | MIF4GD | DDX19B | -2.2878554243944 | 0.01953125 |
| UCEC | MIF4GD | EIF3G | -3.35078334696571 | 0.03125 |
| ESCA | MIF4GD | SLBP | -1.20779658007017 | 0.0322265625 |
| BLCA | MIF4GD | EIF3G | -3.07707559649091 | 0.0323410034179688 |
| THCA | MIF4GD | ERI2 | 1.00775979946092 | 1.13795592860251e-05 |
| BRCA | MIF4GD | PAIP1 | 1.33783668607252 | 1.59729685534959e-08 |
| LIHC | MIF4GD | SLBP | -1.92161263408532 | 1.82457528521744e-08 |
| BRCA | MIF4GD | EIF3G | 1.87948385011271 | 1.9107949115022e-06 |
| PRAD | MIF4GD | DDX25 | 1.2527472475822 | 2.15325156396327e-05 |
| BRCA | MIF4GD | DDX25 | 3.03374654437523 | 2.51798948666808e-19 |
| BRCA | MIF4GD | ERI2 | 1.47959808534493 | 2.63474656161064e-08 |
| HNSC | MIF4GD | DDX25 | 1.22622442798775 | 2.80523191174599e-05 |
| LIHC | MIF4GD | ERI2 | -1.87262453605068 | 4.32830942329488e-06 |
| PRAD | MIF4GD | DDX19B | -5.35187526532367 | 5.10126106041513e-07 |
| THCA | MIF4GD | DDX25 | -1.29240482012627 | 6.1386855605902e-11 |
| THCA | MIF4GD | SLBP | -2.09860049531233 | 7.22868172738035e-09 |
| LUSC | MIF4GD | DDX19B | -4.25679620768829 | 7.78525552645347e-05 |
| LIHC | MIF4GD | DDX19B | -4.37134395144494 | 9.26110880632525e-09 |
Protein-protein interactors with this translation factor (BIOGRID-3.4.160) |
| PPI interactors with MIF4GD |
| HGS, DDX19A, SVIL, UBQLN4, HINFP, DHX16, ILF2, PPIP5K1, PDXDC1, LSM5, HDAC4, PPARG, EXOSC6, PDE4DIP, DDX19B, CTIF, KLK3, PSMC1, Psmd6, CRYBA4, SLBP, DDIAS, C7orf60, SMARCB1, PRE5, APEX1, nsp7ab, CHCHD2, ENKD1, FAM110A, EIF3G, WDYHV1, ATPAF2, MKRN3, C6orf165, AQP1, KIF1B, nsp16, ARHGEF5, EXPH5, TUBGCP6, HAUS5, RICTOR, HPS3, RGL3, HOOK1, RTEL1, |
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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 |
| MIF4GD | BRCA | chr17 | 73264205 | 73264206 | AC | - | Frame_Shift_Del | p.F85fs | 5 |
| MIF4GD | ESCA | chr17 | 73265466 | 73265466 | G | T | Missense_Mutation | p.S56Y | 2 |
| MIF4GD | BLCA | chr17 | 73262901 | 73262901 | C | G | Missense_Mutation | 2 | |
| MIF4GD | UCEC | chr17 | 73262836 | 73262836 | G | A | Nonsense_Mutation | p.R213* | 2 |
| MIF4GD | HNSC | chr17 | 73265430 | 73265430 | C | G | Missense_Mutation | p.R68T | 2 |
| MIF4GD | UCEC | chr17 | 73262994 | 73262994 | T | C | Missense_Mutation | p.N200D | 2 |
| MIF4GD | UCEC | chr17 | 73265484 | 73265484 | C | A | Missense_Mutation | p.R43M | 2 |
| MIF4GD | BLCA | chr17 | 73262901 | 73262901 | C | G | Missense_Mutation | p.E238Q | 2 |
| MIF4GD | COAD | chr17 | 73265494 | 73265494 | C | T | Missense_Mutation | p.V40I | 1 |
| MIF4GD | LUAD | chr17 | 73262985 | 73262985 | G | T | Missense_Mutation | p.R210S | 1 |
| MIF4GD | BLCA | chr17 | 73265518 | 73265518 | C | G | Missense_Mutation | p.E39Q | 1 |
| MIF4GD | SKCM | chr17 | 73265464 | 73265464 | G | T | Missense_Mutation | p.R50S | 1 |
| MIF4GD | COAD | chr17 | 73265439 | 73265439 | G | A | Missense_Mutation | p.T58M | 1 |
| MIF4GD | LUAD | chr17 | 73263692 | 73263692 | A | T | Missense_Mutation | p.M164K | 1 |
| MIF4GD | BLCA | chr17 | 73266270 | 73266270 | C | T | Missense_Mutation | p.E3K | 1 |
| MIF4GD | STAD | chr17 | 73265546 | 73265546 | C | T | Silent | 1 | |
| MIF4GD | LUAD | chr17 | 73265464 | 73265464 | G | A | Missense_Mutation | p.R57C | 1 |
| MIF4GD | BLCA | chr17 | 73263627 | 73263627 | C | G | Missense_Mutation | p.E186Q | 1 |
| MIF4GD | STAD | chr17 | 73265546 | 73265546 | C | T | Silent | p.P29P | 1 |
| MIF4GD | HNSC | chr17 | 73264171 | 73264171 | A | T | Missense_Mutation | 1 | |
| MIF4GD | LUAD | chr17 | 73262985 | 73262985 | G | T | Missense_Mutation | p.R169S | 1 |
| MIF4GD | BLCA | chr17 | 73265503 | 73265503 | C | G | Missense_Mutation | p.E44Q | 1 |
| MIF4GD | STAD | chr17 | 73263620 | 73263620 | T | A | Missense_Mutation | p.E147V | 1 |
| MIF4GD | HNSC | chr17 | 73265430 | 73265430 | C | G | Missense_Mutation | 1 | |
| MIF4GD | LUAD | chr17 | 73263869 | 73263869 | G | T | Silent | p.V102V | 1 |
| MIF4GD | BLCA | chr17 | 73266270 | 73266270 | C | A | Nonsense_Mutation | p.E3* | 1 |
| MIF4GD | UCEC | chr17 | 73262862 | 73262862 | G | A | Missense_Mutation | p.P251S | 1 |
| MIF4GD | HNSC | chr17 | 73264171 | 73264171 | A | T | Missense_Mutation | p.I103N | 1 |
| MIF4GD | LUAD | chr17 | 73263692 | 73263692 | A | T | Missense_Mutation | p.M123K | 1 |
| MIF4GD | BLCA | chr17 | 73262901 | 73262901 | C | G | Missense_Mutation | p.E197Q | 1 |
| MIF4GD | BLCA | chr17 | 73265518 | 73265518 | C | G | Missense_Mutation | 1 | |
| MIF4GD | OV | chr17 | 73263913 | 73263913 | G | A | Nonsense_Mutation | p.Q129* | 1 |
| MIF4GD | BLCA | chr17 | 73263627 | 73263627 | C | G | Missense_Mutation | p.E145Q | 1 |
| MIF4GD | HNSC | chr17 | 73264171 | 73264171 | A | T | Missense_Mutation | p.I62N | 1 |
| MIF4GD | BLCA | chr17 | 73266270 | 73266270 | C | T | Missense_Mutation | 1 | |
| MIF4GD | SARC | chr17 | 73262926 | 73262926 | G | T | Missense_Mutation | 1 | |
| MIF4GD | KIRP | chr17 | 73263949 | 73263949 | G | T | Silent | 1 | |
| MIF4GD | BLCA | chr17 | 73263627 | 73263627 | C | G | Missense_Mutation | 1 | |
| MIF4GD | SARC | chr17 | 73263909 | 73263909 | G | T | Missense_Mutation | 1 | |
| MIF4GD | CESC | chr17 | 73263634 | 73263634 | C | T | Silent | 1 | |
| MIF4GD | LIHC | chr17 | 73263012 | 73263012 | C | T | Missense_Mutation | 1 | |
| MIF4GD | BLCA | chr17 | 73265503 | 73265503 | C | G | Missense_Mutation | 1 | |
| MIF4GD | SARC | chr17 | 73266216 | 73266216 | G | T | Missense_Mutation | 1 | |
| MIF4GD | COAD | chr17 | 73263667 | 73263667 | G | T | Missense_Mutation | p.D131E | 1 |
| MIF4GD | LUAD | chr17 | 73263869 | 73263869 | G | T | Silent | p.V143V | 1 |
| MIF4GD | SARC | chr17 | 73266286 | 73266286 | G | T | Missense_Mutation | 1 |
Copy number variation (CNV) of MIF4GD * 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 MIF4GD * 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 |
| 90207 | LUSC | TCGA-43-2581-01A | MIF4GD | chr17 | 73266195 | - | SDK2 | chr17 | 71443887 | - |
| 78439 | HNSC | TCGA-CV-7416-01A | RSPH3 | chr6 | 159420744 | - | MIF4GD | chr17 | 73264273 | - |
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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 | MIF4GD | 0.000877574143235212 | 0.025 |
| BRCA | MIF4GD | 0.00558204000579513 | 0.15 |
| KIRC | MIF4GD | 0.00611165039993277 | 0.16 |
| PCPG | MIF4GD | 0.0190762856718564 | 0.48 |
| LGG | MIF4GD | 0.0244185118031736 | 0.59 |
| LUAD | MIF4GD | 0.0427188664303575 | 0.98 |
| LIHC | MIF4GD | 0.0496318296603287 | 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 |
| STAD | MIF4GD | 0.016447955621078 | 0.51 |
| LUSC | MIF4GD | 0.0230269171959145 | 0.69 |
| KIRC | MIF4GD | 0.00126676883820088 | 0.042 |
| THYM | MIF4GD | 0.00877898043283677 | 0.28 |
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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 |