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Translation Factor: MRRF (NCBI Gene ID:92399) |
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Gene Summary |
Gene Information | Gene Name: MRRF | Gene ID: 92399 | Gene Symbol | MRRF | Gene ID | 92399 |
Gene Name | mitochondrial ribosome recycling factor | |
Synonyms | MRFF|MTRRF|RRF | |
Cytomap | 9q33.2 | |
Type of Gene | protein-coding | |
Description | ribosome-recycling factor, mitochondrialribosome-releasing factor, mitochondrial | |
Modification date | 20200313 | |
UniProtAcc | Q96E11 |
Child GO biological process term(s) under GO:0006412 |
GO ID | GO term |
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 |
Hgene | MRRF | GO:0032790 | ribosome disassembly | 19716793 |
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 |
MRRF | >1119.25 |
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We searched PubMed using 'MRRF[title] AND translation [title] AND human.' |
Gene | Title | PMID |
MRRF | . | . |
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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. |
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 |
ENST00000344641 | 125033142 | 125033354 | 5CDS-5UTR |
ENST00000344641 | 125042721 | 125042877 | In-frame |
ENST00000344641 | 125047447 | 125047566 | Frame-shift |
ENST00000344641 | 125054027 | 125054119 | Frame-shift |
ENST00000344641 | 125075505 | 125075665 | 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) |
ENST00000344641 | 125042721 | 125042877 | 1964 | 496 | 651 | 262 | 61 | 113 |
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. |
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Gene expression level across TCGA pancancer |
Gene expression level across GTEx pantissue |
Expression level of gene isoforms across TCGA pancancer |
Expression level of gene isoforms across GTEx pantissue |
Cancer(tissue) type-specific expression level of Translation factor using z-score distriution |
Differential expression between tumor and matched normal (in the cancer types with more than 10 matched samples) |
Cancer type | Translation factor | FC | adj.pval |
KICH | MRRF | 1.86992130954506 | 0.0014527440071106 |
LIHC | MRRF | -1.19805818879659 | 0.0305924082275009 |
PRAD | MRRF | -1.56810957454655 | 2.74398347191128e-05 |
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Translation factor expression regulation through miRNA binding |
Cancer type | Gene | miRNA | TargetScan binding score (Context++ score percentile) | Coefficient | Pvalue |
Translation factor expression regulation through methylation in the promoter of Translation factor |
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) |
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 |
Cancer type | Gene | Coefficient | Pvalue |
PCPG | MRRF | 0.106245962 | 0.025971636 |
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Strongly correlated genes belong to cellular important gene groups with MRRF (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 |
KICH | Cell metabolism gene | MRRF | PMPCA | 0.803350973 | 9.62E-22 |
THYM | Cell metabolism gene | MRRF | NUPL2 | 0.836015153 | 4.56E-33 |
THYM | Epifactor | MRRF | DNAJC2 | 0.810895213 | 1.06E-29 |
UCS | Cell metabolism gene | MRRF | NUPL2 | 0.836015153 | 4.56E-33 |
UCS | Epifactor | MRRF | DNAJC2 | 0.810895213 | 1.06E-29 |
UVM | Cell metabolism gene | MRRF | TIMM9 | 0.808685798 | 1.17E-19 |
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Protein 3D structure Visit 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)) |
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)) |
* 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)) |
Cancer type | Translation factor | Interacting protein coding gene | FC | adj.pval |
KIRC | MRRF | MRPL20 | 1.48585631024503 | 0.000111704804180407 |
KICH | MRRF | MRPL9 | 1.16888038960038 | 0.000120222568511963 |
LUAD | MRRF | MRPL20 | -3.00071204707904 | 0.000452706327224566 |
BRCA | MRRF | MRPL20 | -1.74379528461375 | 0.000756034430433012 |
KIRP | MRRF | GFM1 | -3.60557651795202 | 0.00154796987771988 |
KIRP | MRRF | MRPL19 | -1.9689242575519 | 0.00179363833740354 |
BLCA | MRRF | MRPL27 | -4.19270554058168 | 0.00202178955078125 |
STAD | MRRF | MRPS16 | -1.64208084987431 | 0.00239070039242506 |
KICH | MRRF | GFM1 | 1.05246565332639 | 0.00378090143203735 |
PRAD | MRRF | MRPS9 | 1.04379115553269 | 0.00496210155254694 |
HNSC | MRRF | MRPS16 | -2.01564621821803 | 0.00518989327406416 |
KICH | MRRF | MRPL19 | -2.18550705564541 | 0.00672554969787598 |
PRAD | MRRF | ICT1 | -1.54848444909352 | 0.00907723161841939 |
STAD | MRRF | MRPL9 | -1.54523483458273 | 0.0118026207201183 |
LIHC | MRRF | MRPL20 | -1.08735154161025 | 0.0158079482509981 |
CHOL | MRRF | MRPL19 | -2.09295650388558 | 0.0390625 |
BRCA | MRRF | MRPL27 | -1.5584165725499 | 1.16393956539382e-08 |
LUSC | MRRF | MRPL21 | -4.98277643789037 | 1.45947399043856e-08 |
THCA | MRRF | MRPS10 | 1.33413691764991 | 1.55171507174296e-05 |
LUSC | MRRF | MRPS9 | -3.60637641031661 | 1.82498668910368e-07 |
LUAD | MRRF | MRPS9 | -1.32894454884901 | 1.98978698949574e-05 |
BRCA | MRRF | ICT1 | -4.17488220449664 | 2.73719348917167e-14 |
LUAD | MRRF | MRPL27 | -1.39404329671842 | 3.44055922076328e-05 |
LUSC | MRRF | MRPL27 | -1.81809468729316 | 3.90393047420304e-06 |
LUAD | MRRF | GFM1 | -2.84901818322678 | 4.2869535120076e-07 |
LUAD | MRRF | MRPL21 | -1.86897497221853 | 6.16191557420719e-07 |
LUSC | MRRF | ICT1 | -3.23093376049456 | 6.60526357089358e-07 |
BRCA | MRRF | GFM1 | 1.76831243345242 | 7.05963288731276e-10 |
BRCA | MRRF | MRPL21 | -1.5345447607194 | 7.40794680786486e-08 |
Protein-protein interactors with this translation factor (BIOGRID-3.4.160) |
PPI interactors with MRRF |
ICT1, APP, CDV3, MRPL53, RPS19, NDUFA7, SARNP, TSFM, PPIF, SLIRP, PPIB, NDUFA2, RBMS1, SRPRB, SCP2, HCCS, MRRFP1, DBT, MMAB, NFS1, LYRM7, IBA57, MED4, BANP, MKNK2, ANAPC15, TUBA1C, FBXO18, ARX, SKA1, Evpl, Nek2, Cenph, Cbx7, Pdlim5, Tipin, Cdc26, Mis12, Kif22, Haus1, Cep44, CT55, EFTUD2, ATG16L1, SYP, WIPI2, CMTM5, ZNF408, FAM9B, AGTRAP, FHL3, KRT40, nsp13, nsp3, nsp9, ORF8, KIF14, AUH, MDH2, AARS2, ACAD9, ACAT1, ACOT1, ACOT2, AFG3L2, AK4, ALYREF, ARGLU1, ATP5B, ATP5C1, ATP5D, ATPIF1, ATP5J2-PTCD1, ATP5F1, ATP5H, ATP5J, ATP5O, ATPAF1, BCS1L, BRIX1, C17orf80, CARS2, CDK5RAP1, CLPX, COX5A, CS, DAP3, DDX18, DDX28, DDX50, DDX54, DHTKD1, DHX30, DLAT, DLST, EARS2, EBNA1BP2, ECHS1, ECSIT, ELAC2, ERAL1, ETFA, ETFB, FASTKD2, FASTKD5, FLAD1, GADD45GIP1, GARS, GATB, GATC, GCDH, GFM1, GLS, GLUD1, GRSF1, GTPBP10, GTPBP3, GTPBP6, GUF1, HADH, HADHA, HARS2, HINT2, HNRNPA2B1, HNRNPA3, HNRNPAB, HNRNPDL, HNRNPK, HNRNPL, HNRNPR, HSD17B10, HSPA9, HSPD1, IARS2, IDH3A, IVD, KIAA0391, LARS2, LETM1, LONP1, LRPPRC, LUC7L, LUC7L2, LYRM4, MALSU1, ME2, METTL15, RNMTL1, MRPL1, MRPL10, MRPL12, MRPL13, MRPL15, MRPL17, MRPL18, MRPL19, MRPL2, MRPL20, MRPL21, MRPL22, MRPL23, MRPL24, MRPL27, MRPL28, MRPL3, MRPL30, MRPL32, MRPL37, MRPL38, MRPL39, MRPL4, MRPL40, MRPL41, MRPL42, MRPL43, MRPL44, MRPL45, MRPL46, MRPL47, MRPL48, MRPL49, MRPL50, MRPL52, MRPL54, MRPL55, MRPL9, MRPS10, MRPS11, MRPS14, MRPS16, MRPS17, MRPS18B, MRPS18C, MRPS2, MRPS22, MRPS23, MRPS24, MRPS25, MRPS26, MRPS27, MRPS28, MRPS30, MRPS31, MRPS33, MRPS34, MRPS35, MRPS36, MRPS5, MRPS6, MRPS7, MRPS9, MTERF3, MTHFD1L, MTIF2, MTPAP, MTRF1L, NDUFA12, NDUFA5, NDUFA6, NDUFA9, NDUFAF1, NDUFAF2, NDUFAF3, NDUFAF4, NDUFAF5, NDUFS1, NDUFS2, NDUFS3, NDUFS4, NDUFS6, NDUFS7, NDUFS8, NDUFV1, NDUFV2, NDUFV3, NIFK, NIPSNAP1, NME4, NNT, NUBPL, OAT, OGDH, PDE12, PDHA1, PDHB, PDHX, PDK1, PDK3, PDPR, PHB, PMPCA, PNPT1, POLDIP2, POLG, POLRMT, PREPL, PRPF4B, PTCD3, PUS1, PYCR1, PYCR2, WIBG, QRSL1, RBFA, RBM28, RBMX, WBSCR16, RPL36, RSL1D1, RTN4IP1, SHMT2, SLC30A9, SRSF4, STOML2, SUCLA2, SUPV3L1, SYNCRIP, TACO1, TARS2, TEFM, TFAM, THEM4, THG1L, TIMM44, TRMT10C, TRMT11, TRMT61B, TRUB2, C10orf2, U2AF2, VARS2, VWA8, WARS2, YARS2, CLPP, UCHL1, NR3C1, SOCS6, ZNF501, MTIF3, EFNB2, NUDT13, FTSJ2, FGFR1OP2, AHR, ZNF8, NAT1, |
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Clinically associated variants from ClinVar. |
Gene | Chr | Position | RefSeq | VarSeq | RefSeeq | VarType | Pathogenic | Disease | VarInfo |
MRRF | chr9 | 125075600 | A | G | single_nucleotide_variant | Uncertain_significance | not_specified | SO:0001583|missense_variant,SO:0001619|non-coding_transcript_variant,SO:0001627|intron_variant | SO:0001583|missense_variant,SO:0001619|non-coding_transcript_variant,SO:0001627|intron_variant |
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 |
MRRF | KIRC | chr9 | 125033141 | 125033141 | A | T | Splice_Site | 3 | |
MRRF | LIHC | chr9 | 125054104 | 125054104 | G | - | Frame_Shift_Del | p.R179fs | 2 |
MRRF | SKCM | chr9 | 125084878 | 125084878 | C | T | Silent | p.T257T | 2 |
MRRF | SKCM | chr9 | 125075623 | 125075623 | G | A | Silent | p.K223K | 2 |
MRRF | HNSC | chr9 | 125084837 | 125084837 | G | A | Missense_Mutation | p.D244N | 2 |
MRRF | LUAD | chr9 | 125075536 | 125075536 | G | T | Silent | p.V194V | 2 |
MRRF | SKCM | chr9 | 125042722 | 125042722 | C | T | Splice_Site | p.A62_splice | 2 |
MRRF | HNSC | chr9 | 125042818 | 125042818 | C | T | Missense_Mutation | p.S94F | 2 |
MRRF | ESCA | chr9 | 125047552 | 125047552 | G | A | Missense_Mutation | p.A149T | 2 |
MRRF | LUSC | chr9 | 125033303 | 125033303 | A | G | Missense_Mutation | p.M45V | 1 |
MRRF | ESCA | chr9 | 125047541 | 125047541 | T | C | Missense_Mutation | 1 | |
MRRF | STAD | chr9 | 125033202 | 125033202 | T | C | Missense_Mutation | p.V11A | 1 |
MRRF | LIHC | chr9 | 125042730 | 125042730 | A | - | Frame_Shift_Del | p.K65fs | 1 |
MRRF | OV | chr9 | 125075605 | 125075605 | C | G | Missense_Mutation | p.N217K | 1 |
MRRF | HNSC | chr9 | 125084837 | 125084837 | G | A | Missense_Mutation | 1 | |
MRRF | LIHC | chr9 | 125047494 | 125047494 | T | - | Frame_Shift_Del | p.A129fs | 1 |
MRRF | OV | chr9 | 125033218 | 125033218 | C | T | Silent | p.R16 | 1 |
MRRF | HNSC | chr9 | 125042818 | 125042818 | C | T | Missense_Mutation | 1 | |
MRRF | LIHC | chr9 | 125075615 | 125075615 | A | - | Frame_Shift_Del | p.K221fs | 1 |
MRRF | BLCA | chr9 | 125054065 | 125054065 | G | T | Missense_Mutation | 1 | |
MRRF | PAAD | chr9 | 125042786 | 125042786 | C | A | Silent | 1 | |
MRRF | HNSC | chr9 | 125047560 | 125047560 | C | T | Silent | 1 | |
MRRF | LIHC | chr9 | 125047451 | 125047451 | C | - | Frame_Shift_Del | p.S115fs | 1 |
MRRF | BLCA | chr9 | 125042729 | 125042729 | G | C | Silent | 1 | |
MRRF | SARC | chr9 | 125048163 | 125048163 | C | T | RNA | NULL | 1 |
MRRF | HNSC | chr9 | 125042832 | 125042832 | C | G | Missense_Mutation | 1 | |
MRRF | LUAD | chr9 | 125042807 | 125042807 | A | T | Missense_Mutation | p.E90D | 1 |
MRRF | BLCA | chr9 | 125042729 | 125042729 | G | C | Silent | p.G64G | 1 |
MRRF | HNSC | chr9 | 125042832 | 125042832 | C | G | Missense_Mutation | p.L99V | 1 |
MRRF | LUAD | chr9 | 125047485 | 125047485 | G | T | Silent | p.G126G | 1 |
MRRF | CESC | chr9 | 125075632 | 125075632 | C | T | Silent | 1 | |
MRRF | LUAD | chr9 | 125042860 | 125042860 | A | G | Missense_Mutation | p.N108S | 1 |
MRRF | COAD | chr9 | 125042842 | 125042842 | A | C | Missense_Mutation | p.N102T | 1 |
MRRF | SKCM | chr9 | 125042722 | 125042722 | C | T | Missense_Mutation | p.A62V | 1 |
MRRF | HNSC | chr9 | 125047560 | 125047560 | C | T | Silent | p.F151F | 1 |
MRRF | ESCA | chr9 | 125084867 | 125084867 | G | A | Nonsense_Mutation | p.W200* | 1 |
MRRF | LUSC | chr9 | 125047469 | 125047469 | T | C | Missense_Mutation | p.V121A | 1 |
MRRF | ESCA | chr9 | 125047541 | 125047541 | T | C | Missense_Mutation | p.L145S | 1 |
MRRF | SKCM | chr9 | 125054115 | 125054115 | C | T | Missense_Mutation | p.P183S | 1 |
MRRF | LUSC | chr9 | 125054075 | 125054075 | G | C | Silent | p.L169L | 1 |
MRRF | STAD | chr9 | 125033141 | 125033141 | A | T | Splice_Site | . | 1 |
Copy number variation (CNV) of MRRF * Click on the image to open the original image in a new window. |
Fusion gene breakpoints (product of the structural variants (SVs)) across MRRF * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
Fusion genes with this translation factor from FusionGDB2.0. |
FusionGDB2 ID | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
94882 | STAD | TCGA-EQ-A4SO-01A | CDC14B | chr9 | 99381501 | - | MRRF | chr9 | 125075506 | + |
94882 | N/A | BM972978 | MGEA5 | chr10 | 103547843 | - | MRRF | chr9 | 125093607 | - |
100049 | N/A | BG030962 | MRRF | chr9 | 125085310 | + | DIAPH3 | chr13 | 60469285 | + |
85579 | STAD | TCGA-CG-4436-01A | MRRF | chr9 | 125075665 | + | GLIS3 | chr9 | 3937189 | - |
73210 | LUSC | TCGA-66-2754-01A | MRRF | chr9 | 125054119 | - | KIAA0368 | chr9 | 114206774 | - |
95148 | BLCA | TCGA-DK-A3X1-01A | MRRF | chr9 | 125027217 | + | NDUFA8 | chr9 | 124906657 | - |
95595 | SARC | TCGA-DX-A8BV-01A | MRRF | chr9 | 125027217 | + | NR4A1 | chr12 | 52448111 | + |
90011 | COAD | TCGA-DM-A28A-01A | MRRF | chr9 | 125054119 | + | TTLL11 | chr9 | 124633027 | - |
94882 | BRCA | TCGA-E2-A15E-06A | RC3H2 | chr9 | 125652591 | - | MRRF | chr9 | 125033143 | + |
94889 | Non-Cancer | TCGA-HU-A4GC-11A | TTBK2 | chr15 | 43212636 | - | MRRF | chr9 | 125075506 | + |
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Kaplan-Meier plots with logrank tests of overall survival (OS) |
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) |
Cancer type | Translation factor | pval | adj.p |
KIRP | MRRF | 0.00147403583670778 | 0.041 |
TGCT | MRRF | 0.00690306132089501 | 0.19 |
THCA | MRRF | 0.0141606101425267 | 0.37 |
BRCA | MRRF | 0.0376241179995533 | 0.94 |
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Differential gene expression between young and old age groups (Wilcoxon test, pval<0.05) |
Cancer type | Translation factor | pval | adj.p |
STAD | MRRF | 0.0244094451202235 | 0.71 |
LUSC | MRRF | 0.000573537263680879 | 0.019 |
KICH | MRRF | 0.044034233458587 | 1 |
PRAD | MRRF | 0.00671363923281181 | 0.21 |
PAAD | MRRF | 0.00764307713933483 | 0.24 |
OV | MRRF | 0.0302527725705535 | 0.85 |
CESC | MRRF | 0.012426527385324 | 0.37 |
THYM | MRRF | 0.0468019940683807 | 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 |