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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: MRPL10 (NCBI Gene ID:124995)


Gene Summary

check button Gene Summary
Gene InformationGene Name: MRPL10
Gene ID: 124995
Gene Symbol

MRPL10

Gene ID

124995

Gene Namemitochondrial ribosomal protein L10
SynonymsL10MT|MRP-L10|MRP-L8|MRPL8|RPML8
Cytomap

17q21.32

Type of Geneprotein-coding
Description39S ribosomal protein L10, mitochondrial39S ribosomal protein L8, mitochondrialL8mtmitochondrial large ribosomal subunit protein uL10m
Modification date20200313
UniProtAcc

Q7Z7H8


check button Child GO biological process term(s) under GO:0006412
GO IDGO term
GO:0005840Ribosome
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


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Translation Studies in PubMed

check button We searched PubMed using 'MRPL10[title] AND translation [title] AND human.'
GeneTitlePMID
MRPL10..


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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
ENST000003511114590400245904147Frame-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)

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.


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Expression


check buttonGene expression level across TCGA pancancer
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check buttonGene expression level across GTEx pantissue
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check buttonExpression level of gene isoforms across TCGA pancancer
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check buttonExpression level of gene isoforms across GTEx pantissue
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check buttonCancer(tissue) type-specific expression level of Translation factor using z-score distriution
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check buttonDifferential expression between tumor and matched normal (in the cancer types with more than 10 matched samples)
all structure
Cancer typeTranslation factorFCadj.pval
LIHCMRPL10-3.227036179959310.000209845686767642
STADMRPL10-4.874616673958710.0118026207201183
LUSCMRPL10-2.4407157469411.79996309233889e-05
LUADMRPL10-5.605793732115514.11637918366747e-07


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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
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)
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
Cancer typeGeneCoefficientPvalue

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Associated Genes


check button Strongly correlated genes belong to cellular important gene groups with MRPL10 (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
CHOLCell metabolism geneMRPL10NME20.8122941621.26E-11
CHOLTFMRPL10NME20.8122941621.26E-11
TGCTTSGMRPL10PHB0.8296509228.00E-41


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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))
all structure

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
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* 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
LUSCMRPL10MRPL53-7.512588757638570.000291380503797954
KIRCMRPL10MRPL55-1.021634418322580.000291940846845375
KIRCMRPL10MRPL11-1.049668376255570.000354478033746394
LIHCMRPL10MRPL131.544024721076140.000655351190157038
LUSCMRPL10MRPL39-3.504117374290040.000985010025625636
CHOLMRPL10MRPL3-2.684292559906210.00390625
BLCAMRPL10MRPL391.698968519604520.00391769409179688
LUADMRPL10MRPL39-1.10494529815920.00471395891927286
ESCAMRPL10MRPL3-4.978970949082750.0048828125
LUADMRPL10MRPL53-2.947090012910110.00627510264512955
ESCAMRPL10MRPL13-1.077460884749950.0068359375
PRADMRPL10ICT1-1.548484449093520.00907723161841939
ESCAMRPL10MRPL12-1.001749708954810.009765625
CHOLMRPL10MRPL12-3.631305661356590.01171875
STADMRPL10MRPL12-2.485382140707110.020511694252491
STADMRPL10MRPL41.43935391356820.0279771662317216
COADMRPL10MRPL39-1.152859532917560.0357243716716767
STADMRPL10MRPL531.663043603007060.0413399673998356
BLCAMRPL10MRPL22-2.259697477925430.0493659973144531
BRCAMRPL10MRPL22-2.30618232267241.15724909394453e-08
PRADMRPL10MRPL111.125816533946281.15996224044503e-05
LUADMRPL10MRPL12-3.432809009007631.96929418449732e-09
KIRCMRPL10MRPL31.699557622342441.97132191719422e-08
BRCAMRPL10ICT1-4.174882204496642.73719348917167e-14
COADMRPL10MRPL42.777058975144732.98023223876954e-07
LIHCMRPL10MRPL39-1.654616833862163.95799979560965e-08
BRCAMRPL10MRPL55-1.640929106039246.01408870059924e-14
LUSCMRPL10ICT1-3.230933760494566.60526357089358e-07
LUADMRPL10MRPL22-3.643433617326596.84976461567817e-06
LUSCMRPL10MRPL55-1.426655298368467.19742900589893e-05
LUADMRPL10MRPL55-2.504068296944597.3663238952828e-06


check button Protein-protein interactors with this translation factor (BIOGRID-3.4.160)
PPI interactors with MRPL10
USP22, ICT1, APP, MRPL12, MRPL15, MRPL3, MRPL13, MRPL1, MRPL11, MRPL41, MRPL23, ILF3, ABCB7, SLC25A3, ABCC2, HNRNPU, BCS1L, NPM1, REL, TCF4, PNMA1, KLHL12, FAM9B, EGFR, RPS8, MRPL4, HNRNPA1, MRPL39, MRPS30, MRPL47, MRPL22, MRPL50, MRPL9, ACTN2, MRPL42, MRPL45, MRPL2, MRPL51, MRPL55, MRPL44, MRPL34, MRPL30, MRPL49, MRPL32, MRPL16, MRPL27, MRPL17, MRPL40, MRPL28, MRPL48, MRPL38, GADD45GIP1, MRPL24, MRPS18A, MRPL33, MRPL35, MRPL19, MRPL46, MRPL20, MALSU1, MRPL43, MRPL57, MRPL18, UQCC1, MRPL53, MRPL21, MRPL14, ZZEF1, C4BPB, FGF8, RPL36AL, PREPL, LEO1, MRPL36, MRPS11, MRPS14, MRPS5, GATB, PGK1, PSMD12, TAZ, WDR61, ZNF830, ESR2, LARP7, RECQL4, SERBP1, MRM1, HSPD1, PDK1, TRMT61B, AURKAIP1, VCP, RC3H2, SNRNP70, Dppa3, PRKCI, RASA1, IMMP2L, GRSF1, ARHGAP31, ECT2L, ACAD9, AUH, C12orf65, C1QBP, C21orf33, C6orf203, CS, GFM1, GFM2, HINT2, LRPPRC, MDH2, METTL15, METTL17, MRPS12, MRPS26, MRRF, MTERF3, MTG2, MTIF2, MTIF3, MTRF1, MTRF1L, NGRN, PMPCA, PMPCB, SLIRP, TACO1, TBRG4, TFAM, TRUB2, TSFM, TUFM, VWA8, EXD2, CLPP, Apc2, NR3C1, HSCB, UFL1, DDRGK1, AARS2, COX8A, PDHA1, SRSF3, ZNF483, RBMS2, LIN28A, YBX2, RPL13, RPL37, RPL19, YBX1, RPL6, H1FNT, MRPL52, RPL10, YARS2, HERC2, HIST1H2AE, RNMTL1, MRPL37, KLHL22, NEURL4, NEIL1, LONP1, RBPMS, Pcbp1, M, KLF15,


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Mutations


check button Clinically associated variants from ClinVar.
GeneChrPositionRefSeqVarSeqRefSeeqVarTypePathogenicDiseaseVarInfo


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


check button SNVs and Indels
GeneCancer typeChromosomeStartEndRefSeeqMutSeqMutation typeAAchange# samples
MRPL10KIRPchr174590162345901623GAMissense_Mutationp.S255F4
MRPL10LIHCchr174590602445906024GAMissense_Mutationp.T32I3
MRPL10SKCMchr174590181545901815AGMissense_Mutationp.I191T2
MRPL10SKCMchr174590446245904462GAMissense_Mutationp.L121F2
MRPL10UCECchr174590158945901589GASilentp.D2562
MRPL10UCECchr174590401245904012GAMissense_Mutationp.P175S2
MRPL10PAADchr174590411545904115GASilent2
MRPL10UCECchr174590594945905949ACMissense_Mutationp.L47R2
MRPL10LUADchr174590163645901636GAMissense_Mutationp.R251C2
MRPL10PAADchr174590411545904115GASilentp.Y150Y2
MRPL10UCECchr174590596845905968GAMissense_Mutationp.H41Y2
MRPL10HNSCchr174590175745901757CTSilentp.L210L2
MRPL10BLCAchr174590159745901597CAMissense_Mutation1
MRPL10LUADchr174590181645901816TCMissense_Mutationp.I191V1
MRPL10COADchr174590406745904067AGSilentp.S166S1
MRPL10SARCchr174590168145901681GAMissense_Mutation1
MRPL10KIRPchr174590162345901623GAMissense_Mutation1
MRPL10THCAchr174590401145904011GAMissense_Mutation1
MRPL10BLCAchr174590160445901604CTSilent1
MRPL10LUADchr174590163645901636GAMissense_Mutationp.R241C1
MRPL10COADchr174590442045904420CTMissense_Mutationp.V135I1
MRPL10LGGchr174590401645904016GTMissense_Mutationp.F183L1
MRPL10THCAchr174590401145904011GAMissense_Mutationp.P185L1
MRPL10BLCAchr174590443845904438GAMissense_Mutation1
MRPL10LUADchr174590447245904472CAMissense_Mutationp.E107D1
MRPL10ESCAchr174590601945906019GTMissense_Mutationp.Q24K1
MRPL10LGGchr174590401645904016GTMissense_Mutation1
MRPL10UCECchr174590594945905949ACMissense_Mutationp.L57R1
MRPL10BLCAchr174590454445904544GASilentp.R93R1
MRPL10LUADchr174590181645901816TCMissense_Mutationp.I181V1
MRPL10ESCAchr174590411545904115GTNonsense_Mutationp.Y140*1
MRPL10SKCMchr174590442245904422TCMissense_Mutationp.K134R1
MRPL10LIHCchr174590596745905967TCMissense_Mutation1
MRPL10UCECchr174590596845905968GAMissense_Mutationp.H51Y1
MRPL10BLCAchr174590169145901691GCSilentp.L232L1
MRPL10LUSCchr174590168545901685GTMissense_Mutationp.H234Q1
MRPL10ESCAchr174590601945906019GTMissense_Mutation1
MRPL10SKCMchr174590455345904553CTSilentp.R90R1
MRPL10UCECchr174590163545901635CTMissense_Mutationp.R251H1
MRPL10BLCAchr174590160445901604CTSilentp.G261G1
MRPL10OVchr174590441745904417AGMissense_Mutationp.F136L1
MRPL10ESCAchr174590411545904115GTNonsense_Mutationp.Y150X1
MRPL10STADchr174590454545904545CTMissense_Mutationp.R93H1
MRPL10LIHCchr174590408845904088C-Frame_Shift_Delp.G159fs1
MRPL10OVchr174326092143260921GCMissense_Mutationp.P56R1
MRPL10BLCAchr174590159745901597CAMissense_Mutationp.D264Y1
MRPL10GBMchr174590595745905957CTSilentp.R54R1
MRPL10STADchr174590603645906036CTMissense_Mutationp.G28D1
MRPL10LUADchr174590448145904481CGSilentp.L114L1
MRPL10BLCAchr174590443845904438GAMissense_Mutationp.H129Y1
MRPL10HNSCchr174590175745901757CTSilent1
MRPL10STADchr174590445545904455CTMissense_Mutationp.R123Q1
MRPL10BLCAchr174590169145901691GCSilentp.L222L1
MRPL10STADchr174590454545904545CTMissense_Mutationp.R83H1
MRPL10BLCAchr174590454445904544GASilent1
MRPL10LUADchr174590447245904472CAMissense_Mutationp.E117D1
MRPL10CESCchr174590163345901633CTMissense_Mutation1
MRPL10PAADchr174590411545904115GASilentp.Y140Y1
MRPL10HNSCchr174590175745901757CTSilentp.L200L1
MRPL10STADchr174590454245904542CTMissense_Mutationp.R84Q1
MRPL10BLCAchr174590169145901691GCSilent1
MRPL10LUADchr174590412445904124AGSilentp.D147D1
MRPL10CESCchr174590880445908804GAMissense_Mutationp.S25L1
MRPL10PRADchr174590163845901638TAMissense_Mutationp.Q250L1
MRPL10STADchr174590445545904455CTMissense_Mutationp.R113Q1

check buttonCopy number variation (CNV) of MRPL10
* 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 MRPL10
* 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
89826BLCATCGA-HQ-A2OF-01AMRPL10chr1745904003-MTPAPchr1030611546-
87218N/ACS190707MRPL10chr1745905895+PDSS2chr6107679553+
89357N/AES316348MRPL10chr1745900877-PLP1chrX103045970+
92287UCECTCGA-AJ-A23N-01AMRPL10chr1745904003-SKAP1chr1746266862-
76259N/ABE265135RPL23chr1737006343-MRPL10chr1745908870-


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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


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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
HNSCMRPL100.001617527494249530.044
LIHCMRPL100.006449813488832980.17
BRCAMRPL100.04553767822755471
SARCMRPL102.09119174675967e-065.9e-05

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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
LUSCMRPL100.01631037908212650.52
THCAMRPL100.01317172871646190.43
KIRPMRPL100.04949663264089771
BRCAMRPL100.0489081321316171
CHOLMRPL100.02092799206169390.65

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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

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Related Diseases


check button Diseases associated with this translation factor.
(DisGeNet 4.0)
Disease IDDisease Name# PubMedsDisease source