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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: RWDD1 (NCBI Gene ID:51389)


Gene Summary

check button Gene Summary
Gene InformationGene Name: RWDD1
Gene ID: 51389
Gene Symbol

RWDD1

Gene ID

51389

Gene NameRWD domain containing 1
SynonymsCGI-24|PTD013
Cytomap

6q22.1

Type of Geneprotein-coding
DescriptionRWD domain-containing protein 1DRG family-regulatory protein 2
Modification date20200313
UniProtAcc

Q9H446


check button Child GO biological process term(s) under GO:0006412
GO IDGO term
GO:0002181Cytoplasmic translation
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
RWDD1>1119.25


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Translation Studies in PubMed

check button We searched PubMed using 'RWDD1[title] AND translation [title] AND human.'
GeneTitlePMID
RWDD1..


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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
ENST00000466444116905889116906020Frame-shift
ENST00000466444116912050116912113In-frame

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)
ENST000004664441169120501169121135539764826243182203

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.
Q9H4461822032243ChainID=PRO_0000097540;Note=RWD domain-containing protein 1
Q9H446182203142197RegionNote=Interaction with DRG2;Ontology_term=ECO:0000250;evidence=ECO:0000250


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Expression


check buttonGene expression level across TCGA pancancer
all structure

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
all structure

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
ESCARWDD11.430745739530250.009765625
PRADRWDD1-1.370158890114730.0291755363147523
BRCARWDD1-1.137852887662593.18183978181012e-05


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Expression Regulation


check buttonTranslation factor expression regulation through miRNA binding
Cancer typeGenemiRNATargetScan binding score (Context++ score percentile)CoefficientPvalue
CHOLRWDD1hsa-miR-34a-5p690.4021080368906460.00653231377451465


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)
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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
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Cancer typeGeneCoefficientPvalue

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Associated Genes


check button Strongly correlated genes belong to cellular important gene groups with RWDD1 (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)
all structure
Cancer typeGene groupTranslation factorCorrelated geneCoefficientPvalue
DLBCCell metabolism geneRWDD1PSMB10.841706156.72E-14
DLBCEpifactorRWDD1DMAP10.8077786083.96E-12
DLBCIUPHARRWDD1PSMB10.841706156.72E-14
DLBCTFRWDD1THAP30.8043233035.74E-12
THYMCell metabolism geneRWDD1PSMD130.8016386891.39E-28
THYMCell metabolism geneRWDD1PFDN60.8043602536.62E-29
THYMCell metabolism geneRWDD1SNRPD20.8070892693.11E-29
THYMCell metabolism geneRWDD1PSMB70.8089917711.82E-29
THYMCell metabolism geneRWDD1ZNRD10.8126581266.41E-30
THYMCell metabolism geneRWDD1SEC61B0.8191144559.60E-31
THYMCell metabolism geneRWDD1LSM20.8455722721.68E-34
THYMCell metabolism geneRWDD1UROD0.8497449983.69E-35
THYMCell metabolism geneRWDD1PSMB10.8832278082.81E-41
THYMCGCRWDD1TFPT0.8189886969.97E-31
THYMEpifactorRWDD1ZNHIT10.8113253349.40E-30
THYMEpifactorRWDD1TFPT0.8189886969.97E-31
THYMEpifactorRWDD1DMAP10.8210354285.38E-31
THYMEpifactorRWDD1PRMT70.8266551329.47E-32
THYMIUPHARRWDD1PRMT70.8266551329.47E-32
THYMIUPHARRWDD1MMP240.8309965612.37E-32
THYMIUPHARRWDD1CSNK2B0.878396782.76E-40
THYMIUPHARRWDD1PSMB10.8832278082.81E-41
THYMTFRWDD1ZNF4440.8295233.81E-32
THYMTFRWDD1ZNF4280.8337883839.54E-33
THYMTFRWDD1DRAP10.8424616695.03E-34
THYMTFRWDD1THYN10.8549924715.15E-36
THYMTSGRWDD1HTRA20.809912941.41E-29
THYMTSGRWDD1GLTSCR20.8122088727.29E-30
THYMTSGRWDD1AIF10.8206345756.07E-31
THYMTSGRWDD1GNB2L10.8346236167.24E-33
UCSCell metabolism geneRWDD1PSMD130.8016386891.39E-28
UCSCell metabolism geneRWDD1PFDN60.8043602536.62E-29
UCSCell metabolism geneRWDD1SNRPD20.8070892693.11E-29
UCSCell metabolism geneRWDD1PSMB70.8089917711.82E-29
UCSCell metabolism geneRWDD1ZNRD10.8126581266.41E-30
UCSCell metabolism geneRWDD1SEC61B0.8191144559.60E-31
UCSCell metabolism geneRWDD1LSM20.8455722721.68E-34
UCSCell metabolism geneRWDD1UROD0.8497449983.69E-35
UCSCell metabolism geneRWDD1PSMB10.8832278082.81E-41
UCSCGCRWDD1TFPT0.8189886969.97E-31
UCSEpifactorRWDD1ZNHIT10.8113253349.40E-30
UCSEpifactorRWDD1TFPT0.8189886969.97E-31
UCSEpifactorRWDD1DMAP10.8210354285.38E-31
UCSEpifactorRWDD1PRMT70.8266551329.47E-32
UCSIUPHARRWDD1PRMT70.8266551329.47E-32
UCSIUPHARRWDD1MMP240.8309965612.37E-32
UCSIUPHARRWDD1CSNK2B0.878396782.76E-40
UCSIUPHARRWDD1PSMB10.8832278082.81E-41
UCSTFRWDD1ZNF4440.8295233.81E-32
UCSTFRWDD1ZNF4280.8337883839.54E-33
UCSTFRWDD1DRAP10.8424616695.03E-34
UCSTFRWDD1THYN10.8549924715.15E-36
UCSTSGRWDD1HTRA20.809912941.41E-29
UCSTSGRWDD1GLTSCR20.8122088727.29E-30
UCSTSGRWDD1AIF10.8206345756.07E-31
UCSTSGRWDD1GNB2L10.8346236167.24E-33
UVMTFRWDD1HSF20.8064419111.77E-19


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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
LUSCRWDD1RWDD2A2.435287729283720.000201938028703404
LUADRWDD1DRG1-1.388967826652240.00022838170846318
STADRWDD1PFDN51.595451128005610.000234263017773628
PRADRWDD1GCN1L1-7.541731960785640.000376184722398862
KIRCRWDD1GCN1L11.529441280660250.00150654978717842
STADRWDD1ZC3H15-1.049686181731970.00733334058895707
ESCARWDD1EBNA1BP2-1.992001209640510.009765625
KIRCRWDD1DRG1-4.160084217088780.0152218459760014
COADRWDD1RWDD2A-2.461382835748630.0189773440361023
CHOLRWDD1DRG1-2.740369434760790.01953125
BLCARWDD1ZC3H151.074808717139810.0258216857910156
BRCARWDD1EBNA1BP2-6.675699149159611.14170217447768e-18
LIHCRWDD1GCN1L1-1.505469932823762.24402029682138e-06
LUADRWDD1EBNA1BP2-9.219835062797974.60205959480617e-09
BRCARWDD1DRG21.551728762212695.83844264602967e-05
LUADRWDD1GCN1L1-3.114940728714825.86248556550202e-05
THCARWDD1RWDD2A-3.013859810831446.03921940186051e-06
KICHRWDD1EBNA1BP22.412058874359558.16583633422851e-06
HNSCRWDD1PFDN52.512936806289168.21439698484029e-08
LIHCRWDD1EBNA1BP2-9.248329709188659.87002535347663e-07


check button Protein-protein interactors with this translation factor (BIOGRID-3.4.160)
PPI interactors with RWDD1
DRG1, NUDT18, DRG2, XPO1, EGFR, CD74, MAP3K14, P2RY6, DNAJC2, HSPA14, DNAJC1, EP300,


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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
RWDD1LIHCchr6116912097116912097C-Frame_Shift_Delp.I198fs3
RWDD1BLCAchr6116914146116914146GCMissense_Mutationp.G205A2
RWDD1LIHCchr6116901493116901493GAMissense_Mutation2
RWDD1BLCAchr6116892761116892761GAMissense_Mutationp.E6K2
RWDD1BLCAchr6116914217116914217GAMissense_Mutationp.D229N2
RWDD1UCECchr6116910017116910017CAMissense_Mutationp.L95I2
RWDD1UCECchr6116910146116910146ATNonsense_Mutationp.K138*2
RWDD1UCECchr6116914255116914255ACSilentp.S2412
RWDD1OVchr6116914220116914220CAMissense_Mutationp.P230T1
RWDD1BLCAchr6116892761116892761GAMissense_Mutation1
RWDD1SKCMchr6116914170116914170CTMissense_Mutationp.S213F1
RWDD1HNSCchr6116910017116910017CGMissense_Mutation1
RWDD1OVchr6116914221116914221CAMissense_Mutationp.P230Q1
RWDD1BLCAchr6116914217116914217GAMissense_Mutation1
RWDD1SKCMchr6116892810116892810CTMissense_Mutationp.S22F1
RWDD1HNSCchr6116910017116910017CGMissense_Mutationp.L95V1
RWDD1SARCchr6116912049116912049ATSplice_Site1
RWDD1BLCAchr6116914254116914254CTMissense_Mutation1
RWDD1STADchr6116912056116912056CAMissense_Mutationp.Q185K1
RWDD1LIHCchr6116901485116901485CAMissense_Mutation1
RWDD1SKCMchr6116905895116905895CTNonsense_Mutationp.Q49X1
RWDD1STADchr6116911490116911490ACMissense_Mutationp.K157T1
RWDD1SKCMchr6116910006116910006CTMissense_Mutationp.A91V1
RWDD1STADchr6116912077116912077AGMissense_Mutationp.N192D1
RWDD1LIHCchr6116901503116901503AGMissense_Mutationp.E40G1
RWDD1SKCMchr6116911443116911443CTSilentp.F45F1
RWDD1THYMchr6116892691116892691CTMissense_Mutation1
RWDD1SKCMchr6116914170116914170CTMissense_Mutationp.S117F1
RWDD1BLCAchr6116914254116914254CTMissense_Mutationp.S241L1
RWDD1LIHCchr6116910033116910033T-Frame_Shift_Delp.I100fs1
RWDD1SKCMchr6116910104116910104GAMissense_Mutationp.E124K1
RWDD1BLCAchr6116911482116911482GANonsense_Mutationp.W154*1
RWDD1LIHCchr6116911558116911558A-Frame_Shift_Delp.K180fs1
RWDD1SKCMchr6116911443116911443CTSilentp.F141F1
RWDD1CESCchr6116901509116901509GTMissense_Mutation1
RWDD1LUSCchr6116906012116906012GCMissense_Mutationp.A88P1
RWDD1SKCMchr6116910006116910006CTSplice_Sitep.A91_splice1
RWDD1CHOLchr6116901442116901442GAMissense_Mutation1
RWDD1MESOchr6116914158116914158AGMissense_Mutationp.E209G1
RWDD1BLCAchr6116914146116914146GCMissense_Mutation1
RWDD1SKCMchr6116905895116905895CTNonsense_Mutationp.Q49*1
RWDD1ESCAchr6116906012116906012GTMissense_Mutationp.A88S1

check buttonCopy number variation (CNV) of RWDD1
* 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 RWDD1
* 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
89398Non-Cancer2397NHBS1Lchr6135360710-RWDD1chr6116901457+
78751SARCTCGA-SG-A6Z7-01ARWDD1chr6116906020+CEP85Lchr6118845083-
78751N/ACD557821RWDD1chr6116892643+DNAH12chr357357606-
78751LUSCTCGA-77-A5GHRWDD1chr6116906020+FAM26Dchr6116878988+
78751OVTCGA-04-1338-01ARWDD1chr6116901523+FAM26Dchr6116864928+
103224N/ABI494981RWDD1chr6116914438+RASGRF1chr1579299907-
93087N/AAF092134RWDD1chr6116914431+STAU1chr2047745308+
97040BRCATCGA-E9-A1RF-01ARWDD1chr6116892818+WASF1chr6110434663-
97040BRCATCGA-E9-A1RF-01ARWDD1chr6116892818+WASF1chr6110448832-
97040BRCATCGA-E9-A1RF-01ARWDD1chr6116895334+WASF1chr6110448832-
89402STADTCGA-D7-8579TBC1D5chr317783972-RWDD1chr6116914142+


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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
TGCTRWDD10.004917481004369590.14
STADRWDD10.01377603870489140.37
LGGRWDD10.04700326398546571

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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
LUSCRWDD10.008263745269809620.27
PRADRWDD10.0483653756298651
OVRWDD10.02348810460156190.75
SARCRWDD10.03562829155971821

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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