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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: RPSA (NCBI Gene ID:3921)


Gene Summary

check button Gene Summary
Gene InformationGene Name: RPSA
Gene ID: 3921
Gene Symbol

RPSA

Gene ID

3921

Gene Nameribosomal protein SA
Synonyms37LRP|67LR|ICAS|LAMBR|LAMR1|LBP|LBP/p40|LRP|LRP/LR|NEM/1CHD4|SA|lamR|p40
Cytomap

3p22.1

Type of Geneprotein-coding
Description40S ribosomal protein SA37 kDa laminin receptor37/67 kDa laminin receptor67 kDa laminin receptorcolon carcinoma laminin-binding proteinlaminin receptor 1 (67kD, ribosomal protein SA)laminin-binding protein precursor p40multidrug resistance-associat
Modification date20200313
UniProtAcc

P08865


check button Child GO biological process term(s) under GO:0006412
GO IDGO term
GO:0005840Ribosome
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
RPSA>1119.25


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Translation Studies in PubMed

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


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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
ENST000003018213945009639450215Frame-shift
ENST000003018213945224439452490In-frame
ENST000003018213945313939453268In-frame
ENST000003018213945338639453552Frame-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)
ENST000003018213945224439452490118836260729584166
ENST0000030182139453139394532681188608736295166209

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
all structure

check buttonGene expression level across GTEx pantissue
all structure

check buttonExpression level of gene isoforms across TCGA pancancer
all structure

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
all structure

check buttonDifferential expression between tumor and matched normal (in the cancer types with more than 10 matched samples)
all structure
Cancer typeTranslation factorFCadj.pval
LIHCRPSA-2.661818046259880.00010013220697745
CHOLRPSA-1.885012537119620.0078125
PRADRPSA1.151835889908720.0476188245531179


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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
all structure
Cancer typeGenemethyl group bmethyl group aDEG pvalavg methyl in bavg methyl in aavg exp in bavg exp in a
BLCARPSA120.03485805983494160.1351138752052540.252517857142857-0.0488309472427860.139522747338557

check buttonTranslation factor expression regulation through methylation in the gene body of Translation factor (positive regulation)
all structure
Cancer typeGenemethyl group bmethyl group aDEG pvalavg methyl in bavg methyl in aavg exp in bavg exp in a
STADRPSA210.01941087418331130.2500828985507250.1517353086419750.1673659665890480.268608532343272

check buttonTranslation factor expression regulation through copy number variation of Translation factor
all structure
Cancer typeGeneCoefficientPvalue
THCARPSA0.1810892490.007635067
KIRPRPSA-0.0297567450.016038395
SARCRPSA-0.1241223560.019227322

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Associated Genes


check button Strongly correlated genes belong to cellular important gene groups with RPSA (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 geneRPSAFAU0.8025437756.92E-12
DLBCCell metabolism geneRPSASNRPD20.8349928091.62E-13
DLBCCell metabolism geneRPSATIMM130.8500357742.13E-14
DLBCEpifactorRPSAFBL0.8664866521.77E-15
DLBCIUPHARRPSASLC25A260.8518530481.64E-14
DLBCTSGRPSAGLTSCR20.8402812438.12E-14
GBMCell metabolism geneRPSASEC130.8014537268.45E-40
GBMCell metabolism geneRPSALSM30.8185949498.60E-43
HNSCCell metabolism geneRPSAIMPDH20.8121528894.36E-134
HNSCIUPHARRPSAIMPDH20.8121528894.36E-134
KICHCell metabolism geneRPSASNRPD20.8062527835.32E-22
KICHCell metabolism geneRPSAIMPDH20.8273912215.09E-24
KICHIUPHARRPSAIMPDH20.8273912215.09E-24
LGGCell metabolism geneRPSAIMPDH20.815191562.51E-127
LGGIUPHARRPSAIMPDH20.815191562.51E-127
LIHCCell metabolism geneRPSAIMPDH20.8007427279.65E-96
LIHCEpifactorRPSAFBL0.8064892893.96E-98
LIHCIUPHARRPSAIMPDH20.8007427279.65E-96
PRADCell metabolism geneRPSANME20.8003515157.40E-124
PRADCell metabolism geneRPSAFAU0.8157339372.15E-132
PRADCell metabolism geneRPSASNRPD20.8167312815.65E-133
PRADCell metabolism geneRPSATIMM90.8193712371.57E-134
PRADCGCRPSANACA0.8059290597.29E-127
PRADEpifactorRPSAFBL0.8424028482.82E-149
PRADTFRPSANME20.8003515157.40E-124
PRADTFRPSAZNF5810.8197840648.93E-135
PRADTSGRPSAGNB2L10.8624344643.55E-164
THCACell metabolism geneRPSAFAU0.8162211036.29E-138
THYMCell metabolism geneRPSAAPRT0.8000143142.15E-28
THYMCell metabolism geneRPSAIMPDH20.8039277447.45E-29
THYMCell metabolism geneRPSAPSMB30.80866332.00E-29
THYMCell metabolism geneRPSAPGLS0.8121900887.33E-30
THYMCell metabolism geneRPSAPFDN50.8155111812.79E-30
THYMCell metabolism geneRPSAMTMR140.8176372711.49E-30
THYMCell metabolism geneRPSAPOLA20.82274093.20E-31
THYMCell metabolism geneRPSAPSMB70.8243879061.92E-31
THYMCell metabolism geneRPSASSR20.8270863648.27E-32
THYMCell metabolism geneRPSATALDO10.8345350517.45E-33
THYMCell metabolism geneRPSATIMM130.8356722735.11E-33
THYMCell metabolism geneRPSAMVD0.8385751911.92E-33
THYMCell metabolism geneRPSALSM20.8390983091.61E-33
THYMCell metabolism geneRPSAPOLD20.8400227421.17E-33
THYMCell metabolism geneRPSAACOT80.8432079023.87E-34
THYMCell metabolism geneRPSATIMM8B0.8458186591.53E-34
THYMCell metabolism geneRPSAFPGS0.8460828221.40E-34
THYMCell metabolism geneRPSASLC27A50.8490114.83E-35
THYMCell metabolism geneRPSAPSMD130.8507591072.54E-35
THYMCell metabolism geneRPSASNRPD20.8640133921.45E-37
THYMCell metabolism geneRPSAPSMC30.8700828421.13E-38
THYMCell metabolism geneRPSAFAU0.9014292271.89E-45
THYMCGCRPSABAP10.8080498182.38E-29
THYMCGCRPSATFPT0.8333005571.12E-32
THYMCGCRPSASDHAF20.8474538228.52E-35
THYMCGCRPSARBM100.8648235071.04E-37
THYMEpifactorRPSARRP80.8001918282.05E-28
THYMEpifactorRPSACCDC1010.8007282771.78E-28
THYMEpifactorRPSABAP10.8080498182.38E-29
THYMEpifactorRPSAC17orf490.8098426821.43E-29
THYMEpifactorRPSAPRPF310.8179326211.37E-30
THYMEpifactorRPSACXXC10.8188159151.05E-30
THYMEpifactorRPSANOC2L0.8223327743.62E-31
THYMEpifactorRPSATRIM280.8241934382.04E-31
THYMEpifactorRPSAPPP4C0.8296295483.68E-32
THYMEpifactorRPSATFPT0.8333005571.12E-32
THYMEpifactorRPSAMBD30.833314821.11E-32
THYMEpifactorRPSARUVBL20.8343551067.91E-33
THYMEpifactorRPSASS18L20.838024292.32E-33
THYMEpifactorRPSADMAP10.8386634621.86E-33
THYMEpifactorRPSATAF100.8445696462.39E-34
THYMEpifactorRPSAFBL0.8484498315.93E-35
THYMEpifactorRPSABRMS10.848530885.76E-35
THYMIUPHARRPSAIMPDH20.8039277447.45E-29
THYMIUPHARRPSAMFSD2B0.8053656175.02E-29
THYMIUPHARRPSABAP10.8080498182.38E-29
THYMIUPHARRPSATRIM280.8241934382.04E-31
THYMIUPHARRPSAMVD0.8385751911.92E-33
THYMIUPHARRPSATWF20.8393675811.47E-33
THYMIUPHARRPSASLC27A50.8490114.83E-35
THYMIUPHARRPSASLC25A380.8526727391.24E-35
THYMKinaseRPSATRIM280.8241934382.04E-31
THYMTFRPSATHAP30.8113773399.26E-30
THYMTFRPSAZNF4280.8121995337.31E-30
THYMTFRPSACXXC10.8188159151.05E-30
THYMTFRPSAZNF4440.8232946442.70E-31
THYMTFRPSATHYN10.8279840076.23E-32
THYMTFRPSAMBD30.833314821.11E-32
THYMTSGRPSAPFN10.80127361.53E-28
THYMTSGRPSABAP10.8080498182.38E-29
THYMTSGRPSANPRL20.8174595731.57E-30
THYMTSGRPSABRMS10.848530885.76E-35
THYMTSGRPSATSSC40.8597119038.20E-37
THYMTSGRPSAAIP0.8695483231.42E-38
THYMTSGRPSAGNB2L10.8707163698.58E-39
THYMTSGRPSAGLTSCR20.8782398782.97E-40
UCSCell metabolism geneRPSAAPRT0.8000143142.15E-28
UCSCell metabolism geneRPSAIMPDH20.8039277447.45E-29
UCSCell metabolism geneRPSAPSMB30.80866332.00E-29
UCSCell metabolism geneRPSAPGLS0.8121900887.33E-30
UCSCell metabolism geneRPSAPFDN50.8155111812.79E-30
UCSCell metabolism geneRPSAMTMR140.8176372711.49E-30
UCSCell metabolism geneRPSAPOLA20.82274093.20E-31
UCSCell metabolism geneRPSAPSMB70.8243879061.92E-31
UCSCell metabolism geneRPSASSR20.8270863648.27E-32
UCSCell metabolism geneRPSATALDO10.8345350517.45E-33
UCSCell metabolism geneRPSATIMM130.8356722735.11E-33
UCSCell metabolism geneRPSAMVD0.8385751911.92E-33
UCSCell metabolism geneRPSALSM20.8390983091.61E-33
UCSCell metabolism geneRPSAPOLD20.8400227421.17E-33
UCSCell metabolism geneRPSAACOT80.8432079023.87E-34
UCSCell metabolism geneRPSATIMM8B0.8458186591.53E-34
UCSCell metabolism geneRPSAFPGS0.8460828221.40E-34
UCSCell metabolism geneRPSASLC27A50.8490114.83E-35
UCSCell metabolism geneRPSAPSMD130.8507591072.54E-35
UCSCell metabolism geneRPSASNRPD20.8640133921.45E-37
UCSCell metabolism geneRPSAPSMC30.8700828421.13E-38
UCSCell metabolism geneRPSAFAU0.9014292271.89E-45
UCSCGCRPSABAP10.8080498182.38E-29
UCSCGCRPSATFPT0.8333005571.12E-32
UCSCGCRPSASDHAF20.8474538228.52E-35
UCSCGCRPSARBM100.8648235071.04E-37
UCSEpifactorRPSARRP80.8001918282.05E-28
UCSEpifactorRPSACCDC1010.8007282771.78E-28
UCSEpifactorRPSABAP10.8080498182.38E-29
UCSEpifactorRPSAC17orf490.8098426821.43E-29
UCSEpifactorRPSAPRPF310.8179326211.37E-30
UCSEpifactorRPSACXXC10.8188159151.05E-30
UCSEpifactorRPSANOC2L0.8223327743.62E-31
UCSEpifactorRPSATRIM280.8241934382.04E-31
UCSEpifactorRPSAPPP4C0.8296295483.68E-32
UCSEpifactorRPSATFPT0.8333005571.12E-32
UCSEpifactorRPSAMBD30.833314821.11E-32
UCSEpifactorRPSARUVBL20.8343551067.91E-33
UCSEpifactorRPSASS18L20.838024292.32E-33
UCSEpifactorRPSADMAP10.8386634621.86E-33
UCSEpifactorRPSATAF100.8445696462.39E-34
UCSEpifactorRPSAFBL0.8484498315.93E-35
UCSEpifactorRPSABRMS10.848530885.76E-35
UCSIUPHARRPSAIMPDH20.8039277447.45E-29
UCSIUPHARRPSAMFSD2B0.8053656175.02E-29
UCSIUPHARRPSABAP10.8080498182.38E-29
UCSIUPHARRPSATRIM280.8241934382.04E-31
UCSIUPHARRPSAMVD0.8385751911.92E-33
UCSIUPHARRPSATWF20.8393675811.47E-33
UCSIUPHARRPSASLC27A50.8490114.83E-35
UCSIUPHARRPSASLC25A380.8526727391.24E-35
UCSKinaseRPSATRIM280.8241934382.04E-31
UCSTFRPSATHAP30.8113773399.26E-30
UCSTFRPSAZNF4280.8121995337.31E-30
UCSTFRPSACXXC10.8188159151.05E-30
UCSTFRPSAZNF4440.8232946442.70E-31
UCSTFRPSATHYN10.8279840076.23E-32
UCSTFRPSAMBD30.833314821.11E-32
UCSTSGRPSAPFN10.80127361.53E-28
UCSTSGRPSABAP10.8080498182.38E-29
UCSTSGRPSANPRL20.8174595731.57E-30
UCSTSGRPSABRMS10.848530885.76E-35
UCSTSGRPSATSSC40.8597119038.20E-37
UCSTSGRPSAAIP0.8695483231.42E-38
UCSTSGRPSAGNB2L10.8707163698.58E-39
UCSTSGRPSAGLTSCR20.8782398782.97E-40
UVMCell metabolism geneRPSALTA4H0.8423687621.21E-22
UVMIUPHARRPSALTA4H0.8423687621.21E-22
UVMTSGRPSAST130.8244371695.66E-21


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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
check button
* 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
KIRPRPSARPL18A-1.516513928088850.00016188295558095
KICHRPSARPS27A1.753966937859560.000187873840332031
KIRPRPSARPS16-1.359570436175170.00019507110118866
STADRPSARPS231.850767606645760.000364991836249828
COADRPSARPS31.487303751430140.000411599874496461
KIRPRPSARPS11-1.018615705651030.00105937570333481
LIHCRPSARPL8-4.845882849745580.00110314154326131
PRADRPSARPL18A1.406001757484990.00205137828390396
KICHRPSARPL191.369011828940890.00250792503356934
KICHRPSARPS121.269973817584310.00308787822723389
LUADRPSARPL19-1.313980266157250.00993159558412698
THCARPSARPS16-6.163227981565770.0115764821363307
LUSCRPSARPS231.467511698910470.0174932185880974
BLCARPSARPS12-1.478046734404210.0204124450683594
BLCARPSARPS27A-1.047474700691880.0258216857910156
HNSCRPSARPS3-4.735058190951350.0273726439852453
COADRPSARPS111.353075489982040.0312207043170929
LUSCRPSARPL19-2.146698895166660.044366810398747
UCECRPSARPS23-2.036581598140070.046875
KIRCRPSARPL19-2.734852712766761.33980982873695e-10
BRCARPSARPS12-4.912393274782441.85340619742495e-09
KIRCRPSARPL35-1.064752380593922.72286325678163e-08
KIRCRPSARPL8-1.182524599717735.64962994208288e-07
KIRPRPSARPL8-1.530036923501196.0301274061203e-05
KIRCRPSARPS16-1.661498698893847.8509870430991e-09
BRCARPSARPS27A-4.285121482004247.8788217967112e-14
KIRPRPSARPL35-1.529811019754969.0546440333128e-05
KIRCRPSARPS3-1.295608479263879.05905681935088e-10
KIRCRPSARPL18A-4.430793049608439.2516163152192e-11


check button Protein-protein interactors with this translation factor (BIOGRID-3.4.160)
PPI interactors with RPSA
CBX5, RPS21, TRIB3, CD4, HDAC5, PCNA, CLEC4G, VHL, SIRT7, KARS, NEDD4, TINF2, ACD, POT1, CUL1, COPS5, CAND1, PPP2R1A, APEX1, RPL5, RPL7, RPS3A, RPS6, RPS4X, RPLP0, RPL10A, RPL10, RPL11, RPL12, RPL13, RPL14, RPL18A, RPL18, RPL19, RPL23, RPL24, RPL27, RPL30, RPL31, RPL37A, RPL3, RPL4, RPL6, RPL7A, RPL8, RPS15A, RPS15, RPS16, RPS17, RPS23, RPS24, RPS25, RPS28, RPS3, RPS5, RPS8, RPL21, RPS2, RPLP1, RPL9, RPS26, RPL15, RPS20, RPL23A, RPLP2, RPL22, RPS14, RPS13, RPS7, RPS10, RPS19, RPS9, RPL35, RPL17, RPL29, RPL32, RPS27A, RPS29, EEF1A1, HNRNPA1, EIF4A1, PABPC1, HNRNPM, NHP2L1, SLC25A5, DHX9, HSPA5, SSR4, SLC25A4, RPN1, VDAC2, RBM8A, DKC1, PDHB, TCP1, RPLP0P6, CCT4, RPS27L, NENF, CLTC, CCT6A, ECE1, HSPA4, RPL10L, HIST1H2AA, RBMX, CCDC68, HNRNPA0, ESR1, CTNNB1, HSP90AA1, HSP90AB1, FN1, VCAM1, TP63, IL7R, RNF8, BRCA1, UBL4A, ITGA4, NKX3-1, BAG3, ANKH, C6orf106, SLC2A5, ACADVL, ABCD1, CALM2, HBG2, PROS1, DCTN6, GNMT, RNF114, HNRNPD, TARDBP, DYNC1LI2, DYNLL1, FAU, GNB2L1, PRUNE2, PTBP1, RPS12, RPS18, SYNCRIP, TSR1, XRCC6, rev, SUP35, ZBTB1, CUL7, OBSL1, RNF2, LUZP4, WDR76, FBXW11, HIST1H1A, LARP7, RPL26L1, RPSAP58, U2SURP, SF3B1, SF3B2, ZNF768, ZNF574, ZNF121, ZNF358, ZNF146, ZNF629, KRI1, LTV1, UTP23, DHX57, BMS1, ZNF777, CDR2L, CHERP, KRR1, ZBTB11, ZCRB1, CDR2, IMP3, GZF1, SRSF10, PURB, ZNF335, HSPB1, EIF4A2, LAGE3, RPL13A, RPL35A, RPL38, LOC101929876, RPS27, EEF1A2, PNO1, RPL27A, RPL34, RPL36, RPS11, UQCRC2, SFN, NTRK1, EWSR1, XPO1, HNRNPU, NPM1, LIMA1, Eif3a, Eif3e, Dctn3, Osgep, Rpl35, Rrbp1, Sesn2, GAN, MCM2, CDC73, CRBN, ZNF746, RRS1, YBX1, SLC9A1, CYLD, SPTA1, TRIM25, CCND2, PRNP, HDAC6, EIF4G2, PSMD1, SNAPC1, FBXO7, WDR77, HDAC4, YAF2, UBE2M, PRPF8, EFTUD2, AAR2, PIH1D1, TNIP2, CHD3, CHD4, RIOK1, ESR2, HEXIM1, MEPCE, SNAI1, RECQL4, GPC1, REST, MYC, Prkaa1, KRT17, METTL14, KIAA1429, RC3H1, RC3H2, ATG16L1, PSMA3, ACTC1, PHB, FAF1, NR2C2, PPP1CC, ZDHHC18, ZDHHC23, ATXN3, SNRNP70, ITFG1, HMGB1, PPP1CA, BIRC3, WWP2, LRRK2, CCDC13, ARIH2, PINK1, YAP1, TFCP2, FANCD2, NGB, E6, PEA15, LINC01554, ZC3H18, MAP2K3, RIPK1, MAU2, NEK4, LRRC31, DUX4, CIT, ANLN, CHMP4B, ECT2, KIF14, KIF20A, PRC1, MKI67, LRRC59, INS, NDN, AIMP2, MAFB, BRD4, NUPR1, CIC, Apc2, RBM39, LGALS9, IFI16, RIN3, DDX42, CTTN, CPSF7, NSRP1, PSPC1, YY1, PPP1R10, PPIL4, CCNT1, CDK9, LRPAP1, NUDT21, NUFIP2, PDIA6, EIF5A, GLUD1, TOP1, PIP4K2A, SART1, RCL1, RBM25, CSNK1D, C1orf35, OGT, SPOP, PARK2, UFL1, DDRGK1, FZR1, TSC2, WDR5, MAP4K3, NAA40, BGLT3, NGDN, WDR74, FTSJ3, CTCF, NAT10, SURF6, EPB41L5, UTP3, MPHOSPH10, SMURF2, AATF, GLYR1, STAU2, HIST1H2AG, PAK1IP1, DHX36, RRP12, NOP10, SREK1, PAPD5, DDX27, SSB, SRSF5, LIN28A, TTF1, ZNF16, PPAN-P2RY11, DDX31, DDX10, ZC3H8, LARP1B, FAM111B, NKRF, METTL17, YTHDF1, LARP1, PURA, GAR1, NOP16, SF3B5, RPL26, ZNF512, OASL, MAK16, GLTSCR2, RPL7L1, NOL10, PRDM15, POP1, RPS4Y2, GTPBP4, RSBN1, RSL1D1, CCDC137, HTRA4, ZC3HAV1, DHX30, NOL12, PRKRIR, NIFK, BTF3, EIF3E, Htatsf1, Pard6g, NLRP7, E, nsp1, nsp10, nsp4, ORF10, ORF7b, ORF8, nsp6, S, FGD5, RCHY1, CCNF, NBR1, TAX1BP1, CALCOCO2, PDE4B, SP1, TLX1,


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Mutations


check button Clinically associated variants from ClinVar.
GeneChrPositionRefSeqVarSeqRefSeeqVarTypePathogenicDiseaseVarInfo
RPSAchr339449137TCsingle_nucleotide_variantBenignAsplenia,_isolated_congenital|not_specifiedSO:0001623|5_prime_UTR_variantSO:0001623|5_prime_UTR_variant
RPSAchr339449169CTsingle_nucleotide_variantPathogenicAsplenia,_isolated_congenitalSO:0001587|nonsenseSO:0001587|nonsense
RPSAchr339449244AGsingle_nucleotide_variantUncertain_significancenot_providedSO:0001583|missense_variantSO:0001583|missense_variant
RPSAchr339450065CTsingle_nucleotide_variantBenignAsplenia,_isolated_congenitalSO:0001627|intron_variantSO:0001627|intron_variant
RPSAchr339450124CAsingle_nucleotide_variantPathogenicAsplenia,_isolated_congenitalSO:0001583|missense_variantSO:0001583|missense_variant
RPSAchr339450124CGsingle_nucleotide_variantUncertain_significancenot_providedSO:0001583|missense_variantSO:0001583|missense_variant
RPSAchr339450135CTsingle_nucleotide_variantPathogenicAsplenia,_isolated_congenitalSO:0001583|missense_variantSO:0001583|missense_variant
RPSAchr339450232TCsingle_nucleotide_variantBenignnot_providedSO:0001575|splice_donor_variant,SO:0001627|intron_variantSO:0001575|splice_donor_variant,SO:0001627|intron_variant
RPSAchr339452307TCsingle_nucleotide_variantBenignnot_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
RPSAchr339452493ACsingle_nucleotide_variantUncertain_significancenot_specifiedSO:0001627|intron_variantSO:0001627|intron_variant
RPSAchr339452498TAsingle_nucleotide_variantUncertain_significanceAsplenia,_isolated_congenitalSO:0001627|intron_variantSO:0001627|intron_variant
RPSAchr339453160GAsingle_nucleotide_variantBenignAsplenia,_isolated_congenital|not_specified|not_providedSO:0001819|synonymous_variantSO:0001819|synonymous_variant
RPSAchr339453179CGsingle_nucleotide_variantPathogenicAsplenia,_isolated_congenitalSO:0001583|missense_variantSO:0001583|missense_variant
RPSAchr339453179CTsingle_nucleotide_variantPathogenicAsplenia,_isolated_congenitalSO:0001583|missense_variantSO:0001583|missense_variant
RPSAchr339453197CTsingle_nucleotide_variantPathogenicAsplenia,_isolated_congenitalSO:0001583|missense_variantSO:0001583|missense_variant
RPSAchr339453229GGGTCATDuplicationPathogenicAsplenia,_isolated_congenitalSO:0001589|frameshift_variantSO:0001589|frameshift_variant
RPSAchr339453278TCsingle_nucleotide_variantLikely_benignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
RPSAchr339453367CCTDuplicationBenignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant


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


check button SNVs and Indels
GeneCancer typeChromosomeStartEndRefSeeqMutSeqMutation typeAAchange# samples
RPSAGBMchr192401029424010294CGMissense_Mutationp.Q111E8
RPSAPCPGchr33945351539453515AGSilent4
RPSAPAADchr33945020239450202GTMissense_Mutationp.R80M3
RPSABRCAchr33945238439452384ACMissense_Mutationp.H131P3
RPSAUCSchr33944916039449160GAMissense_Mutationp.D6N3
RPSASTADchr33945319839453198GAMissense_Mutationp.R186H2
RPSAKIRPchr33945355339453556GTAT-Frame_Shift_Delp.265_265del2
RPSAPAADchr33945342539453425GASilentp.V222V2
RPSAPRADchr33945013739450137TGSilentp.L58L2
RPSAUCECchr33945343439453434GTMissense_Mutationp.E225D2
RPSAUCECchr33945384739453847TCSilentp.T2922
RPSASKCMchr33944916539449165CTSilentp.V7V2
RPSASKCMchr33944916639449166CTSilentp.L8L2
RPSASKCMchr33944917639449176AGMissense_Mutationp.K11R2
RPSAPAADchr33945342539453425GASilent1
RPSABLCAchr33945348639453486CTMissense_Mutation1
RPSASKCMchr33945231239452312CGMissense_Mutationp.T107S1
RPSAGBMchr192401041224010412CAMissense_Mutationp.T150K1
RPSAPAADchr33945020239450202GTMissense_Mutation1
RPSABLCAchr33945352639453526CTMissense_Mutation1
RPSAGBMchr33945012239450122GASilent1
RPSABLCAchr33945019339450193TCMissense_Mutationp.I77T1
RPSASTADchr33945321239453212CTMissense_Mutationp.R191C1
RPSABLCAchr33945348639453486CTMissense_Mutationp.P243S1
RPSASTADchr33945243039452430GASilentp.A146A1
RPSAKIRPchr33945355339453556GTAT-Splice_Sitep.E270_splice1
RPSABLCAchr33945349839453498GTMissense_Mutationp.D247Y1
RPSASTADchr33944925339449253TCMissense_Mutationp.Y37H1
RPSALGGchr33944820439448204CTSplice_Site.1
RPSABLCAchr33945352639453526CTMissense_Mutationp.S256F1
RPSAUCECchr33945384739453847TCSilentp.T297T1
RPSALIHCchr33945315739453157TCSilentp.G172G1
RPSASARCchr33945316039453160GASilent1
RPSALIHCchr33945229139452291C-Frame_Shift_Delp.A100fs1
RPSASARCchr33944982639449826GARNANULL1
RPSACESCchr33944922339449223GAMissense_Mutation1
RPSALUADchr33944925539449255CTSilentp.Y37Y1
RPSAESCAchr33945247739452477CAMissense_Mutationp.P162Q1
RPSAUCSchr33944916039449160GAMissense_Mutation1
RPSALUADchr33945381139453811CTSilentp.P280P1
RPSALUADchr33945230539452305CAMissense_Mutationp.P105T1
RPSABLCAchr33945019339450193TCMissense_Mutation1
RPSAGBMchr192401032224010322GAMissense_Mutationp.R120Q1

check buttonCopy number variation (CNV) of RPSA
* 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 RPSA
* 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
78208ESCATCGA-VR-A8EQGTF2IRD1chr773868506+RPSAchr339450096+
78208N/AEC570254RBFOX2chr2236404899-RPSAchr339453429+
98309N/ABG033899RPSAchr339453803+LINC00593chr1569993751-
96707N/ABP281426RPSAchr339452315+PXKchr358376366+
79205UCECTCGA-AP-A05H-01ARPSAchr339450215+WIBGchr1256308150-
78213N/ABM014604RPSAP58chr1924010795+RPSAchr339449111+


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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
TGCTRPSA0.0007601660674083250.021
KIRCRPSA9.97359134933862e-072.8e-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
BRCARPSA0.006131864185935390.2
PAADRPSA0.0116211264938010.37
THYMRPSA0.01330909468848740.41

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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
P08865DB04985TigapotideBiotechInvestigational
P08865DB04985Tigapotide

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Related Diseases


check button Diseases associated with this translation factor.
(DisGeNet 4.0)
Disease IDDisease Name# PubMedsDisease source
C0152013Adenocarcinoma of lung (disorder)1CTD_human
C0685889Splenic Hypoplasia1CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT