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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: RPL35A (NCBI Gene ID:6165)


Gene Summary

check button Gene Summary
Gene InformationGene Name: RPL35A
Gene ID: 6165
Gene Symbol

RPL35A

Gene ID

6165

Gene Nameribosomal protein L35a
SynonymsDBA5|L35A|eL33
Cytomap

3q29

Type of Geneprotein-coding
Description60S ribosomal protein L35acell growth-inhibiting gene 33 proteinlarge ribosomal subunit protein eL33
Modification date20200313
UniProtAcc

P18077


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
RPL35A>1119.25


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Translation Studies in PubMed

check button We searched PubMed using 'RPL35A[title] AND translation [title] AND human.'
GeneTitlePMID
RPL35A..


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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
ENST00000448864197678029197678182In-frame
ENST00000464167197678029197678182In-frame
ENST00000448864197680873197681018Frame-shift
ENST00000464167197680873197681018Frame-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)
ENST00000448864197678029197678182566150302110454
ENST000004641671976780291976781821454279431110454

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.
P180774541110ChainID=PRO_0000192796;Note=60S ribosomal protein L35a
P180774541110ChainID=PRO_0000192796;Note=60S ribosomal protein L35a
P1807745488Modified residueNote=N6-acetyllysine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:19608861;Dbxref=PMID:19608861
P1807745488Modified residueNote=N6-acetyllysine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:19608861;Dbxref=PMID:19608861
P180774542727Natural variantID=VAR_055446;Note=In DBA5. Missing;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:18535205;Dbxref=PMID:18535205
P180774542727Natural variantID=VAR_055446;Note=In DBA5. Missing;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:18535205;Dbxref=PMID:18535205
P180774543333Natural variantID=VAR_055447;Note=In DBA5%3B may result in aberrant splicing. V->I;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:18535205;Dbxref=dbSNP:rs116840808,PMID:18535205
P180774543333Natural variantID=VAR_055447;Note=In DBA5%3B may result in aberrant splicing. V->I;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:18535205;Dbxref=dbSNP:rs116840808,PMID:18535205


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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
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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
KIRCRPL35A-2.332468134253783.7449081319937e-09


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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

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

check buttonTranslation factor expression regulation through copy number variation of Translation factor
all structure
Cancer typeGeneCoefficientPvalue
STADRPL35A-0.0538858390.022268706

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Associated Genes


check button Strongly correlated genes belong to cellular important gene groups with RPL35A (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
CHOLCell metabolism geneRPL35APOLR2H0.8125825171.22E-11
CHOLCell metabolism geneRPL35ASNRPD20.8203397735.35E-12
DLBCCell metabolism geneRPL35ATIMM90.8216117238.34E-13
DLBCCell metabolism geneRPL35AFAU0.8311181052.64E-13
DLBCTSGRPL35AGNB2L10.8377514661.13E-13
GBMCell metabolism geneRPL35ASSR20.815372523.32E-42
GBMCell metabolism geneRPL35APSMA50.8173255321.47E-42
GBMCell metabolism geneRPL35ASSR40.8195085985.84E-43
GBMCell metabolism geneRPL35APIGC0.8288850729.59E-45
GBMTSGRPL35AGAS50.8462690492.33E-48
LGGCell metabolism geneRPL35AFAU0.8463619261.43E-146
LGGCGCRPL35ANACA0.8127111335.92E-126
LGGTSGRPL35AGNB2L10.8108178866.40E-125
LIHCCell metabolism geneRPL35ASNRPD20.8031900959.50E-97
LIHCCell metabolism geneRPL35APOLR2H0.8497855373.86E-119
LIHCEpifactorRPL35AFBL0.8158717893.33E-102
PCPGCell metabolism geneRPL35APOLR2H0.8083907331.91E-44
PRADCell metabolism geneRPL35APOLR2H0.8049062052.64E-126
PRADCell metabolism geneRPL35AFAU0.816138961.25E-132
PRADCell metabolism geneRPL35ASNRPD20.8334570162.79E-143
PRADCell metabolism geneRPL35ATIMM90.8404168396.50E-148
PRADCGCRPL35ANACA0.8298841645.51E-141
PRADEpifactorRPL35AFBL0.8212448341.19E-135
PRADTSGRPL35AGNB2L10.8316110684.35E-142
THCACell metabolism geneRPL35AFAU0.8080248914.41E-133
THCACell metabolism geneRPL35APFDN50.8261860313.72E-144
THCACell metabolism geneRPL35ASNRPD20.8271906838.33E-145
THYMCell metabolism geneRPL35ADPM20.8039100957.49E-29
THYMCell metabolism geneRPL35ASNRPD30.807128643.08E-29
THYMCell metabolism geneRPL35AITPA0.8127788096.19E-30
THYMCell metabolism geneRPL35ASNRPE0.8134347915.12E-30
THYMCell metabolism geneRPL35APSMB30.8137228194.71E-30
THYMCell metabolism geneRPL35APSME10.8154362.86E-30
THYMCell metabolism geneRPL35ASEC61G0.8173521211.62E-30
THYMCell metabolism geneRPL35AOAZ10.8181111341.30E-30
THYMCell metabolism geneRPL35AACOT80.8184122421.18E-30
THYMCell metabolism geneRPL35APSMB10.8196947448.06E-31
THYMCell metabolism geneRPL35ASMPD20.8255255861.35E-31
THYMCell metabolism geneRPL35ATALDO10.8296114963.71E-32
THYMCell metabolism geneRPL35APSMC30.8305069842.78E-32
THYMCell metabolism geneRPL35APSMD130.8367464243.56E-33
THYMCell metabolism geneRPL35APSMB70.8448932582.13E-34
THYMCell metabolism geneRPL35ALSM20.8546567535.86E-36
THYMCell metabolism geneRPL35APOLR2H0.8592126339.99E-37
THYMCell metabolism geneRPL35ATIMM130.8602557266.61E-37
THYMCell metabolism geneRPL35ATIMM8B0.8605320695.92E-37
THYMCell metabolism geneRPL35APFDN50.8640822371.41E-37
THYMCell metabolism geneRPL35AFAU0.8725867173.79E-39
THYMCell metabolism geneRPL35ASLC27A50.8833954812.59E-41
THYMCell metabolism geneRPL35ASNRPD20.8857282768.28E-42
THYMCell metabolism geneRPL35ASSR20.9023639661.10E-45
THYMCGCRPL35ASDHAF20.8148339593.41E-30
THYMCGCRPL35ATFPT0.8168896951.86E-30
THYMEpifactorRPL35APPP4C0.8016686691.38E-28
THYMEpifactorRPL35AC17orf490.8126940336.34E-30
THYMEpifactorRPL35ATFPT0.8168896951.86E-30
THYMEpifactorRPL35ARRP80.8204579916.40E-31
THYMEpifactorRPL35ASIRT60.8246935371.75E-31
THYMEpifactorRPL35ATAF100.8249199741.63E-31
THYMEpifactorRPL35ABRMS10.840311691.06E-33
THYMEpifactorRPL35AFBL0.9112588854.65E-48
THYMIUPHARRPL35AMFSD2B0.8188544251.04E-30
THYMIUPHARRPL35APSMB10.8196947448.06E-31
THYMIUPHARRPL35ASIRT60.8246935371.75E-31
THYMIUPHARRPL35ASMPD20.8255255861.35E-31
THYMIUPHARRPL35ASLC27A50.8833954812.59E-41
THYMTFRPL35AZNF7870.8005328171.87E-28
THYMTFRPL35AREXO40.801418921.47E-28
THYMTFRPL35ATHAP30.8056164324.68E-29
THYMTFRPL35AZNF5810.8125392126.63E-30
THYMTFRPL35AZNF4280.8227433773.19E-31
THYMTSGRPL35ASIRT60.8246935371.75E-31
THYMTSGRPL35ATSSC40.8363511424.07E-33
THYMTSGRPL35ABRMS10.840311691.06E-33
THYMTSGRPL35AGNB2L10.873307742.76E-39
UCSCell metabolism geneRPL35ADPM20.8039100957.49E-29
UCSCell metabolism geneRPL35ASNRPD30.807128643.08E-29
UCSCell metabolism geneRPL35AITPA0.8127788096.19E-30
UCSCell metabolism geneRPL35ASNRPE0.8134347915.12E-30
UCSCell metabolism geneRPL35APSMB30.8137228194.71E-30
UCSCell metabolism geneRPL35APSME10.8154362.86E-30
UCSCell metabolism geneRPL35ASEC61G0.8173521211.62E-30
UCSCell metabolism geneRPL35AOAZ10.8181111341.30E-30
UCSCell metabolism geneRPL35AACOT80.8184122421.18E-30
UCSCell metabolism geneRPL35APSMB10.8196947448.06E-31
UCSCell metabolism geneRPL35ASMPD20.8255255861.35E-31
UCSCell metabolism geneRPL35ATALDO10.8296114963.71E-32
UCSCell metabolism geneRPL35APSMC30.8305069842.78E-32
UCSCell metabolism geneRPL35APSMD130.8367464243.56E-33
UCSCell metabolism geneRPL35APSMB70.8448932582.13E-34
UCSCell metabolism geneRPL35ALSM20.8546567535.86E-36
UCSCell metabolism geneRPL35APOLR2H0.8592126339.99E-37
UCSCell metabolism geneRPL35ATIMM130.8602557266.61E-37
UCSCell metabolism geneRPL35ATIMM8B0.8605320695.92E-37
UCSCell metabolism geneRPL35APFDN50.8640822371.41E-37
UCSCell metabolism geneRPL35AFAU0.8725867173.79E-39
UCSCell metabolism geneRPL35ASLC27A50.8833954812.59E-41
UCSCell metabolism geneRPL35ASNRPD20.8857282768.28E-42
UCSCell metabolism geneRPL35ASSR20.9023639661.10E-45
UCSCGCRPL35ASDHAF20.8148339593.41E-30
UCSCGCRPL35ATFPT0.8168896951.86E-30
UCSEpifactorRPL35APPP4C0.8016686691.38E-28
UCSEpifactorRPL35AC17orf490.8126940336.34E-30
UCSEpifactorRPL35ATFPT0.8168896951.86E-30
UCSEpifactorRPL35ARRP80.8204579916.40E-31
UCSEpifactorRPL35ASIRT60.8246935371.75E-31
UCSEpifactorRPL35ATAF100.8249199741.63E-31
UCSEpifactorRPL35ABRMS10.840311691.06E-33
UCSEpifactorRPL35AFBL0.9112588854.65E-48
UCSIUPHARRPL35AMFSD2B0.8188544251.04E-30
UCSIUPHARRPL35APSMB10.8196947448.06E-31
UCSIUPHARRPL35ASIRT60.8246935371.75E-31
UCSIUPHARRPL35ASMPD20.8255255861.35E-31
UCSIUPHARRPL35ASLC27A50.8833954812.59E-41
UCSTFRPL35AZNF7870.8005328171.87E-28
UCSTFRPL35AREXO40.801418921.47E-28
UCSTFRPL35ATHAP30.8056164324.68E-29
UCSTFRPL35AZNF5810.8125392126.63E-30
UCSTFRPL35AZNF4280.8227433773.19E-31
UCSTSGRPL35ASIRT60.8246935371.75E-31
UCSTSGRPL35ATSSC40.8363511424.07E-33
UCSTSGRPL35ABRMS10.840311691.06E-33
UCSTSGRPL35AGNB2L10.873307742.76E-39
UVMCell metabolism geneRPL35ALTA4H0.8669014632.70E-25
UVMIUPHARRPL35ASLC25A260.8281666852.64E-21
UVMIUPHARRPL35ALTA4H0.8669014632.70E-25
UVMTSGRPL35AST130.8370130614.02E-22


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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
KIRPRPL35ARPL18A-1.516513928088850.00016188295558095
KICHRPL35ARPS27A1.753966937859560.000187873840332031
KIRPRPL35ARPS16-1.359570436175170.00019507110118866
COADRPL35ARPS31.487303751430140.000411599874496461
KIRPRPL35ARPS11-1.018615705651030.00105937570333481
LIHCRPL35ARPL8-4.845882849745580.00110314154326131
PRADRPL35ARPL18A1.406001757484990.00205137828390396
KICHRPL35ARPL191.369011828940890.00250792503356934
KICHRPL35ARPS121.269973817584310.00308787822723389
LUADRPL35ARPL19-1.313980266157250.00993159558412698
THCARPL35ARPS16-6.163227981565770.0115764821363307
BLCARPL35ARPS12-1.478046734404210.0204124450683594
BLCARPL35ARPS27A-1.047474700691880.0258216857910156
HNSCRPL35ARPS3-4.735058190951350.0273726439852453
COADRPL35ARPS111.353075489982040.0312207043170929
LUSCRPL35ARPL19-2.146698895166660.044366810398747
KIRCRPL35ARPL19-2.734852712766761.33980982873695e-10
BRCARPL35ARPS12-4.912393274782441.85340619742495e-09
KIRPRPL35ARPL37-1.174216219471392.26888805627823e-05
KIRCRPL35ARPL35-1.064752380593922.72286325678163e-08
KIRCRPL35ARPL8-1.182524599717735.64962994208288e-07
KIRPRPL35ARPL8-1.530036923501196.0301274061203e-05
KIRCRPL35ARPS16-1.661498698893847.8509870430991e-09
BRCARPL35ARPS27A-4.285121482004247.8788217967112e-14
KIRCRPL35ARPL37-2.871988220584648.03913394748564e-12
KIRPRPL35ARPL35-1.529811019754969.0546440333128e-05
KIRCRPL35ARPS3-1.295608479263879.05905681935088e-10
KIRCRPL35ARPL18A-4.430793049608439.2516163152192e-11


check button Protein-protein interactors with this translation factor (BIOGRID-3.4.160)
PPI interactors with RPL35A
PSTPIP1, CNBP, SH3GL3, NOP56, RAD21, HDGF, ARRB2, CUL3, CUL4B, CUL1, CAND1, PAN2, IGSF8, ICAM1, rev, ASB2, UBC, ABCE1, HNRNPUL2, RNPS1, RPL10A, RPL12, RPL15, RPL17, MTHFD1, NUMA1, RPL10, RPL11, RPL13, RPL13A, RPL14, RPL18, RPL18A, RPL19, RPL21, RPL22, RPL23, RPL23A, RPL24, RPL27, RPL27A, RPL3, RPL31, RPL32, RPL34, RPL35, RPL36AL, RPL37, RPL4, RPL6, RPL7, RPL7A, RPL8, RPL9, RPLP0, RPLP2, RPS11, RPS12, RPS13, RPS15, RPS16, RPS19, RPS2, RPS20, RPS25, RPS3, RPS4X, RPS8, RPS9, RPSA, UBA52, RPL36, RPL39, RPL5, RPS10, RPS14, RPS15A, RPS18, RPS27, RPS27L, RPS3A, RPS5, RPS6, RTF1, Eif3a, Rrbp1, MCM2, RRS1, RBM34, KIAA0020, PTPN6, NCL, CYLD, COX15, TRIM25, MTF1, CFTR, CBX3, TFDP1, WDR5, TRIM14, HBP1, BMP4, KRAS, TRIP4, API5, ARNT, CTNNB1, HNF1B, MAP2K1, PCBP1, PPIE, AAR2, PIH1D1, EFTUD2, TNIP2, MEPCE, LARP7, HERC2, KCMF1, RNF181, AGR2, RECQL4, DCPS, REST, MYC, METTL14, ACTC1, ZBTB7A, PHB, NR2C2, CTCF, VRK1, HIST1H4A, SNRNP70, PTPN21, ITFG1, BIRC3, STAU1, NFX1, WWP2, Hsp22, SOX2, CMTR1, ARIH2, PLEKHA4, FANCD2, ZC3H18, GRB7, MAP3K14, NCK1, M, nsp13, nsp4, nsp5, nsp6, ORF3a, ORF6, ORF7a, ORF7b, S, ESR1, HTRA2, IMMP2L, NEK4, CIT, ANLN, CHMP4C, ECT2, KIF14, KIF20A, KIF23, PRC1, MTERF3, Rnf183, MAFB, Apc2, RBM39, FBP1, LGALS9, BKRF1, DNAJC2, DNAJC17, DNAJC8, HSCB, LIN28A, SETD8, FBXL19, RPL26L1, HIST1H2AI, CPSF3L, RALY, S100A7, S100A8, DDX58, PARK2, UFL1, DDRGK1, TRIM37, USP15, HTRA4, FZR1, PAGE4, UHRF1, CHORDC1, SH3GL1, WDHD1, NAA50, XPNPEP1, CYB5R3, UBE2T, CD3EAP, ARF5, PRKRA, UBLCP1, OXSR1, C12orf57, SRRT, RPRD1B, YY1, RECQL, PPP1R8, EIF4G2, SCML2, RBM33, WDR3, MAVS, PDS5A, NARS, GLS, NSDHL, BRD4, TLN1, SF3A3, RAB5B, FEN1, DUSP3, WDR36, VAMP3, ACAA1, TTLL12, RNF20, CTNNBL1, ETF1, SF1, LZIC, PPP2R5D, SMCHD1, CCDC51, RAB5A, DACH1, MDC1, PHF3, ZC3H11A, DDX46, TOMM34, BLVRB, FAM49B, NDRG1, RAB4A, ATG3, LETM1, GTF2F1, RAP1B, RAP1A, PAPSS1, SF3A1, EFHD1, SAR1B, NDUFB8, UBP1, PTRH2, PKN2, ZMPSTE24, TPP2, HIBCH, SYAP1, SRP68, MLLT4, HDLBP, BRD3, DBNL, COQ9, CKAP5, KIF2A, PIN1, PRPF38B, WIBG, LASP1, XRCC1, TERF2, HMGN5, LRRC40, AK4, IDH3G, TPX2, TBCE, EIF2A, ALDH6A1, PTPN1, SPPL3, SNX27, PRPF40A, RAVER1, MCTS1, PPP1R12A, SYMPK, NAA15, RAC3, ZBTB10, EEF1A2, SLC4A7, EIF2AK2, USP28, SCCPDH, SCAF4, GINS1, HARS2, RBM12, PDS5B, SBDS, ADARB1, KITLG, ACTB, PSMG3, MAGEB2, TMOD1, BTF3, FBXW7, Cpsf6, NLRP7, DPP4, RCHY1, N, KLF12, FOS,


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Mutations


check button Clinically associated variants from ClinVar.
GeneChrPositionRefSeqVarSeqRefSeeqVarTypePathogenicDiseaseVarInfo
RPL35Achr3197677088TGsingle_nucleotide_variantUncertain_significanceDiamond-Blackfan_anemia_5SO:0001623|5_prime_UTR_variant,SO:0001627|intron_variantSO:0001623|5_prime_UTR_variant,SO:0001627|intron_variant
RPL35Achr3197677092GAsingle_nucleotide_variantUncertain_significanceDiamond-Blackfan_anemia_5SO:0001623|5_prime_UTR_variant,SO:0001627|intron_variantSO:0001623|5_prime_UTR_variant,SO:0001627|intron_variant
RPL35Achr3197677108GCsingle_nucleotide_variantLikely_benignnot_specifiedSO:0001623|5_prime_UTR_variant,SO:0001627|intron_variantSO:0001623|5_prime_UTR_variant,SO:0001627|intron_variant
RPL35Achr3197677666GAsingle_nucleotide_variantBenignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
RPL35Achr3197677804AGsingle_nucleotide_variantBenignDiamond-Blackfan_anemia_5SO:0001627|intron_variantSO:0001627|intron_variant
RPL35Achr3197677808CTsingle_nucleotide_variantUncertain_significanceDiamond-Blackfan_anemia_5SO:0001623|5_prime_UTR_variant,SO:0001627|intron_variantSO:0001623|5_prime_UTR_variant,SO:0001627|intron_variant
RPL35Achr3197678023GTsingle_nucleotide_variantLikely_benignDiamond-Blackfan_anemia_5SO:0001627|intron_variantSO:0001627|intron_variant
RPL35Achr3197678025CGsingle_nucleotide_variantUncertain_significanceDiamond-Blackfan_anemia_5SO:0001627|intron_variantSO:0001627|intron_variant
RPL35Achr3197678039CTsingle_nucleotide_variantBenign/Likely_benignDiamond-Blackfan_anemia_5|not_specifiedSO:0001819|synonymous_variant,SO:0001627|intron_variantSO:0001819|synonymous_variant,SO:0001627|intron_variant
RPL35Achr3197678052GAsingle_nucleotide_variantUncertain_significanceDiamond-Blackfan_anemia_5SO:0001583|missense_variant,SO:0001627|intron_variantSO:0001583|missense_variant,SO:0001627|intron_variant
RPL35Achr3197678059ATsingle_nucleotide_variantUncertain_significanceDiamond-Blackfan_anemia_5SO:0001583|missense_variant,SO:0001627|intron_variantSO:0001583|missense_variant,SO:0001627|intron_variant
RPL35Achr3197678073CTsingle_nucleotide_variantUncertain_significanceDiamond-Blackfan_anemia_5SO:0001583|missense_variant,SO:0001627|intron_variantSO:0001583|missense_variant,SO:0001627|intron_variant
RPL35Achr3197678075GAsingle_nucleotide_variantLikely_benignDiamond-Blackfan_anemia_5SO:0001819|synonymous_variant,SO:0001627|intron_variantSO:0001819|synonymous_variant,SO:0001627|intron_variant
RPL35Achr3197678095CTCTCMicrosatelliteConflicting_interpretations_of_pathogenicityDiamond-Blackfan_anemia_5|not_providedSO:0001822|inframe_deletion,SO:0001627|intron_variantSO:0001822|inframe_deletion,SO:0001627|intron_variant
RPL35Achr3197678107TCsingle_nucleotide_variantUncertain_significanceDiamond-Blackfan_anemia_5SO:0001583|missense_variant,SO:0001627|intron_variantSO:0001583|missense_variant,SO:0001627|intron_variant
RPL35Achr3197678115GAsingle_nucleotide_variantPathogenicDiamond-Blackfan_anemia_5SO:0001583|missense_variant,SO:0001627|intron_variantSO:0001583|missense_variant,SO:0001627|intron_variant
RPL35Achr3197678131AGsingle_nucleotide_variantUncertain_significanceDiamond-Blackfan_anemia_5SO:0001583|missense_variant,SO:0001627|intron_variantSO:0001583|missense_variant,SO:0001627|intron_variant
RPL35Achr3197678134CAGCDeletionPathogenicDiamond-Blackfan_anemia_5SO:0001589|frameshift_variant,SO:0001627|intron_variantSO:0001589|frameshift_variant,SO:0001627|intron_variant
RPL35Achr3197678183GAsingle_nucleotide_variantLikely_pathogenicDiamond-Blackfan_anemia_5SO:0001575|splice_donor_variant,SO:0001627|intron_variantSO:0001575|splice_donor_variant,SO:0001627|intron_variant
RPL35Achr3197680892CTsingle_nucleotide_variantLikely_benignDiamond-Blackfan_anemia_5SO:0001819|synonymous_variant,SO:0001627|intron_variantSO:0001819|synonymous_variant,SO:0001627|intron_variant
RPL35Achr3197680893GTsingle_nucleotide_variantLikely_benignDiamond-Blackfan_anemia_5|not_providedSO:0001583|missense_variant,SO:0001627|intron_variantSO:0001583|missense_variant,SO:0001627|intron_variant
RPL35Achr3197680921GAsingle_nucleotide_variantPathogenicDiamond-Blackfan_anemia_5SO:0001587|nonsense,SO:0001627|intron_variantSO:0001587|nonsense,SO:0001627|intron_variant
RPL35Achr3197680965GCGDeletionPathogenicDiamond-Blackfan_anemia_5SO:0001589|frameshift_variant,SO:0001627|intron_variantSO:0001589|frameshift_variant,SO:0001627|intron_variant
RPL35Achr3197680975GAsingle_nucleotide_variantBenignDiamond-Blackfan_anemia_5SO:0001583|missense_variant,SO:0001627|intron_variantSO:0001583|missense_variant,SO:0001627|intron_variant
RPL35Achr3197680980AGsingle_nucleotide_variantUncertain_significanceDiamond-Blackfan_anemia_5SO:0001583|missense_variant,SO:0001627|intron_variantSO:0001583|missense_variant,SO:0001627|intron_variant
RPL35Achr3197680991TCsingle_nucleotide_variantBenignDiamond-Blackfan_anemia_5SO:0001819|synonymous_variant,SO:0001627|intron_variantSO:0001819|synonymous_variant,SO:0001627|intron_variant
RPL35Achr3197681013CTsingle_nucleotide_variantPathogenicDiamond-Blackfan_anemia_5SO:0001587|nonsense,SO:0001627|intron_variantSO:0001587|nonsense,SO:0001627|intron_variant
RPL35Achr3197681022ATsingle_nucleotide_variantUncertain_significanceDiamond-Blackfan_anemia_5SO:0001627|intron_variantSO:0001627|intron_variant
RPL35Achr3197681207GTGDeletionLikely_benignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
RPL35Achr3197681217TGsingle_nucleotide_variantLikely_benignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
RPL35Achr3197681227CAsingle_nucleotide_variantBenignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
RPL35Achr3197682555CTsingle_nucleotide_variantBenignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
RPL35Achr3197682573CTsingle_nucleotide_variantLikely_benignnot_providedSO:0001627|intron_variantSO:0001627|intron_variant
RPL35Achr3197682650CTsingle_nucleotide_variantBenign/Likely_benignDiamond-Blackfan_anemia_5|not_specifiedSO:0001624|3_prime_UTR_variant,SO:0001627|intron_variantSO:0001624|3_prime_UTR_variant,SO:0001627|intron_variant
RPL35Achr3197682658CAsingle_nucleotide_variantBenignDiamond-Blackfan_anemia_5SO:0001624|3_prime_UTR_variant,SO:0001627|intron_variantSO:0001624|3_prime_UTR_variant,SO:0001627|intron_variant
RPL35Achr3197682665TAsingle_nucleotide_variantLikely_benignDiamond-Blackfan_anemia_5SO:0001624|3_prime_UTR_variant,SO:0001627|intron_variantSO:0001624|3_prime_UTR_variant,SO:0001627|intron_variant
RPL35Achr3197682779GCsingle_nucleotide_variantLikely_benignnot_providedSO:0001624|3_prime_UTR_variant,SO:0001627|intron_variantSO:0001624|3_prime_UTR_variant,SO:0001627|intron_variant
RPL35Achr3197682904CTsingle_nucleotide_variantBenignnot_providedSO:0001624|3_prime_UTR_variant,SO:0001627|intron_variantSO:0001624|3_prime_UTR_variant,SO: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
RPL35AUCECchr3197678094197678094GAMissense_Mutationp.A26T2
RPL35ALIHCchr3197678080197678080A-Frame_Shift_Delp.Q21fs2
RPL35AUCECchr3197678155197678155GTMissense_Mutationp.R46I2
RPL35APAADchr3197680900197680900CAMissense_Mutationp.P64Q2
RPL35ASTADchr3197678109197678109GAMissense_Mutation2
RPL35ASTADchr3197678109197678109GAMissense_Mutationp.E31K2
RPL35ABLCAchr3197678160197678160GAMissense_Mutationp.A48T2
RPL35ASTADchr3197678096197678098TCT-In_Frame_Delp.26_27del1
RPL35ADLBCchr3197678057197678057CTSilentp.G13G1
RPL35ASTADchr3197678096197678098TCT-In_Frame_Delp.L28del1
RPL35ALIHCchr3197678059197678059AGMissense_Mutationp.Y14C1
RPL35APAADchr3197680900197680900CAMissense_Mutation1
RPL35APRADchr3197678115197678115GAMissense_Mutationp.V33I1
RPL35ASKCMchr3197680974197680974CTNonsense_Mutationp.R89X1
RPL35ASKCMchr3197680974197680974CTNonsense_Mutationp.R89*1
RPL35ABLCAchr3197678160197678160GAMissense_Mutation1

check buttonCopy number variation (CNV) of RPL35A
* 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 RPL35A
* 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
101977N/ABF852302AKAP13chr1586198989-RPL35Achr3197678052+
101977N/ACA776035DOCK7chr162976292-RPL35Achr3197677087+
101977N/ABF893174FN1chr2216235227+RPL35Achr3197677064+
101977LUSCTCGA-85-8664-01AFYTTD1chr3197503872+RPL35Achr3197680874+
101977BRCATCGA-B6-A0RS-01AIQCGchr3197686400-RPL35Achr3197680874+
101977N/ACF124693IQCGchr3197677092+RPL35Achr3197677062+
101977N/ACF124701IQCGchr3197677092+RPL35Achr3197677063+
101977N/AEC559816PLCE1chr1095836863-RPL35Achr3197680874+
101977N/AEC575683PRKG1chr1053344421-RPL35Achr3197677112+
100056N/ADA779835RPL35Achr3197681003+BPTFchr1765914828+
97959N/ABF217777RPL35Achr3197682676+BRCC3chrX154304656+
97709N/AAA554649RPL35Achr3197682722+BRIP1chr1759808433+
102061N/ABI858652RPL35Achr3197682722+C2CD3chr1173861358+
100981N/AEC582733RPL35Achr3197682722+CDH4chr2060512275+
91133N/ABI856029RPL35Achr3197682722+GNG7chr192607528+
102962N/ABG576138RPL35Achr3197682722+KMT2Echr7104712086-
90754N/AAA737125RPL35Achr3197682658+LARSchr5145518569-
100295OVTCGA-23-1120-01ARPL35Achr3197681018+LPPchr3188202380+
99013N/ABG034739RPL35Achr3197682708+MAPK6chr1552320159-
102773N/ACB048671RPL35Achr3197682722+MELKchr936616408-
98486N/ABF687716RPL35Achr3197682718+NXNchr17724159+
85212N/AHI579411RPL35Achr3197682722+PSME4chr254126133+
93718STADTCGA-BR-A4QI-01ARPL35Achr3197681018+RAF1chr312633291-
89746N/ABM015835RPL35Achr3197682722+SLC25A17chr2241087369+
101977N/AEC573461SHROOM2chrX9916539-RPL35Achr3197678028+
101977STADTCGA-CD-5813SPARCL1chr488414733-RPL35Achr3197677806+
101977STADTCGA-CD-5813-01ASPARCL1chr488414734-RPL35Achr3197677807+
101977N/ACB857203USP39chr285868097-RPL35Achr3197677059+
101977N/AAK092633ZNF391chr627358698+RPL35Achr3197680924+


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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
HNSCRPL35A0.004146418185305830.12
MESORPL35A0.00715059610938590.19
BRCARPL35A0.01007654402132040.26

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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
LUSCRPL35A0.001913366550788470.061
LAMLRPL35A0.03266816884219440.98
BRCARPL35A0.003510591455468410.11
ESCARPL35A0.000720361506484230.024

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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
C1260899Anemia, Diamond-Blackfan2GENOMICS_ENGLAND
C2675859Diamond-Blackfan Anemia 51CTD_human;GENOMICS_ENGLAND;UNIPROT