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Center for Computational Systems Medicine
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Gene summary

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Gene structures and expression levels

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Exon skipping events with PSIs in TCGA

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Exon skipping events with PSIs in GTEx

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Open reading frame (ORF) annotation in the exon skipping event

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Exon skipping events in the canonical protein sequence

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SNVs in the skipped exons with depth of coverage

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Splicing Quantitative Trait Loci (sQTLs) in the skipped exons

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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon

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Related drugs with this gene

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Related diseases with this gene

Gene summary for NOP58

check button Gene summary
Gene informationGene symbol

NOP58

Gene ID

51602

Gene nameNOP58 ribonucleoprotein
SynonymsHSPC120|NOP5|NOP5/NOP58
Cytomap

2q33.1

Type of geneprotein-coding
Descriptionnucleolar protein 58NOP58 ribonucleoprotein homolognucleolar protein 5nucleolar protein NOP5/NOP58
Modification date20180523
UniProtAcc

Q9Y2X3

ContextPubMed: NOP58 [Title/Abstract] AND exon [Title/Abstract] AND skip [Title/Abstract]
- Title (PMID)

check button Gene ontology of each this gene with evidence of Inferred from Direct Assay (IDA) from Entrez
GeneGO IDGO termPubMed ID

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Exon skipping events across known transcript of Ensembl for NOP58 from UCSC genome browser

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.
all structure

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Gene isoform structures and expression levels for NOP58

check button Expression levels of gene isoforms across TCGA.
gencode gene structure

check button Expression levels of gene isoforms across GTEx.
gencode gene structure


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Exon skipping events with PSIs in TCGA for NOP58

check button Information of exkip skipping event in TCGA.
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_3325122203130501:203130709:203139835:203139912:203142672:203142725203139835:203139912ENSG00000055044.6ENST00000472050.1,ENST00000488403.1,ENST00000426814.1
exon_skip_3325142203139884:203139912:203142672:203142725:203147073:203147195203142672:203142725ENSG00000055044.6ENST00000472050.1,ENST00000264279.5,ENST00000488403.1,ENST00000492688.1
exon_skip_3325202203142674:203142725:203142934:203143052:203147073:203147195203142934:203143052ENSG00000055044.6ENST00000467734.1,ENST00000426814.1
exon_skip_3325212203142672:203142725:203147073:203147195:203149067:203149101203147073:203147195ENSG00000055044.6ENST00000264279.5,ENST00000488403.1,ENST00000492688.1
exon_skip_3325252203149160:203149204:203152382:203152447:203155045:203155095203152382:203152447ENSG00000055044.6ENST00000264279.5,ENST00000433543.2,ENST00000492688.1
exon_skip_3325282203152382:203152447:203155045:203155180:203155847:203155993203155045:203155180ENSG00000055044.6ENST00000264279.5,ENST00000433543.2
exon_skip_3325292203155847:203155993:203157499:203157626:203160396:203160560203157499:203157626ENSG00000055044.6ENST00000264279.5
exon_skip_3325302203155847:203155993:203157499:203157626:203162101:203162236203157499:203157626ENSG00000055044.6ENST00000433543.2
exon_skip_3325332203157499:203157626:203160396:203160560:203162101:203162236203160396:203160560ENSG00000055044.6ENST00000264279.5
exon_skip_3325442203162567:203162629:203164956:203165090:203167643:203167780203164956:203165090ENSG00000055044.6ENST00000264279.5

check button PSI values of skipped exons in TCGA.
psi tcga

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Exon skipping events with PSIs in GTEx for NOP58

check button Information of exkip skipping event in GTEx
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_3325122203130501:203130709:203139835:203139912:203142672:203142725203139835:203139912ENSG00000055044.6ENST00000426814.1,ENST00000488403.1,ENST00000472050.1
exon_skip_3325142203139884:203139912:203142672:203142725:203147073:203147195203142672:203142725ENSG00000055044.6ENST00000264279.5,ENST00000488403.1,ENST00000472050.1,ENST00000492688.1
exon_skip_3325202203142674:203142725:203142934:203143052:203147073:203147195203142934:203143052ENSG00000055044.6ENST00000426814.1,ENST00000467734.1
exon_skip_3325212203142672:203142725:203147073:203147195:203149067:203149101203147073:203147195ENSG00000055044.6ENST00000264279.5,ENST00000488403.1,ENST00000492688.1
exon_skip_3325252203149160:203149204:203152382:203152447:203155045:203155095203152382:203152447ENSG00000055044.6ENST00000264279.5,ENST00000492688.1,ENST00000433543.2
exon_skip_3325282203152382:203152447:203155045:203155180:203155847:203155993203155045:203155180ENSG00000055044.6ENST00000264279.5,ENST00000433543.2
exon_skip_3325292203155847:203155993:203157499:203157626:203160396:203160560203157499:203157626ENSG00000055044.6ENST00000264279.5
exon_skip_3325302203155847:203155993:203157499:203157626:203162101:203162236203157499:203157626ENSG00000055044.6ENST00000433543.2
exon_skip_3325332203157499:203157626:203160396:203160560:203162101:203162236203160396:203160560ENSG00000055044.6ENST00000264279.5
exon_skip_3325442203162567:203162629:203164956:203165090:203167643:203167780203164956:203165090ENSG00000055044.6ENST00000264279.5

check button PSI values of skipped exons in GTEx.
psi gtex

* Skipped exon sequences.

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Open reading frame (ORF) annotation in the exon skipping event for NOP58

check button Open reading frame (ORF) of individual exon skipping events in TCGA based on the Ensembl gene structure combined from isoforms.
ENSTStart of skipped exonEnd of skipped exonORF
ENST00000264279203142672203142725Frame-shift
ENST00000264279203147073203147195Frame-shift
ENST00000264279203152382203152447Frame-shift
ENST00000264279203157499203157626Frame-shift
ENST00000264279203160396203160560Frame-shift
ENST00000264279203164956203165090Frame-shift
ENST00000264279203155045203155180In-frame

check button Open reading frame (ORF) of individual exon skipping events in GTEx based on the Ensembl gene structure combined from isoforms.
ENSTStart of skipped exonEnd of skipped exonORF
ENST00000264279203142672203142725Frame-shift
ENST00000264279203147073203147195Frame-shift
ENST00000264279203152382203152447Frame-shift
ENST00000264279203157499203157626Frame-shift
ENST00000264279203160396203160560Frame-shift
ENST00000264279203164956203165090Frame-shift
ENST00000264279203155045203155180In-frame

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Infer the effects of exon skipping event on protein functional features for NOP58

check button Exon skipping at the protein sequence level and followed lost functional features.
* Click on the image to enlarge it in a new window.
prot feature distribution

check button Loci of skipped exons in TCGA across genomic, transcript, and protein sequence levels of In-frame cases.
ENSTLength of mRNALength of AA seq.Genomic startGenomic endmRNA startmRNA endAA startAA end
ENST000002642792063529203155045203155180726860166211

check button Loci of skipped exons in GTEx across genomic, transcript, and protein sequence levels of In-frame cases.
ENSTLength of mRNALength of AA seq.Genomic startGenomic endmRNA startmRNA endAA startAA end
ENST000002642792063529203155045203155180726860166211

check button Lost protein functional features of individual exon skipping events in TCGA.
UniProt acc.Start of exon skipping (AA)End of exon skipping (AA)Protein feature start (AA)Protein feature end (AA)Category of protein featureDescription of feature
Q9Y2X31662111529ChainID=PRO_0000219023;Note=Nucleolar protein 58
Q9Y2X3166211202221Sequence conflictNote=LTYCKCLQKVGDRKNYASAK->YHTASVYRKLAIGRLCLCQ;Ontology_term=ECO:0000305;evidence=ECO:0000305


check button Lost protein functional features of individual exon skipping events in GTEx.
UniProt acc.Start of exon skipping (AA)End of exon skipping (AA)Protein feature start (AA)Protein feature end (AA)Category of protein featureDescription of feature
Q9Y2X31662111529ChainID=PRO_0000219023;Note=Nucleolar protein 58
Q9Y2X3166211202221Sequence conflictNote=LTYCKCLQKVGDRKNYASAK->YHTASVYRKLAIGRLCLCQ;Ontology_term=ECO:0000305;evidence=ECO:0000305


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SNVs in the skipped exons for NOP58

check button - Lollipop plot for presenting exon skipping associated SNVs.
* Click on the image to enlarge it in a new window.
lollipop

check button - Differential PSIs between mutated versus non-mutated samples.
NOP58_LIHC_exon_skip_332544_psi_boxplot.png
boxplot
NOP58_STAD_exon_skip_332544_psi_boxplot.png
boxplot

check button - Non-synonymous mutations located in the skipped exons in TCGA.
Cancer typeSampleESIDSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange
LIHCTCGA-DD-A3A0-01exon_skip_332512
203139836203139912203139908203139908Frame_Shift_DelA-p.K40fs
LIHCTCGA-DD-A1EG-01203157500203157626203157546203157546Frame_Shift_DelA-p.Q276fs
LIHCTCGA-DD-A39Y-01203157500203157626203157546203157546Frame_Shift_DelA-p.Q276fs
BLCATCGA-XF-AAMG-01exon_skip_332533
203160397203160560203160445203160464Frame_Shift_DelTTGGAGCTGAAAAGGCACTT-p.LGAEKAL319fs
LIHCTCGA-G3-A3CJ-01exon_skip_332544
203164957203165090203165009203165009Frame_Shift_DelA-p.K442fs
LIHCTCGA-DD-A3A0-01exon_skip_332544
203164957203165090203165060203165060Frame_Shift_DelA-p.K458fs
LIHCTCGA-DD-A39Y-01exon_skip_332544
203164957203165090203165066203165066Frame_Shift_DelA-p.K461fs
STADTCGA-F1-6177-01exon_skip_332544
203164957203165090203165008203165009Frame_Shift_Ins-Ap.S440fs
STADTCGA-F1-6177-01exon_skip_332544
203164957203165090203165009203165010Frame_Shift_Ins-Ap.S440fs
SKCMTCGA-EE-A2MF-06exon_skip_332514
203142673203142725203142701203142701Nonsense_MutationCTp.Q51*
SKCMTCGA-EE-A2MF-06exon_skip_332514
203142673203142725203142701203142701Nonsense_MutationCTp.Q51X
UCECTCGA-BS-A0UF-01203157500203157626203157506203157506Nonsense_MutationGTp.E263*
COADTCGA-G4-6303-01203157500203157626203157515203157515Nonsense_MutationGTp.E266X
STADTCGA-D7-A4YV-01203157500203157626203157521203157521Nonsense_MutationCTp.R268*
STADTCGA-D7-A4YV-01203157500203157626203157521203157521Nonsense_MutationCTp.R268X
HNSCTCGA-CR-7368-01203157500203157626203157551203157551Nonsense_MutationCTp.R278*
STADTCGA-BR-8360-01exon_skip_332512
203139836203139912203139835203139835Splice_SiteGT.
UCECTCGA-DI-A0WH-01203157500203157626203157628203157628Splice_SiteTCp.G303_splice

check button - Depth of coverage in the three exons composing exon skipping event
Depth of coverage in three exonsMutation description
NOP58_203162567_203162629_203164956_203165090_203167643_203167780_TCGA-F1-6177-01Sample: TCGA-F1-6177-01
Cancer type: STAD
ESID: exon_skip_332544
Skipped exon start: 203164957
Skipped exon end: 203165090
Mutation start: 203165008
Mutation end: 203165009
Mutation type: Frame_Shift_Ins
Reference seq: -
Mutation seq: A
AAchange: p.S440fs
NOP58_203162567_203162629_203164956_203165090_203167643_203167780_TCGA-F1-6177-01Sample: TCGA-F1-6177-01
Cancer type: STAD
ESID: exon_skip_332544
Skipped exon start: 203164957
Skipped exon end: 203165090
Mutation start: 203165009
Mutation end: 203165010
Mutation type: Frame_Shift_Ins
Reference seq: -
Mutation seq: A
AAchange: p.S440fs
exon_skip_105325_STAD_TCGA-F1-6177-01.png
boxplot
exon_skip_105326_STAD_TCGA-F1-6177-01.png
boxplot
exon_skip_285856_STAD_TCGA-F1-6177-01.png
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exon_skip_303345_STAD_TCGA-F1-6177-01.png
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exon_skip_319572_STAD_TCGA-F1-6177-01.png
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exon_skip_332544_STAD_TCGA-F1-6177-01.png
boxplot
exon_skip_377238_STAD_TCGA-F1-6177-01.png
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exon_skip_383047_STAD_TCGA-F1-6177-01.png
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exon_skip_423141_STAD_TCGA-F1-6177-01.png
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exon_skip_423142_STAD_TCGA-F1-6177-01.png
boxplot
exon_skip_470537_STAD_TCGA-F1-6177-01.png
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exon_skip_477308_STAD_TCGA-F1-6177-01.png
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exon_skip_494000_STAD_TCGA-F1-6177-01.png
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exon_skip_74586_STAD_TCGA-F1-6177-01.png
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exon_skip_77151_STAD_TCGA-F1-6177-01.png
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exon_skip_77155_STAD_TCGA-F1-6177-01.png
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exon_skip_9828_STAD_TCGA-F1-6177-01.png
boxplot

check button - Non-synonymous mutations located in the skipped exons in CCLE.
SampleSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange
SKMEL30_SKIN203155046203155180203155078203155084Frame_Shift_DelAACTACA-p.NYI178fs
HCC1569_BREAST203164957203165090203165009203165009Frame_Shift_DelA-p.K442fs
DG75_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE203164957203165090203165009203165009Frame_Shift_DelA-p.K442fs
HMC18_BREAST203164957203165090203164993203165025In_Frame_DelACTTCCAACCTGTTCTAAAAAACGCAAAATAGA-p.LPTCSKKRKIE436del
HEC1_ENDOMETRIUM203147074203147195203147093203147093Missense_MutationGTp.E65D
SNU349_KIDNEY203147074203147195203147115203147115Missense_MutationAGp.K73E
SNU1077_ENDOMETRIUM203147074203147195203147133203147133Missense_MutationACp.I79L
TT2609C02_THYROID203152383203152447203152420203152420Missense_MutationGAp.V158I
LNCAPCLONEFGC_PROSTATE203152383203152447203152427203152427Missense_MutationCAp.T160K
CCK81_LARGE_INTESTINE203155046203155180203155081203155081Missense_MutationTCp.Y179H
SKGIIIA_CERVIX203155046203155180203155163203155163Missense_MutationAGp.K206R
L1236_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE203155046203155180203155172203155172Missense_MutationATp.Q209L
HEC59_ENDOMETRIUM203157500203157626203157537203157537Missense_MutationAGp.E273G
NCIH1155_LUNG203157500203157626203157543203157543Missense_MutationTCp.L275P
NCIH2081_LUNG203160397203160560203160496203160496Missense_MutationCTp.P336L
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE203164957203165090203165027203165027Missense_MutationCGp.Q447E
CFPAC1_PANCREAS203164957203165090203165031203165031Missense_MutationTCp.V448A
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE203164957203165090203165084203165084Missense_MutationGAp.V466I
SNU81_LARGE_INTESTINE203155046203155180203155069203155069Nonsense_MutationGTp.E175*
SNU1040_LARGE_INTESTINE203155046203155180203155090203155090Nonsense_MutationCTp.R182*
JHUEM7_ENDOMETRIUM203157500203157626203157551203157551Nonsense_MutationCTp.R278*

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for NOP58

check button sQTL information located at the skipped exons.
Exon skip IDChromosomeThree exonsSkippped exonENSTCancer typeSNP idLocationDNA change (ref/var)P-value

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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for NOP58


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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for NOP58


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RelatedDrugs for NOP58

check button Approved drugs targeting this gene.
(DrugBank Version 5.1.0 2018-04-02)
GeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for NOP58

check button Diseases associated with this gene.
(DisGeNet 4.0)
GeneDisease IDDisease name# pubmedsSource