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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 LYN

check button Gene summary
Gene informationGene symbol

LYN

Gene ID

4067

Gene nameLYN proto-oncogene, Src family tyrosine kinase
SynonymsJTK8|p53Lyn|p56Lyn
Cytomap

8q12.1

Type of geneprotein-coding
Descriptiontyrosine-protein kinase Lynlck/Yes-related novel protein tyrosine kinasev-yes-1 Yamaguchi sarcoma viral related oncogene homolog
Modification date20180523
UniProtAcc

P07948

ContextPubMed: LYN [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
LYN

GO:0006468

protein phosphorylation

11517336

LYN

GO:0006974

cellular response to DNA damage stimulus

10891478|11517336

LYN

GO:0018108

peptidyl-tyrosine phosphorylation

7682714|11782428

LYN

GO:0046777

protein autophosphorylation

7682714

LYN

GO:0051272

positive regulation of cellular component movement

16467205

LYN

GO:0070304

positive regulation of stress-activated protein kinase signaling cascade

10891478


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Exon skipping events across known transcript of Ensembl for LYN 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 LYN

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 LYN

check button Information of exkip skipping event in TCGA.
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_483603856792393:56792662:56854413:56854487:56859006:5685905256854413:56854487ENSG00000254087.3ENST00000520220.2
exon_skip_483610856854413:56854487:56859006:56859052:56860176:5686028256859006:56859052ENSG00000254087.3ENST00000520220.2
exon_skip_483611856854413:56854550:56859006:56859052:56860176:5686028256859006:56859052ENSG00000254087.3ENST00000520050.1,ENST00000519728.1
exon_skip_483612856860176:56860282:56863017:56863116:56863239:5686330756863017:56863116ENSG00000254087.3ENST00000520050.1,ENST00000520220.2,ENST00000519728.1
exon_skip_483614856866390:56866543:56879273:56879456:56882275:5688235256879273:56879456ENSG00000254087.3ENST00000520220.2,ENST00000519728.1

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

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Exon skipping events with PSIs in GTEx for LYN

check button Information of exkip skipping event in GTEx
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_483603856792393:56792662:56854413:56854487:56859006:5685905256854413:56854487ENSG00000254087.3ENST00000520220.2
exon_skip_483610856854413:56854487:56859006:56859052:56860176:5686028256859006:56859052ENSG00000254087.3ENST00000520220.2
exon_skip_483611856854413:56854550:56859006:56859052:56860176:5686028256859006:56859052ENSG00000254087.3ENST00000519728.1,ENST00000520050.1
exon_skip_483612856860176:56860282:56863017:56863116:56863239:5686330756863017:56863116ENSG00000254087.3ENST00000519728.1,ENST00000520220.2,ENST00000520050.1
exon_skip_483614856866390:56866543:56879273:56879456:56882275:5688235256879273:56879456ENSG00000254087.3ENST00000519728.1,ENST00000520220.2

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 LYN

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
ENST000005197285685900656859052Frame-shift
ENST000005197285686301756863116In-frame
ENST000005197285687927356879456In-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
ENST000005197285685900656859052Frame-shift
ENST000005197285686301756863116In-frame
ENST000005197285687927356879456In-frame

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

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
ENST000005197282314512568630175686311658167995127
ENST000005197282314512568792735687945610871269263324

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
ENST000005197282314512568630175686311658167995127
ENST000005197282314512568792735687945610871269263324

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
P07948951278995Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:1W1F
P079489512797104Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:1W1F
P0794895127110114Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:1W1F
P0794895127118120Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:1W1F
P07948951272512ChainID=PRO_0000088129;Note=Tyrosine-protein kinase Lyn
P079489512763123DomainNote=SH3;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00192
P0794895127105107TurnOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:1W1F
P0794895127115117TurnOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:1W1F
P07948263324260266Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5XY1
P07948263324270277Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5XY1
P07948263324305309Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5XY1
P07948263324311320Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5XY1
P07948263324275275Binding siteNote=ATP;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00159
P079482633242512ChainID=PRO_0000088129;Note=Tyrosine-protein kinase Lyn
P07948263324247501DomainNote=Protein kinase;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00159
P07948263324284296HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5XY1
P07948263324306306Modified residueNote=Phosphotyrosine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:19369195;Dbxref=PMID:19369195
P07948263324316316Modified residueNote=Phosphotyrosine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:19369195;Dbxref=PMID:19369195
P07948263324275275MutagenesisNote=Loss of activity and no effect on localization to the cell membrane. Abundant localization in the nucleus%3B when associated with A-2 and A-3. K->A;Ontology_term=ECO:0000269,ECO:0000269,ECO:0000269,ECO:0000269;evidence=ECO:0000269|PubMed:11435302,ECO
P07948263324275275MutagenesisNote=Loss of kinase activity. K->L%2CR;Ontology_term=ECO:0000269,ECO:0000269,ECO:0000269,ECO:0000269;evidence=ECO:0000269|PubMed:11435302,ECO:0000269|PubMed:11517336,ECO:0000269|PubMed:15173188,ECO:0000269|PubMed:18817770;Dbxref=PMID:11435302,PMID:1151733
P07948263324267269TurnOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5XY1


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
P07948951278995Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:1W1F
P079489512797104Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:1W1F
P0794895127110114Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:1W1F
P0794895127118120Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:1W1F
P07948951272512ChainID=PRO_0000088129;Note=Tyrosine-protein kinase Lyn
P079489512763123DomainNote=SH3;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00192
P0794895127105107TurnOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:1W1F
P0794895127115117TurnOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:1W1F
P07948263324260266Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5XY1
P07948263324270277Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5XY1
P07948263324305309Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5XY1
P07948263324311320Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5XY1
P07948263324275275Binding siteNote=ATP;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00159
P079482633242512ChainID=PRO_0000088129;Note=Tyrosine-protein kinase Lyn
P07948263324247501DomainNote=Protein kinase;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00159
P07948263324284296HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5XY1
P07948263324306306Modified residueNote=Phosphotyrosine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:19369195;Dbxref=PMID:19369195
P07948263324316316Modified residueNote=Phosphotyrosine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:19369195;Dbxref=PMID:19369195
P07948263324275275MutagenesisNote=Loss of activity and no effect on localization to the cell membrane. Abundant localization in the nucleus%3B when associated with A-2 and A-3. K->A;Ontology_term=ECO:0000269,ECO:0000269,ECO:0000269,ECO:0000269;evidence=ECO:0000269|PubMed:11435302,ECO
P07948263324275275MutagenesisNote=Loss of kinase activity. K->L%2CR;Ontology_term=ECO:0000269,ECO:0000269,ECO:0000269,ECO:0000269;evidence=ECO:0000269|PubMed:11435302,ECO:0000269|PubMed:11517336,ECO:0000269|PubMed:15173188,ECO:0000269|PubMed:18817770;Dbxref=PMID:11435302,PMID:1151733
P07948263324267269TurnOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5XY1


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SNVs in the skipped exons for LYN

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.

check button - Non-synonymous mutations located in the skipped exons in TCGA.
Cancer typeSampleESIDSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange
LIHCTCGA-G3-A3CJ-01exon_skip_483611
exon_skip_483610
56859007568590525685902356859023Frame_Shift_DelT-p.L30fs
HNSCTCGA-F7-A624-01exon_skip_483612
56863018568631165686305456863054Frame_Shift_DelA-p.T86fs
LIHCTCGA-DD-A39Y-01exon_skip_483612
56863018568631165686305456863054Frame_Shift_DelA-p.T86fs
STADTCGA-VQ-A8P2-01exon_skip_483612
56863018568631165686305456863054Frame_Shift_DelA-p.T107fs
STADTCGA-VQ-A8P2-01exon_skip_483612
56863018568631165686305456863054Frame_Shift_DelA-p.T86fs
UCECTCGA-AP-A0LT-01exon_skip_483612
56863018568631165686305456863054Frame_Shift_DelA-p.T107fs
HNSCTCGA-CR-7370-01exon_skip_483614
56879274568794565687942056879420Nonsense_MutationGTp.E292*
HNSCTCGA-CR-7370-01exon_skip_483614
56879274568794565687942056879420Nonsense_MutationGTp.E313*
LUSCTCGA-66-2754-01exon_skip_483614
56879274568794565687927356879273Splice_SiteGTp.G264_splice

check button - Depth of coverage in the three exons composing exon skipping event
Depth of coverage in three exonsMutation description

check button - Non-synonymous mutations located in the skipped exons in CCLE.
SampleSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange
SUPHD1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE56863018568631165686305456863054Frame_Shift_DelA-p.T107fs
KM12_LARGE_INTESTINE56863018568631165686305456863054Frame_Shift_DelA-p.T107fs
KMS12BM_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE56854414568544875685449056854492In_Frame_DelACG-p.R25del
FARAGE_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE56859007568590525685901056859010Missense_MutationCGp.P46A
MHHPREB1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE56859007568590525685902356859023Missense_MutationTCp.L50P
NCIH1155_LUNG56863018568631165686308556863085Missense_MutationGAp.V118M
SNUC1_LARGE_INTESTINE56863018568631165686309856863098Missense_MutationATp.N122I
MFE319_ENDOMETRIUM56879274568794565687929656879296Missense_MutationGTp.K271N
SKNDZ_AUTONOMIC_GANGLIA56879274568794565687930356879303Missense_MutationGTp.V274L
NCIH524_LUNG56879274568794565687930956879309Missense_MutationATp.T276S
LS411N_LARGE_INTESTINE56879274568794565687939456879394Missense_MutationGAp.R304K

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

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 LYN


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


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RelatedDrugs for LYN

check button Approved drugs targeting this gene.
(DrugBank Version 5.1.0 2018-04-02)
GeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
P07948DB06616BosutinibTyrosine-protein kinase Lynsmall moleculeapproved
P07948DB09079NintedanibTyrosine-protein kinase Lynsmall moleculeapproved
P07948DB01254DasatinibTyrosine-protein kinase Lynsmall moleculeapproved|investigational
P07948DB08901PonatinibTyrosine-protein kinase Lynsmall moleculeapproved|investigational
P07948DB12010FostamatinibTyrosine-protein kinase Lynsmall moleculeapproved|investigational

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RelatedDiseases for LYN

check button Diseases associated with this gene.
(DisGeNet 4.0)
GeneDisease IDDisease name# pubmedsSource
LYNC0019693HIV Infections1CTD_human