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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:LYN-TGS1 (FusionGDB2 ID:50448)

Fusion Gene Summary for LYN-TGS1

check button Fusion gene summary
Fusion gene informationFusion gene name: LYN-TGS1
Fusion gene ID: 50448
HgeneTgene
Gene symbol

LYN

TGS1

Gene ID

4067

286826

Gene nameLYN proto-oncogene, Src family tyrosine kinaselin-9 DREAM MuvB core complex component
SynonymsJTK8|p53Lyn|p56LynBARA|BARPsv|Lin-9|TGS|TGS1|TGS2
Cytomap

8q12.1

1q42.12

Type of geneprotein-codingprotein-coding
Descriptiontyrosine-protein kinase Lynlck/Yes-related novel protein tyrosine kinasev-yes-1 Yamaguchi sarcoma viral related oncogene homologprotein lin-9 homologTUDOR gene similar proteinbeta subunit-associated regulator of apoptosislin-9 homologpRB-associated proteinrb related pathway actortype I interferon receptor beta chain-associated protein
Modification date2020032720200313
UniProtAcc

P07948

.
Ensembl transtripts involved in fusion geneENST00000420292, ENST00000519728, 
ENST00000520220, 
ENST00000260129, 
Fusion gene scores* DoF score11 X 7 X 7=5395 X 6 X 5=150
# samples 136
** MAII scorelog2(13/539*10)=-2.05177364972405
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/150*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: LYN [Title/Abstract] AND TGS1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointLYN(56879456)-TGS1(56723440), # samples:5
Anticipated loss of major functional domain due to fusion event.
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneLYN

GO:0006468

protein phosphorylation

11517336

HgeneLYN

GO:0006974

cellular response to DNA damage stimulus

10891478|11517336

HgeneLYN

GO:0018108

peptidyl-tyrosine phosphorylation

7682714|11782428

HgeneLYN

GO:0046777

protein autophosphorylation

7682714

HgeneLYN

GO:0051272

positive regulation of cellular component movement

16467205

HgeneLYN

GO:0070304

positive regulation of stress-activated protein kinase signaling cascade

10891478


check buttonFusion gene breakpoints across LYN (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across TGS1 (3'-gene)
* 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 gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4HNSCTCGA-CQ-6228LYNchr8

56879456

+TGS1chr8

56723440

+
ChimerDB4HNSCTCGA-CV-7242LYNchr8

56879456

+TGS1chr8

56723440

+
ChimerDB4LGGTCGA-HT-7602LYNchr8

56879456

+TGS1chr8

56723440

+
ChimerDB4OVTCGA-24-1565-01ALYNchr8

56879456

+TGS1chr8

56723440

+
ChimerDB4SKCMTCGA-FS-A1ZA-06ALYNchr8

56879456

+TGS1chr8

56723440

+


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Fusion Gene ORF analysis for LYN-TGS1

check button Open reading frame (ORF) analsis of fusion genes 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.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
3UTR-3CDSENST00000420292ENST00000260129LYNchr8

56879456

+TGS1chr8

56723440

+
In-frameENST00000519728ENST00000260129LYNchr8

56879456

+TGS1chr8

56723440

+
In-frameENST00000520220ENST00000260129LYNchr8

56879456

+TGS1chr8

56723440

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000519728LYNchr856879456+ENST00000260129TGS1chr856723440+24311269501687545
ENST00000520220LYNchr856879456+ENST00000260129TGS1chr856723440+23461184281602524

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score
ENST00000519728ENST00000260129LYNchr856879456+TGS1chr856723440+0.0009823150.9990177
ENST00000520220ENST00000260129LYNchr856879456+TGS1chr856723440+0.0013247360.9986753

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Fusion Genomic Features for LYN-TGS1


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)
LYNchr856879456+TGS1chr856723439+8.97E-080.9999999
LYNchr856879456+TGS1chr856723439+8.97E-080.9999999

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.
genomic feature

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.
genomic feature of top 1%

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Fusion Protein Features for LYN-TGS1


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr8:56879456/chr8:56723440)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
LYN

P07948

.
FUNCTION: Non-receptor tyrosine-protein kinase that transmits signals from cell surface receptors and plays an important role in the regulation of innate and adaptive immune responses, hematopoiesis, responses to growth factors and cytokines, integrin signaling, but also responses to DNA damage and genotoxic agents. Functions primarily as negative regulator, but can also function as activator, depending on the context. Required for the initiation of the B-cell response, but also for its down-regulation and termination. Plays an important role in the regulation of B-cell differentiation, proliferation, survival and apoptosis, and is important for immune self-tolerance. Acts downstream of several immune receptors, including the B-cell receptor, CD79A, CD79B, CD5, CD19, CD22, FCER1, FCGR2, FCGR1A, TLR2 and TLR4. Plays a role in the inflammatory response to bacterial lipopolysaccharide. Mediates the responses to cytokines and growth factors in hematopoietic progenitors, platelets, erythrocytes, and in mature myeloid cells, such as dendritic cells, neutrophils and eosinophils. Acts downstream of EPOR, KIT, MPL, the chemokine receptor CXCR4, as well as the receptors for IL3, IL5 and CSF2. Plays an important role in integrin signaling. Regulates cell proliferation, survival, differentiation, migration, adhesion, degranulation, and cytokine release. Down-regulates signaling pathways by phosphorylation of immunoreceptor tyrosine-based inhibitory motifs (ITIM), that then serve as binding sites for phosphatases, such as PTPN6/SHP-1, PTPN11/SHP-2 and INPP5D/SHIP-1, that modulate signaling by dephosphorylation of kinases and their substrates. Phosphorylates LIME1 in response to CD22 activation. Phosphorylates BTK, CBL, CD5, CD19, CD72, CD79A, CD79B, CSF2RB, DOK1, HCLS1, LILRB3/PIR-B, MS4A2/FCER1B, SYK and TEC. Promotes phosphorylation of SIRPA, PTPN6/SHP-1, PTPN11/SHP-2 and INPP5D/SHIP-1. Mediates phosphorylation of the BCR-ABL fusion protein. Required for rapid phosphorylation of FER in response to FCER1 activation. Mediates KIT phosphorylation. Acts as an effector of EPOR (erythropoietin receptor) in controlling KIT expression and may play a role in erythroid differentiation during the switch between proliferation and maturation. Depending on the context, activates or inhibits several signaling cascades. Regulates phosphatidylinositol 3-kinase activity and AKT1 activation. Regulates activation of the MAP kinase signaling cascade, including activation of MAP2K1/MEK1, MAPK1/ERK2, MAPK3/ERK1, MAPK8/JNK1 and MAPK9/JNK2. Mediates activation of STAT5A and/or STAT5B. Phosphorylates LPXN on 'Tyr-72'. Kinase activity facilitates TLR4-TLR6 heterodimerization and signal initiation. Phosphorylates SCIMP on 'Tyr-107'; this enhances binding of SCIMP to TLR4, promoting the phosphorylation of TLR4, and a selective cytokine response to lipopolysaccharide in macrophages (By similarity). Phosphorylates CLNK (By similarity). {ECO:0000250|UniProtKB:P25911, ECO:0000269|PubMed:10574931, ECO:0000269|PubMed:10748115, ECO:0000269|PubMed:10891478, ECO:0000269|PubMed:11435302, ECO:0000269|PubMed:11517336, ECO:0000269|PubMed:11825908, ECO:0000269|PubMed:14726379, ECO:0000269|PubMed:15795233, ECO:0000269|PubMed:16467205, ECO:0000269|PubMed:17640867, ECO:0000269|PubMed:17977829, ECO:0000269|PubMed:18056483, ECO:0000269|PubMed:18070987, ECO:0000269|PubMed:18235045, ECO:0000269|PubMed:18577747, ECO:0000269|PubMed:18802065, ECO:0000269|PubMed:19290919, ECO:0000269|PubMed:20037584, ECO:0000269|PubMed:7687428}.FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.

check buttonRetention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page


* Minus value of BPloci means that the break pointn is located before the CDS.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneLYNchr8:56879456chr8:56723440ENST00000519728+913129_226324513.0DomainSH2
HgeneLYNchr8:56879456chr8:56723440ENST00000519728+91363_123324513.0DomainSH3
HgeneLYNchr8:56879456chr8:56723440ENST00000520220+913129_226303492.0DomainSH2
HgeneLYNchr8:56879456chr8:56723440ENST00000520220+91363_123303492.0DomainSH3
HgeneLYNchr8:56879456chr8:56723440ENST00000519728+913253_261324513.0Nucleotide bindingATP
HgeneLYNchr8:56879456chr8:56723440ENST00000520220+913253_261303492.0Nucleotide bindingATP

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneLYNchr8:56879456chr8:56723440ENST00000519728+913247_501324513.0DomainProtein kinase
HgeneLYNchr8:56879456chr8:56723440ENST00000520220+913247_501303492.0DomainProtein kinase
TgeneTGS1chr8:56879456chr8:56723440ENST00000260129913611_624714854.0Compositional biasNote=Lys-rich
TgeneTGS1chr8:56879456chr8:56723440ENST00000260129913631_846714854.0RegionNote=Sufficient for catalytic activity


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Fusion Gene Sequence for LYN-TGS1


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>50448_50448_1_LYN-TGS1_LYN_chr8_56879456_ENST00000519728_TGS1_chr8_56723440_ENST00000260129_length(transcript)=2431nt_BP=1269nt
TCGGCCGAGCCCAGAGACAGCCAGTTCCTCTCCCGCCGCGCCGGGCCGCGCTGCCGCTCGCTCCCCGGCCGTGGCGCCTCCGGGCCAGAC
GCGCTGCAGCCTCCAGCCCGCGGCAAGCGGGGCGGCCGCGCCACCCCCGGCCCCGCGCCAGCAGCCCCTCGCCGCGCGTCCAGCGTTCCC
GGCCAGCAGCCTCCCCATACGCAGGTCCTGCTGGGCCGCCCCGTCGCGCCCCCCACTCTGAACTCAAGTCACCGTGGAGCTCCGCCGCCC
CGAAACTTTCACCGCGAGCGGGAAATATGGGATGTATAAAATCAAAAGGGAAAGACAGCTTGAGTGACGATGGAGTAGATTTGAAGACTC
AACCAGTACGTAATACTGAAAGAACTATTTATGTGAGAGATCCAACGTCCAATAAACAGCAAAGGCCAGTTCCAGAATCTCAGCTTTTAC
CTGGACAGAGGTTTCAAACTAAAGATCCAGAGGAACAAGGAGACATTGTGGTAGCCTTGTACCCCTATGATGGCATCCACCCGGACGACT
TGTCTTTCAAGAAAGGAGAGAAGATGAAAGTCCTGGAGGAGCATGGAGAATGGTGGAAAGCAAAGTCCCTTTTAACAAAAAAAGAAGGCT
TCATCCCCAGCAACTATGTGGCCAAACTCAACACCTTAGAAACAGAAGAGTGGTTTTTCAAGGATATAACCAGGAAGGACGCAGAAAGGC
AGCTTTTGGCACCAGGAAATAGCGCTGGAGCTTTCCTTATTAGAGAAAGTGAAACATTAAAAGGAAGCTTCTCTCTGTCTGTCAGAGACT
TTGACCCTGTGCATGGTGATGTTATTAAGCACTACAAAATTAGAAGTCTGGATAATGGGGGCTATTACATCTCTCCACGAATCACTTTTC
CCTGTATCAGCGACATGATTAAACATTACCAAAAGCAGGCAGATGGCTTGTGCAGAAGATTGGAGAAGGCTTGTATTAGTCCCAAGCCAC
AGAAGCCATGGGATAAAGATGCCTGGGAGATCCCCCGGGAGTCCATCAAGTTGGTGAAAAGGCTTGGCGCTGGGCAGTTTGGGGAAGTCT
GGATGGGTTACTATAACAACAGTACCAAGGTGGCTGTGAAAACCCTGAAGCCAGGAACTATGTCTGTGCAAGCCTTCCTGGAAGAAGCCA
ACCTCATGAAGACCCTGCAGCATGACAAGCTCGTGAGGCTCTACGCTGTGGTCACCAGGGAGGAGCCCATTTACATCATCACCGAGTACA
TGGCCAAGGTGATTGCCATTGATATCGATCCTGTTAAGATTGCCCTTGCTCGCAATAATGCAGAAGTTTATGGGATAGCAGATAAGATAG
AGTTCATCTGTGGAGATTTCTTGCTGCTGGCTTCTTTTTTAAAGGCTGATGTTGTGTTCCTCAGCCCACCTTGGGGAGGGCCAGACTATG
CCACTGCAGAGACCTTTGACATTAGAACAATGATGTCTCCTGATGGCTTTGAAATTTTCAGACTTTCTAAGAAGATCACTAATAATATTG
TTTATTTTCTTCCAAGAAATGCTGATATTGACCAGGTGGCATCCTTAGCTGGGCCTGGAGGGCAAGTGGAAATAGAACAGAACTTCCTTA
ACAACAAATTGAAGACAATCACTGCATATTTTGGTGACCTAATTCGAAGACCAGCCTCTGAAACCTAACTATGCAGCAGTGCGAGGACAA
AAGATCATGGAGTGGTCAAAATATTCAGATGAGACATTTGGCATGTCTTCCTTTATTCACTGATATTTTCTACCCATGGTCTTATATCAC
CGTATGAAATGGAAACTTACAGGACTTAAATATCAGTGAAATATTTTGAGATCTTTGAATAATTCCTTTAGAGGAATTATACAAAATTAA
TATATATGAGTCCTTTGTAATTTATTTTTTTTTGAGACAGGATCTCACTTTTACCGCCCAGGCTGGAGTGCAGTGCCATGATCACAGCTC
ACTGCAGGTTCAGCCTTCTGAGTTCAAGCAATCCTTCTGTCTCAGTCTCCTCAGTAGCTGGGGCTTTAGGTGGGCACTGCCACACCGTAC
TAATTTTTGTATTTTTTGTAGAGACGAGGTCCCACCATGTTGCCCAGGCTGGTGTCAAACTCCTGGGCTCAGTCAGTCCCCCCATCTCAC
CCTCCCCAAGTGCTGGAATTACAGGCGTGAGCTACTGTGCCCAGCCTTACGGACATCCTTTTGAATTATCTTTTTCACTCATAGAATATG
AATACATTTATTTAGACTTTTTCTAGAACTTTCCTGTTTTCATGTCTTTGCTTCATCTGGAATTGGCTTAACACCCTTTTATAAAGTTTG
TGTTTGTAAAATTTCCATTGTGACATCAATACGCAATATATTTTGTAATATAGGAGTTTCTATTTTTTTATTAAAATGGCAATGAAAGCA

>50448_50448_1_LYN-TGS1_LYN_chr8_56879456_ENST00000519728_TGS1_chr8_56723440_ENST00000260129_length(amino acids)=545AA_BP=406
MPLAPRPWRLRARRAAASSPRQAGRPRHPRPRASSPSPRVQRSRPAASPYAGPAGPPRRAPHSELKSPWSSAAPKLSPRAGNMGCIKSKG
KDSLSDDGVDLKTQPVRNTERTIYVRDPTSNKQQRPVPESQLLPGQRFQTKDPEEQGDIVVALYPYDGIHPDDLSFKKGEKMKVLEEHGE
WWKAKSLLTKKEGFIPSNYVAKLNTLETEEWFFKDITRKDAERQLLAPGNSAGAFLIRESETLKGSFSLSVRDFDPVHGDVIKHYKIRSL
DNGGYYISPRITFPCISDMIKHYQKQADGLCRRLEKACISPKPQKPWDKDAWEIPRESIKLVKRLGAGQFGEVWMGYYNNSTKVAVKTLK
PGTMSVQAFLEEANLMKTLQHDKLVRLYAVVTREEPIYIITEYMAKVIAIDIDPVKIALARNNAEVYGIADKIEFICGDFLLLASFLKAD
VVFLSPPWGGPDYATAETFDIRTMMSPDGFEIFRLSKKITNNIVYFLPRNADIDQVASLAGPGGQVEIEQNFLNNKLKTITAYFGDLIRR

--------------------------------------------------------------
>50448_50448_2_LYN-TGS1_LYN_chr8_56879456_ENST00000520220_TGS1_chr8_56723440_ENST00000260129_length(transcript)=2346nt_BP=1184nt
AGTTCCTCTCCCGCCGCGCCGGGCCGCGCTGCCGCTCGCTCCCCGGCCGTGGCGCCTCCGGGCCAGACGCGCTGCAGCCTCCAGCCCGCG
GCAAGCGGGGCGGCCGCGCCACCCCCGGCCCCGCGCCAGCAGCCCCTCGCCGCGCGTCCAGCGTTCCCGGCCAGCAGCCTCCCCATACGC
AGGTCCTGCTGGGCCGCCCCGTCGCGCCCCCCACTCTGAACTCAAGTCACCGTGGAGCTCCGCCGCCCCGAAACTTTCACCGCGAGCGGG
AAATATGGGATGTATAAAATCAAAAGGGAAAGACAGCTTGAGTGACGATGGAGTAGATTTGAAGACTCAACCAGTTCCAGAATCTCAGCT
TTTACCTGGACAGAGGTTTCAAACTAAAGATCCAGAGGAACAAGGAGACATTGTGGTAGCCTTGTACCCCTATGATGGCATCCACCCGGA
CGACTTGTCTTTCAAGAAAGGAGAGAAGATGAAAGTCCTGGAGGAGCATGGAGAATGGTGGAAAGCAAAGTCCCTTTTAACAAAAAAAGA
AGGCTTCATCCCCAGCAACTATGTGGCCAAACTCAACACCTTAGAAACAGAAGAGTGGTTTTTCAAGGATATAACCAGGAAGGACGCAGA
AAGGCAGCTTTTGGCACCAGGAAATAGCGCTGGAGCTTTCCTTATTAGAGAAAGTGAAACATTAAAAGGAAGCTTCTCTCTGTCTGTCAG
AGACTTTGACCCTGTGCATGGTGATGTTATTAAGCACTACAAAATTAGAAGTCTGGATAATGGGGGCTATTACATCTCTCCACGAATCAC
TTTTCCCTGTATCAGCGACATGATTAAACATTACCAAAAGCAGGCAGATGGCTTGTGCAGAAGATTGGAGAAGGCTTGTATTAGTCCCAA
GCCACAGAAGCCATGGGATAAAGATGCCTGGGAGATCCCCCGGGAGTCCATCAAGTTGGTGAAAAGGCTTGGCGCTGGGCAGTTTGGGGA
AGTCTGGATGGGTTACTATAACAACAGTACCAAGGTGGCTGTGAAAACCCTGAAGCCAGGAACTATGTCTGTGCAAGCCTTCCTGGAAGA
AGCCAACCTCATGAAGACCCTGCAGCATGACAAGCTCGTGAGGCTCTACGCTGTGGTCACCAGGGAGGAGCCCATTTACATCATCACCGA
GTACATGGCCAAGGTGATTGCCATTGATATCGATCCTGTTAAGATTGCCCTTGCTCGCAATAATGCAGAAGTTTATGGGATAGCAGATAA
GATAGAGTTCATCTGTGGAGATTTCTTGCTGCTGGCTTCTTTTTTAAAGGCTGATGTTGTGTTCCTCAGCCCACCTTGGGGAGGGCCAGA
CTATGCCACTGCAGAGACCTTTGACATTAGAACAATGATGTCTCCTGATGGCTTTGAAATTTTCAGACTTTCTAAGAAGATCACTAATAA
TATTGTTTATTTTCTTCCAAGAAATGCTGATATTGACCAGGTGGCATCCTTAGCTGGGCCTGGAGGGCAAGTGGAAATAGAACAGAACTT
CCTTAACAACAAATTGAAGACAATCACTGCATATTTTGGTGACCTAATTCGAAGACCAGCCTCTGAAACCTAACTATGCAGCAGTGCGAG
GACAAAAGATCATGGAGTGGTCAAAATATTCAGATGAGACATTTGGCATGTCTTCCTTTATTCACTGATATTTTCTACCCATGGTCTTAT
ATCACCGTATGAAATGGAAACTTACAGGACTTAAATATCAGTGAAATATTTTGAGATCTTTGAATAATTCCTTTAGAGGAATTATACAAA
ATTAATATATATGAGTCCTTTGTAATTTATTTTTTTTTGAGACAGGATCTCACTTTTACCGCCCAGGCTGGAGTGCAGTGCCATGATCAC
AGCTCACTGCAGGTTCAGCCTTCTGAGTTCAAGCAATCCTTCTGTCTCAGTCTCCTCAGTAGCTGGGGCTTTAGGTGGGCACTGCCACAC
CGTACTAATTTTTGTATTTTTTGTAGAGACGAGGTCCCACCATGTTGCCCAGGCTGGTGTCAAACTCCTGGGCTCAGTCAGTCCCCCCAT
CTCACCCTCCCCAAGTGCTGGAATTACAGGCGTGAGCTACTGTGCCCAGCCTTACGGACATCCTTTTGAATTATCTTTTTCACTCATAGA
ATATGAATACATTTATTTAGACTTTTTCTAGAACTTTCCTGTTTTCATGTCTTTGCTTCATCTGGAATTGGCTTAACACCCTTTTATAAA
GTTTGTGTTTGTAAAATTTCCATTGTGACATCAATACGCAATATATTTTGTAATATAGGAGTTTCTATTTTTTTATTAAAATGGCAATGA

>50448_50448_2_LYN-TGS1_LYN_chr8_56879456_ENST00000520220_TGS1_chr8_56723440_ENST00000260129_length(amino acids)=524AA_BP=385
MPLAPRPWRLRARRAAASSPRQAGRPRHPRPRASSPSPRVQRSRPAASPYAGPAGPPRRAPHSELKSPWSSAAPKLSPRAGNMGCIKSKG
KDSLSDDGVDLKTQPVPESQLLPGQRFQTKDPEEQGDIVVALYPYDGIHPDDLSFKKGEKMKVLEEHGEWWKAKSLLTKKEGFIPSNYVA
KLNTLETEEWFFKDITRKDAERQLLAPGNSAGAFLIRESETLKGSFSLSVRDFDPVHGDVIKHYKIRSLDNGGYYISPRITFPCISDMIK
HYQKQADGLCRRLEKACISPKPQKPWDKDAWEIPRESIKLVKRLGAGQFGEVWMGYYNNSTKVAVKTLKPGTMSVQAFLEEANLMKTLQH
DKLVRLYAVVTREEPIYIITEYMAKVIAIDIDPVKIALARNNAEVYGIADKIEFICGDFLLLASFLKADVVFLSPPWGGPDYATAETFDI

--------------------------------------------------------------

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Fusion Gene PPI Analysis for LYN-TGS1


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for LYN-TGS1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for LYN-TGS1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource