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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-EXT1 (FusionGDB2 ID:50441)

Fusion Gene Summary for LYN-EXT1

check button Fusion gene summary
Fusion gene informationFusion gene name: LYN-EXT1
Fusion gene ID: 50441
HgeneTgene
Gene symbol

LYN

EXT1

Gene ID

4067

2131

Gene nameLYN proto-oncogene, Src family tyrosine kinaseexostosin glycosyltransferase 1
SynonymsJTK8|p53Lyn|p56LynEXT|LGCR|LGS|TRPS2|TTV
Cytomap

8q12.1

8q24.11

Type of geneprotein-codingprotein-coding
Descriptiontyrosine-protein kinase Lynlck/Yes-related novel protein tyrosine kinasev-yes-1 Yamaguchi sarcoma viral related oncogene homologexostosin-1Glucuronosyl-N-acetylglucosaminyl-proteoglycan 4-alpha-N- acetylglucosaminyltransferaseLanger-Giedion syndrome chromosome regionN-acetylglucosaminyl-proteoglycan 4-beta-glucuronosyltransferaseexostoses (multiple) 1glucuronosyl-N-acetylgluc
Modification date2020032720200313
UniProtAcc

P07948

Q16394

Ensembl transtripts involved in fusion geneENST00000519728, ENST00000420292, 
ENST00000520220, 
ENST00000378204, 
Fusion gene scores* DoF score11 X 7 X 7=53915 X 10 X 7=1050
# samples 1317
** MAII scorelog2(13/539*10)=-2.05177364972405
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(17/1050*10)=-2.62678267641578
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: LYN [Title/Abstract] AND EXT1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointLYN(56854550)-EXT1(118842588), # samples:1
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

TgeneEXT1

GO:0006024

glycosaminoglycan biosynthetic process

12907669

TgeneEXT1

GO:0015012

heparan sulfate proteoglycan biosynthetic process

9620772|10639137

TgeneEXT1

GO:0033692

cellular polysaccharide biosynthetic process

12907669


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 EXT1 (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
ChimerDB4STADTCGA-FP-8211-01ALYNchr8

56854550

+EXT1chr8

118842588

-


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Fusion Gene ORF analysis for LYN-EXT1

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
In-frameENST00000519728ENST00000378204LYNchr8

56854550

+EXT1chr8

118842588

-
intron-3CDSENST00000420292ENST00000378204LYNchr8

56854550

+EXT1chr8

118842588

-
intron-3CDSENST00000520220ENST00000378204LYNchr8

56854550

+EXT1chr8

118842588

-

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)
ENST00000519728LYNchr856854550+ENST00000378204EXT1chr8118842588-6727428501504484

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
ENST00000519728ENST00000378204LYNchr856854550+EXT1chr8118842588-0.0005494170.9994506

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Fusion Genomic Features for LYN-EXT1


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)

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.

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Fusion Protein Features for LYN-EXT1


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/chr8:56854550/chr8:118842588)
- 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

EXT1

Q16394

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: Glycosyltransferase required for the biosynthesis of heparan-sulfate. The EXT1/EXT2 complex possesses substantially higher glycosyltransferase activity than EXT1 or EXT2 alone. Appears to be a tumor suppressor. Required for the exosomal release of SDCBP, CD63 and syndecan (PubMed:22660413). {ECO:0000269|PubMed:11518722, ECO:0000269|PubMed:22660413}.

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
TgeneEXT1chr8:56854550chr8:118842588ENST00000378204211544_549388747.0RegionSubstrate binding
TgeneEXT1chr8:56854550chr8:118842588ENST00000378204211565_567388747.0RegionSubstrate binding
TgeneEXT1chr8:56854550chr8:118842588ENST00000378204211650_654388747.0RegionSubstrate binding
TgeneEXT1chr8:56854550chr8:118842588ENST00000378204211688_701388747.0RegionSubstrate binding

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneLYNchr8:56854550chr8:118842588ENST00000519728+213129_22644513.0DomainSH2
HgeneLYNchr8:56854550chr8:118842588ENST00000519728+213247_50144513.0DomainProtein kinase
HgeneLYNchr8:56854550chr8:118842588ENST00000519728+21363_12344513.0DomainSH3
HgeneLYNchr8:56854550chr8:118842588ENST00000520220+113129_2260492.0DomainSH2
HgeneLYNchr8:56854550chr8:118842588ENST00000520220+113247_5010492.0DomainProtein kinase
HgeneLYNchr8:56854550chr8:118842588ENST00000520220+11363_1230492.0DomainSH3
HgeneLYNchr8:56854550chr8:118842588ENST00000519728+213253_26144513.0Nucleotide bindingATP
HgeneLYNchr8:56854550chr8:118842588ENST00000520220+113253_2610492.0Nucleotide bindingATP
TgeneEXT1chr8:56854550chr8:118842588ENST000003782042111_7388747.0Topological domainCytoplasmic
TgeneEXT1chr8:56854550chr8:118842588ENST0000037820421129_746388747.0Topological domainLumenal
TgeneEXT1chr8:56854550chr8:118842588ENST000003782042118_28388747.0TransmembraneHelical%3B Signal-anchor for type II membrane protein


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Fusion Gene Sequence for LYN-EXT1


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.
>50441_50441_1_LYN-EXT1_LYN_chr8_56854550_ENST00000519728_EXT1_chr8_118842588_ENST00000378204_length(transcript)=6727nt_BP=428nt
TCGGCCGAGCCCAGAGACAGCCAGTTCCTCTCCCGCCGCGCCGGGCCGCGCTGCCGCTCGCTCCCCGGCCGTGGCGCCTCCGGGCCAGAC
GCGCTGCAGCCTCCAGCCCGCGGCAAGCGGGGCGGCCGCGCCACCCCCGGCCCCGCGCCAGCAGCCCCTCGCCGCGCGTCCAGCGTTCCC
GGCCAGCAGCCTCCCCATACGCAGGTCCTGCTGGGCCGCCCCGTCGCGCCCCCCACTCTGAACTCAAGTCACCGTGGAGCTCCGCCGCCC
CGAAACTTTCACCGCGAGCGGGAAATATGGGATGTATAAAATCAAAAGGGAAAGACAGCTTGAGTGACGATGGAGTAGATTTGAAGACTC
AACCAGTACGTAATACTGAAAGAACTATTTATGTGAGAGATCCAACGTCCAATAAACAGCAAAGGCCAATTCCTTCTACAATCAGGTCTA
TTCATCAGGATAAAATCCTAGCACTTAGACAGCAGACACAATTCTTGTGGGAGGCTTATTTTTCTTCAGTTGAGAAGATTGTATTAACTA
CACTAGAGATTATTCAGGACAGAATATTCAAGCACATATCACGTAACAGTTTAATATGGAACAAACATCCTGGAGGATTGTTCGTACTAC
CACAGTATTCATCTTATCTGGGAGATTTTCCTTACTACTATGCTAATTTAGGTTTAAAGCCCCCCTCCAAATTCACTGCAGTCATCCATG
CGGTGACCCCCCTGGTCTCTCAGTCCCAGCCAGTGTTGAAGCTTCTCGTGGCTGCAGCCAAGTCCCAGTACTGTGCCCAGATCATAGTTC
TATGGAATTGTGACAAGCCCCTACCAGCCAAACACCGCTGGCCTGCCACTGCTGTGCCTGTCGTCGTCATTGAAGGAGAGAGCAAGGTTA
TGAGCAGCCGTTTTCTGCCCTACGACAACATCATCACAGACGCCGTGCTCAGCCTTGACGAGGACACGGTGCTTTCAACAACAGAGGTGG
ATTTCGCCTTCACAGTGTGGCAGAGCTTCCCTGAGAGGATTGTGGGGTACCCCGCGCGCAGCCACTTCTGGGATAACTCTAAGGAGCGGT
GGGGATACACATCAAAGTGGACGAACGACTACTCCATGGTGTTGACAGGAGCTGCTATTTACCACAAATATTATCACTACCTATACTCCC
ATTACCTGCCAGCCAGCCTGAAGAACATGGTGGACCAATTGGCCAATTGTGAGGACATTCTCATGAACTTCCTGGTGTCTGCTGTGACAA
AATTGCCTCCAATCAAAGTGACCCAGAAGAAGCAGTATAAGGAGACAATGATGGGACAGACTTCTCGGGCTTCCCGTTGGGCTGACCCTG
ACCACTTTGCCCAGCGACAGAGCTGCATGAATACGTTTGCCAGCTGGTTTGGCTACATGCCGCTGATCCACTCTCAGATGAGGCTCGACC
CCGTCCTCTTTAAAGACCAGGTCTCTATTTTGAGGAAGAAATACCGAGACATTGAGCGACTTTGAGGAATCCGGCTGAGTGGGGGAGGGG
AAGCAAGAAGGGATGGGGGTCAAGCTGCTCTCTCTTCCCAGTGCAGATCCACTCATCAGCAGAGCCAGATTGTGCCAACTATCCAAAAAC
TTAGATGAGCAGAATGACAAAAAAAAAAAGGCCAATGAGAACTCAACTCCTGGCTCCTGGGACTGCACCAGACTGCTCCAAACTCACCTC
ACTGGCTTCTGTGTCCCAAGACTAGGTTGTGTACAGTTTAATTATGGAACATTAAATAATTATTTTTGAAATGATTGCTATGCAGGTTTA
AACTTTTTTAATGATCAAAACTATTAAAAACCAGAGTTCTTTGTTTAATCAAAATTGTGTTGGTTGTGAATATTTCAAAGCTGCTATTCC
TTTTCCCACAGACATCATTGTCATGGCCATGTAGGGTGCCCTGCAGTTTCAAAAGCTCAAACTTCGTGGAAAACACAATAAGTCACTCTA
CCCATTATCAAGAAATAACTGAGCATAAGTTGTAACTTCATTATTCAACTTTGCCAGTGCAAATTGTTTTCCACTTCGAATCTTCAAATC
CACTTGAACTTTTATCTCTAAAATGTCGCTGCATGAAAGAAAGTATTACGACTTCCAGGTAGGCAGTTCTAACTGAAATCTCTATGTTTG
AGATAGATATATATGATAATCGTTTTTCATTGGGGGGGTGGGGGGAATTAGTACCAAGAAAACACTAGTATAATTAAGAAATGTTCAGTT
TGCACAAAGAACTATCCAGATAACCCACCAGCATGTTAGTGAGATGGAAATACAGACCCACAACAGTAACCCAATACTTGCAGGGGTTGG
GGGCACGGTTATAGATTCAACCATTGACCTAAGTCTGCGTAGCACTGGGAAGAGGCTTTGGTTTAGAAGCCAAGGAATAATGAGTATATT
GGGGAGAACAGATTATTTACAAGATGAACTCTTTAATGTTTGTGAGAATCTCAAGTTTCAGAGTTTCTCTTTTGAGAAAGAAAAAGGGGT
AATAAGGTAGAAATTCACACCAATGAACAAGAGGATTGCTGCAAAGTAACTGAGGAGATGTCTCGCCATTGGGACCCTAATGCCATTTTT
GGTCAAACATTGTTTTGAGCAAGAATCTGGCAAACAAAATAATCAACAACAAATGTGAATATAGTTTCATTTACTTTTAATTTTTAAATC
TGTGGAAAAGTTTAGTTGTGCTTCTTGTTAAAAAGAACATTTCTATCCCTGAAAATGCTATCTTGGGCTTATGATTATTGTTAAACTCCA
AGTATAAACTGAAAAAAAAAACATATCCCTAACTCTGTTATGAAAAATGGAGACTTCTGATATTAAATGCTTTCTTCTACTTGGAAGAGG
CCAGAGAAAACAGGGAAGAGAAAGACATTATTGAGTTTGACCATGTATTATGCTGAATAAACAATAAGCACTTTAGAGTCCCTCCCTCAA
ACTCTCATACATTTCATATTTCTTTTCCATTTATTTTCAGTTTTGTTTTAGAAGAAAAGTTCATCAGAGAATTTTGTTCTGATAATTTCA
AGTGGCCATCTTAGGTCAGTGGAAACCGTAAGTCCATTGGACTTTACCTCATCCTTTCTTTGTAGACATCTGGGAGAGGAAGAGGAGCTT
GTAATGATAGCACGGGGATGGTGCTGTAAACAGGAGTGAAAGTGTTTGTGGAAGTCCAGAGAAGTGACTCAACAGGCTACCTAGCTGCAG
AACAAGGAGTAGAGCCCACATATCCAGATGGTGTTTTGAGAGGTGCGTAGACAGTGAAATTCAATTAAAGAGAGGATTTTCTCCTCAGCC
TCATGACTCAGAACAGCTCCCTAAATACCTCTCTCATCTAATTGGACCCATCCATAGTCCATTCTCAAACATGTGACATTTTCCCCTAAG
TAGATGTGATTATCTCTTAGGCATTTGTTGAAAAATAATTCTTAGGTCCATGGTGCTTGCACTTGTGTCTTTTCTATAAAATGTTTGGTC
TTACAGGTTTCATGTCATTTAAGCTGCACTTCTCAGCAAGTTAAAAGATTAGCAGTTAATCTTTATTCATTTGGCCTTTGTGAATTTGTA
TTTAAATTATTTTTTTCAGGATTGGCAAATTATTCTTGTTTCTCCTTTACCAAAAAATAAATGCGATATTTTGTTCAATGACCCCAAAAC
CAACTTGAAACTTAGGTGGTCATATTGGCTTGCAAAGCAATGTCCCTAATTGTACCAGTCAGTCACACAAGTGGATTCAAGGACCTGCTT
TGCCAGATTGACCTGTCACCAAGCTCACAACACATATCCTCCACAAACAACATGTGTTATGTGAAGAAAAATGGTAATTATAAATAAGAA
CAGGATATAACACACCTTTCATCCACTTTAAATCTCCACAGTTTCATTTTATGTCATTCTCTGAGCAAATCTCTTTGGGATGTGAGCTAG
CGTGTTCTTCTCCCATTTGGAATATAAGGCTGGGAATAGAACAATGCTTAACAAATCAGTGAAGCTCGACAGTAATATGTAATTTTAATT
CAGTTAGGAAAGAGTTGTATTGCATTGCAACAAGTTGACAAATCATAGCCATCTCTGTAGGGTGTCAGGAATTATCTCCTGGTCAACTTT
AATGATAACTAGGGGTCCCTAAGTGGGCTAACATGTGCTGCATTGGAGAGAAGCCAAGGGCTGAGAGTACAGTGCCAACCACGTAATGAA
TTGCTTGCAGAAATTCCAAAGAGGACTCAGCCACTTATGGATTTCCACACAGCATCTTTTCCCAGCTCCACATTAAGACACAGGATCTTA
AAAGTAATTTTTTAAAAGCTGGCTGTGTATTTATTTATATGAAAGTGTTATAAATATCAAAGCTTACAAATACATTAATACATATCACCT
TTGTTGAAGCTAGCAAAATGGCTCAAAATTGAGACTGTAGAGAAAAATCCATGAAATAATCACGATAGTCATACCACAAAAGATAGCATA
GCTAGGTGGGCCTACCTGGTCGTATCAACACACTTTCAGATAGATGCTTCAAAAAAAAAGGGAAAGCTTGTTACTGGAATCTTATGTGCA
TTACAGTTTAATTTCTTCTTGTGACAAATGGTGCTCAAAGAAGGATCAATCCGGTTGCATCCTTCAATTTCCCTTTTAGAATGACTTTTG
GTTTTCATTACAGTAGGCTATGTTAGCCTTTATTTTGGTGGTTCTCAAATACCTGGTGACTTGAAAGAGTATTATGCTGGTGGCCTTTCA
TAAAGGTTACTGAACTTTAATCAGGGGTGAGATGAATGAATGTGAATAGGCCTATATACTATTTTTTTTAATTAAAAAAAAAAAAAACAG
GGCACTTGATTTAAGAACAAACCTGTTTAAAGGGCAGGATCAGGGGGAAGACAGCCTTACTAGGTTGGAATCTGAATGAGATTCTTGCTG
GACAAGGCTGAATTATGGATGCAAAAGCCAAGCAAACTTCCCAGACCTGGAAGTGTCTTGTGTTCCCTTGGGTCTCTTGAGATCTCCAGT
ATTTAAAAGTAGCAGTTATTGCCATGAACTCTCAAATAAAAATGCTCCTGCCTCTTACTTGTGAATATAATCAACATGCAGCCAGTACAT
CAGGACCGCAGTTGCTGAATTCATTTACCTAGTTCCCCTTTACAGCGACTATGGACAAGAACCTTTCAGTTGGTTTTGTCATTCTTGGCC
AGATTTAACCAAGAAATTTCTTTCACTATCAGCCTCATTTTCTCAGGCATGCTTACAGGGACAAAGTTGTTTTGAGTTGAGTTCTCAGCA
AATAAGCATTAATATCAAACTGTGCTAAACTTGTCTCACTTGGTATAAGAACTTCAGCATAAAGAGATTAGTTTATCCTTTGACACCAAG
TCTTTTTTTTTTCTTTGAGACAGAGTCTTGCCCTGTCACCCAGGCTGGAATGCATTGGTGTGATCTCAGCTCAGTCACTGCAACCTCCGC
CTCCCCGGTTCAAGCAATTCTCCTGCCTCACCCTGCTTAGTAGTTGGGATTACAGGCATGTGCTACCACACTGGGCTAATTTTTGTATAT
TTATTAGAGACAGGGTTTTGCTATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCCACCTGCCTCTGCCTCCCAAAGTGCT
GAGATTACAGGTGTAAGCCACTGCGCCTGGCCCCCCTTTTTTTTTTCTTTAAAAAAAAAAAAAAGCTTGGGGGATTAAGTACCCTAAGAT
AGTGGTCTCTCCCATCAGTTCAATAATGCTGTACAGAACCTCTGGATAAAAAAGCTGTTATTTACACCATAATTGTGATGATGGATTTGA
CTCCTCAAAACCATCTCTCCCCTTTTTGCCCTTTCCAAAAATCAAAGGCTTTTGTCTCCATGAGTTTTACCTAGTAGGGATTGTAGTTGT
CACTGGTCTAGAGTTCCAATACATTTTATATCAGGAACCTCAGTGAGCTACCCAGAATTGGAACTTAACATGGCCCAGCAACTAGGAGAA
GAAGGCAAACCTTGAGAAAGCTGAGCCCTCAGGATAGCACAGTCTCACCCTTGTTTAAAATCAAGTCAGGCTAGCCTTTCAGTCACTCTG
GTTTTGTAATGATTTGCCTTTTAGGCCTCAGGCCATTTGATTTCTGCAATAGTTTTCTGTTCTTCTCCTACAGGAATACATCCCTGTCCT
TTCGGTTGTAACTATTACTAAAACTAGGGCTATGCAAATGACCTGGTTACCATGTAATGAACCTTGTGTACTTATTTTGAGAGAACAATA
TGTATAGGATATGTTGAGGGGCAGAAAGAAAGACATCAAAAACTGGAACTATTTTAGGTGGCAAATTGTAACGCAAAAAACAAAAGTATA
CCTTATTTTGTATACGATGTACACTTGGGACAGAGTTTTCTAATATGTTGCCAATGTTTTTGTAGTGTCACCACAGGTCTTTTCTGAAGT
GTTTTTCCCATTTGTTATAGAGTATTAATGACTTAGCGTAATTAAGCCCTCAAGTATGTGTGAGAGAGCGCGTGTGAGAAAATACAAAGC
CATAGATATTGATTTACTTCACTGACCTGTGTAACTTTATGTCTGGGTTTCGCCATCCAAGATAGATTGTTTTATAGAGAGTGTCACCAA

>50441_50441_1_LYN-EXT1_LYN_chr8_56854550_ENST00000519728_EXT1_chr8_118842588_ENST00000378204_length(amino acids)=484AA_BP=126
MPLAPRPWRLRARRAAASSPRQAGRPRHPRPRASSPSPRVQRSRPAASPYAGPAGPPRRAPHSELKSPWSSAAPKLSPRAGNMGCIKSKG
KDSLSDDGVDLKTQPVRNTERTIYVRDPTSNKQQRPIPSTIRSIHQDKILALRQQTQFLWEAYFSSVEKIVLTTLEIIQDRIFKHISRNS
LIWNKHPGGLFVLPQYSSYLGDFPYYYANLGLKPPSKFTAVIHAVTPLVSQSQPVLKLLVAAAKSQYCAQIIVLWNCDKPLPAKHRWPAT
AVPVVVIEGESKVMSSRFLPYDNIITDAVLSLDEDTVLSTTEVDFAFTVWQSFPERIVGYPARSHFWDNSKERWGYTSKWTNDYSMVLTG
AAIYHKYYHYLYSHYLPASLKNMVDQLANCEDILMNFLVSAVTKLPPIKVTQKKQYKETMMGQTSRASRWADPDHFAQRQSCMNTFASWF

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Fusion Gene PPI Analysis for LYN-EXT1


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-EXT1


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-EXT1


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