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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:MYL9-AAR2 (FusionGDB2 ID:56499)

Fusion Gene Summary for MYL9-AAR2

check button Fusion gene summary
Fusion gene informationFusion gene name: MYL9-AAR2
Fusion gene ID: 56499
HgeneTgene
Gene symbol

MYL9

AAR2

Gene ID

10398

25980

Gene namemyosin light chain 9AAR2 splicing factor
SynonymsLC20|MLC-2C|MLC2|MRLC1|MYRL2C20orf4|CGI-23
Cytomap

20q11.23

20q11.23

Type of geneprotein-codingprotein-coding
Descriptionmyosin regulatory light polypeptide 920 kDa myosin light chainepididymis secretory sperm binding proteinmyosin RLCmyosin regulatory light chain 1myosin regulatory light chain 2, smooth muscle isoformmyosin regulatory light chain 9myosin regulatory protein AAR2 homologAAR2 splicing factor homolog
Modification date2020031320200313
UniProtAcc

P24844

Q9Y312

Ensembl transtripts involved in fusion geneENST00000279022, ENST00000346786, 
ENST00000320849, ENST00000373932, 
ENST00000397286, 
Fusion gene scores* DoF score4 X 3 X 4=482 X 2 X 2=8
# samples 42
** MAII scorelog2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: MYL9 [Title/Abstract] AND AAR2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointMYL9(35173471)-AAR2(34858455), # samples:2
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

check buttonFusion gene breakpoints across MYL9 (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 AAR2 (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
ChimerDB4OVTCGA-61-2002-01AMYL9chr20

35173471

+AAR2chr20

34858455

+


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Fusion Gene ORF analysis for MYL9-AAR2

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
5CDS-intronENST00000279022ENST00000320849MYL9chr20

35173471

+AAR2chr20

34858455

+
5CDS-intronENST00000279022ENST00000373932MYL9chr20

35173471

+AAR2chr20

34858455

+
5CDS-intronENST00000346786ENST00000320849MYL9chr20

35173471

+AAR2chr20

34858455

+
5CDS-intronENST00000346786ENST00000373932MYL9chr20

35173471

+AAR2chr20

34858455

+
In-frameENST00000279022ENST00000397286MYL9chr20

35173471

+AAR2chr20

34858455

+
In-frameENST00000346786ENST00000397286MYL9chr20

35173471

+AAR2chr20

34858455

+

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)
ENST00000279022MYL9chr2035173471+ENST00000397286AAR2chr2034858455+6742883942131
ENST00000346786MYL9chr2035173471+ENST00000397286AAR2chr2034858455+6612753811127

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
ENST00000279022ENST00000397286MYL9chr2035173471+AAR2chr2034858455+0.21338040.78661966
ENST00000346786ENST00000397286MYL9chr2035173471+AAR2chr2034858455+0.146354290.8536457

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Fusion Genomic Features for MYL9-AAR2


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.
genomic feature of top 1%

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Fusion Protein Features for MYL9-AAR2


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/chr20:35173471/chr20:34858455)
- 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
MYL9

P24844

AAR2

Q9Y312

FUNCTION: Myosin regulatory subunit that plays an important role in regulation of both smooth muscle and nonmuscle cell contractile activity via its phosphorylation. Implicated in cytokinesis, receptor capping, and cell locomotion (PubMed:11942626, PubMed:2526655). In myoblasts, may regulate PIEZO1-dependent cortical actomyosin assembly involved in myotube formation (By similarity). {ECO:0000250|UniProtKB:Q9CQ19, ECO:0000269|PubMed:11942626, ECO:0000269|PubMed:2526655}.FUNCTION: Component of the U5 snRNP complex that is required for spliceosome assembly and for pre-mRNA splicing. {ECO:0000250|UniProtKB:P32357}.

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
HgeneMYL9chr20:35173471chr20:34858455ENST00000279022+2442_5361173.0Calcium binding.
HgeneMYL9chr20:35173471chr20:34858455ENST00000346786+2342_5361119.0Calcium binding.
HgeneMYL9chr20:35173471chr20:34858455ENST00000279022+2429_6461173.0DomainEF-hand 1
HgeneMYL9chr20:35173471chr20:34858455ENST00000346786+2329_6461119.0DomainEF-hand 1

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneMYL9chr20:35173471chr20:34858455ENST00000279022+24134_16961173.0DomainEF-hand 3
HgeneMYL9chr20:35173471chr20:34858455ENST00000279022+2498_13361173.0DomainEF-hand 2
HgeneMYL9chr20:35173471chr20:34858455ENST00000346786+23134_16961119.0DomainEF-hand 3
HgeneMYL9chr20:35173471chr20:34858455ENST00000346786+2398_13361119.0DomainEF-hand 2


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Fusion Gene Sequence for MYL9-AAR2


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.
>56499_56499_1_MYL9-AAR2_MYL9_chr20_35173471_ENST00000279022_AAR2_chr20_34858455_ENST00000397286_length(transcript)=674nt_BP=288nt
GCCCCCGCCTGGAGTCCAGACCCGACGGCCGGCCCAGTTCCACGCACCCAGCGAGCCCAAGCGCCTTCTCCGCACCAGGGAAGCCCCACC
CACCAGAAGCCAAGATGTCCAGCAAGCGGGCCAAAGCCAAGACCACCAAGAAGCGGCCACAGCGGGCCACATCCAATGTCTTCGCAATGT
TTGACCAGTCCCAGATCCAGGAGTTTAAGGAGGCTTTCAACATGATTGACCAGAACCGTGATGGCTTCATTGACAAGGAGGACCTGCACG
ACATGCTGGCCTCGCTGGAGACAGAGTCTCGCTGTGTCACCCAGACTGAAGTGCAGTGACTTAATCATAGCTCGCTGCAGCCTTGAACTC
CTGGGCTCATACGATCCACCCACCTCAGCCTCCAGAGTAGCTGGGACTACAGGAAGATATCATCACACCCGGCTAATTAACAACAACAAA
AAAAATTGTAGGGATAAAGTCTTTCTATGTTGCCCAGGCTGGTCTTGAACTCCTAGCCTCAAGCAATCCTCCCACTTTGGCCTCTCAAAA
TGTTGGGATTACAGGCGTGAGTCGCCACACCCGGCCCACGGCATCACTTTTATCTGCCACAGCATATTTCATTCTGTGTTTATACCTTGG

>56499_56499_1_MYL9-AAR2_MYL9_chr20_35173471_ENST00000279022_AAR2_chr20_34858455_ENST00000397286_length(amino acids)=131AA_BP=1
MEAEVGGSYEPRSSRLQRAMIKSLHFSLGDTARLCLQRGQHVVQVLLVNEAITVLVNHVESLLKLLDLGLVKHCEDIGCGPLWPLLGGLG

--------------------------------------------------------------
>56499_56499_2_MYL9-AAR2_MYL9_chr20_35173471_ENST00000346786_AAR2_chr20_34858455_ENST00000397286_length(transcript)=661nt_BP=275nt
GTCCAGACCCGACGGCCGGCCCAGTTCCACGCACCCAGCGAGCCCAAGCGCCTTCTCCGCACCAGGGAAGCCCCACCCACCAGAAGCCAA
GATGTCCAGCAAGCGGGCCAAAGCCAAGACCACCAAGAAGCGGCCACAGCGGGCCACATCCAATGTCTTCGCAATGTTTGACCAGTCCCA
GATCCAGGAGTTTAAGGAGGCTTTCAACATGATTGACCAGAACCGTGATGGCTTCATTGACAAGGAGGACCTGCACGACATGCTGGCCTC
GCTGGAGACAGAGTCTCGCTGTGTCACCCAGACTGAAGTGCAGTGACTTAATCATAGCTCGCTGCAGCCTTGAACTCCTGGGCTCATACG
ATCCACCCACCTCAGCCTCCAGAGTAGCTGGGACTACAGGAAGATATCATCACACCCGGCTAATTAACAACAACAAAAAAAATTGTAGGG
ATAAAGTCTTTCTATGTTGCCCAGGCTGGTCTTGAACTCCTAGCCTCAAGCAATCCTCCCACTTTGGCCTCTCAAAATGTTGGGATTACA
GGCGTGAGTCGCCACACCCGGCCCACGGCATCACTTTTATCTGCCACAGCATATTTCATTCTGTGTTTATACCTTGGTATAACCACTCTC

>56499_56499_2_MYL9-AAR2_MYL9_chr20_35173471_ENST00000346786_AAR2_chr20_34858455_ENST00000397286_length(amino acids)=127AA_BP=1
MEAEVGGSYEPRSSRLQRAMIKSLHFSLGDTARLCLQRGQHVVQVLLVNEAITVLVNHVESLLKLLDLGLVKHCEDIGCGPLWPLLGGLG

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

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Fusion Gene PPI Analysis for MYL9-AAR2


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 MYL9-AAR2


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 MYL9-AAR2


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