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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:LPIN2-MYOM1 (FusionGDB2 ID:49539)

Fusion Gene Summary for LPIN2-MYOM1

check button Fusion gene summary
Fusion gene informationFusion gene name: LPIN2-MYOM1
Fusion gene ID: 49539
HgeneTgene
Gene symbol

LPIN2

MYOM1

Gene ID

9663

8736

Gene namelipin 2myomesin 1
Synonyms-SKELEMIN
Cytomap

18p11.31

18p11.31

Type of geneprotein-codingprotein-coding
Descriptionphosphatidate phosphatase LPIN2myomesin-1190 kDa connectin-associated protein190 kDa titin-associated proteinEH-myomesinmyomesin (M-protein) 1 (190kD)myomesin 1 (skelemin) 185kDamyomesin 1 variant 1myomesin 1, 185kDamyomesin family member 1
Modification date2020032820200313
UniProtAcc

Q92539

P52179

Ensembl transtripts involved in fusion geneENST00000581568, ENST00000261596, 
ENST00000261606, ENST00000356443, 
ENST00000400569, ENST00000582016, 
Fusion gene scores* DoF score9 X 5 X 8=36010 X 11 X 8=880
# samples 1213
** MAII scorelog2(12/360*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(13/880*10)=-2.75899190049621
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: LPIN2 [Title/Abstract] AND MYOM1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointLPIN2(3013085)-MYOM1(3102628), # samples:3
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 LPIN2 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across MYOM1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

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
ChimerDB4LIHCTCGA-PD-A5DF-01ALPIN2chr18

2982666

-MYOM1chr18

3102628

-
ChimerDB4LIHCTCGA-PD-A5DF-01ALPIN2chr18

3013085

-MYOM1chr18

3102628

-
ChimerDB4LUADTCGA-97-A4M3-01ALPIN2chr18

3013085

-MYOM1chr18

3102628

-
ChimerDB4STADTCGA-VQ-A8PE-01ALPIN2chr18

3013085

-MYOM1chr18

3193956

-
ChimerDB4UCECTCGA-AX-A3FX-01ALPIN2chr18

3013085

-MYOM1chr18

3102628

-
ChimerDB4UCSTCGA-N8-A4PP-01ALPIN2chr18

3013085

-MYOM1chr18

3079340

-
ChimerDB4UCSTCGA-N8-A4PPLPIN2chr18

3013085

-MYOM1chr18

3079340

-


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Fusion Gene ORF analysis for LPIN2-MYOM1

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
5UTR-3CDSENST00000581568ENST00000261606LPIN2chr18

2982666

-MYOM1chr18

3102628

-
5UTR-3CDSENST00000581568ENST00000356443LPIN2chr18

2982666

-MYOM1chr18

3102628

-
5UTR-3CDSENST00000581568ENST00000400569LPIN2chr18

2982666

-MYOM1chr18

3102628

-
5UTR-intronENST00000581568ENST00000582016LPIN2chr18

2982666

-MYOM1chr18

3102628

-
intron-3CDSENST00000261596ENST00000261606LPIN2chr18

2982666

-MYOM1chr18

3102628

-
intron-3CDSENST00000261596ENST00000261606LPIN2chr18

3013085

-MYOM1chr18

3102628

-
intron-3CDSENST00000261596ENST00000261606LPIN2chr18

3013085

-MYOM1chr18

3193956

-
intron-3CDSENST00000261596ENST00000261606LPIN2chr18

3013085

-MYOM1chr18

3079340

-
intron-3CDSENST00000261596ENST00000356443LPIN2chr18

2982666

-MYOM1chr18

3102628

-
intron-3CDSENST00000261596ENST00000356443LPIN2chr18

3013085

-MYOM1chr18

3102628

-
intron-3CDSENST00000261596ENST00000356443LPIN2chr18

3013085

-MYOM1chr18

3193956

-
intron-3CDSENST00000261596ENST00000356443LPIN2chr18

3013085

-MYOM1chr18

3079340

-
intron-3CDSENST00000261596ENST00000400569LPIN2chr18

2982666

-MYOM1chr18

3102628

-
intron-3CDSENST00000261596ENST00000400569LPIN2chr18

3013085

-MYOM1chr18

3102628

-
intron-3CDSENST00000261596ENST00000400569LPIN2chr18

3013085

-MYOM1chr18

3193956

-
intron-3CDSENST00000261596ENST00000400569LPIN2chr18

3013085

-MYOM1chr18

3079340

-
intron-3CDSENST00000581568ENST00000261606LPIN2chr18

3013085

-MYOM1chr18

3102628

-
intron-3CDSENST00000581568ENST00000261606LPIN2chr18

3013085

-MYOM1chr18

3193956

-
intron-3CDSENST00000581568ENST00000261606LPIN2chr18

3013085

-MYOM1chr18

3079340

-
intron-3CDSENST00000581568ENST00000356443LPIN2chr18

3013085

-MYOM1chr18

3102628

-
intron-3CDSENST00000581568ENST00000356443LPIN2chr18

3013085

-MYOM1chr18

3193956

-
intron-3CDSENST00000581568ENST00000356443LPIN2chr18

3013085

-MYOM1chr18

3079340

-
intron-3CDSENST00000581568ENST00000400569LPIN2chr18

3013085

-MYOM1chr18

3102628

-
intron-3CDSENST00000581568ENST00000400569LPIN2chr18

3013085

-MYOM1chr18

3193956

-
intron-3CDSENST00000581568ENST00000400569LPIN2chr18

3013085

-MYOM1chr18

3079340

-
intron-intronENST00000261596ENST00000582016LPIN2chr18

2982666

-MYOM1chr18

3102628

-
intron-intronENST00000261596ENST00000582016LPIN2chr18

3013085

-MYOM1chr18

3102628

-
intron-intronENST00000261596ENST00000582016LPIN2chr18

3013085

-MYOM1chr18

3193956

-
intron-intronENST00000261596ENST00000582016LPIN2chr18

3013085

-MYOM1chr18

3079340

-
intron-intronENST00000581568ENST00000582016LPIN2chr18

3013085

-MYOM1chr18

3102628

-
intron-intronENST00000581568ENST00000582016LPIN2chr18

3013085

-MYOM1chr18

3193956

-
intron-intronENST00000581568ENST00000582016LPIN2chr18

3013085

-MYOM1chr18

3079340

-

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)

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

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Fusion Genomic Features for LPIN2-MYOM1


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.

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 LPIN2-MYOM1


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/:3013085/:3102628)
- 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
LPIN2

Q92539

MYOM1

P52179

FUNCTION: Acts as a magnesium-dependent phosphatidate phosphatase enzyme which catalyzes the conversion of phosphatidic acid to diacylglycerol during triglyceride, phosphatidylcholine and phosphatidylethanolamine biosynthesis in the reticulum endoplasmic membrane. Plays important roles in controlling the metabolism of fatty acids at different levels. Acts also as a nuclear transcriptional coactivator for PPARGC1A to modulate lipid metabolism. {ECO:0000250|UniProtKB:Q99PI5}.FUNCTION: Major component of the vertebrate myofibrillar M band. Binds myosin, titin, and light meromyosin. This binding is dose dependent.

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

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for LPIN2-MYOM1


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.

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Fusion Gene PPI Analysis for LPIN2-MYOM1


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 LPIN2-MYOM1


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 LPIN2-MYOM1


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