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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 20016

FusionGeneSummary for LPIN2_MYOM1

check button Fusion gene summary
Fusion gene informationFusion gene name: LPIN2_MYOM1
Fusion gene ID: 20016
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 date2018052320180523
UniProtAcc

Q92539

P52179

Ensembl transtripts involved in fusion geneENST00000261596, ENST00000581568, 
ENST00000400569, ENST00000356443, 
ENST00000261606, ENST00000582016, 
Fusion gene scores* DoF score7 X 4 X 7=1965 X 5 X 5=125
# samples 107
** MAII scorelog2(10/196*10)=-0.970853654340483
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/125*10)=-0.836501267717121
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]

Functional or gene categories assigned by FusionGDB annotation
* 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 button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
TCGARVLIHCTCGA-PD-A5DF-01ALPIN2chr18

2982666

-MYOM1chr18

3102628

-
TCGARVLUADTCGA-97-A4M3-01ALPIN2chr18

3013085

-MYOM1chr18

3102628

-
TCGARVUCSTCGA-N8-A4PP-01ALPIN2chr18

3013085

-MYOM1chr18

3079340

-
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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
intron-3CDSENST00000261596ENST00000400569LPIN2chr18

2982666

-MYOM1chr18

3102628

-
intron-3CDSENST00000261596ENST00000356443LPIN2chr18

2982666

-MYOM1chr18

3102628

-
intron-3CDSENST00000261596ENST00000261606LPIN2chr18

2982666

-MYOM1chr18

3102628

-
intron-intronENST00000261596ENST00000582016LPIN2chr18

2982666

-MYOM1chr18

3102628

-
5UTR-3CDSENST00000581568ENST00000400569LPIN2chr18

2982666

-MYOM1chr18

3102628

-
5UTR-3CDSENST00000581568ENST00000356443LPIN2chr18

2982666

-MYOM1chr18

3102628

-
5UTR-3CDSENST00000581568ENST00000261606LPIN2chr18

2982666

-MYOM1chr18

3102628

-
5UTR-intronENST00000581568ENST00000582016LPIN2chr18

2982666

-MYOM1chr18

3102628

-
intron-3CDSENST00000261596ENST00000400569LPIN2chr18

3013085

-MYOM1chr18

3102628

-
intron-3CDSENST00000261596ENST00000356443LPIN2chr18

3013085

-MYOM1chr18

3102628

-
intron-3CDSENST00000261596ENST00000261606LPIN2chr18

3013085

-MYOM1chr18

3102628

-
intron-intronENST00000261596ENST00000582016LPIN2chr18

3013085

-MYOM1chr18

3102628

-
intron-3CDSENST00000581568ENST00000400569LPIN2chr18

3013085

-MYOM1chr18

3102628

-
intron-3CDSENST00000581568ENST00000356443LPIN2chr18

3013085

-MYOM1chr18

3102628

-
intron-3CDSENST00000581568ENST00000261606LPIN2chr18

3013085

-MYOM1chr18

3102628

-
intron-intronENST00000581568ENST00000582016LPIN2chr18

3013085

-MYOM1chr18

3102628

-
intron-3CDSENST00000261596ENST00000400569LPIN2chr18

3013085

-MYOM1chr18

3079340

-
intron-3CDSENST00000261596ENST00000356443LPIN2chr18

3013085

-MYOM1chr18

3079340

-
intron-3CDSENST00000261596ENST00000261606LPIN2chr18

3013085

-MYOM1chr18

3079340

-
intron-intronENST00000261596ENST00000582016LPIN2chr18

3013085

-MYOM1chr18

3079340

-
intron-3CDSENST00000581568ENST00000400569LPIN2chr18

3013085

-MYOM1chr18

3079340

-
intron-3CDSENST00000581568ENST00000356443LPIN2chr18

3013085

-MYOM1chr18

3079340

-
intron-3CDSENST00000581568ENST00000261606LPIN2chr18

3013085

-MYOM1chr18

3079340

-
intron-intronENST00000581568ENST00000582016LPIN2chr18

3013085

-MYOM1chr18

3079340

-

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FusionProtFeatures for LPIN2_MYOM1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
LPIN2

Q92539

MYOM1

P52179

Plays important roles in controlling the metabolism offatty acids at different levels. Acts as a magnesium-dependentphosphatidate phosphatase enzyme which catalyzes the conversion ofphosphatidic acid to diacylglycerol during triglyceride,phosphatidylcholine and phosphatidylethanolamine biosynthesis inthe reticulum endoplasmic membrane. Acts also as a nucleartranscriptional coactivator for PPARGC1A to modulate lipidmetabolism (By similarity). {ECO:0000250}. Major component of the vertebrate myofibrillar M band.Binds myosin, titin, and light meromyosin. This binding is dosedependent.

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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FusionGeneSequence for LPIN2_MYOM1


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI 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
LPIN2PPP1CA, FBXW11, LPIN3MYOM1CLK1


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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RelatedDrugs for LPIN2_MYOM1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for LPIN2_MYOM1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneLPIN2C1864997Majeed syndrome1CTD_human;ORPHANET;UNIPROT