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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: 19481

FusionGeneSummary for LARP4_RYR3

check button Fusion gene summary
Fusion gene informationFusion gene name: LARP4_RYR3
Fusion gene ID: 19481
HgeneTgene
Gene symbol

LARP4

RYR3

Gene ID

113251

6263

Gene nameLa ribonucleoprotein domain family member 4ryanodine receptor 3
SynonymsPP13296RYR-3
Cytomap

12q13.12

15q13.3-q14

Type of geneprotein-codingprotein-coding
Descriptionla-related protein 4c-Mpl binding proteinryanodine receptor 3brain ryanodine receptor-calcium release channelbrain-type ryanodine receptortype 3 ryanodine receptor
Modification date2018052720180523
UniProtAcc

Q71RC2

Q15413

Ensembl transtripts involved in fusion geneENST00000293618, ENST00000429001, 
ENST00000398473, ENST00000518444, 
ENST00000347328, ENST00000522085, 
ENST00000518561, 
ENST00000415757, 
ENST00000389232, ENST00000559917, 
Fusion gene scores* DoF score8 X 4 X 6=1923 X 3 X 3=27
# samples 83
** MAII scorelog2(8/192*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: LARP4 [Title/Abstract] AND RYR3 [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
TCGARVBRCATCGA-BH-A5IZ-01ALARP4chr12

50794811

+RYR3chr15

34028436

+
* 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
Frame-shiftENST00000293618ENST00000415757LARP4chr12

50794811

+RYR3chr15

34028436

+
Frame-shiftENST00000293618ENST00000389232LARP4chr12

50794811

+RYR3chr15

34028436

+
5CDS-intronENST00000293618ENST00000559917LARP4chr12

50794811

+RYR3chr15

34028436

+
Frame-shiftENST00000429001ENST00000415757LARP4chr12

50794811

+RYR3chr15

34028436

+
Frame-shiftENST00000429001ENST00000389232LARP4chr12

50794811

+RYR3chr15

34028436

+
5CDS-intronENST00000429001ENST00000559917LARP4chr12

50794811

+RYR3chr15

34028436

+
Frame-shiftENST00000398473ENST00000415757LARP4chr12

50794811

+RYR3chr15

34028436

+
Frame-shiftENST00000398473ENST00000389232LARP4chr12

50794811

+RYR3chr15

34028436

+
5CDS-intronENST00000398473ENST00000559917LARP4chr12

50794811

+RYR3chr15

34028436

+
Frame-shiftENST00000518444ENST00000415757LARP4chr12

50794811

+RYR3chr15

34028436

+
Frame-shiftENST00000518444ENST00000389232LARP4chr12

50794811

+RYR3chr15

34028436

+
5CDS-intronENST00000518444ENST00000559917LARP4chr12

50794811

+RYR3chr15

34028436

+
Frame-shiftENST00000347328ENST00000415757LARP4chr12

50794811

+RYR3chr15

34028436

+
Frame-shiftENST00000347328ENST00000389232LARP4chr12

50794811

+RYR3chr15

34028436

+
5CDS-intronENST00000347328ENST00000559917LARP4chr12

50794811

+RYR3chr15

34028436

+
Frame-shiftENST00000522085ENST00000415757LARP4chr12

50794811

+RYR3chr15

34028436

+
Frame-shiftENST00000522085ENST00000389232LARP4chr12

50794811

+RYR3chr15

34028436

+
5CDS-intronENST00000522085ENST00000559917LARP4chr12

50794811

+RYR3chr15

34028436

+
5UTR-3CDSENST00000518561ENST00000415757LARP4chr12

50794811

+RYR3chr15

34028436

+
5UTR-3CDSENST00000518561ENST00000389232LARP4chr12

50794811

+RYR3chr15

34028436

+
5UTR-intronENST00000518561ENST00000559917LARP4chr12

50794811

+RYR3chr15

34028436

+

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FusionProtFeatures for LARP4_RYR3


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
LARP4

Q71RC2

RYR3

Q15413

RNA binding protein that binds to the poly-A tract ofmRNA molecules (PubMed:21098120). Associates with the 40Sribosomal subunit and with polysomes (PubMed:21098120). Plays arole in the regulation of mRNA translation (PubMed:21098120).Plays a role in the regulation of cell morphology and cytoskeletalorganization (PubMed:21834987, PubMed:27615744).{ECO:0000269|PubMed:21098120, ECO:0000269|PubMed:21834987,ECO:0000269|PubMed:27615744}. Calcium channel that mediates the release of Ca(2+) fromthe sarcoplasmic reticulum into the cytoplasm in muscle andthereby plays a role in triggering muscle contraction. Mayregulate Ca(2+) release by other calcium channels. Calcium channelthat mediates Ca(2+)-induced Ca(2+) release from the endoplasmicreticulum in non-muscle cells. Contributes to cellular calcium ionhomeostasis (By similarity). Plays a role in cellular calciumsignaling. {ECO:0000250, ECO:0000269|PubMed:12354756}.

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 LARP4_RYR3


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 LARP4_RYR3


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
LARP4ELAVL1, SIRT7, CUL3, COPS6, APP, MPG, TARDBP, LIN28A, LIN28B, CRX, BHLHE40, EGFR, GNB2L1, NTRK1, MYO1C, NPM1, RPL10, AKAP1, RNF126, G3BP1RYR3RYR2, FKBP1A, CUL1, CFTR, HNF1A, BMI1, FKBP1B


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 LARP4_RYR3


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 LARP4_RYR3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneLARP4C0032460Polycystic Ovary Syndrome1CTD_human