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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:PLA2G6-SCARF2 (FusionGDB2 ID:65471)

Fusion Gene Summary for PLA2G6-SCARF2

check button Fusion gene summary
Fusion gene informationFusion gene name: PLA2G6-SCARF2
Fusion gene ID: 65471
HgeneTgene
Gene symbol

PLA2G6

SCARF2

Gene ID

8398

91179

Gene namephospholipase A2 group VIscavenger receptor class F member 2
SynonymsCaI-PLA2|GVI|INAD1|IPLA2-VIA|NBIA2|NBIA2A|NBIA2B|PARK14|PLA2|PNPLA9|iPLA2|iPLA2betaNSR1|SREC-II|SREC2|SRECRP-1|VDEGS
Cytomap

22q13.1

22q11.21

Type of geneprotein-codingprotein-coding
Description85/88 kDa calcium-independent phospholipase A285 kDa calcium-independent phospholipase A2GVI PLA2iPLA2-betaintracellular membrane-associated calcium-independent phospholipase A2 betaneurodegeneration with brain iron accumulation 2patatin-like phosphscavenger receptor class F member 2scavenger receptor expressed by endothelial cells 2 protein
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000332509, ENST00000335539, 
ENST00000402064, ENST00000490473, 
ENST00000436218, ENST00000447598, 
ENST00000435484, ENST00000417303, 
ENST00000405555, ENST00000266214, 
Fusion gene scores* DoF score9 X 12 X 6=6482 X 2 X 2=8
# samples 132
** MAII scorelog2(13/648*10)=-2.31748218985617
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: PLA2G6 [Title/Abstract] AND SCARF2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPLA2G6(38538057)-SCARF2(20780307), # 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
HgenePLA2G6

GO:0019731

antibacterial humoral response

18714013


check buttonFusion gene breakpoints across PLA2G6 (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 SCARF2 (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
ChimerDB4HNSCTCGA-CV-7421-01APLA2G6chr22

38538057

-SCARF2chr22

20780307

-
ChimerDB4HNSCTCGA-CV-7421PLA2G6chr22

38538057

-SCARF2chr22

20780307

-


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Fusion Gene ORF analysis for PLA2G6-SCARF2

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-3CDSENST00000332509ENST00000405555PLA2G6chr22

38538057

-SCARF2chr22

20780307

-
intron-3CDSENST00000332509ENST00000266214PLA2G6chr22

38538057

-SCARF2chr22

20780307

-
intron-3CDSENST00000335539ENST00000405555PLA2G6chr22

38538057

-SCARF2chr22

20780307

-
intron-3CDSENST00000335539ENST00000266214PLA2G6chr22

38538057

-SCARF2chr22

20780307

-
intron-3CDSENST00000402064ENST00000405555PLA2G6chr22

38538057

-SCARF2chr22

20780307

-
intron-3CDSENST00000402064ENST00000266214PLA2G6chr22

38538057

-SCARF2chr22

20780307

-
intron-3CDSENST00000490473ENST00000405555PLA2G6chr22

38538057

-SCARF2chr22

20780307

-
intron-3CDSENST00000490473ENST00000266214PLA2G6chr22

38538057

-SCARF2chr22

20780307

-
intron-3CDSENST00000436218ENST00000405555PLA2G6chr22

38538057

-SCARF2chr22

20780307

-
intron-3CDSENST00000436218ENST00000266214PLA2G6chr22

38538057

-SCARF2chr22

20780307

-
intron-3CDSENST00000447598ENST00000405555PLA2G6chr22

38538057

-SCARF2chr22

20780307

-
intron-3CDSENST00000447598ENST00000266214PLA2G6chr22

38538057

-SCARF2chr22

20780307

-
intron-3CDSENST00000435484ENST00000405555PLA2G6chr22

38538057

-SCARF2chr22

20780307

-
intron-3CDSENST00000435484ENST00000266214PLA2G6chr22

38538057

-SCARF2chr22

20780307

-
intron-3CDSENST00000417303ENST00000405555PLA2G6chr22

38538057

-SCARF2chr22

20780307

-
intron-3CDSENST00000417303ENST00000266214PLA2G6chr22

38538057

-SCARF2chr22

20780307

-

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 PLA2G6-SCARF2


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 PLA2G6-SCARF2


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
..
FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

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 PLA2G6-SCARF2


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 PLA2G6-SCARF2


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 PLA2G6-SCARF2


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 PLA2G6-SCARF2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePLA2G6C0270724Infantile Neuroaxonal Dystrophy7CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgenePLA2G6C1857747NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2 (disorder)5CTD_human;GENOMICS_ENGLAND;UNIPROT
HgenePLA2G6C2751842PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE4CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgenePLA2G6C0005586Bipolar Disorder1PSYGENET
HgenePLA2G6C0027960Nevus1CTD_human
HgenePLA2G6C0033975Psychotic Disorders1PSYGENET
HgenePLA2G6C0036341Schizophrenia1PSYGENET
HgenePLA2G6C0349204Nonorganic psychosis1PSYGENET
TgeneSCARF2C1833136Marden Walker like syndrome3CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT