FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:MDGA1-PTGDS (FusionGDB2 ID:52034)

Fusion Gene Summary for MDGA1-PTGDS

check button Fusion gene summary
Fusion gene informationFusion gene name: MDGA1-PTGDS
Fusion gene ID: 52034
HgeneTgene
Gene symbol

MDGA1

PTGDS

Gene ID

266727

5730

Gene nameMAM domain containing glycosylphosphatidylinositol anchor 1prostaglandin D2 synthase
SynonymsGPIM|MAMDC3L-PGDS|LPGDS|PDS|PGD2|PGDS|PGDS2
Cytomap

6p21.2

9q34.3

Type of geneprotein-codingprotein-coding
DescriptionMAM domain-containing glycosylphosphatidylinositol anchor protein 1GPI and MAM proteinMAM domain-containing protein 3glycosylphosphatidylinositol-MAMprostaglandin-H2 D-isomerasePGD2 synthasebeta-trace proteincerebrin-28glutathione-independent PGD synthaseglutathione-independent PGD synthetaselipocalin-type prostaglandin D synthaseprostaglandin D synthaseprostaglandin D2 synthase 21kDa (brain)
Modification date2020031320200313
UniProtAcc

Q8NFP4

.
Ensembl transtripts involved in fusion geneENST00000297153, ENST00000434837, 
ENST00000505425, ENST00000510077, 
ENST00000224167, ENST00000371625, 
ENST00000460340, 
Fusion gene scores* DoF score4 X 5 X 4=804 X 4 X 2=32
# samples 54
** MAII scorelog2(5/80*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/32*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: MDGA1 [Title/Abstract] AND PTGDS [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointMDGA1(37623476)-PTGDS(139874697), # samples:1
Anticipated loss of major functional domain due to fusion event.MDGA1-PTGDS seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
MDGA1-PTGDS seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
MDGA1-PTGDS seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
* 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
HgeneMDGA1

GO:0099179

regulation of synaptic membrane adhesion

28641112

HgeneMDGA1

GO:1905606

regulation of presynapse assembly

28641112

TgenePTGDS

GO:0001516

prostaglandin biosynthetic process

20667974


check buttonFusion gene breakpoints across MDGA1 (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 PTGDS (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
ChimerDB4STADTCGA-BR-8080-01AMDGA1chr6

37623476

-PTGDSchr9

139874697

+


Top

Fusion Gene ORF analysis for MDGA1-PTGDS

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-shiftENST00000297153ENST00000224167MDGA1chr6

37623476

-PTGDSchr9

139874697

+
Frame-shiftENST00000297153ENST00000371625MDGA1chr6

37623476

-PTGDSchr9

139874697

+
5CDS-intronENST00000297153ENST00000460340MDGA1chr6

37623476

-PTGDSchr9

139874697

+
Frame-shiftENST00000434837ENST00000224167MDGA1chr6

37623476

-PTGDSchr9

139874697

+
Frame-shiftENST00000434837ENST00000371625MDGA1chr6

37623476

-PTGDSchr9

139874697

+
5CDS-intronENST00000434837ENST00000460340MDGA1chr6

37623476

-PTGDSchr9

139874697

+
Frame-shiftENST00000505425ENST00000224167MDGA1chr6

37623476

-PTGDSchr9

139874697

+
Frame-shiftENST00000505425ENST00000371625MDGA1chr6

37623476

-PTGDSchr9

139874697

+
5CDS-intronENST00000505425ENST00000460340MDGA1chr6

37623476

-PTGDSchr9

139874697

+
intron-3CDSENST00000510077ENST00000224167MDGA1chr6

37623476

-PTGDSchr9

139874697

+
intron-3CDSENST00000510077ENST00000371625MDGA1chr6

37623476

-PTGDSchr9

139874697

+
intron-intronENST00000510077ENST00000460340MDGA1chr6

37623476

-PTGDSchr9

139874697

+

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

Top

Fusion Genomic Features for MDGA1-PTGDS


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.

Top

Fusion Protein Features for MDGA1-PTGDS


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
MDGA1

Q8NFP4

.
FUNCTION: Required for radial migration of cortical neurons in the superficial layer of the neocortex (By similarity). Plays a role in the formation or maintenance of inhibitory synapses. May function by inhibiting the activity of NLGN2. {ECO:0000250, ECO:0000269|PubMed:23248271}.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


Top

Fusion Gene Sequence for MDGA1-PTGDS


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.

Top

Fusion Gene PPI Analysis for MDGA1-PTGDS


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


Top

Related Drugs for MDGA1-PTGDS


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

Top

Related Diseases for MDGA1-PTGDS


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneMDGA1C0036341Schizophrenia2PSYGENET
HgeneMDGA1C0005586Bipolar Disorder1PSYGENET
TgenePTGDSC0005586Bipolar Disorder2PSYGENET