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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:ADAMTSL4-MAT2A (FusionGDB2 ID:2259)

Fusion Gene Summary for ADAMTSL4-MAT2A

check button Fusion gene summary
Fusion gene informationFusion gene name: ADAMTSL4-MAT2A
Fusion gene ID: 2259
HgeneTgene
Gene symbol

ADAMTSL4

MAT2A

Gene ID

54507

4144

Gene nameADAMTS like 4methionine adenosyltransferase 2A
SynonymsADAMTSL-4|ECTOL2|TSRC1MATA2|MATII|SAMS2
Cytomap

1q21.2

2p11.2

Type of geneprotein-codingprotein-coding
DescriptionADAMTS-like protein 4thrombospondin repeat-containing protein 1S-adenosylmethionine synthase isoform type-2MAT 2MAT-IIadoMet synthase 2adoMet synthetase 2methionine adenosyltransferase 2methionine adenosyltransferase II, alphatesticular tissue protein Li 121
Modification date2020031320200313
UniProtAcc

Q6UY14

P31153

Ensembl transtripts involved in fusion geneENST00000369041, ENST00000483335, 
ENST00000271643, ENST00000369039, 
ENST00000369038, 
ENST00000306434, 
ENST00000409017, ENST00000490878, 
Fusion gene scores* DoF score3 X 3 X 2=182 X 2 X 1=4
# samples 32
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(2/4*10)=2.32192809488736
Context

PubMed: ADAMTSL4 [Title/Abstract] AND MAT2A [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointADAMTSL4(150533101)-MAT2A(85769334), # samples:1
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
HgeneADAMTSL4

GO:0043065

positive regulation of apoptotic process

16364318

TgeneMAT2A

GO:0006556

S-adenosylmethionine biosynthetic process

10644686|25075345

TgeneMAT2A

GO:0034214

protein hexamerization

25075345

TgeneMAT2A

GO:0051291

protein heterooligomerization

25075345


check buttonFusion gene breakpoints across ADAMTSL4 (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 MAT2A (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
ChiTaRS5.0N/AAA992625ADAMTSL4chr1

150533101

-MAT2Achr2

85769334

-


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Fusion Gene ORF analysis for ADAMTSL4-MAT2A

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-3CDSENST00000369041ENST00000306434ADAMTSL4chr1

150533101

-MAT2Achr2

85769334

-
intron-3CDSENST00000369041ENST00000409017ADAMTSL4chr1

150533101

-MAT2Achr2

85769334

-
intron-intronENST00000369041ENST00000490878ADAMTSL4chr1

150533101

-MAT2Achr2

85769334

-
intron-3CDSENST00000483335ENST00000306434ADAMTSL4chr1

150533101

-MAT2Achr2

85769334

-
intron-3CDSENST00000483335ENST00000409017ADAMTSL4chr1

150533101

-MAT2Achr2

85769334

-
intron-intronENST00000483335ENST00000490878ADAMTSL4chr1

150533101

-MAT2Achr2

85769334

-
3UTR-3CDSENST00000271643ENST00000306434ADAMTSL4chr1

150533101

-MAT2Achr2

85769334

-
3UTR-3CDSENST00000271643ENST00000409017ADAMTSL4chr1

150533101

-MAT2Achr2

85769334

-
3UTR-intronENST00000271643ENST00000490878ADAMTSL4chr1

150533101

-MAT2Achr2

85769334

-
3UTR-3CDSENST00000369039ENST00000306434ADAMTSL4chr1

150533101

-MAT2Achr2

85769334

-
3UTR-3CDSENST00000369039ENST00000409017ADAMTSL4chr1

150533101

-MAT2Achr2

85769334

-
3UTR-intronENST00000369039ENST00000490878ADAMTSL4chr1

150533101

-MAT2Achr2

85769334

-
3UTR-3CDSENST00000369038ENST00000306434ADAMTSL4chr1

150533101

-MAT2Achr2

85769334

-
3UTR-3CDSENST00000369038ENST00000409017ADAMTSL4chr1

150533101

-MAT2Achr2

85769334

-
3UTR-intronENST00000369038ENST00000490878ADAMTSL4chr1

150533101

-MAT2Achr2

85769334

-

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 ADAMTSL4-MAT2A


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 ADAMTSL4-MAT2A


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
ADAMTSL4

Q6UY14

MAT2A

P31153

FUNCTION: Positive regulation of apoptosis. May facilitate FBN1 microfibril biogenesis. {ECO:0000269|PubMed:16364318, ECO:0000269|PubMed:21989719}.FUNCTION: Catalyzes the formation of S-adenosylmethionine from methionine and ATP. The reaction comprises two steps that are both catalyzed by the same enzyme: formation of S-adenosylmethionine (AdoMet) and triphosphate, and subsequent hydrolysis of the triphosphate. {ECO:0000269|PubMed:10644686, ECO:0000269|PubMed:23189196, ECO:0000269|PubMed:25075345}.

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 ADAMTSL4-MAT2A


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 ADAMTSL4-MAT2A


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 ADAMTSL4-MAT2A


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneMAT2AP31153DB00118AdemetionineCofactorSmall moleculeApproved|Investigational|Nutraceutical
TgeneMAT2AP31153DB00118AdemetionineCofactorSmall moleculeApproved|Investigational|Nutraceutical
TgeneMAT2AP31153DB00118AdemetionineCofactorSmall moleculeApproved|Investigational|Nutraceutical

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Related Diseases for ADAMTSL4-MAT2A


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneADAMTSL4C1644196Ectopia Lentis with Ectopia of Pupil1CTD_human;GENOMICS_ENGLAND
HgeneADAMTSL4C3541474ECTOPIA LENTIS 2, ISOLATED, AUTOSOMAL RECESSIVE1CTD_human;GENOMICS_ENGLAND
TgeneMAT2AC4707243Familial thoracic aortic aneurysm and aortic dissection1CLINGEN;GENOMICS_ENGLAND;ORPHANET