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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:MTSS1L-DGCR8

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: MTSS1L-DGCR8
FusionPDB ID: 55914
FusionGDB2.0 ID: 55914
HgeneTgene
Gene symbol

MTSS1L

DGCR8

Gene ID

92154

54487

Gene nameMTSS I-BAR domain containing 2DGCR8 microprocessor complex subunit
SynonymsABBA|ABBA-1|ABBA1|MTSS1LC22orf12|DGCRK6|Gy1|pasha
Cytomap

16q22.1

22q11.21

Type of geneprotein-codingprotein-coding
Descriptionprotein MTSS 2MTSS1-like proteinMTSS1L, I-BAR domain containingactin-bundling with BAIAP2 homology protein 1metastasis suppressor 1-likemicroprocessor complex subunit DGCR8DiGeorge syndrome critical region 8DiGeorge syndrome critical region gene 8
Modification date2020031320200320
UniProtAcc.

Q8WYQ5

Ensembl transtripts involved in fusion geneENST idsENST00000338779, ENST00000351989, 
ENST00000383024, ENST00000407755, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 7 X 6=2529 X 8 X 6=432
# samples 79
** MAII scorelog2(7/252*10)=-1.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/432*10)=-2.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: MTSS1L [Title/Abstract] AND DGCR8 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MTSS1L(70719625)-DGCR8(20077498), # samples:1
Anticipated loss of major functional domain due to fusion event.MTSS1L-DGCR8 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
MTSS1L-DGCR8 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
MTSS1L-DGCR8 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
MTSS1L-DGCR8 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame 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
HgeneMTSS1L

GO:0036120

cellular response to platelet-derived growth factor stimulus

20875796

HgeneMTSS1L

GO:0090630

activation of GTPase activity

20875796

TgeneDGCR8

GO:0031053

primary miRNA processing

15531877|15574589|24449907|24910438


check buttonFusion gene breakpoints across MTSS1L (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across DGCR8 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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
ChimerDB4OVTCGA-13-1497MTSS1Lchr16

70719625

-DGCR8chr22

20077498

+


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000338779MTSS1Lchr1670719625-ENST00000351989DGCR8chr2220077498+3406344291642537
ENST00000338779MTSS1Lchr1670719625-ENST00000383024DGCR8chr2220077498+3311344291543504
ENST00000338779MTSS1Lchr1670719625-ENST00000407755DGCR8chr2220077498+3308344291543504

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
ENST00000338779ENST00000351989MTSS1Lchr1670719625-DGCR8chr2220077498+0.0023713550.9976286
ENST00000338779ENST00000383024MTSS1Lchr1670719625-DGCR8chr2220077498+0.0017432410.99825674
ENST00000338779ENST00000407755MTSS1Lchr1670719625-DGCR8chr2220077498+0.0017664640.99823356

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>55914_55914_1_MTSS1L-DGCR8_MTSS1L_chr16_70719625_ENST00000338779_DGCR8_chr22_20077498_ENST00000351989_length(amino acids)=537AA_BP=37
MRRELPAPRPPRRPPAPLRHGPRRPPEARDPGARRGRPLSAAWRREARPGLGASARAAWPPPLRCSPRSVRLAAAAARPSQSMETAEKEC
GALGGLFQAIVNDMKKHDPPLSSIPCLHYKKMKDNEEREQSSDLTPSGDVSPVKPLSRSAELEFPLDEPDSMGADPGPPDEKDPLGAEAA
PGALGQVKAKVEVCKDESVDLEEFRSYLEKRFDFEQVTVKKFRTWAERRQFNREMKRKQAESERPILPANQKLITLSVQDAPTKKEFVIN
PNGKSEVCILHEYMQRVLKVRPVYNFFECENPSEPFGASVTIDGVTYGSGTASSKKLAKNKAARATLEILIPDFVKQTSEEKPKDSEELE
YFNHISIEDSRVYELTSKAGLLSPYQILHECLKRNHGMGDTSIKFEVVPGKNQKSEYVMACGKHTVRGWCKNKRVGKQLASQKILQLLHP

--------------------------------------------------------------

>55914_55914_2_MTSS1L-DGCR8_MTSS1L_chr16_70719625_ENST00000338779_DGCR8_chr22_20077498_ENST00000383024_length(amino acids)=504AA_BP=37
MRRELPAPRPPRRPPAPLRHGPRRPPEARDPGARRGRPLSAAWRREARPGLGASARAAWPPPLRCSPRSVRLAAAAARPSQSMETAEKEC
GALGGLFQAIVNDMKKHDPPLSSIPCLHYKKMKDNEEREQSSDLTPSGDVSPVKPLSRSAELEFPLDEPDSMGADPGPPDEKDPLGAEAA
PGALGQVKAKVEVCKDESVDLEEFRSYLEKRFDFEQVTVKKFRTWAERRQFNREMKRKQAESERPILPANQKLITLSVQDAPTKKEFVIN
PNGKSEVCILHEYMQRVLKVRPVYNFFECARATLEILIPDFVKQTSEEKPKDSEELEYFNHISIEDSRVYELTSKAGLLSPYQILHECLK
RNHGMGDTSIKFEVVPGKNQKSEYVMACGKHTVRGWCKNKRVGKQLASQKILQLLHPHVKNWGSLLRMYGRESSKMVKQETSDKSVIELQ

--------------------------------------------------------------

>55914_55914_3_MTSS1L-DGCR8_MTSS1L_chr16_70719625_ENST00000338779_DGCR8_chr22_20077498_ENST00000407755_length(amino acids)=504AA_BP=37
MRRELPAPRPPRRPPAPLRHGPRRPPEARDPGARRGRPLSAAWRREARPGLGASARAAWPPPLRCSPRSVRLAAAAARPSQSMETAEKEC
GALGGLFQAIVNDMKKHDPPLSSIPCLHYKKMKDNEEREQSSDLTPSGDVSPVKPLSRSAELEFPLDEPDSMGADPGPPDEKDPLGAEAA
PGALGQVKAKVEVCKDESVDLEEFRSYLEKRFDFEQVTVKKFRTWAERRQFNREMKRKQAESERPILPANQKLITLSVQDAPTKKEFVIN
PNGKSEVCILHEYMQRVLKVRPVYNFFECARATLEILIPDFVKQTSEEKPKDSEELEYFNHISIEDSRVYELTSKAGLLSPYQILHECLK
RNHGMGDTSIKFEVVPGKNQKSEYVMACGKHTVRGWCKNKRVGKQLASQKILQLLHPHVKNWGSLLRMYGRESSKMVKQETSDKSVIELQ

--------------------------------------------------------------

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Fusion Protein Functional Features


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr16:70719625/chr22:20077498)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.DGCR8

Q8WYQ5

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: Component of the microprocessor complex that acts as a RNA- and heme-binding protein that is involved in the initial step of microRNA (miRNA) biogenesis. Component of the microprocessor complex that is required to process primary miRNA transcripts (pri-miRNAs) to release precursor miRNA (pre-miRNA) in the nucleus. Within the microprocessor complex, DGCR8 function as a molecular anchor necessary for the recognition of pri-miRNA at dsRNA-ssRNA junction and directs DROSHA to cleave 11 bp away form the junction to release hairpin-shaped pre-miRNAs that are subsequently cut by the cytoplasmic DICER to generate mature miRNAs (PubMed:26027739, PubMed:26748718). The heme-bound DGCR8 dimer binds pri-miRNAs as a cooperative trimer (of dimers) and is active in triggering pri-miRNA cleavage, whereas the heme-free DGCR8 monomer binds pri-miRNAs as a dimer and is much less active. Both double-stranded and single-stranded regions of a pri-miRNA are required for its binding (PubMed:15531877, PubMed:15574589, PubMed:15589161, PubMed:16751099, PubMed:16906129, PubMed:16963499, PubMed:17159994). Specifically recognizes and binds N6-methyladenosine (m6A)-containing pri-miRNAs, a modification required for pri-miRNAs processing (PubMed:25799998). Involved in the silencing of embryonic stem cell self-renewal (By similarity). {ECO:0000250|UniProtKB:Q9EQM6, ECO:0000269|PubMed:15531877, ECO:0000269|PubMed:15574589, ECO:0000269|PubMed:15589161, ECO:0000269|PubMed:16751099, ECO:0000269|PubMed:16906129, ECO:0000269|PubMed:16963499, ECO:0000269|PubMed:17159994, ECO:0000269|PubMed:25799998, ECO:0000269|PubMed:26027739, ECO:0000269|PubMed:26748718}.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneDGCR8chr16:70719625chr22:20077498ENST00000351989314511_578341.0774.0DomainDRBM 1
TgeneDGCR8chr16:70719625chr22:20077498ENST00000351989314620_685341.0774.0DomainDRBM 2
TgeneDGCR8chr16:70719625chr22:20077498ENST00000383024313511_578341.0741.0DomainDRBM 1
TgeneDGCR8chr16:70719625chr22:20077498ENST00000383024313620_685341.0741.0DomainDRBM 2
TgeneDGCR8chr16:70719625chr22:20077498ENST00000407755212511_578341.0741.0DomainDRBM 1
TgeneDGCR8chr16:70719625chr22:20077498ENST00000407755212620_685341.0741.0DomainDRBM 2

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneMTSS1Lchr16:70719625chr22:20077498ENST00000338779-115135_15923.0748.0Coiled coilOntology_term=ECO:0000255
HgeneMTSS1Lchr16:70719625chr22:20077498ENST00000338779-115252_38323.0748.0Compositional biasNote=Ser-rich
HgeneMTSS1Lchr16:70719625chr22:20077498ENST00000338779-1151_25223.0748.0DomainIMD
HgeneMTSS1Lchr16:70719625chr22:20077498ENST00000338779-115719_73623.0748.0DomainNote=WH2
TgeneDGCR8chr16:70719625chr22:20077498ENST00000351989314301_334341.0774.0DomainWW
TgeneDGCR8chr16:70719625chr22:20077498ENST00000383024313301_334341.0741.0DomainWW
TgeneDGCR8chr16:70719625chr22:20077498ENST00000407755212301_334341.0741.0DomainWW
TgeneDGCR8chr16:70719625chr22:20077498ENST000003519893141_275341.0774.0RegionNote=Necessary for nuclear localization and retention
TgeneDGCR8chr16:70719625chr22:20077498ENST00000351989314276_751341.0774.0RegionNote=Necessary for heme-binding and pri-miRNA processing
TgeneDGCR8chr16:70719625chr22:20077498ENST000003830243131_275341.0741.0RegionNote=Necessary for nuclear localization and retention
TgeneDGCR8chr16:70719625chr22:20077498ENST00000383024313276_751341.0741.0RegionNote=Necessary for heme-binding and pri-miRNA processing
TgeneDGCR8chr16:70719625chr22:20077498ENST000004077552121_275341.0741.0RegionNote=Necessary for nuclear localization and retention
TgeneDGCR8chr16:70719625chr22:20077498ENST00000407755212276_751341.0741.0RegionNote=Necessary for heme-binding and pri-miRNA processing


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
MTSS1L
DGCR8


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to MTSS1L-DGCR8


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to MTSS1L-DGCR8


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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