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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:MYSM1-TM2D1 (FusionGDB2 ID:56523)

Fusion Gene Summary for MYSM1-TM2D1

check button Fusion gene summary
Fusion gene informationFusion gene name: MYSM1-TM2D1
Fusion gene ID: 56523
HgeneTgene
Gene symbol

MYSM1

TM2D1

Gene ID

114803

83941

Gene nameMyb like, SWIRM and MPN domains 1TM2 domain containing 1
Synonyms2A-DUB|2ADUB|BMFS4BBP
Cytomap

1p32.1

1p31.3

Type of geneprotein-codingprotein-coding
Descriptionhistone H2A deubiquitinase MYSM1myb-like, SWIRM and MPN domain-containing protein 1TM2 domain-containing protein 1Beta-amyloid peptide binding proteinamyloid-beta-binding proteinbeta-amyloid-binding proteinhBBP
Modification date2020032020200313
UniProtAcc

Q5VVJ2

.
Ensembl transtripts involved in fusion geneENST00000472487, ENST00000493821, 
ENST00000606498, ENST00000294613, 
ENST00000371180, ENST00000472989, 
ENST00000371177, 
Fusion gene scores* DoF score9 X 11 X 6=5946 X 6 X 3=108
# samples 116
** MAII scorelog2(11/594*10)=-2.43295940727611
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/108*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: MYSM1 [Title/Abstract] AND TM2D1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointMYSM1(59158533)-TM2D1(62189456), # samples:1
Anticipated loss of major functional domain due to fusion event.MYSM1-TM2D1 seems lost the major protein functional domain in Hgene partner, which is a transcription factor due to the frame-shifted ORF.
MYSM1-TM2D1 seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor 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

check buttonFusion gene breakpoints across MYSM1 (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 TM2D1 (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-8080-01AMYSM1chr1

59158533

-TM2D1chr1

62189456

-


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Fusion Gene ORF analysis for MYSM1-TM2D1

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-shiftENST00000472487ENST00000606498MYSM1chr1

59158533

-TM2D1chr1

62189456

-
Frame-shiftENST00000472487ENST00000294613MYSM1chr1

59158533

-TM2D1chr1

62189456

-
Frame-shiftENST00000472487ENST00000371180MYSM1chr1

59158533

-TM2D1chr1

62189456

-
5CDS-intronENST00000472487ENST00000472989MYSM1chr1

59158533

-TM2D1chr1

62189456

-
5CDS-intronENST00000472487ENST00000371177MYSM1chr1

59158533

-TM2D1chr1

62189456

-
intron-3CDSENST00000493821ENST00000606498MYSM1chr1

59158533

-TM2D1chr1

62189456

-
intron-3CDSENST00000493821ENST00000294613MYSM1chr1

59158533

-TM2D1chr1

62189456

-
intron-3CDSENST00000493821ENST00000371180MYSM1chr1

59158533

-TM2D1chr1

62189456

-
intron-intronENST00000493821ENST00000472989MYSM1chr1

59158533

-TM2D1chr1

62189456

-
intron-intronENST00000493821ENST00000371177MYSM1chr1

59158533

-TM2D1chr1

62189456

-

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 MYSM1-TM2D1


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 MYSM1-TM2D1


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
MYSM1

Q5VVJ2

.
FUNCTION: Metalloprotease with deubiquitinase activity that plays important regulator roles in hematopoietic stem cell function, blood cell production and immune response (PubMed:24062447, PubMed:26220525, PubMed:28115216). Participates in the normal programming of B-cell responses to antigen after the maturation process (By similarity). Within the cytoplasm, plays critical roles in the repression of innate immunity and autoimmunity (PubMed:33086059). Removes 'Lys-63'-linked polyubiquitins from TRAF3 and TRAF6 complexes (By similarity). Attenuates NOD2-mediated inflammation and tissue injury by promoting 'Lys-63'-linked deubiquitination of RIPK2 component (By similarity). Suppresses the CGAS-STING1 signaling pathway by cleaving STING1 'Lys-63'-linked ubiquitin chains (PubMed:33086059). In the nucleus, acts as a hematopoietic transcription regulator derepressing a range of genes essential for normal stem cell differentiation including EBF1 and PAX5 in B-cells, ID2 in NK-cell progenitor or FLT3 in dendritic cell precursors (PubMed:24062447). Deubiquitinates monoubiquitinated histone H2A, a specific tag for epigenetic transcriptional repression, leading to dissociation of histone H1 from the nucleosome (PubMed:17707232). {ECO:0000250|UniProtKB:Q69Z66, ECO:0000269|PubMed:17707232, ECO:0000269|PubMed:22169041, ECO:0000269|PubMed:24062447, ECO:0000269|PubMed:26220525, ECO:0000269|PubMed:28115216, ECO:0000269|PubMed:33086059}.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 MYSM1-TM2D1


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 MYSM1-TM2D1


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 MYSM1-TM2D1


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 MYSM1-TM2D1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneMYSM1C4748257BONE MARROW FAILURE SYNDROME 43GENOMICS_ENGLAND;UNIPROT
HgeneMYSM1C0021051Immunologic Deficiency Syndromes1GENOMICS_ENGLAND
HgeneMYSM1C0030312Pancytopenia1GENOMICS_ENGLAND
HgeneMYSM1C1855710Bone marrow hypocellularity1GENOMICS_ENGLAND
HgeneMYSM1C1858085Malar flattening1GENOMICS_ENGLAND
HgeneMYSM1C4022738Neurodevelopmental delay1GENOMICS_ENGLAND