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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:TMEM50B-DONSON (FusionGDB2 ID:91508)

Fusion Gene Summary for TMEM50B-DONSON

check button Fusion gene summary
Fusion gene informationFusion gene name: TMEM50B-DONSON
Fusion gene ID: 91508
HgeneTgene
Gene symbol

TMEM50B

DONSON

Gene ID

757

29980

Gene nametransmembrane protein 50BDNA replication fork stabilization factor DONSON
SynonymsC21orf4|HCVP7TP3B17|C21orf60|MIMIS|MISSLA
Cytomap

21q22.11

21q22.11

Type of geneprotein-codingprotein-coding
Descriptiontransmembrane protein 50BHCV p7-trans-regulated protein 3HCV p7-transregulated protein 3protein downstream neighbor of Sondownstream neighbor of SON
Modification date2020031320200313
UniProtAcc.

Q9NYP3

Ensembl transtripts involved in fusion geneENST00000468874, ENST00000542230, 
ENST00000303113, ENST00000453626, 
ENST00000303071, ENST00000432378, 
Fusion gene scores* DoF score10 X 7 X 6=4202 X 3 X 3=18
# samples 113
** MAII scorelog2(11/420*10)=-1.93288580414146
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: TMEM50B [Title/Abstract] AND DONSON [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointTMEM50B(34804967)-DONSON(34951868), # samples:1
TMEM50B(34837649)-DONSON(34945678), # 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

check buttonFusion gene breakpoints across TMEM50B (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 DONSON (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
ChimerDB4BRCATCGA-B6-A0IO-01ATMEM50Bchr21

34804967

-DONSONchr21

34951868

-
ChimerDB4ESCATCGA-L5-A88VTMEM50Bchr21

34837649

-DONSONchr21

34945678

-


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Fusion Gene ORF analysis for TMEM50B-DONSON

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-3CDSENST00000468874ENST00000303113TMEM50Bchr21

34804967

-DONSONchr21

34951868

-
intron-intronENST00000468874ENST00000453626TMEM50Bchr21

34804967

-DONSONchr21

34951868

-
intron-intronENST00000468874ENST00000303071TMEM50Bchr21

34804967

-DONSONchr21

34951868

-
intron-intronENST00000468874ENST00000432378TMEM50Bchr21

34804967

-DONSONchr21

34951868

-
intron-3CDSENST00000542230ENST00000303113TMEM50Bchr21

34804967

-DONSONchr21

34951868

-
intron-intronENST00000542230ENST00000453626TMEM50Bchr21

34804967

-DONSONchr21

34951868

-
intron-intronENST00000542230ENST00000303071TMEM50Bchr21

34804967

-DONSONchr21

34951868

-
intron-intronENST00000542230ENST00000432378TMEM50Bchr21

34804967

-DONSONchr21

34951868

-
intron-intronENST00000468874ENST00000303113TMEM50Bchr21

34837649

-DONSONchr21

34945678

-
intron-intronENST00000468874ENST00000453626TMEM50Bchr21

34837649

-DONSONchr21

34945678

-
intron-intronENST00000468874ENST00000303071TMEM50Bchr21

34837649

-DONSONchr21

34945678

-
intron-intronENST00000468874ENST00000432378TMEM50Bchr21

34837649

-DONSONchr21

34945678

-
5CDS-intronENST00000542230ENST00000303113TMEM50Bchr21

34837649

-DONSONchr21

34945678

-
5CDS-intronENST00000542230ENST00000453626TMEM50Bchr21

34837649

-DONSONchr21

34945678

-
5CDS-intronENST00000542230ENST00000303071TMEM50Bchr21

34837649

-DONSONchr21

34945678

-
5CDS-intronENST00000542230ENST00000432378TMEM50Bchr21

34837649

-DONSONchr21

34945678

-

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 TMEM50B-DONSON


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 TMEM50B-DONSON


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
.DONSON

Q9NYP3

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: Replisome component that maintains genome stability by protecting stalled or damaged replication forks. After the induction of replication stress, required for the stabilization of stalled replication forks, the efficient activation of the intra-S-phase and G/2M cell-cycle checkpoints and the maintenance of genome stability. {ECO:0000269|PubMed:28191891}.

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 TMEM50B-DONSON


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 TMEM50B-DONSON


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 TMEM50B-DONSON


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 TMEM50B-DONSON


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneDONSONC1855079Microcephaly-Micromelia Syndrome2GENOMICS_ENGLAND
TgeneDONSONC4539873MICROCEPHALY, SHORT STATURE, AND LIMB ABNORMALITIES2GENOMICS_ENGLAND;UNIPROT
TgeneDONSONC0009402Colorectal Carcinoma1CTD_human
TgeneDONSONC0009404Colorectal Neoplasms1CTD_human
TgeneDONSONC0013336Dwarfism1CTD_human
TgeneDONSONC0025958Microcephaly1CTD_human
TgeneDONSONC1956147Microlissencephaly1CTD_human
TgeneDONSONC3853041Severe Congenital Microcephaly1CTD_human