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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:SHC3-MYH10 (FusionGDB2 ID:81079)

Fusion Gene Summary for SHC3-MYH10

check button Fusion gene summary
Fusion gene informationFusion gene name: SHC3-MYH10
Fusion gene ID: 81079
HgeneTgene
Gene symbol

SHC3

MYH10

Gene ID

53358

4628

Gene nameSHC adaptor protein 3myosin heavy chain 10
SynonymsN-Shc|NSHC|RAI|SHCCNMMHC-IIB|NMMHCB
Cytomap

9q22.1

17p13.1

Type of geneprotein-codingprotein-coding
DescriptionSHC-transforming protein 3SH2 domain protein C3SHC (Src homology 2 domain containing) transforming protein 3SHC-transforming protein CShc3 p51neuronal Shcprotein Raisrc homology 2 domain-containing transforming protein C3myosin-10cellular myosin heavy chain, type Bmyosin heavy chain, nonmuscle type Bmyosin, heavy chain 10, non-musclemyosin, heavy polypeptide 10, non-musclenonmuscle myosin II heavy chain-Bnonmuscle myosin heavy chain IIB
Modification date2020031320200313
UniProtAcc.

P35580

Ensembl transtripts involved in fusion geneENST00000375835, ENST00000375830, 
ENST00000375831, 
ENST00000360416, 
ENST00000379980, ENST00000396239, 
ENST00000269243, 
Fusion gene scores* DoF score4 X 4 X 3=4812 X 12 X 7=1008
# samples 414
** MAII scorelog2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(14/1008*10)=-2.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SHC3 [Title/Abstract] AND MYH10 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSHC3(91727470)-MYH10(8452105), # samples:1
Anticipated loss of major functional domain due to fusion event.SHC3-MYH10 seems lost the major protein functional domain in Hgene partner, which is a essential gene 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
TgeneMYH10

GO:0000281

mitotic cytokinesis

15774463

TgeneMYH10

GO:0030048

actin filament-based movement

15845534


check buttonFusion gene breakpoints across SHC3 (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 MYH10 (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
ChimerDB4ESCATCGA-LN-A7HVSHC3chr9

91727470

-MYH10chr17

8452105

-


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Fusion Gene ORF analysis for SHC3-MYH10

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-shiftENST00000375835ENST00000360416SHC3chr9

91727470

-MYH10chr17

8452105

-
Frame-shiftENST00000375835ENST00000379980SHC3chr9

91727470

-MYH10chr17

8452105

-
Frame-shiftENST00000375835ENST00000396239SHC3chr9

91727470

-MYH10chr17

8452105

-
Frame-shiftENST00000375835ENST00000269243SHC3chr9

91727470

-MYH10chr17

8452105

-
5UTR-3CDSENST00000375830ENST00000360416SHC3chr9

91727470

-MYH10chr17

8452105

-
5UTR-3CDSENST00000375830ENST00000379980SHC3chr9

91727470

-MYH10chr17

8452105

-
5UTR-3CDSENST00000375830ENST00000396239SHC3chr9

91727470

-MYH10chr17

8452105

-
5UTR-3CDSENST00000375830ENST00000269243SHC3chr9

91727470

-MYH10chr17

8452105

-
intron-3CDSENST00000375831ENST00000360416SHC3chr9

91727470

-MYH10chr17

8452105

-
intron-3CDSENST00000375831ENST00000379980SHC3chr9

91727470

-MYH10chr17

8452105

-
intron-3CDSENST00000375831ENST00000396239SHC3chr9

91727470

-MYH10chr17

8452105

-
intron-3CDSENST00000375831ENST00000269243SHC3chr9

91727470

-MYH10chr17

8452105

-

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 SHC3-MYH10


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 SHC3-MYH10


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
.MYH10

P35580

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: Cellular myosin that appears to play a role in cytokinesis, cell shape, and specialized functions such as secretion and capping. Involved with LARP6 in the stabilization of type I collagen mRNAs for CO1A1 and CO1A2. During cell spreading, plays an important role in cytoskeleton reorganization, focal contacts formation (in the central part but not the margins of spreading cells), and lamellipodial extension; this function is mechanically antagonized by MYH9. {ECO:0000269|PubMed:20052411, ECO:0000269|PubMed:20603131}.

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 SHC3-MYH10


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 SHC3-MYH10


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 SHC3-MYH10


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 SHC3-MYH10


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneMYH10C0017668Focal glomerulosclerosis1CTD_human
TgeneMYH10C0086432Hyalinosis, Segmental Glomerular1CTD_human
TgeneMYH10C2936786Aqueductal Stenosis1GENOMICS_ENGLAND