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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:MYH11-APOBEC3G

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: MYH11-APOBEC3G
FusionPDB ID: 56283
FusionGDB2.0 ID: 56283
HgeneTgene
Gene symbol

MYH11

APOBEC3G

Gene ID

4629

60489

Gene namemyosin heavy chain 11apolipoprotein B mRNA editing enzyme catalytic subunit 3G
SynonymsAAT4|FAA4|SMHC|SMMHCA3G|ARCD|ARP-9|ARP9|CEM-15|CEM15|MDS019|bK150C2.7|dJ494G10.1
Cytomap

16p13.11

22q13.1

Type of geneprotein-codingprotein-coding
Descriptionmyosin-11epididymis secretory sperm binding proteinmyosin heavy chain, smooth muscle isoformmyosin, heavy chain 11, smooth musclemyosin, heavy polypeptide 11, smooth muscleDNA dC->dU-editing enzyme APOBEC-3GAPOBEC-related cytidine deaminaseAPOBEC-related protein 9DNA dC->dU editing enzymeapolipoprotein B editing enzyme catalytic polypeptide-like 3Gapolipoprotein B mRNA editing enzyme cytidine deaminaseapolipoprotein B
Modification date2020032220200313
UniProtAcc

P35749

.
Ensembl transtripts involved in fusion geneENST idsENST00000300036, ENST00000396324, 
ENST00000452625, ENST00000576790, 
ENST00000573908, 
ENST00000461827, 
ENST00000407997, ENST00000452957, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score31 X 31 X 8=76883 X 3 X 2=18
# samples 323
** MAII scorelog2(32/7688*10)=-4.58646452588639
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 (manual curation of fusion genes in FusionPDB)

PubMed: MYH11 [Title/Abstract] AND APOBEC3G [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MYH11(15931765)-APOBEC3G(39482284), # samples:1
Anticipated loss of major functional domain due to fusion event.MYH11-APOBEC3G 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.
MYH11-APOBEC3G 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.
MYH11-APOBEC3G 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.
MYH11-APOBEC3G 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.
MYH11-APOBEC3G seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
MYH11-APOBEC3G seems lost the major protein functional domain in Tgene 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
TgeneAPOBEC3G

GO:0002230

positive regulation of defense response to virus by host

17121840

TgeneAPOBEC3G

GO:0009972

cytidine deamination

16378963

TgeneAPOBEC3G

GO:0010529

negative regulation of transposition

16527742

TgeneAPOBEC3G

GO:0045071

negative regulation of viral genome replication

16378963|17121840

TgeneAPOBEC3G

GO:0045087

innate immune response

17121840

TgeneAPOBEC3G

GO:0045869

negative regulation of single stranded viral RNA replication via double stranded DNA intermediate

16571802|17121840|21835787

TgeneAPOBEC3G

GO:0048525

negative regulation of viral process

17121840

TgeneAPOBEC3G

GO:0051607

defense response to virus

12808465|21835787|22915799

TgeneAPOBEC3G

GO:0070383

DNA cytosine deamination

16527742|16571802|21835787


check buttonFusion gene breakpoints across MYH11 (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 APOBEC3G (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
ChimerDB4KIRCTCGA-B0-5100-01AMYH11chr16

15931765

-APOBEC3Gchr22

39482284

+


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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)
ENST00000452625MYH11chr1615931765-ENST00000452957APOBEC3Gchr2239482284+116243361852263
ENST00000452625MYH11chr1615931765-ENST00000407997APOBEC3Gchr2239482284+117543361852263
ENST00000576790MYH11chr1615931765-ENST00000452957APOBEC3Gchr2239482284+118445583874263
ENST00000576790MYH11chr1615931765-ENST00000407997APOBEC3Gchr2239482284+119745583874263

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
ENST00000452625ENST00000452957MYH11chr1615931765-APOBEC3Gchr2239482284+0.0061855170.99381447
ENST00000452625ENST00000407997MYH11chr1615931765-APOBEC3Gchr2239482284+0.0061862050.99381375
ENST00000576790ENST00000452957MYH11chr1615931765-APOBEC3Gchr2239482284+0.00598430.9940157
ENST00000576790ENST00000407997MYH11chr1615931765-APOBEC3Gchr2239482284+0.0059322950.99406767

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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

>56283_56283_1_MYH11-APOBEC3G_MYH11_chr16_15931765_ENST00000452625_APOBEC3G_chr22_39482284_ENST00000407997_length(amino acids)=263AA_BP=124
MEIWDQQGTMAQKGQLSDDEKFLFVDKNFINSPVAQADWAAKRLVWVPSEKQGFEAASIKEEKGDEVVVELVENGKKVTVGKDDIQKMNP
PKFSKVEDMAELTCLNEASVLHNLRERYFSGLIYAPHKHGFLEGRHAELCFLDVIPFWKLDLDQDYRVTCFTSWSPCFSCAQEMAKFISK

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

>56283_56283_2_MYH11-APOBEC3G_MYH11_chr16_15931765_ENST00000452625_APOBEC3G_chr22_39482284_ENST00000452957_length(amino acids)=263AA_BP=124
MEIWDQQGTMAQKGQLSDDEKFLFVDKNFINSPVAQADWAAKRLVWVPSEKQGFEAASIKEEKGDEVVVELVENGKKVTVGKDDIQKMNP
PKFSKVEDMAELTCLNEASVLHNLRERYFSGLIYAPHKHGFLEGRHAELCFLDVIPFWKLDLDQDYRVTCFTSWSPCFSCAQEMAKFISK

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

>56283_56283_3_MYH11-APOBEC3G_MYH11_chr16_15931765_ENST00000576790_APOBEC3G_chr22_39482284_ENST00000407997_length(amino acids)=263AA_BP=124
MEIWDQQGTMAQKGQLSDDEKFLFVDKNFINSPVAQADWAAKRLVWVPSEKQGFEAASIKEEKGDEVVVELVENGKKVTVGKDDIQKMNP
PKFSKVEDMAELTCLNEASVLHNLRERYFSGLIYAPHKHGFLEGRHAELCFLDVIPFWKLDLDQDYRVTCFTSWSPCFSCAQEMAKFISK

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

>56283_56283_4_MYH11-APOBEC3G_MYH11_chr16_15931765_ENST00000576790_APOBEC3G_chr22_39482284_ENST00000452957_length(amino acids)=263AA_BP=124
MEIWDQQGTMAQKGQLSDDEKFLFVDKNFINSPVAQADWAAKRLVWVPSEKQGFEAASIKEEKGDEVVVELVENGKKVTVGKDDIQKMNP
PKFSKVEDMAELTCLNEASVLHNLRERYFSGLIYAPHKHGFLEGRHAELCFLDVIPFWKLDLDQDYRVTCFTSWSPCFSCAQEMAKFISK

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

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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/chr16:15931765/chr22:39482284)
- 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
MYH11

P35749

.
FUNCTION: Muscle contraction.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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneMYH11chr16:15931765chr22:39482284ENST00000300036-24131_81115.01973.0DomainMyosin N-terminal SH3-like
HgeneMYH11chr16:15931765chr22:39482284ENST00000396324-24231_81115.01980.0DomainMyosin N-terminal SH3-like
HgeneMYH11chr16:15931765chr22:39482284ENST00000452625-24331_81115.02132.0DomainMyosin N-terminal SH3-like
HgeneMYH11chr16:15931765chr22:39482284ENST00000576790-24231_81115.01912.6666666666667DomainMyosin N-terminal SH3-like

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneMYH11chr16:15931765chr22:39482284ENST00000300036-241844_1934115.01973.0Coiled coilOntology_term=ECO:0000255
HgeneMYH11chr16:15931765chr22:39482284ENST00000396324-242844_1934115.01980.0Coiled coilOntology_term=ECO:0000255
HgeneMYH11chr16:15931765chr22:39482284ENST00000452625-243844_1934115.02132.0Coiled coilOntology_term=ECO:0000255
HgeneMYH11chr16:15931765chr22:39482284ENST00000576790-242844_1934115.01912.6666666666667Coiled coilOntology_term=ECO:0000255
HgeneMYH11chr16:15931765chr22:39482284ENST00000300036-241786_815115.01973.0DomainIQ
HgeneMYH11chr16:15931765chr22:39482284ENST00000300036-24185_783115.01973.0DomainMyosin motor
HgeneMYH11chr16:15931765chr22:39482284ENST00000396324-242786_815115.01980.0DomainIQ
HgeneMYH11chr16:15931765chr22:39482284ENST00000396324-24285_783115.01980.0DomainMyosin motor
HgeneMYH11chr16:15931765chr22:39482284ENST00000452625-243786_815115.02132.0DomainIQ
HgeneMYH11chr16:15931765chr22:39482284ENST00000452625-24385_783115.02132.0DomainMyosin motor
HgeneMYH11chr16:15931765chr22:39482284ENST00000576790-242786_815115.01912.6666666666667DomainIQ
HgeneMYH11chr16:15931765chr22:39482284ENST00000576790-24285_783115.01912.6666666666667DomainMyosin motor
HgeneMYH11chr16:15931765chr22:39482284ENST00000300036-241178_185115.01973.0Nucleotide bindingATP
HgeneMYH11chr16:15931765chr22:39482284ENST00000396324-242178_185115.01980.0Nucleotide bindingATP
HgeneMYH11chr16:15931765chr22:39482284ENST00000452625-243178_185115.02132.0Nucleotide bindingATP
HgeneMYH11chr16:15931765chr22:39482284ENST00000576790-242178_185115.01912.6666666666667Nucleotide bindingATP
HgeneMYH11chr16:15931765chr22:39482284ENST00000300036-2411935_1972115.01973.0RegionNote=C-terminal
HgeneMYH11chr16:15931765chr22:39482284ENST00000300036-241661_683115.01973.0RegionActin-binding
HgeneMYH11chr16:15931765chr22:39482284ENST00000300036-241762_776115.01973.0RegionActin-binding
HgeneMYH11chr16:15931765chr22:39482284ENST00000396324-2421935_1972115.01980.0RegionNote=C-terminal
HgeneMYH11chr16:15931765chr22:39482284ENST00000396324-242661_683115.01980.0RegionActin-binding
HgeneMYH11chr16:15931765chr22:39482284ENST00000396324-242762_776115.01980.0RegionActin-binding
HgeneMYH11chr16:15931765chr22:39482284ENST00000452625-2431935_1972115.02132.0RegionNote=C-terminal
HgeneMYH11chr16:15931765chr22:39482284ENST00000452625-243661_683115.02132.0RegionActin-binding
HgeneMYH11chr16:15931765chr22:39482284ENST00000452625-243762_776115.02132.0RegionActin-binding
HgeneMYH11chr16:15931765chr22:39482284ENST00000576790-2421935_1972115.01912.6666666666667RegionNote=C-terminal
HgeneMYH11chr16:15931765chr22:39482284ENST00000576790-242661_683115.01912.6666666666667RegionActin-binding
HgeneMYH11chr16:15931765chr22:39482284ENST00000576790-242762_776115.01912.6666666666667RegionActin-binding
TgeneAPOBEC3Gchr16:15931765chr22:39482284ENST0000040799748214_328245.0385.0DomainCMP/dCMP-type deaminase 2
TgeneAPOBEC3Gchr16:15931765chr22:39482284ENST000004079974829_138245.0385.0DomainCMP/dCMP-type deaminase 1
TgeneAPOBEC3Gchr16:15931765chr22:39482284ENST0000045295748214_328245.0385.0DomainCMP/dCMP-type deaminase 2
TgeneAPOBEC3Gchr16:15931765chr22:39482284ENST000004529574829_138245.0385.0DomainCMP/dCMP-type deaminase 1
TgeneAPOBEC3Gchr16:15931765chr22:39482284ENST00000407997481_60245.0385.0RegionNote=Essential for cytoplasmic localization
TgeneAPOBEC3Gchr16:15931765chr22:39482284ENST0000040799748209_336245.0385.0RegionNote=Necessary for homooligomerization
TgeneAPOBEC3Gchr16:15931765chr22:39482284ENST00000452957481_60245.0385.0RegionNote=Essential for cytoplasmic localization
TgeneAPOBEC3Gchr16:15931765chr22:39482284ENST0000045295748209_336245.0385.0RegionNote=Necessary for homooligomerization


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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
MYH11all structure
APOBEC3G


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
TgeneAPOBEC3Gchr16:15931765chr22:39482284ENST0000040799748213_215245.0385.0DNA
TgeneAPOBEC3Gchr16:15931765chr22:39482284ENST0000045295748213_215245.0385.0DNA


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Related Drugs to MYH11-APOBEC3G


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 MYH11-APOBEC3G


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
HgeneMYH11C4707243Familial thoracic aortic aneurysm and aortic dissection10CLINGEN;GENOMICS_ENGLAND
HgeneMYH11C0023467Leukemia, Myelocytic, Acute2CTD_human
HgeneMYH11C0023479Acute myelomonocytic leukemia2CTD_human;ORPHANET
HgeneMYH11C0026998Acute Myeloid Leukemia, M12CTD_human
HgeneMYH11C1851504Aortic aneurysm, familial thoracic 42CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneMYH11C1879321Acute Myeloid Leukemia (AML-M2)2CTD_human
HgeneMYH11C1608393Megacystis microcolon intestinal hypoperistalsis syndrome1GENOMICS_ENGLAND;ORPHANET