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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:ZNF789-MEAF6 (FusionGDB2 ID:102251)

Fusion Gene Summary for ZNF789-MEAF6

check button Fusion gene summary
Fusion gene informationFusion gene name: ZNF789-MEAF6
Fusion gene ID: 102251
HgeneTgene
Gene symbol

ZNF789

MEAF6

Gene ID

285989

64769

Gene namezinc finger protein 789MYST/Esa1 associated factor 6
Synonyms-C1orf149|CENP-28|EAF6|NY-SAR-91
Cytomap

7q22.1

1p34.3

Type of geneprotein-codingprotein-coding
Descriptionzinc finger protein 789chromatin modification-related protein MEAF6Esa1p-associated factor 6 homologcentromere protein 28protein EAF6 homologsarcoma antigen NY-SAR-91
Modification date2020031320200313
UniProtAcc.

Q9HAF1

Ensembl transtripts involved in fusion geneENST00000493485, ENST00000494186, 
ENST00000331410, ENST00000483089, 
ENST00000448667, ENST00000379724, 
ENST00000373075, ENST00000296214, 
ENST00000373074, ENST00000475828, 
ENST00000373073, ENST00000448519, 
Fusion gene scores* DoF score5 X 4 X 4=806 X 5 X 5=150
# samples 66
** MAII scorelog2(6/80*10)=-0.415037499278844
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/150*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ZNF789 [Title/Abstract] AND MEAF6 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointZNF789(99070679)-MEAF6(37967597), # 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
TgeneMEAF6

GO:0043968

histone H2A acetylation

14966270

TgeneMEAF6

GO:0043981

histone H4-K5 acetylation

16387653

TgeneMEAF6

GO:0043982

histone H4-K8 acetylation

16387653

TgeneMEAF6

GO:0043983

histone H4-K12 acetylation

16387653

TgeneMEAF6

GO:0043984

histone H4-K16 acetylation

16387653

TgeneMEAF6

GO:0044154

histone H3-K14 acetylation

16387653


check buttonFusion gene breakpoints across ZNF789 (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 MEAF6 (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-A4IY-01AZNF789chr7

99070679

+MEAF6chr1

37967597

-


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Fusion Gene ORF analysis for ZNF789-MEAF6

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
5UTR-3CDSENST00000493485ENST00000373075ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-3CDSENST00000493485ENST00000296214ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-3CDSENST00000493485ENST00000373074ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-5UTRENST00000493485ENST00000475828ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-5UTRENST00000493485ENST00000373073ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-5UTRENST00000493485ENST00000448519ZNF789chr7

99070679

+MEAF6chr1

37967597

-
intron-3CDSENST00000494186ENST00000373075ZNF789chr7

99070679

+MEAF6chr1

37967597

-
intron-3CDSENST00000494186ENST00000296214ZNF789chr7

99070679

+MEAF6chr1

37967597

-
intron-3CDSENST00000494186ENST00000373074ZNF789chr7

99070679

+MEAF6chr1

37967597

-
intron-5UTRENST00000494186ENST00000475828ZNF789chr7

99070679

+MEAF6chr1

37967597

-
intron-5UTRENST00000494186ENST00000373073ZNF789chr7

99070679

+MEAF6chr1

37967597

-
intron-5UTRENST00000494186ENST00000448519ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-3CDSENST00000331410ENST00000373075ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-3CDSENST00000331410ENST00000296214ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-3CDSENST00000331410ENST00000373074ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-5UTRENST00000331410ENST00000475828ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-5UTRENST00000331410ENST00000373073ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-5UTRENST00000331410ENST00000448519ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-3CDSENST00000483089ENST00000373075ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-3CDSENST00000483089ENST00000296214ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-3CDSENST00000483089ENST00000373074ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-5UTRENST00000483089ENST00000475828ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-5UTRENST00000483089ENST00000373073ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-5UTRENST00000483089ENST00000448519ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-3CDSENST00000448667ENST00000373075ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-3CDSENST00000448667ENST00000296214ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-3CDSENST00000448667ENST00000373074ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-5UTRENST00000448667ENST00000475828ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-5UTRENST00000448667ENST00000373073ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-5UTRENST00000448667ENST00000448519ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-3CDSENST00000379724ENST00000373075ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-3CDSENST00000379724ENST00000296214ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-3CDSENST00000379724ENST00000373074ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-5UTRENST00000379724ENST00000475828ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-5UTRENST00000379724ENST00000373073ZNF789chr7

99070679

+MEAF6chr1

37967597

-
5UTR-5UTRENST00000379724ENST00000448519ZNF789chr7

99070679

+MEAF6chr1

37967597

-

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 ZNF789-MEAF6


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 ZNF789-MEAF6


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
.MEAF6

Q9HAF1

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 NuA4 histone acetyltransferase complex which is involved in transcriptional activation of select genes principally by acetylation of nucleosomal histone H4 and H2A (PubMed:14966270). This modification may both alter nucleosome - DNA interactions and promote interaction of the modified histones with other proteins which positively regulate transcription (PubMed:14966270). Component of HBO1 complexes, which specifically mediate acetylation of histone H3 at 'Lys-14' (H3K14ac), and have reduced activity toward histone H4 (PubMed:16387653, PubMed:24065767). Component of the MOZ/MORF complex which has a histone H3 acetyltransferase activity (PubMed:18794358). {ECO:0000269|PubMed:14966270, ECO:0000269|PubMed:16387653, ECO:0000269|PubMed:18794358, ECO:0000269|PubMed:24065767}.

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 ZNF789-MEAF6


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 ZNF789-MEAF6


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 ZNF789-MEAF6


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 ZNF789-MEAF6


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