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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:HLTF-HDAC4 (FusionGDB2 ID:36739)

Fusion Gene Summary for HLTF-HDAC4

check button Fusion gene summary
Fusion gene informationFusion gene name: HLTF-HDAC4
Fusion gene ID: 36739
HgeneTgene
Gene symbol

HLTF

HDAC4

Gene ID

6596

9759

Gene namehelicase like transcription factorhistone deacetylase 4
SynonymsHIP116|HIP116A|HLTF1|RNF80|SMARCA3|SNF2L3|ZBU1AHO3|BDMR|HA6116|HD4|HDAC-4|HDAC-A|HDACA
Cytomap

3q24

2q37.3

Type of geneprotein-codingprotein-coding
Descriptionhelicase-like transcription factorDNA-binding protein/plasminogen activator inhibitor-1 regulatorRING finger protein 80RING-type E3 ubiquitin transferase HLTFSNF2-like 3SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfahistone deacetylase 4histone deacetylase A
Modification date2020032220200329
UniProtAcc

Q14527

P56524

Ensembl transtripts involved in fusion geneENST00000310053, ENST00000392912, 
ENST00000465259, ENST00000481663, 
ENST00000494055, 
ENST00000345617, 
ENST00000541256, ENST00000543185, 
ENST00000553145, 
Fusion gene scores* DoF score6 X 7 X 4=16811 X 11 X 4=484
# samples 711
** MAII scorelog2(7/168*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/484*10)=-2.13750352374993
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: HLTF [Title/Abstract] AND HDAC4 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointHLTF(148750135)-HDAC4(240180097), # samples:3
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
TgeneHDAC4

GO:0000122

negative regulation of transcription by RNA polymerase II

10869435|16236793

TgeneHDAC4

GO:0006338

chromatin remodeling

18850004

TgeneHDAC4

GO:0006476

protein deacetylation

27708256

TgeneHDAC4

GO:0016575

histone deacetylation

10869435

TgeneHDAC4

GO:0033235

positive regulation of protein sumoylation

17696781

TgeneHDAC4

GO:0034983

peptidyl-lysine deacetylation

18614528

TgeneHDAC4

GO:0045892

negative regulation of transcription, DNA-templated

10869435

TgeneHDAC4

GO:0070932

histone H3 deacetylation

12590135

TgeneHDAC4

GO:0070933

histone H4 deacetylation

12590135


check buttonFusion gene breakpoints across HLTF (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 HDAC4 (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
ChiTaRS5.0N/ABE768509HLTFchr3

148750135

+HDAC4chr2

240180097

-
ChiTaRS5.0N/ABE768592HLTFchr3

148750135

+HDAC4chr2

240180097

-
ChiTaRS5.0N/ABE768701HLTFchr3

148750135

+HDAC4chr2

240180097

-


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Fusion Gene ORF analysis for HLTF-HDAC4

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-intronENST00000310053ENST00000345617HLTFchr3

148750135

+HDAC4chr2

240180097

-
intron-intronENST00000310053ENST00000541256HLTFchr3

148750135

+HDAC4chr2

240180097

-
intron-intronENST00000310053ENST00000543185HLTFchr3

148750135

+HDAC4chr2

240180097

-
intron-intronENST00000310053ENST00000553145HLTFchr3

148750135

+HDAC4chr2

240180097

-
intron-intronENST00000392912ENST00000345617HLTFchr3

148750135

+HDAC4chr2

240180097

-
intron-intronENST00000392912ENST00000541256HLTFchr3

148750135

+HDAC4chr2

240180097

-
intron-intronENST00000392912ENST00000543185HLTFchr3

148750135

+HDAC4chr2

240180097

-
intron-intronENST00000392912ENST00000553145HLTFchr3

148750135

+HDAC4chr2

240180097

-
intron-intronENST00000465259ENST00000345617HLTFchr3

148750135

+HDAC4chr2

240180097

-
intron-intronENST00000465259ENST00000541256HLTFchr3

148750135

+HDAC4chr2

240180097

-
intron-intronENST00000465259ENST00000543185HLTFchr3

148750135

+HDAC4chr2

240180097

-
intron-intronENST00000465259ENST00000553145HLTFchr3

148750135

+HDAC4chr2

240180097

-
intron-intronENST00000481663ENST00000345617HLTFchr3

148750135

+HDAC4chr2

240180097

-
intron-intronENST00000481663ENST00000541256HLTFchr3

148750135

+HDAC4chr2

240180097

-
intron-intronENST00000481663ENST00000543185HLTFchr3

148750135

+HDAC4chr2

240180097

-
intron-intronENST00000481663ENST00000553145HLTFchr3

148750135

+HDAC4chr2

240180097

-
intron-intronENST00000494055ENST00000345617HLTFchr3

148750135

+HDAC4chr2

240180097

-
intron-intronENST00000494055ENST00000541256HLTFchr3

148750135

+HDAC4chr2

240180097

-
intron-intronENST00000494055ENST00000543185HLTFchr3

148750135

+HDAC4chr2

240180097

-
intron-intronENST00000494055ENST00000553145HLTFchr3

148750135

+HDAC4chr2

240180097

-

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 HLTF-HDAC4


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 HLTF-HDAC4


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/:148750135/:240180097)
- 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
HLTF

Q14527

HDAC4

P56524

FUNCTION: Has both helicase and E3 ubiquitin ligase activities. Possesses intrinsic ATP-dependent nucleosome-remodeling activity; This activity may be required for transcriptional activation or repression of specific target promoters (By similarity). These may include the SERPINE1 and HIV-1 promoters and the SV40 enhancer, to which this protein can bind directly. Plays a role in error-free postreplication repair (PRR) of damaged DNA and maintains genomic stability through acting as a ubiquitin ligase for 'Lys-63'-linked polyubiquitination of chromatin-bound PCNA. {ECO:0000250, ECO:0000269|PubMed:10391891, ECO:0000269|PubMed:18316726, ECO:0000269|PubMed:18719106, ECO:0000269|PubMed:7876228, ECO:0000269|PubMed:8672239, ECO:0000269|PubMed:9126292}.FUNCTION: Responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4). Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events. Histone deacetylases act via the formation of large multiprotein complexes. Involved in muscle maturation via its interaction with the myocyte enhancer factors such as MEF2A, MEF2C and MEF2D. Involved in the MTA1-mediated epigenetic regulation of ESR1 expression in breast cancer. Deacetylates HSPA1A and HSPA1B at 'Lys-77' leading to their preferential binding to co-chaperone STUB1 (PubMed:27708256). {ECO:0000269|PubMed:10523670, ECO:0000269|PubMed:24413532, ECO:0000269|PubMed:27708256}.

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 HLTF-HDAC4


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 HLTF-HDAC4


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 HLTF-HDAC4


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 HLTF-HDAC4


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