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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:HDAC7-VDR (FusionGDB2 ID:35865)

Fusion Gene Summary for HDAC7-VDR

check button Fusion gene summary
Fusion gene informationFusion gene name: HDAC7-VDR
Fusion gene ID: 35865
HgeneTgene
Gene symbol

HDAC7

VDR

Gene ID

51564

7421

Gene namehistone deacetylase 7vitamin D receptor
SynonymsHD7|HD7A|HDAC7ANR1I1|PPP1R163
Cytomap

12q13.11

12q13.11

Type of geneprotein-codingprotein-coding
Descriptionhistone deacetylase 7histone deacetylase 7Avitamin D3 receptor1,25-dihydroxyvitamin D3 receptornuclear receptor subfamily 1 group I member 1protein phosphatase 1, regulatory subunit 163vitamin D (1,25- dihydroxyvitamin D3) receptorvitamin D nuclear receptor variant 1
Modification date2020032720200329
UniProtAcc

Q8WUI4

.
Ensembl transtripts involved in fusion geneENST00000080059, ENST00000354334, 
ENST00000552960, ENST00000380610, 
ENST00000427332, ENST00000488927, 
ENST00000229022, ENST00000395324, 
ENST00000535672, ENST00000549336, 
ENST00000550325, 
Fusion gene scores* DoF score11 X 8 X 6=5285 X 7 X 5=175
# samples 158
** MAII scorelog2(15/528*10)=-1.81557542886257
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/175*10)=-1.12928301694497
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: HDAC7 [Title/Abstract] AND VDR [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointHDAC7(48213550)-VDR(48258960), # samples:2
Anticipated loss of major functional domain due to fusion event.HDAC7-VDR seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
HDAC7-VDR seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
HDAC7-VDR seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
HDAC7-VDR seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF.
HDAC7-VDR seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
HDAC7-VDR seems lost the major protein functional domain in Tgene partner, which is a transcription factor due to the frame-shifted ORF.
HDAC7-VDR seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor 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
HgeneHDAC7

GO:0032703

negative regulation of interleukin-2 production

17360565

TgeneVDR

GO:0000122

negative regulation of transcription by RNA polymerase II

17426122

TgeneVDR

GO:0008285

negative regulation of cell proliferation

16549446

TgeneVDR

GO:0010980

positive regulation of vitamin D 24-hydroxylase activity

16549446

TgeneVDR

GO:0038183

bile acid signaling pathway

12016314

TgeneVDR

GO:0045892

negative regulation of transcription, DNA-templated

11891224

TgeneVDR

GO:0070561

vitamin D receptor signaling pathway

16549446


check buttonFusion gene breakpoints across HDAC7 (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 VDR (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

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
ChimerDB4ACCTCGA-OR-A5JM-01AHDAC7chr12

48213550

-VDRchr12

48258960

-
ChimerDB4UCECTCGA-EY-A54A-01AHDAC7chr12

48191167

-VDRchr12

48240591

-


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Fusion Gene ORF analysis for HDAC7-VDR

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-shiftENST00000080059ENST00000229022HDAC7chr12

48213550

-VDRchr12

48258960

-
Frame-shiftENST00000080059ENST00000229022HDAC7chr12

48191167

-VDRchr12

48240591

-
Frame-shiftENST00000080059ENST00000395324HDAC7chr12

48213550

-VDRchr12

48258960

-
Frame-shiftENST00000080059ENST00000395324HDAC7chr12

48191167

-VDRchr12

48240591

-
Frame-shiftENST00000080059ENST00000535672HDAC7chr12

48213550

-VDRchr12

48258960

-
Frame-shiftENST00000080059ENST00000535672HDAC7chr12

48191167

-VDRchr12

48240591

-
Frame-shiftENST00000080059ENST00000549336HDAC7chr12

48213550

-VDRchr12

48258960

-
Frame-shiftENST00000080059ENST00000549336HDAC7chr12

48191167

-VDRchr12

48240591

-
Frame-shiftENST00000080059ENST00000550325HDAC7chr12

48213550

-VDRchr12

48258960

-
Frame-shiftENST00000080059ENST00000550325HDAC7chr12

48191167

-VDRchr12

48240591

-
Frame-shiftENST00000354334ENST00000229022HDAC7chr12

48213550

-VDRchr12

48258960

-
Frame-shiftENST00000354334ENST00000229022HDAC7chr12

48191167

-VDRchr12

48240591

-
Frame-shiftENST00000354334ENST00000395324HDAC7chr12

48213550

-VDRchr12

48258960

-
Frame-shiftENST00000354334ENST00000395324HDAC7chr12

48191167

-VDRchr12

48240591

-
Frame-shiftENST00000354334ENST00000535672HDAC7chr12

48213550

-VDRchr12

48258960

-
Frame-shiftENST00000354334ENST00000535672HDAC7chr12

48191167

-VDRchr12

48240591

-
Frame-shiftENST00000354334ENST00000549336HDAC7chr12

48213550

-VDRchr12

48258960

-
Frame-shiftENST00000354334ENST00000549336HDAC7chr12

48191167

-VDRchr12

48240591

-
Frame-shiftENST00000354334ENST00000550325HDAC7chr12

48213550

-VDRchr12

48258960

-
Frame-shiftENST00000354334ENST00000550325HDAC7chr12

48191167

-VDRchr12

48240591

-
Frame-shiftENST00000552960ENST00000229022HDAC7chr12

48213550

-VDRchr12

48258960

-
Frame-shiftENST00000552960ENST00000229022HDAC7chr12

48191167

-VDRchr12

48240591

-
Frame-shiftENST00000552960ENST00000395324HDAC7chr12

48213550

-VDRchr12

48258960

-
Frame-shiftENST00000552960ENST00000395324HDAC7chr12

48191167

-VDRchr12

48240591

-
Frame-shiftENST00000552960ENST00000535672HDAC7chr12

48213550

-VDRchr12

48258960

-
Frame-shiftENST00000552960ENST00000535672HDAC7chr12

48191167

-VDRchr12

48240591

-
Frame-shiftENST00000552960ENST00000549336HDAC7chr12

48213550

-VDRchr12

48258960

-
Frame-shiftENST00000552960ENST00000549336HDAC7chr12

48191167

-VDRchr12

48240591

-
Frame-shiftENST00000552960ENST00000550325HDAC7chr12

48213550

-VDRchr12

48258960

-
Frame-shiftENST00000552960ENST00000550325HDAC7chr12

48191167

-VDRchr12

48240591

-
In-frameENST00000380610ENST00000229022HDAC7chr12

48191167

-VDRchr12

48240591

-
In-frameENST00000380610ENST00000395324HDAC7chr12

48191167

-VDRchr12

48240591

-
In-frameENST00000380610ENST00000535672HDAC7chr12

48191167

-VDRchr12

48240591

-
In-frameENST00000380610ENST00000549336HDAC7chr12

48191167

-VDRchr12

48240591

-
In-frameENST00000380610ENST00000550325HDAC7chr12

48191167

-VDRchr12

48240591

-
In-frameENST00000427332ENST00000229022HDAC7chr12

48191167

-VDRchr12

48240591

-
In-frameENST00000427332ENST00000395324HDAC7chr12

48191167

-VDRchr12

48240591

-
In-frameENST00000427332ENST00000535672HDAC7chr12

48191167

-VDRchr12

48240591

-
In-frameENST00000427332ENST00000549336HDAC7chr12

48191167

-VDRchr12

48240591

-
In-frameENST00000427332ENST00000550325HDAC7chr12

48191167

-VDRchr12

48240591

-
intron-3CDSENST00000380610ENST00000229022HDAC7chr12

48213550

-VDRchr12

48258960

-
intron-3CDSENST00000380610ENST00000395324HDAC7chr12

48213550

-VDRchr12

48258960

-
intron-3CDSENST00000380610ENST00000535672HDAC7chr12

48213550

-VDRchr12

48258960

-
intron-3CDSENST00000380610ENST00000549336HDAC7chr12

48213550

-VDRchr12

48258960

-
intron-3CDSENST00000380610ENST00000550325HDAC7chr12

48213550

-VDRchr12

48258960

-
intron-3CDSENST00000427332ENST00000229022HDAC7chr12

48213550

-VDRchr12

48258960

-
intron-3CDSENST00000427332ENST00000395324HDAC7chr12

48213550

-VDRchr12

48258960

-
intron-3CDSENST00000427332ENST00000535672HDAC7chr12

48213550

-VDRchr12

48258960

-
intron-3CDSENST00000427332ENST00000549336HDAC7chr12

48213550

-VDRchr12

48258960

-
intron-3CDSENST00000427332ENST00000550325HDAC7chr12

48213550

-VDRchr12

48258960

-
intron-3CDSENST00000488927ENST00000229022HDAC7chr12

48213550

-VDRchr12

48258960

-
intron-3CDSENST00000488927ENST00000229022HDAC7chr12

48191167

-VDRchr12

48240591

-
intron-3CDSENST00000488927ENST00000395324HDAC7chr12

48213550

-VDRchr12

48258960

-
intron-3CDSENST00000488927ENST00000395324HDAC7chr12

48191167

-VDRchr12

48240591

-
intron-3CDSENST00000488927ENST00000535672HDAC7chr12

48213550

-VDRchr12

48258960

-
intron-3CDSENST00000488927ENST00000535672HDAC7chr12

48191167

-VDRchr12

48240591

-
intron-3CDSENST00000488927ENST00000549336HDAC7chr12

48213550

-VDRchr12

48258960

-
intron-3CDSENST00000488927ENST00000549336HDAC7chr12

48191167

-VDRchr12

48240591

-
intron-3CDSENST00000488927ENST00000550325HDAC7chr12

48213550

-VDRchr12

48258960

-
intron-3CDSENST00000488927ENST00000550325HDAC7chr12

48191167

-VDRchr12

48240591

-

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 HDAC7-VDR


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.
genomic feature

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 HDAC7-VDR


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/chr12:48213550/chr12:48258960)
- 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
HDAC7

Q8WUI4

.
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 by repressing transcription of myocyte enhancer factors such as MEF2A, MEF2B and MEF2C. During muscle differentiation, it shuttles into the cytoplasm, allowing the expression of myocyte enhancer factors (By similarity). May be involved in Epstein-Barr virus (EBV) latency, possibly by repressing the viral BZLF1 gene. Positively regulates the transcriptional repressor activity of FOXP3 (PubMed:17360565). Serves as a corepressor of RARA, causing its deacetylation and inhibition of RARE DNA element binding (PubMed:28167758). In association with RARA, plays a role in the repression of microRNA-10a and thereby in the inflammatory response (PubMed:28167758). {ECO:0000250|UniProtKB:Q8C2B3, ECO:0000269|PubMed:12239305, ECO:0000269|PubMed:17360565, ECO:0000269|PubMed:28167758}.FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.

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
TgeneVDRchr12:48191167chr12:48240591ENST00000229022711416_424251428.0Motif9aaTAD
TgeneVDRchr12:48191167chr12:48240591ENST00000395324610416_424251428.0Motif9aaTAD
TgeneVDRchr12:48191167chr12:48240591ENST00000549336610416_424251428.0Motif9aaTAD
TgeneVDRchr12:48191167chr12:48240591ENST00000550325610416_424301478.0Motif9aaTAD
TgeneVDRchr12:48191167chr12:48240591ENST00000229022711271_278251428.0RegionNote=Vitamin D3 binding
TgeneVDRchr12:48191167chr12:48240591ENST00000395324610271_278251428.0RegionNote=Vitamin D3 binding
TgeneVDRchr12:48191167chr12:48240591ENST00000549336610271_278251428.0RegionNote=Vitamin D3 binding

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneHDAC7chr12:48191167chr12:48240591ENST00000080059-626197_203192992.0Compositional biasNote=Poly-Ser
HgeneHDAC7chr12:48191167chr12:48240591ENST00000080059-626368_373192992.0Compositional biasNote=Poly-Pro
HgeneHDAC7chr12:48191167chr12:48240591ENST00000354334-625197_203192955.0Compositional biasNote=Poly-Ser
HgeneHDAC7chr12:48191167chr12:48240591ENST00000354334-625368_373192955.0Compositional biasNote=Poly-Pro
HgeneHDAC7chr12:48191167chr12:48240591ENST00000427332-626197_203153953.0Compositional biasNote=Poly-Ser
HgeneHDAC7chr12:48191167chr12:48240591ENST00000427332-626368_373153953.0Compositional biasNote=Poly-Pro
HgeneHDAC7chr12:48191167chr12:48240591ENST00000552960-525197_203175975.0Compositional biasNote=Poly-Ser
HgeneHDAC7chr12:48191167chr12:48240591ENST00000552960-525368_373175975.0Compositional biasNote=Poly-Pro
HgeneHDAC7chr12:48191167chr12:48240591ENST00000080059-626918_952192992.0MotifNuclear export signal
HgeneHDAC7chr12:48191167chr12:48240591ENST00000354334-625918_952192955.0MotifNuclear export signal
HgeneHDAC7chr12:48191167chr12:48240591ENST00000427332-626918_952153953.0MotifNuclear export signal
HgeneHDAC7chr12:48191167chr12:48240591ENST00000552960-525918_952175975.0MotifNuclear export signal
HgeneHDAC7chr12:48191167chr12:48240591ENST00000080059-6261_268192992.0RegionTranscription repression 1
HgeneHDAC7chr12:48191167chr12:48240591ENST00000080059-626218_546192992.0RegionTranscription repression 2
HgeneHDAC7chr12:48191167chr12:48240591ENST00000080059-626518_865192992.0RegionNote=Histone deacetylase
HgeneHDAC7chr12:48191167chr12:48240591ENST00000354334-6251_268192955.0RegionTranscription repression 1
HgeneHDAC7chr12:48191167chr12:48240591ENST00000354334-625218_546192955.0RegionTranscription repression 2
HgeneHDAC7chr12:48191167chr12:48240591ENST00000354334-625518_865192955.0RegionNote=Histone deacetylase
HgeneHDAC7chr12:48191167chr12:48240591ENST00000427332-6261_268153953.0RegionTranscription repression 1
HgeneHDAC7chr12:48191167chr12:48240591ENST00000427332-626218_546153953.0RegionTranscription repression 2
HgeneHDAC7chr12:48191167chr12:48240591ENST00000427332-626518_865153953.0RegionNote=Histone deacetylase
HgeneHDAC7chr12:48191167chr12:48240591ENST00000552960-5251_268175975.0RegionTranscription repression 1
HgeneHDAC7chr12:48191167chr12:48240591ENST00000552960-525218_546175975.0RegionTranscription repression 2
HgeneHDAC7chr12:48191167chr12:48240591ENST00000552960-525518_865175975.0RegionNote=Histone deacetylase
TgeneVDRchr12:48191167chr12:48240591ENST0000022902271121_96251428.0DNA bindingNuclear receptor
TgeneVDRchr12:48191167chr12:48240591ENST0000039532461021_96251428.0DNA bindingNuclear receptor
TgeneVDRchr12:48191167chr12:48240591ENST0000054933661021_96251428.0DNA bindingNuclear receptor
TgeneVDRchr12:48191167chr12:48240591ENST0000055032561021_96301478.0DNA bindingNuclear receptor
TgeneVDRchr12:48191167chr12:48240591ENST00000229022711127_423251428.0DomainNR LBD
TgeneVDRchr12:48191167chr12:48240591ENST00000395324610127_423251428.0DomainNR LBD
TgeneVDRchr12:48191167chr12:48240591ENST00000549336610127_423251428.0DomainNR LBD
TgeneVDRchr12:48191167chr12:48240591ENST00000550325610127_423301478.0DomainNR LBD
TgeneVDRchr12:48191167chr12:48240591ENST00000229022711227_237251428.0RegionNote=Vitamin D3 binding
TgeneVDRchr12:48191167chr12:48240591ENST0000022902271197_126251428.0RegionNote=Hinge
TgeneVDRchr12:48191167chr12:48240591ENST00000395324610227_237251428.0RegionNote=Vitamin D3 binding
TgeneVDRchr12:48191167chr12:48240591ENST0000039532461097_126251428.0RegionNote=Hinge
TgeneVDRchr12:48191167chr12:48240591ENST00000549336610227_237251428.0RegionNote=Vitamin D3 binding
TgeneVDRchr12:48191167chr12:48240591ENST0000054933661097_126251428.0RegionNote=Hinge
TgeneVDRchr12:48191167chr12:48240591ENST00000550325610227_237301478.0RegionNote=Vitamin D3 binding
TgeneVDRchr12:48191167chr12:48240591ENST00000550325610271_278301478.0RegionNote=Vitamin D3 binding
TgeneVDRchr12:48191167chr12:48240591ENST0000055032561097_126301478.0RegionNote=Hinge
TgeneVDRchr12:48191167chr12:48240591ENST0000022902271124_44251428.0Zinc fingerNR C4-type
TgeneVDRchr12:48191167chr12:48240591ENST0000022902271160_84251428.0Zinc fingerNR C4-type
TgeneVDRchr12:48191167chr12:48240591ENST0000039532461024_44251428.0Zinc fingerNR C4-type
TgeneVDRchr12:48191167chr12:48240591ENST0000039532461060_84251428.0Zinc fingerNR C4-type
TgeneVDRchr12:48191167chr12:48240591ENST0000054933661024_44251428.0Zinc fingerNR C4-type
TgeneVDRchr12:48191167chr12:48240591ENST0000054933661060_84251428.0Zinc fingerNR C4-type
TgeneVDRchr12:48191167chr12:48240591ENST0000055032561024_44301478.0Zinc fingerNR C4-type
TgeneVDRchr12:48191167chr12:48240591ENST0000055032561060_84301478.0Zinc fingerNR C4-type


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Fusion Gene Sequence for HDAC7-VDR


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 HDAC7-VDR


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
HgeneHDAC7chr12:48191167chr12:48240591ENST00000080059-62649_149192.33333333333334992.0MEF2A
HgeneHDAC7chr12:48191167chr12:48240591ENST00000354334-62549_149192.33333333333334955.0MEF2A
HgeneHDAC7chr12:48191167chr12:48240591ENST00000427332-62649_149153.33333333333334953.0MEF2A
HgeneHDAC7chr12:48191167chr12:48240591ENST00000552960-52549_149175.33333333333334975.0MEF2A
HgeneHDAC7chr12:48191167chr12:48240591ENST00000080059-6261_98192.33333333333334992.0MEF2C
HgeneHDAC7chr12:48191167chr12:48240591ENST00000354334-6251_98192.33333333333334955.0MEF2C
HgeneHDAC7chr12:48191167chr12:48240591ENST00000427332-6261_98153.33333333333334953.0MEF2C
HgeneHDAC7chr12:48191167chr12:48240591ENST00000552960-5251_98175.33333333333334975.0MEF2C


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with
HgeneHDAC7chr12:48191167chr12:48240591ENST00000080059-626877_952192.33333333333334992.0SIN3A
HgeneHDAC7chr12:48191167chr12:48240591ENST00000354334-625877_952192.33333333333334955.0SIN3A
HgeneHDAC7chr12:48191167chr12:48240591ENST00000427332-626877_952153.33333333333334953.0SIN3A
HgeneHDAC7chr12:48191167chr12:48240591ENST00000552960-525877_952175.33333333333334975.0SIN3A


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 HDAC7-VDR


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 HDAC7-VDR


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