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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:UHRF2-VLDLR (FusionGDB2 ID:96074)

Fusion Gene Summary for UHRF2-VLDLR

check button Fusion gene summary
Fusion gene informationFusion gene name: UHRF2-VLDLR
Fusion gene ID: 96074
HgeneTgene
Gene symbol

UHRF2

VLDLR

Gene ID

115426

7436

Gene nameubiquitin like with PHD and ring finger domains 2very low density lipoprotein receptor
SynonymsNIRF|RNF107|TDRD23|URF2CAMRQ1|CARMQ1|CHRMQ1|VLDL-R|VLDLRCH
Cytomap

9p24.1

9p24.2

Type of geneprotein-codingprotein-coding
DescriptionE3 ubiquitin-protein ligase UHRF2Np95-like ring finger proteinRING finger protein 107RING-type E3 ubiquitin transferase UHRF2np95/ICBP90-like RING finger proteinnuclear protein 97nuclear zinc finger protein NP97ubiquitin-like PHD and RING finger dovery low-density lipoprotein receptorVLDL receptor
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000276893, ENST00000381373, 
ENST00000485617, 
ENST00000382100, 
ENST00000382099, ENST00000478776, 
Fusion gene scores* DoF score7 X 5 X 5=1751 X 1 X 1=1
# samples 61
** MAII scorelog2(6/175*10)=-1.54432051622381
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: UHRF2 [Title/Abstract] AND VLDLR [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointUHRF2(6434173)-VLDLR(2635453), # samples:1
Anticipated loss of major functional domain due to fusion event.UHRF2-VLDLR seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
UHRF2-VLDLR seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
UHRF2-VLDLR seems lost the major protein functional domain in Hgene 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
HgeneUHRF2

GO:0016567

protein ubiquitination

14741369

HgeneUHRF2

GO:0051865

protein autoubiquitination

14741369

HgeneUHRF2

GO:0071158

positive regulation of cell cycle arrest

15178429

TgeneVLDLR

GO:0006898

receptor-mediated endocytosis

10571240

TgeneVLDLR

GO:0034436

glycoprotein transport

10571240

TgeneVLDLR

GO:0034447

very-low-density lipoprotein particle clearance

8083232


check buttonFusion gene breakpoints across UHRF2 (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 VLDLR (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
ChimerDB4KIRCTCGA-BP-4983-01AUHRF2chr9

6434173

+VLDLRchr9

2635453

+


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Fusion Gene ORF analysis for UHRF2-VLDLR

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-shiftENST00000276893ENST00000382100UHRF2chr9

6434173

+VLDLRchr9

2635453

+
Frame-shiftENST00000276893ENST00000382099UHRF2chr9

6434173

+VLDLRchr9

2635453

+
5CDS-intronENST00000276893ENST00000478776UHRF2chr9

6434173

+VLDLRchr9

2635453

+
intron-3CDSENST00000381373ENST00000382100UHRF2chr9

6434173

+VLDLRchr9

2635453

+
intron-3CDSENST00000381373ENST00000382099UHRF2chr9

6434173

+VLDLRchr9

2635453

+
intron-intronENST00000381373ENST00000478776UHRF2chr9

6434173

+VLDLRchr9

2635453

+
intron-3CDSENST00000485617ENST00000382100UHRF2chr9

6434173

+VLDLRchr9

2635453

+
intron-3CDSENST00000485617ENST00000382099UHRF2chr9

6434173

+VLDLRchr9

2635453

+
intron-intronENST00000485617ENST00000478776UHRF2chr9

6434173

+VLDLRchr9

2635453

+

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 UHRF2-VLDLR


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)
UHRF2chr96434173+VLDLRchr92635452+0.0003162610.99968374
UHRF2chr96434173+VLDLRchr92635452+0.0003162610.99968374

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 UHRF2-VLDLR


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
..
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: 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.
- 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 UHRF2-VLDLR


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 UHRF2-VLDLR


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 UHRF2-VLDLR


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 UHRF2-VLDLR


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneVLDLRC0036341Schizophrenia3PSYGENET
TgeneVLDLRC4551552Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 13CTD_human;GENOMICS_ENGLAND
TgeneVLDLRC0266470Cerebellar Hypoplasia2GENOMICS_ENGLAND
TgeneVLDLRC0004352Autistic Disorder1CTD_human
TgeneVLDLRC0028754Obesity1CTD_human
TgeneVLDLRC0394006Dysequilibrium syndrome1ORPHANET
TgeneVLDLRC0400966Non-alcoholic Fatty Liver Disease1CTD_human
TgeneVLDLRC3241937Nonalcoholic Steatohepatitis1CTD_human