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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:VMP1-DHCR7 (FusionGDB2 ID:97529)

Fusion Gene Summary for VMP1-DHCR7

check button Fusion gene summary
Fusion gene informationFusion gene name: VMP1-DHCR7
Fusion gene ID: 97529
HgeneTgene
Gene symbol

VMP1

DHCR7

Gene ID

81671

1717

Gene namevacuole membrane protein 17-dehydrocholesterol reductase
SynonymsEPG3|TANGO5|TMEM49SLOS
Cytomap

17q23.1

11q13.4

Type of geneprotein-codingprotein-coding
Descriptionvacuole membrane protein 1ectopic P-granules autophagy protein 3 homologtransmembrane protein 49transport and golgi organization 5 homolog7-dehydrocholesterol reductase7-DHC reductasedelta-7-dehydrocholesterol reductasedelta7-sterol reductaseputative sterol reductase SR-2sterol delta-7-reductasesterol reductase SR-2
Modification date2020032720200313
UniProtAcc.

Q9UBM7

Ensembl transtripts involved in fusion geneENST00000262291, ENST00000537567, 
ENST00000539763, ENST00000536180, 
ENST00000545362, ENST00000588617, 
ENST00000407721, ENST00000355527, 
Fusion gene scores* DoF score34 X 17 X 12=69367 X 6 X 5=210
# samples 387
** MAII scorelog2(38/6936*10)=-4.19003257489089
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/210*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: VMP1 [Title/Abstract] AND DHCR7 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointVMP1(57918685)-DHCR7(71152487), # samples:2
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

check buttonFusion gene breakpoints across VMP1 (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 DHCR7 (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
ChimerDB4BRCATCGA-E9-A22D-01AVMP1chr17

57918685

+DHCR7chr11

71152487

-
ChimerDB4BRCATCGA-E9-A22D-01AVMP1chr17

57918685

+DHCR7chr11

71152487

-
ChimerDB4BRCATCGA-E9-A22D-01AVMP1chr17

57915573

+DHCR7chr11

71152486

-


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Fusion Gene ORF analysis for VMP1-DHCR7

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-3CDSENST00000262291ENST00000407721VMP1chr17

57918685

+DHCR7chr11

71152487

-
intron-3CDSENST00000262291ENST00000355527VMP1chr17

57918685

+DHCR7chr11

71152487

-
intron-3CDSENST00000537567ENST00000407721VMP1chr17

57918685

+DHCR7chr11

71152487

-
intron-3CDSENST00000537567ENST00000355527VMP1chr17

57918685

+DHCR7chr11

71152487

-
intron-3CDSENST00000539763ENST00000407721VMP1chr17

57918685

+DHCR7chr11

71152487

-
intron-3CDSENST00000539763ENST00000355527VMP1chr17

57918685

+DHCR7chr11

71152487

-
intron-3CDSENST00000536180ENST00000407721VMP1chr17

57918685

+DHCR7chr11

71152487

-
intron-3CDSENST00000536180ENST00000355527VMP1chr17

57918685

+DHCR7chr11

71152487

-
intron-3CDSENST00000545362ENST00000407721VMP1chr17

57918685

+DHCR7chr11

71152487

-
intron-3CDSENST00000545362ENST00000355527VMP1chr17

57918685

+DHCR7chr11

71152487

-
intron-3CDSENST00000588617ENST00000407721VMP1chr17

57918685

+DHCR7chr11

71152487

-
intron-3CDSENST00000588617ENST00000355527VMP1chr17

57918685

+DHCR7chr11

71152487

-
intron-3CDSENST00000262291ENST00000407721VMP1chr17

57915573

+DHCR7chr11

71152486

-
intron-3CDSENST00000262291ENST00000355527VMP1chr17

57915573

+DHCR7chr11

71152486

-
intron-3CDSENST00000537567ENST00000407721VMP1chr17

57915573

+DHCR7chr11

71152486

-
intron-3CDSENST00000537567ENST00000355527VMP1chr17

57915573

+DHCR7chr11

71152486

-
intron-3CDSENST00000539763ENST00000407721VMP1chr17

57915573

+DHCR7chr11

71152486

-
intron-3CDSENST00000539763ENST00000355527VMP1chr17

57915573

+DHCR7chr11

71152486

-
intron-3CDSENST00000536180ENST00000407721VMP1chr17

57915573

+DHCR7chr11

71152486

-
intron-3CDSENST00000536180ENST00000355527VMP1chr17

57915573

+DHCR7chr11

71152486

-
intron-3CDSENST00000545362ENST00000407721VMP1chr17

57915573

+DHCR7chr11

71152486

-
intron-3CDSENST00000545362ENST00000355527VMP1chr17

57915573

+DHCR7chr11

71152486

-
3UTR-3CDSENST00000588617ENST00000407721VMP1chr17

57915573

+DHCR7chr11

71152486

-
3UTR-3CDSENST00000588617ENST00000355527VMP1chr17

57915573

+DHCR7chr11

71152486

-

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 VMP1-DHCR7


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 VMP1-DHCR7


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
.DHCR7

Q9UBM7

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: 7-dehydrocholesterol reductase of the cholesterol biosynthetic pathway reducing the C7-C8 double bond of cholesta-5,7-dien-3beta-ol (7-dehydrocholesterol/7-DHC) and cholesta-5,7,24-trien-3beta-ol, two intermidiates in that pathway. {ECO:0000269|PubMed:25637936, ECO:0000269|PubMed:9465114, ECO:0000269|PubMed:9634533}.

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 VMP1-DHCR7


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 VMP1-DHCR7


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 VMP1-DHCR7


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneDHCR7Q9UBM7DB00157NADHSmall moleculeApproved|Nutraceutical
TgeneDHCR7Q9UBM7DB00157NADHSmall moleculeApproved|Nutraceutical

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Related Diseases for VMP1-DHCR7


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneDHCR7C0175694Smith-Lemli-Opitz Syndrome35CLINGEN;CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneDHCR7C0282643Smith-Lemli-Opitz Syndrome, Type I11CTD_human
TgeneDHCR7C0282644Smith-Lemli-Opitz Syndrome, Type II11CTD_human
TgeneDHCR7C27133477-Dehydrocholesterol Reductase Deficiency11CTD_human
TgeneDHCR7C0004352Autistic Disorder1CTD_human
TgeneDHCR7C0005944Metabolic Bone Disorder1CTD_human
TgeneDHCR7C0023890Liver Cirrhosis1CTD_human
TgeneDHCR7C0029453Osteopenia1CTD_human
TgeneDHCR7C0036875Disorders of Sex Development1GENOMICS_ENGLAND
TgeneDHCR7C0086543Cataract1GENOMICS_ENGLAND
TgeneDHCR7C0239946Fibrosis, Liver1CTD_human
TgeneDHCR7C3714756Intellectual Disability1GENOMICS_ENGLAND