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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 15754

FusionGeneSummary for H19_VCPIP1

check button Fusion gene summary
Fusion gene informationFusion gene name: H19_VCPIP1
Fusion gene ID: 15754
HgeneTgene
Gene symbol

H19

VCPIP1

Gene ID

283120

80124

Gene nameH19, imprinted maternally expressed transcriptvalosin containing protein interacting protein 1
SynonymsASM|ASM1|BWS|D11S813E|LINC00008|NCRNA00008|WT2DUBA3|VCIP135
Cytomap

11p15.5

8q13.1

Type of genencRNAprotein-coding
DescriptionH19, imprinted maternally expressed transcript (non-protein coding)H19, imprinted maternally expressed untranslated mRNAlong intergenic non-protein coding RNA 8deubiquitinating protein VCIP135VCP/p47 complex-interacting 135-kDa proteinvalosin-containing protein p97/p47 complex-interacting protein 1valosin-containing protein p97/p47 complex-interacting protein p135
Modification date2018052720180522
UniProtAcc

Q96JH7

Ensembl transtripts involved in fusion geneENST00000390168, ENST00000310421, 
Fusion gene scores* DoF score19 X 23 X 1=4371 X 1 X 1=1
# samples 301
** MAII scorelog2(30/437*10)=-0.542670779004717
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: H19 [Title/Abstract] AND VCPIP1 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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
TgeneVCPIP1

GO:0035871

protein K11-linked deubiquitination

23827681

TgeneVCPIP1

GO:0071108

protein K48-linked deubiquitination

23827681


check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS3.1DA444649H19chr11

2018562

-VCPIP1chr8

67546796

-
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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-3CDSENST00000390168ENST00000310421H19chr11

2018562

-VCPIP1chr8

67546796

-

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FusionProtFeatures for H19_VCPIP1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
H19

VCPIP1

Q96JH7

Lectin that binds to various sugars: galactose > mannose= fucose > N-acetylglucosamine > N-acetylgalactosamine(PubMed:10224141). Acts as a chemoattractant, probably involved inthe regulation of cell migration (PubMed:28301481).{ECO:0000269|PubMed:10224141, ECO:0000269|PubMed:28301481}. Acts as a deubiquitinating enzyme. Necessary for VCP-mediated reassembly of Golgi stacks after mitosis. May play a rolein VCP-mediated formation of transitional endoplasmic reticulum(tER). Mediates dissociation of the ternary complex containingSTX5A, NSFL1C and VCP (By similarity). Hydrolyzes 'Lys-11'- and'Lys-48'-linked polyubiquitin chains. {ECO:0000250,ECO:0000269|PubMed:23827681}.

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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FusionGeneSequence for H19_VCPIP1


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for H19_VCPIP1


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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RelatedDrugs for H19_VCPIP1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for H19_VCPIP1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneH19C0019188Hepatitis, Animal1CTD_human
HgeneH19C0023904Liver Neoplasms, Experimental1CTD_human
HgeneH19C0175693Russell-Silver syndrome1CTD_human