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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: 3461

FusionGeneSummary for ATP6V1B2_ATP6V1B2

check button Fusion gene summary
Fusion gene informationFusion gene name: ATP6V1B2_ATP6V1B2
Fusion gene ID: 3461
HgeneTgene
Gene symbol

ATP6V1B2

ATP6V1B2

Gene ID

526

526

Gene nameATPase H+ transporting V1 subunit B2ATPase H+ transporting V1 subunit B2
SynonymsATP6B1B2|ATP6B2|DOOD|HO57|VATB|VPP3|Vma2|ZLS2ATP6B1B2|ATP6B2|DOOD|HO57|VATB|VPP3|Vma2|ZLS2
Cytomap

8p21.3

8p21.3

Type of geneprotein-codingprotein-coding
DescriptionV-type proton ATPase subunit B, brain isoformATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B2H+ transporting two-sector ATPaseV-ATPase B2 subunitV-ATPase subunit B 2endomembrane proton pump 58 kDa subunittesticular secretory protein Li 65V-type proton ATPase subunit B, brain isoformATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B2H+ transporting two-sector ATPaseV-ATPase B2 subunitV-ATPase subunit B 2endomembrane proton pump 58 kDa subunittesticular secretory protein Li 65
Modification date2018052220180522
UniProtAcc

P21281

P21281

Ensembl transtripts involved in fusion geneENST00000276390, ENST00000276390, 
Fusion gene scores* DoF score2 X 2 X 2=81 X 1 X 1=1
# samples 21
** MAII scorelog2(2/8*10)=1.32192809488736log2(1/1*10)=3.32192809488736
Context

PubMed: ATP6V1B2 [Title/Abstract] AND ATP6V1B2 [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

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
ChiTaRS3.1BF591113ATP6V1B2chr8

20077869

-ATP6V1B2chr8

20078119

-
* 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
5CDS-3UTRENST00000276390ENST00000276390ATP6V1B2chr8

20077869

-ATP6V1B2chr8

20078119

-

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FusionProtFeatures for ATP6V1B2_ATP6V1B2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ATP6V1B2

P21281

ATP6V1B2

P21281

Non-catalytic subunit of the peripheral V1 complex ofvacuolar ATPase. V-ATPase is responsible for acidifying a varietyof intracellular compartments in eukaryotic cells. Non-catalytic subunit of the peripheral V1 complex ofvacuolar ATPase. V-ATPase is responsible for acidifying a varietyof intracellular compartments in eukaryotic cells.

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 ATP6V1B2_ATP6V1B2


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 ATP6V1B2_ATP6V1B2


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 ATP6V1B2_ATP6V1B2


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 ATP6V1B2_ATP6V1B2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneATP6V1B2C0024301Lymphoma, Follicular1CTD_human
HgeneATP6V1B2C0029408Degenerative polyarthritis1CTD_human
HgeneATP6V1B2C0796013Zimmerman Laband syndrome1CTD_human;ORPHANET
HgeneATP6V1B2C4225321ZIMMERMANN-LABAND SYNDROME 21UNIPROT
TgeneATP6V1B2C0024301Lymphoma, Follicular1CTD_human
TgeneATP6V1B2C0029408Degenerative polyarthritis1CTD_human
TgeneATP6V1B2C0796013Zimmerman Laband syndrome1CTD_human;ORPHANET
TgeneATP6V1B2C4225321ZIMMERMANN-LABAND SYNDROME 21UNIPROT