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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: 25894

FusionGeneSummary for PANK2_VAMP3

check button Fusion gene summary
Fusion gene informationFusion gene name: PANK2_VAMP3
Fusion gene ID: 25894
HgeneTgene
Gene symbol

PANK2

VAMP3

Gene ID

80025

9341

Gene namepantothenate kinase 2vesicle associated membrane protein 3
SynonymsC20orf48|HARP|HSS|NBIA1|PKANCEB
Cytomap

20p13

1p36.23

Type of geneprotein-codingprotein-coding
Descriptionpantothenate kinase 2, mitochondrialHallervorden-Spatz syndromepantothenic acid kinase 2vesicle-associated membrane protein 3VAMP-3cellubrevinsynaptobrevin-3
Modification date2018052220180527
UniProtAcc

Q9BZ23

Q15836

Ensembl transtripts involved in fusion geneENST00000497424, ENST00000316562, 
ENST00000610179, ENST00000464452, 
ENST00000054666, ENST00000470357, 
Fusion gene scores* DoF score6 X 4 X 4=964 X 4 X 3=48
# samples 64
** MAII scorelog2(6/96*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PANK2 [Title/Abstract] AND VAMP3 [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
TgeneVAMP3

GO:0042147

retrograde transport, endosome to Golgi

18195106

TgeneVAMP3

GO:1903531

negative regulation of secretion by cell

12130530


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
ChiTaRS3.1BF896192PANK2chr20

3870763

+VAMP3chr1

7839660

+
* 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-intronENST00000497424ENST00000054666PANK2chr20

3870763

+VAMP3chr1

7839660

+
intron-intronENST00000497424ENST00000470357PANK2chr20

3870763

+VAMP3chr1

7839660

+
intron-intronENST00000316562ENST00000054666PANK2chr20

3870763

+VAMP3chr1

7839660

+
intron-intronENST00000316562ENST00000470357PANK2chr20

3870763

+VAMP3chr1

7839660

+
intron-intronENST00000610179ENST00000054666PANK2chr20

3870763

+VAMP3chr1

7839660

+
intron-intronENST00000610179ENST00000470357PANK2chr20

3870763

+VAMP3chr1

7839660

+
intron-intronENST00000464452ENST00000054666PANK2chr20

3870763

+VAMP3chr1

7839660

+
intron-intronENST00000464452ENST00000470357PANK2chr20

3870763

+VAMP3chr1

7839660

+

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FusionProtFeatures for PANK2_VAMP3


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
PANK2

Q9BZ23

VAMP3

Q15836

SNARE involved in vesicular transport from the lateendosomes to the trans-Golgi network.{ECO:0000269|PubMed:18195106}.

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 PANK2_VAMP3


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 PANK2_VAMP3


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 PANK2_VAMP3


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 PANK2_VAMP3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePANK2C0018523Hallervorden-Spatz Syndrome5CTD_human;UNIPROT
HgenePANK2C0524851Neurodegenerative Disorders2CTD_human
HgenePANK2C0027746Nerve Degeneration1CTD_human
HgenePANK2C0036341Schizophrenia1PSYGENET
HgenePANK2C2931845Neurodegeneration with brain iron accumulation (NBIA)1CTD_human
TgeneVAMP3C0005586Bipolar Disorder1PSYGENET
TgeneVAMP3C1839839MAJOR AFFECTIVE DISORDER 21PSYGENET