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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: 26774

FusionGeneSummary for PFN2_HLCS

check button Fusion gene summary
Fusion gene informationFusion gene name: PFN2_HLCS
Fusion gene ID: 26774
HgeneTgene
Gene symbol

PFN2

HLCS

Gene ID

5217

3141

Gene nameprofilin 2holocarboxylase synthetase
SynonymsD3S1319E|PFLHCS
Cytomap

3q25.1

21q22.13

Type of geneprotein-codingprotein-coding
Descriptionprofilin-2profilin IIbiotin--protein ligasebiotin apo-protein ligasebiotin--[acetyl-CoA-carboxylase] ligasebiotin--[methylcrotonoyl-CoA-carboxylase] ligasebiotin--[methylmalonyl-CoA-carboxytransferase] ligaseholocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase
Modification date2018052320180519
UniProtAcc

P35080

P50747

Ensembl transtripts involved in fusion geneENST00000452853, ENST00000239940, 
ENST00000423691, ENST00000481767, 
ENST00000494827, ENST00000490975, 
ENST00000497148, ENST00000475518, 
ENST00000481275, ENST00000498307, 
ENST00000489155, ENST00000461930, 
ENST00000461868, 
ENST00000336648, 
ENST00000399120, ENST00000482273, 
Fusion gene scores* DoF score3 X 3 X 1=95 X 4 X 4=80
# samples 35
** MAII scorelog2(3/9*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(5/80*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PFN2 [Title/Abstract] AND HLCS [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
HgenePFN2

GO:0030837

negative regulation of actin filament polymerization

7758455

HgenePFN2

GO:0032781

positive regulation of ATPase activity

7758455

HgenePFN2

GO:0050821

protein stabilization

18573880

TgeneHLCS

GO:0009305

protein biotinylation

7842009

TgeneHLCS

GO:0016570

histone modification

14613969

TgeneHLCS

GO:0070781

response to biotin

17904341

TgeneHLCS

GO:0071110

histone biotinylation

14613969


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
ChiTaRS3.1BF366959PFN2chr3

149685233

+HLCSchr21

38268133

+
* 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-intronENST00000452853ENST00000336648PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000452853ENST00000399120PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000452853ENST00000482273PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000239940ENST00000336648PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000239940ENST00000399120PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000239940ENST00000482273PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000423691ENST00000336648PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000423691ENST00000399120PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000423691ENST00000482273PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000481767ENST00000336648PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000481767ENST00000399120PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000481767ENST00000482273PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000494827ENST00000336648PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000494827ENST00000399120PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000494827ENST00000482273PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000490975ENST00000336648PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000490975ENST00000399120PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000490975ENST00000482273PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000497148ENST00000336648PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000497148ENST00000399120PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000497148ENST00000482273PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000475518ENST00000336648PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000475518ENST00000399120PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000475518ENST00000482273PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000481275ENST00000336648PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000481275ENST00000399120PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000481275ENST00000482273PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000498307ENST00000336648PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000498307ENST00000399120PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000498307ENST00000482273PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000489155ENST00000336648PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000489155ENST00000399120PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000489155ENST00000482273PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000461930ENST00000336648PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000461930ENST00000399120PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000461930ENST00000482273PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000461868ENST00000336648PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000461868ENST00000399120PFN2chr3

149685233

+HLCSchr21

38268133

+
intron-intronENST00000461868ENST00000482273PFN2chr3

149685233

+HLCSchr21

38268133

+

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FusionProtFeatures for PFN2_HLCS


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
PFN2

P35080

HLCS

P50747

Binds to actin and affects the structure of thecytoskeleton. At high concentrations, profilin prevents thepolymerization of actin, whereas it enhances it at lowconcentrations. By binding to PIP2, it inhibits the formation ofIP3 and DG. Post-translational modification of specific protein byattachment of biotin. Acts on various carboxylases such as acetyl-CoA-carboxylase, pyruvate carboxylase, propionyl CoA carboxylase,and 3-methylcrotonyl CoA carboxylase.

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 PFN2_HLCS


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 PFN2_HLCS


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 PFN2_HLCS


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneHLCSP50747DB00121BiotinBiotin--protein ligasesmall moleculeapproved|investigational|nutraceutical

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RelatedDiseases for PFN2_HLCS


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneHLCSC0268581Holocarboxylase Synthetase Deficiency10CTD_human;ORPHANET;UNIPROT