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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: 27945

FusionGeneSummary for POLN_PITPNC1

check button Fusion gene summary
Fusion gene informationFusion gene name: POLN_PITPNC1
Fusion gene ID: 27945
HgeneTgene
Gene symbol

POLN

PITPNC1

Gene ID

353497

26207

Gene nameDNA polymerase nuphosphatidylinositol transfer protein cytoplasmic 1
SynonymsPOL4PM-RDGB-beta|MRDGBbeta|RDGB-BETA|RDGBB|RDGBB1
Cytomap

4p16.3

17q24.2

Type of geneprotein-codingprotein-coding
DescriptionDNA polymerase nuDNA polymerase NDNA polymerase POL4Ppolymerase (DNA directed) nupolymerase (DNA) nucytoplasmic phosphatidylinositol transfer protein 1M-rdgB betamammalian rdgB homolog betaretinal degeneration B beta 1retinal degeneration B homolog beta
Modification date2018052320180523
UniProtAcc

Q7Z5Q5

Q9UKF7

Ensembl transtripts involved in fusion geneENST00000382865, ENST00000511885, 
ENST00000515357, 
ENST00000580974, 
ENST00000299954, ENST00000335257, 
ENST00000581322, 
Fusion gene scores* DoF score3 X 3 X 1=923 X 12 X 9=2484
# samples 326
** MAII scorelog2(3/9*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(26/2484*10)=-3.25608164519203
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: POLN [Title/Abstract] AND PITPNC1 [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
HgenePOLN

GO:0019985

translesion synthesis

20102227

TgenePITPNC1

GO:0015914

phospholipid transport

22822086


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
ChiTaRS3.1AW902492POLNchr4

2091761

-PITPNC1chr17

65479397

+
* 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-intronENST00000382865ENST00000580974POLNchr4

2091761

-PITPNC1chr17

65479397

+
intron-intronENST00000382865ENST00000299954POLNchr4

2091761

-PITPNC1chr17

65479397

+
intron-intronENST00000382865ENST00000335257POLNchr4

2091761

-PITPNC1chr17

65479397

+
intron-intronENST00000382865ENST00000581322POLNchr4

2091761

-PITPNC1chr17

65479397

+
intron-intronENST00000511885ENST00000580974POLNchr4

2091761

-PITPNC1chr17

65479397

+
intron-intronENST00000511885ENST00000299954POLNchr4

2091761

-PITPNC1chr17

65479397

+
intron-intronENST00000511885ENST00000335257POLNchr4

2091761

-PITPNC1chr17

65479397

+
intron-intronENST00000511885ENST00000581322POLNchr4

2091761

-PITPNC1chr17

65479397

+
intron-intronENST00000515357ENST00000580974POLNchr4

2091761

-PITPNC1chr17

65479397

+
intron-intronENST00000515357ENST00000299954POLNchr4

2091761

-PITPNC1chr17

65479397

+
intron-intronENST00000515357ENST00000335257POLNchr4

2091761

-PITPNC1chr17

65479397

+
intron-intronENST00000515357ENST00000581322POLNchr4

2091761

-PITPNC1chr17

65479397

+

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FusionProtFeatures for POLN_PITPNC1


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

Q7Z5Q5

PITPNC1

Q9UKF7

DNA polymerase with very low fidelity that catalyzesconsiderable misincorporation by inserting dTTP opposite a Gtemplate, and dGTP opposite a T template (PubMed:16787914,PubMed:17118716). Is the least accurate of the DNA polymerase Afamily (i.e. POLG, POLN and POLQ) (PubMed:17118716). Can performaccurate translesion DNA synthesis (TLS) past a 5S-thymine glycol.Can perform efficient strand displacement past a nick or a gap andgives rise to an amount of product similar to that on non-damagedtemplate. Has no exonuclease activity (PubMed:16787914). Error-prone DNA polymerase that preferentially misincorporates dTregardless of template sequence (PubMed:25775266). May play a rolein TLS during interstrand cross-link (ICL) repair(PubMed:19908865). May be involved in TLS when genomic replicationis blocked by extremely large major groove DNA lesions. Mayfunction in the bypass of some DNA-protein and DNA-DNA cross-links. May have a role in cellular tolerance to DNA cross-linkingagents (PubMed:20102227). Involved in the repair of DNA cross-links and double-strand break (DSB) resistance. Participates inFANCD2-mediated repair. Forms a complex with HELQ helicase thatparticipates in homologous recombination (HR) repair and isessential for cellular protection against DNA cross-links(PubMed:19995904). {ECO:0000269|PubMed:16787914,ECO:0000269|PubMed:17118716, ECO:0000269|PubMed:19908865,ECO:0000269|PubMed:19995904, ECO:0000269|PubMed:20102227,ECO:0000269|PubMed:25775266}. Phosphatidylinositol transfer proteins mediate themonomeric transport of lipids by shielding a lipid from theaqueous environment and binding the lipid in a hydrophobic cavity.Able to transfer phosphatidylinositol in vitro.{ECO:0000269|PubMed:10531358}.

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 POLN_PITPNC1


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 POLN_PITPNC1


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 POLN_PITPNC1


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 POLN_PITPNC1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource