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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: 25329

FusionGeneSummary for OAZ1_PLP1

check button Fusion gene summary
Fusion gene informationFusion gene name: OAZ1_PLP1
Fusion gene ID: 25329
HgeneTgene
Gene symbol

OAZ1

PLP1

Gene ID

4946

5354

Gene nameornithine decarboxylase antizyme 1proteolipid protein 1
SynonymsAZ1|AZI|OAZGPM6C|HLD1|MMPL|PLP|PLP/DM20|PMD|SPG2
Cytomap

19p13.3

Xq22.2

Type of geneprotein-codingprotein-coding
Descriptionornithine decarboxylase antizyme 1ODC-Azantizyme 1myelin proteolipid proteinlipophilinmajor myelin proteolipid protein
Modification date2018052320180523
UniProtAcc

P54368

P60201

Ensembl transtripts involved in fusion geneENST00000582888, ENST00000602676, 
ENST00000322297, ENST00000583542, 
ENST00000588673, 
ENST00000418604, 
ENST00000303958, ENST00000361621, 
ENST00000466486, 
Fusion gene scores* DoF score8 X 6 X 4=1929 X 8 X 2=144
# samples 99
** MAII scorelog2(9/192*10)=-1.09310940439148
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/144*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: OAZ1 [Title/Abstract] AND PLP1 [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
HgeneOAZ1

GO:0045732

positive regulation of protein catabolic process

17900240


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
ChiTaRS3.1DA327340OAZ1chr19

2269577

+PLP1chrX

103031802

+
* 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
5UTR-5UTRENST00000582888ENST00000418604OAZ1chr19

2269577

+PLP1chrX

103031802

+
5UTR-5UTRENST00000582888ENST00000303958OAZ1chr19

2269577

+PLP1chrX

103031802

+
5UTR-5UTRENST00000582888ENST00000361621OAZ1chr19

2269577

+PLP1chrX

103031802

+
5UTR-intronENST00000582888ENST00000466486OAZ1chr19

2269577

+PLP1chrX

103031802

+
5UTR-5UTRENST00000602676ENST00000418604OAZ1chr19

2269577

+PLP1chrX

103031802

+
5UTR-5UTRENST00000602676ENST00000303958OAZ1chr19

2269577

+PLP1chrX

103031802

+
5UTR-5UTRENST00000602676ENST00000361621OAZ1chr19

2269577

+PLP1chrX

103031802

+
5UTR-intronENST00000602676ENST00000466486OAZ1chr19

2269577

+PLP1chrX

103031802

+
5UTR-5UTRENST00000322297ENST00000418604OAZ1chr19

2269577

+PLP1chrX

103031802

+
5UTR-5UTRENST00000322297ENST00000303958OAZ1chr19

2269577

+PLP1chrX

103031802

+
5UTR-5UTRENST00000322297ENST00000361621OAZ1chr19

2269577

+PLP1chrX

103031802

+
5UTR-intronENST00000322297ENST00000466486OAZ1chr19

2269577

+PLP1chrX

103031802

+
5UTR-5UTRENST00000583542ENST00000418604OAZ1chr19

2269577

+PLP1chrX

103031802

+
5UTR-5UTRENST00000583542ENST00000303958OAZ1chr19

2269577

+PLP1chrX

103031802

+
5UTR-5UTRENST00000583542ENST00000361621OAZ1chr19

2269577

+PLP1chrX

103031802

+
5UTR-intronENST00000583542ENST00000466486OAZ1chr19

2269577

+PLP1chrX

103031802

+
intron-5UTRENST00000588673ENST00000418604OAZ1chr19

2269577

+PLP1chrX

103031802

+
intron-5UTRENST00000588673ENST00000303958OAZ1chr19

2269577

+PLP1chrX

103031802

+
intron-5UTRENST00000588673ENST00000361621OAZ1chr19

2269577

+PLP1chrX

103031802

+
intron-intronENST00000588673ENST00000466486OAZ1chr19

2269577

+PLP1chrX

103031802

+

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FusionProtFeatures for OAZ1_PLP1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
OAZ1

P54368

PLP1

P60201

Ornithine decarboxylase (ODC) antizyme protein thatnegatively regulates ODC activity and intracellular polyaminebiosynthesis and uptake in response to increased intracellularpolyamine levels. Binds to ODC monomers, inhibiting the assemblyof the functional ODC homodimer, and targets the monomers forubiquitin-independent proteolytic destruction by the 26Sproteasome (PubMed:17900240, PubMed:26305948, PubMed:26443277).Triggers ODC degradation by inducing the exposure of a crypticproteasome-interacting surface of ODC (PubMed:26305948).Stabilizes AZIN2 by interfering with its ubiquitination(PubMed:17900240). Also inhibits cellular uptake of polyamines byinactivating the polyamine uptake transporter. SMAD1/OAZ1/PSMB4complex mediates the degradation of the CREBBP/EP300 repressorSNIP1. Involved in the translocation of AZIN2 from ER-Golgiintermediate compartment (ERGIC) to the cytosol (PubMed:12097147).{ECO:0000269|PubMed:12097147, ECO:0000269|PubMed:17900240,ECO:0000269|PubMed:26305948, ECO:0000269|PubMed:26443277}. This is the major myelin protein from the centralnervous system. It plays an important role in the formation ormaintenance of the multilamellar structure of myelin.

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 OAZ1_PLP1


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 OAZ1_PLP1


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 OAZ1_PLP1


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 OAZ1_PLP1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgenePLP1C0205711Pelizaeus-Merzbacher Disease31CTD_human;HPO;UNIPROT
TgenePLP1C1839264SPASTIC PARAPLEGIA 2, X-LINKED (disorder)9CTD_human;ORPHANET;UNIPROT
TgenePLP1C0036341Schizophrenia4PSYGENET
TgenePLP1C0009171Cocaine Abuse2PSYGENET
TgenePLP1C2673482Increased susceptibility to schizophrenia1PSYGENET