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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: 31524

FusionGeneSummary for RNF213_PPM1L

check button Fusion gene summary
Fusion gene informationFusion gene name: RNF213_PPM1L
Fusion gene ID: 31524
HgeneTgene
Gene symbol

RNF213

PPM1L

Gene ID

57674

151742

Gene namering finger protein 213protein phosphatase, Mg2+/Mn2+ dependent 1L
SynonymsALO17|C17orf27|KIAA1618|MYMY2|MYSTR|NET57PP2C-epsilon|PP2CE|PPM1-LIKE
Cytomap

17q25.3

3q25.33-q26.1

Type of geneprotein-codingprotein-coding
DescriptionE3 ubiquitin-protein ligase RNF213ALK lymphoma oligomerization partner on chromosome 17RING-type E3 ubiquitin transferase RNF213mysterinprotein phosphatase 1LPP2C epsilonProtein phosphatase 2C epsilon isoformprotein phosphatase 2C isoform epsilon
Modification date2018052720180519
UniProtAcc

Q63HN8

Q5SGD2

Ensembl transtripts involved in fusion geneENST00000508628, ENST00000456466, 
ENST00000582970, ENST00000319921, 
ENST00000336301, ENST00000427003, 
ENST00000497343, ENST00000498165, 
ENST00000464260, ENST00000295839, 
ENST00000480117, 
Fusion gene scores* DoF score22 X 22 X 12=58082 X 2 X 2=8
# samples 302
** MAII scorelog2(30/5808*10)=-4.27500704749987
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: RNF213 [Title/Abstract] AND PPM1L [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
HgeneRNF213

GO:0016567

protein ubiquitination

21799892

HgeneRNF213

GO:0051260

protein homooligomerization

24658080|26126547

HgeneRNF213

GO:0051865

protein autoubiquitination

21799892


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
ChiTaRS3.1AK025676RNF213chr17

78368151

+PPM1Lchr3

160744481

+
* 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
3UTR-intronENST00000508628ENST00000497343RNF213chr17

78368151

+PPM1Lchr3

160744481

+
3UTR-intronENST00000508628ENST00000498165RNF213chr17

78368151

+PPM1Lchr3

160744481

+
3UTR-intronENST00000508628ENST00000464260RNF213chr17

78368151

+PPM1Lchr3

160744481

+
3UTR-intronENST00000508628ENST00000295839RNF213chr17

78368151

+PPM1Lchr3

160744481

+
3UTR-intronENST00000508628ENST00000480117RNF213chr17

78368151

+PPM1Lchr3

160744481

+
intron-intronENST00000456466ENST00000497343RNF213chr17

78368151

+PPM1Lchr3

160744481

+
intron-intronENST00000456466ENST00000498165RNF213chr17

78368151

+PPM1Lchr3

160744481

+
intron-intronENST00000456466ENST00000464260RNF213chr17

78368151

+PPM1Lchr3

160744481

+
intron-intronENST00000456466ENST00000295839RNF213chr17

78368151

+PPM1Lchr3

160744481

+
intron-intronENST00000456466ENST00000480117RNF213chr17

78368151

+PPM1Lchr3

160744481

+
3UTR-intronENST00000582970ENST00000497343RNF213chr17

78368151

+PPM1Lchr3

160744481

+
3UTR-intronENST00000582970ENST00000498165RNF213chr17

78368151

+PPM1Lchr3

160744481

+
3UTR-intronENST00000582970ENST00000464260RNF213chr17

78368151

+PPM1Lchr3

160744481

+
3UTR-intronENST00000582970ENST00000295839RNF213chr17

78368151

+PPM1Lchr3

160744481

+
3UTR-intronENST00000582970ENST00000480117RNF213chr17

78368151

+PPM1Lchr3

160744481

+
intron-intronENST00000319921ENST00000497343RNF213chr17

78368151

+PPM1Lchr3

160744481

+
intron-intronENST00000319921ENST00000498165RNF213chr17

78368151

+PPM1Lchr3

160744481

+
intron-intronENST00000319921ENST00000464260RNF213chr17

78368151

+PPM1Lchr3

160744481

+
intron-intronENST00000319921ENST00000295839RNF213chr17

78368151

+PPM1Lchr3

160744481

+
intron-intronENST00000319921ENST00000480117RNF213chr17

78368151

+PPM1Lchr3

160744481

+
3UTR-intronENST00000336301ENST00000497343RNF213chr17

78368151

+PPM1Lchr3

160744481

+
3UTR-intronENST00000336301ENST00000498165RNF213chr17

78368151

+PPM1Lchr3

160744481

+
3UTR-intronENST00000336301ENST00000464260RNF213chr17

78368151

+PPM1Lchr3

160744481

+
3UTR-intronENST00000336301ENST00000295839RNF213chr17

78368151

+PPM1Lchr3

160744481

+
3UTR-intronENST00000336301ENST00000480117RNF213chr17

78368151

+PPM1Lchr3

160744481

+
3UTR-intronENST00000427003ENST00000497343RNF213chr17

78368151

+PPM1Lchr3

160744481

+
3UTR-intronENST00000427003ENST00000498165RNF213chr17

78368151

+PPM1Lchr3

160744481

+
3UTR-intronENST00000427003ENST00000464260RNF213chr17

78368151

+PPM1Lchr3

160744481

+
3UTR-intronENST00000427003ENST00000295839RNF213chr17

78368151

+PPM1Lchr3

160744481

+
3UTR-intronENST00000427003ENST00000480117RNF213chr17

78368151

+PPM1Lchr3

160744481

+

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FusionProtFeatures for RNF213_PPM1L


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
RNF213

Q63HN8

PPM1L

Q5SGD2

Acts as a suppressor of the SAPK signaling pathways byassociating with and dephosphorylating MAP3K7/TAK1 and MAP3K5, andby attenuating the association between MAP3K7/TAK1 and MAP2K4 orMAP2K6. {ECO:0000269|PubMed:17456047}.

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 RNF213_PPM1L


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 RNF213_PPM1L


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 RNF213_PPM1L


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 RNF213_PPM1L


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneRNF213C1846689MOYAMOYA DISEASE 23UNIPROT
TgenePPM1LC0028754Obesity1CTD_human