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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: 28991

FusionGeneSummary for PRRC2C_PRRX1

check button Fusion gene summary
Fusion gene informationFusion gene name: PRRC2C_PRRX1
Fusion gene ID: 28991
HgeneTgene
Gene symbol

PRRC2C

PRRX1

Gene ID

23215

5396

Gene nameproline rich coiled-coil 2Cpaired related homeobox 1
SynonymsBAT2-iso|BAT2D1|BAT2L2|XTP2AGOTC|PHOX1|PMX1|PRX-1|PRX1
Cytomap

1q24.3

1q24.2

Type of geneprotein-codingprotein-coding
Descriptionprotein PRRC2CBAT2 domain containing 1BAT2 domain-containing protein 1HBV X-transactivated gene 2 proteinHBV XAg-transactivated protein 2HBxAg transactivated protein 2HLA-B-associated transcript 2-like 2proline-rich and coiled-coil-containing protepaired mesoderm homeobox protein 1homeobox protein PHOX1paired mesoderm homeobox 1 isoform pmx-1b
Modification date2018052320180519
UniProtAcc

Q9Y520

P54821

Ensembl transtripts involved in fusion geneENST00000426496, ENST00000392078, 
ENST00000476522, ENST00000367742, 
ENST00000338920, 
ENST00000367760, 
ENST00000239461, ENST00000497230, 
ENST00000476867, 
Fusion gene scores* DoF score12 X 13 X 5=7803 X 3 X 2=18
# samples 173
** MAII scorelog2(17/780*10)=-2.19793937761191
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: PRRC2C [Title/Abstract] AND PRRX1 [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

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
TCGALDPRADTCGA-KK-A5A1-01APRRC2Cchr1

171454874

+PRRX1chr1

170688867

+
* 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-3CDSENST00000426496ENST00000367760PRRC2Cchr1

171454874

+PRRX1chr1

170688867

+
5UTR-3CDSENST00000426496ENST00000239461PRRC2Cchr1

171454874

+PRRX1chr1

170688867

+
5UTR-3CDSENST00000426496ENST00000497230PRRC2Cchr1

171454874

+PRRX1chr1

170688867

+
5UTR-intronENST00000426496ENST00000476867PRRC2Cchr1

171454874

+PRRX1chr1

170688867

+
5UTR-3CDSENST00000392078ENST00000367760PRRC2Cchr1

171454874

+PRRX1chr1

170688867

+
5UTR-3CDSENST00000392078ENST00000239461PRRC2Cchr1

171454874

+PRRX1chr1

170688867

+
5UTR-3CDSENST00000392078ENST00000497230PRRC2Cchr1

171454874

+PRRX1chr1

170688867

+
5UTR-intronENST00000392078ENST00000476867PRRC2Cchr1

171454874

+PRRX1chr1

170688867

+
3UTR-3CDSENST00000476522ENST00000367760PRRC2Cchr1

171454874

+PRRX1chr1

170688867

+
3UTR-3CDSENST00000476522ENST00000239461PRRC2Cchr1

171454874

+PRRX1chr1

170688867

+
3UTR-3CDSENST00000476522ENST00000497230PRRC2Cchr1

171454874

+PRRX1chr1

170688867

+
3UTR-intronENST00000476522ENST00000476867PRRC2Cchr1

171454874

+PRRX1chr1

170688867

+
5UTR-3CDSENST00000367742ENST00000367760PRRC2Cchr1

171454874

+PRRX1chr1

170688867

+
5UTR-3CDSENST00000367742ENST00000239461PRRC2Cchr1

171454874

+PRRX1chr1

170688867

+
5UTR-3CDSENST00000367742ENST00000497230PRRC2Cchr1

171454874

+PRRX1chr1

170688867

+
5UTR-intronENST00000367742ENST00000476867PRRC2Cchr1

171454874

+PRRX1chr1

170688867

+
5UTR-3CDSENST00000338920ENST00000367760PRRC2Cchr1

171454874

+PRRX1chr1

170688867

+
5UTR-3CDSENST00000338920ENST00000239461PRRC2Cchr1

171454874

+PRRX1chr1

170688867

+
5UTR-3CDSENST00000338920ENST00000497230PRRC2Cchr1

171454874

+PRRX1chr1

170688867

+
5UTR-intronENST00000338920ENST00000476867PRRC2Cchr1

171454874

+PRRX1chr1

170688867

+

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FusionProtFeatures for PRRC2C_PRRX1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
PRRC2C

Q9Y520

PRRX1

P54821

Acts as a transcriptional regulator of muscle creatinekinase (MCK) and so has a role in the establishment of diversemesodermal muscle types. The protein binds to an A/T-rich elementin the muscle creatine enhancer (By similarity). {ECO:0000250}.

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 PRRC2C_PRRX1


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 PRRC2C_PRRX1


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
PRRC2CELAVL1, SIRT7, HINFP, ITGA4, TARDBP, PARK2, LGR4, CSNK2A2, SHFM1, AURKA, AURKB, CEP57, HAUS2, CEP76, LGALS3BP, TP53, QPRT, FBL, RABGGTB, PRMT8, ZFP41, NTRK1, SRPK2, RPL10, C10orf12, FOXK2, ATOH1, JPH4, SNRNP70, CHCHD10, TRPC4AP, SFPQ, CYLD, TRIM25, G3BP1PRRX1GTF2I


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 PRRC2C_PRRX1


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 PRRC2C_PRRX1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgenePRRX1C1876185Dysgnathia complex2CTD_human;ORPHANET;UNIPROT
TgenePRRX1C0004238Atrial Fibrillation1CTD_human
TgenePRRX1C0033578Prostatic Neoplasms1CTD_human
TgenePRRX1C3494422Retrognathia1CTD_human