FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:C19orf25-REEP6 (FusionGDB2 ID:11240)

Fusion Gene Summary for C19orf25-REEP6

check button Fusion gene summary
Fusion gene informationFusion gene name: C19orf25-REEP6
Fusion gene ID: 11240
HgeneTgene
Gene symbol

C19orf25

REEP6

Gene ID

148223

92840

Gene namechromosome 19 open reading frame 25receptor accessory protein 6
Synonyms-C19orf32|DP1L1|REEP6.1|REEP6.2|RP77|TB2L1|Yip2f
Cytomap

19p13.3

19p13.3

Type of geneprotein-codingprotein-coding
DescriptionUPF0449 protein C19orf25receptor expression-enhancing protein 6deleted in polyposis 1-like 1polyposis locus protein 1-like 1
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000588427, ENST00000436106, 
ENST00000588871, ENST00000427685, 
ENST00000588849, ENST00000586564, 
ENST00000592872, ENST00000585675, 
ENST00000591027, 
ENST00000233596, 
Fusion gene scores* DoF score10 X 4 X 9=3602 X 3 X 2=12
# samples 123
** MAII scorelog2(12/360*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/12*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: C19orf25 [Title/Abstract] AND REEP6 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointC19orf25(1478773)-REEP6(1497173), # samples:1
Anticipated loss of major functional domain due to fusion event.C19orf25-REEP6 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
* 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 buttonFusion gene breakpoints across C19orf25 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across REEP6 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4TGCTTCGA-XE-AANI-01AC19orf25chr19

1478773

-REEP6chr19

1497173

+


Top

Fusion Gene ORF analysis for C19orf25-REEP6

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
Frame-shiftENST00000588427ENST00000233596C19orf25chr19

1478773

-REEP6chr19

1497173

+
Frame-shiftENST00000436106ENST00000233596C19orf25chr19

1478773

-REEP6chr19

1497173

+
Frame-shiftENST00000588871ENST00000233596C19orf25chr19

1478773

-REEP6chr19

1497173

+
intron-3CDSENST00000427685ENST00000233596C19orf25chr19

1478773

-REEP6chr19

1497173

+
Frame-shiftENST00000588849ENST00000233596C19orf25chr19

1478773

-REEP6chr19

1497173

+
Frame-shiftENST00000586564ENST00000233596C19orf25chr19

1478773

-REEP6chr19

1497173

+
Frame-shiftENST00000592872ENST00000233596C19orf25chr19

1478773

-REEP6chr19

1497173

+
In-frameENST00000585675ENST00000233596C19orf25chr19

1478773

-REEP6chr19

1497173

+
5UTR-3CDSENST00000591027ENST00000233596C19orf25chr19

1478773

-REEP6chr19

1497173

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

Top

Fusion Genomic Features for C19orf25-REEP6


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)
C19orf25chr191478772-REEP6chr191497172+3.28E-050.9999672
C19orf25chr191478772-REEP6chr191497172+3.28E-050.9999672

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

Top

Fusion Protein Features for C19orf25-REEP6


check button Go to

FGviewer for the breakpoints of chr19:1478773-chr19:1497173

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
..
FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

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
HgeneC19orf25chr19:1478773chr19:1497173ENST00000436106-2381_10943.333333333333336119.0Coiled coilOntology_term=ECO:0000255
HgeneC19orf25chr19:1478773chr19:1497173ENST00000585675-2381_10943.333333333333336119.0Coiled coilOntology_term=ECO:0000255
HgeneC19orf25chr19:1478773chr19:1497173ENST00000586564-1281_10943.333333333333336119.0Coiled coilOntology_term=ECO:0000255
HgeneC19orf25chr19:1478773chr19:1497173ENST00000592872-2381_10943.333333333333336119.0Coiled coilOntology_term=ECO:0000255
TgeneREEP6chr19:1478773chr19:1497173ENST000002335963544_64172.33333333333334185.0TransmembraneHelical
TgeneREEP6chr19:1478773chr19:1497173ENST000002335963589_109172.33333333333334185.0TransmembraneHelical


Top

Fusion Gene Sequence for C19orf25-REEP6


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

Top

Fusion Gene PPI Analysis for C19orf25-REEP6


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


Top

Related Drugs for C19orf25-REEP6


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

Top

Related Diseases for C19orf25-REEP6


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneREEP6C4310626RETINITIS PIGMENTOSA 774CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneREEP6C0035334Retinitis Pigmentosa2GENOMICS_ENGLAND;ORPHANET