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![]() | Fusion Gene Summary |
![]() | Fusion Gene ORF analysis |
![]() | Fusion Genomic Features |
![]() | Fusion Protein Features |
![]() | Fusion Gene Sequence |
![]() | Fusion Gene PPI analysis |
![]() | Related Drugs |
![]() | Related Diseases |
Fusion gene:BRE-PEX14 (FusionGDB2 ID:HG9577TG5195) |
Fusion Gene Summary for BRE-PEX14 |
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Fusion gene information | Fusion gene name: BRE-PEX14 | Fusion gene ID: hg9577tg5195 | Hgene | Tgene | Gene symbol | BRE | PEX14 | Gene ID | 9577 | 5195 |
Gene name | BRISC and BRCA1 A complex member 2 | peroxisomal biogenesis factor 14 | |
Synonyms | BRCC4|BRCC45|BRE | NAPP2|PBD13A|Pex14p|dJ734G22.2 | |
Cytomap | ('BRE')('PEX14') 2p23.2 | 1p36.22 | |
Type of gene | protein-coding | protein-coding | |
Description | BRISC and BRCA1-A complex member 2BRCA1-A complex subunit BREBRCA1/BRCA2-containing complex subunit 45BRCA1/BRCA2-containing complex, subunit 4brain and reproductive organ-expressed (TNFRSF1A modulator)brain and reproductive organ-expressed protein | peroxisomal membrane protein PEX14NF-E2 associated polypeptide 2PTS1 receptor docking proteinperoxin-14peroxisomal membrane anchor protein PEX14peroxisomal membrane anchor protein Pex14p | |
Modification date | 20200313 | 20200313 | |
UniProtAcc | . | . | |
Ensembl transtripts involved in fusion gene | ENST00000342045, ENST00000344773, ENST00000361704, ENST00000379624, ENST00000379632, ENST00000603461, | ||
Fusion gene scores | * DoF score | 13 X 9 X 8=936 | 13 X 10 X 7=910 |
# samples | 15 | 13 | |
** MAII score | log2(15/936*10)=-2.64154602908752 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(13/910*10)=-2.8073549220576 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: BRE [Title/Abstract] AND PEX14 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | BRE(28117551)-PEX14(10596270), # samples:1 | ||
Anticipated loss of major functional domain due to fusion event. | BRE-PEX14 seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF. BRE-PEX14 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) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | BRE | GO:0043066 | negative regulation of apoptotic process | 15465831 |
Tgene | PEX14 | GO:0016561 | protein import into peroxisome matrix, translocation | 21525035 |
Tgene | PEX14 | GO:0032091 | negative regulation of protein binding | 21976670 |
Tgene | PEX14 | GO:0034453 | microtubule anchoring | 21525035 |
Tgene | PEX14 | GO:0036250 | peroxisome transport along microtubule | 21525035 |
Tgene | PEX14 | GO:0043433 | negative regulation of DNA-binding transcription factor activity | 11863372 |
Tgene | PEX14 | GO:0044721 | protein import into peroxisome matrix, substrate release | 21976670 |
Tgene | PEX14 | GO:0045892 | negative regulation of transcription, DNA-templated | 11863372 |
Tgene | PEX14 | GO:0065003 | protein-containing complex assembly | 21525035 |
![]() * 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. |
Source | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
ChimerDB4 | STAD | TCGA-FP-8209-01A | BRE | chr2 | 28117551 | + | PEX14 | chr1 | 10596270 | + |
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Fusion Gene ORF analysis for BRE-PEX14 |
![]() * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
ORF | Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
5CDS-3UTR | ENST00000342045 | ENST00000492696 | BRE | chr2 | 28117551 | + | PEX14 | chr1 | 10596270 | + |
5CDS-3UTR | ENST00000344773 | ENST00000492696 | BRE | chr2 | 28117551 | + | PEX14 | chr1 | 10596270 | + |
5CDS-3UTR | ENST00000361704 | ENST00000492696 | BRE | chr2 | 28117551 | + | PEX14 | chr1 | 10596270 | + |
5CDS-3UTR | ENST00000379624 | ENST00000492696 | BRE | chr2 | 28117551 | + | PEX14 | chr1 | 10596270 | + |
5CDS-3UTR | ENST00000379632 | ENST00000492696 | BRE | chr2 | 28117551 | + | PEX14 | chr1 | 10596270 | + |
5CDS-intron | ENST00000342045 | ENST00000538836 | BRE | chr2 | 28117551 | + | PEX14 | chr1 | 10596270 | + |
5CDS-intron | ENST00000344773 | ENST00000538836 | BRE | chr2 | 28117551 | + | PEX14 | chr1 | 10596270 | + |
5CDS-intron | ENST00000361704 | ENST00000538836 | BRE | chr2 | 28117551 | + | PEX14 | chr1 | 10596270 | + |
5CDS-intron | ENST00000379624 | ENST00000538836 | BRE | chr2 | 28117551 | + | PEX14 | chr1 | 10596270 | + |
5CDS-intron | ENST00000379632 | ENST00000538836 | BRE | chr2 | 28117551 | + | PEX14 | chr1 | 10596270 | + |
Frame-shift | ENST00000342045 | ENST00000356607 | BRE | chr2 | 28117551 | + | PEX14 | chr1 | 10596270 | + |
Frame-shift | ENST00000344773 | ENST00000356607 | BRE | chr2 | 28117551 | + | PEX14 | chr1 | 10596270 | + |
Frame-shift | ENST00000361704 | ENST00000356607 | BRE | chr2 | 28117551 | + | PEX14 | chr1 | 10596270 | + |
Frame-shift | ENST00000379624 | ENST00000356607 | BRE | chr2 | 28117551 | + | PEX14 | chr1 | 10596270 | + |
Frame-shift | ENST00000379632 | ENST00000356607 | BRE | chr2 | 28117551 | + | PEX14 | chr1 | 10596270 | + |
intron-3CDS | ENST00000603461 | ENST00000356607 | BRE | chr2 | 28117551 | + | PEX14 | chr1 | 10596270 | + |
intron-3UTR | ENST00000603461 | ENST00000492696 | BRE | chr2 | 28117551 | + | PEX14 | chr1 | 10596270 | + |
intron-intron | ENST00000603461 | ENST00000538836 | BRE | chr2 | 28117551 | + | PEX14 | chr1 | 10596270 | + |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | Seq length (transcript) | BP loci (transcript) | Predicted start (transcript) | Predicted stop (transcript) | Seq length (amino acids) |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
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Fusion Genomic Features for BRE-PEX14 |
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Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | 1-p | p (fusion gene breakpoint) |
BRE | chr2 | 28117551 | + | PEX14 | chr1 | 10596269 | + | 0.000673419 | 0.9993266 |
BRE | chr2 | 28117551 | + | PEX14 | chr1 | 10596269 | + | 0.000673419 | 0.9993266 |
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Fusion Protein Features for BRE-PEX14 |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:28117551/:10596270) - FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels. - How to search 1. Put your fusion gene symbol. 2. Press the tab key until there will be shown the breakpoint information filled. 4. Go down and press 'Search' tab twice. 4. Go down to have the hyperlink of the search result. 5. Click the hyperlink. 6. See the FGviewer result for your fusion gene. |
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Hgene | Tgene |
. | . |
FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}. | FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}. |
![]() * 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. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
- In-frame and not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
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Fusion Gene Sequence for BRE-PEX14 |
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Fusion Gene PPI Analysis for BRE-PEX14 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Related Drugs for BRE-PEX14 |
![]() (DrugBank Version 5.1.8 2021-05-08) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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Related Diseases for BRE-PEX14 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Tgene | C3554004 | PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER) | 5 | CTD_human;GENOMICS_ENGLAND | |
Tgene | C1832200 | Peroxisome biogenesis disorders | 4 | CTD_human;GENOMICS_ENGLAND | |
Tgene | C0043459 | Zellweger Syndrome | 2 | CTD_human;GENOMICS_ENGLAND | |
Tgene | C0751594 | Zellweger-Like Syndrome | 2 | CTD_human | |
Tgene | C3658299 | Zellweger Spectrum | 2 | CTD_human | |
Tgene | C0010093 | Corpus Luteum Cyst | 1 | CTD_human | |
Tgene | C0029927 | Ovarian Cysts | 1 | CTD_human |