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in Kim Lab

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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:FAF1-PRDX6 (FusionGDB2 ID:HG11124TG9588)

Fusion Gene Summary for FAF1-PRDX6

check button Fusion gene summary
Fusion gene informationFusion gene name: FAF1-PRDX6
Fusion gene ID: hg11124tg9588
HgeneTgene
Gene symbol

FAF1

PRDX6

Gene ID

11124

9588

Gene nameFas associated factor 1peroxiredoxin 6
SynonymsCGI-03|HFAF1s|UBXD12|UBXN3A|hFAF11-Cys|AOP2|HEL-S-128m|NSGPx|PRX|aiPLA2|p29
Cytomap('FAF1')('PRDX6')

1p32.3

1q25.1

Type of geneprotein-codingprotein-coding
DescriptionFAS-associated factor 1Fas (TNFRSF6) associated factor 1TNFRSF6-associated factor 1UBX domain protein 3AUBX domain-containing protein 12UBX domain-containing protein 3Aperoxiredoxin-61-Cys PRX1-Cys peroxiredoxin24 kDa proteinacidic calcium-independent phospholipase A2antioxidant protein 2epididymis secretory sperm binding protein Li 128mliver 2D page spot 40non-selenium glutathione peroxidasered blood cells pag
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000371778, ENST00000396153, 
ENST00000545823, ENST00000472808, 
Fusion gene scores* DoF score23 X 21 X 9=43474 X 5 X 3=60
# samples 315
** MAII scorelog2(31/4347*10)=-3.80967997500385
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/60*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: FAF1 [Title/Abstract] AND PRDX6 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointFAF1(51032748)-PRDX6(173450464), # samples:1
Anticipated loss of major functional domain due to fusion event.FAF1-PRDX6 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
FAF1-PRDX6 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
FAF1-PRDX6 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
FAF1-PRDX6 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
FAF1-PRDX6 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
FAF1-PRDX6 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism 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
HgeneFAF1

GO:0010942

positive regulation of cell death

15596450


check buttonFusion gene breakpoints across FAF1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure
check buttonFusion gene breakpoints across PRDX6 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check button Fusion gene information
* 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
ChimerDB4STADTCGA-CG-5717FAF1chr1

51032748

-PRDX6chr1

173450464

+


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Fusion Gene ORF analysis for FAF1-PRDX6

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
5CDS-3UTRENST00000371778ENST00000470017FAF1chr1

51032748

-PRDX6chr1

173450464

+
5CDS-3UTRENST00000396153ENST00000470017FAF1chr1

51032748

-PRDX6chr1

173450464

+
5CDS-3UTRENST00000545823ENST00000470017FAF1chr1

51032748

-PRDX6chr1

173450464

+
5UTR-3CDSENST00000472808ENST00000340385FAF1chr1

51032748

-PRDX6chr1

173450464

+
5UTR-3UTRENST00000472808ENST00000470017FAF1chr1

51032748

-PRDX6chr1

173450464

+
Frame-shiftENST00000371778ENST00000340385FAF1chr1

51032748

-PRDX6chr1

173450464

+
In-frameENST00000396153ENST00000340385FAF1chr1

51032748

-PRDX6chr1

173450464

+
In-frameENST00000545823ENST00000340385FAF1chr1

51032748

-PRDX6chr1

173450464

+

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)
ENST00000396153FAF1chr151032748-ENST00000340385PRDX6chr1173450464+324417201402299719
ENST00000545823FAF1chr151032748-ENST00000340385PRDX6chr1173450464+22166921501271373

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
ENST00000396153ENST00000340385FAF1chr151032748-PRDX6chr1173450464+0.00043660.9995634
ENST00000545823ENST00000340385FAF1chr151032748-PRDX6chr1173450464+0.0002402960.99975973

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Fusion Genomic Features for FAF1-PRDX6


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)
FAF1chr151032748-PRDX6chr1173450464+0.0006526980.99934727
FAF1chr151032748-PRDX6chr1173450464+0.0006526980.99934727

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.
genomic feature

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.
genomic feature of top 1%

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Fusion Protein Features for FAF1-PRDX6


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr1:51032748/chr1:173450464)
- 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.
FGviewer

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

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
HgeneFAF1chr1:51032748chr1:173450464ENST00000371778-14201_57422651.0DomainUBA
HgeneFAF1chr1:51032748chr1:173450464ENST00000396153-13191_57422651.0DomainUBA
TgenePRDX6chr1:51032748chr1:173450464ENST000003403850531_4031225.0RegionRequired and sufficient for targeting to lysosomes and lamellar bodies

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneFAF1chr1:51032748chr1:173450464ENST00000371778-1420569_646422651.0DomainUBX
HgeneFAF1chr1:51032748chr1:173450464ENST00000396153-1319569_646422651.0DomainUBX
TgenePRDX6chr1:51032748chr1:173450464ENST00000340385055_16931225.0DomainThioredoxin


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Fusion Gene Sequence for FAF1-PRDX6


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.
>28245_28245_1_FAF1-PRDX6_FAF1_chr1_51032748_ENST00000396153_PRDX6_chr1_173450464_ENST00000340385_length(transcript)=3244nt_BP=1720nt
AGGGGCGGAGGCGGCGGCCAGGGAGGAAGCGGAGGAGGCGGAGGCGGCCGCGGCGTTCGCCCGCCCGCTCGCTCGCTCGGTTTCCCCGCC
CCCGCCGGGCTTAACGCCGCTGAAGGTATCCGGGTGCGCGCTGTCGCAACCTGCCCTCATCCTGGCCCGCGACTGTAAGACCGGACCCAC
ATCCAGACCAATCTTCCTGTCCGGGCTGCTGCGACGCGGGCTCCGCAGGTTGCAGGCGGGCGGCCGGGGCGCCTGAAGGTTACCGAGTGC
ATGAGCGCCTAGCGCTTCCCGCGCTGCCCCGCCCGCTGGCCCGCCGACCCGCCCGCCGGCTCGCCCGCCAGCCCCTCGGCGCCCGGCGGC
GGCGGCGGCGGTGGCGGCGACGGTCGCAGGAGGTGCCGTCTGCCTCCCAGGTGCGCGCTTCGCTCCCGGAGCCGCGGAACTCGGCGGCCG
CCATGGCGTCCAACATGGACCGGGAGATGATCCTGGCGGATTTTCAGGCATGTACTGGCATTGAAAACATTGACGAAGCTATTACATTGC
TTGAACAAAATAATTGGGACTTAGTGGCAGCTATCAATGGTGTAATACCACAGGAAAATGGCATTCTACAAAGTGAATATGGAGGTGAGA
CCATACCAGGACCTGCATTTAATCCAGCAAGTCATCCAGCTTCAGCTCCTACTTCCTCTTCTTCTTCAGCGTTTCGACCTGTAATGCCAT
CCAGGCAGATTGTAGAAAGGCAACCTCGGATGCTGGACTTCAGGGTTGAATACAGAGACAGAAATGTTGATGTGGTACTTGAAGACACCT
GTACTGTTGGAGAGATTAAACAGATTCTAGAAAATGAACTTCAGATACCTGTGTCCAAAATGCTGTTAAAAGGCTGGAAGACGGGAGATG
TGGAAGACAGTACGGTCCTAAAATCTCTACACTTGCCAAAAAACAACAGTCTTTATGTCCTTACACCAGATTTGCCACCACCTTCATCAT
CTAGTCATGCTGGTGCCCTGCAGGAGTCATTAAATCAAAACTTCATGCTGATCATCACCCACCGAGAAGTCCAGCGGGAGTACAACCTGA
ACTTCTCAGGAAGCAGTACTATTCAAGAGGTAAAGAGAAATGTGTATGACCTTACAAGTATCCCCGTTCGCCACCAATTATGGGAGGGCT
GGCCAACTTCTGCTACAGACGACTCAATGTGTCTTGCTGAATCAGGGCTCTCTTATCCCTGCCATCGACTTACAGTGGGAAGAAGATCTT
CACCTGCACAGACCCGGGAACAGTCGGAAGAACAAATCACCGATGTTCATATGGTTAGTGATAGCGATGGAGATGACTTTGAAGATGCTA
CAGAATTTGGGGTGGATGATGGAGAAGTATTTGGCATGGCGTCATCTGCCTTGAGAAAATCTCCAATGATGCCAGAAAACGCAGAAAATG
AAGGAGATGCCTTATTACAATTTACAGCAGAGTTTTCTTCAAGATATGGTGATTGCCATCCTGTATTTTTTATTGGCTCATTAGAAGCTG
CTTTTCAAGAGGCCTTCTATGTGAAAGCCCGAGATAGAAAGCTTCTTGCTATCTACCTCCACCATGATGAAAGTGTGTTAACCAACGTGT
TCTGCTCACAAATGCTTTGTGCTGAATCCATTGTTTCTTATCTGAGTCAAAATTTTATAACCTGGGCTTGGGATCTGACAAAGGACTCCA
ACAGAGCAAGATGGGGCATTCTCTTCTCCCACCCTCGGGACTTTACCCCAGTGTGCACCACAGAGCTTGGCAGAGCTGCAAAGCTGGCAC
CAGAATTTGCCAAGAGGAATGTTAAGTTGATTGCCCTTTCAATAGACAGTGTTGAGGACCATCTTGCCTGGAGCAAGGATATCAATGCTT
ACAATTGTGAAGAGCCCACAGAAAAGTTACCTTTTCCCATCATCGATGATAGGAATCGGGAGCTTGCCATCCTGTTGGGCATGCTGGATC
CAGCAGAGAAGGATGAAAAGGGCATGCCTGTGACAGCTCGTGTGGTGTTTGTTTTTGGTCCTGATAAGAAGCTGAAGCTGTCTATCCTCT
ACCCAGCTACCACTGGCAGGAACTTTGATGAGATTCTCAGGGTAGTCATCTCTCTCCAGCTGACAGCAGAAAAAAGGGTTGCCACCCCAG
TTGATTGGAAGGATGGGGATAGTGTGATGGTCCTTCCAACCATCCCTGAAGAAGAAGCCAAAAAACTTTTCCCGAAAGGAGTCTTCACCA
AAGAGCTCCCATCTGGCAAGAAATACCTCCGCTACACACCCCAGCCTTAAGTCTCTTGGAGAAGCTGGTGCTGTGAGCCAGAGGATGTCA
GCTGCCAATTGTGTTTTCCTGCAGCAATTCCATAAACACATCCTGGTGTCATCACAGCCAAGGTTTTTAGGTTGCTATACCAATGGCTTA
TTAAATGAAAATGGCACTAAAAGTTTCTTGAGATTCTTTATACTCTCTGCCTTCAGCAATCAATTCCATTCATACATCAGCACTCTGCTG
GTTCTGTTTGAAATATGTTCTGTATTTAAAACTCAAATCTTGTTGGATCTCTGCAGGGCTTGTGACCAATGAAGTCATATTTGTTGATGG
TTGACAAAGCTTGCTTCACTCCATCAGAGAATGACTATCAATTTTTTTTTAACTGTCCTATCACGTCCTCTCCTGTCACCCATTTTGAAG
AGTGGCAGAACTTGAAGTTCAACTTCCTCTGTAAATATCCAAGTATAAAGCCCAGGAACTTCTAGAATAACCCAGATGCGCTTTAATTTT
TTTTAATATGTTTTGATCACAGAACTTCTAGAATAACCCAGATGCTCTTTCATATTCTTTTAATACATCTTGATCACAGCTGGGGGAAAA
AAAGCTTTTTAATTCTATACCTTCCTAGTAGATAAGTGAAGAGCAGGGAAAGAGACCTTTAAATATTTTGCTATAAAAAAATTTGTGATA
AGTTTCTATCAAAATGGGGAGATTGCAGAAAAGGCTTCCCTTGGCTCCCAAGGAGGTGTAGCAGGTGTGAGCAATATTAGTGCCATGTGC
CTTTCACACAGGGTTTGCATTTATCAGTCTGTTTTCCGATGATGTGTACATGAAAGAGTACACCATGTGAAGAGAAGAGAGAATGATTGA
AAATGTTTTAGTATAGAACTCTTCTTGCAGTGGGTTGCTATTTTCTAGATTTTACTTTTTAGGGAACAAAATAAAATCCTTTGTTAAAAC
TGGG

>28245_28245_1_FAF1-PRDX6_FAF1_chr1_51032748_ENST00000396153_PRDX6_chr1_173450464_ENST00000340385_length(amino acids)=719AA_BP=526
MPSSWPATVRPDPHPDQSSCPGCCDAGSAGCRRAAGAPEGYRVHERLALPALPRPLARRPARRLARQPLGARRRRRRWRRRSQEVPSASQ
VRASLPEPRNSAAAMASNMDREMILADFQACTGIENIDEAITLLEQNNWDLVAAINGVIPQENGILQSEYGGETIPGPAFNPASHPASAP
TSSSSSAFRPVMPSRQIVERQPRMLDFRVEYRDRNVDVVLEDTCTVGEIKQILENELQIPVSKMLLKGWKTGDVEDSTVLKSLHLPKNNS
LYVLTPDLPPPSSSSHAGALQESLNQNFMLIITHREVQREYNLNFSGSSTIQEVKRNVYDLTSIPVRHQLWEGWPTSATDDSMCLAESGL
SYPCHRLTVGRRSSPAQTREQSEEQITDVHMVSDSDGDDFEDATEFGVDDGEVFGMASSALRKSPMMPENAENEGDALLQFTAEFSSRYG
DCHPVFFIGSLEAAFQEAFYVKARDRKLLAIYLHHDESVLTNVFCSQMLCAESIVSYLSQNFITWAWDLTKDSNRARWGILFSHPRDFTP
VCTTELGRAAKLAPEFAKRNVKLIALSIDSVEDHLAWSKDINAYNCEEPTEKLPFPIIDDRNRELAILLGMLDPAEKDEKGMPVTARVVF
VFGPDKKLKLSILYPATTGRNFDEILRVVISLQLTAEKRVATPVDWKDGDSVMVLPTIPEEEAKKLFPKGVFTKELPSGKKYLRYTPQP

--------------------------------------------------------------
>28245_28245_2_FAF1-PRDX6_FAF1_chr1_51032748_ENST00000545823_PRDX6_chr1_173450464_ENST00000340385_length(transcript)=2216nt_BP=692nt
ATACAAAGCAGGCTTGAGATGTATCCTTGCATATTTGAAGGTTCTGTGGTTATGATGAGCTGAAATGACCACTGATTAATACAGTAGCTC
TCTAAAATAATGAGGTTTCTCCACTAACGGAACCTCTTTATTTATCAAACTTATAATAAAATGAGGAATCTGCTTGAGATGTGTCTTGCT
GAATCAGGGCTCTCTTATCCCTGCCATCGACTTACAGTGGGAAGAAGATCTTCACCTGCACAGACCCGGGAACAGTCGGAAGAACAAATC
ACCGATGTTCATATGGTTAGTGATAGCGATGGAGATGACTTTGAAGATGCTACAGAATTTGGGGTGGATGATGGAGAAGTATTTGGCATG
GCGTCATCTGCCTTGAGAAAATCTCCAATGATGCCAGAAAACGCAGAAAATGAAGGAGATGCCTTATTACAATTTACAGCAGAGTTTTCT
TCAAGATATGGTGATTGCCATCCTGTATTTTTTATTGGCTCATTAGAAGCTGCTTTTCAAGAGGCCTTCTATGTGAAAGCCCGAGATAGA
AAGCTTCTTGCTATCTACCTCCACCATGATGAAAGTGTGTTAACCAACGTGTTCTGCTCACAAATGCTTTGTGCTGAATCCATTGTTTCT
TATCTGAGTCAAAATTTTATAACCTGGGCTTGGGATCTGACAAAGGACTCCAACAGAGCAAGATGGGGCATTCTCTTCTCCCACCCTCGG
GACTTTACCCCAGTGTGCACCACAGAGCTTGGCAGAGCTGCAAAGCTGGCACCAGAATTTGCCAAGAGGAATGTTAAGTTGATTGCCCTT
TCAATAGACAGTGTTGAGGACCATCTTGCCTGGAGCAAGGATATCAATGCTTACAATTGTGAAGAGCCCACAGAAAAGTTACCTTTTCCC
ATCATCGATGATAGGAATCGGGAGCTTGCCATCCTGTTGGGCATGCTGGATCCAGCAGAGAAGGATGAAAAGGGCATGCCTGTGACAGCT
CGTGTGGTGTTTGTTTTTGGTCCTGATAAGAAGCTGAAGCTGTCTATCCTCTACCCAGCTACCACTGGCAGGAACTTTGATGAGATTCTC
AGGGTAGTCATCTCTCTCCAGCTGACAGCAGAAAAAAGGGTTGCCACCCCAGTTGATTGGAAGGATGGGGATAGTGTGATGGTCCTTCCA
ACCATCCCTGAAGAAGAAGCCAAAAAACTTTTCCCGAAAGGAGTCTTCACCAAAGAGCTCCCATCTGGCAAGAAATACCTCCGCTACACA
CCCCAGCCTTAAGTCTCTTGGAGAAGCTGGTGCTGTGAGCCAGAGGATGTCAGCTGCCAATTGTGTTTTCCTGCAGCAATTCCATAAACA
CATCCTGGTGTCATCACAGCCAAGGTTTTTAGGTTGCTATACCAATGGCTTATTAAATGAAAATGGCACTAAAAGTTTCTTGAGATTCTT
TATACTCTCTGCCTTCAGCAATCAATTCCATTCATACATCAGCACTCTGCTGGTTCTGTTTGAAATATGTTCTGTATTTAAAACTCAAAT
CTTGTTGGATCTCTGCAGGGCTTGTGACCAATGAAGTCATATTTGTTGATGGTTGACAAAGCTTGCTTCACTCCATCAGAGAATGACTAT
CAATTTTTTTTTAACTGTCCTATCACGTCCTCTCCTGTCACCCATTTTGAAGAGTGGCAGAACTTGAAGTTCAACTTCCTCTGTAAATAT
CCAAGTATAAAGCCCAGGAACTTCTAGAATAACCCAGATGCGCTTTAATTTTTTTTAATATGTTTTGATCACAGAACTTCTAGAATAACC
CAGATGCTCTTTCATATTCTTTTAATACATCTTGATCACAGCTGGGGGAAAAAAAGCTTTTTAATTCTATACCTTCCTAGTAGATAAGTG
AAGAGCAGGGAAAGAGACCTTTAAATATTTTGCTATAAAAAAATTTGTGATAAGTTTCTATCAAAATGGGGAGATTGCAGAAAAGGCTTC
CCTTGGCTCCCAAGGAGGTGTAGCAGGTGTGAGCAATATTAGTGCCATGTGCCTTTCACACAGGGTTTGCATTTATCAGTCTGTTTTCCG
ATGATGTGTACATGAAAGAGTACACCATGTGAAGAGAAGAGAGAATGATTGAAAATGTTTTAGTATAGAACTCTTCTTGCAGTGGGTTGC
TATTTTCTAGATTTTACTTTTTAGGGAACAAAATAAAATCCTTTGTTAAAACTGGG

>28245_28245_2_FAF1-PRDX6_FAF1_chr1_51032748_ENST00000545823_PRDX6_chr1_173450464_ENST00000340385_length(amino acids)=373AA_BP=180
MRNLLEMCLAESGLSYPCHRLTVGRRSSPAQTREQSEEQITDVHMVSDSDGDDFEDATEFGVDDGEVFGMASSALRKSPMMPENAENEGD
ALLQFTAEFSSRYGDCHPVFFIGSLEAAFQEAFYVKARDRKLLAIYLHHDESVLTNVFCSQMLCAESIVSYLSQNFITWAWDLTKDSNRA
RWGILFSHPRDFTPVCTTELGRAAKLAPEFAKRNVKLIALSIDSVEDHLAWSKDINAYNCEEPTEKLPFPIIDDRNRELAILLGMLDPAE
KDEKGMPVTARVVFVFGPDKKLKLSILYPATTGRNFDEILRVVISLQLTAEKRVATPVDWKDGDSVMVLPTIPEEEAKKLFPKGVFTKEL
PSGKKYLRYTPQP

--------------------------------------------------------------

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Fusion Gene PPI Analysis for FAF1-PRDX6


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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Related Drugs for FAF1-PRDX6


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

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Related Diseases for FAF1-PRDX6


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneC0011616Contact Dermatitis1CTD_human
TgeneC0013080Down Syndrome1CTD_human
TgeneC0024121Lung Neoplasms1CTD_human
TgeneC0035222Respiratory Distress Syndrome, Adult1CTD_human
TgeneC0036341Schizophrenia1PSYGENET
TgeneC0151744Myocardial Ischemia1CTD_human
TgeneC0162351Contact hypersensitivity1CTD_human
TgeneC0242379Malignant neoplasm of lung1CTD_human
TgeneC0432416Down Syndrome, Partial Trisomy 211CTD_human
TgeneC0432417Trisomy 21, Meiotic Nondisjunction1CTD_human
TgeneC0751081Trisomy 21, Mitotic Nondisjunction1CTD_human
TgeneC2239176Liver carcinoma1CTD_human