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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:SAV1-PELI2 (FusionGDB2 ID:79273)

Fusion Gene Summary for SAV1-PELI2

check button Fusion gene summary
Fusion gene informationFusion gene name: SAV1-PELI2
Fusion gene ID: 79273
HgeneTgene
Gene symbol

SAV1

PELI2

Gene ID

60485

57161

Gene namesalvador family WW domain containing protein 1pellino E3 ubiquitin protein ligase family member 2
SynonymsSAV|WW45|WWP4-
Cytomap

14q22.1

14q22.3

Type of geneprotein-codingprotein-coding
Descriptionprotein salvador homolog 11700040G09Rik45 kDa WW domain proteinWW domain-containing adaptor 45hWW45salvador homolog 1E3 ubiquitin-protein ligase pellino homolog 2RING-type E3 ubiquitin transferase pellino homolog 2pellino homolog 2pellino-2protein pellino homolog 2
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000324679, ENST00000267460, 
Fusion gene scores* DoF score8 X 6 X 6=2882 X 2 X 2=8
# samples 82
** MAII scorelog2(8/288*10)=-1.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: SAV1 [Title/Abstract] AND PELI2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSAV1(51111462)-PELI2(56645053), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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
TgenePELI2

GO:0001934

positive regulation of protein phosphorylation

12804775

TgenePELI2

GO:0043410

positive regulation of MAPK cascade

12804775


check buttonFusion gene breakpoints across SAV1 (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 PELI2 (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 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
ChimerDB4LUSCTCGA-85-8355-01ASAV1chr14

51111462

-PELI2chr14

56645053

+


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Fusion Gene ORF analysis for SAV1-PELI2

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
In-frameENST00000324679ENST00000267460SAV1chr14

51111462

-PELI2chr14

56645053

+

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)
ENST00000324679SAV1chr1451111462-ENST00000267460PELI2chr1456645053+671611703642355663

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
ENST00000324679ENST00000267460SAV1chr1451111462-PELI2chr1456645053+0.0004411120.99955887

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Fusion Genomic Features for SAV1-PELI2


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)
SAV1chr1451111461-PELI2chr1456645052+3.78E-050.9999622
SAV1chr1451111461-PELI2chr1456645052+3.78E-050.9999622

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 SAV1-PELI2


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/chr14:51111462/chr14:56645053)
- 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
HgeneSAV1chr14:51111462chr14:56645053ENST00000324679-35199_232268384.0DomainWW 1
HgeneSAV1chr14:51111462chr14:56645053ENST00000324679-35234_267268384.0DomainWW 2

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneSAV1chr14:51111462chr14:56645053ENST00000324679-35344_373268384.0Coiled coilOntology_term=ECO:0000255
HgeneSAV1chr14:51111462chr14:56645053ENST00000324679-35321_368268384.0DomainSARAH
TgenePELI2chr14:51111462chr14:56645053ENST000002674600615_20225421.0DomainNote=FHA%3B atypical


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Fusion Gene Sequence for SAV1-PELI2


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.
>79273_79273_1_SAV1-PELI2_SAV1_chr14_51111462_ENST00000324679_PELI2_chr14_56645053_ENST00000267460_length(transcript)=6716nt_BP=1170nt
ACGGGATGTAGGCGGCGGCGGCGGTAGTGGTAGCGGTTATTCGGCGGCCCGCGGCGGACCATGGCCCTGGCCCTGGCCCGGCGTCGCTGG
GCTTTCCTCACGGCGTCCCCGAGCAGCGTCGCAGAGCGGGCCGACTTCCGGGAAGGAACTGACCAGCGACTGAGCGGCGGCCGGCGCGCT
TAGCGCCCTGAACATGCGGCAGTCCCTGCGGGCGACCCCGGGCTCCGGACAGGCGGCGGCGGAGGCGGCGGCTCGGGAGGGAAGGAGGCG
GCGGCGCCGGCGGAGGTGGCGGCGGAGACGGCCGGCGCCCGGCGCGGAGCCCTAGGGAGGCAGTTCAGCGCGGCCTCGGGCCTCGTCGAG
AAGGATGCTGTCCCGAAAGAAAACCAAAAACGAAGTGTCCAAGCCGGCCGAGGTGCAGGGGAAGTACGTGAAGAAGGAGACGTCGCCTCT
GCTTCGGAATCTTATGCCTTCATTCATCCGGCATGGTCCAACAATTCCAAGACGAACTGATATCTGTCTTCCAGATTCAAGCCCTAATGC
CTTTTCAACTTCTGGAGATGTAGTTTCAAGAAACCAGAGTTTCCTTAGAACTCCAATTCAAAGAACACCTCATGAAATAATGAGAAGAGA
AAGCAACAGATTATCTGCACCTTCTTATCTTGCCAGAAGTCTAGCAGATGTCCCTAGAGAGTATGGTTCTTCTCAGTCATTTGTAACGGA
AGTTAGTTTTGCTGTTGAAAATGGAGACTCTGGTTCCCGATATTATTATTCAGACAATTTTTTTGATGGTCAGAGAAAGCGGCCACTTGG
AGATCGTGCACATGAAGACTACAGATATTATGAATACAACCATGATCTCTTCCAAAGAATGCCACAGAATCAGGGGAGGCATGCTTCAGG
TATTGGGAGAGTTGCTGCTACATCTTTAGGAAATTTGACTAACCATGGTTCTGAAGATTTACCCCTTCCTCCTGGCTGGTCTGTGGACTG
GACAATGAGAGGGAGAAAATATTATATAGATCATAACACAAATACAACTCACTGGAGCCATCCTCTTGAGCGAGAAGGACTTCCTCCTGG
ATGGGAACGAGTTGAGTCATCCGAATTTGGAACCTATTATGTAGATCACACAAATAAGAAGGCCCAATACAGGCATCCCTGTGCTCCTAG
GTACAATGGTGCTTTACCCAATGGAGATAGAGGACGGAGGAAAAGTAGATTTGCCCTCTACAAGCGGCCCAAGGCAAATGGTGTCAAACC
CAGCACCGTCCATGTGATATCCACGCCCCAGGCATCCAAGGCTATCAGCTGCAAAGGTCAACACAGTATATCCTACACTTTGTCAAGGAA
TCAGACTGTGGTGGTGGAGTACACACATGATAAGGATACGGATATGTTTCAGGTGGGCAGATCAACAGAAAGCCCTATCGACTTCGTTGT
CACAGACACGATTTCTGGCAGCCAGAACACGGACGAAGCCCAGATCACACAGAGCACCATATCCAGGTTCGCCTGCAGGATCGTGTGCGA
CAGGAATGAACCTTACACAGCACGGATATTCGCCGCCGGATTTGACTCTTCCAAAAACATATTTCTTGGAGAAAAGGCAGCAAAGTGGAA
AAACCCCGACGGCCACATGGATGGGCTCACTACTAATGGCGTCCTGGTGATGCATCCACGAGGGGGCTTCACCGAGGAGTCCCAGCCCGG
GGTCTGGCGCGAGATCTCTGTCTGTGGAGATGTGTACACCTTGCGAGAAACCAGGTCGGCCCAGCAACGAGGAAAGCTGGTGGAAAGTGA
GACCAACGTCCTGCAGGACGGCTCCCTCATTGACCTGTGTGGGGCCACTCTCCTCTGGAGAACAGCAGATGGGCTTTTTCATACTCCAAC
TCAGAAGCACATAGAAGCCCTCCGGCAGGAGATTAACGCCGCCCGGCCTCAGTGTCCTGTGGGGCTCAACACCCTGGCCTTCCCCAGCAT
CAACAGGAAAGAGGTGGTGGAGGAGAAGCAGCCCTGGGCATATCTCAGTTGTGGCCACGTGCACGGGTACCACAACTGGGGCCATCGGAG
TGACACGGAGGCCAACGAGAGGGAGTGTCCCATGTGCAGGACTGTGGGCCCCTATGTGCCTCTCTGGCTTGGCTGTGAGGCAGGATTTTA
TGTAGACGCAGGACCGCCAACTCATGCTTTCACTCCCTGTGGACACGTGTGCTCGGAGAAGTCTGCAAAATACTGGTCTCAGATCCCGTT
GCCTCATGGAACTCATGCATTTCACGCTGCTTGCCCTTTCTGTGCTACACAGCTGGTTGGGGAGCAAAACTGCATCAAATTAATTTTCCA
AGGTCCAATTGACTGACGCCCTTGACAGCCATCTACGACTTTATTAACAGGTTACTGTGAAGATTTTGCCACTAACTCTAGATTTTACCT
TTTTGTAATGCTGTTTATCAGAGGAGGGTGACAGGGGCTGGAAATAAAGAGAGGGGACATGGTGATGAAACATGGCAGGAGTGTAACAGA
TACCAGTGGTGTGTTGCATGCTCAAAACAGCAGCGTCGTCATTGAAGTCTGCTTGATTAAACCATAATATCTTTGTAATAATTGGATTTA
AAATGCTATGCTTCTATTTTTAACCTTGGGTTTTTAACCAAGTTTTTTTTTTTTTGTAATCTTGGACAAGACTTTAAATCATATTTTACA
GATGTAGAAGAAATTTATTCAAAAGTGTGGGCTCATGAAGTTCACTTCAGTGCAGTGTGGTGTAGGTGTTACGCGAAGGGCGCACAGTGT
CTAGAAATACTTGATCGTGGCTCAAACCTGACCAGACAGCAGAGGGGCGGCTCTGTACAGTGTGACTGGTGGACAGATGGCCTTAGGCAC
AGGTGGTTTTGAAATCTGGGGCTTTTTCTGATTTATTTTTCTGACTTGTTGGGGGAGAGAATATTCATAACTTGTGGGCTTTTTTTTTTT
TTAACTTCAGTGGAATTTACTTTAGATATTCATTCATCAAATACATGGGACTTCACAAACAATTTTCCATAACTTTTTAGCCTGTCTTTT
GTTATTTCTGCCTAATATGATTTGCCCCGATACTCATCTTGCACGGCCAGAACTGTTTGGTTGATTAAAATACATCAGCTCTTAAAAACT
CATTAACTGAGGGTAATTACAGTAGTAGACATGGTCTGGGTACTATACTACCATGTTTATTTGCTGACTGAATTAAGATTTAAGAATGAT
TAAAAATAAGCTTTTACTTTTTAAAACCACTTGAGGTTTCATAAAGCTTGGGGTTTTTTTTTTTCCTTTGTTAAGAAAGCCAACCAATCA
CAATGATATAGTCATTGTTGTGCACTCCCTTTTCACCATCTGTCACCTTCCCTTGCAGCTTAAGGAGCCCAGTAAGTTTTGAAAATGTTT
GCGAATCAAACTAAATTTAAGTGGGATGATTAGATATACACAACACCAAGTGGTACATCTGCAGAGATAATTCAAAATTCCTGCTTTTGA
GAGAGCAAATGAGTGTTGCTGAGGAATAATTAAATGAGAATTTCATAGGAGCTCCACCATTCCTGTTACTTTCATTTCATTTTGATTAAT
AATTCTTGGATGCTTGGCATCGATCGTATCACTGCTCCTAGAAGGTAAAGATCCTTTAGGACATGAGACTGGTAGAAGCTGGCTGAGATA
AAATAAGTATTTATTTAAACTAATGTTCTCTTAATTTGACCATTGCAGATTTGGGTGACTTTTTTTTAACCTTTGTACATATACGTAATT
TATATGATTCTAATGTACTATATCCATACTTGAATTGGTTTTTTCGTATTTTGCCTACTGGCAAATATTTTGCCTATTTTCAGTCGTTCT
AACCTATTTGAATACGCTTTTCCTTAAAGTGATACGATAATATTACTCTTGATTGCTGCTGCTTAATTTGATGTAATATGTTTAAAGTTC
AGCCTCTCAGTTTTAATATAGCTTTATTTTTCAGTGGAGATCATTGTTTAGGATGAGACATTTTTGGTTTTGGTTTTGTTTGGGTAAATT
TTAAATGGTGTGAAAATCGATGACAACAGTCCTCTTACAGATAGCTTGCTGTATTCTGTATAGCTTACTCTACCTGCAGACAGAAAATGA
AAGAAAAAAATGGACTTGCCTAGAATAATATATTGAATGCCTTTTGATTTAGCCAGAGTCTCTGATGATTAGCTTTCACTGATAGAGTAT
GTCTTTTCAGCCTGTAATTCTTTGGGCCCCAAAGAATGACAAAGGAGGCACTCGTTCTCTTTTCTTGCTGTATGCCTAGAAAGTGGTTGA
AGGATTCTTGATGCCCTAAAACCATCTTGTAAGCTAAATGGTCTTGCATCCAGAAAGGCCAGATTTTACCTACCAAGAAAAAAAGATATT
TTTCCAGAGAGTTAGGTATATCATAATTTTCCATTTCAAGTCCTGTTTATAAGTCTAGTCATTCTGCAACGTGACATATCCCCCAAAATG
AAGTTACCTTCCAAGTTGGACACGTCCCGTAGTTGGGCATATGTCTAACTAAAAGTTTCTGACTTTTAGTAAATTCAGCTTAAATATAAG
TTGAAATTTGGGAAATAATTTCCAAGCTCTTGGAAGGGGTAACAGTGAACCGCCCTCCATGGGCTCCACATCTTTTCCTTTGGCTTCCAA
AGTCAGGTCCCGCCCACCCTGCCTAAGGAACTGCAGAGAGGTGGCAAATCAGCAAAAAGGACACCAGGCTCTTCTTGGCCACTTGTAGGA
AGATCCCTTTACAATTTTGACTAAGGAGATTTTTTTTTTCACAGTTGAGTTAGTTTGTGAAAATAAAGAACTCTGTAGCTCACCAAGGTG
GAGAAACGCAATTCAGAAAAGTAATTTCTCCAAGGTCACTTCTTTTTTTATGTCTTGCCATCACTTTAAAGGACTAGCCCCACTCCCCCA
TGTGTATACACAAGGAAATTGCAGACCAATTAGTTGTCTTGGCCTGACTCTAATGCCTTTTGCAAGTAGCTTTCCAGAAGTAAAAGTCCC
AGTGATGTATTCCCATAGAAATATTTTTCAGTTGTTTATGTCGTTTACTACAAAAAAAAAGATTCAGAGTGGATGGAGTACAACTCTGAG
TATTTTTCTAGTCCGGAATTTTTTATTAATAATCGGTGCTGCCGGGTCATGCATGCTGCAACTCTCAACATTTCCCTTATTTGGTTCAGC
TTTTAGCAAAAAGGGCTACAGTTCACCCTGCAGAGTATTAAGGTTTCTGGATTTTTTTCTCCCAACTGTGGCCCAAAAGAATTAAAATCT
GTTAATATAAATAGAGAACATATTTATCATTCCTCGATAGTTAATTATAGACTTTGGTACCTTTGTGCCTCAGGGAAGCCACGTGATATA
ACTGGTTATAGAATTTCAGGGTTAGGGTTTAAAGAAAGGAGAAAGCCATTGGAAAAATGATGGGCTCCATTAAGGAGACTAATGAATCTG
GATGCAGAAATATGTCAGAAACTGGCATAAACATGATTGTAGTAGAATTTATTTTCCAGTACCAATAGGGAAATTATTTTAAGTTATTAC
ATTTACTGTATTGGGAAACTTGAGGAGAACTCTTTAGTTCATAAAGCTTCAATGTCTTTTTTTTTTTTTTCATGGAAAAACTCAAACCTC
TGTTATTTGGGAGCTCAGTATTGTGTGGACACTTACGAGAGTTTTCTGCTTAATTGAAGTGTAATATAGGTTGTAGAATTGTTACCTGCA
GTTCTATGGTTTTGTTTCACTTCTTTTCTTTTTTAAAGCCATTCTGTTCTTTGGATGTGCTTGAAAGGGTGTGTGATTACACCATTGTTA
ATGCTGGGTAAAAACTATCTTCTTGCAGCCTTGCCTCATAACAGTGGAATTTCTGATAGACAAACCACAGGACTTTGATTTTAAGCCAAA
TCCATCTCCATCCCTTTACTGTCAATCTTCTGTCCCAGTAGTTTAGCCTTTGTGGCTTAGGTTATGATGCGCCTCCTTCTGTGCGACCAA
TGAGACGACTTCAGCATCTTTTTAAAATAATCTAAGCATCATTGAAGCAGTAACACAAAAAAAAGGTTCAGTATTTTCTTTTTAGTATAA
CTTACATCCTTTCAAATAAGTCTTTGCCCTCATGAAGAATCCCTAGAGGAAGATAAGGAAAATAAGTATTTTCCAGTTTTGCTTGACAGT
TTCTAAACAAACAAAAATAAACTCAATGAAAGGAAAGATGTTTCTTTTTAGCTGAGATGACAGATTGCTTCTCTGTATTAAATAGTCTAG
AAGTTAAGGGGATGGTCACATTTACCATGTATTGTGTTATTAGCAGTTAAATTTTATGAATATGTTTGTAAAATTGTTGTTTTATATTTC
ATGTCAAATTGAAAAGTTTATTTCTTCACTATTGTACCTGTGGAAATACAAGCCATTTTACAGGAAAAAATCTTCAAAAACTATTAAATG
GATATCAGCCTGTTTGTGAGCCATTGTCTTCAGATTCTGTGGTTGTCACTGAGTTCATTAGGACATTTAGTAGGTTGATACGAGTAGAAC
TGATTTTTTTCACTTCTCTAACTTCCAAGTTAATCTCCAGCTGTTGAGTTTATTAATTGTTTTATATTCTGCACAATACATATTTAAACC

>79273_79273_1_SAV1-PELI2_SAV1_chr14_51111462_ENST00000324679_PELI2_chr14_56645053_ENST00000267460_length(amino acids)=663AA_BP=268
MLSRKKTKNEVSKPAEVQGKYVKKETSPLLRNLMPSFIRHGPTIPRRTDICLPDSSPNAFSTSGDVVSRNQSFLRTPIQRTPHEIMRRES
NRLSAPSYLARSLADVPREYGSSQSFVTEVSFAVENGDSGSRYYYSDNFFDGQRKRPLGDRAHEDYRYYEYNHDLFQRMPQNQGRHASGI
GRVAATSLGNLTNHGSEDLPLPPGWSVDWTMRGRKYYIDHNTNTTHWSHPLEREGLPPGWERVESSEFGTYYVDHTNKKAQYRHPCAPRY
NGALPNGDRGRRKSRFALYKRPKANGVKPSTVHVISTPQASKAISCKGQHSISYTLSRNQTVVVEYTHDKDTDMFQVGRSTESPIDFVVT
DTISGSQNTDEAQITQSTISRFACRIVCDRNEPYTARIFAAGFDSSKNIFLGEKAAKWKNPDGHMDGLTTNGVLVMHPRGGFTEESQPGV
WREISVCGDVYTLRETRSAQQRGKLVESETNVLQDGSLIDLCGATLLWRTADGLFHTPTQKHIEALRQEINAARPQCPVGLNTLAFPSIN
RKEVVEEKQPWAYLSCGHVHGYHNWGHRSDTEANERECPMCRTVGPYVPLWLGCEAGFYVDAGPPTHAFTPCGHVCSEKSAKYWSQIPLP

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Fusion Gene PPI Analysis for SAV1-PELI2


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 SAV1-PELI2


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 SAV1-PELI2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource