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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:SACS-MIPEP (FusionGDB2 ID:78507)

Fusion Gene Summary for SACS-MIPEP

check button Fusion gene summary
Fusion gene informationFusion gene name: SACS-MIPEP
Fusion gene ID: 78507
HgeneTgene
Gene symbol

SACS

MIPEP

Gene ID

26278

4285

Gene namesacsin molecular chaperonemitochondrial intermediate peptidase
SynonymsARSACS|DNAJC29|PPP1R138|SPAX6COXPD31|HMIP|MIP
Cytomap

13q12.12

13q12.12

Type of geneprotein-codingprotein-coding
DescriptionsacsindnaJ homolog subfamily C member 29protein phosphatase 1, regulatory subunit 138spastic ataxia of Charlevoix-Saguenay (sacsin)mitochondrial intermediate peptidase
Modification date2020031320200313
UniProtAcc.

Q99797

Ensembl transtripts involved in fusion geneENST00000382298, ENST00000402364, 
ENST00000382292, ENST00000476776, 
ENST00000382172, ENST00000469167, 
Fusion gene scores* DoF score13 X 9 X 5=58510 X 7 X 7=490
# samples 1314
** MAII scorelog2(13/585*10)=-2.16992500144231
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(14/490*10)=-1.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SACS [Title/Abstract] AND MIPEP [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSACS(23985359)-MIPEP(24415627), # samples:3
Anticipated loss of major functional domain due to fusion event.SACS-MIPEP seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
SACS-MIPEP seems lost the major protein functional domain in Tgene 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 SACS (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 MIPEP (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
ChimerDB4LUSCTCGA-46-3767-01ASACSchr13

23985359

-MIPEPchr13

24415627

-
ChimerDB4LUSCTCGA-46-3767SACSchr13

23985358

-MIPEPchr13

24415627

-
ChimerDB4LUSCTCGA-46-3767SACSchr13

23985359

-MIPEPchr13

24415627

-
ChimerDB4LUSCTCGA-46-3767-01ASACSchr13

23985359

-MIPEPchr13

24415627

-


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Fusion Gene ORF analysis for SACS-MIPEP

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-shiftENST00000382298ENST00000382172SACSchr13

23985359

-MIPEPchr13

24415627

-
5CDS-intronENST00000382298ENST00000469167SACSchr13

23985359

-MIPEPchr13

24415627

-
intron-3CDSENST00000402364ENST00000382172SACSchr13

23985359

-MIPEPchr13

24415627

-
intron-intronENST00000402364ENST00000469167SACSchr13

23985359

-MIPEPchr13

24415627

-
Frame-shiftENST00000382292ENST00000382172SACSchr13

23985359

-MIPEPchr13

24415627

-
5CDS-intronENST00000382292ENST00000469167SACSchr13

23985359

-MIPEPchr13

24415627

-
intron-3CDSENST00000476776ENST00000382172SACSchr13

23985359

-MIPEPchr13

24415627

-
intron-intronENST00000476776ENST00000469167SACSchr13

23985359

-MIPEPchr13

24415627

-
Frame-shiftENST00000382298ENST00000382172SACSchr13

23985358

-MIPEPchr13

24415627

-
5CDS-intronENST00000382298ENST00000469167SACSchr13

23985358

-MIPEPchr13

24415627

-
intron-3CDSENST00000402364ENST00000382172SACSchr13

23985358

-MIPEPchr13

24415627

-
intron-intronENST00000402364ENST00000469167SACSchr13

23985358

-MIPEPchr13

24415627

-
Frame-shiftENST00000382292ENST00000382172SACSchr13

23985358

-MIPEPchr13

24415627

-
5CDS-intronENST00000382292ENST00000469167SACSchr13

23985358

-MIPEPchr13

24415627

-
intron-3CDSENST00000476776ENST00000382172SACSchr13

23985358

-MIPEPchr13

24415627

-
intron-intronENST00000476776ENST00000469167SACSchr13

23985358

-MIPEPchr13

24415627

-

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

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Fusion Genomic Features for SACS-MIPEP


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)

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.

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Fusion Protein Features for SACS-MIPEP


check button Go to

FGviewer for the breakpoints of :-:

.
- 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
.MIPEP

Q99797

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: Cleaves proteins, imported into the mitochondrion, to their mature size.

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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Fusion Gene Sequence for SACS-MIPEP


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.

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Fusion Gene PPI Analysis for SACS-MIPEP


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 SACS-MIPEP


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 SACS-MIPEP


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSACSC1849140SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE15CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneSACSC0751776Atypical Inclusion-Body Disease1CTD_human
HgeneSACSC0751777Familial Progressive Myoclonic Epilepsy1CTD_human
HgeneSACSC0751778Myoclonic Epilepsies, Progressive1CTD_human
HgeneSACSC0751779Action Myoclonus-Renal Failure Syndrome1CTD_human
HgeneSACSC0751780Biotin-Responsive Encephalopathy1CTD_human
HgeneSACSC0751781Dentatorubral-Pallidoluysian Atrophy1CTD_human
HgeneSACSC0751782May-White Syndrome1CTD_human
HgeneSACSC3714756Intellectual Disability1GENOMICS_ENGLAND
TgeneMIPEPC4310661COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 312CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT