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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:CERS5-INO80C

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CERS5-INO80C
FusionPDB ID: 15986
FusionGDB2.0 ID: 15986
HgeneTgene
Gene symbol

CERS5

INO80C

Gene ID

253782

125476

Gene nameceramide synthase 6INO80 complex subunit C
SynonymsCERS5|LASS6C18orf37|IES6|hIes6
Cytomap

2q24.3

18q12.2

Type of geneprotein-codingprotein-coding
Descriptionceramide synthase 6LAG1 homolog, ceramide synthase 6longevity assurance homolog 6INO80 complex subunit CIES6 homolog
Modification date2020031320200313
UniProtAcc

Q8N5B7

Q6PI98

Ensembl transtripts involved in fusion geneENST idsENST00000317551, ENST00000422340, 
ENST00000547852, 
ENST00000586489, 
ENST00000441607, ENST00000590757, 
ENST00000334598, ENST00000592173, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score8 X 6 X 7=3363 X 3 X 3=27
# samples 103
** MAII scorelog2(10/336*10)=-1.74846123300404
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context (manual curation of fusion genes in FusionPDB)

PubMed: CERS5 [Title/Abstract] AND INO80C [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CERS5(50560883)-INO80C(33060527), # samples:1
Anticipated loss of major functional domain due to fusion event.CERS5-INO80C 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.
CERS5-INO80C 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.
* 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
HgeneCERS5

GO:0046513

ceramide biosynthetic process

17609214|17977534


check buttonFusion gene breakpoints across CERS5 (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 INO80C (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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
ChimerDB4ESCATCGA-L5-A8NKCERS5chr12

50560883

-INO80Cchr18

33060527

-


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000317551CERS5chr1250560883-ENST00000592173INO80Cchr1833060527-33523224730158
ENST00000317551CERS5chr1250560883-ENST00000334598INO80Cchr1833060527-10233224730158

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
ENST00000317551ENST00000592173CERS5chr1250560883-INO80Cchr1833060527-0.0038776260.9961223
ENST00000317551ENST00000334598CERS5chr1250560883-INO80Cchr1833060527-0.0162971110.9837029

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>15986_15986_1_CERS5-INO80C_CERS5_chr12_50560883_ENST00000317551_INO80C_chr18_33060527_ENST00000334598_length(amino acids)=158AA_BP=1
MFFLPATAPPWPECTKLGSLNGKGLAAFSTGPVLNSEGTILFSLMASMLIPARRAASRRRCPPPAGTPRGCAGRGGNRSRRPAPPDQPSS

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

>15986_15986_2_CERS5-INO80C_CERS5_chr12_50560883_ENST00000317551_INO80C_chr18_33060527_ENST00000592173_length(amino acids)=158AA_BP=1
MFFLPATAPPWPECTKLGSLNGKGLAAFSTGPVLNSEGTILFSLMASMLIPARRAASRRRCPPPAGTPRGCAGRGGNRSRRPAPPDQPSS

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

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Fusion Protein Functional Features


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/chr12:50560883/chr18:33060527)
- 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
CERS5

Q8N5B7

INO80C

Q6PI98

FUNCTION: Ceramide synthase that catalyzes formation of ceramide from sphinganine and acyl-CoA substrates, with high selectivity toward palmitoyl-CoA (hexadecanoyl-CoA; C16:0-CoA) as acyl donor (PubMed:16951403, PubMed:18541923, PubMed:22144673, PubMed:22661289, PubMed:23530041, PubMed:26887952, PubMed:29632068, PubMed:31916624). Can use other acyl donors, but with less efficiency (By similarity). {ECO:0000250|UniProtKB:Q9D6K9, ECO:0000269|PubMed:16951403, ECO:0000269|PubMed:18541923, ECO:0000269|PubMed:22144673, ECO:0000269|PubMed:22661289, ECO:0000269|PubMed:23530041, ECO:0000269|PubMed:26887952, ECO:0000269|PubMed:29632068, ECO:0000269|PubMed:31916624}.FUNCTION: Proposed core component of the chromatin remodeling INO80 complex which is involved in transcriptional regulation, DNA replication and probably DNA repair.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneCERS5chr12:50560883chr18:33060527ENST00000317551-1101_4665.66666666666667393.0Topological domainLumenal
HgeneCERS5chr12:50560883chr18:33060527ENST00000317551-11047_6765.66666666666667393.0TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneCERS5chr12:50560883chr18:33060527ENST00000317551-110139_34065.66666666666667393.0DomainTLC
HgeneCERS5chr12:50560883chr18:33060527ENST00000317551-11075_13665.66666666666667393.0RegionHomeobox-like
HgeneCERS5chr12:50560883chr18:33060527ENST00000317551-110332_39265.66666666666667393.0Topological domainCytoplasmic
HgeneCERS5chr12:50560883chr18:33060527ENST00000317551-110148_16865.66666666666667393.0TransmembraneHelical
HgeneCERS5chr12:50560883chr18:33060527ENST00000317551-110183_20365.66666666666667393.0TransmembraneHelical
HgeneCERS5chr12:50560883chr18:33060527ENST00000317551-110214_23465.66666666666667393.0TransmembraneHelical
HgeneCERS5chr12:50560883chr18:33060527ENST00000317551-110272_29265.66666666666667393.0TransmembraneHelical
HgeneCERS5chr12:50560883chr18:33060527ENST00000317551-110311_33165.66666666666667393.0TransmembraneHelical


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
CERS5
INO80C


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to CERS5-INO80C


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to CERS5-INO80C


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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