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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:SNHG1-SLC27A5 (FusionGDB2 ID:84556)

Fusion Gene Summary for SNHG1-SLC27A5

check button Fusion gene summary
Fusion gene informationFusion gene name: SNHG1-SLC27A5
Fusion gene ID: 84556
HgeneTgene
Gene symbol

SNHG1

SLC27A5

Gene ID

23642

10998

Gene namesmall nucleolar RNA host gene 1solute carrier family 27 member 5
SynonymsLINC00057|NCRNA00057|U22HG|UHG|lncRNA16ACSB|ACSVL6|BACS|BAL|FACVL3|FATP-5|FATP5|VLACSR|VLCS-H2|VLCSH2
Cytomap

11q12.3

19q13.43

Type of genencRNAprotein-coding
DescriptionU22 snoRNA hostlong intergenic non-protein coding RNA 57small nucleolar RNA host gene 1 (non-protein coding)bile acyl-CoA synthetaseBA-CoA ligaseVLACS-relatedbile acid-CoA ligasecholate--CoA ligasefatty acid transport protein 5fatty-acid-Coenzyme A ligase, very long-chain 3solute carrier family 27 (fatty acid transporter), member 5very long-chain acyl-C
Modification date2020031520200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000383926, ENST00000363981, 
ENST00000364799, ENST00000365607, 
ENST00000384147, ENST00000384693, 
ENST00000384706, ENST00000384756, 
ENST00000516331, 
ENST00000263093, 
ENST00000601355, ENST00000594786, 
ENST00000599700, 
Fusion gene scores* DoF score18 X 13 X 5=11703 X 2 X 3=18
# samples 183
** MAII scorelog2(18/1170*10)=-2.70043971814109
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: SNHG1 [Title/Abstract] AND SLC27A5 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSNHG1(62621379)-SLC27A5(59023364), # 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
TgeneSLC27A5

GO:0000038

very long-chain fatty acid metabolic process

10479480

TgeneSLC27A5

GO:0006699

bile acid biosynthetic process

11980911


check buttonFusion gene breakpoints across SNHG1 (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 SLC27A5 (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
ChiTaRS5.0N/ADA285853SNHG1chr11

62621379

-SLC27A5chr19

59023364

-


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Fusion Gene ORF analysis for SNHG1-SLC27A5

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-5UTRENST00000383926ENST00000263093SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
5CDS-5UTRENST00000383926ENST00000601355SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
5CDS-intronENST00000383926ENST00000594786SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
5CDS-intronENST00000383926ENST00000599700SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-5UTRENST00000363981ENST00000263093SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-5UTRENST00000363981ENST00000601355SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-5UTRENST00000364799ENST00000263093SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-5UTRENST00000364799ENST00000601355SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-5UTRENST00000365607ENST00000263093SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-5UTRENST00000365607ENST00000601355SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-5UTRENST00000384147ENST00000263093SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-5UTRENST00000384147ENST00000601355SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-5UTRENST00000384693ENST00000263093SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-5UTRENST00000384693ENST00000601355SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-5UTRENST00000384706ENST00000263093SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-5UTRENST00000384706ENST00000601355SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-5UTRENST00000384756ENST00000263093SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-5UTRENST00000384756ENST00000601355SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-5UTRENST00000516331ENST00000263093SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-5UTRENST00000516331ENST00000601355SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-intronENST00000363981ENST00000594786SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-intronENST00000363981ENST00000599700SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-intronENST00000364799ENST00000594786SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-intronENST00000364799ENST00000599700SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-intronENST00000365607ENST00000594786SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-intronENST00000365607ENST00000599700SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-intronENST00000384147ENST00000594786SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-intronENST00000384147ENST00000599700SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-intronENST00000384693ENST00000594786SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-intronENST00000384693ENST00000599700SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-intronENST00000384706ENST00000594786SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-intronENST00000384706ENST00000599700SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-intronENST00000384756ENST00000594786SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-intronENST00000384756ENST00000599700SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-intronENST00000516331ENST00000594786SNHG1chr11

62621379

-SLC27A5chr19

59023364

-
intron-intronENST00000516331ENST00000599700SNHG1chr11

62621379

-SLC27A5chr19

59023364

-

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 SNHG1-SLC27A5


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 SNHG1-SLC27A5


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/:62621379/:59023364)
- 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

- 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 SNHG1-SLC27A5


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 SNHG1-SLC27A5


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 SNHG1-SLC27A5


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 SNHG1-SLC27A5


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