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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:SART1-DRD4 (FusionGDB2 ID:78726)

Fusion Gene Summary for SART1-DRD4

check button Fusion gene summary
Fusion gene informationFusion gene name: SART1-DRD4
Fusion gene ID: 78726
HgeneTgene
Gene symbol

SART1

DRD4

Gene ID

9092

1815

Gene namespliceosome associated factor 1, recruiter of U4/U6.U5 tri-snRNPdopamine receptor D4
SynonymsAra1|HAF|HOMS1|SART1259|SNRNP110|Snu66D4DR
Cytomap

11q13.1

11p15.5

Type of geneprotein-codingprotein-coding
DescriptionU4/U6.U5 tri-snRNP-associated protein 1IgE autoantigenSART-1SART1(259) proteinSART1(800) proteinSART1, U4/U6.U5 tri-snRNP-associated protein 1SNU66 homologU4/U6.U5 tri-snRNP-associated 110 kDa proteinhSART-1hSnu66hypoxia associated factorsmall D(4) dopamine receptorD(2C) dopamine receptordopamine D4 receptorseven transmembrane helix receptor
Modification date2020031320200329
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000312397, ENST00000528573, 
ENST00000176183, ENST00000528733, 
Fusion gene scores* DoF score5 X 5 X 3=754 X 5 X 3=60
# samples 57
** MAII scorelog2(5/75*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/60*10)=0.222392421336448
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: SART1 [Title/Abstract] AND DRD4 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSART1(65744524)-DRD4(637540), # samples:1
Anticipated loss of major functional domain due to fusion event.SART1-DRD4 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
SART1-DRD4 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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
HgeneSART1

GO:0000398

mRNA splicing, via spliceosome

28781166

HgeneSART1

GO:0045585

positive regulation of cytotoxic T cell differentiation

10209962

TgeneDRD4

GO:0000187

activation of MAPK activity

9843378|15755724

TgeneDRD4

GO:0007195

adenylate cyclase-inhibiting dopamine receptor signaling pathway

7512953|9003072|9843378

TgeneDRD4

GO:0007212

dopamine receptor signaling pathway

1840645

TgeneDRD4

GO:0032417

positive regulation of sodium:proton antiporter activity

7512953

TgeneDRD4

GO:0033674

positive regulation of kinase activity

15755724

TgeneDRD4

GO:0034776

response to histamine

16839358

TgeneDRD4

GO:0050482

arachidonic acid secretion

7512953

TgeneDRD4

GO:0050709

negative regulation of protein secretion

16839358

TgeneDRD4

GO:1901386

negative regulation of voltage-gated calcium channel activity

7921596


check buttonFusion gene breakpoints across SART1 (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 DRD4 (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/ABQ186689SART1chr11

65744524

+DRD4chr11

637540

+


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Fusion Gene ORF analysis for SART1-DRD4

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-shiftENST00000312397ENST00000176183SART1chr11

65744524

+DRD4chr11

637540

+
5CDS-intronENST00000312397ENST00000528733SART1chr11

65744524

+DRD4chr11

637540

+
intron-3CDSENST00000528573ENST00000176183SART1chr11

65744524

+DRD4chr11

637540

+
intron-intronENST00000528573ENST00000528733SART1chr11

65744524

+DRD4chr11

637540

+

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 SART1-DRD4


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 SART1-DRD4


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
..
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: 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.

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 SART1-DRD4


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 SART1-DRD4


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 SART1-DRD4


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 SART1-DRD4


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneDRD4C0001973Alcoholic Intoxication, Chronic5PSYGENET
TgeneDRD4C0005586Bipolar Disorder5PSYGENET
TgeneDRD4C0011570Mental Depression5PSYGENET
TgeneDRD4C0011581Depressive disorder5PSYGENET
TgeneDRD4C0041696Unipolar Depression5PSYGENET
TgeneDRD4C0525045Mood Disorders5PSYGENET
TgeneDRD4C1269683Major Depressive Disorder5PSYGENET
TgeneDRD4C0024809Marijuana Abuse4PSYGENET
TgeneDRD4C0041671Attention Deficit Disorder4CTD_human
TgeneDRD4C0085159Seasonal Affective Disorder4PSYGENET
TgeneDRD4C1263846Attention deficit hyperactivity disorder4CTD_human
TgeneDRD4C1321905Minimal Brain Dysfunction4CTD_human
TgeneDRD4C0001969Alcoholic Intoxication3PSYGENET
TgeneDRD4C0085762Alcohol abuse2PSYGENET
TgeneDRD4C0003477Separation Anxiety Disorder1CTD_human
TgeneDRD4C0008074Child Development Disorders, Pervasive1CTD_human
TgeneDRD4C0008701Chronic Motor or Vocal Tic Disorder1CTD_human
TgeneDRD4C0012734Disruptive Behavior Disorder1CTD_human
TgeneDRD4C0029121Oppositional Defiant Disorder1CTD_human
TgeneDRD4C0036341Schizophrenia1CTD_human
TgeneDRD4C0040188Tic disorder1CTD_human
TgeneDRD4C0040702Transient Tic Disorder1CTD_human
TgeneDRD4C0233477Dysphoric mood1PSYGENET
TgeneDRD4C0236733Amphetamine-Related Disorders1CTD_human
TgeneDRD4C0236804Amphetamine Addiction1CTD_human
TgeneDRD4C0236807Amphetamine Abuse1CTD_human
TgeneDRD4C0236964Attention Deficit and Disruptive Behavior Disorders1CTD_human
TgeneDRD4C0338468Tic Disorders, Vocal1CTD_human
TgeneDRD4C0524528Pervasive Development Disorder1CTD_human
TgeneDRD4C0751553Childhood Tic Disorders1CTD_human
TgeneDRD4C0751554Motor Tic Disorders1CTD_human
TgeneDRD4C3160814Cannabis use1PSYGENET