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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:SRGAP3-LHFPL4 (FusionGDB2 ID:85794)

Fusion Gene Summary for SRGAP3-LHFPL4

check button Fusion gene summary
Fusion gene informationFusion gene name: SRGAP3-LHFPL4
Fusion gene ID: 85794
HgeneTgene
Gene symbol

SRGAP3

LHFPL4

Gene ID

23380

375612

Gene nameSLIT-ROBO Rho GTPase activating protein 2LHFPL tetraspan subfamily member 3
SynonymsARHGAP34|FNBP2|SRGAP2A|SRGAP3LHFPL4
Cytomap

1q32.1

7q22.2-q22.3

Type of geneprotein-codingprotein-coding
DescriptionSLIT-ROBO Rho GTPase-activating protein 2SLIT-ROBO GAP2formin-binding protein 2rho GTPase-activating protein 34LHFPL tetraspan subfamily member 3 proteinLHFP-like protein 3lipoma HMGIC fusion partner-like 3 proteinlipoma HMGIC fusion partner-like 4
Modification date2020031320200313
UniProtAcc.

Q7Z7J7

Ensembl transtripts involved in fusion geneENST00000383836, ENST00000360413, 
ENST00000433332, 
ENST00000287585, 
ENST00000495730, 
Fusion gene scores* DoF score12 X 10 X 10=12003 X 3 X 3=27
# samples 185
** MAII scorelog2(18/1200*10)=-2.73696559416621
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/27*10)=0.888968687611256
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: SRGAP3 [Title/Abstract] AND LHFPL4 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSRGAP3(9290569)-LHFPL4(9547887), # samples:5
Anticipated loss of major functional domain due to fusion event.SRGAP3-LHFPL4 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
SRGAP3-LHFPL4 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
SRGAP3-LHFPL4 seems lost the major protein functional domain in Hgene 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
HgeneSRGAP3

GO:0043547

positive regulation of GTPase activity

21148482

HgeneSRGAP3

GO:0046847

filopodium assembly

22559944

HgeneSRGAP3

GO:0051014

actin filament severing

21148482

HgeneSRGAP3

GO:0060996

dendritic spine development

22559944

HgeneSRGAP3

GO:2001223

negative regulation of neuron migration

22559944


check buttonFusion gene breakpoints across SRGAP3 (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 LHFPL4 (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
ChimerDB4UCECTCGA-EO-A1Y7-01ASRGAP3chr3

9290569

-LHFPL4chr3

9547887

-
ChimerDB4UCECTCGA-KJ-A3U4-01ASRGAP3chr3

9290569

-LHFPL4chr3

9547887

-
ChimerDB4UCECTCGA-KJ-A3U4-01ASRGAP3chr3

9290569

-LHFPL4chr3

9547887

-
ChimerDB4UCECTCGA-A5-A2K4-01ASRGAP3chr3

9054992

-LHFPL4chr3

9547887

-
ChimerDB4UCECTCGA-EO-A1Y7-01ASRGAP3chr3

9290569

-LHFPL4chr3

9547887

-
ChimerDB4UCECTCGA-KJ-A3U4-01ASRGAP3chr3

9290569

-LHFPL4chr3

9547887

-


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Fusion Gene ORF analysis for SRGAP3-LHFPL4

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-shiftENST00000383836ENST00000287585SRGAP3chr3

9290569

-LHFPL4chr3

9547887

-
5CDS-intronENST00000383836ENST00000495730SRGAP3chr3

9290569

-LHFPL4chr3

9547887

-
Frame-shiftENST00000360413ENST00000287585SRGAP3chr3

9290569

-LHFPL4chr3

9547887

-
5CDS-intronENST00000360413ENST00000495730SRGAP3chr3

9290569

-LHFPL4chr3

9547887

-
intron-3CDSENST00000433332ENST00000287585SRGAP3chr3

9290569

-LHFPL4chr3

9547887

-
intron-intronENST00000433332ENST00000495730SRGAP3chr3

9290569

-LHFPL4chr3

9547887

-
Frame-shiftENST00000383836ENST00000287585SRGAP3chr3

9054992

-LHFPL4chr3

9547887

-
5CDS-intronENST00000383836ENST00000495730SRGAP3chr3

9054992

-LHFPL4chr3

9547887

-
Frame-shiftENST00000360413ENST00000287585SRGAP3chr3

9054992

-LHFPL4chr3

9547887

-
5CDS-intronENST00000360413ENST00000495730SRGAP3chr3

9054992

-LHFPL4chr3

9547887

-
intron-3CDSENST00000433332ENST00000287585SRGAP3chr3

9054992

-LHFPL4chr3

9547887

-
intron-intronENST00000433332ENST00000495730SRGAP3chr3

9054992

-LHFPL4chr3

9547887

-

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 SRGAP3-LHFPL4


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 SRGAP3-LHFPL4


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
.LHFPL4

Q7Z7J7

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: Plays a role in the regulation of inhibitory synapse formation and function by being involved in maintening gamma-aminobutyric acid receptors (GABAARs) clustering and their associated scaffold proteins at inhibitory synaptic sites. Acts in concert with NLGN2 to recruit or stabilize GABAARs. {ECO:0000250|UniProtKB:Q5U4E0}.

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 SRGAP3-LHFPL4


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 SRGAP3-LHFPL4


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 SRGAP3-LHFPL4


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 SRGAP3-LHFPL4


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSRGAP3C1519086Pilomyxoid astrocytoma2ORPHANET
HgeneSRGAP3C0020796Profound Mental Retardation1CTD_human
HgeneSRGAP3C0025363Mental Retardation, Psychosocial1CTD_human
HgeneSRGAP3C0036341Schizophrenia1PSYGENET
HgeneSRGAP3C0795806Chromosome 3, monosomy 3p1GENOMICS_ENGLAND
HgeneSRGAP3C0917816Mental deficiency1CTD_human
HgeneSRGAP3C1535926Neurodevelopmental Disorders1CTD_human
HgeneSRGAP3C2931337Chromosome 3, monosomy 3p251CTD_human
HgeneSRGAP3C3714756Intellectual Disability1CTD_human