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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:LNX1-GABRB1 (FusionGDB2 ID:45630)

Fusion Gene Summary for LNX1-GABRB1

check button Fusion gene summary
Fusion gene informationFusion gene name: LNX1-GABRB1
Fusion gene ID: 45630
HgeneTgene
Gene symbol

LNX1

GABRB1

Gene ID

84708

2560

Gene nameligand of numb-protein X 1gamma-aminobutyric acid type A receptor subunit beta1
SynonymsLNX|MPDZ|PDZRN2EIEE45
Cytomap

4q12

4p12

Type of geneprotein-codingprotein-coding
DescriptionE3 ubiquitin-protein ligase LNXPDZ domain-containing ring finger protein 2RING-type E3 ubiquitin transferase LNXligand of numb-protein X 1, E3 ubiquitin protein ligasemulti-PDZ-domain-containing protein, E3 ubiquitin-protein ligase LNXnumb-binding prgamma-aminobutyric acid receptor subunit beta-1gamma-aminobutyric acid (GABA) A receptor, beta 1gamma-aminobutyric acid type A receptor beta1 subunit
Modification date2020032720200313
UniProtAcc

Q8TBB1

P18505

Ensembl transtripts involved in fusion geneENST00000306888, ENST00000263925, 
ENST00000504605, 
ENST00000295454, 
ENST00000538619, ENST00000509366, 
Fusion gene scores* DoF score12 X 7 X 7=5885 X 2 X 4=40
# samples 135
** MAII scorelog2(13/588*10)=-2.17730453180791
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/40*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: LNX1 [Title/Abstract] AND GABRB1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointLNX1(54439790)-GABRB1(47322144), # samples:2
Anticipated loss of major functional domain due to fusion event.LNX1-GABRB1 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
LNX1-GABRB1 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
TgeneGABRB1

GO:1902476

chloride transmembrane transport

9039914


check buttonFusion gene breakpoints across LNX1 (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 GABRB1 (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
ChimerDB4BRCATCGA-A8-A09A-01ALNX1chr4

54439790

-GABRB1chr4

47322144

+
ChimerDB4BRCATCGA-A8-A09A-01ALNX1chr4

54439790

-GABRB1chr4

47322144

+


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Fusion Gene ORF analysis for LNX1-GABRB1

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
intron-3CDSENST00000306888ENST00000295454LNX1chr4

54439790

-GABRB1chr4

47322144

+
intron-3CDSENST00000306888ENST00000538619LNX1chr4

54439790

-GABRB1chr4

47322144

+
intron-intronENST00000306888ENST00000509366LNX1chr4

54439790

-GABRB1chr4

47322144

+
Frame-shiftENST00000263925ENST00000295454LNX1chr4

54439790

-GABRB1chr4

47322144

+
Frame-shiftENST00000263925ENST00000538619LNX1chr4

54439790

-GABRB1chr4

47322144

+
5CDS-intronENST00000263925ENST00000509366LNX1chr4

54439790

-GABRB1chr4

47322144

+
intron-3CDSENST00000504605ENST00000295454LNX1chr4

54439790

-GABRB1chr4

47322144

+
intron-3CDSENST00000504605ENST00000538619LNX1chr4

54439790

-GABRB1chr4

47322144

+
intron-intronENST00000504605ENST00000509366LNX1chr4

54439790

-GABRB1chr4

47322144

+

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 LNX1-GABRB1


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)
LNX1chr454439789-GABRB1chr447322143+1.31E-050.9999869
LNX1chr454439789-GABRB1chr447322143+1.31E-050.9999869

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 LNX1-GABRB1


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
LNX1

Q8TBB1

GABRB1

P18505

FUNCTION: E3 ubiquitin-protein ligase that mediates ubiquitination and subsequent proteasomal degradation of NUMB. E3 ubiquitin ligases accept ubiquitin from an E2 ubiquitin-conjugating enzyme in the form of a thioester and then directly transfers the ubiquitin to targeted substrates. Mediates ubiquitination of isoform p66 and isoform p72 of NUMB, but not that of isoform p71 or isoform p65. {ECO:0000250|UniProtKB:O70263}.; FUNCTION: Isoform 2 provides an endocytic scaffold for IGSF5/JAM4. {ECO:0000250|UniProtKB:O70263}.FUNCTION: Component of the heteropentameric receptor for GABA, the major inhibitory neurotransmitter in the vertebrate brain. Functions also as histamine receptor and mediates cellular responses to histamine. Functions as receptor for diazepines and various anesthetics, such as pentobarbital; these are bound at a separate allosteric effector binding site. Functions as ligand-gated chloride channel. {ECO:0000269|PubMed:26950270}.

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 LNX1-GABRB1


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 LNX1-GABRB1


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 LNX1-GABRB1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneGABRB1P18505DB00898EthanolSmall moleculeApproved
TgeneGABRB1P18505DB01440gamma-Hydroxybutyric acidAgonistSmall moleculeApproved|Illicit|Investigational
TgeneGABRB1P18505DB00431LindaneAntagonistSmall moleculeApproved|Withdrawn

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Related Diseases for LNX1-GABRB1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneGABRB1C0001973Alcoholic Intoxication, Chronic5PSYGENET
TgeneGABRB1C4310691EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 453CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneGABRB1C0004352Autistic Disorder2CTD_human
TgeneGABRB1C0005586Bipolar Disorder2PSYGENET
TgeneGABRB1C0036341Schizophrenia2PSYGENET
TgeneGABRB1C0019147Hepatic Coma1CTD_human
TgeneGABRB1C0019151Hepatic Encephalopathy1CTD_human
TgeneGABRB1C0035222Respiratory Distress Syndrome, Adult1CTD_human
TgeneGABRB1C0270496Schizoaffective disorder, bipolar type1PSYGENET
TgeneGABRB1C0751197Fulminant Hepatic Failure with Cerebral Edema1CTD_human
TgeneGABRB1C0751198Hepatic Stupor1CTD_human