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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:LAMB2-LAMB2 (FusionGDB2 ID:43699)

Fusion Gene Summary for LAMB2-LAMB2

check button Fusion gene summary
Fusion gene informationFusion gene name: LAMB2-LAMB2
Fusion gene ID: 43699
HgeneTgene
Gene symbol

LAMB2

LAMB2

Gene ID

84823

84823

Gene namelamin B2lamin B2
SynonymsEPM9|LAMB2|LMN2EPM9|LAMB2|LMN2
Cytomap

19p13.3

19p13.3

Type of geneprotein-codingprotein-coding
Descriptionlamin-B2epididymis secretory sperm binding proteinlamin B3lamin-B2epididymis secretory sperm binding proteinlamin B3
Modification date2020031320200313
UniProtAcc

P55268

P55268

Ensembl transtripts involved in fusion geneENST00000418109, ENST00000305544, 
ENST00000464891, 
ENST00000418109, 
ENST00000305544, ENST00000464891, 
Fusion gene scores* DoF score6 X 6 X 2=723 X 4 X 2=24
# samples 74
** MAII scorelog2(7/72*10)=-0.0406419844973459
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/24*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: LAMB2 [Title/Abstract] AND LAMB2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointLAMB2(49158646)-LAMB2(49159420), # samples:1
LAMB2(49166576)-LAMB2(49165945), # 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

check buttonFusion gene breakpoints across LAMB2 (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 LAMB2 (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/AAW996518LAMB2chr3

49158646

-LAMB2chr3

49159420

-
ChiTaRS5.0N/ABF803132LAMB2chr3

49166576

+LAMB2chr3

49165945

-


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Fusion Gene ORF analysis for LAMB2-LAMB2

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-3CDSENST00000418109ENST00000418109LAMB2chr3

49158646

-LAMB2chr3

49159420

-
intron-3CDSENST00000418109ENST00000305544LAMB2chr3

49158646

-LAMB2chr3

49159420

-
intron-intronENST00000418109ENST00000464891LAMB2chr3

49158646

-LAMB2chr3

49159420

-
intron-3CDSENST00000305544ENST00000418109LAMB2chr3

49158646

-LAMB2chr3

49159420

-
intron-3CDSENST00000305544ENST00000305544LAMB2chr3

49158646

-LAMB2chr3

49159420

-
intron-intronENST00000305544ENST00000464891LAMB2chr3

49158646

-LAMB2chr3

49159420

-
intron-3CDSENST00000464891ENST00000418109LAMB2chr3

49158646

-LAMB2chr3

49159420

-
intron-3CDSENST00000464891ENST00000305544LAMB2chr3

49158646

-LAMB2chr3

49159420

-
intron-intronENST00000464891ENST00000464891LAMB2chr3

49158646

-LAMB2chr3

49159420

-
intron-3CDSENST00000418109ENST00000418109LAMB2chr3

49166576

+LAMB2chr3

49165945

-
intron-3CDSENST00000418109ENST00000305544LAMB2chr3

49166576

+LAMB2chr3

49165945

-
intron-intronENST00000418109ENST00000464891LAMB2chr3

49166576

+LAMB2chr3

49165945

-
intron-3CDSENST00000305544ENST00000418109LAMB2chr3

49166576

+LAMB2chr3

49165945

-
intron-3CDSENST00000305544ENST00000305544LAMB2chr3

49166576

+LAMB2chr3

49165945

-
intron-intronENST00000305544ENST00000464891LAMB2chr3

49166576

+LAMB2chr3

49165945

-
intron-3CDSENST00000464891ENST00000418109LAMB2chr3

49166576

+LAMB2chr3

49165945

-
intron-3CDSENST00000464891ENST00000305544LAMB2chr3

49166576

+LAMB2chr3

49165945

-
intron-intronENST00000464891ENST00000464891LAMB2chr3

49166576

+LAMB2chr3

49165945

-

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 LAMB2-LAMB2


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 LAMB2-LAMB2


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
LAMB2

P55268

LAMB2

P55268

FUNCTION: Binding to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components.FUNCTION: Binding to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components.

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 LAMB2-LAMB2


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 LAMB2-LAMB2


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 LAMB2-LAMB2


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 LAMB2-LAMB2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneLAMB2C1836876Pierson syndrome6CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneLAMB2C3280113NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES4CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneLAMB2C0009241Cognition Disorders1CTD_human
HgeneLAMB2C0033578Prostatic Neoplasms1CTD_human
HgeneLAMB2C0268747Diffuse mesangial sclerosis (disorder)1CTD_human
HgeneLAMB2C0376358Malignant neoplasm of prostate1CTD_human
HgeneLAMB2C0751882Myasthenic Syndromes, Congenital1GENOMICS_ENGLAND
HgeneLAMB2C3489732Familial mesangial sclerosis1CTD_human
HgeneLAMB2C3501249Nephrotic Syndrome, Congenital, With Ocular Abnormalities And Congenital Myasthenic Syndrome1CTD_human
TgeneLAMB2C1836876Pierson syndrome6CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneLAMB2C3280113NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES4CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneLAMB2C0009241Cognition Disorders1CTD_human
TgeneLAMB2C0033578Prostatic Neoplasms1CTD_human
TgeneLAMB2C0268747Diffuse mesangial sclerosis (disorder)1CTD_human
TgeneLAMB2C0376358Malignant neoplasm of prostate1CTD_human
TgeneLAMB2C0751882Myasthenic Syndromes, Congenital1GENOMICS_ENGLAND
TgeneLAMB2C3489732Familial mesangial sclerosis1CTD_human
TgeneLAMB2C3501249Nephrotic Syndrome, Congenital, With Ocular Abnormalities And Congenital Myasthenic Syndrome1CTD_human