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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:LIPA-TMEM132A (FusionGDB2 ID:45378)

Fusion Gene Summary for LIPA-TMEM132A

check button Fusion gene summary
Fusion gene informationFusion gene name: LIPA-TMEM132A
Fusion gene ID: 45378
HgeneTgene
Gene symbol

LIPA

TMEM132A

Gene ID

10648

54972

Gene namesecretoglobin family 1D member 1transmembrane protein 132A
SynonymsLIPA|LPHA|LPNAGBP|HSPA5BP1
Cytomap

11q12.3

11q12.2

Type of geneprotein-codingprotein-coding
Descriptionsecretoglobin family 1D member 1lipophilin A (uteroglobin family member)lipophilin-Aprostatein-like lipophilin Atransmembrane protein 132AGRP78-binding proteinHSPA5-binding protein 1glucose-regulated protein, 78kDaheat shock 70kDa protein 5 (glucose-regulated protein, 78kDa) binding protein 1heat shock 70kDa protein 5 binding protein 1
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000371837, ENST00000487618, 
ENST00000336233, ENST00000456827, 
ENST00000453848, ENST00000005286, 
ENST00000543732, 
Fusion gene scores* DoF score9 X 10 X 3=2703 X 3 X 2=18
# samples 103
** MAII scorelog2(10/270*10)=-1.43295940727611
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: LIPA [Title/Abstract] AND TMEM132A [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointLIPA(91005433)-TMEM132A(60694676), # samples:3
Anticipated loss of major functional domain due to fusion event.LIPA-TMEM132A 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

check buttonFusion gene breakpoints across LIPA (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 TMEM132A (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
ChimerDB4BLCATCGA-FD-A62N-01ALIPAchr10

91005433

-TMEM132Achr11

60694676

+
ChimerDB4BLCATCGA-FD-A62N-01ALIPAchr10

91005433

-TMEM132Achr11

60694676

+
ChimerDB4BLCATCGA-FD-A62N-01ALIPAchr10

91005433

-TMEM132Achr11

60694676

+


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Fusion Gene ORF analysis for LIPA-TMEM132A

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-3CDSENST00000371837ENST00000453848LIPAchr10

91005433

-TMEM132Achr11

60694676

+
intron-3CDSENST00000371837ENST00000005286LIPAchr10

91005433

-TMEM132Achr11

60694676

+
intron-intronENST00000371837ENST00000543732LIPAchr10

91005433

-TMEM132Achr11

60694676

+
intron-3CDSENST00000487618ENST00000453848LIPAchr10

91005433

-TMEM132Achr11

60694676

+
intron-3CDSENST00000487618ENST00000005286LIPAchr10

91005433

-TMEM132Achr11

60694676

+
intron-intronENST00000487618ENST00000543732LIPAchr10

91005433

-TMEM132Achr11

60694676

+
Frame-shiftENST00000336233ENST00000453848LIPAchr10

91005433

-TMEM132Achr11

60694676

+
Frame-shiftENST00000336233ENST00000005286LIPAchr10

91005433

-TMEM132Achr11

60694676

+
5CDS-intronENST00000336233ENST00000543732LIPAchr10

91005433

-TMEM132Achr11

60694676

+
Frame-shiftENST00000456827ENST00000453848LIPAchr10

91005433

-TMEM132Achr11

60694676

+
Frame-shiftENST00000456827ENST00000005286LIPAchr10

91005433

-TMEM132Achr11

60694676

+
5CDS-intronENST00000456827ENST00000543732LIPAchr10

91005433

-TMEM132Achr11

60694676

+

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 LIPA-TMEM132A


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)
LIPAchr1091005432-TMEM132Achr1160694675+0.0004721660.9995278
LIPAchr1091005432-TMEM132Achr1160694675+0.0004721660.9995278

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 LIPA-TMEM132A


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 LIPA-TMEM132A


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 LIPA-TMEM132A


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 LIPA-TMEM132A


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 LIPA-TMEM132A


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneLIPAC0043208Wolman Disease6GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneLIPAC0008384Cholesterol Ester Storage Disease3CTD_human;GENOMICS_ENGLAND;ORPHANET
HgeneLIPAC2936797Acid cholesteryl ester hydrolase deficiency, type 22CTD_human;GENOMICS_ENGLAND
HgeneLIPAC0008370Cholestasis1GENOMICS_ENGLAND
HgeneLIPAC0010054Coronary Arteriosclerosis1CTD_human
HgeneLIPAC0020305Hydrops Fetalis1GENOMICS_ENGLAND
HgeneLIPAC0220756Niemann-Pick Disease, Type C1CTD_human
HgeneLIPAC0268247Niemann-Pick Disease, Type D1CTD_human
HgeneLIPAC1956346Coronary Artery Disease1CTD_human
HgeneLIPAC3179455Niemann-Pick Disease, Type C11CTD_human