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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:ALDH18A1-PDLIM1 (FusionGDB2 ID:3942)

Fusion Gene Summary for ALDH18A1-PDLIM1

check button Fusion gene summary
Fusion gene informationFusion gene name: ALDH18A1-PDLIM1
Fusion gene ID: 3942
HgeneTgene
Gene symbol

ALDH18A1

PDLIM1

Gene ID

5832

9124

Gene namealdehyde dehydrogenase 18 family member A1PDZ and LIM domain 1
SynonymsADCL3|ARCL3A|GSAS|P5CS|PYCS|SPG9|SPG9A|SPG9BCLIM1|CLP-36|CLP36|HEL-S-112|hCLIM1
Cytomap

10q24.1

10q23.33

Type of geneprotein-codingprotein-coding
Descriptiondelta-1-pyrroline-5-carboxylate synthaseSpastic paraplegia-9 (spastic paraparesis with amyotrophy, cataracts and gastroesophageal reflux)aldehyde dehydrogenase family 18 member A1delta-1-pyrroline-5-carboxylate synthetasedelta1-pyrroline-5-carboxlate PDZ and LIM domain protein 1LIM domain protein CLP-36carboxyl terminal LIM domain protein 1elfinepididymis secretory protein Li 112
Modification date2020031320200327
UniProtAcc

P54886

.
Ensembl transtripts involved in fusion geneENST00000371224, ENST00000371221, 
ENST00000483788, 
ENST00000329399, 
ENST00000477757, 
Fusion gene scores* DoF score10 X 10 X 3=30010 X 5 X 6=300
# samples 1111
** MAII scorelog2(11/300*10)=-1.44745897697122
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/300*10)=-1.44745897697122
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ALDH18A1 [Title/Abstract] AND PDLIM1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointALDH18A1(97416354)-PDLIM1(97031541), # samples:2
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 ALDH18A1 (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 PDLIM1 (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
ChimerDB4LUSCTCGA-66-2781-01AALDH18A1chr10

97416354

-PDLIM1chr10

97031541

-
ChimerDB4LUSCTCGA-66-2781ALDH18A1chr10

97416353

-PDLIM1chr10

97031541

-
ChimerDB4LUSCTCGA-66-2781ALDH18A1chr10

97416354

-PDLIM1chr10

97031541

-


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Fusion Gene ORF analysis for ALDH18A1-PDLIM1

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
5UTR-3CDSENST00000371224ENST00000329399ALDH18A1chr10

97416354

-PDLIM1chr10

97031541

-
5UTR-intronENST00000371224ENST00000477757ALDH18A1chr10

97416354

-PDLIM1chr10

97031541

-
5UTR-3CDSENST00000371221ENST00000329399ALDH18A1chr10

97416354

-PDLIM1chr10

97031541

-
5UTR-intronENST00000371221ENST00000477757ALDH18A1chr10

97416354

-PDLIM1chr10

97031541

-
intron-3CDSENST00000483788ENST00000329399ALDH18A1chr10

97416354

-PDLIM1chr10

97031541

-
intron-intronENST00000483788ENST00000477757ALDH18A1chr10

97416354

-PDLIM1chr10

97031541

-
5UTR-3CDSENST00000371224ENST00000329399ALDH18A1chr10

97416353

-PDLIM1chr10

97031541

-
5UTR-intronENST00000371224ENST00000477757ALDH18A1chr10

97416353

-PDLIM1chr10

97031541

-
5UTR-3CDSENST00000371221ENST00000329399ALDH18A1chr10

97416353

-PDLIM1chr10

97031541

-
5UTR-intronENST00000371221ENST00000477757ALDH18A1chr10

97416353

-PDLIM1chr10

97031541

-
intron-3CDSENST00000483788ENST00000329399ALDH18A1chr10

97416353

-PDLIM1chr10

97031541

-
intron-intronENST00000483788ENST00000477757ALDH18A1chr10

97416353

-PDLIM1chr10

97031541

-

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 ALDH18A1-PDLIM1


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 ALDH18A1-PDLIM1


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
ALDH18A1

P54886

.
FUNCTION: Bifunctional enzyme that converts glutamate to glutamate 5-semialdehyde, an intermediate in the biosynthesis of proline, ornithine and arginine. {ECO:0000269|PubMed:10037775, ECO:0000269|PubMed:11092761, ECO:0000269|PubMed:26297558, ECO:0000269|PubMed:26320891}.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 ALDH18A1-PDLIM1


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 ALDH18A1-PDLIM1


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 ALDH18A1-PDLIM1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneALDH18A1P54886DB00142Glutamic acidSmall moleculeApproved|Nutraceutical
HgeneALDH18A1P54886DB00142Glutamic acidSmall moleculeApproved|Nutraceutical
HgeneALDH18A1P54886DB00142Glutamic acidSmall moleculeApproved|Nutraceutical
HgeneALDH18A1P54886DB00142Glutamic acidSmall moleculeApproved|Nutraceutical

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Related Diseases for ALDH18A1-PDLIM1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneALDH18A1C0268354De Barsy syndrome11CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneALDH18A1C4225268CUTIS LAXA, AUTOSOMAL DOMINANT 36GENOMICS_ENGLAND;UNIPROT
HgeneALDH18A1C1832669SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder)4CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneALDH18A1C4225272SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE3CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneALDH18A1C0152013Adenocarcinoma of lung (disorder)1CTD_human
HgeneALDH18A1C0268350Cutis Laxa, Autosomal Dominant1CTD_human;ORPHANET